Colon Cancer: Gene >> CYFIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22918852:22918852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759931816
CDS Mutation	c.1366G>A
AA Mutation	p.Ala456Thr(p.A456T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22917909:22917909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1553T>C
AA Mutation	p.Val518Ala(p.V518A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22928021:22928021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1118C>T
AA Mutation	p.Thr373Met(p.T373M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22873612:22873612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3328C>T
AA Mutation	p.Arg1110Cys(p.R1110C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22873622:22873622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3318C>G
AA Mutation	p.Asp1106Glu(p.D1106E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22918758:22918758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1460T>G
AA Mutation	p.Phe487Cys(p.F487C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22939302:22939302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778270959
CDS Mutation	c.685G>A
AA Mutation	p.Glu229Lys(p.E229K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22939220:22939220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750340297
CDS Mutation	c.767C>T
AA Mutation	p.Thr256Met(p.T256M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22874614:22874614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3146G>T
AA Mutation	p.Arg1049Ile(p.R1049I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22882909:22882909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763053554
CDS Mutation	c.2779G>A
AA Mutation	p.Ala927Thr(p.A927T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22912183:22912183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2078C>T
AA Mutation	p.Ala693Val(p.A693V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22939239:22939239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.748G>A
AA Mutation	p.Glu250Lys(p.E250K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610365
Start	22874634:22874634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3126A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610365
Start	22926048:22926048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779224600
CDS Mutation	c.1293C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610365
Start	22927987:22927987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1152C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610365
Start	22879916:22879916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3039C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610365
Start	22918796:22918796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768369679
CDS Mutation	c.1422C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610365
Start	22917833:22917833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761659015
CDS Mutation	c.1629C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610365
Start	22943181:22943181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530221441
CDS Mutation	c.561G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000610365
Start	22944582:22944582(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.363delA
AA Mutation	p.Lys121AsnfsTer2(p.K121Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CYFIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22870165:22870165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371607573
CDS Mutation	c.3625C>T
AA Mutation	p.Arg1209Cys(p.R1209C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22943338:22943338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746030413
CDS Mutation	c.404G>A
AA Mutation	p.Arg135His(p.R135H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000610365
Start	22909220:22909220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2362G>A
AA Mutation	p.Glu788Lys(p.E788K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript