Colon Cancer: Gene >> BLK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259089
Start	11563095:11563095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751422253
CDS Mutation	c.1297C>T
AA Mutation	p.Arg433Trp(p.R433W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259089
Start	11556766:11556766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.881A>C
AA Mutation	p.Glu294Ala(p.E294A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259089
Start	11543333:11543333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.109C>T
AA Mutation	p.Pro37Ser(p.P37S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000259089
Start	11555405:11555405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.693G>T
AA Mutation	p.Gln231His(p.Q231H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000259089
Start	11554880:11554880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610C>T
AA Mutation	p.His204Tyr(p.H204Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000259089
Start	11546094:11546094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166C>A
AA Mutation	p.Leu56Met(p.L56M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000259089
Start	11563030:11563030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1232T>C
AA Mutation	p.Val411Ala(p.V411A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000259089
Start	11549055:11549055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371256341
CDS Mutation	c.301G>A
AA Mutation	p.Val101Ile(p.V101I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000259089
Start	11550236:11550236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.446T>G
AA Mutation	p.Leu149Arg(p.L149R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259089
Start	11555468:11555468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201158722
CDS Mutation	c.756C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259089
Start	11557984:11557984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.975G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000259089
Start	11555420:11555420(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.712delC
AA Mutation	p.Arg238GlyfsTer27(p.R238Gfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000259089
Start	11550251:11550251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.463delA
AA Mutation	p.Thr155ProfsTer10(p.T155Pfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BLK

Mutation ID	1
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000259089
Start	11562978:11562978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1181-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript