Colon Cancer: Gene >> HGFAC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382774
Start	3444331:3444331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619C>A
AA Mutation	p.Arg207Ser(p.R207S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382774
Start	3449403:3449403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1952T>G
AA Mutation	p.Leu651Arg(p.L651R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382774
Start	3444864:3444864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.887G>T
AA Mutation	p.Gly296Val(p.G296V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382774
Start	3442766:3442766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.152C>T
AA Mutation	p.Ala51Val(p.A51V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382774
Start	3447552:3447552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759083816
CDS Mutation	c.1416C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382774
Start	3449290:3449290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754099232
CDS Mutation	c.1839C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382774
Start	3448013:3448013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200335063
CDS Mutation	c.1614G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382774
Start	3449389:3449389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1938G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382774
Start	3444127:3444127(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.568delC
AA Mutation	p.Arg190GlyfsTer57(p.R190Gfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382774
Start	3442867:3442867(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs777946425
CDS Mutation	c.257delC
AA Mutation	p.Pro86ArgfsTer161(p.P86Rfs*161)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000382774
Start	3447491:3447492(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs777027535
CDS Mutation	c.1362dupC
AA Mutation	p.Arg455GlnfsTer91(p.R455Qfs*91)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HGFAC

No Mutation Annotation!