Colon Cancer: Gene >> STK36

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218679980:218679980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1036G>A
AA Mutation	p.Ala346Thr(p.A346T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218676082:218676082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.488C>T
AA Mutation	p.Thr163Ile(p.T163I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218690528:218690528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1737G>T
AA Mutation	p.Glu579Asp(p.E579D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218699344:218699344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141876461
CDS Mutation	c.3800A>G
AA Mutation	p.His1267Arg(p.H1267R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218697090:218697090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142521346
CDS Mutation	c.2638G>A
AA Mutation	p.Val880Ile(p.V880I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218697580:218697580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2879G>T
AA Mutation	p.Cys960Phe(p.C960F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218673641:218673641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.101T>C
AA Mutation	p.Phe34Ser(p.F34S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218673740:218673740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.200T>C
AA Mutation	p.Leu67Pro(p.L67P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218698910:218698910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3366G>T
AA Mutation	p.Glu1122Asp(p.E1122D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000295709
Start	218701867:218701867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3806T>C
AA Mutation	p.Val1269Ala(p.V1269A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218698735:218698735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746785758
CDS Mutation	c.3191C>T
AA Mutation	p.Ser1064Leu(p.S1064L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295709
Start	218697923:218697923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781197058
CDS Mutation	c.2979G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295709
Start	218673935:218673935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185827846
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295709
Start	218692590:218692590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140295724
CDS Mutation	c.1923G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295709
Start	218693734:218693734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2160C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295709
Start	218694584:218694584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2460G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295709
Start	218699237:218699237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762005504
CDS Mutation	c.3693C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295709
Start	218679639:218679639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761675217
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295709
Start	218698736:218698736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770915285
CDS Mutation	c.3192G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295709
Start	218673708:218673708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000295709
Start	218697194:218697194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2742G>A
AA Mutation	p.Trp914Ter(p.W914*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> STK36

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218692687:218692687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751003140
CDS Mutation	c.2020G>A
AA Mutation	p.Asp674Asn(p.D674N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218679584:218679584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.803A>C
AA Mutation	p.Asp268Ala(p.D268A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218698612:218698612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3068A>G
AA Mutation	p.Tyr1023Cys(p.Y1023C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295709
Start	218697092:218697092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2640T>C
Mutation Classification	Silent
Feature Type	Transcript