Colon Cancer: Gene >> FNBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000446176
Start	129908984:129908984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1201G>A
AA Mutation	p.Asp401Asn(p.D401N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000446176
Start	129902934:129902934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1363G>T
AA Mutation	p.Asp455Tyr(p.D455Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000446176
Start	129900001:129900001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1651G>A
AA Mutation	p.Ala551Thr(p.A551T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000446176
Start	129925029:129925029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.918A>C
AA Mutation	p.Glu306Asp(p.E306D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000446176
Start	129957395:129957395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200418146
CDS Mutation	c.478G>A
AA Mutation	p.Ala160Thr(p.A160T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000446176
Start	129900078:129900078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1574A>G
AA Mutation	p.Glu525Gly(p.E525G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000446176
Start	129895909:129895909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374562503
CDS Mutation	c.1775G>A
AA Mutation	p.Arg592Gln(p.R592Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000446176
Start	129978500:129978500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774615028
CDS Mutation	c.310C>T
AA Mutation	p.Arg104Cys(p.R104C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000446176
Start	129979370:129979370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145C>A
AA Mutation	p.Leu49Ile(p.L49I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000446176
Start	129927339:129927339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645A>C
AA Mutation	p.Lys215Asn(p.K215N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000446176
Start	129958537:129958537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750439648
CDS Mutation	c.362G>A
AA Mutation	p.Arg121His(p.R121H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446176
Start	129957396:129957396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374689208
CDS Mutation	c.477C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446176
Start	129978581:129978581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446176
Start	129908922:129908922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1263A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446176
Start	129895980:129895980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781328311
CDS Mutation	c.1704G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000446176
Start	129978606:129978606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765621679
CDS Mutation	c.204G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000446176
Start	129924985:129924985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962T>G
AA Mutation	p.Leu321Ter(p.L321*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000446176
Start	129924963:129924964(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.983dupA
AA Mutation	p.Asn328LysfsTer2(p.N328Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FNBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000446176
Start	129927215:129927215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778471637
CDS Mutation	c.769G>A
AA Mutation	p.Glu257Lys(p.E257K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000446176
Start	129958515:129958515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384G>T
AA Mutation	p.Glu128Asp(p.E128D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript