Colon Cancer: Gene >> CCT5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280326
Start	10255961:10255961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338C>A
AA Mutation	p.Ala113Asp(p.A113D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280326
Start	10261572:10261572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768768696
CDS Mutation	c.1006G>A
AA Mutation	p.Ala336Thr(p.A336T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280326
Start	10255982:10255982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.359C>T
AA Mutation	p.Ala120Val(p.A120V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000280326
Start	10258481:10258481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.819T>G
AA Mutation	p.Asp273Glu(p.D273E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000280326
Start	10263216:10263216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1400G>A
AA Mutation	p.Gly467Asp(p.G467D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000280326
Start	10263176:10263176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1360G>A
AA Mutation	p.Ala454Thr(p.A454T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280326
Start	10258228:10258228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754143874
CDS Mutation	c.648C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280326
Start	10262510:10262510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771307325
CDS Mutation	c.1209C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CCT5

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280326
Start	10262540:10262540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1239C>T
Mutation Classification	Silent
Feature Type	Transcript