ClinVar Miner

List of variants in gene HOXB13 reported as likely benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 167
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HGVS dbSNP gnomAD frequency
NM_006361.6(HOXB13):c.735G>A (p.Lys245=) rs138675188 0.00147
NM_006361.6(HOXB13):c.411C>T (p.Tyr137=) rs377339084 0.00022
NM_006361.6(HOXB13):c.567C>T (p.Asn189=) rs143945091 0.00022
NM_006361.6(HOXB13):c.6G>A (p.Glu2=) rs371544984 0.00015
NM_006361.6(HOXB13):c.634G>A (p.Ala212Thr) rs145059285 0.00014
NM_006361.6(HOXB13):c.474G>A (p.Pro158=) rs35033273 0.00013
NM_006361.6(HOXB13):c.849C>T (p.Thr283=) rs374736844 0.00009
NM_006361.6(HOXB13):c.303C>G (p.Ala101=) rs150413396 0.00008
NM_006361.6(HOXB13):c.177G>A (p.Pro59=) rs779780541 0.00004
NM_006361.6(HOXB13):c.606C>T (p.Ser202=) rs370633734 0.00004
NM_006361.6(HOXB13):c.210C>T (p.Pro70=) rs768670673 0.00003
NM_006361.6(HOXB13):c.105C>T (p.Ser35=) rs1175466694 0.00002
NM_006361.6(HOXB13):c.271C>A (p.Arg91=) rs749195398 0.00002
NM_006361.6(HOXB13):c.454C>T (p.Leu152=) rs140373548 0.00002
NM_006361.6(HOXB13):c.804G>T (p.Arg268=) rs779692736 0.00002
NM_006361.6(HOXB13):c.150C>G (p.Pro50=) rs1321649246 0.00001
NM_006361.6(HOXB13):c.183G>A (p.Lys61=) rs541519790 0.00001
NM_006361.6(HOXB13):c.216G>A (p.Gly72=) rs769145488 0.00001
NM_006361.6(HOXB13):c.246C>T (p.Tyr82=) rs1597934677 0.00001
NM_006361.6(HOXB13):c.258G>C (p.Gly86=) rs754872559 0.00001
NM_006361.6(HOXB13):c.285C>T (p.Ser95=) rs750529308 0.00001
NM_006361.6(HOXB13):c.315C>A (p.Thr105=) rs2038235885 0.00001
NM_006361.6(HOXB13):c.33A>T (p.Gly11=) rs773581479 0.00001
NM_006361.6(HOXB13):c.360C>T (p.Tyr120=) rs777265653 0.00001
NM_006361.6(HOXB13):c.387C>T (p.Phe129=) rs1230906460 0.00001
NM_006361.6(HOXB13):c.393G>A (p.Pro131=) rs1480179424 0.00001
NM_006361.6(HOXB13):c.39G>A (p.Lys13=) rs1555558715 0.00001
NM_006361.6(HOXB13):c.408C>T (p.Thr136=) rs781228991 0.00001
NM_006361.6(HOXB13):c.417T>C (p.Pro139=) rs758708152 0.00001
NM_006361.6(HOXB13):c.468A>G (p.Gly156=) rs902238751 0.00001
NM_006361.6(HOXB13):c.489G>C (p.Leu163=) rs199561305 0.00001
NM_006361.6(HOXB13):c.492G>A (p.Leu164=) rs762580646 0.00001
NM_006361.6(HOXB13):c.507C>T (p.Tyr169=) rs373766741 0.00001
NM_006361.6(HOXB13):c.57G>A (p.Leu19=) rs1027470378 0.00001
NM_006361.6(HOXB13):c.633C>T (p.Cys211=) rs760440566 0.00001
NM_006361.6(HOXB13):c.666G>A (p.Pro222=) rs1230526859 0.00001
NM_006361.6(HOXB13):c.705T>C (p.Tyr235=) rs923773143 0.00001
NM_006361.6(HOXB13):c.738G>A (p.Arg246=) rs1242916911 0.00001
NM_006361.6(HOXB13):c.73C>A (p.Arg25=) rs1597935204 0.00001
NM_006361.6(HOXB13):c.783C>A (p.Thr261=) rs1249659597 0.00001
NM_006361.6(HOXB13):c.802C>A (p.Arg268=) rs768168209 0.00001
NM_006361.6(HOXB13):c.825C>T (p.Leu275=) rs750156094 0.00001
NM_006361.6(HOXB13):c.87C>T (p.Ala29=) rs1343907541 0.00001
NM_006361.6(HOXB13):c.93C>T (p.Ser31=) rs1290541379 0.00001
NM_006361.6(HOXB13):c.96T>A (p.Pro32=) rs752661579 0.00001
NM_006361.6(HOXB13):c.99G>C (p.Leu33=) rs570672959 0.00001
NM_006361.6(HOXB13):c.102C>T (p.Thr34=)
NM_006361.6(HOXB13):c.114G>A (p.Ala38=) rs1597935079
NM_006361.6(HOXB13):c.114G>C (p.Ala38=) rs1597935079
NM_006361.6(HOXB13):c.117G>A (p.Ala39=)
NM_006361.6(HOXB13):c.117G>T (p.Ala39=) rs1597935062
NM_006361.6(HOXB13):c.123G>A (p.Thr41=) rs1597935055
NM_006361.6(HOXB13):c.123G>T (p.Thr41=)
NM_006361.6(HOXB13):c.126G>C (p.Leu42=)
NM_006361.6(HOXB13):c.12C>A (p.Gly4=) rs1597935395
NM_006361.6(HOXB13):c.138C>G (p.Val46=) rs1597935033
NM_006361.6(HOXB13):c.138C>T (p.Val46=) rs1597935033
NM_006361.6(HOXB13):c.147C>A (p.Ala49=)
NM_006361.6(HOXB13):c.159G>T (p.Leu53=) rs1265294177
NM_006361.6(HOXB13):c.165C>T (p.Gly55=) rs1597934949
NM_006361.6(HOXB13):c.177G>T (p.Pro59=) rs779780541
NM_006361.6(HOXB13):c.189C>T (p.Cys63=) rs1597934839
NM_006361.6(HOXB13):c.18T>C (p.Tyr6=)
NM_006361.6(HOXB13):c.195A>C (p.Pro65=) rs1597934828
NM_006361.6(HOXB13):c.195A>T (p.Pro65=)
NM_006361.6(HOXB13):c.207G>A (p.Val69=)
NM_006361.6(HOXB13):c.219G>C (p.Thr73=)
NM_006361.6(HOXB13):c.231C>T (p.Pro77=) rs770545259
NM_006361.6(HOXB13):c.243T>C (p.Gly81=)
NM_006361.6(HOXB13):c.24C>T (p.Thr8=) rs748740551
NM_006361.6(HOXB13):c.261C>T (p.Tyr87=) rs1197613952
NM_006361.6(HOXB13):c.282G>A (p.Arg94=) rs2143073149
NM_006361.6(HOXB13):c.288G>T (p.Ser96=) rs767708021
NM_006361.6(HOXB13):c.303C>T (p.Ala101=)
NM_006361.6(HOXB13):c.315C>T (p.Thr105=) rs2038235885
NM_006361.6(HOXB13):c.318G>A (p.Leu106=)
NM_006361.6(HOXB13):c.321C>A (p.Ala107=) rs1555558636
NM_006361.6(HOXB13):c.321C>T (p.Ala107=)
NM_006361.6(HOXB13):c.324G>A (p.Ala108=) rs768311961
NM_006361.6(HOXB13):c.324G>T (p.Ala108=)
NM_006361.6(HOXB13):c.327C>T (p.Tyr109=) rs749101324
NM_006361.6(HOXB13):c.330C>T (p.Pro110=) rs33993186
NM_006361.6(HOXB13):c.333G>A (p.Ala111=)
NM_006361.6(HOXB13):c.336G>A (p.Glu112=) rs1597934464
NM_006361.6(HOXB13):c.339T>A (p.Thr113=)
NM_006361.6(HOXB13):c.342C>T (p.Pro114=) rs1344504139
NM_006361.6(HOXB13):c.345G>T (p.Thr115=) rs758798025
NM_006361.6(HOXB13):c.348C>G (p.Ala116=) rs753116559
NM_006361.6(HOXB13):c.348C>T (p.Ala116=) rs753116559
NM_006361.6(HOXB13):c.351G>C (p.Gly117=) rs1597934408
NM_006361.6(HOXB13):c.354A>G (p.Glu118=)
NM_006361.6(HOXB13):c.357G>A (p.Glu119=) rs1597934370
NM_006361.6(HOXB13):c.363C>G (p.Pro121=) rs1597934347
NM_006361.6(HOXB13):c.372C>T (p.Pro124=)
NM_006361.6(HOXB13):c.384C>T (p.Ala128=) rs1445231138
NM_006361.6(HOXB13):c.408C>A (p.Thr136=)
NM_006361.6(HOXB13):c.408C>G (p.Thr136=)
NM_006361.6(HOXB13):c.430C>T (p.Leu144=) rs1471084758
NM_006361.6(HOXB13):c.435C>T (p.Asp145=)
NM_006361.6(HOXB13):c.441T>C (p.Ser147=)
NM_006361.6(HOXB13):c.447G>T (p.Val149=) rs1597934186
NM_006361.6(HOXB13):c.456G>A (p.Leu152=) rs755437330
NM_006361.6(HOXB13):c.456G>C (p.Leu152=) rs755437330
NM_006361.6(HOXB13):c.459T>G (p.Gly153=) rs1597934161
NM_006361.6(HOXB13):c.465T>C (p.Pro155=)
NM_006361.6(HOXB13):c.474G>C (p.Pro158=) rs35033273
NM_006361.6(HOXB13):c.483C>T (p.Asp161=)
NM_006361.6(HOXB13):c.486C>G (p.Ser162=) rs2143071654
NM_006361.6(HOXB13):c.487C>T (p.Leu163=)
NM_006361.6(HOXB13):c.489G>A (p.Leu163=) rs199561305
NM_006361.6(HOXB13):c.490T>C (p.Leu164=) rs555788633
NM_006361.6(HOXB13):c.510G>A (p.Gln170=)
NM_006361.6(HOXB13):c.522C>G (p.Leu174=) rs1408338112
NM_006361.6(HOXB13):c.522C>T (p.Leu174=) rs1408338112
NM_006361.6(HOXB13):c.528T>G (p.Gly176=) rs1597933899
NM_006361.6(HOXB13):c.52T>C (p.Leu18=)
NM_006361.6(HOXB13):c.552C>T (p.Cys184=) rs1597933837
NM_006361.6(HOXB13):c.573A>G (p.Pro191=) rs1597933773
NM_006361.6(HOXB13):c.60A>G (p.Gly20=) rs1597935240
NM_006361.6(HOXB13):c.618C>T (p.His206=)
NM_006361.6(HOXB13):c.627C>T (p.Asp209=) rs1175181412
NM_006361.6(HOXB13):c.636C>T (p.Ala212=) rs1597932953
NM_006361.6(HOXB13):c.639T>C (p.Phe213=) rs1597932949
NM_006361.6(HOXB13):c.63G>A (p.Ala21=) rs368505949
NM_006361.6(HOXB13):c.63G>C (p.Ala21=) rs368505949
NM_006361.6(HOXB13):c.642T>A (p.Arg214=)
NM_006361.6(HOXB13):c.645C>A (p.Arg215=)
NM_006361.6(HOXB13):c.645C>G (p.Arg215=) rs931880786
NM_006361.6(HOXB13):c.645C>T (p.Arg215=) rs931880786
NM_006361.6(HOXB13):c.666G>C (p.Pro222=) rs1230526859
NM_006361.6(HOXB13):c.666G>T (p.Pro222=) rs1230526859
NM_006361.6(HOXB13):c.669C>T (p.Tyr223=)
NM_006361.6(HOXB13):c.672C>T (p.Ser224=)
NM_006361.6(HOXB13):c.678G>A (p.Gly226=) rs200362093
NM_006361.6(HOXB13):c.682T>C (p.Leu228=) rs1555558471
NM_006361.6(HOXB13):c.693G>A (p.Leu231=)
NM_006361.6(HOXB13):c.696G>A (p.Glu232=) rs1597932804
NM_006361.6(HOXB13):c.697C>A (p.Arg233=) rs778481913
NM_006361.6(HOXB13):c.702G>A (p.Glu234=)
NM_006361.6(HOXB13):c.706G>T (p.Ala236Ser)
NM_006361.6(HOXB13):c.708G>A (p.Ala236=) rs555201890
NM_006361.6(HOXB13):c.711T>C (p.Ala237=) rs1555558465
NM_006361.6(HOXB13):c.717G>A (p.Lys239=) rs1597932762
NM_006361.6(HOXB13):c.720C>T (p.Phe240=) rs1597932759
NM_006361.6(HOXB13):c.747C>T (p.Ile249=) rs761824576
NM_006361.6(HOXB13):c.750G>A (p.Ser250=) rs764201750
NM_006361.6(HOXB13):c.750G>C (p.Ser250=) rs764201750
NM_006361.6(HOXB13):c.759C>T (p.Thr253=)
NM_006361.6(HOXB13):c.75G>A (p.Arg25=) rs1053531133
NM_006361.6(HOXB13):c.765C>T (p.Leu255=) rs1597932610
NM_006361.6(HOXB13):c.768G>A (p.Ser256=) rs917899187
NM_006361.6(HOXB13):c.786C>A (p.Ile262=) rs2038215864
NM_006361.6(HOXB13):c.798C>T (p.Asn266=) rs990843946
NM_006361.6(HOXB13):c.801C>T (p.Arg267=) rs1358131965
NM_006361.6(HOXB13):c.807C>T (p.Val269=) rs1289659465
NM_006361.6(HOXB13):c.810A>G (p.Lys270=) rs2143065422
NM_006361.6(HOXB13):c.816G>A (p.Lys272=) rs1597932452
NM_006361.6(HOXB13):c.81G>A (p.Leu27=)
NM_006361.6(HOXB13):c.81G>T (p.Leu27=) rs1319038051
NM_006361.6(HOXB13):c.831G>A (p.Lys277=)
NM_006361.6(HOXB13):c.843C>T (p.Ser281=) rs763047500
NM_006361.6(HOXB13):c.849C>A (p.Thr283=)
NM_006361.6(HOXB13):c.84C>A (p.Val28=) rs2038241798
NM_006361.6(HOXB13):c.84C>T (p.Val28=) rs2038241798
NM_006361.6(HOXB13):c.96T>C (p.Pro32=)
NM_006361.6(HOXB13):c.9C>G (p.Pro3=) rs1597935416
NM_006361.6(HOXB13):c.9C>T (p.Pro3=)

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