Colon Cancer: Gene >> AMH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221496
Start	2249678:2249678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371130597
CDS Mutation	c.346C>T
AA Mutation	p.Arg116Trp(p.R116W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221496
Start	2250433:2250433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509C>A
AA Mutation	p.Pro170His(p.P170H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221496
Start	2251744:2251744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1470C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221496
Start	2249539:2249539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759994294
CDS Mutation	c.207C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AMH

No Mutation Annotation!