Colon Cancer: Gene >> SKA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314759
Start	21168297:21168297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.434G>A
AA Mutation	p.Ser145Asn(p.S145N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314759
Start	21161872:21161872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747G>T
AA Mutation	p.Glu249Asp(p.E249D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314759
Start	21168048:21168048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.683A>T
AA Mutation	p.Tyr228Phe(p.Y228F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314759
Start	21172660:21172660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.125G>T
AA Mutation	p.Arg42Ile(p.R42I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000314759
Start	21168141:21168141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590T>C
AA Mutation	p.Leu197Pro(p.L197P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000314759
Start	21168271:21168271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.460C>T
AA Mutation	p.Arg154Cys(p.R154C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000314759
Start	21168229:21168229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146011474
CDS Mutation	c.502G>A
AA Mutation	p.Val168Ile(p.V168I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314759
Start	21159959:21159959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000314759
Start	21158088:21158088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.953C>A
AA Mutation	p.Ser318Ter(p.S318*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SKA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314759
Start	21158020:21158020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1021T>G
AA Mutation	p.Leu341Val(p.L341V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314759
Start	21168120:21168120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611C>A
AA Mutation	p.Pro204Gln(p.P204Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314759
Start	21168145:21168145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.586T>C
AA Mutation	p.Ser196Pro(p.S196P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314759
Start	21172656:21172656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129T>G
AA Mutation	p.Ile43Met(p.I43M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript