Colon Cancer: Gene >> DLG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399506
Start	7196840:7196840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000G>A
AA Mutation	p.Glu334Lys(p.E334K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399506
Start	7191918:7191918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1951C>T
AA Mutation	p.Arg651Cys(p.R651C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399506
Start	7190758:7190758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747146441
CDS Mutation	c.2125G>A
AA Mutation	p.Glu709Lys(p.E709K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399506
Start	7193503:7193503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1673A>G
AA Mutation	p.Lys558Arg(p.K558R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399506
Start	7196902:7196902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764739020
CDS Mutation	c.938G>A
AA Mutation	p.Arg313Gln(p.R313Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399506
Start	7203717:7203717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>T
AA Mutation	p.Ala104Ser(p.A104S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399506
Start	7203733:7203733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294G>T
AA Mutation	p.Lys98Asn(p.K98N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399506
Start	7203312:7203312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523G>A
AA Mutation	p.Ala175Thr(p.A175T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399506
Start	7203762:7203762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265G>A
AA Mutation	p.Gly89Ser(p.G89S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000399506
Start	7190811:7190811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2072T>C
AA Mutation	p.Ile691Thr(p.I691T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399506
Start	7191979:7191979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1890C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399506
Start	7208213:7208213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.57G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399506
Start	7193538:7193538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201604329
CDS Mutation	c.1638C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399506
Start	7193532:7193532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374550329
CDS Mutation	c.1644C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399506
Start	7194450:7194450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1347C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399506
Start	7196835:7196835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1005C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399506
Start	7196543:7196543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1116T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	start_lost
Transcription ID	ENST00000399506
Start	7217145:7217145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3G>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DLG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399506
Start	7193537:7193537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760656143
CDS Mutation	c.1639G>A
AA Mutation	p.Ala547Thr(p.A547T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399506
Start	7196902:7196902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764739020
CDS Mutation	c.938G>A
AA Mutation	p.Arg313Gln(p.R313Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript