Colon Cancer: Gene >> HAND1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231121
Start	154477599:154477599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374536409
CDS Mutation	c.410G>A
AA Mutation	p.Arg137His(p.R137H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231121
Start	154477585:154477585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424T>G
AA Mutation	p.Tyr142Asp(p.Y142D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000231121
Start	154477479:154477479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747099689
CDS Mutation	c.530G>A
AA Mutation	p.Arg177Gln(p.R177Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000231121
Start	154477683:154477683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.326G>A
AA Mutation	p.Ser109Asn(p.S109N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000231121
Start	154475853:154475853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601C>T
AA Mutation	p.Arg201Cys(p.R201C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HAND1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231121
Start	154477492:154477492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517C>T
AA Mutation	p.Arg173Cys(p.R173C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript