Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RSPH14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216036
Start	23059536:23059536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771042436
CDS Mutation	c.973G>A
AA Mutation	p.Glu325Lys(p.E325K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216036
Start	23061932:23061932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667G>A
AA Mutation	p.Gly223Ser(p.G223S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216036
Start	23063920:23063920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375976017
CDS Mutation	c.635G>A
AA Mutation	p.Arg212His(p.R212H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216036
Start	23140348:23140348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73C>A
AA Mutation	p.His25Asn(p.H25N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216036
Start	23063924:23063924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145095630
CDS Mutation	c.631G>A
AA Mutation	p.Ala211Thr(p.A211T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216036
Start	23064120:23064120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RSPH14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216036
Start	23059476:23059476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1033G>A
AA Mutation	p.Glu345Lys(p.E345K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216036
Start	23063961:23063961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.594G>T
AA Mutation	p.Lys198Asn(p.K198N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216036
Start	23063928:23063928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627G>A
Mutation Classification	Silent
Feature Type	Transcript