Mutation

Primary Site >> Stomach Cancer

Gene >> FANCM

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45175297:45175297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2543C>T
AA Mutation	p.Thr848Ile(p.T848I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45176024:45176024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3270A>T
AA Mutation	p.Gln1090His(p.Q1090H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45176040:45176040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3286C>T
AA Mutation	p.Pro1096Ser(p.P1096S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45187806:45187806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4698G>A
AA Mutation	p.Met1566Ile(p.M1566I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45176680:45176680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3926A>T
AA Mutation	p.His1309Leu(p.H1309L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45136161:45136161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130G>A
AA Mutation	p.Ala44Thr(p.A44T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45148930:45148930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853A>C
AA Mutation	p.Lys285Gln(p.K285Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45196208:45196208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5377G>A
AA Mutation	p.Ala1793Thr(p.A1793T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45176190:45176190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142077813
CDS Mutation	c.3436G>A
AA Mutation	p.Asp1146Asn(p.D1146N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45188937:45188937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4915A>G
AA Mutation	p.Lys1639Glu(p.K1639E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45173161:45173161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142763060
CDS Mutation	c.2267G>A
AA Mutation	p.Arg756His(p.R756H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45176116:45176116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3362G>A
AA Mutation	p.Ser1121Asn(p.S1121N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45181686:45181686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749332566
CDS Mutation	c.4367G>A
AA Mutation	p.Arg1456His(p.R1456H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45181468:45181468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4261G>A
AA Mutation	p.Glu1421Lys(p.E1421K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45189310:45189310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5288T>G
AA Mutation	p.Phe1763Cys(p.F1763C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45196527:45196527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5696A>G
AA Mutation	p.Glu1899Gly(p.E1899G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45173122:45173122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2228C>A
AA Mutation	p.Pro743His(p.P743H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45159186:45159186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1487T>G
AA Mutation	p.Leu496Arg(p.L496R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45167061:45167061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1900A>G
AA Mutation	p.Asn634Asp(p.N634D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000267430
Start	45198751:45198751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759078220
CDS Mutation	c.5824G>A
AA Mutation	p.Ala1942Thr(p.A1942T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267430
Start	45137148:45137148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.588T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267430
Start	45176216:45176216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3462T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267430
Start	45199924:45199924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6063G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267430
Start	45176868:45176868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4114A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267430
Start	45196456:45196456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5625C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267430
Start	45176525:45176525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3771T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267430
Start	45198843:45198843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5916A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267430
Start	45176752:45176752(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs746983128
CDS Mutation	c.4005delA
AA Mutation	p.Val1336LeufsTer2(p.V1336Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267430
Start	45175939:45175939(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs778191984
CDS Mutation	c.3190delA
AA Mutation	p.Ser1064ValfsTer31(p.S1064Vfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267430
Start	45175337:45175337(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2589delA
AA Mutation	p.Asp864IlefsTer12(p.D864Ifs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267430
Start	45176698:45176699(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3950dupA
AA Mutation	p.Asn1317LysfsTer2(p.N1317Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267430
Start	45173084:45173085(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2201_2202dupCT
AA Mutation	p.Glu735LeufsTer26(p.E735Lfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	33
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000267430
Start	45196262:45196263(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5431_5432insCTCAAAAAA
AA Mutation	p.Leu1811delinsProGlnLysIle(p.L1811delinsPQKI)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript