Colon Cancer: Gene >> CCT6A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275603
Start	56055751:56055751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.464C>A
AA Mutation	p.Ser155Tyr(p.S155Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000275603
Start	56058028:56058028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650G>A
AA Mutation	p.Arg217Gln(p.R217Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000275603
Start	56060903:56060903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1310T>C
AA Mutation	p.Val437Ala(p.V437A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000275603
Start	56060861:56060861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1268T>A
AA Mutation	p.Ile423Asn(p.I423N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000275603
Start	56058658:56058658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.924A>T
AA Mutation	p.Glu308Asp(p.E308D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000275603
Start	56060896:56060896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1303C>A
AA Mutation	p.Leu435Ile(p.L435I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000275603
Start	56058408:56058408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772A>C
AA Mutation	p.Lys258Gln(p.K258Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000275603
Start	56060833:56060833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1240G>A
AA Mutation	p.Val414Met(p.V414M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275603
Start	56058661:56058661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000275603
Start	56058450:56058450(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.820delA
AA Mutation	p.Ile274Ter(p.I274*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000275603
Start	56058378:56058378(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.748delT
AA Mutation	p.Tyr250ThrfsTer11(p.Y250Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CCT6A

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000275603
Start	56058450:56058450(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.820delA
AA Mutation	p.Ile274Ter(p.I274*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000275603
Start	56058462:56058462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826G>T
AA Mutation	p.Glu276Ter(p.E276*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript