Mutation

Primary Site >> Stomach Cancer

Gene >> WWC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168431322:168431322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141513893
CDS Mutation	c.2158G>A
AA Mutation	p.Ala720Thr(p.A720T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265293
Start	168464729:168464729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2917C>T
AA Mutation	p.Pro973Ser(p.P973S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168385246:168385246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781547786
CDS Mutation	c.265C>T
AA Mutation	p.Arg89Trp(p.R89W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168428769:168428769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778406863
CDS Mutation	c.1982G>A
AA Mutation	p.Arg661Gln(p.R661Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168428763:168428763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374770777
CDS Mutation	c.1976C>T
AA Mutation	p.Ala659Val(p.A659V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168455392:168455392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2695T>C
AA Mutation	p.Ser899Pro(p.S899P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168371503:168371503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>T
AA Mutation	p.Val67Phe(p.V67F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168385364:168385364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775504769
CDS Mutation	c.383A>G
AA Mutation	p.Tyr128Cys(p.Y128C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168397779:168397779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.489A>C
AA Mutation	p.Glu163Asp(p.E163D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265293
Start	168423754:168423754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1496C>T
AA Mutation	p.Thr499Ile(p.T499I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265293
Start	168399541:168399541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.564A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265293
Start	168460727:168460727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754970817
CDS Mutation	c.2901C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265293
Start	168408602:168408602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140218628
CDS Mutation	c.816G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265293
Start	168423883:168423883(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1629delC
AA Mutation	p.Ser544ProfsTer29(p.S544Pfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265293
Start	168468964:168468964(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3293delT
AA Mutation	p.Phe1098SerfsTer6(p.F1098Sfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000265293
Start	168423690:168423690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1432C>T
AA Mutation	p.Gln478Ter(p.Q478*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000265293
Start	168431356:168431356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2192G>A
AA Mutation	p.Trp731Ter(p.W731*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000265293
Start	168371481:168371481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177G>A
AA Mutation	p.Trp59Ter(p.W59*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000265293
Start	168428032:168428032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1811-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	20
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000265293
Start	168408468:168408507(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.721-38_722delGGAAGGCGCATCACTAACCCTGCTCTCCCCTCCTTCAGAG
Mutation Classification	Splice_Site
Feature Type	Transcript