Colon Cancer: Gene >> ABCF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287844
Start	151223733:151223733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145078285
CDS Mutation	c.667C>T
AA Mutation	p.Arg223Cys(p.R223C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287844
Start	151219110:151219110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.971A>C
AA Mutation	p.Gln324Pro(p.Q324P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000287844
Start	151221579:151221579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753104612
CDS Mutation	c.920C>T
AA Mutation	p.Thr307Met(p.T307M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287844
Start	151218765:151218765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775988044
CDS Mutation	c.1126G>A
AA Mutation	p.Val376Met(p.V376M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287844
Start	151215058:151215058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555G>T
AA Mutation	p.Asp519Tyr(p.D519Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287844
Start	151215056:151215056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545658338
CDS Mutation	c.1557C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287844
Start	151218766:151218766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139539137
CDS Mutation	c.1125C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ABCF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287844
Start	151219132:151219132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759491541
CDS Mutation	c.949C>T
AA Mutation	p.Arg317Trp(p.R317W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287844
Start	151218590:151218590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198A>G
AA Mutation	p.Asn400Asp(p.N400D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287844
Start	151224858:151224858(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.285delT
AA Mutation	p.His96MetfsTer13(p.H96Mfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript