Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RDH12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267502
Start	67733796:67733796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.899C>T
AA Mutation	p.Ala300Val(p.A300V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267502
Start	67725175:67725175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264G>T
AA Mutation	p.Lys88Asn(p.K88N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267502
Start	67727091:67727091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115356583
CDS Mutation	c.559G>A
AA Mutation	p.Asp187Asn(p.D187N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267502
Start	67726080:67726080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373A>G
AA Mutation	p.Asn125Asp(p.N125D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RDH12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267502
Start	67725212:67725212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148334092
CDS Mutation	c.301G>A
AA Mutation	p.Asp101Asn(p.D101N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267502
Start	67725175:67725175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264G>T
AA Mutation	p.Lys88Asn(p.K88N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript