Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.13562278C>TCA603378190GRIN2Bc.*505G>A (p.=)
gnomAD
12g.13562280G>CCA603378191GRIN2Bc.*503C>G (p.=)
gnomAD
12g.13562282A>TCA603378192GRIN2Bc.*501T>A (p.=)
gnomAD
12g.13562284G>CCA685661385GRIN2Bc.*499C>G (p.=)
12g.13562285A>TCA233131942GRIN2Bc.*498T>A (p.=)
dbSNP
12g.13562295G>ACA944929855GRIN2Bc.*488C>T (p.=)
12g.13562302T>CCA233131945GRIN2Bc.*481A>G (p.=)
dbSNP
12g.13562302_13562303delCA685661390GRIN2Bc.*479_*480del (p.=)
dbSNP
12g.13562303_13562316dupCA685661407GRIN2Bc.*467_*480dup (p.=)
dbSNP
12g.13562310C>GCA685661408GRIN2Bc.*473G>C (p.=)
12g.13562312C>TCA233131948GRIN2Bc.*471G>A (p.=)
dbSNP gnomAD
12g.13562319T>CCA233131959GRIN2Bc.*464A>G (p.=)
dbSNP
12g.13562320G>ACA944929860GRIN2Bc.*463C>T (p.=)
12g.13562321T>CCA233131971GRIN2Bc.*462A>G (p.=)
dbSNP gnomAD
12g.13562328T>CCA685661418GRIN2Bc.*455A>G (p.=)
12g.13562329G>ACA653981735GRIN2Bc.*454C>T (p.=)
COSMIC
12g.13562329G>TCA944929863GRIN2Bc.*454C>A (p.=)
12g.13562334C>TCA233131987GRIN2Bc.*449G>A (p.=)
dbSNP gnomAD
12g.13562336C>TCA233131991GRIN2Bc.*447G>A (p.=)
dbSNP
12g.13562342T>ACA685661424GRIN2Bc.*441A>T (p.=)
12g.13562342T>CCA233132002GRIN2Bc.*441A>G (p.=)
dbSNP gnomAD
12g.13562343G>ACA233132006GRIN2Bc.*440C>T (p.=)
dbSNP
12g.13562350C>TCA233132011GRIN2Bc.*433G>A (p.=)
dbSNP
12g.13562358C>TCA233132014GRIN2Bc.*425G>A (p.=)
dbSNP
12g.13562359C>TCA944929868GRIN2Bc.*424G>A (p.=)
12g.13562362A>GCA233132019GRIN2Bc.*421T>C (p.=)
dbSNP
12g.13562370delCA233132041GRIN2Bc.*413del (p.=)
dbSNP
12g.13562370G>CCA233132046GRIN2Bc.*413C>G (p.=)
dbSNP gnomAD
12g.13562371A>CCA233132054GRIN2Bc.*412T>G (p.=)
dbSNP
12g.13562374A>CCA10641392GRIN2Bc.*409T>G (p.=)
ClinVar dbSNP gnomAD
12g.13562374A>GCA603378194GRIN2Bc.*409T>C (p.=)
gnomAD

Number of alleles fetched