Colon Cancer: Gene >> ABHD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352732
Start	89155472:89155472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476T>C
AA Mutation	p.Val159Ala(p.V159A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000352732
Start	89193299:89193299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1061C>T
AA Mutation	p.Thr354Ile(p.T354I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000352732
Start	89175970:89175970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150079355
CDS Mutation	c.697G>A
AA Mutation	p.Val233Met(p.V233M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000352732
Start	89175824:89175824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551A>G
AA Mutation	p.Glu184Gly(p.E184G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000352732
Start	89195268:89195268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123G>C
AA Mutation	p.Gly375Arg(p.G375R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352732
Start	89151725:89151725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.243C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352732
Start	89193270:89193270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs74029947
CDS Mutation	c.1032C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352732
Start	89175963:89175963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763642629
CDS Mutation	c.690C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352732
Start	89155450:89155450(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.458delA
AA Mutation	p.Asn153MetfsTer8(p.N153Mfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ABHD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352732
Start	89151816:89151816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373748122
CDS Mutation	c.334G>A
AA Mutation	p.Asp112Asn(p.D112N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000352732
Start	89116415:89116415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772771831
CDS Mutation	c.88G>A
AA Mutation	p.Val30Ile(p.V30I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript