Colon Cancer: Gene >> HEPACAM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298251
Start	124923992:124923992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446A>G
AA Mutation	p.Gln149Arg(p.Q149R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298251
Start	124924001:124924001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542132168
CDS Mutation	c.437C>T
AA Mutation	p.Ser146Leu(p.S146L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298251
Start	124924898:124924898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.257A>T
AA Mutation	p.Glu86Val(p.E86V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298251
Start	124935961:124935961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549252759
CDS Mutation	c.46C>T
AA Mutation	p.Arg16Cys(p.R16C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000298251
Start	124923819:124923819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201870421
CDS Mutation	c.619G>A
AA Mutation	p.Val207Met(p.V207M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298251
Start	124924840:124924840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.315C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298251
Start	124923417:124923417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.726C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298251
Start	124924840:124924840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.315C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000298251
Start	124922389:124922389(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.947delA
AA Mutation	p.Lys316ArgfsTer87(p.K316Rfs*87)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298251
Start	124923847:124923847(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.591delC
AA Mutation	p.Asp198ThrfsTer57(p.D198Tfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HEPACAM

No Mutation Annotation!