Colon Cancer: Gene >> NOP56

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329276
Start	2653376:2653376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.191C>T
AA Mutation	p.Ala64Val(p.A64V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000329276
Start	2657217:2657217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1418A>G
AA Mutation	p.Glu473Gly(p.E473G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329276
Start	2657172:2657172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763810400
CDS Mutation	c.1373C>T
AA Mutation	p.Ala458Val(p.A458V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329276
Start	2657995:2657995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1486A>C
AA Mutation	p.Met496Leu(p.M496L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329276
Start	2657934:2657934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541896402
CDS Mutation	c.1425G>A
AA Mutation	p.Met475Ile(p.M475I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329276
Start	2657179:2657179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1380G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329276
Start	2656793:2656793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146878231
CDS Mutation	c.1179C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329276
Start	2657209:2657209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1410G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329276
Start	2654930:2654930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329276
Start	2658150:2658150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546429113
CDS Mutation	c.1641T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329276
Start	2658036:2658036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1527G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329276
Start	2655629:2655629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147425088
CDS Mutation	c.792C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NOP56

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329276
Start	2658104:2658104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1595C>A
AA Mutation	p.Pro532His(p.P532H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329276
Start	2656537:2656537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1147G>A
AA Mutation	p.Asp383Asn(p.D383N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329276
Start	2657136:2657136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143140440
CDS Mutation	c.1337G>A
AA Mutation	p.Arg446His(p.R446H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329276
Start	2653309:2653309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.124T>G
AA Mutation	p.Phe42Val(p.F42V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000329276
Start	2657986:2657986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1477G>T
AA Mutation	p.Glu493Ter(p.E493*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript