Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLC33A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359479
Start	155828235:155828235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767960891
CDS Mutation	c.1625C>T
AA Mutation	p.Ser542Leu(p.S542L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359479
Start	155828295:155828295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1565T>G
AA Mutation	p.Phe522Cys(p.F522C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359479
Start	155853847:155853847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151G>A
AA Mutation	p.Ala51Thr(p.A51T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359479
Start	155842549:155842549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359479
Start	155853629:155853629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.369A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359479
Start	155853385:155853385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC33A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359479
Start	155829753:155829753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1417C>G
AA Mutation	p.Pro473Ala(p.P473A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359479
Start	155828235:155828235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767960891
CDS Mutation	c.1625C>T
AA Mutation	p.Ser542Leu(p.S542L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript