Colon Cancer: Gene >> HINFP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350777
Start	119134164:119134164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558542812
CDS Mutation	c.1220G>A
AA Mutation	p.Arg407Gln(p.R407Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350777
Start	119134095:119134095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1151A>G
AA Mutation	p.His384Arg(p.H384R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350777
Start	119133147:119133147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1067G>A
AA Mutation	p.Arg356Gln(p.R356Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350777
Start	119127081:119127081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.137G>A
AA Mutation	p.Gly46Asp(p.G46D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000350777
Start	119130927:119130927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384C>A
AA Mutation	p.His128Gln(p.H128Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000350777
Start	119132953:119132953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.965G>A
AA Mutation	p.Ser322Asn(p.S322N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000350777
Start	119127040:119127040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.96C>A
AA Mutation	p.Phe32Leu(p.F32L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350777
Start	119132677:119132677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.771C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350777
Start	119134415:119134415(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1475delC
AA Mutation	p.Pro492GlnfsTer17(p.P492Qfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HINFP

No Mutation Annotation!