Colon Cancer: Gene >> FRK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000606080
Start	115942568:115942568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1364C>T
AA Mutation	p.Pro455Leu(p.P455L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000606080
Start	115942569:115942569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1363C>G
AA Mutation	p.Pro455Ala(p.P455A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000606080
Start	115956603:115956603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.807G>T
AA Mutation	p.Met269Ile(p.M269I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000606080
Start	115968670:115968670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536G>A
AA Mutation	p.Arg179Gln(p.R179Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000606080
Start	115942507:115942507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1425G>T
AA Mutation	p.Lys475Asn(p.K475N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000606080
Start	116003962:116003962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.381G>T
AA Mutation	p.Glu127Asp(p.E127D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000606080
Start	115968657:115968657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745410841
CDS Mutation	c.549T>G
AA Mutation	p.Phe183Leu(p.F183L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000606080
Start	115956586:115956586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824T>C
AA Mutation	p.Leu275Pro(p.L275P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000606080
Start	115968595:115968595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611T>G
AA Mutation	p.Leu204Arg(p.L204R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000606080
Start	115942584:115942584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1348T>C
AA Mutation	p.Tyr450His(p.Y450H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000606080
Start	115967553:115967553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797C>A
AA Mutation	p.Pro266Gln(p.P266Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000606080
Start	116060301:116060301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11T>C
AA Mutation	p.Ile4Thr(p.I4T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000606080
Start	116060018:116060018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FRK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000606080
Start	115968644:115968644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562G>A
AA Mutation	p.Glu188Lys(p.E188K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000606080
Start	115942495:115942495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1437A>G
Mutation Classification	Silent
Feature Type	Transcript