Mutation

Primary Site >> Stomach Cancer

Gene >> FANCA

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389301
Start	89739195:89739195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201225325
CDS Mutation	c.4105G>A
AA Mutation	p.Val1369Met(p.V1369M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000389301
Start	89791403:89791403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1359G>T
AA Mutation	p.Lys453Asn(p.K453N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389301
Start	89805311:89805311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.678G>T
AA Mutation	p.Gln226His(p.Q226H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389301
Start	89769984:89769984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2357C>T
AA Mutation	p.Ala786Val(p.A786V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389301
Start	89765013:89765013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2655G>T
AA Mutation	p.Glu885Asp(p.E885D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000389301
Start	89783008:89783008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1565A>G
AA Mutation	p.Lys522Arg(p.K522R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000389301
Start	89740098:89740098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3830G>C
AA Mutation	p.Ser1277Thr(p.S1277T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000389301
Start	89782860:89782860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1625A>C
AA Mutation	p.Glu542Ala(p.E542A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000389301
Start	89791431:89791431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144234991
CDS Mutation	c.1331C>T
AA Mutation	p.Ala444Val(p.A444V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389301
Start	89764944:89764944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2724C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389301
Start	89742878:89742878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3687A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389301
Start	89805302:89805302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.687C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389301
Start	89767205:89767206(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2535_2536dupCT
AA Mutation	p.Cys846SerfsTer44(p.C846Sfs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000389301
Start	89803257:89803257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.792+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript