NM_002880.4(RAF1):c.-209G>A
|
rs727504351
|
0.00035
|
NM_002880.4(RAF1):c.212A>G (p.Asn71Ser)
|
rs184022679
|
0.00029
|
NM_002880.4(RAF1):c.1721A>G (p.Tyr574Cys)
|
rs370242565
|
0.00012
|
NM_002880.4(RAF1):c.1537-13G>A
|
rs369039413
|
0.00011
|
NM_002880.4(RAF1):c.935T>C (p.Val312Ala)
|
rs370243307
|
0.00010
|
NM_002880.4(RAF1):c.1814C>T (p.Ser605Phe)
|
rs730881004
|
0.00006
|
NM_002880.4(RAF1):c.1663G>C (p.Asp555His)
|
rs371704292
|
0.00004
|
NM_002880.4(RAF1):c.1109-17G>C
|
rs770431112
|
0.00003
|
NM_002880.4(RAF1):c.1921A>G (p.Thr641Ala)
|
rs1183812590
|
0.00003
|
NM_002880.3(RAF1):c.-361G>T
|
rs727504376
|
0.00002
|
NM_002880.4(RAF1):c.1193+17C>T
|
rs753928357
|
0.00002
|
NM_002880.4(RAF1):c.313C>G (p.His105Asp)
|
rs397516818
|
0.00002
|
NM_002880.4(RAF1):c.819C>G (p.Asp273Glu)
|
rs771675427
|
0.00002
|
NM_002880.4(RAF1):c.952C>T (p.Arg318Trp)
|
rs759433668
|
0.00002
|
NM_002880.4(RAF1):c.-4A>C
|
rs368465923
|
0.00001
|
NM_002880.4(RAF1):c.1063A>G (p.Ile355Val)
|
rs727504719
|
0.00001
|
NM_002880.4(RAF1):c.1247A>G (p.Asn416Ser)
|
rs774198365
|
0.00001
|
NM_002880.4(RAF1):c.1334T>G (p.Leu445Arg)
|
rs757591797
|
0.00001
|
NM_002880.4(RAF1):c.1355C>T (p.Thr452Met)
|
rs555781462
|
0.00001
|
NM_002880.4(RAF1):c.1688G>A (p.Arg563Gln)
|
rs727504827
|
0.00001
|
NM_002880.4(RAF1):c.1741A>G (p.Met581Val)
|
rs752063874
|
0.00001
|
NM_002880.4(RAF1):c.1895_1918del (p.Glu632_Thr640delinsAla)
|
rs2058255431
|
0.00001
|
NM_002880.4(RAF1):c.1910G>A (p.Cys637Tyr)
|
rs769639669
|
0.00001
|
NM_002880.4(RAF1):c.1928C>T (p.Pro643Leu)
|
rs1382398408
|
0.00001
|
NM_002880.4(RAF1):c.321T>C (p.Gly107=)
|
rs201937982
|
0.00001
|
NM_002880.4(RAF1):c.331C>T (p.Arg111Cys)
|
rs773801570
|
0.00001
|
NM_002880.4(RAF1):c.424-6T>C
|
rs983999914
|
0.00001
|
NM_002880.4(RAF1):c.482A>G (p.Asn161Ser)
|
rs775781057
|
0.00001
|
NM_002880.4(RAF1):c.536A>G (p.Lys179Arg)
|
rs1271531726
|
0.00001
|
NM_002880.4(RAF1):c.845G>A (p.Arg282Gln)
|
rs752713997
|
0.00001
|
NM_002880.4(RAF1):c.974A>C (p.Gln325Pro)
|
rs764719098
|
0.00001
|
NM_002880.3(RAF1):c.(?_-26)-50_(1370_?)+72dup
|
|
|
NM_002880.3(RAF1):c.1804-11_1804-7dup
|
rs727503382
|
|
NM_002880.4(RAF1):c.-40C>T
|
rs727503385
|
|
NM_002880.4(RAF1):c.1016G>A (p.Ser339Asn)
|
rs1057518084
|
|
NM_002880.4(RAF1):c.1144C>T (p.Pro382Ser)
|
rs1575546471
|
|
NM_002880.4(RAF1):c.1193+13C>T
|
|
|
NM_002880.4(RAF1):c.1194-17TCCCC[2]
|
rs2058496555
|
|
NM_002880.4(RAF1):c.124_125delinsAT (p.Ala42Ile)
|
rs876657965
|
|
NM_002880.4(RAF1):c.1483C>T (p.Arg495Cys)
|
|
|
NM_002880.4(RAF1):c.1528C>T (p.Leu510Phe)
|
rs397516816
|
|
NM_002880.4(RAF1):c.1613T>C (p.Leu538Ser)
|
rs730881011
|
|
NM_002880.4(RAF1):c.1673T>C (p.Ile558Thr)
|
rs1559399152
|
|
NM_002880.4(RAF1):c.1708C>G (p.Leu570Val)
|
rs876657966
|
|
NM_002880.4(RAF1):c.1720_1760dup (p.Asp587_Cys588insIleArgThrAlaProLysGlnTer)
|
rs2058275378
|
|
NM_002880.4(RAF1):c.1724A>C (p.Lys575Thr)
|
rs767890715
|
|
NM_002880.4(RAF1):c.172A>C (p.Ile58Leu)
|
rs147984543
|
|
NM_002880.4(RAF1):c.1770G>C (p.Lys590Asn)
|
rs773583951
|
|
NM_002880.4(RAF1):c.1842G>A (p.Pro614=)
|
rs200235582
|
|
NM_002880.4(RAF1):c.1927C>T (p.Pro643Ser)
|
rs876657967
|
|
NM_002880.4(RAF1):c.207+10C>T
|
rs2059446210
|
|
NM_002880.4(RAF1):c.226A>G (p.Met76Val)
|
rs730880999
|
|
NM_002880.4(RAF1):c.237T>G (p.His79Gln)
|
rs876661384
|
|
NM_002880.4(RAF1):c.321-4delinsTG
|
rs2125421173
|
|
NM_002880.4(RAF1):c.325_327del (p.Lys109del)
|
rs1418886913
|
|
NM_002880.4(RAF1):c.329C>T (p.Ala110Val)
|
rs397516819
|
|
NM_002880.4(RAF1):c.379C>G (p.Gln127Glu)
|
rs397516820
|
|
NM_002880.4(RAF1):c.388T>A (p.Phe130Ile)
|
rs397516821
|
|
NM_002880.4(RAF1):c.419A>G (p.Asn140Ser)
|
rs876657968
|
|
NM_002880.4(RAF1):c.424G>T (p.Ala142Ser)
|
rs1553614748
|
|
NM_002880.4(RAF1):c.512A>G (p.Lys171Arg)
|
rs876657969
|
|
NM_002880.4(RAF1):c.68_70del (p.Asp23del)
|
rs749549707
|
|
NM_002880.4(RAF1):c.752T>A (p.Leu251His)
|
rs1553613787
|
|
NM_002880.4(RAF1):c.775T>G (p.Ser259Ala)
|
rs3730271
|
|
NM_002880.4(RAF1):c.776C>A (p.Ser259Tyr)
|
rs397516827
|
|
NM_002880.4(RAF1):c.784A>C (p.Asn262His)
|
rs1575573204
|
|
NM_002880.4(RAF1):c.837T>A (p.Asp279Glu)
|
rs2125381916
|
|
NM_002880.4(RAF1):c.856G>A (p.Glu286Lys)
|
rs147453956
|
|
NM_002880.4(RAF1):c.991-17A>G
|
|
|
Single allele
|
|
|