Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MFF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000353339
Start	227340346:227340346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201498602
CDS Mutation	c.484C>T
AA Mutation	p.Arg162Cys(p.R162C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000353339
Start	227347380:227347380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748C>T
AA Mutation	p.Arg250Cys(p.R250C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000353339
Start	227355741:227355741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.877G>A
AA Mutation	p.Ala293Thr(p.A293T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000353339
Start	227330724:227330724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373709042
CDS Mutation	c.137G>A
AA Mutation	p.Arg46Gln(p.R46Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000353339
Start	227357056:227357056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.968T>G
AA Mutation	p.Val323Gly(p.V323G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353339
Start	227347238:227347238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555978161
CDS Mutation	c.606G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353339
Start	227330764:227330764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775384816
CDS Mutation	c.177C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000353339
Start	227330681:227330681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94C>T
AA Mutation	p.Arg32Ter(p.R32*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MFF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000353339
Start	227347350:227347350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.718C>A
AA Mutation	p.Gln240Lys(p.Q240K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000353339
Start	227340346:227340346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201498602
CDS Mutation	c.484C>T
AA Mutation	p.Arg162Cys(p.R162C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000353339
Start	227340377:227340377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515C>A
AA Mutation	p.Ser172Tyr(p.S172Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353339
Start	227332531:227332531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.372A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000353339
Start	227352512:227352512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.753-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript