Colon Cancer: Gene >> CSNK1A1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379800
Start	37104581:37104581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676G>A
AA Mutation	p.Ala226Thr(p.A226T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379800
Start	37104787:37104787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470A>G
AA Mutation	p.Asp157Gly(p.D157G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379800
Start	37104948:37104948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.309C>A
AA Mutation	p.Phe103Leu(p.F103L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379800
Start	37104466:37104466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.791G>A
AA Mutation	p.Arg264His(p.R264H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379800
Start	37104407:37104407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776982240
CDS Mutation	c.850C>A
AA Mutation	p.Leu284Ile(p.L284I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379800
Start	37105249:37105249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8A>C
AA Mutation	p.Asn3Thr(p.N3T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379800
Start	37104412:37104412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759977373
CDS Mutation	c.845G>A
AA Mutation	p.Arg282His(p.R282H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379800
Start	37104955:37104955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302T>A
AA Mutation	p.Phe101Tyr(p.F101Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000379800
Start	37104376:37104376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.881A>T
AA Mutation	p.Tyr294Phe(p.Y294F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379800
Start	37104489:37104489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379800
Start	37104903:37104903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379800
Start	37105242:37105242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768049929
CDS Mutation	c.15C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379800
Start	37104300:37104300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.957C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379800
Start	37104300:37104300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000379800
Start	37105024:37105024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.233G>A
AA Mutation	p.Trp78Ter(p.W78*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379800
Start	37104267:37104268(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs551077397
CDS Mutation	c.989dupA
AA Mutation	p.Asn330LysfsTer4(p.N330Kfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379800
Start	37104566:37104567(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs769712615
CDS Mutation	c.690dupA
AA Mutation	p.Gln231ThrfsTer4(p.Q231Tfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CSNK1A1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379800
Start	37105136:37105136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121G>A
AA Mutation	p.Glu41Lys(p.E41K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379800
Start	37104457:37104457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546173732
CDS Mutation	c.800G>A
AA Mutation	p.Arg267His(p.R267H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379800
Start	37104348:37104348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.909G>C
AA Mutation	p.Gln303His(p.Q303H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379800
Start	37104865:37104865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375626846
CDS Mutation	c.392A>G
AA Mutation	p.Asn131Ser(p.N131S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379800
Start	37104489:37104489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379800
Start	37104360:37104360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781264924
CDS Mutation	c.897G>A
Mutation Classification	Silent
Feature Type	Transcript