Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GRID1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85728013:85728013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1375C>A
AA Mutation	p.Gln459Lys(p.Q459K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85647356:85647356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2039G>A
AA Mutation	p.Gly680Asp(p.G680D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85723109:85723109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138984541
CDS Mutation	c.1891C>T
AA Mutation	p.Arg631Cys(p.R631C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85724523:85724523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1687T>G
AA Mutation	p.Phe563Val(p.F563V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85856142:85856142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000T>A
AA Mutation	p.Phe334Ile(p.F334I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	86206376:86206376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779659096
CDS Mutation	c.508G>A
AA Mutation	p.Asp170Asn(p.D170N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85602454:85602454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2849A>G
AA Mutation	p.Asn950Ser(p.N950S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85647231:85647231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753413551
CDS Mutation	c.2164G>A
AA Mutation	p.Val722Met(p.V722M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85724569:85724569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1641G>T
AA Mutation	p.Lys547Asn(p.K547N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85620015:85620015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2212G>A
AA Mutation	p.Ala738Thr(p.A738T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000327946
Start	86206648:86206648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.236C>A
AA Mutation	p.Ala79Asp(p.A79D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85724388:85724388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536754961
CDS Mutation	c.1822G>A
AA Mutation	p.Ala608Thr(p.A608T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85869104:85869104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760195348
CDS Mutation	c.857C>T
AA Mutation	p.Pro286Leu(p.P286L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	86138848:86138848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.697C>A
AA Mutation	p.Pro233Thr(p.P233T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	86138985:86138985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768009874
CDS Mutation	c.560G>A
AA Mutation	p.Arg187Gln(p.R187Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	86138884:86138884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201655919
CDS Mutation	c.661C>T
AA Mutation	p.Arg221Trp(p.R221W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	86138866:86138866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368448368
CDS Mutation	c.679G>A
AA Mutation	p.Ala227Thr(p.A227T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	86206402:86206402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771100097
CDS Mutation	c.482G>A
AA Mutation	p.Arg161His(p.R161H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85647284:85647284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771133372
CDS Mutation	c.2111C>T
AA Mutation	p.Thr704Met(p.T704M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85602656:85602656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569741039
CDS Mutation	c.2647C>T
AA Mutation	p.Leu883Phe(p.L883F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85602667:85602667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536785868
CDS Mutation	c.2636G>A
AA Mutation	p.Arg879His(p.R879H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85602592:85602592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2711A>T
AA Mutation	p.Glu904Val(p.E904V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85916199:85916199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.767T>C
AA Mutation	p.Val256Ala(p.V256A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327946
Start	85602447:85602447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200390116
CDS Mutation	c.2856G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327946
Start	85602612:85602612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148112222
CDS Mutation	c.2691G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327946
Start	86138822:86138822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327946
Start	85602390:85602390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2913C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327946
Start	85724545:85724545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1665C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327946
Start	86206377:86206377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368572646
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327946
Start	85613512:85613512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763283212
CDS Mutation	c.2496C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327946
Start	85647331:85647331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2064T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327946
Start	85602522:85602522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2781C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327946
Start	85724422:85724422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1788G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327946
Start	85854565:85854565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1164G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000327946
Start	85724424:85724424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1786C>T
AA Mutation	p.Gln596Ter(p.Q596*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GRID1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85727868:85727868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1520A>C
AA Mutation	p.Glu507Ala(p.E507A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85727955:85727955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1433T>A
AA Mutation	p.Leu478Gln(p.L478Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	85723108:85723108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191266908
CDS Mutation	c.1892G>A
AA Mutation	p.Arg631His(p.R631H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000327946
Start	85916238:85916238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.728C>G
AA Mutation	p.Ala243Gly(p.A243G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327946
Start	86138979:86138979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.566G>A
AA Mutation	p.Gly189Asp(p.G189D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327946
Start	85724608:85724608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1602G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327946
Start	85619944:85619944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112935027
CDS Mutation	c.2283C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327946
Start	85602612:85602612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148112222
CDS Mutation	c.2691G>A
Mutation Classification	Silent
Feature Type	Transcript