Colon Cancer: Gene >> AFP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395792
Start	73438184:73438184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.148T>G
AA Mutation	p.Phe50Val(p.F50V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395792
Start	73449364:73449364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1088C>T
AA Mutation	p.Pro363Leu(p.P363L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395792
Start	73452428:73452428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1456A>G
AA Mutation	p.Ile486Val(p.I486V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395792
Start	73436330:73436330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68G>T
AA Mutation	p.Arg23Ile(p.R23I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000395792
Start	73450745:73450745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748956575
CDS Mutation	c.1420G>A
AA Mutation	p.Glu474Lys(p.E474K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000395792
Start	73450752:73450752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376466369
CDS Mutation	c.1427C>T
AA Mutation	p.Ala476Val(p.A476V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000395792
Start	73440735:73440735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754667512
CDS Mutation	c.404C>T
AA Mutation	p.Ser135Leu(p.S135L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000395792
Start	73452603:73452603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369625484
CDS Mutation	c.1631C>T
AA Mutation	p.Ala544Val(p.A544V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000395792
Start	73450104:73450104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1260G>T
AA Mutation	p.Gln420His(p.Q420H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395792
Start	73452466:73452466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1494C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395792
Start	73452415:73452415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371460704
CDS Mutation	c.1443C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395792
Start	73447655:73447655(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs779815391
CDS Mutation	c.1043delA
AA Mutation	p.Asn348IlefsTer22(p.N348Ifs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395792
Start	73447654:73447655(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1043dupA
AA Mutation	p.Asn348LysfsTer10(p.N348Kfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395792
Start	73440751:73440752(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.420_421insAATTTCTTTCTCAT
AA Mutation	p.Val141AsnfsTer24(p.V141Nfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395792
Start	73453890:73453891(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1778_1779insAATGCTATTTT
AA Mutation	p.Glu594MetfsTer10(p.E594Mfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> AFP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395792
Start	73449391:73449391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1115G>T
AA Mutation	p.Arg372Ile(p.R372I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395792
Start	73452602:73452602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1630G>A
AA Mutation	p.Ala544Thr(p.A544T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript