Colon Cancer: Gene >> NBPF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318249
Start	21481665:21481665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753276257
CDS Mutation	c.1502C>T
AA Mutation	p.Ser501Leu(p.S501L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318249
Start	21445193:21445193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199755595
CDS Mutation	c.107G>A
AA Mutation	p.Arg36Gln(p.R36Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318249
Start	21468796:21468796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757791248
CDS Mutation	c.242G>A
AA Mutation	p.Arg81His(p.R81H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318249
Start	21483292:21483292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1808T>C
AA Mutation	p.Val603Ala(p.V603A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318249
Start	21471575:21471575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318249
Start	21470714:21470714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756854649
CDS Mutation	c.426C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318249
Start	21483251:21483251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1767G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318249
Start	21483320:21483321(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1842dupT
AA Mutation	p.Thr615TyrfsTer25(p.T615Yfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NBPF3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318249
Start	21481708:21481708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1545C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000318249
Start	21481663:21481663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1500T>G
AA Mutation	p.Tyr500Ter(p.Y500*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript