Colon Cancer: Gene >> CCT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258091
Start	73249174:73249174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139247672
CDS Mutation	c.967A>G
AA Mutation	p.Met323Val(p.M323V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258091
Start	73244607:73244607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258091
Start	73239723:73239723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.87C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_retained_variant
Transcription ID	ENST00000258091
Start	73252860:73252860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756429492
CDS Mutation	c.1631G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258091
Start	73249902:73249902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1056G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258091
Start	73239693:73239693(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.61delC
AA Mutation	p.Gln21SerfsTer3(p.Q21Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CCT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258091
Start	73247922:73247922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779T>C
AA Mutation	p.Val260Ala(p.V260A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript