Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EXPH5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108514509:108514509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998C>T
AA Mutation	p.Ala333Val(p.A333V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108511288:108511288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146870938
CDS Mutation	c.4219G>A
AA Mutation	p.Glu1407Lys(p.E1407K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108513125:108513125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2382A>C
AA Mutation	p.Gln794His(p.Q794H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108513696:108513696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1811C>A
AA Mutation	p.Ser604Tyr(p.S604Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108514128:108514128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1379C>A
AA Mutation	p.Ser460Tyr(p.S460Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108510228:108510228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5279C>A
AA Mutation	p.Pro1760His(p.P1760H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108510511:108510511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4996G>A
AA Mutation	p.Val1666Met(p.V1666M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108512271:108512271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3236A>T
AA Mutation	p.Asn1079Ile(p.N1079I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108511751:108511751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761525773
CDS Mutation	c.3756A>G
AA Mutation	p.Ile1252Met(p.I1252M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108510930:108510930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4577A>G
AA Mutation	p.Asp1526Gly(p.D1526G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108510204:108510204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5303G>C
AA Mutation	p.Ser1768Thr(p.S1768T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108511389:108511389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4118A>G
AA Mutation	p.Lys1373Arg(p.K1373R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108513214:108513214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2293A>C
AA Mutation	p.Ser765Arg(p.S765R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108514704:108514704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.803A>C
AA Mutation	p.Asn268Thr(p.N268T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108514849:108514849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.658G>T
AA Mutation	p.Ala220Ser(p.A220S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108513159:108513159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2348T>C
AA Mutation	p.Ile783Thr(p.I783T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265843
Start	108510091:108510091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5416C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265843
Start	108514559:108514559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773292363
CDS Mutation	c.948T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265843
Start	108514190:108514190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767269195
CDS Mutation	c.1317C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265843
Start	108514610:108514610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.897G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265843
Start	108510953:108510953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4554G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265843
Start	108514781:108514781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.726C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265843
Start	108514475:108514475(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1032delT
AA Mutation	p.Pro345GlnfsTer45(p.P345Qfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000265843
Start	108513730:108513730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1777A>T
AA Mutation	p.Lys593Ter(p.K593*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000265843
Start	108511369:108511369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4138G>T
AA Mutation	p.Glu1380Ter(p.E1380*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000265843
Start	108510415:108510415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755280942
CDS Mutation	c.5092C>T
AA Mutation	p.Arg1698Ter(p.R1698*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000265843
Start	108512743:108512743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2764G>T
AA Mutation	p.Glu922Ter(p.E922*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EXPH5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108514548:108514548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537870251
CDS Mutation	c.959C>T
AA Mutation	p.Ser320Leu(p.S320L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108511908:108511908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3599G>T
AA Mutation	p.Arg1200Ile(p.R1200I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108514358:108514358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1149G>T
AA Mutation	p.Glu383Asp(p.E383D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108528155:108528155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.473C>A
AA Mutation	p.Pro158His(p.P158H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108511930:108511930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3577G>C
AA Mutation	p.Gly1193Arg(p.G1193R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265843
Start	108514401:108514401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1106C>T
AA Mutation	p.Ser369Leu(p.S369L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265843
Start	108509642:108509642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548865935
CDS Mutation	c.5865G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265843
Start	108514781:108514781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.726C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265843
Start	108509990:108509990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5517C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265843
Start	108514547:108514547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770593653
CDS Mutation	c.960G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000265843
Start	108511285:108511285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4222G>T
AA Mutation	p.Glu1408Ter(p.E1408*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript