Colon Cancer: Gene >> BCKDK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219794
Start	31112005:31112005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755584594
CDS Mutation	c.1072G>A
AA Mutation	p.Ala358Thr(p.A358T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219794
Start	31109527:31109527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.212C>T
AA Mutation	p.Thr71Met(p.T71M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219794
Start	31110488:31110488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631C>T
AA Mutation	p.His211Tyr(p.H211Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000219794
Start	31110715:31110715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762515151
CDS Mutation	c.670C>T
AA Mutation	p.Arg224Cys(p.R224C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000219794
Start	31112222:31112222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766922526
CDS Mutation	c.1196G>A
AA Mutation	p.Arg399Gln(p.R399Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000219794
Start	31109311:31109311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.88C>T
AA Mutation	p.Arg30Cys(p.R30C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000219794
Start	31110093:31110093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.392G>A
AA Mutation	p.Arg131His(p.R131H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000219794
Start	31111894:31111894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201445468
CDS Mutation	c.961G>A
AA Mutation	p.Ala321Thr(p.A321T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219794
Start	31112235:31112235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377552512
CDS Mutation	c.1209C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219794
Start	31110711:31110711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219794
Start	31112154:31112154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749211768
CDS Mutation	c.1128C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219794
Start	31110436:31110436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756441659
CDS Mutation	c.579G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219794
Start	31109546:31109546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BCKDK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219794
Start	31109566:31109566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251G>A
AA Mutation	p.Gly84Asp(p.G84D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript