Colon Cancer: Gene >> GP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000401815
Start	194397808:194397808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475G>A
AA Mutation	p.Asp159Asn(p.D159N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000401815
Start	194397682:194397682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601C>A
AA Mutation	p.Leu201Ile(p.L201I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000401815
Start	194397829:194397829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454G>A
AA Mutation	p.Ala152Thr(p.A152T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000401815
Start	194397007:194397007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778829280
CDS Mutation	c.1276G>A
AA Mutation	p.Asp426Asn(p.D426N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000401815
Start	194398053:194398053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.230A>C
AA Mutation	p.Gln77Pro(p.Q77P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000401815
Start	194397754:194397754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529T>G
AA Mutation	p.Leu177Val(p.L177V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000401815
Start	194398257:194398257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26C>T
AA Mutation	p.Ala9Val(p.A9V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000401815
Start	194397489:194397489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.794C>T
AA Mutation	p.Ser265Leu(p.S265L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000401815
Start	194397936:194397936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.347C>T
AA Mutation	p.Ala116Val(p.A116V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000401815
Start	194397844:194397844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439A>G
AA Mutation	p.Asn147Asp(p.N147D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401815
Start	194397935:194397935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.348G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401815
Start	194397452:194397452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401815
Start	194397754:194397754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401815
Start	194397569:194397569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401815
Start	194397950:194397950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.333G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401815
Start	194398190:194398190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759843994
CDS Mutation	c.93C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000401815
Start	194397651:194397651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.632C>T
AA Mutation	p.Ser211Leu(p.S211L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000401815
Start	194397773:194397773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510G>A
Mutation Classification	Silent
Feature Type	Transcript