Colon Cancer: Gene >> UBAP2L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154227331:154227331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.140A>T
AA Mutation	p.Asp47Val(p.D47V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154251607:154251607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375698253
CDS Mutation	c.1618G>A
AA Mutation	p.Ala540Thr(p.A540T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154234729:154234729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771701488
CDS Mutation	c.418C>T
AA Mutation	p.Arg140Trp(p.R140W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154254003:154254003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1768C>T
AA Mutation	p.Pro590Ser(p.P590S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154255694:154255694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746135849
CDS Mutation	c.2096C>T
AA Mutation	p.Thr699Met(p.T699M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154260957:154260957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2644C>G
AA Mutation	p.Pro882Ala(p.P882A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154251064:154251064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528881045
CDS Mutation	c.1237G>A
AA Mutation	p.Ala413Thr(p.A413T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154237032:154237032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.599A>G
AA Mutation	p.Asn200Ser(p.N200S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154251182:154251182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202092808
CDS Mutation	c.1355C>T
AA Mutation	p.Pro452Leu(p.P452L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154255157:154255157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1915A>G
AA Mutation	p.Thr639Ala(p.T639A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154270263:154270263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3232G>A
AA Mutation	p.Ala1078Thr(p.A1078T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154253913:154253913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1678A>T
AA Mutation	p.Thr560Ser(p.T560S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361546
Start	154255701:154255701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2103G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361546
Start	154243273:154243273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748375079
CDS Mutation	c.813G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361546
Start	154227332:154227332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> UBAP2L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154246260:154246260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899C>G
AA Mutation	p.Ser300Cys(p.S300C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154251634:154251634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1645C>A
AA Mutation	p.Leu549Met(p.L549M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361546
Start	154251599:154251599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1610C>T
AA Mutation	p.Thr537Ile(p.T537I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361546
Start	154268768:154268768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2982G>A
Mutation Classification	Silent
Feature Type	Transcript