Colon Cancer: Gene >> CCNL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000400809
Start	1398315:1398315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391G>A
AA Mutation	p.Ala131Thr(p.A131T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000400809
Start	1387274:1387274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151152085
CDS Mutation	c.1520G>A
AA Mutation	p.Arg507His(p.R507H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000400809
Start	1395452:1395452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536C>G
AA Mutation	p.Ala179Gly(p.A179G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000400809
Start	1395419:1395419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569G>A
AA Mutation	p.Cys190Tyr(p.C190Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000400809
Start	1387488:1387488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146517668
CDS Mutation	c.1306G>A
AA Mutation	p.Ala436Thr(p.A436T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000400809
Start	1399165:1399165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142A>T
AA Mutation	p.Thr48Ser(p.T48S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000400809
Start	1390797:1390797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.728C>T
AA Mutation	p.Ala243Val(p.A243V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000400809
Start	1395417:1395417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767154963
CDS Mutation	c.571G>A
AA Mutation	p.Val191Ile(p.V191I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000400809
Start	1390260:1390260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.976A>G
AA Mutation	p.Thr326Ala(p.T326A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CCNL2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400809
Start	1390348:1390348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888T>C
Mutation Classification	Silent
Feature Type	Transcript