Colon Cancer: Gene >> NUPL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258742
Start	23200500:23200500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027G>A
AA Mutation	p.Ala343Thr(p.A343T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258742
Start	23200620:23200620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1147G>T
AA Mutation	p.Asp383Tyr(p.D383Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258742
Start	23200422:23200422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949T>A
AA Mutation	p.Ser317Thr(p.S317T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258742
Start	23199477:23199477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629G>C
AA Mutation	p.Gly210Ala(p.G210A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258742
Start	23200207:23200207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.734A>C
AA Mutation	p.Asn245Thr(p.N245T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258742
Start	23185154:23185154(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.212delG
AA Mutation	p.Gly71AlafsTer51(p.G71Afs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258742
Start	23196734:23196734(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.580delA
AA Mutation	p.Ser194ValfsTer2(p.S194Vfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NUPL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258742
Start	23182165:23182165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.80G>T
AA Mutation	p.Gly27Val(p.G27V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258742
Start	23200693:23200693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1220C>G
AA Mutation	p.Thr407Ser(p.T407S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript