Colon Cancer: Gene >> ANLN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265748
Start	36396279:36396279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774828191
CDS Mutation	c.32G>A
AA Mutation	p.Arg11Gln(p.R11Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265748
Start	36419306:36419306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1696A>C
AA Mutation	p.Asn566His(p.N566H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265748
Start	36452581:36452581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3356A>C
AA Mutation	p.Lys1119Thr(p.K1119T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265748
Start	36406532:36406532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748050195
CDS Mutation	c.839C>T
AA Mutation	p.Ala280Val(p.A280V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265748
Start	36399364:36399364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576328951
CDS Mutation	c.458G>A
AA Mutation	p.Arg153Gln(p.R153Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265748
Start	36415842:36415842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778648455
CDS Mutation	c.1480G>A
AA Mutation	p.Glu494Lys(p.E494K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265748
Start	36421869:36421869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767615862
CDS Mutation	c.2176G>A
AA Mutation	p.Glu726Lys(p.E726K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265748
Start	36422679:36422679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772500301
CDS Mutation	c.2346C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265748
Start	36419296:36419296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34371129
CDS Mutation	c.1686G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265748
Start	36424715:36424715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2682T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265748
Start	36399176:36399176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146340773
CDS Mutation	c.270G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265748
Start	36399333:36399333(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.430delA
AA Mutation	p.Thr144HisfsTer18(p.T144Hfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000265748
Start	36420228:36420229(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1929_1930insGTAAGCTGATTGATTCATC
AA Mutation	p.Lys644ValfsTer3(p.K644Vfs*3)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265748
Start	36399106:36399107(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.207dupA
AA Mutation	p.Arg70ThrfsTer4(p.R70Tfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265748
Start	36399157:36399158(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.251_252insCTTGAGGG
AA Mutation	p.Lys85LeufsTer45(p.K85Lfs*45)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ANLN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265748
Start	36417094:36417094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772690246
CDS Mutation	c.1537G>A
AA Mutation	p.Glu513Lys(p.E513K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265748
Start	36439220:36439220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2900C>A
AA Mutation	p.Ser967Tyr(p.S967Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265748
Start	36424721:36424721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2688G>T
AA Mutation	p.Lys896Asn(p.K896N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265748
Start	36417102:36417102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139579665
CDS Mutation	c.1545G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265748
Start	36449730:36449731(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3148dupT
AA Mutation	p.Cys1050LeufsTer8(p.C1050Lfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000265748
Start	36420745:36420745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2163+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript