Colon Cancer: Gene >> HNMT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280097
Start	138005173:138005173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471C>A
AA Mutation	p.Phe157Leu(p.F157L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280097
Start	138013841:138013841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590A>G
AA Mutation	p.Gln197Arg(p.Q197R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280097
Start	138013828:138013828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.577G>T
AA Mutation	p.Asp193Tyr(p.D193Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000280097
Start	138002188:138002188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423G>A
AA Mutation	p.Met141Ile(p.M141I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280097
Start	138013821:138013822(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.574dupC
AA Mutation	p.Gln192ProfsTer3(p.Q192Pfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HNMT

No Mutation Annotation!