Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SFRP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220772
Start	41308760:41308760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400G>A
AA Mutation	p.Glu134Lys(p.E134K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220772
Start	41265267:41265267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761465184
CDS Mutation	c.845C>T
AA Mutation	p.Thr282Met(p.T282M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220772
Start	41309063:41309063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.97G>A
AA Mutation	p.Glu33Lys(p.E33K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220772
Start	41308635:41308635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761271626
CDS Mutation	c.525C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220772
Start	41308743:41308743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.417G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SFRP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220772
Start	41309057:41309057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.103G>A
AA Mutation	p.Asp35Asn(p.D35N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220772
Start	41308777:41308777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383C>T
AA Mutation	p.Pro128Leu(p.P128L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220772
Start	41308703:41308703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457G>A
AA Mutation	p.Glu153Lys(p.E153K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript