Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.70831747A=CA1259751238CD207c.790T= (p.Trp264=)
2g.70831747A>CCA347179454CD207c.790T>G (p.Trp264Gly)
2g.70831747A>GCA117413CD207c.790T>C (p.Trp264Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.70831747A>TCA347179455CD207c.790T>A (p.Trp264Arg)
2g.70831748G>ACA426673156CD207c.789C>T (p.Asp263=)
dbSNP gnomAD v4
2g.70831748G>CCA347179456CD207c.789C>G (p.Asp263Glu)
2g.70831748G=CA1259751239CD207c.789C= (p.Asp263=)
2g.70831748G>TCA347179457CD207c.789C>A (p.Asp263Glu)
2g.70831749T>ACA347179458CD207c.788A>T (p.Asp263Val)
2g.70831749T>CCA347179459CD207c.788A>G (p.Asp263Gly)
2g.70831749T>GCA347179460CD207c.788A>C (p.Asp263Ala)
2g.70831750C>ACA347179464CD207c.787G>T (p.Asp263Tyr)
2g.70831750C>GCA347179463CD207c.787G>C (p.Asp263His)
2g.70831750C>TCA347179461CD207c.787G>A (p.Asp263Asn)
2g.70831751C>ACA426673157CD207c.786G>T (p.Gly262=)
dbSNP gnomAD v2 gnomAD v4
2g.70831751C=CA1259751240CD207c.786G= (p.Gly262=)
2g.70831751C>GCA426673158CD207c.786G>C (p.Gly262=)
2g.70831751C>TCA426673159CD207c.786G>A (p.Gly262=)
gnomAD v4 COSMIC
2g.70831752C>ACA347179465CD207c.785G>T (p.Gly262Val)
2g.70831752C>GCA347179466CD207c.785G>C (p.Gly262Ala)
gnomAD v4
2g.70831752C>TCA347179467CD207c.785G>A (p.Gly262Glu)
gnomAD v4
2g.70831753C>ACA347179468CD207c.784G>T (p.Gly262Trp)
2g.70831753C=CA1259751241CD207c.784G= (p.Gly262=)
2g.70831753C>GCA347179469CD207c.784G>C (p.Gly262Arg)
2g.70831753C>TCA1700298CD207c.784G>A (p.Gly262Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.70831754T>ACA347179470CD207c.783A>T (p.Glu261Asp)
2g.70831754T>CCA426673160CD207c.783A>G (p.Glu261=)
gnomAD v4
2g.70831754T>GCA347179471CD207c.783A>C (p.Glu261Asp)
2g.70831755T>ACA347179472CD207c.782A>T (p.Glu261Val)
2g.70831755T>CCA347179473CD207c.782A>G (p.Glu261Gly)
2g.70831755T>GCA347179474CD207c.782A>C (p.Glu261Ala)
2g.70831756C>ACA347179476CD207c.781G>T (p.Glu261Ter)
2g.70831756C=CA1259751242CD207c.781G= (p.Glu261=)
2g.70831756C>GCA347179475CD207c.781G>C (p.Glu261Gln)
2g.70831756C>TCA1700299CD207c.781G>A (p.Glu261Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.70831757C>ACA347179477CD207c.780G>T (p.Met260Ile)
2g.70831757C>GCA347179478CD207c.780G>C (p.Met260Ile)
2g.70831757C>TCA347179480CD207c.780G>A (p.Met260Ile)
2g.70831758A=CA1259751243CD207c.779T= (p.Met260=)
2g.70831758A>CCA347179482CD207c.779T>G (p.Met260Arg)
2g.70831758A>GCA347179483CD207c.779T>C (p.Met260Thr)
dbSNP gnomAD v2 gnomAD v4
2g.70831758A>TCA347179484CD207c.779T>A (p.Met260Lys)
2g.70831759T>ACA347179485CD207c.778A>T (p.Met260Leu)
2g.70831759T>CCA347179486CD207c.778A>G (p.Met260Val)
dbSNP
2g.70831759T>GCA347179487CD207c.778A>C (p.Met260Leu)
2g.70831759T=CA1259751244CD207c.778A= (p.Met260=)
2g.70831760C>ACA426673161CD207c.777G>T (p.Gly259=)
2g.70831760C=CA1259751245CD207c.777G= (p.Gly259=)
2g.70831760C>GCA426673163CD207c.777G>C (p.Gly259=)
dbSNP gnomAD v2 gnomAD v4
2g.70831760C>TCA426673162CD207c.777G>A (p.Gly259=)
COSMIC

Number of alleles fetched