Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904001C>ACA414906073F8c.5903G>T (p.Ser1968Ile)
c.5798G>T (p.Ser1933Ile)
Xg.154904001C=CA2466828164F8c.5903G= (p.Ser1968=)
c.5798G= (p.Ser1933=)
Xg.154904001C>GCA414906078F8c.5903G>C (p.Ser1968Thr)
c.5798G>C (p.Ser1933Thr)
Xg.154904001C>TCA337318263F8c.5903G>A (p.Ser1968Asn)
c.5798G>A (p.Ser1933Asn)
 ClinVar dbSNP COSMIC COSMIC
Xg.154904002T>ACA414906093F8c.5902A>T (p.Ser1968Cys)
c.5797A>T (p.Ser1933Cys)
Xg.154904002T>CCA414906101F8c.5902A>G (p.Ser1968Gly)
c.5797A>G (p.Ser1933Gly)
Xg.154904002T>GCA414906098F8c.5902A>C (p.Ser1968Arg)
c.5797A>C (p.Ser1933Arg)
Xg.154904003G>ACA519356253F8c.5901C>T (p.Gly1967=)
c.5796C>T (p.Gly1932=)
 gnomAD v4
Xg.154904003G>CCA519356255F8c.5901C>G (p.Gly1967=)
c.5796C>G (p.Gly1932=)
Xg.154904003G>TCA519356256F8c.5901C>A (p.Gly1967=)
c.5796C>A (p.Gly1932=)
Xg.154904004C>ACA414906106F8c.5900G>T (p.Gly1967Val)
c.5795G>T (p.Gly1932Val)
Xg.154904004C=CA2466828165F8c.5900G= (p.Gly1967=)
c.5795G= (p.Gly1932=)
Xg.154904004C>GCA414906108F8c.5900G>C (p.Gly1967Ala)
c.5795G>C (p.Gly1932Ala)
Xg.154904004C>TCA255188F8c.5900G>A (p.Gly1967Asp)
c.5795G>A (p.Gly1932Asp)
 ClinVar dbSNP
Xg.154904005C>ACA414906111F8c.5899G>T (p.Gly1967Cys)
c.5794G>T (p.Gly1932Cys)
Xg.154904005C>GCA414906113F8c.5899G>C (p.Gly1967Arg)
c.5794G>C (p.Gly1932Arg)
Xg.154904005C>TCA414906115F8c.5899G>A (p.Gly1967Ser)
c.5794G>A (p.Gly1932Ser)
Xg.154904006C>ACA414906123F8c.5898G>T (p.Met1966Ile)
c.5793G>T (p.Met1931Ile)
Xg.154904006C>GCA414906126F8c.5898G>C (p.Met1966Ile)
c.5793G>C (p.Met1931Ile)
Xg.154904006C>TCA414906131F8c.5898G>A (p.Met1966Ile)
c.5793G>A (p.Met1931Ile)
Xg.154904007A>CCA414906135F8c.5897T>G (p.Met1966Arg)
c.5792T>G (p.Met1931Arg)
Xg.154904007A>GCA414906137F8c.5897T>C (p.Met1966Thr)
c.5792T>C (p.Met1931Thr)
 gnomAD v4
Xg.154904007A>TCA414906132F8c.5897T>A (p.Met1966Lys)
c.5792T>A (p.Met1931Lys)
Xg.154904008T>ACA414906143F8c.5896A>T (p.Met1966Leu)
c.5791A>T (p.Met1931Leu)
 gnomAD v4
Xg.154904008T>CCA414906149F8c.5896A>G (p.Met1966Val)
c.5791A>G (p.Met1931Val)
 dbSNP
Xg.154904008T>GCA414906151F8c.5896A>C (p.Met1966Leu)
c.5791A>C (p.Met1931Leu)
 ClinVar dbSNP
Xg.154904008T=CA2466828166F8c.5896A= (p.Met1966=)
c.5791A= (p.Met1931=)
Xg.154904009G>ACA519356259F8c.5895C>T (p.Ser1965=)
c.5790C>T (p.Ser1930=)
Xg.154904009G>CCA414906154F8c.5895C>G (p.Ser1965Arg)
c.5790C>G (p.Ser1930Arg)
Xg.154904009G>TCA414906156F8c.5895C>A (p.Ser1965Arg)
c.5790C>A (p.Ser1930Arg)
 dbSNP
Xg.154904010C>ACA414906159F8c.5894G>T (p.Ser1965Ile)
c.5789G>T (p.Ser1930Ile)
 dbSNP
Xg.154904010C=CA2466828167F8c.5894G= (p.Ser1965=)
c.5789G= (p.Ser1930=)
Xg.154904010C>GCA414906162F8c.5894G>C (p.Ser1965Thr)
c.5789G>C (p.Ser1930Thr)
Xg.154904010C>TCA414906165F8c.5894G>A (p.Ser1965Asn)
c.5789G>A (p.Ser1930Asn)
Xg.154904011T>ACA414906168F8c.5893A>T (p.Ser1965Cys)
c.5788A>T (p.Ser1930Cys)
Xg.154904011T>CCA414906178F8c.5893A>G (p.Ser1965Gly)
c.5788A>G (p.Ser1930Gly)
Xg.154904011T>GCA414906179F8c.5893A>C (p.Ser1965Arg)
c.5788A>C (p.Ser1930Arg)
Xg.154904012G>ACA519356261F8c.5892C>T (p.Leu1964=)
c.5787C>T (p.Leu1929=)
 gnomAD v4
Xg.154904012G>CCA519356263F8c.5892C>G (p.Leu1964=)
c.5787C>G (p.Leu1929=)
Xg.154904012G>TCA519356264F8c.5892C>A (p.Leu1964=)
c.5787C>A (p.Leu1929=)
Xg.154904013A=CA2466828168F8c.5891T= (p.Leu1964=)
c.5786T= (p.Leu1929=)
Xg.154904013A>CCA414906182F8c.5891T>G (p.Leu1964Arg)
c.5786T>G (p.Leu1929Arg)
Xg.154904013A>GCA414906184F8c.5891T>C (p.Leu1964Pro)
c.5786T>C (p.Leu1929Pro)
 dbSNP
Xg.154904013A>TCA414906180F8c.5891T>A (p.Leu1964His)
c.5786T>A (p.Leu1929His)
Xg.154904014G>ACA414906186F8c.5890C>T (p.Leu1964Phe)
c.5785C>T (p.Leu1929Phe)
Xg.154904014G>CCA414906189F8c.5890C>G (p.Leu1964Val)
c.5785C>G (p.Leu1929Val)
 gnomAD v4
Xg.154904014G>TCA414906191F8c.5890C>A (p.Leu1964Ile)
c.5785C>A (p.Leu1929Ile)
Xg.154904015C>ACA519717768F8c.5889G>T (p.Leu1963=)
c.5784G>T (p.Leu1928=)
Xg.154904015C>GCA519717776F8c.5889G>C (p.Leu1963=)
c.5784G>C (p.Leu1928=)
Xg.154904015C>TCA519717772F8c.5889G>A (p.Leu1963=)
c.5784G>A (p.Leu1928=)

Number of alleles fetched