Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HIST1H1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244573
Start	26017220:26017220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762712997
CDS Mutation	c.513A>C
AA Mutation	p.Lys171Asn(p.K171N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000244573
Start	26017369:26017369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.364G>T
AA Mutation	p.Gly122Cys(p.G122C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000244573
Start	26017285:26017285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.448G>A
AA Mutation	p.Val150Ile(p.V150I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000244573
Start	26017384:26017384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>A
AA Mutation	p.Val117Met(p.V117M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000244573
Start	26017119:26017119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614C>T
AA Mutation	p.Ala205Val(p.A205V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000244573
Start	26017219:26017219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370624155
CDS Mutation	c.514C>A
AA Mutation	p.Pro172Thr(p.P172T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244573
Start	26017220:26017220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.513A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244573
Start	26017597:26017597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200744524
CDS Mutation	c.136C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244573
Start	26017133:26017133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.600G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HIST1H1A

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244573
Start	26017253:26017253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.480G>A
Mutation Classification	Silent
Feature Type	Transcript