Colon Cancer: Gene >> AIFM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287295
Start	130130020:130130020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1720G>A
AA Mutation	p.Val574Met(p.V574M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287295
Start	130149558:130149558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.260C>A
AA Mutation	p.Thr87Asn(p.T87N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287295
Start	130165650:130165650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7C>T
AA Mutation	p.Arg3Trp(p.R3W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287295
Start	130129985:130129985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1755G>A
AA Mutation	p.Met585Ile(p.M585I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287295
Start	130136097:130136097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1253T>G
AA Mutation	p.Phe418Cys(p.F418C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287295
Start	130139859:130139859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.794G>T
AA Mutation	p.Arg265Ile(p.R265I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000287295
Start	130130082:130130082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1658C>T
AA Mutation	p.Ala553Val(p.A553V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000287295
Start	130129615:130129615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1784G>A
AA Mutation	p.Gly595Asp(p.G595D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287295
Start	130138621:130138621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768118991
CDS Mutation	c.939C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287295
Start	130149479:130149479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368967639
CDS Mutation	c.339C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000287295
Start	130147878:130147878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> AIFM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287295
Start	130130113:130130113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1627A>T
AA Mutation	p.Ile543Phe(p.I543F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287295
Start	130139819:130139819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834G>T
AA Mutation	p.Lys278Asn(p.K278N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287295
Start	130140565:130140565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.749A>C
AA Mutation	p.Gln250Pro(p.Q250P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287295
Start	130133390:130133390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1371C>T
Mutation Classification	Silent
Feature Type	Transcript