Colon Cancer: Gene >> FAF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396153
Start	50490594:50490594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1647A>C
AA Mutation	p.Glu549Asp(p.E549D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396153
Start	50655522:50655522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.664A>G
AA Mutation	p.Arg222Gly(p.R222G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396153
Start	50584714:50584714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371330134
CDS Mutation	c.938C>T
AA Mutation	p.Ala313Val(p.A313V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396153
Start	50705872:50705872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571A>C
AA Mutation	p.Asn191His(p.N191H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396153
Start	50857969:50857969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.74A>G
AA Mutation	p.Glu25Gly(p.E25G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000396153
Start	50475528:50475528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1805T>G
AA Mutation	p.Phe602Cys(p.F602C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000396153
Start	50491798:50491798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1498G>A
AA Mutation	p.Glu500Lys(p.E500K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000396153
Start	50539663:50539663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370024425
CDS Mutation	c.1334C>T
AA Mutation	p.Thr445Met(p.T445M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000396153
Start	50596137:50596137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538524843
CDS Mutation	c.824G>A
AA Mutation	p.Arg275Gln(p.R275Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396153
Start	50583699:50583699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.984A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396153
Start	50583705:50583705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140546895
CDS Mutation	c.978C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396153
Start	50788110:50788110(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.257delC
AA Mutation	p.Pro86LeufsTer2(p.P86Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396153
Start	50788176:50788177(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.190_191insATTTCTGTCT
AA Mutation	p.Pro64HisfsTer7(p.P64Hfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FAF1

No Mutation Annotation!