Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CYFIP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157300860:157300860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.533A>G
AA Mutation	p.Lys178Arg(p.K178R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157296685:157296685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753263281
CDS Mutation	c.298G>A
AA Mutation	p.Glu100Lys(p.E100K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157300758:157300758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431G>A
AA Mutation	p.Cys144Tyr(p.C144Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157382601:157382601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3126G>T
AA Mutation	p.Glu1042Asp(p.E1042D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157383319:157383319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3242T>C
AA Mutation	p.Leu1081Pro(p.L1081P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157333441:157333441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2455A>G
AA Mutation	p.Ile819Val(p.I819V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157307829:157307829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.864G>C
AA Mutation	p.Lys288Asn(p.K288N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157341083:157341083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2674G>A
AA Mutation	p.Ala892Thr(p.A892T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157339128:157339128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2532C>G
AA Mutation	p.Ser844Arg(p.S844R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157315053:157315053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315C>T
AA Mutation	p.Arg439Cys(p.R439C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157389250:157389250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3344C>T
AA Mutation	p.Ser1115Phe(p.S1115F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157307842:157307842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.877A>G
AA Mutation	p.Ser293Gly(p.S293G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157392953:157392953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371399881
CDS Mutation	c.3790C>T
AA Mutation	p.Arg1264Cys(p.R1264C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616178
Start	157325600:157325600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2019G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616178
Start	157339131:157339131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761084028
CDS Mutation	c.2535C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616178
Start	157389329:157389329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769817015
CDS Mutation	c.3423C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616178
Start	157285436:157285436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.75G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616178
Start	157341133:157341133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2724G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616178
Start	157296705:157296705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.318G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616178
Start	157392952:157392952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3789G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616178
Start	157319845:157319845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1440C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616178
Start	157339119:157339119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371132555
CDS Mutation	c.2523G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000616178
Start	157325556:157325556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1975C>T
AA Mutation	p.Arg659Ter(p.R659*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000616178
Start	157320671:157320671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1540C>T
AA Mutation	p.Arg514Ter(p.R514*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000616178
Start	157320701:157320701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1570C>T
AA Mutation	p.Arg524Ter(p.R524*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000616178
Start	157319855:157319856(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1450_1451insGA
AA Mutation	p.Gln484ArgfsTer7(p.Q484Rfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000616178
Start	157319857:157319858(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1452_1453insAAT
AA Mutation	p.Gln484_Asp485insAsn(p.Q484_D485insN)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CYFIP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157392851:157392851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749706783
CDS Mutation	c.3688G>A
AA Mutation	p.Asp1230Asn(p.D1230N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157304313:157304313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.742T>C
AA Mutation	p.Tyr248His(p.Y248H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000616178
Start	157359107:157359107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2851G>A
AA Mutation	p.Ala951Thr(p.A951T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616178
Start	157339131:157339131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761084028
CDS Mutation	c.2535C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616178
Start	157359052:157359052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764090706
CDS Mutation	c.2796C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616178
Start	157330760:157330760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2250T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616178
Start	157389386:157389386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267600516
CDS Mutation	c.3480C>T
Mutation Classification	Silent
Feature Type	Transcript