Colon Cancer: Gene >> MST1R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49896349:49896349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769911110
CDS Mutation	c.2495G>A
AA Mutation	p.Arg832Gln(p.R832Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49891263:49891263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3578C>A
AA Mutation	p.Ala1193Asp(p.A1193D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49890024:49890024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752084153
CDS Mutation	c.3847C>T
AA Mutation	p.Arg1283Trp(p.R1283W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49902981:49902981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629G>T
AA Mutation	p.Ser210Ile(p.S210I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49902982:49902982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.628A>G
AA Mutation	p.Ser210Gly(p.S210G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49896238:49896238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772475555
CDS Mutation	c.2606A>G
AA Mutation	p.Asn869Ser(p.N869S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49903404:49903404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206C>T
AA Mutation	p.Ala69Val(p.A69V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49902591:49902591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1019C>T
AA Mutation	p.Ala340Val(p.A340V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49903014:49903014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.596T>C
AA Mutation	p.Val199Ala(p.V199A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49899191:49899191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531433657
CDS Mutation	c.1303C>T
AA Mutation	p.Arg435Cys(p.R435C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49891260:49891260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560835056
CDS Mutation	c.3581G>A
AA Mutation	p.Arg1194His(p.R1194H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49887338:49887338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541003810
CDS Mutation	c.4172G>A
AA Mutation	p.Arg1391Gln(p.R1391Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49897406:49897406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2057T>C
AA Mutation	p.Leu686Pro(p.L686P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49895203:49895203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780949671
CDS Mutation	c.3235C>T
AA Mutation	p.Arg1079Trp(p.R1079W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000296474
Start	49891814:49891814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3296G>C
AA Mutation	p.Gly1099Ala(p.G1099A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296474
Start	49899212:49899212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296474
Start	49887544:49887544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3966A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296474
Start	49896794:49896800(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2274_2280delACCTGGT
AA Mutation	p.Ser761ProfsTer11(p.S761Pfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296474
Start	49896810:49896810(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2264delG
AA Mutation	p.Gly755ValfsTer19(p.G755Vfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000296474
Start	49896194:49896194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2649+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MST1R

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296474
Start	49895806:49895806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2871G>A
Mutation Classification	Silent
Feature Type	Transcript