Colon Cancer: Gene >> NUTM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34357478:34357478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200540515
CDS Mutation	c.3386G>A
AA Mutation	p.Arg1129His(p.R1129H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34355557:34355557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150270874
CDS Mutation	c.1465G>A
AA Mutation	p.Ala489Thr(p.A489T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34355967:34355967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1875G>T
AA Mutation	p.Gln625His(p.Q625H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34356860:34356860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2768T>C
AA Mutation	p.Leu923Pro(p.L923P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34354494:34354494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775619864
CDS Mutation	c.1040G>A
AA Mutation	p.Arg347His(p.R347H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34348472:34348472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147118207
CDS Mutation	c.520C>T
AA Mutation	p.Pro174Ser(p.P174S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34354488:34354488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139446732
CDS Mutation	c.1034G>A
AA Mutation	p.Arg345His(p.R345H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34350762:34350762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784C>T
AA Mutation	p.Pro262Ser(p.P262S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34350748:34350748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.770T>C
AA Mutation	p.Leu257Pro(p.L257P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34354481:34354481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1027G>C
AA Mutation	p.Ala343Pro(p.A343P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34348013:34348013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.61G>A
AA Mutation	p.Ala21Thr(p.A21T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34348299:34348299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199644358
CDS Mutation	c.347C>T
AA Mutation	p.Ser116Leu(p.S116L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34354666:34354666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61737333
CDS Mutation	c.1212G>A
AA Mutation	p.Met404Ile(p.M404I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333756
Start	34348133:34348133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752993555
CDS Mutation	c.181C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333756
Start	34356534:34356534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2442A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333756
Start	34355070:34355070(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1332delA
AA Mutation	p.Lys444AsnfsTer8(p.K444Nfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333756
Start	34355644:34355644(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1556delG
AA Mutation	p.Gly519AlafsTer26(p.G519Afs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333756
Start	34356879:34356879(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2791delC
AA Mutation	p.Gln931LysfsTer53(p.Q931Kfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333756
Start	34356176:34356176(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2088delC
AA Mutation	p.Met697TrpfsTer28(p.M697Wfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NUTM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34348023:34348023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71C>A
AA Mutation	p.Pro24Gln(p.P24Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34356802:34356802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2710C>A
AA Mutation	p.Leu904Ile(p.L904I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333756
Start	34354664:34354664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1210A>C
AA Mutation	p.Met404Leu(p.M404L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333756
Start	34355826:34355826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1734C>G
Mutation Classification	Silent
Feature Type	Transcript