Colon Cancer: Gene >> NEFL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000610854
Start	24956284:24956284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232G>A
AA Mutation	p.Ala78Thr(p.A78T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000610854
Start	24955861:24955861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655G>A
AA Mutation	p.Glu219Lys(p.E219K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000610854
Start	24954305:24954305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1045G>A
AA Mutation	p.Asp349Asn(p.D349N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000610854
Start	24955834:24955834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.682G>A
AA Mutation	p.Glu228Lys(p.E228K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000610854
Start	24956001:24956001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.515G>A
AA Mutation	p.Arg172His(p.R172H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000610854
Start	24953506:24953506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558065942
CDS Mutation	c.1459G>A
AA Mutation	p.Glu487Lys(p.E487K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000610854
Start	24955689:24955689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.827C>T
AA Mutation	p.Ala276Val(p.A276V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000610854
Start	24955819:24955819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.697G>A
AA Mutation	p.Glu233Lys(p.E233K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000610854
Start	24955771:24955771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745G>A
AA Mutation	p.Val249Met(p.V249M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000610854
Start	24955794:24955794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722C>T
AA Mutation	p.Ala241Val(p.A241V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000610854
Start	24954287:24954287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1063G>A
AA Mutation	p.Glu355Lys(p.E355K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610854
Start	24955586:24955586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.930T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610854
Start	24955721:24955721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.795C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610854
Start	24955955:24955955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.561C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610854
Start	24954222:24954222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1128C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610854
Start	24956453:24956453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.63G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NEFL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000610854
Start	24956001:24956001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.515G>A
AA Mutation	p.Arg172His(p.R172H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000610854
Start	24956273:24956273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.243C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000610854
Start	24952923:24952923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1519G>T
AA Mutation	p.Glu507Ter(p.E507*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000610854
Start	24952911:24952911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1531G>T
AA Mutation	p.Gly511Ter(p.G511*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript