Colon Cancer: Gene >> PSG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000405312
Start	43205533:43205533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4G>T
AA Mutation	p.Gly2Trp(p.G2W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000405312
Start	43194514:43194514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768586725
CDS Mutation	c.1069G>A
AA Mutation	p.Glu357Lys(p.E357K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000405312
Start	43203936:43203936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380G>A
AA Mutation	p.Arg127Gln(p.R127Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000405312
Start	43204017:43204017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299G>T
AA Mutation	p.Arg100Ile(p.R100I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000405312
Start	43194467:43194467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1116T>G
AA Mutation	p.Phe372Leu(p.F372L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000405312
Start	43195045:43195045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189743457
CDS Mutation	c.938G>A
AA Mutation	p.Arg313Gln(p.R313Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000405312
Start	43198180:43198180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777453397
CDS Mutation	c.526G>A
AA Mutation	p.Ala176Thr(p.A176T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000405312
Start	43204057:43204057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259C>G
AA Mutation	p.Gln87Glu(p.Q87E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000405312
Start	43195024:43195024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374621539
CDS Mutation	c.959G>A
AA Mutation	p.Arg320His(p.R320H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000405312
Start	43194502:43194502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749563398
CDS Mutation	c.1081C>T
AA Mutation	p.Arg361Trp(p.R361W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405312
Start	43203977:43203977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372928608
CDS Mutation	c.339G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405312
Start	43204061:43204061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77454946
CDS Mutation	c.255C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405312
Start	43204226:43204226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533600298
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405312
Start	43203932:43203932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375869018
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405312
Start	43204082:43204082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183355892
CDS Mutation	c.234C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405312
Start	43194413:43194413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1170G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000405312
Start	43194491:43194492(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1091_1092insGTTTTGGAAG
AA Mutation	p.Tyr364Ter(p.Y364*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PSG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000405312
Start	43195078:43195078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905G>A
AA Mutation	p.Arg302Lys(p.R302K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000405312
Start	43198131:43198131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.575G>T
AA Mutation	p.Arg192Met(p.R192M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405312
Start	43194422:43194422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776868878
CDS Mutation	c.1161G>A
Mutation Classification	Silent
Feature Type	Transcript