Mutation

Primary Site >> Stomach Cancer

Gene >> TRPV4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261740
Start	109794354:109794354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1466C>T
AA Mutation	p.Ala489Val(p.A489V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261740
Start	109803027:109803027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676T>C
AA Mutation	p.Phe226Leu(p.F226L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261740
Start	109814547:109814547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250G>A
AA Mutation	p.Asp84Asn(p.D84N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261740
Start	109786756:109786756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750416252
CDS Mutation	c.2290G>A
AA Mutation	p.Val764Met(p.V764M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261740
Start	109808400:109808400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.455C>A
AA Mutation	p.Pro152His(p.P152H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261740
Start	109808443:109808443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412C>A
AA Mutation	p.Pro138Thr(p.P138T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261740
Start	109814571:109814571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777647151
CDS Mutation	c.226C>T
AA Mutation	p.Arg76Cys(p.R76C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261740
Start	109814630:109814630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767169716
CDS Mutation	c.167G>A
AA Mutation	p.Arg56His(p.R56H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261740
Start	109794390:109794390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1430C>A
AA Mutation	p.Ser477Tyr(p.S477Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261740
Start	109800660:109800660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811C>T
AA Mutation	p.Arg271Cys(p.R271C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261740
Start	109803089:109803089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614G>A
AA Mutation	p.Gly205Asp(p.G205D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261740
Start	109788714:109788714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1894C>A
AA Mutation	p.Leu632Met(p.L632M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261740
Start	109784371:109784371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2403G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261740
Start	109788628:109788628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1980C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261740
Start	109788460:109788460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2148C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261740
Start	109792679:109792679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747018354
CDS Mutation	c.1797G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261740
Start	109798674:109798674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761716884
CDS Mutation	c.1092C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261740
Start	109783743:109783743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2494C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261740
Start	109808369:109808369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.486C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261740
Start	109800631:109800632(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.839dupG
AA Mutation	p.Tyr281LeufsTer53(p.Y281Lfs*53)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261740
Start	109783652:109783653(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2584dupC
AA Mutation	p.Arg862ProfsTer6(p.R862Pfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript