Colon Cancer: Gene >> NOC2L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327044
Start	956154:956154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548C>T
AA Mutation	p.Thr183Ile(p.T183I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327044
Start	948183:948183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747085379
CDS Mutation	c.1607G>A
AA Mutation	p.Ser536Asn(p.S536N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327044
Start	945088:945088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2112G>T
AA Mutation	p.Glu704Asp(p.E704D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327044
Start	952464:952464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1139A>G
AA Mutation	p.Tyr380Cys(p.Y380C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327044
Start	951192:951192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112703241
CDS Mutation	c.1378C>T
AA Mutation	p.Arg460Cys(p.R460C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000327044
Start	955922:955922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.698+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000327044
Start	957186:957188(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.265_267delGAG
AA Mutation	p.Glu89del(p.E89del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000327044
Start	957005:957006(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.372_374dupGGA
AA Mutation	p.Glu124dup(p.E124dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NOC2L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327044
Start	959009:959009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.99A>C
AA Mutation	p.Glu33Asp(p.E33D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327044
Start	951206:951206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760523219
CDS Mutation	c.1364G>A
AA Mutation	p.Arg455Gln(p.R455Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327044
Start	957154:957154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372783720
CDS Mutation	c.299C>T
AA Mutation	p.Ser100Leu(p.S100L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327044
Start	946222:946222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148962722
CDS Mutation	c.1868G>A
AA Mutation	p.Arg623His(p.R623H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327044
Start	946256:946256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1834G>A
AA Mutation	p.Gly612Arg(p.G612R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327044
Start	956926:956926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769695147
CDS Mutation	c.454G>A
AA Mutation	p.Ala152Thr(p.A152T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript