Colon Cancer: Gene >> HNRNPUL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301785
Start	62722836:62722836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.959T>C
AA Mutation	p.Val320Ala(p.V320A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301785
Start	62722700:62722700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.996C>A
AA Mutation	p.Phe332Leu(p.F332L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301785
Start	62724376:62724376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589C>T
AA Mutation	p.Arg197Trp(p.R197W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000301785
Start	62724292:62724292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673C>A
AA Mutation	p.Arg225Ser(p.R225S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301785
Start	62720038:62720038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1765A>C
AA Mutation	p.Met589Leu(p.M589L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301785
Start	62722824:62722824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761674867
CDS Mutation	c.971G>A
AA Mutation	p.Arg324His(p.R324H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301785
Start	62722364:62722364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1112A>C
AA Mutation	p.Glu371Ala(p.E371A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301785
Start	62720072:62720072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1731G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301785
Start	62715933:62715933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748222976
CDS Mutation	c.1986C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301785
Start	62715900:62715900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367678403
CDS Mutation	c.2019C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301785
Start	62722688:62722688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1008C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000301785
Start	62717010:62717010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1960C>T
AA Mutation	p.Arg654Ter(p.R654*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000301785
Start	62726880:62726880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.277G>T
AA Mutation	p.Glu93Ter(p.E93*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPUL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301785
Start	62722377:62722377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099T>G
AA Mutation	p.Phe367Val(p.F367V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000301785
Start	62724424:62724424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541G>T
AA Mutation	p.Asp181Tyr(p.D181Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript