Colon Cancer: Gene >> CD320

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301458
Start	8303896:8303896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461G>A
AA Mutation	p.Gly154Asp(p.G154D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301458
Start	8302599:8302599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.713T>G
AA Mutation	p.Leu238Arg(p.L238R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301458
Start	8305150:8305150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149G>A
AA Mutation	p.Ser50Asn(p.S50N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301458
Start	8303971:8303971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139064611
CDS Mutation	c.386G>A
AA Mutation	p.Arg129His(p.R129H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301458
Start	8302522:8302522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790T>A
AA Mutation	p.Leu264Ile(p.L264I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301458
Start	8305113:8305113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CD320

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301458
Start	8302808:8302808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760066815
CDS Mutation	c.675C>T
Mutation Classification	Silent
Feature Type	Transcript