Colon Cancer: Gene >> B4GALT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356836
Start	43984920:43984920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755791825
CDS Mutation	c.605C>T
AA Mutation	p.Ala202Val(p.A202V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356836
Start	43990419:43990419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753720865
CDS Mutation	c.1090C>T
AA Mutation	p.Arg364Trp(p.R364W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356836
Start	43984964:43984964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.649G>A
AA Mutation	p.Val217Met(p.V217M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356836
Start	43985546:43985546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766675284
CDS Mutation	c.893G>A
AA Mutation	p.Arg298His(p.R298H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356836
Start	43985611:43985611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.958A>G
AA Mutation	p.Asn320Asp(p.N320D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356836
Start	43984921:43984921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356836
Start	43990340:43990340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs79144559
CDS Mutation	c.1011C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> B4GALT2

No Mutation Annotation!