Colon Cancer: Gene >> ABHD12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339157
Start	25323398:25323398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349C>A
AA Mutation	p.Pro117Thr(p.P117T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339157
Start	25300856:25300856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775599343
CDS Mutation	c.1186C>T
AA Mutation	p.His396Tyr(p.H396Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339157
Start	25308475:25308475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41306784
CDS Mutation	c.769C>T
AA Mutation	p.Arg257Trp(p.R257W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339157
Start	25339250:25339250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.293C>G
AA Mutation	p.Ala98Gly(p.A98G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339157
Start	25320311:25320311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535070738
CDS Mutation	c.430G>A
AA Mutation	p.Val144Ile(p.V144I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000339157
Start	25306878:25306878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905T>C
AA Mutation	p.Leu302Pro(p.L302P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ABHD12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339157
Start	25309534:25309534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.661A>G
AA Mutation	p.Thr221Ala(p.T221A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript