Mutation

Primary Site >> Stomach Cancer

Gene >> TMTC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000539277
Start	29556977:29556977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1556C>T
AA Mutation	p.Ala519Val(p.A519V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000539277
Start	29604202:29604202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144467040
CDS Mutation	c.1226C>T
AA Mutation	p.Ala409Val(p.A409V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000539277
Start	29767938:29767938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761374402
CDS Mutation	c.440C>T
AA Mutation	p.Thr147Met(p.T147M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000539277
Start	29512108:29512108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2443G>A
AA Mutation	p.Ala815Thr(p.A815T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000539277
Start	29512113:29512113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2438G>C
AA Mutation	p.Arg813Thr(p.R813T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000539277
Start	29751724:29751724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880C>T
AA Mutation	p.Pro294Ser(p.P294S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000539277
Start	29506970:29506970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2525C>T
AA Mutation	p.Ala842Val(p.A842V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000539277
Start	29633239:29633239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1036G>C
AA Mutation	p.Val346Leu(p.V346L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000539277
Start	29516395:29516395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2261A>G
AA Mutation	p.Tyr754Cys(p.Y754C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000539277
Start	29604249:29604249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372059579
CDS Mutation	c.1179G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000539277
Start	29517540:29517540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2056T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000539277
Start	29536303:29536303(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1691delA
AA Mutation	p.Lys564ArgfsTer8(p.K564Rfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000539277
Start	29517509:29517524(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2072_2087delCACTGTATTACAACAC
AA Mutation	p.Ala691ValfsTer34(p.A691Vfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript