Colon Cancer: Gene >> CSNK2A2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262506
Start	58197633:58197633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104G>A
AA Mutation	p.Gly35Asp(p.G35D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262506
Start	58167776:58167776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.533G>A
AA Mutation	p.Gly178Asp(p.G178D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262506
Start	58196821:58196821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128T>C
AA Mutation	p.Val43Ala(p.V43A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262506
Start	58197637:58197637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.100T>C
AA Mutation	p.Trp34Arg(p.W34R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262506
Start	58165676:58165676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.860A>T
AA Mutation	p.His287Leu(p.H287L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262506
Start	58174477:58174477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403C>T
AA Mutation	p.Arg135Trp(p.R135W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262506
Start	58196786:58196786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.163T>G
AA Mutation	p.Phe55Val(p.F55V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262506
Start	58186777:58186777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.296T>A
AA Mutation	p.Ile99Asn(p.I99N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262506
Start	58166677:58166677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.734G>A
AA Mutation	p.Arg245His(p.R245H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262506
Start	58186827:58186827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246G>T
AA Mutation	p.Glu82Asp(p.E82D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262506
Start	58197690:58197690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.47T>C
AA Mutation	p.Val16Ala(p.V16A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262506
Start	58186843:58186843(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.230delA
AA Mutation	p.Lys77ArgfsTer3(p.K77Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CSNK2A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262506
Start	58186835:58186835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238A>C
AA Mutation	p.Lys80Gln(p.K80Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript