Colon Cancer: Gene >> MTHFR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376590
Start	11795236:11795236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.893G>A
AA Mutation	p.Gly298Asp(p.G298D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376590
Start	11794793:11794793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102G>T
AA Mutation	p.Ala368Ser(p.A368S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376590
Start	11794471:11794471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1234T>C
AA Mutation	p.Ser412Pro(p.S412P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376590
Start	11800271:11800271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.527T>C
AA Mutation	p.Val176Ala(p.V176A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376590
Start	11801193:11801193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.443T>G
AA Mutation	p.Leu148Arg(p.L148R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376590
Start	11793991:11793991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1446C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376590
Start	11794403:11794403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1302C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376590
Start	11794020:11794020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1417C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MTHFR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376590
Start	11801217:11801217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.419G>A
AA Mutation	p.Gly140Asp(p.G140D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376590
Start	11794825:11794825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1070G>A
AA Mutation	p.Arg357His(p.R357H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript