Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.78304841_78304844delCA2690397189PSAT1c.298_301del (p.Asp100MetfsTer3)
gnomAD v4
9g.78304842A=CA1857665729PSAT1c.299A= (p.Asp100=)
9g.78304842A>CCA114739PSAT1c.299A>C (p.Asp100Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
9g.78304842A>GCA373872313PSAT1c.299A>G (p.Asp100Gly)
9g.78304842A>TCA373872314PSAT1c.299A>T (p.Asp100Val)
9g.78304843C>ACA373872316PSAT1c.300C>A (p.Asp100Glu)
9g.78304843C>GCA373872318PSAT1c.300C>G (p.Asp100Glu)
9g.78304843C>TCA465542957PSAT1c.300C>T (p.Asp100=)
9g.78304844T>ACA373872320PSAT1c.301T>A (p.Tyr101Asn)
9g.78304844T>CCA373872321PSAT1c.301T>C (p.Tyr101His)
dbSNP
9g.78304844T>GCA373872323PSAT1c.301T>G (p.Tyr101Asp)
9g.78304844T=CA1857665730PSAT1c.301T= (p.Tyr101=)
9g.78304845A>CCA373872328PSAT1c.302A>C (p.Tyr101Ser)
9g.78304845A>GCA373872326PSAT1c.302A>G (p.Tyr101Cys)
gnomAD v4
9g.78304845A>TCA373872325PSAT1c.302A>T (p.Tyr101Phe)
9g.78304846T>ACA373872330PSAT1c.303T>A (p.Tyr101Ter)
9g.78304846T>CCA465542958PSAT1c.303T>C (p.Tyr101=)
dbSNP
9g.78304846T>GCA373872332PSAT1c.303T>G (p.Tyr101Ter)
9g.78304846T=CA1857665731PSAT1c.303T= (p.Tyr101=)
9g.78304847G>ACA373872334PSAT1c.304G>A (p.Val102Met)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.78304847G>CCA373872335PSAT1c.304G>C (p.Val102Leu)
9g.78304847G=CA1857665732PSAT1c.304G= (p.Val102=)
9g.78304847G>TCA373872337PSAT1c.304G>T (p.Val102Leu)
9g.78304848T>ACA373872339PSAT1c.305T>A (p.Val102Glu)
9g.78304848T>CCA373872340PSAT1c.305T>C (p.Val102Ala)
9g.78304848T>GCA373872343PSAT1c.305T>G (p.Val102Gly)
9g.78304849G>ACA465542960PSAT1c.306G>A (p.Val102=)
9g.78304849G>CCA465542961PSAT1c.306G>C (p.Val102=)
9g.78304849G>TCA465542959PSAT1c.306G>T (p.Val102=)
COSMIC
9g.78304850G>ACA5095577PSAT1c.307G>A (p.Val103Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
9g.78304850G>CCA5095576PSAT1c.307G>C (p.Val103Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.78304850G=CA1857665733PSAT1c.307G= (p.Val103=)
9g.78304850G>TCA373872346PSAT1c.307G>T (p.Val103Leu)
ClinVar dbSNP
9g.78304851T>ACA373872347PSAT1c.308T>A (p.Val103Glu)
9g.78304851T>CCA373872349PSAT1c.308T>C (p.Val103Ala)
9g.78304851T>GCA373872350PSAT1c.308T>G (p.Val103Gly)
9g.78304852G>ACA465542964PSAT1c.309G>A (p.Val103=)
gnomAD v4
9g.78304852G>CCA465542963PSAT1c.309G>C (p.Val103=)
gnomAD v4
9g.78304852G>TCA465542962PSAT1c.309G>T (p.Val103=)
9g.78304853A>CCA373872353PSAT1c.310A>C (p.Thr104Pro)
9g.78304853A>GCA373872354PSAT1c.310A>G (p.Thr104Ala)
9g.78304853A>TCA373872352PSAT1c.310A>T (p.Thr104Ser)
9g.78304854C>ACA373872355PSAT1c.311C>A (p.Thr104Lys)
COSMIC
9g.78304854C=CA1857665734PSAT1c.311C= (p.Thr104=)
9g.78304854C>GCA373872356PSAT1c.311C>G (p.Thr104Arg)
9g.78304854C>TCA194441078PSAT1c.311C>T (p.Thr104Ile)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.78304855A=CA1857665735PSAT1c.312A= (p.Thr104=)
9g.78304855A>CCA465542965PSAT1c.312A>C (p.Thr104=)
9g.78304855A>GCA194441104PSAT1c.312A>G (p.Thr104=)
dbSNP gnomAD v2 gnomAD v4
9g.78304855A>TCA465542966PSAT1c.312A>T (p.Thr104=)
dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched