Colon Cancer: Gene >> CCT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295688
Start	156320948:156320948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771827407
CDS Mutation	c.500G>A
AA Mutation	p.Arg167Gln(p.R167Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000295688
Start	156310952:156310952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747605804
CDS Mutation	c.1399C>T
AA Mutation	p.Arg467Trp(p.R467W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295688
Start	156309270:156309270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373870763
CDS Mutation	c.1567G>A
AA Mutation	p.Val523Ile(p.V523I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295688
Start	156335861:156335861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.59G>T
AA Mutation	p.Arg20Ile(p.R20I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295688
Start	156338158:156338158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.27G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295688
Start	156312212:156312212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.984G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295688
Start	156312104:156312104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1092T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295688
Start	156320857:156320857(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.591delA
AA Mutation	p.Lys197AsnfsTer23(p.K197Nfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295688
Start	156312061:156312061(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1135delG
AA Mutation	p.Ala379LeufsTer9(p.A379Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295688
Start	156312146:156312147(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1049dupT
AA Mutation	p.Leu350PhefsTer9(p.L350Ffs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CCT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295688
Start	156312046:156312046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746203604
CDS Mutation	c.1150C>A
AA Mutation	p.Leu384Ile(p.L384I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000295688
Start	156310952:156310952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747605804
CDS Mutation	c.1399C>T
AA Mutation	p.Arg467Trp(p.R467W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295688
Start	156317181:156317181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.959A>C
AA Mutation	p.Asn320Thr(p.N320T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript