Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.112913935T>ACA341826731SLC16A1c.1459A>T (p.Lys487Ter)
1g.112913935T>CCA341826729SLC16A1c.1459A>G (p.Lys487Glu)
1g.112913935T>GCA341826730SLC16A1c.1459A>C (p.Lys487Gln)
1g.112913936C>ACA341826732SLC16A1c.1458G>T (p.Gln486His)
1g.112913936C>GCA341826733SLC16A1c.1458G>C (p.Gln486His)
1g.112913936C>TCA419708015SLC16A1c.1458G>A (p.Gln486=)
1g.112913937T>ACA341826734SLC16A1c.1457A>T (p.Gln486Leu)
1g.112913937T>CCA341826735SLC16A1c.1457A>G (p.Gln486Arg)
gnomAD v4
1g.112913937T>GCA341826736SLC16A1c.1457A>C (p.Gln486Pro)
1g.112913937dupCA1005896138SLC16A1c.1457dup (p.Lys487GlufsTer20)
gnomAD v3 gnomAD v4
1g.112913938G>ACA341826737SLC16A1c.1456C>T (p.Gln486Ter)
gnomAD v4
1g.112913938G>CCA341826738SLC16A1c.1456C>G (p.Gln486Glu)
1g.112913938G>TCA341826739SLC16A1c.1456C>A (p.Gln486Lys)
1g.112913939G>ACA419708016SLC16A1c.1455C>T (p.Asp485=)
1g.112913939G>CCA341826740SLC16A1c.1455C>G (p.Asp485Glu)
1g.112913939G>TCA341826741SLC16A1c.1455C>A (p.Asp485Glu)
1g.112913940T>ACA341826744SLC16A1c.1454A>T (p.Asp485Val)
1g.112913940T>CCA341826743SLC16A1c.1454A>G (p.Asp485Gly)
1g.112913940T>GCA341826742SLC16A1c.1454A>C (p.Asp485Ala)
1g.112913941C>ACA341826745SLC16A1c.1453G>T (p.Asp485Tyr)
ClinVar
1g.112913941C>GCA341826746SLC16A1c.1453G>C (p.Asp485His)
1g.112913941C>TCA341826747SLC16A1c.1453G>A (p.Asp485Asn)
ClinVar gnomAD v4
1g.112913942C>ACA419708017SLC16A1c.1452G>T (p.Pro484=)
1g.112913942C=CA1140474901SLC16A1c.1452G= (p.Pro484=)
1g.112913942C>GCA419708018SLC16A1c.1452G>C (p.Pro484=)
1g.112913942C>TCA1011240SLC16A1c.1452G>A (p.Pro484=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.112913943G>ACA1011241SLC16A1c.1451C>T (p.Pro484Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.112913943G>CCA341826748SLC16A1c.1451C>G (p.Pro484Arg)
1g.112913943G=CA1189548320SLC16A1c.1451C= (p.Pro484=)
1g.112913943G>TCA341826749SLC16A1c.1451C>A (p.Pro484Gln)
1g.112913944G>ACA341826750SLC16A1c.1450C>T (p.Pro484Ser)
gnomAD v4
1g.112913944G>CCA29390615SLC16A1c.1450C>G (p.Pro484Ala)
dbSNP
1g.112913944G=CA1189548321SLC16A1c.1450C= (p.Pro484=)
1g.112913944G>TCA341826751SLC16A1c.1450C>A (p.Pro484Thr)
1g.112913945A=CA1189548322SLC16A1c.1449T= (p.Ser483=)
1g.112913945A>CCA29390616SLC16A1c.1449T>G (p.Ser483=)
dbSNP
1g.112913945A>GCA419708020SLC16A1c.1449T>C (p.Ser483=)
1g.112913945A>TCA419708022SLC16A1c.1449T>A (p.Ser483=)
1g.112913946G>ACA341826752SLC16A1c.1448C>T (p.Ser483Phe)
1g.112913946G>CCA341826753SLC16A1c.1448C>G (p.Ser483Cys)
COSMIC
1g.112913946G>TCA341826754SLC16A1c.1448C>A (p.Ser483Tyr)
1g.112913947A>CCA341826756SLC16A1c.1447T>G (p.Ser483Ala)
1g.112913947A>GCA341826757SLC16A1c.1447T>C (p.Ser483Pro)
1g.112913947A>TCA341826755SLC16A1c.1447T>A (p.Ser483Thr)
ClinVar
1g.112913948T>ACA341826758SLC16A1c.1446A>T (p.Glu482Asp)
1g.112913948T>CCA419708024SLC16A1c.1446A>G (p.Glu482=)
1g.112913948T>GCA341826759SLC16A1c.1446A>C (p.Glu482Asp)
dbSNP gnomAD v4
1g.112913948T=CA1189548323SLC16A1c.1446A= (p.Glu482=)
1g.112913949T>ACA341826760SLC16A1c.1445A>T (p.Glu482Val)
1g.112913949T>CCA341826761SLC16A1c.1445A>G (p.Glu482Gly)

Number of alleles fetched