Colon Cancer: Gene >> CLMN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95204399:95204399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.950C>A
AA Mutation	p.Thr317Asn(p.T317N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95203799:95203799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78561092
CDS Mutation	c.1550G>A
AA Mutation	p.Arg517His(p.R517H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95203125:95203125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2224G>A
AA Mutation	p.Ala742Thr(p.A742T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95204262:95204262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774934404
CDS Mutation	c.1087C>T
AA Mutation	p.Arg363Cys(p.R363C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95203677:95203677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1672G>T
AA Mutation	p.Ala558Ser(p.A558S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95203743:95203743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1606G>T
AA Mutation	p.Asp536Tyr(p.D536Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95203077:95203077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2272G>A
AA Mutation	p.Glu758Lys(p.E758K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95203572:95203572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182308272
CDS Mutation	c.1777G>A
AA Mutation	p.Glu593Lys(p.E593K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95193903:95193903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2786T>C
AA Mutation	p.Val929Ala(p.V929A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95204117:95204117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1232G>A
AA Mutation	p.Arg411Lys(p.R411K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95202858:95202858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2491G>T
AA Mutation	p.Asp831Tyr(p.D831Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298912
Start	95210771:95210771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.717G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298912
Start	95203027:95203027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201976115
CDS Mutation	c.2322C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298912
Start	95213224:95213224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143229821
CDS Mutation	c.603G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298912
Start	95202894:95202894(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2455delC
AA Mutation	p.His819MetfsTer29(p.H819Mfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298912
Start	95196612:95196612(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2594delA
AA Mutation	p.Lys865ArgfsTer10(p.K865Rfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000298912
Start	95210843:95210843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645G>A
AA Mutation	p.Trp215Ter(p.W215*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CLMN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95204412:95204412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139154234
CDS Mutation	c.937C>T
AA Mutation	p.Arg313Cys(p.R313C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95203653:95203653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1696T>G
AA Mutation	p.Phe566Val(p.F566V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95204427:95204427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.922G>A
AA Mutation	p.Glu308Lys(p.E308K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298912
Start	95193861:95193861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2828G>T
AA Mutation	p.Arg943Leu(p.R943L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298912
Start	95203912:95203912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201041933
CDS Mutation	c.1437G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298912
Start	95204236:95204236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753946996
CDS Mutation	c.1113G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298912
Start	95196612:95196612(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2594delA
AA Mutation	p.Lys865ArgfsTer10(p.K865Rfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript