ClinVar Miner

List of variants in gene SPINT2 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 90
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HGVS dbSNP gnomAD frequency
NM_021102.4(SPINT2):c.592+3A>G rs111990687 0.00365
NM_021102.4(SPINT2):c.698G>A (p.Arg233His) rs115746965 0.00290
NM_021102.4(SPINT2):c.331C>T (p.Pro111Ser) rs141683432 0.00190
NM_021102.4(SPINT2):c.715G>A (p.Gly239Arg) rs143567268 0.00097
NM_021102.4(SPINT2):c.554-16G>A rs369303695 0.00038
NM_021102.4(SPINT2):c.391+13A>G rs371302405 0.00019
NM_021102.4(SPINT2):c.129G>A (p.Val43=) rs777327266 0.00007
NM_021102.4(SPINT2):c.337+20C>T rs759143848 0.00007
NM_021102.4(SPINT2):c.546C>T (p.Arg182=) rs201542510 0.00006
NM_021102.4(SPINT2):c.554-7C>T rs373006737 0.00006
NM_021102.4(SPINT2):c.593-9C>T rs538522427 0.00006
NM_021102.4(SPINT2):c.663C>A (p.Ile221=) rs377497678 0.00006
NM_021102.4(SPINT2):c.392-15C>T rs376086427 0.00004
NM_021102.4(SPINT2):c.592+20C>T rs572380002 0.00004
NM_021102.4(SPINT2):c.702C>T (p.Thr234=) rs774389164 0.00003
NM_021102.4(SPINT2):c.107-10C>T rs200870624 0.00002
NM_021102.4(SPINT2):c.553+11A>G rs368915701 0.00002
NM_021102.4(SPINT2):c.141C>T (p.Cys47=) rs190085217 0.00001
NM_021102.4(SPINT2):c.168C>T (p.Tyr56=) rs767551161 0.00001
NM_021102.4(SPINT2):c.171T>C (p.Asn57=) rs755846896 0.00001
NM_021102.4(SPINT2):c.216C>T (p.Asp72=) rs756781647 0.00001
NM_021102.4(SPINT2):c.277+18G>A rs765086874 0.00001
NM_021102.4(SPINT2):c.393A>G (p.Glu131=) rs759003195 0.00001
NM_021102.4(SPINT2):c.474C>T (p.Cys158=) rs1255750053 0.00001
NM_021102.4(SPINT2):c.593-15C>G rs1968722610 0.00001
NM_021102.4(SPINT2):c.106+10G>C
NM_021102.4(SPINT2):c.106+20del
NM_021102.4(SPINT2):c.107-19G>A
NM_021102.4(SPINT2):c.120G>A (p.Val40=) rs2146274899
NM_021102.4(SPINT2):c.123G>C (p.Ser41=)
NM_021102.4(SPINT2):c.144G>T (p.Arg48=)
NM_021102.4(SPINT2):c.177T>C (p.Thr59=)
NM_021102.4(SPINT2):c.180C>T (p.Asp60=)
NM_021102.4(SPINT2):c.186C>A (p.Ser62=)
NM_021102.4(SPINT2):c.222C>T (p.Asn74=)
NM_021102.4(SPINT2):c.235C>T (p.Leu79=)
NM_021102.4(SPINT2):c.240C>G (p.Thr80=) rs112235785
NM_021102.4(SPINT2):c.277+10C>T
NM_021102.4(SPINT2):c.277+18_277+29del
NM_021102.4(SPINT2):c.278-16C>G
NM_021102.4(SPINT2):c.278-20G>A rs924108835
NM_021102.4(SPINT2):c.278-8C>T
NM_021102.4(SPINT2):c.288G>A (p.Thr96=)
NM_021102.4(SPINT2):c.288G>T (p.Thr96=)
NM_021102.4(SPINT2):c.330C>G (p.Val110=)
NM_021102.4(SPINT2):c.338-14T>C
NM_021102.4(SPINT2):c.338-17A>G
NM_021102.4(SPINT2):c.387T>C (p.Tyr129=) rs2146278816
NM_021102.4(SPINT2):c.391+10C>T
NM_021102.4(SPINT2):c.391+16G>A
NM_021102.4(SPINT2):c.391+17G>A
NM_021102.4(SPINT2):c.391+17G>T
NM_021102.4(SPINT2):c.392-4C>T
NM_021102.4(SPINT2):c.396C>T (p.Tyr132=)
NM_021102.4(SPINT2):c.399C>T (p.Cys133=)
NM_021102.4(SPINT2):c.402C>T (p.Thr134=)
NM_021102.4(SPINT2):c.408C>T (p.Asn136=) rs368856630
NM_021102.4(SPINT2):c.417T>G (p.Thr139=)
NM_021102.4(SPINT2):c.453T>C (p.Phe151=)
NM_021102.4(SPINT2):c.456C>T (p.Asp152=) rs373558499
NM_021102.4(SPINT2):c.45C>T (p.Ala15=)
NM_021102.4(SPINT2):c.553+13C>T
NM_021102.4(SPINT2):c.553+15C>T
NM_021102.4(SPINT2):c.553+18C>T
NM_021102.4(SPINT2):c.592+15A>G
NM_021102.4(SPINT2):c.592+17C>T
NM_021102.4(SPINT2):c.592+18C>T
NM_021102.4(SPINT2):c.592+8G>A
NM_021102.4(SPINT2):c.593-11C>G
NM_021102.4(SPINT2):c.593-11C>T
NM_021102.4(SPINT2):c.593-12T>C
NM_021102.4(SPINT2):c.593-13C>G
NM_021102.4(SPINT2):c.593-16C>T
NM_021102.4(SPINT2):c.593-17C>G
NM_021102.4(SPINT2):c.593-18C>G
NM_021102.4(SPINT2):c.593-8G>A
NM_021102.4(SPINT2):c.601C>T (p.Leu201=) rs2146281080
NM_021102.4(SPINT2):c.606G>T (p.Ala202=)
NM_021102.4(SPINT2):c.654C>G (p.Val218=)
NM_021102.4(SPINT2):c.654C>T (p.Val218=)
NM_021102.4(SPINT2):c.693C>A (p.Ala231=)
NM_021102.4(SPINT2):c.696G>T (p.Leu232=)
NM_021102.4(SPINT2):c.699C>A (p.Arg233=)
NM_021102.4(SPINT2):c.705C>A (p.Val235=)
NM_021102.4(SPINT2):c.714C>T (p.Ser238=)
NM_021102.4(SPINT2):c.729G>A (p.Glu243=) rs199831478
NM_021102.4(SPINT2):c.756G>A (p.Leu252=)
NM_021102.4(SPINT2):c.75C>A (p.Val25=)
NM_021102.4(SPINT2):c.81G>T (p.Ala27=)
NM_021102.4(SPINT2):c.88C>A (p.Arg30=)

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