Colon Cancer: Gene >> AKR7L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000420396
Start	19269609:19269609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.575G>T
AA Mutation	p.Arg192Met(p.R192M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000420396
Start	19269586:19269586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598G>C
AA Mutation	p.Ala200Pro(p.A200P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000420396
Start	19269311:19269311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747136876
CDS Mutation	c.662G>A
AA Mutation	p.Arg221His(p.R221H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420396
Start	19269364:19269364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.609G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420396
Start	19274000:19274000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.75G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420396
Start	19269614:19269614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.570A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420396
Start	19273913:19273913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774966138
CDS Mutation	c.162C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AKR7L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000420396
Start	19269311:19269311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.662G>C
AA Mutation	p.Arg221Pro(p.R221P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420396
Start	19268680:19268680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375904032
CDS Mutation	c.723C>T
Mutation Classification	Silent
Feature Type	Transcript