Colon Cancer: Gene >> VIPR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325123
Start	42536152:42536152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779447235
CDS Mutation	c.1245C>G
AA Mutation	p.Asn415Lys(p.N415K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325123
Start	42532293:42532293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748019905
CDS Mutation	c.970C>T
AA Mutation	p.Arg324Trp(p.R324W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325123
Start	42528005:42528005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751164992
CDS Mutation	c.518C>T
AA Mutation	p.Thr173Met(p.T173M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325123
Start	42535051:42535051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200064877
CDS Mutation	c.1087A>G
AA Mutation	p.Asn363Asp(p.N363D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325123
Start	42535086:42535086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1122C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325123
Start	42519251:42519251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325123
Start	42535035:42535035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371839610
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VIPR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325123
Start	42532273:42532273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200704872
CDS Mutation	c.950G>A
AA Mutation	p.Arg317Gln(p.R317Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325123
Start	42535053:42535053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1089T>G
AA Mutation	p.Asn363Lys(p.N363K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript