Colon Cancer: Gene >> NOL8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442668
Start	92318623:92318623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186223201
CDS Mutation	c.481C>T
AA Mutation	p.Arg161Cys(p.R161C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000442668
Start	92298285:92298285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3425G>C
AA Mutation	p.Trp1142Ser(p.W1142S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000442668
Start	92324041:92324041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749766188
CDS Mutation	c.121A>G
AA Mutation	p.Thr41Ala(p.T41A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000442668
Start	92306926:92306926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2785A>G
AA Mutation	p.Asn929Asp(p.N929D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000442668
Start	92319351:92319351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287C>T
AA Mutation	p.Ala96Val(p.A96V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000442668
Start	92315288:92315288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544769426
CDS Mutation	c.1337A>G
AA Mutation	p.Asn446Ser(p.N446S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000442668
Start	92315178:92315178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759194714
CDS Mutation	c.1447C>T
AA Mutation	p.Arg483Cys(p.R483C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000442668
Start	92301614:92301614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772631824
CDS Mutation	c.3112G>A
AA Mutation	p.Ala1038Thr(p.A1038T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000442668
Start	92311186:92311186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747719597
CDS Mutation	c.2432C>T
AA Mutation	p.Ser811Leu(p.S811L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000442668
Start	92310557:92310557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2591A>G
AA Mutation	p.Gln864Arg(p.Q864R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000442668
Start	92314479:92314479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748873347
CDS Mutation	c.2146G>A
AA Mutation	p.Gly716Ser(p.G716S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442668
Start	92319305:92319305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.333A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442668
Start	92315786:92315786(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.839delA
AA Mutation	p.Asn280IlefsTer29(p.N280Ifs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained;inframe_insertion
Transcription ID	ENST00000442668
Start	92301722:92301723(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3003_3004insAATTAAGTT
AA Mutation	p.Phe1001_Gln1002insAsnTerVal(p.F1001_Q1002insN*V)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442668
Start	92297865:92297866(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3474dupA
AA Mutation	p.Asp1159ArgfsTer17(p.D1159Rfs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442668
Start	92301578:92301579(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3147dupT
AA Mutation	p.Asp1050Ter(p.D1050*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NOL8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442668
Start	92315515:92315515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110G>A
AA Mutation	p.Met370Ile(p.M370I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000442668
Start	92306925:92306925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2786A>C
AA Mutation	p.Asn929Thr(p.N929T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000442668
Start	92315576:92315576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372632723
CDS Mutation	c.1049C>A
AA Mutation	p.Ser350Tyr(p.S350Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442668
Start	92323454:92323454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201912608
CDS Mutation	c.189G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442668
Start	92301737:92301737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747762980
CDS Mutation	c.2989C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000442668
Start	92297880:92297880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3460C>T
AA Mutation	p.Arg1154Ter(p.R1154*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442668
Start	92301804:92301805(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2921dupA
AA Mutation	p.Lys975GlufsTer6(p.K975Efs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript