Colon Cancer: Gene >> TSSK1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434797:113434797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43G>T
AA Mutation	p.Gly15Trp(p.G15W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434074:113434074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.766G>A
AA Mutation	p.Asp256Asn(p.D256N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434061:113434061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535839960
CDS Mutation	c.779G>A
AA Mutation	p.Arg260Gln(p.R260Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434118:113434118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.722T>C
AA Mutation	p.Leu241Pro(p.L241P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434724:113434724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116C>T
AA Mutation	p.Ala39Val(p.A39V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434563:113434563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373083902
CDS Mutation	c.277G>A
AA Mutation	p.Ala93Thr(p.A93T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434197:113434197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643C>T
AA Mutation	p.Pro215Ser(p.P215S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434506:113434506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334G>A
AA Mutation	p.Glu112Lys(p.E112K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434483:113434483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357G>T
AA Mutation	p.Gln119His(p.Q119H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434101:113434101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739G>A
AA Mutation	p.Asp247Asn(p.D247N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434443:113434443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397G>A
AA Mutation	p.Val133Ile(p.V133I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434238:113434238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.602G>A
AA Mutation	p.Ser201Asn(p.S201N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434206:113434206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770870954
CDS Mutation	c.634G>A
AA Mutation	p.Gly212Ser(p.G212S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434188:113434188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.652G>A
AA Mutation	p.Asp218Asn(p.D218N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434508:113434508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332A>T
AA Mutation	p.Asp111Val(p.D111V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000390666
Start	113434123:113434123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000390666
Start	113434273:113434273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.567C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000390666
Start	113434207:113434207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147355003
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000390666
Start	113434831:113434831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192415501
CDS Mutation	c.9C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000390666
Start	113434723:113434723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.117G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000390666
Start	113434576:113434576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.264C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000390666
Start	113433811:113433811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000390666
Start	113433765:113433765(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs771835235
CDS Mutation	c.1075delC
AA Mutation	p.Gln359AsnfsTer43(p.Q359Nfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TSSK1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000390666
Start	113434131:113434131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55738530
CDS Mutation	c.709C>T
AA Mutation	p.Arg237Cys(p.R237C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000390666
Start	113434429:113434429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000390666
Start	113434762:113434762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000390666
Start	113434815:113434815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767886872
CDS Mutation	c.25C>T
AA Mutation	p.Arg9Ter(p.R9*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript