Colon Cancer: Gene >> AMT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273588
Start	49419057:49419057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.791T>A
AA Mutation	p.Leu264Gln(p.L264Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273588
Start	49420214:49420214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.468G>T
AA Mutation	p.Met156Ile(p.M156I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273588
Start	49422392:49422392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749087037
CDS Mutation	c.59C>T
AA Mutation	p.Pro20Leu(p.P20L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273588
Start	49417573:49417573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1179C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273588
Start	49422251:49422251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754165977
CDS Mutation	c.111G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273588
Start	49419374:49419374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377552553
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273588
Start	49419305:49419305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.651C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AMT

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273588
Start	49420331:49420331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351G>A
Mutation Classification	Silent
Feature Type	Transcript