Colon Cancer: Gene >> NMUR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152405056:152405056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58G>T
AA Mutation	p.Asp20Tyr(p.D20Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152404393:152404393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.721C>A
AA Mutation	p.Leu241Ile(p.L241I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152392354:152392354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759161756
CDS Mutation	c.1085G>A
AA Mutation	p.Arg362Gln(p.R362Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152404995:152404995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768254421
CDS Mutation	c.119G>A
AA Mutation	p.Arg40Gln(p.R40Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152404852:152404852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262G>A
AA Mutation	p.Ala88Thr(p.A88T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152395548:152395548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369018357
CDS Mutation	c.848C>T
AA Mutation	p.Pro283Leu(p.P283L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152392276:152392276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1163T>C
AA Mutation	p.Met388Thr(p.M388T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152404690:152404690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424G>A
AA Mutation	p.Val142Met(p.V142M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152404992:152404992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779708928
CDS Mutation	c.122G>A
AA Mutation	p.Arg41His(p.R41H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152404762:152404762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352G>T
AA Mutation	p.Gly118Cys(p.G118C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152404442:152404442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.672C>A
AA Mutation	p.Phe224Leu(p.F224L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152404512:152404512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200730009
CDS Mutation	c.602C>T
AA Mutation	p.Ser201Leu(p.S201L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152404444:152404444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.670T>G
AA Mutation	p.Phe224Val(p.F224V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152404783:152404783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331C>T
AA Mutation	p.Pro111Ser(p.P111S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152404635:152404635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.479G>A
AA Mutation	p.Arg160Gln(p.R160Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255262
Start	152404880:152404880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.234G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255262
Start	152395532:152395532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.864A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255262
Start	152392413:152392413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1026C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255262
Start	152395562:152395562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000255262
Start	152392199:152392199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1240A>T
AA Mutation	p.Lys414Ter(p.K414*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255262
Start	152392451:152392452(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.987_988insGAGAGGG
AA Mutation	p.Leu330GlufsTer27(p.L330Efs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NMUR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152404500:152404500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614C>T
AA Mutation	p.Thr205Met(p.T205M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152392228:152392228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1211G>T
AA Mutation	p.Arg404Ile(p.R404I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000255262
Start	152405099:152405099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.15A>C
AA Mutation	p.Glu5Asp(p.E5D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255262
Start	152404463:152404463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.651C>A
Mutation Classification	Silent
Feature Type	Transcript