Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.124500125A= | CA1878468051 | NR5A1 | c.835T= (p.Trp279=) c.187T= (p.Trp63=) c.574T= (p.Trp192=) | |
9 | g.124500125A>C | CA374885235 | NR5A1 | c.835T>G (p.Trp279Gly) c.187T>G (p.Trp63Gly) c.574T>G (p.Trp192Gly) | |
9 | g.124500125A>G | CA374885237 | NR5A1 | c.835T>C (p.Trp279Arg) c.187T>C (p.Trp63Arg) c.574T>C (p.Trp192Arg) | |
9 | g.124500125A>T | CA16618733 | NR5A1 | c.835T>A (p.Trp279Arg) c.187T>A (p.Trp63Arg) c.574T>A (p.Trp192Arg) | ClinVar dbSNP |
9 | g.124500126G>A | CA467207910 | NR5A1 | c.834C>T (p.Asp278=) c.186C>T (p.Asp62=) c.573C>T (p.Asp191=) | |
9 | g.124500126G>C | CA374885243 | NR5A1 | c.834C>G (p.Asp278Glu) c.186C>G (p.Asp62Glu) c.573C>G (p.Asp191Glu) | |
9 | g.124500126G>T | CA374885245 | NR5A1 | c.834C>A (p.Asp278Glu) c.186C>A (p.Asp62Glu) c.573C>A (p.Asp191Glu) | |
9 | g.124500127T>A | CA374885249 | NR5A1 | c.833A>T (p.Asp278Val) c.185A>T (p.Asp62Val) c.572A>T (p.Asp191Val) | |
9 | g.124500127T>C | CA374885251 | NR5A1 | c.833A>G (p.Asp278Gly) c.185A>G (p.Asp62Gly) c.572A>G (p.Asp191Gly) | |
9 | g.124500127T>G | CA374885253 | NR5A1 | c.833A>C (p.Asp278Ala) c.185A>C (p.Asp62Ala) c.572A>C (p.Asp191Ala) | |
9 | g.124500128C>A | CA374885257 | NR5A1 | c.832G>T (p.Asp278Tyr) c.184G>T (p.Asp62Tyr) c.571G>T (p.Asp191Tyr) | |
9 | g.124500128C>G | CA374885260 | NR5A1 | c.832G>C (p.Asp278His) c.184G>C (p.Asp62His) c.571G>C (p.Asp191His) | |
9 | g.124500128C>T | CA374885263 | NR5A1 | c.832G>A (p.Asp278Asn) c.184G>A (p.Asp62Asn) c.571G>A (p.Asp191Asn) | COSMIC COSMIC |
9 | g.124500129C>A | CA467207923 | NR5A1 | c.831G>T (p.Val277=) c.183G>T (p.Val61=) c.570G>T (p.Val190=) | |
9 | g.124500129C>G | CA467207920 | NR5A1 | c.831G>C (p.Val277=) c.183G>C (p.Val61=) c.570G>C (p.Val190=) | |
9 | g.124500129C>T | CA467207917 | NR5A1 | c.831G>A (p.Val277=) c.183G>A (p.Val61=) c.570G>A (p.Val190=) | COSMIC COSMIC |
9 | g.124500130A>C | CA374885269 | NR5A1 | c.830T>G (p.Val277Gly) c.182T>G (p.Val61Gly) c.569T>G (p.Val190Gly) | |
9 | g.124500130A>G | CA374885273 | NR5A1 | c.830T>C (p.Val277Ala) c.182T>C (p.Val61Ala) c.569T>C (p.Val190Ala) | |
9 | g.124500130A>T | CA374885267 | NR5A1 | c.830T>A (p.Val277Glu) c.182T>A (p.Val61Glu) c.569T>A (p.Val190Glu) | |
9 | g.124500131C>A | CA374885276 | NR5A1 | c.829G>T (p.Val277Leu) c.181G>T (p.Val61Leu) c.568G>T (p.Val190Leu) | gnomAD v4 |
9 | g.124500131C>G | CA374885280 | NR5A1 | c.829G>C (p.Val277Leu) c.181G>C (p.Val61Leu) c.568G>C (p.Val190Leu) | |
9 | g.124500131C>T | CA374885283 | NR5A1 | c.829G>A (p.Val277Met) c.181G>A (p.Val61Met) c.568G>A (p.Val190Met) | gnomAD v4 |
9 | g.124500132G>A | CA5235388 | NR5A1 | c.828C>T (p.Ile276=) c.180C>T (p.Ile60=) c.567C>T (p.Ile189=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.124500132G>C | CA374885290 | NR5A1 | c.828C>G (p.Ile276Met) c.180C>G (p.Ile60Met) c.567C>G (p.Ile189Met) | |
9 | g.124500132G= | CA1878468057 | NR5A1 | c.828C= (p.Ile276=) c.180C= (p.Ile60=) c.567C= (p.Ile189=) | |
9 | g.124500132G>T | CA467207927 | NR5A1 | c.828C>A (p.Ile276=) c.180C>A (p.Ile60=) c.567C>A (p.Ile189=) | |
9 | g.124500133A>C | CA374885299 | NR5A1 | c.827T>G (p.Ile276Ser) c.179T>G (p.Ile60Ser) c.566T>G (p.Ile189Ser) | |
9 | g.124500133A>G | CA374885295 | NR5A1 | c.827T>C (p.Ile276Thr) c.179T>C (p.Ile60Thr) c.566T>C (p.Ile189Thr) | |
9 | g.124500133A>T | CA374885294 | NR5A1 | c.827T>A (p.Ile276Asn) c.179T>A (p.Ile60Asn) c.566T>A (p.Ile189Asn) | |
9 | g.124500134T>A | CA374885302 | NR5A1 | c.826A>T (p.Ile276Phe) c.178A>T (p.Ile60Phe) c.565A>T (p.Ile189Phe) | |
9 | g.124500134T>C | CA374885305 | NR5A1 | c.826A>G (p.Ile276Val) c.178A>G (p.Ile60Val) c.565A>G (p.Ile189Val) | dbSNP gnomAD v4 |
9 | g.124500134T>G | CA374885308 | NR5A1 | c.826A>C (p.Ile276Leu) c.178A>C (p.Ile60Leu) c.565A>C (p.Ile189Leu) | gnomAD v4 |
9 | g.124500134T= | CA1878468062 | NR5A1 | c.826A= (p.Ile276=) c.178A= (p.Ile60=) c.565A= (p.Ile189=) | |
9 | g.124500135G>A | CA467207934 | NR5A1 | c.825C>T (p.Ser275=) c.177C>T (p.Ser59=) c.564C>T (p.Ser188=) | gnomAD v4 |
9 | g.124500135G>C | CA467207935 | NR5A1 | c.825C>G (p.Ser275=) c.177C>G (p.Ser59=) c.564C>G (p.Ser188=) | |
9 | g.124500135G>T | CA467207937 | NR5A1 | c.825C>A (p.Ser275=) c.177C>A (p.Ser59=) c.564C>A (p.Ser188=) | |
9 | g.124500136G>A | CA374885313 | NR5A1 | c.824C>T (p.Ser275Phe) c.176C>T (p.Ser59Phe) c.563C>T (p.Ser188Phe) | dbSNP |
9 | g.124500136G>C | CA374885314 | NR5A1 | c.824C>G (p.Ser275Cys) c.176C>G (p.Ser59Cys) c.563C>G (p.Ser188Cys) | gnomAD v4 |
9 | g.124500136G= | CA1878468065 | NR5A1 | c.824C= (p.Ser275=) c.176C= (p.Ser59=) c.563C= (p.Ser188=) | |
9 | g.124500136G>T | CA374885316 | NR5A1 | c.824C>A (p.Ser275Tyr) c.176C>A (p.Ser59Tyr) c.563C>A (p.Ser188Tyr) | |
9 | g.124500137A>C | CA374885321 | NR5A1 | c.823T>G (p.Ser275Ala) c.175T>G (p.Ser59Ala) c.562T>G (p.Ser188Ala) | |
9 | g.124500137A>G | CA374885327 | NR5A1 | c.823T>C (p.Ser275Pro) c.175T>C (p.Ser59Pro) c.562T>C (p.Ser188Pro) | |
9 | g.124500137A>T | CA374885325 | NR5A1 | c.823T>A (p.Ser275Thr) c.175T>A (p.Ser59Thr) c.562T>A (p.Ser188Thr) | |
9 | g.124500138G>A | CA467207943 | NR5A1 | c.822C>T (p.Ile274=) c.174C>T (p.Ile58=) c.561C>T (p.Ile187=) | |
9 | g.124500138G>C | CA374885330 | NR5A1 | c.822C>G (p.Ile274Met) c.174C>G (p.Ile58Met) c.561C>G (p.Ile187Met) | |
9 | g.124500138G>T | CA467207944 | NR5A1 | c.822C>A (p.Ile274=) c.174C>A (p.Ile58=) c.561C>A (p.Ile187=) | |
9 | g.124500139A= | CA1878468069 | NR5A1 | c.821T= (p.Ile274=) c.173T= (p.Ile58=) c.560T= (p.Ile187=) | |
9 | g.124500139A>C | CA374885334 | NR5A1 | c.821T>G (p.Ile274Ser) c.173T>G (p.Ile58Ser) c.560T>G (p.Ile187Ser) | |
9 | g.124500139A>G | CA199728548 | NR5A1 | c.821T>C (p.Ile274Thr) c.173T>C (p.Ile58Thr) c.560T>C (p.Ile187Thr) | dbSNP gnomAD v4 |
9 | g.124500139A>T | CA374885338 | NR5A1 | c.821T>A (p.Ile274Asn) c.173T>A (p.Ile58Asn) c.560T>A (p.Ile187Asn) |