Mutation

Primary Site >> Stomach Cancer

Gene >> CHD1L

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369258
Start	147254967:147254967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.338A>T
AA Mutation	p.Glu113Val(p.E113V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369258
Start	147276121:147276121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587620686
CDS Mutation	c.1403G>A
AA Mutation	p.Arg468Gln(p.R468Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369258
Start	147280184:147280184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1698G>T
AA Mutation	p.Glu566Asp(p.E566D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369258
Start	147286359:147286359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2080C>T
AA Mutation	p.Pro694Ser(p.P694S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369258
Start	147294510:147294510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2608A>G
AA Mutation	p.Thr870Ala(p.T870A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000369258
Start	147286300:147286300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2021T>C
AA Mutation	p.Met674Thr(p.M674T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369258
Start	147280036:147280036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1550T>C
AA Mutation	p.Ile517Thr(p.I517T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369258
Start	147284477:147284477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368838337
CDS Mutation	c.1832G>A
AA Mutation	p.Arg611Gln(p.R611Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369258
Start	147276150:147276150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1432A>T
AA Mutation	p.Ile478Leu(p.I478L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369258
Start	147285336:147285336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1867G>T
AA Mutation	p.Gly623Cys(p.G623C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369258
Start	147284479:147284479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1834T>C
AA Mutation	p.Ser612Pro(p.S612P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript