Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.43030351C=CA3117757897GRXCR1c.694-10C= (n.694-10C=)
c.331-10C= (n.331-10C=)
 dbSNP
4g.43030351C>GCA2670496242GRXCR1c.694-10C>G (n.694-10C>G)
c.331-10C>G (n.331-10C>G)
 dbSNP gnomAD v4
4g.43030355A=CA3117757932GRXCR1c.694-6A= (n.694-6A=)
c.331-6A= (n.331-6A=)
 dbSNP
4g.43030355A>CCA2670496243GRXCR1c.694-6A>C (n.694-6A>C)
c.331-6A>C (n.331-6A>C)
 dbSNP gnomAD v4
4g.43030356T>ACA551142782GRXCR1c.694-5T>A (n.694-5T>A)
c.331-5T>A (n.331-5T>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.43030356T>CCA2904510GRXCR1c.694-5T>C (n.694-5T>C)
c.331-5T>C (n.331-5T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.43030356T>GCA2980005650GRXCR1c.694-5T>G (n.694-5T>G)
c.331-5T>G (n.331-5T>G)
4g.43030356T=CA1453107613GRXCR1c.694-5T= (n.694-5T=)
c.331-5T= (n.331-5T=)
 dbSNP
4g.43030361_43030369delCA2578077017GRXCR1c.694_702del
c.331_339del
 gnomAD v4
4g.43030357A=CA1453107614GRXCR1c.694-4A= (n.694-4A=)
c.331-4A= (n.331-4A=)
 dbSNP
4g.43030357A>GCA1453107615GRXCR1c.694-4A>G (n.694-4A>G)
c.331-4A>G (n.331-4A>G)
 dbSNP
4g.43030358C=CA1453107616GRXCR1c.694-3C= (n.694-3C=)
c.331-3C= (n.331-3C=)
 dbSNP
4g.43030358C>GCA1453107617GRXCR1c.694-3C>G (n.694-3C>G)
c.331-3C>G (n.331-3C>G)
 dbSNP
4g.43030359A>CCA356791686GRXCR1c.694-2A>C (n.694-2A>C)
c.331-2A>C (n.331-2A>C)
4g.43030359A>GCA356791687GRXCR1c.694-2A>G (n.694-2A>G)
c.331-2A>G (n.331-2A>G)
4g.43030359A>TCA356791688GRXCR1c.694-2A>T (n.694-2A>T)
c.331-2A>T (n.331-2A>T)
4g.43030363_43030364delCA2580616094GRXCR1c.696_697del
c.333_334del
 ClinVar dbSNP
4g.43030360G>ACA356791689GRXCR1c.694-1G>A (n.694-1G>A)
c.331-1G>A (n.331-1G>A)
 COSMIC
4g.43030360G>CCA356791690GRXCR1c.694-1G>C (n.694-1G>C)
c.331-1G>C (n.331-1G>C)
4g.43030360G>TCA356791691GRXCR1c.694-1G>T (n.694-1G>T)
c.331-1G>T (n.331-1G>T)
4g.43030361A=CA1453107618GRXCR1c.694A= (p.Arg232=)
c.331A= (p.Arg111=)
 dbSNP
4g.43030361A>CCA439192085GRXCR1c.694A>C (p.Arg232=)
c.331A>C (p.Arg111=)
 dbSNP
4g.43030361A>GCA356791692GRXCR1c.694A>G (p.Arg232Gly)
c.331A>G (p.Arg111Gly)
 dbSNP gnomAD v4
4g.43030361A>TCA356791693GRXCR1c.694A>T (p.Arg232Ter)
c.331A>T (p.Arg111Ter)
4g.43030362G>ACA356791694GRXCR1c.695G>A (p.Arg232Lys)
c.332G>A (p.Arg111Lys)
4g.43030362G>CCA356791695GRXCR1c.695G>C (p.Arg232Thr)
c.332G>C (p.Arg111Thr)
4g.43030362G>TCA356791696GRXCR1c.695G>T (p.Arg232Ile)
c.332G>T (p.Arg111Ile)
4g.43030363A>CCA356791697GRXCR1c.696A>C (p.Arg232Ser)
c.333A>C (p.Arg111Ser)
4g.43030363A>GCA439192086GRXCR1c.696A>G (p.Arg232=)
c.333A>G (p.Arg111=)
4g.43030363A>TCA356791698GRXCR1c.696A>T (p.Arg232Ser)
c.333A>T (p.Arg111Ser)
4g.43030364G>ACA356791701GRXCR1c.697G>A (p.Val233Ile)
c.334G>A (p.Val112Ile)
 dbSNP gnomAD v2 gnomAD v4
4g.43030364G>CCA356791699GRXCR1c.697G>C (p.Val233Leu)
c.334G>C (p.Val112Leu)
4g.43030364G=CA1453107619GRXCR1c.697G= (p.Val233=)
c.334G= (p.Val112=)
 dbSNP
4g.43030364G>TCA356791700GRXCR1c.697G>T (p.Val233Leu)
c.334G>T (p.Val112Leu)
4g.43030365T>ACA356791702GRXCR1c.698T>A (p.Val233Glu)
c.335T>A (p.Val112Glu)
4g.43030365T>CCA356791703GRXCR1c.698T>C (p.Val233Ala)
c.335T>C (p.Val112Ala)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.43030365T>GCA356791704GRXCR1c.698T>G (p.Val233Gly)
c.335T>G (p.Val112Gly)
4g.43030365T=CA1453107620GRXCR1c.698T= (p.Val233=)
c.335T= (p.Val112=)
 dbSNP
4g.43030366A=CA1453107621GRXCR1c.699A= (p.Val233=)
c.336A= (p.Val112=)
 dbSNP
4g.43030366A>CCA439192087GRXCR1c.699A>C (p.Val233=)
c.336A>C (p.Val112=)
4g.43030366A>GCA2904511GRXCR1c.699A>G (p.Val233=)
c.336A>G (p.Val112=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.43030366A>TCA439192088GRXCR1c.699A>T (p.Val233=)
c.336A>T (p.Val112=)
4g.43030367C>ACA356791705GRXCR1c.700C>A (p.Gln234Lys)
c.337C>A (p.Gln113Lys)
 dbSNP gnomAD v4
4g.43030367C=CA1453107622GRXCR1c.700C= (p.Gln234=)
c.337C= (p.Gln113=)
 dbSNP
4g.43030367C>GCA356791706GRXCR1c.700C>G (p.Gln234Glu)
c.337C>G (p.Gln113Glu)
4g.43030367C>TCA2904512GRXCR1c.700C>T (p.Gln234Ter)
c.337C>T (p.Gln113Ter)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.43030368A>CCA356791709GRXCR1c.701A>C (p.Gln234Pro)
c.338A>C (p.Gln113Pro)
4g.43030368A>GCA356791707GRXCR1c.701A>G (p.Gln234Arg)
c.338A>G (p.Gln113Arg)
4g.43030368A>TCA356791708GRXCR1c.701A>T (p.Gln234Leu)
c.338A>T (p.Gln113Leu)
4g.43030369G>ACA439192089GRXCR1c.702G>A (p.Gln234=)
c.339G>A (p.Gln113=)

Number of alleles fetched