Colon Cancer: Gene >> FSD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221856
Start	4310513:4310513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780907933
CDS Mutation	c.407C>T
AA Mutation	p.Ala136Val(p.A136V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221856
Start	4323033:4323033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148882494
CDS Mutation	c.1087G>A
AA Mutation	p.Glu363Lys(p.E363K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221856
Start	4306205:4306205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.119C>T
AA Mutation	p.Ser40Leu(p.S40L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000221856
Start	4311962:4311962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752149632
CDS Mutation	c.611G>A
AA Mutation	p.Arg204Gln(p.R204Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000221856
Start	4318922:4318922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776511823
CDS Mutation	c.1010G>A
AA Mutation	p.Arg337His(p.R337H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000221856
Start	4323435:4323435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375153495
CDS Mutation	c.1379C>T
AA Mutation	p.Thr460Met(p.T460M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000221856
Start	4318425:4318425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879G>T
AA Mutation	p.Met293Ile(p.M293I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221856
Start	4323179:4323179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1233C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221856
Start	4311849:4311849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749088245
CDS Mutation	c.498C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221856
Start	4323158:4323158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776188536
CDS Mutation	c.1212G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FSD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221856
Start	4311862:4311862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760189878
CDS Mutation	c.511G>A
AA Mutation	p.Asp171Asn(p.D171N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221856
Start	4305968:4305968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.38A>C
AA Mutation	p.Lys13Thr(p.K13T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221856
Start	4307968:4307968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761135570
CDS Mutation	c.330C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221856
Start	4318419:4318419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376149637
CDS Mutation	c.873C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221856
Start	4318482:4318482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144756712
CDS Mutation	c.936G>A
Mutation Classification	Silent
Feature Type	Transcript