Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CABIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24064062:24064062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1912T>C
AA Mutation	p.Tyr638His(p.Y638H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24043019:24043019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461A>T
AA Mutation	p.Asn154Ile(p.N154I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24166870:24166870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148733148
CDS Mutation	c.5239C>T
AA Mutation	p.Arg1747Trp(p.R1747W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24056275:24056275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177C>T
AA Mutation	p.Arg393Trp(p.R393W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24165609:24165609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4990C>G
AA Mutation	p.Leu1664Val(p.L1664V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24050893:24050893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.725G>T
AA Mutation	p.Gly242Val(p.G242V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24098045:24098045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3970C>T
AA Mutation	p.His1324Tyr(p.H1324Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24165553:24165553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4934G>A
AA Mutation	p.Arg1645His(p.R1645H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24167002:24167002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201053897
CDS Mutation	c.5371G>A
AA Mutation	p.Glu1791Lys(p.E1791K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24119631:24119631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4565G>A
AA Mutation	p.Arg1522His(p.R1522H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24056213:24056213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748459908
CDS Mutation	c.1115A>C
AA Mutation	p.Lys372Thr(p.K372T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24098081:24098081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4006T>C
AA Mutation	p.Ser1336Pro(p.S1336P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24171947:24171947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763783967
CDS Mutation	c.5992C>T
AA Mutation	p.Arg1998Trp(p.R1998W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24060047:24060047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567361031
CDS Mutation	c.1523C>T
AA Mutation	p.Ala508Val(p.A508V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24095979:24095979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767920054
CDS Mutation	c.3835G>A
AA Mutation	p.Asp1279Asn(p.D1279N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24050899:24050899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777390432
CDS Mutation	c.731G>A
AA Mutation	p.Arg244Gln(p.R244Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24171840:24171840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5885C>T
AA Mutation	p.Ala1962Val(p.A1962V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24036110:24036110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.25G>A
AA Mutation	p.Ala9Thr(p.A9T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24060089:24060089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1565G>A
AA Mutation	p.Ser522Asn(p.S522N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24171774:24171774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374113751
CDS Mutation	c.5819C>A
AA Mutation	p.Pro1940His(p.P1940H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24166648:24166648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749933147
CDS Mutation	c.5017C>T
AA Mutation	p.Arg1673Cys(p.R1673C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24085124:24085124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3236T>C
AA Mutation	p.Met1079Thr(p.M1079T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24059241:24059241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1277A>G
AA Mutation	p.Asp426Gly(p.D426G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24166657:24166657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5026C>T
AA Mutation	p.Pro1676Ser(p.P1676S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24176135:24176135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6065C>T
AA Mutation	p.Ala2022Val(p.A2022V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24171792:24171792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5837C>T
AA Mutation	p.Thr1946Ile(p.T1946I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24036098:24036098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13G>A
AA Mutation	p.Ala5Thr(p.A5T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24167270:24167270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139783753
CDS Mutation	c.5639G>A
AA Mutation	p.Arg1880His(p.R1880H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24091586:24091586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3529G>C
AA Mutation	p.Glu1177Gln(p.E1177Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263119
Start	24171850:24171850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5895G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263119
Start	24055071:24055071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774566464
CDS Mutation	c.1005C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263119
Start	24072482:24072482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2604G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263119
Start	24166686:24166686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5055G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263119
Start	24062978:24062978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1716T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263119
Start	24095942:24095942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3798G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000263119
Start	24171758:24171758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5803C>T
AA Mutation	p.Arg1935Ter(p.R1935*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CABIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24041257:24041257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.329T>C
AA Mutation	p.Met110Thr(p.M110T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24084733:24084733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3065C>A
AA Mutation	p.Pro1022Gln(p.P1022Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263119
Start	24043081:24043081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750428201
CDS Mutation	c.523A>G
AA Mutation	p.Thr175Ala(p.T175A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263119
Start	24070862:24070862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771270819
CDS Mutation	c.2295C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263119
Start	24050939:24050939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758954607
CDS Mutation	c.771G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263119
Start	24113615:24113615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374980657
CDS Mutation	c.4167G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000263119
Start	24165540:24165540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4921C>T
AA Mutation	p.Arg1641Ter(p.R1641*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript