Colon Cancer: Gene >> PARVG

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000422871
Start	44196156:44196156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.585G>T
AA Mutation	p.Lys195Asn(p.K195N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000422871
Start	44187827:44187827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752515984
CDS Mutation	c.196C>T
AA Mutation	p.Arg66Cys(p.R66C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000422871
Start	44206416:44206416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.986C>G
AA Mutation	p.Ala329Gly(p.A329G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000422871
Start	44190659:44190659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199889732
CDS Mutation	c.497C>T
AA Mutation	p.Thr166Ile(p.T166I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000422871
Start	44187850:44187850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745544487
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000422871
Start	44190594:44190594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000422871
Start	44206420:44206420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191035480
CDS Mutation	c.990G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000422871
Start	44183404:44183404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000422871
Start	44196397:44196397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000422871
Start	44206382:44206382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs73428406
CDS Mutation	c.952C>T
AA Mutation	p.Gln318Ter(p.Q318*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PARVG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000422871
Start	44196160:44196160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768880557
CDS Mutation	c.589G>A
AA Mutation	p.Val197Ile(p.V197I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000422871
Start	44206420:44206420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191035480
CDS Mutation	c.990G>A
Mutation Classification	Silent
Feature Type	Transcript