Mutation

Primary Site >> Stomach Cancer

Gene >> CYP26A1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93074936:93074936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572G>A
AA Mutation	p.Arg191His(p.R191H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000224356
Start	93074308:93074308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190C>T
AA Mutation	p.Arg64Trp(p.R64W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93075020:93075020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656G>A
AA Mutation	p.Arg219His(p.R219H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93074974:93074974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610G>A
AA Mutation	p.Gly204Arg(p.G204R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93075162:93075162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.719G>A
AA Mutation	p.Arg240Gln(p.R240Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93074410:93074410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292C>T
AA Mutation	p.Arg98Trp(p.R98W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93074005:93074005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71C>T
AA Mutation	p.Ala24Val(p.A24V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93077186:93077186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1376T>C
AA Mutation	p.Leu459Pro(p.L459P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93074486:93074486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.368G>A
AA Mutation	p.Gly123Asp(p.G123D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93077228:93077228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1418C>T
AA Mutation	p.Thr473Ile(p.T473I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93077188:93077188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378G>A
AA Mutation	p.Ala460Thr(p.A460T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93074851:93074851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.487A>G
AA Mutation	p.Ser163Gly(p.S163G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000224356
Start	93074434:93074434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316C>T
AA Mutation	p.Arg106Trp(p.R106W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000224356
Start	93074424:93074424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757303454
CDS Mutation	c.306C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000224356
Start	93074967:93074967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000224356
Start	93077292:93077293(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1486dupG
AA Mutation	p.Glu496GlyfsTer11(p.E496Gfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000224356
Start	93074096:93074097(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.166dupG
AA Mutation	p.Glu56GlyfsTer72(p.E56Gfs*72)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript