Colon Cancer: Gene >> TRPM5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000155858
Start	2415939:2415939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1095G>T
AA Mutation	p.Lys365Asn(p.K365N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000155858
Start	2421160:2421160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.337G>A
AA Mutation	p.Ala113Thr(p.A113T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000155858
Start	2411716:2411716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2526C>A
AA Mutation	p.Phe842Leu(p.F842L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000155858
Start	2407161:2407161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3076C>T
AA Mutation	p.Arg1026Trp(p.R1026W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000155858
Start	2407769:2407769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772292156
CDS Mutation	c.2926G>A
AA Mutation	p.Ala976Thr(p.A976T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000155858
Start	2413135:2413135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775413241
CDS Mutation	c.2095C>T
AA Mutation	p.Arg699Trp(p.R699W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000155858
Start	2414140:2414140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768526088
CDS Mutation	c.1811G>A
AA Mutation	p.Arg604His(p.R604H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000155858
Start	2420289:2420289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763955838
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000155858
Start	2415328:2415328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1272C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000155858
Start	2422983:2422983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000155858
Start	2412825:2412825(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2284delC
AA Mutation	p.Gln762ArgfsTer35(p.Q762Rfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRPM5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000155858
Start	2415967:2415967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1067T>C
AA Mutation	p.Val356Ala(p.V356A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000155858
Start	2405548:2405548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756022087
CDS Mutation	c.3370G>A
AA Mutation	p.Ala1124Thr(p.A1124T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000155858
Start	2418200:2418200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873C>A
AA Mutation	p.Phe291Leu(p.F291L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript