Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SHF

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000290894
Start 45172001:45172001(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.967T>C
AA Mutation p.Trp323Arg(p.W323R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000290894
Start 45172261:45172261(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140713703
CDS Mutation c.851G>A
AA Mutation p.Arg284Gln(p.R284Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000290894
Start 45178242:45178242(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.368G>A
AA Mutation p.Gly123Glu(p.G123E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000290894
Start 45178291:45178291(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.319G>T
AA Mutation p.Asp107Tyr(p.D107Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000290894
Start 45168083:45168083(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1136A>C
AA Mutation p.Lys379Thr(p.K379T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000290894
Start 45171926:45171926(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1042C>T
AA Mutation p.Arg348Cys(p.R348C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000290894
Start 45198790:45198791(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.284dupA
AA Mutation p.Asp95GlufsTer19(p.D95Efs*19)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> SHF

No Mutation Annotation!