Mutation

Primary Site >> Stomach Cancer

Gene >> HDC

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267845
Start	50242379:50242379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758313706
CDS Mutation	c.1870A>C
AA Mutation	p.Met624Leu(p.M624L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267845
Start	50254573:50254573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.533A>G
AA Mutation	p.Glu178Gly(p.E178G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267845
Start	50242651:50242651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1598C>A
AA Mutation	p.Pro533His(p.P533H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267845
Start	50252703:50252703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772945540
CDS Mutation	c.859C>T
AA Mutation	p.Arg287Trp(p.R287W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000267845
Start	50254135:50254135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758334668
CDS Mutation	c.715G>A
AA Mutation	p.Val239Ile(p.V239I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000267845
Start	50252459:50252459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765088806
CDS Mutation	c.1012G>A
AA Mutation	p.Ala338Thr(p.A338T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000267845
Start	50248325:50248325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1060A>G
AA Mutation	p.Ser354Gly(p.S354G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000267845
Start	50248256:50248256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129C>G
AA Mutation	p.His377Asp(p.H377D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000267845
Start	50242909:50242909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370055047
CDS Mutation	c.1340G>A
AA Mutation	p.Arg447His(p.R447H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267845
Start	50242737:50242737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765392492
CDS Mutation	c.1512G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267845
Start	50242581:50242581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1668G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267845
Start	50243158:50243158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1227G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267845
Start	50242353:50242353(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1896delA
AA Mutation	p.Lys632AsnfsTer85(p.K632Nfs*85)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267845
Start	50242352:50242353(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1896dupA
AA Mutation	p.Leu633ThrfsTer12(p.L633Tfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript