Mutation

Primary Site >> Stomach Cancer

Gene >> TRPC6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101472239:101472239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2103A>C
AA Mutation	p.Glu701Asp(p.E701D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101583370:101583370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134A>G
AA Mutation	p.Gln45Arg(p.Q45R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101491729:101491729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750400201
CDS Mutation	c.955A>C
AA Mutation	p.Lys319Gln(p.K319Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101504298:101504298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671T>G
AA Mutation	p.Ile224Ser(p.I224S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101504754:101504754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.215T>G
AA Mutation	p.Leu72Arg(p.L72R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101504542:101504542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.427A>C
AA Mutation	p.Asn143His(p.N143H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101476433:101476433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753943966
CDS Mutation	c.1612G>A
AA Mutation	p.Ala538Thr(p.A538T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101504766:101504766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369866012
CDS Mutation	c.203G>A
AA Mutation	p.Arg68Gln(p.R68Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101472300:101472300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2042C>T
AA Mutation	p.Ala681Val(p.A681V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101504622:101504622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.347A>C
AA Mutation	p.Lys116Thr(p.K116T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101504675:101504675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294G>T
AA Mutation	p.Glu98Asp(p.E98D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101476503:101476503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1542G>C
AA Mutation	p.Trp514Cys(p.W514C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101504770:101504770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200031940
CDS Mutation	c.199C>T
AA Mutation	p.Arg67Trp(p.R67W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101472298:101472298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2044A>G
AA Mutation	p.Ile682Val(p.I682V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101483038:101483038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1421A>G
AA Mutation	p.Glu474Gly(p.E474G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000344327
Start	101472174:101472174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2168T>C
AA Mutation	p.Leu723Ser(p.L723S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344327
Start	101504081:101504081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344327
Start	101504123:101504123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344327
Start	101504734:101504734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344327
Start	101504582:101504582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.387G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344327
Start	101488958:101488958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1272C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344327
Start	101455042:101455042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61890853
CDS Mutation	c.2544C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344327
Start	101491610:101491610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745979751
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344327
Start	101453713:101453713(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2581delA
AA Mutation	p.Arg861GlyfsTer12(p.R861Gfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000344327
Start	101491556:101491556(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1128delA
AA Mutation	p.Lys376AsnfsTer3(p.K376Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344327
Start	101483016:101483016(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1443delA
AA Mutation	p.Lys481AsnfsTer6(p.K481Nfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000344327
Start	101504725:101504725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244C>T
AA Mutation	p.Arg82Ter(p.R82*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript