Colon Cancer: Gene >> HCRTR1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373706
Start	31625118:31625118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1087G>A
AA Mutation	p.Gly363Ser(p.G363S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373706
Start	31621549:31621549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695C>T
AA Mutation	p.Ala232Val(p.A232V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373706
Start	31625003:31625003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.972C>A
AA Mutation	p.Phe324Leu(p.F324L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373706
Start	31625075:31625075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765422061
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373706
Start	31619225:31619225(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.37delG
AA Mutation	p.Val13SerfsTer65(p.V13Sfs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373706
Start	31619699:31619700(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.367_368insG
AA Mutation	p.Pro123ArgfsTer69(p.P123Rfs*69)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HCRTR1

No Mutation Annotation!