Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SORD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267814
Start	45073382:45073382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764998822
CDS Mutation	c.926C>T
AA Mutation	p.Ser309Leu(p.S309L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267814
Start	45072335:45072335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.805A>G
AA Mutation	p.Asn269Asp(p.N269D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267814
Start	45073455:45073455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.999G>T
AA Mutation	p.Glu333Asp(p.E333D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267814
Start	45061190:45061190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.389G>A
AA Mutation	p.Cys130Tyr(p.C130Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000267814
Start	45072372:45072372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.842C>T
AA Mutation	p.Thr281Ile(p.T281I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267814
Start	45073398:45073398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746503166
CDS Mutation	c.942G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267814
Start	45061167:45061167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11542063
CDS Mutation	c.366G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SORD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267814
Start	45073505:45073505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1049G>T
AA Mutation	p.Cys350Phe(p.C350F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267814
Start	45061174:45061174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754952217
CDS Mutation	c.373G>A
AA Mutation	p.Asp125Asn(p.D125N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267814
Start	45073382:45073382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764998822
CDS Mutation	c.926C>T
AA Mutation	p.Ser309Leu(p.S309L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267814
Start	45073494:45073494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038C>A
Mutation Classification	Silent
Feature Type	Transcript