Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.136676051_136677087delCA277954AGPAT2c.366_588+534del
c.366_492+910del
n.294_516+534del
ClinVar
9g.136676957_136676960delCA16043673AGPAT2c.492+4_492+7del (n.492+4_492+7del)
n.420+4_420+7del
ClinVar dbSNP gnomAD v2 gnomAD v4
9g.136676960C>ACA375581657AGPAT2c.492+1G>T (n.492+1G>T)
n.420+1G>T
gnomAD v4
9g.136676960C>GCA375581661AGPAT2c.492+1G>C (n.492+1G>C)
n.420+1G>C
gnomAD v4
9g.136676960C>TCA16042196AGPAT2c.492+1G>A (n.492+1G>A)
n.420+1G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.136676962_136676978delCA2692654878AGPAT2c.477_492+1del
n.405_420+1del
gnomAD v4
9g.136676961G>ACA201629785AGPAT2c.492C>T (p.Asn164=)
n.420C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.136676961G>CCA201629794AGPAT2c.492C>G (p.Asn164Lys)
n.420C>G
dbSNP gnomAD v4
9g.136676961G>TCA375581678AGPAT2c.492C>A (p.Asn164Lys)
n.420C>A
9g.136676962T>ACA375581682AGPAT2c.491A>T (p.Asn164Ile)
n.419A>T
gnomAD v4
9g.136676962T>CCA375581686AGPAT2c.491A>G (p.Asn164Ser)
n.419A>G
9g.136676962T>GCA375581683AGPAT2c.491A>C (p.Asn164Thr)
n.419A>C
gnomAD v4
9g.136676963T>ACA375581690AGPAT2c.490A>T (p.Asn164Tyr)
n.418A>T
9g.136676963T>CCA375581692AGPAT2c.490A>G (p.Asn164Asp)
n.418A>G
9g.136676963T>GCA375581694AGPAT2c.490A>C (p.Asn164His)
n.418A>C
9g.136676964C>ACA375581699AGPAT2c.489G>T (p.Glu163Asp)
n.417G>T
9g.136676964C>GCA375581700AGPAT2c.489G>C (p.Glu163Asp)
n.417G>C
9g.136676964C>TCA467739418AGPAT2c.489G>A (p.Glu163=)
n.417G>A
9g.136676965T>ACA375581701AGPAT2c.488A>T (p.Glu163Val)
n.416A>T
9g.136676965T>CCA375581702AGPAT2c.488A>G (p.Glu163Gly)
n.416A>G
9g.136676965T>GCA375581705AGPAT2c.488A>C (p.Glu163Ala)
n.416A>C
9g.136676966C>ACA375581709AGPAT2c.487G>T (p.Glu163Ter)
n.415G>T
9g.136676966C>GCA375581719AGPAT2c.487G>C (p.Glu163Gln)
n.415G>C
gnomAD v4
9g.136676966C>TCA201629800AGPAT2c.487G>A (p.Glu163Lys)
n.415G>A
dbSNP gnomAD v3 gnomAD v4
9g.136676968delCA5342989AGPAT2c.487del (p.Glu163ArgfsTer?)
n.415del
dbSNP ExAC gnomAD v2 gnomAD v4
9g.136676967C>ACA375581728AGPAT2c.486G>T (p.Arg162Ser)
n.414G>T
9g.136676967C>GCA375581735AGPAT2c.486G>C (p.Arg162Ser)
n.414G>C
9g.136676967C>TCA467739430AGPAT2c.486G>A (p.Arg162=)
n.414G>A
9g.136676968C>ACA375581738AGPAT2c.485G>T (p.Arg162Met)
n.413G>T
9g.136676968C>GCA5342990AGPAT2c.485G>C (p.Arg162Thr)
n.413G>C
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136676968C>TCA375581739AGPAT2c.485G>A (p.Arg162Lys)
n.413G>A
gnomAD v4
9g.136676969T>ACA375581741AGPAT2c.484A>T (p.Arg162Trp)
n.412A>T
9g.136676969T>CCA375581749AGPAT2c.484A>G (p.Arg162Gly)
n.412A>G
9g.136676969T>GCA467739447AGPAT2c.484A>C (p.Arg162=)
n.412A>C
9g.136676970G>ACA5342991AGPAT2c.483C>T (p.Val161=)
n.411C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.136676970G>CCA467739453AGPAT2c.483C>G (p.Val161=)
n.411C>G
9g.136676970G>TCA467739455AGPAT2c.483C>A (p.Val161=)
n.411C>A
dbSNP gnomAD v2 gnomAD v4
9g.136676971A>CCA375581756AGPAT2c.482T>G (p.Val161Gly)
n.410T>G
dbSNP gnomAD v3 gnomAD v4
9g.136676971A>GCA375581758AGPAT2c.482T>C (p.Val161Ala)
n.410T>C
9g.136676971A>TCA375581760AGPAT2c.482T>A (p.Val161Asp)
n.410T>A
9g.136676972C>ACA375581763AGPAT2c.481G>T (p.Val161Phe)
n.409G>T
9g.136676972C>GCA375581769AGPAT2c.481G>C (p.Val161Leu)
n.409G>C
9g.136676972C>TCA375581774AGPAT2c.481G>A (p.Val161Ile)
n.409G>A
9g.136676973C>ACA375581779AGPAT2c.480G>T (p.Met160Ile)
n.408G>T
9g.136676973C>GCA375581782AGPAT2c.480G>C (p.Met160Ile)
n.408G>C
9g.136676973C>TCA5342992AGPAT2c.480G>A (p.Met160Ile)
n.408G>A
dbSNP ExAC gnomAD v2 gnomAD v4
9g.136676974A>CCA375581800AGPAT2c.479T>G (p.Met160Arg)
n.407T>G
9g.136676974A>GCA375581791AGPAT2c.479T>C (p.Met160Thr)
n.407T>C
dbSNP gnomAD v3 gnomAD v4
9g.136676974A>TCA375581799AGPAT2c.479T>A (p.Met160Lys)
n.407T>A
9g.136676975T>ACA375581801AGPAT2c.478A>T (p.Met160Leu)
n.406A>T

Number of alleles fetched