Colon Cancer: Gene >> AKAP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50193556:50193556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157G>A
AA Mutation	p.Cys386Tyr(p.C386Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50192965:50192965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1748A>G
AA Mutation	p.Gln583Arg(p.Q583R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50193906:50193906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.807G>C
AA Mutation	p.Lys269Asn(p.K269N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50193950:50193950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.763C>T
AA Mutation	p.Pro255Ser(p.P255S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50196906:50196906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781841685
CDS Mutation	c.261G>T
AA Mutation	p.Lys87Asn(p.K87N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50192466:50192466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2247G>T
AA Mutation	p.Gln749His(p.Q749H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50194141:50194141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572C>T
AA Mutation	p.Pro191Leu(p.P191L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50194103:50194103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610G>T
AA Mutation	p.Ala204Ser(p.A204S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50193771:50193771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942C>A
AA Mutation	p.Asp314Glu(p.D314E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50193416:50193416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1297G>A
AA Mutation	p.Ala433Thr(p.A433T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50192800:50192800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1913T>G
AA Mutation	p.Leu638Arg(p.L638R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50194271:50194271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442C>A
AA Mutation	p.His148Asn(p.H148N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50196968:50196968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>T
AA Mutation	p.Gly67Cys(p.G67C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358526
Start	50192943:50192943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1770C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358526
Start	50194278:50194278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358526
Start	50193792:50193792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.921C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358526
Start	50192634:50192634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782361715
CDS Mutation	c.2079C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358526
Start	50192893:50192893(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1820delC
AA Mutation	p.Pro607LeufsTer25(p.P607Lfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358526
Start	50193983:50193983(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.730delA
AA Mutation	p.Ser244AlafsTer38(p.S244Afs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000358526
Start	50193555:50193555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1158C>A
AA Mutation	p.Cys386Ter(p.C386*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358526
Start	50192610:50192611(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2102_2103insCCAAG
AA Mutation	p.Glu702GlnfsTer5(p.E702Qfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000358526
Start	50192612:50192613(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2100_2101insCTTCAT
AA Mutation	p.Leu700_Val701insLeuHis(p.L700_V701insLH)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> AKAP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50194277:50194277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.436G>A
AA Mutation	p.Glu146Lys(p.E146K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50196909:50196909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258G>T
AA Mutation	p.Glu86Asp(p.E86D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358526
Start	50194370:50194370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343C>A
AA Mutation	p.Leu115Ile(p.L115I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358526
Start	50192637:50192637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2076G>A
Mutation Classification	Silent
Feature Type	Transcript