All variants in the SRY gene

Information The variants shown are described using the NM_003140.2 transcript reference sequence.

38 entries on 1 page. Showing entries 1 - 38.
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AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

DB-ID     

dbSNP ID     

gnomAD frequency     

gnomAD homozygote count     
c.-45A>G r.(=) p.(=) g.2655689T>C - - 1/62438 unknown
c.-42C>G r.(=) p.(=) g.2655686G>C - - 1/63347 unknown
c.-9T>A r.(=) p.(=) g.2655653A>T - rs754712640 1/66795 unknown
c.-6T>C r.(=) p.(=) g.2655650A>G - rs754209742 2/66874 unknown
c.-3A>G r.(=) p.(=) g.2655647T>C - rs766867548 2/66947 unknown
c.14C>T r.(?) p.(Ala5Val) g.2655631G>A - - 1/67099 unknown
c.53G>A r.(?) p.(Ser18Asn) g.2655592C>T - rs104894971 3/67281 unknown
c.63G>T r.(?) p.(Val21=) g.2655582C>A - rs751006997 1/67275 unknown
c.71A>T r.(?) p.(Asn24Ile) g.2655574T>A - - 1/67298 unknown
c.85C>T r.(?) p.(Arg29Trp) g.2655560G>A - - 1/67272 unknown
c.100T>C r.(?) p.(Phe34Leu) g.2655545A>G - - 1/67303 unknown
c.148G>A r.(?) p.(Glu50Lys) g.2655497C>T - rs767481926 1/67311 unknown
c.154A>G r.(?) p.(Ser52Gly) g.2655491T>C - - 2/67318 unknown
c.155G>A r.(?) p.(Ser52Asn) g.2655490C>T - - 1/67306 unknown
c.170A>G r.(?) p.(Gln57Arg) g.2655475T>C - rs762003265 1/67274 unknown
c.174T>G r.(?) p.(Asp58Glu) g.2655471A>C - rs773764555 29/67262 unknown
c.200T>A r.(?) p.(Phe67Tyr) g.2655445A>T - - 1/67204 unknown
c.205G>C r.(?) p.(Val69Leu) g.2655440C>G - rs763174397 1/67164 unknown
c.216C>T r.(?) p.(Arg72=) g.2655429G>A - - 1/67107 unknown
c.219T>G r.(?) p.(Asp73Glu) g.2655426A>C - rs776339584 1/67129 unknown
c.251G>C r.(?) p.(Arg84Thr) g.2655394C>G - rs770778716 1/67033 unknown
c.254T>A r.(?) p.(Met85Lys) g.2655391A>T - rs746931713 1/67050 unknown
c.270C>G r.(?) p.(Ile90Met) g.2655375G>C - rs104894959 1/66846 unknown
c.297A>T r.(?) p.(Lys99Asn) g.2655348T>A - - 1/65826 unknown
c.339A>C r.(?) p.(Ala113=) g.2655306T>G - rs773247144 1/63063 unknown
c.364G>A r.(?) p.(Glu122Lys) g.2655281C>T - rs771449441 1/62407 unknown
c.408G>A r.(?) p.(Lys136=) g.2655237C>T - - 1/61506 unknown
c.465C>T r.(?) p.(Ser155=) g.2655180G>A - rs11575897 334/61202 unknown
c.544C>T r.(?) p.(His182Tyr) g.2655101G>A - - 1/66434 unknown
c.552G>A r.(?) p.(Pro184=) g.2655093C>T - - 1/66687 unknown
c.560A>G r.(?) p.(Asn187Ser) g.2655085T>C - rs780561417 1/66935 unknown
c.585G>C r.(?) p.(Arg195=) g.2655060C>G - - 1/67167 unknown
c.589C>T r.(?) p.(Arg197Cys) g.2655056G>A - rs756606002 2/67175 unknown
c.*5A>T r.(=) p.(=) g.2655025T>A - - 1/67250 unknown
c.*16T>C r.(=) p.(=) g.2655014A>G - - 2/67241 unknown
c.*21T>C r.(=) p.(=) g.2655009A>G - - 1/67218 unknown
c.*27G>C r.(=) p.(=) g.2655003C>G - rs750874990 1/67181 unknown
c.*51C>G r.(=) p.(=) g.2654979G>C - rs781744002 2/66651 unknown
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