ClinVar Miner

List of variants in gene NIN studied for not specified

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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_020921.4(NIN):c.933G>C (p.Leu311=) rs8020503 0.99252
NM_020921.4(NIN):c.5628+5T>C rs3015485 0.99236
NM_020921.4(NIN):c.3374A>C (p.Gln1125Pro) rs12882191 0.79682
NM_020921.4(NIN):c.3959G>A (p.Gly1320Glu) rs2073347 0.78250
NM_020921.4(NIN):c.5637G>A (p.Gln1879=) rs11376 0.56301
NM_020921.4(NIN):c.1128T>C (p.Val376=) rs17793018 0.52775
NM_020921.4(NIN):c.2616C>A (p.Ala872=) rs2073349 0.35221
NM_020921.4(NIN):c.3090A>T (p.Ser1030=) rs2073348 0.28854
NM_020921.4(NIN):c.3331C>G (p.Pro1111Ala) rs2236316 0.20068
NM_020921.4(NIN):c.5800C>G (p.Gln1934Glu) rs2295847 0.10087
NM_020921.4(NIN):c.5509T>A (p.Ser1837Thr) rs12717411 0.02104
NM_020921.4(NIN):c.3459G>A (p.Arg1153=) rs41310342 0.01853
NM_020921.4(NIN):c.819C>T (p.Phe273=) rs61755581 0.01567
NM_020921.4(NIN):c.1728G>A (p.Pro576=) rs61755036 0.01477
NM_020921.4(NIN):c.2651A>G (p.Lys884Arg) rs41299191 0.01436
NM_020921.4(NIN):c.4866A>C (p.Glu1622Asp) rs77959782 0.01304
NM_020921.4(NIN):c.600T>C (p.Gly200=) rs61740039 0.00982
NM_020921.4(NIN):c.3454G>T (p.Val1152Phe) rs61742284 0.00858
NM_020921.4(NIN):c.4674G>A (p.Thr1558=) rs45578537 0.00828
NM_020921.4(NIN):c.264A>T (p.Pro88=) rs61755037 0.00815
NM_020921.4(NIN):c.5903C>T (p.Thr1968Met) rs61744312 0.00758
NM_020921.4(NIN):c.5188T>C (p.Leu1730=) rs61741547 0.00749
NM_020921.4(NIN):c.2988G>A (p.Ala996=) rs80291668 0.00645
NM_020921.4(NIN):c.6068A>G (p.Asn2023Ser) rs61747997 0.00620
NM_020921.4(NIN):c.4395T>C (p.Thr1465=) rs74594049 0.00510
NM_020921.4(NIN):c.4837C>T (p.Arg1613Cys) rs61755995 0.00434
NM_020921.4(NIN):c.2676G>A (p.Gln892=) rs78234652 0.00358
NM_020921.4(NIN):c.3197T>A (p.Val1066Asp) rs78280523 0.00316
NM_020921.4(NIN):c.2987C>T (p.Ala996Val) rs41313507 0.00235
NM_020921.4(NIN):c.4288A>T (p.Ile1430Leu) rs41299193 0.00217
NM_020921.4(NIN):c.612G>A (p.Arg204=) rs150057118 0.00118
NM_020921.4(NIN):c.5996G>A (p.Arg1999His) rs141405524 0.00097
NM_020921.4(NIN):c.4937G>A (p.Arg1646His) rs149669464 0.00096
NM_020921.4(NIN):c.3487G>C (p.Val1163Leu) rs139059875 0.00088
NM_020921.4(NIN):c.421G>A (p.Gly141Ser) rs143800977 0.00057
NM_020921.4(NIN):c.3647G>A (p.Arg1216Gln) rs192017781 0.00034
NM_020921.4(NIN):c.2244C>T (p.Ser748=) rs200278498 0.00009
NM_020921.4(NIN):c.3403G>A (p.Val1135Ile) rs150722174 0.00009
NM_020921.4(NIN):c.3749T>C (p.Leu1250Pro) rs896607535 0.00008
NM_020921.4(NIN):c.3954T>C (p.Asn1318=) rs142326581 0.00006
NM_020921.4(NIN):c.4898G>A (p.Arg1633Gln) rs375891968 0.00006
NM_020921.4(NIN):c.471G>A (p.Ala157=) rs200517297 0.00005
NM_020921.4(NIN):c.1063A>G (p.Asn355Asp) rs372422633 0.00004
NM_020921.4(NIN):c.3997G>A (p.Glu1333Lys) rs369577037 0.00003
NM_020921.4(NIN):c.5264C>T (p.Ala1755Val) rs758555048 0.00002
NM_020921.4(NIN):c.2494G>A (p.Ala832Thr) rs370154746 0.00001
NM_020921.4(NIN):c.2654C>G (p.Thr885Arg) rs776499143 0.00001
NM_020921.4(NIN):c.3196G>A (p.Val1066Ile) rs143976273 0.00001
NM_020921.4(NIN):c.4240G>A (p.Gly1414Arg) rs951191260 0.00001
NM_020921.4(NIN):c.1435G>A (p.Glu479Lys) rs2141730313
NM_020921.4(NIN):c.3007C>G (p.Arg1003Gly) rs751569014
NM_020921.4(NIN):c.3026G>A (p.Ser1009Asn) rs866350711
NM_020921.4(NIN):c.3326A>C (p.Asp1109Ala) rs797045742
NM_020921.4(NIN):c.3641G>A (p.Cys1214Tyr) rs797045743
NM_020921.4(NIN):c.447G>A (p.Thr149=) rs547438612
NM_020921.4(NIN):c.4868A>G (p.Lys1623Arg) rs2140718932
NM_020921.4(NIN):c.5302G>T (p.Val1768Phe) rs151233126
NM_020921.4(NIN):c.606G>C (p.Leu202=) rs2141867314

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