Colon Cancer: Gene >> APLNR

Mutation ID	1
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000257254
Start	57236055:57236055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200854787
CDS Mutation	c.950G>A
AA Mutation	p.Arg317His(p.R317H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000257254
Start	57236298:57236298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199589565
CDS Mutation	c.707G>A
AA Mutation	p.Arg236His(p.R236H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000257254
Start	57236224:57236224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.781T>C
AA Mutation	p.Trp261Arg(p.W261R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000257254
Start	57236820:57236820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.185G>A
AA Mutation	p.Arg62His(p.R62H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000257254
Start	57236554:57236554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451G>A
AA Mutation	p.Ala151Thr(p.A151T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000257254
Start	57236107:57236107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs7943508
CDS Mutation	c.898G>A
AA Mutation	p.Val300Ile(p.V300I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000257254
Start	57236503:57236503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373170562
CDS Mutation	c.502C>T
AA Mutation	p.Arg168Cys(p.R168C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant;NMD_transcript_variant
Transcription ID	ENST00000257254
Start	57236879:57236879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.126C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant;NMD_transcript_variant
Transcription ID	ENST00000257254
Start	57236867:57236867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138964036
CDS Mutation	c.138C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant;NMD_transcript_variant
Transcription ID	ENST00000257254
Start	57236462:57236462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749605299
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> APLNR

Mutation ID	1
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000257254
Start	57236832:57236832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753846480
CDS Mutation	c.173G>A
AA Mutation	p.Arg58Gln(p.R58Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant;NMD_transcript_variant
Transcription ID	ENST00000257254
Start	57236012:57236012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771763352
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript