Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LRRIQ3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74155839:74155839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601A>T
AA Mutation	p.Asn201Tyr(p.N201Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74041600:74041600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1331C>G
AA Mutation	p.Ala444Gly(p.A444G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74155775:74155775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.665T>C
AA Mutation	p.Val222Ala(p.V222A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74041238:74041238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1693T>G
AA Mutation	p.Leu565Val(p.L565V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74041357:74041357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374700532
CDS Mutation	c.1574G>A
AA Mutation	p.Arg525His(p.R525H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74183443:74183443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770907166
CDS Mutation	c.242G>A
AA Mutation	p.Gly81Glu(p.G81E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74109508:74109508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.753A>C
AA Mutation	p.Arg251Ser(p.R251S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74041660:74041660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757451201
CDS Mutation	c.1271A>G
AA Mutation	p.Asp424Gly(p.D424G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74041856:74041856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1075T>C
AA Mutation	p.Tyr359His(p.Y359H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74074707:74074707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.951A>C
AA Mutation	p.Lys317Asn(p.K317N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74041352:74041352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1579C>A
AA Mutation	p.Leu527Ile(p.L527I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74182572:74182572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571959184
CDS Mutation	c.539G>A
AA Mutation	p.Arg180Gln(p.R180Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74183635:74183635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50G>T
AA Mutation	p.Ser17Ile(p.S17I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74183660:74183660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.25G>A
AA Mutation	p.Glu9Lys(p.E9K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74155752:74155752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688T>G
AA Mutation	p.Leu230Val(p.L230V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74109435:74109435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826C>T
AA Mutation	p.Pro276Ser(p.P276S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354431
Start	74155782:74155782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374358600
CDS Mutation	c.658T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354431
Start	74041509:74041509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1422A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354431
Start	74182697:74182697(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs749244073
CDS Mutation	c.414delA
AA Mutation	p.Gly139AspfsTer20(p.G139Dfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354431
Start	74041797:74041797(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs751977298
CDS Mutation	c.1134delT
AA Mutation	p.Pro379LeufsTer26(p.P379Lfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354431
Start	74041707:74041707(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1224delT
AA Mutation	p.Phe408LeufsTer8(p.F408Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354431
Start	74155814:74155815(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.625dupA
AA Mutation	p.Ile209AsnfsTer2(p.I209Nfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354431
Start	74041381:74041382(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1549_1550insATTTTTCTGCTTT
AA Mutation	p.Leu517TyrfsTer11(p.L517Yfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LRRIQ3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74041683:74041683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1248A>T
AA Mutation	p.Lys416Asn(p.K416N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74155762:74155762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.678A>G
AA Mutation	p.Ile226Met(p.I226M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74041594:74041594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1337C>A
AA Mutation	p.Ala446Glu(p.A446E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74041398:74041398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1533G>C
AA Mutation	p.Lys511Asn(p.K511N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74041426:74041426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1505C>A
AA Mutation	p.Ala502Asp(p.A502D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74074732:74074732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.926C>A
AA Mutation	p.Ser309Tyr(p.S309Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74182772:74182772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.339G>T
AA Mutation	p.Lys113Asn(p.K113N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74041238:74041238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1693T>G
AA Mutation	p.Leu565Val(p.L565V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74182681:74182681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430C>A
AA Mutation	p.Leu144Ile(p.L144I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000354431
Start	74041246:74041246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1685G>T
AA Mutation	p.Arg562Ile(p.R562I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354431
Start	74183532:74183532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.153T>C
Mutation Classification	Silent
Feature Type	Transcript