Colon Cancer: Gene >> GNL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373062
Start	37566880:37566880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199557756
CDS Mutation	c.2171G>A
AA Mutation	p.Arg724His(p.R724H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373062
Start	37569124:37569124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1595A>C
AA Mutation	p.Asn532Thr(p.N532T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373062
Start	37568851:37568851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1868G>T
AA Mutation	p.Arg623Ile(p.R623I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373062
Start	37583895:37583895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608C>G
AA Mutation	p.Ser203Cys(p.S203C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373062
Start	37576521:37576521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.945C>A
AA Mutation	p.Phe315Leu(p.F315L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373062
Start	37590764:37590764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326T>G
AA Mutation	p.Val109Gly(p.V109G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373062
Start	37566942:37566942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754537333
CDS Mutation	c.2109C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373062
Start	37568306:37568306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370049441
CDS Mutation	c.1920A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373062
Start	37592728:37592728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.228A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373062
Start	37587388:37587388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373062
Start	37568946:37568946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200495851
CDS Mutation	c.1773C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000373062
Start	37593844:37593844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201910888
CDS Mutation	c.67C>T
AA Mutation	p.Arg23Ter(p.R23*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_lost
Transcription ID	ENST00000373062
Start	37566855:37566855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2196A>C
AA Mutation	p.Ter732TyrextTer7(p.*732Yext*7)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GNL2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373062
Start	37587311:37587311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.569G>T
AA Mutation	p.Arg190Ile(p.R190I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript