Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SPERT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310521
Start	45714274:45714274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1249G>A
AA Mutation	p.Val417Met(p.V417M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310521
Start	45713224:45713224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199A>T
AA Mutation	p.Ser67Cys(p.S67C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310521
Start	45713447:45713447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376455643
CDS Mutation	c.422G>A
AA Mutation	p.Arg141His(p.R141H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310521
Start	45714322:45714322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1297G>A
AA Mutation	p.Ala433Thr(p.A433T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310521
Start	45713306:45713306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.281G>A
AA Mutation	p.Arg94His(p.R94H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310521
Start	45714145:45714145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1120C>T
AA Mutation	p.Arg374Trp(p.R374W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310521
Start	45714079:45714079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054G>A
AA Mutation	p.Gly352Ser(p.G352S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000310521
Start	45713695:45713695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.670G>A
AA Mutation	p.Ala224Thr(p.A224T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000310521
Start	45713776:45713776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143200378
CDS Mutation	c.751C>T
AA Mutation	p.Arg251Trp(p.R251W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000310521
Start	45713426:45713426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754097956
CDS Mutation	c.401G>A
AA Mutation	p.Arg134His(p.R134H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000310521
Start	45713251:45713251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226G>A
AA Mutation	p.Ala76Thr(p.A76T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310521
Start	45713250:45713250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779454032
CDS Mutation	c.225C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310521
Start	45713832:45713832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.807G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SPERT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310521
Start	45713239:45713239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761413589
CDS Mutation	c.214G>A
AA Mutation	p.Ala72Thr(p.A72T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310521
Start	45714274:45714274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1249G>A
AA Mutation	p.Val417Met(p.V417M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310521
Start	45713194:45713194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.169G>A
AA Mutation	p.Glu57Lys(p.E57K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310521
Start	45713673:45713673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.648G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310521
Start	45713397:45713397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372C>T
Mutation Classification	Silent
Feature Type	Transcript