Colon Cancer: Gene >> NEK11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383366
Start	131109815:131109815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>A
AA Mutation	p.Asp117Asn(p.D117N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383366
Start	131165484:131165484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142330323
CDS Mutation	c.1141C>T
AA Mutation	p.Arg381Trp(p.R381W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000383366
Start	131168926:131168926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1273G>T
AA Mutation	p.Gly425Cys(p.G425C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000383366
Start	131152642:131152642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809A>C
AA Mutation	p.Lys270Thr(p.K270T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000383366
Start	131109822:131109822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356A>T
AA Mutation	p.Lys119Ile(p.K119I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383366
Start	131228583:131228583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1455C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383366
Start	131152436:131152436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759501857
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383366
Start	131133912:131133912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000383366
Start	131168848:131168848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1195G>T
AA Mutation	p.Gly399Ter(p.G399*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000383366
Start	131273573:131273573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1717G>T
AA Mutation	p.Glu573Ter(p.E573*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000383366
Start	131165439:131165439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096G>T
AA Mutation	p.Glu366Ter(p.E366*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NEK11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383366
Start	131029716:131029716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8A>C
AA Mutation	p.Lys3Thr(p.K3T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383366
Start	131228604:131228604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145914506
CDS Mutation	c.1476G>T
AA Mutation	p.Glu492Asp(p.E492D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript