Colon Cancer: Gene >> HIST1H1C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343677
Start	26056115:26056115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314T>G
AA Mutation	p.Phe105Cys(p.F105C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343677
Start	26055975:26055975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.454A>G
AA Mutation	p.Lys152Glu(p.K152E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343677
Start	26055861:26055861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.568G>A
AA Mutation	p.Ala190Thr(p.A190T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343677
Start	26056256:26056256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550065694
CDS Mutation	c.173C>A
AA Mutation	p.Ser58Tyr(p.S58Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343677
Start	26055990:26055990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527943061
CDS Mutation	c.439C>T
AA Mutation	p.Pro147Ser(p.P147S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343677
Start	26056102:26056102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343677
Start	26056192:26056192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343677
Start	26056153:26056153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.276T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343677
Start	26056029:26056029(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.400delG
AA Mutation	p.Ala134GlnfsTer33(p.A134Qfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000343677
Start	26055808:26055810(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.619_621delAAG
AA Mutation	p.Lys207del(p.K207del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HIST1H1C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343677
Start	26056230:26056230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561654336
CDS Mutation	c.199G>A
AA Mutation	p.Ala67Thr(p.A67T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript