Colon Cancer: Gene >> SLK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	104002464:104002464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286A>C
AA Mutation	p.Lys429Thr(p.K429T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	104021692:104021692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3520G>A
AA Mutation	p.Glu1174Lys(p.E1174K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	104001563:104001563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.984A>T
AA Mutation	p.Glu328Asp(p.E328D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	104003121:104003121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1943C>T
AA Mutation	p.Thr648Ile(p.T648I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	104001497:104001497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.918G>T
AA Mutation	p.Glu306Asp(p.E306D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	104020593:104020593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775081236
CDS Mutation	c.3427C>T
AA Mutation	p.Arg1143Cys(p.R1143C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	104005631:104005631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2420T>C
AA Mutation	p.Val807Ala(p.V807A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	103993023:103993023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404T>C
AA Mutation	p.Val135Ala(p.V135A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	104002283:104002283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140715399
CDS Mutation	c.1105C>T
AA Mutation	p.Arg369Cys(p.R369C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	104002968:104002968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1790C>A
AA Mutation	p.Thr597Asn(p.T597N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	104003200:104003200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2022A>C
AA Mutation	p.Lys674Asn(p.K674N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	103999909:103999909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.825G>T
AA Mutation	p.Lys275Asn(p.K275N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	103990729:103990729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.205T>G
AA Mutation	p.Ser69Ala(p.S69A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369755
Start	104002507:104002507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1329C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369755
Start	104003401:104003401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2223G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369755
Start	104002255:104002255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1077T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369755
Start	104018250:104018251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2975_2976delAG
AA Mutation	p.Glu992ValfsTer4(p.E992Vfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000369755
Start	104008273:104008273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777801234
CDS Mutation	c.2701C>T
AA Mutation	p.Arg901Ter(p.R901*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000369755
Start	104003351:104003351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2173G>T
AA Mutation	p.Glu725Ter(p.E725*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369755
Start	104018249:104018250(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2975_2976dupAG
AA Mutation	p.Cys993SerfsTer3(p.C993Sfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	103993048:103993048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.429G>T
AA Mutation	p.Leu143Phe(p.L143F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	104003042:104003042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1864A>C
AA Mutation	p.Asn622His(p.N622H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	104002214:104002214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759799710
CDS Mutation	c.1036G>A
AA Mutation	p.Ala346Thr(p.A346T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369755
Start	104025621:104025621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3609C>A
AA Mutation	p.Phe1203Leu(p.F1203L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369755
Start	104003206:104003206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2028T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369755
Start	104010833:104010833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2802G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000369755
Start	104002646:104002646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1468G>T
AA Mutation	p.Glu490Ter(p.E490*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript