Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PSMA8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308268
Start	26133985:26133985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.20G>A
AA Mutation	p.Arg7Lys(p.R7K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308268
Start	26178918:26178918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584C>A
AA Mutation	p.Ala195Asp(p.A195D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308268
Start	26192388:26192388(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.753delA
AA Mutation	p.Lys251AsnfsTer9(p.K251Nfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000308268
Start	26144568:26144568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376403017
CDS Mutation	c.112C>T
AA Mutation	p.Arg38Ter(p.R38*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000308268
Start	26158143:26158143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749936851
CDS Mutation	c.394C>T
AA Mutation	p.Arg132Ter(p.R132*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000308268
Start	26178845:26178845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511C>T
AA Mutation	p.Arg171Ter(p.R171*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308268
Start	26179084:26179085(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.638dupA
AA Mutation	p.Asn213LysfsTer3(p.N213Kfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PSMA8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308268
Start	26192387:26192387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.747G>T
AA Mutation	p.Lys249Asn(p.K249N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308268
Start	26178941:26178941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607T>G
AA Mutation	p.Leu203Val(p.L203V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308268
Start	26133989:26133989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.24G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000308268
Start	26178863:26178863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139896833
CDS Mutation	c.529C>T
AA Mutation	p.Arg177Ter(p.R177*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000308268
Start	26144568:26144568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376403017
CDS Mutation	c.112C>T
AA Mutation	p.Arg38Ter(p.R38*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000308268
Start	26192334:26192334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.694G>T
AA Mutation	p.Glu232Ter(p.E232*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript