Colon Cancer: Gene >> HNRNPR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302271
Start	23310951:23310951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1405G>A
AA Mutation	p.Asp469Asn(p.D469N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302271
Start	23310984:23310984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1372T>A
AA Mutation	p.Tyr458Asn(p.Y458N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302271
Start	23321623:23321623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.716T>C
AA Mutation	p.Val239Ala(p.V239A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302271
Start	23310959:23310959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1397G>A
AA Mutation	p.Gly466Asp(p.G466D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302271
Start	23323595:23323595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200469820
CDS Mutation	c.636C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302271
Start	23311000:23311000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1356T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302271
Start	23310916:23310916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765435170
CDS Mutation	c.1440C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302271
Start	23310575:23310576(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1780_1781delTG
AA Mutation	p.Trp594GlyfsTer15(p.W594Gfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000302271
Start	23310831:23310831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1525C>T
AA Mutation	p.Arg509Ter(p.R509*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302271
Start	23313620:23313621(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1099_1100insAGAGATTAAA
AA Mutation	p.Leu367GlnfsTer19(p.L367Qfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPR

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302271
Start	23311260:23311260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1230G>A
Mutation Classification	Silent
Feature Type	Transcript