Colon Cancer: Gene >> CCT4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394440
Start	61872251:61872251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771250995
CDS Mutation	c.1322G>A
AA Mutation	p.Arg441Gln(p.R441Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394440
Start	61872491:61872491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1223C>T
AA Mutation	p.Ala408Val(p.A408V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394440
Start	61876131:61876131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881G>A
AA Mutation	p.Gly294Glu(p.G294E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394440
Start	61873244:61873244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140356041
CDS Mutation	c.967A>G
AA Mutation	p.Met323Val(p.M323V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394440
Start	61883525:61883525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394440
Start	61878932:61878932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.459A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394440
Start	61872223:61872223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778508965
CDS Mutation	c.1350C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394440
Start	61888394:61888394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.114T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394440
Start	61872105:61872105(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1468delA
AA Mutation	p.Thr490LeufsTer30(p.T490Lfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained;inframe_insertion
Transcription ID	ENST00000394440
Start	61872186:61872187(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1386_1387insAATTAATCAATATTT
AA Mutation	p.Pro462_Ser463insAsnTerSerIlePhe(p.P462_S463insN*SIF)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000394440
Start	61873295:61873295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.918-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CCT4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394440
Start	61872555:61872555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769218948
CDS Mutation	c.1159A>G
AA Mutation	p.Thr387Ala(p.T387A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394440
Start	61869533:61869533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1512G>T
AA Mutation	p.Leu504Phe(p.L504F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript