Colon Cancer: Gene >> CDK11B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407249
Start	1637130:1637130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778552932
CDS Mutation	c.1682G>A
AA Mutation	p.Arg561His(p.R561H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000407249
Start	1641945:1641945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.850G>A
AA Mutation	p.Asp284Asn(p.D284N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000407249
Start	1636785:1636785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1853C>T
AA Mutation	p.Ala618Val(p.A618V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000407249
Start	1637175:1637175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1637T>A
AA Mutation	p.Leu546Gln(p.L546Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000407249
Start	1638542:1638542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1339G>T
AA Mutation	p.Gly447Cys(p.G447C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000407249
Start	1636714:1636714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1924T>G
AA Mutation	p.Ser642Ala(p.S642A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000407249
Start	1640297:1640297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1270A>G
AA Mutation	p.Lys424Glu(p.K424E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000407249
Start	1636982:1636982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1754G>A
AA Mutation	p.Arg585Gln(p.R585Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000407249
Start	1641991:1641991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.804G>T
AA Mutation	p.Glu268Asp(p.E268D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407249
Start	1637783:1637783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1482T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407249
Start	1636951:1636951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1785C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407249
Start	1640439:1640439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1128G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407249
Start	1637148:1637161(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1651_1664delAAACACCTGCACGA
AA Mutation	p.Lys551GlnfsTer7(p.K551Qfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000407249
Start	1637843:1637845(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1420_1422delGAG
AA Mutation	p.Glu474del(p.E474del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000407249
Start	1637846:1637848(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1417_1419delAAG
AA Mutation	p.Lys473del(p.K473del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CDK11B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407249
Start	1645213:1645213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.544C>T
AA Mutation	p.Arg182Trp(p.R182W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript