Colon Cancer: Gene >> GLYR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321919
Start	4805259:4805259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1639G>A
AA Mutation	p.Val547Met(p.V547M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321919
Start	4812112:4812112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1256C>T
AA Mutation	p.Ala419Val(p.A419V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321919
Start	4814622:4814622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.932C>G
AA Mutation	p.Ala311Gly(p.A311G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321919
Start	4817645:4817645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859C>A
AA Mutation	p.Leu287Ile(p.L287I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321919
Start	4812180:4812180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188639121
CDS Mutation	c.1188C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321919
Start	4805271:4805278(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1620_1627delTGACAACG
AA Mutation	p.Asp541TyrfsTer183(p.D541Yfs*183)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000321919
Start	4832914:4832914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GLYR1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321919
Start	4814582:4814582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775989603
CDS Mutation	c.972C>T
Mutation Classification	Silent
Feature Type	Transcript