Colon Cancer: Gene >> TACR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305249
Start	75198595:75198595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749162463
CDS Mutation	c.340G>A
AA Mutation	p.Ala114Thr(p.A114T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305249
Start	75049641:75049641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1015A>G
AA Mutation	p.Thr339Ala(p.T339A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305249
Start	75120761:75120761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397G>A
AA Mutation	p.Ala133Thr(p.A133T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305249
Start	75051396:75051396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.787C>T
AA Mutation	p.Pro263Ser(p.P263S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305249
Start	75198862:75198862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.73T>C
AA Mutation	p.Phe25Leu(p.F25L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305249
Start	75120594:75120594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199842504
CDS Mutation	c.564G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305249
Start	75049600:75049600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1056C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305249
Start	75198755:75198755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305249
Start	75198599:75198599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305249
Start	75049684:75049684(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.972delC
AA Mutation	p.Phe325SerfsTer12(p.F325Sfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305249
Start	75198925:75198926(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.9_10insCAGAAAATAGTTCGTCACT
AA Mutation	p.Val4GlnfsTer21(p.V4Qfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TACR1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305249
Start	75198734:75198734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201G>A
Mutation Classification	Silent
Feature Type	Transcript