Colon Cancer: Gene >> ITPRIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278071
Start	104315745:104315745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307T>C
AA Mutation	p.Trp103Arg(p.W103R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278071
Start	104315267:104315267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.785T>C
AA Mutation	p.Leu262Pro(p.L262P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278071
Start	104315265:104315265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776290130
CDS Mutation	c.787G>A
AA Mutation	p.Gly263Arg(p.G263R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278071
Start	104315970:104315970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775756816
CDS Mutation	c.82G>A
AA Mutation	p.Ala28Thr(p.A28T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278071
Start	104314614:104314614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750228977
CDS Mutation	c.1438G>A
AA Mutation	p.Gly480Ser(p.G480S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278071
Start	104315419:104315419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278071
Start	104315164:104315164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278071
Start	104315701:104315701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278071
Start	104314714:104314714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746212406
CDS Mutation	c.1338C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278071
Start	104315911:104315911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372515030
CDS Mutation	c.141G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278071
Start	104315668:104315669(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs759638581
CDS Mutation	c.383dupG
AA Mutation	p.Ala129ArgfsTer19(p.A129Rfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ITPRIP

No Mutation Annotation!