Colon Cancer: Gene >> POR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394893
Start	75985672:75985672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781994682
CDS Mutation	c.1492C>T
AA Mutation	p.Arg498Trp(p.R498W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394893
Start	75985193:75985193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs72557936
CDS Mutation	c.1384G>A
AA Mutation	p.Ala462Thr(p.A462T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394893
Start	75981112:75981112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769916309
CDS Mutation	c.581G>A
AA Mutation	p.Arg194Gln(p.R194Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394893
Start	75984927:75984927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs72557929
CDS Mutation	c.1217G>A
AA Mutation	p.Arg406His(p.R406H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394893
Start	75980472:75980472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500C>T
AA Mutation	p.Ser167Phe(p.S167F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394893
Start	75983535:75983535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846G>T
AA Mutation	p.Lys282Asn(p.K282N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394893
Start	75982259:75982259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.767T>C
AA Mutation	p.Ile256Thr(p.I256T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000394893
Start	75981129:75981129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598G>A
AA Mutation	p.Ala200Thr(p.A200T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394893
Start	75986050:75986050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1797C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394893
Start	75985133:75985133(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1329delC
AA Mutation	p.Ile444SerfsTer101(p.I444Sfs*101)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> POR

No Mutation Annotation!