Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.27750943A>CCA411032795MN1n.460T>G
c.3935T>G (p.Phe1312Cys)
c.288T>G
n.291T>G
22g.27750943A>GCA411032797MN1n.460T>C
c.3935T>C (p.Phe1312Ser)
c.288T>C
n.291T>C
22g.27750943A>TCA411032799MN1n.460T>A
c.3935T>A (p.Phe1312Tyr)
c.288T>A
n.291T>A
22g.27750944A=CA2399818104MN1n.459T=
c.3934T= (p.Phe1312=)
c.287T=
n.290T=
22g.27750944A>CCA411032801MN1n.459T>G
c.3934T>G (p.Phe1312Val)
c.287T>G
n.290T>G
22g.27750944A>GCA411032802MN1n.459T>C
c.3934T>C (p.Phe1312Leu)
c.287T>C
n.290T>C
 dbSNP gnomAD v3 gnomAD v4
22g.27750944A>TCA411032803MN1n.459T>A
c.3934T>A (p.Phe1312Ile)
c.287T>A
n.290T>A
22g.27750945T>ACA411032805MN1n.458A>T
c.3933A>T (p.Arg1311Ser)
c.286A>T
n.289A>T
22g.27750945T>CCA513939240MN1n.458A>G
c.3933A>G (p.Arg1311=)
c.286A>G
n.289A>G
22g.27750945T>GCA411032807MN1n.458A>C
c.3933A>C (p.Arg1311Ser)
c.286A>C
n.289A>C
22g.27750946C>ACA411032809MN1n.457G>T
c.3932G>T (p.Arg1311Ile)
c.285G>T
n.288G>T
 gnomAD v4
22g.27750946C=CA2399818105MN1n.457G=
c.3932G= (p.Arg1311=)
c.285G=
n.288G=
22g.27750946C>GCA411032811MN1n.457G>C
c.3932G>C (p.Arg1311Thr)
c.285G>C
n.288G>C
22g.27750946C>TCA322870756MN1n.457G>A
c.3932G>A (p.Arg1311Lys)
c.285G>A
n.288G>A
 dbSNP
22g.27750947T>ACA411032814MN1n.456A>T
c.3931A>T (p.Arg1311Ter)
c.284A>T
n.287A>T
22g.27750947T>CCA411032816MN1n.456A>G
c.3931A>G (p.Arg1311Gly)
c.284A>G
n.287A>G
22g.27750947T>GCA513939241MN1n.456A>C
c.3931A>C (p.Arg1311=)
c.284A>C
n.287A>C
22g.27750948G>ACA10165933MN1n.455C>T
c.3930C>T (p.Asn1310=)
c.283C>T
n.286C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
22g.27750948G>CCA411032822MN1n.455C>G
c.3930C>G (p.Asn1310Lys)
c.283C>G
n.286C>G
22g.27750948G=CA2399818106MN1n.455C=
c.3930C= (p.Asn1310=)
c.283C=
n.286C=
22g.27750948G>TCA411032826MN1n.455C>A
c.3930C>A (p.Asn1310Lys)
c.283C>A
n.286C>A
22g.27750949T>ACA411032835MN1n.454A>T
c.3929A>T (p.Asn1310Ile)
c.282A>T
n.285A>T
22g.27750949T>CCA411032832MN1n.454A>G
c.3929A>G (p.Asn1310Ser)
c.282A>G
n.285A>G
22g.27750949T>GCA411032830MN1n.454A>C
c.3929A>C (p.Asn1310Thr)
c.282A>C
n.285A>C
22g.27750950dupCA2655934855MN1n.454dup
c.3929dup (p.Asn1310LysfsTer?)
c.282dup
n.285dup
 gnomAD v4
22g.27750950T>ACA411032839MN1n.453A>T
c.3928A>T (p.Asn1310Tyr)
c.281A>T
n.284A>T
22g.27750950T>CCA411032844MN1n.453A>G
c.3928A>G (p.Asn1310Asp)
c.281A>G
n.284A>G
22g.27750950T>GCA411032848MN1n.453A>C
c.3928A>C (p.Asn1310His)
c.281A>C
n.284A>C
22g.27750950_27750951delCA2739290371MN1n.452_453del
c.3927_3928del (p.Asn1310GlnfsTer?)
c.280_281del
n.283_284del
22g.27750951G>ACA513939242MN1n.452C>T
c.3927C>T (p.Ser1309=)
c.280C>T
n.283C>T
22g.27750951G>CCA513939243MN1n.452C>G
c.3927C>G (p.Ser1309=)
c.280C>G
n.283C>G
22g.27750951G>TCA513939244MN1n.452C>A
c.3927C>A (p.Ser1309=)
c.280C>A
n.283C>A
22g.27750952G>ACA411032852MN1n.451C>T
c.3926C>T (p.Ser1309Phe)
c.279C>T
n.282C>T
22g.27750952G>CCA411032855MN1n.451C>G
c.3926C>G (p.Ser1309Cys)
c.279C>G
n.282C>G
 gnomAD v4
22g.27750952G>TCA411032859MN1n.451C>A
c.3926C>A (p.Ser1309Tyr)
c.279C>A
n.282C>A
22g.27750953A=CA2399818107MN1n.450T=
c.3925T= (p.Ser1309=)
c.278T=
n.281T=
22g.27750953A>CCA411032873MN1n.450T>G
c.3925T>G (p.Ser1309Ala)
c.278T>G
n.281T>G
22g.27750953A>GCA411032863MN1n.450T>C
c.3925T>C (p.Ser1309Pro)
c.278T>C
n.281T>C
22g.27750953A>TCA10165934MN1n.450T>A
c.3925T>A (p.Ser1309Thr)
c.278T>A
n.281T>A
 dbSNP ExAC gnomAD v2
22g.27750954G>ACA513939246MN1n.449C>T
c.3924C>T (p.Ile1308=)
c.277C>T
n.280C>T
22g.27750954G>CCA411032878MN1n.449C>G
c.3924C>G (p.Ile1308Met)
c.277C>G
n.280C>G
 COSMIC
22g.27750954G>TCA513939245MN1n.449C>A
c.3924C>A (p.Ile1308=)
c.277C>A
n.280C>A
22g.27750955A>CCA411032883MN1n.448T>G
c.3923T>G (p.Ile1308Ser)
c.276T>G
n.279T>G
22g.27750955A>GCA411032888MN1n.448T>C
c.3923T>C (p.Ile1308Thr)
c.276T>C
n.279T>C
22g.27750955A>TCA411032891MN1n.448T>A
c.3923T>A (p.Ile1308Asn)
c.276T>A
n.279T>A
22g.27750956T>ACA411032896MN1n.447A>T
c.3922A>T (p.Ile1308Phe)
c.275A>T
n.278A>T
22g.27750956T>CCA411032899MN1n.447A>G
c.3922A>G (p.Ile1308Val)
c.275A>G
n.278A>G
 gnomAD v4
22g.27750956T>GCA411032903MN1n.447A>C
c.3922A>C (p.Ile1308Leu)
c.275A>C
n.278A>C
22g.27750957G>ACA322870762MN1n.446C>T
c.3921C>T (p.Asp1307=)
c.274C>T
n.277C>T
 dbSNP
22g.27750957G>CCA411032908MN1n.446C>G
c.3921C>G (p.Asp1307Glu)
c.274C>G
n.277C>G

Number of alleles fetched