chr8:24956248:C>T Detail (hg38) (NEFL)

Information

Genome

Assembly Position
hg19 chr8:24,813,762-24,813,762 View the variant detail on this assembly version.
hg38 chr8:24,956,248-24,956,248

HGVS

Type Transcript Protein
RefSeq NM_006158.4:c.268G>A NP_006149.2:p.Glu90Lys
Ensemble ENST00000610854.2:c.268G>A ENST00000610854.2:p.Glu90Lys
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 162280 OMIM
HGNC 7739 HGNC
Ensembl ENSG00000277586 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2022-08-23 criteria provided, single submitter not provided germline not provided Detail
Pathogenic 2022-08-23 criteria provided, single submitter Charcot-Marie-Tooth disease type 2E germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.480 Charcot-Marie-Tooth disease, demyelinating, Type 1F Mutations in the neurofilament light chain gene (NEFL) cause early onset severe ... UNIPROT 12566280 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_006158.5(NEFL):c.268G>A (p.Glu90Lys) AND not provided ClinVar Detail
NM_006158.5(NEFL):c.268G>A (p.Glu90Lys) AND Charcot-Marie-Tooth disease type 2E ClinVar Detail
Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth ... DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs58332872 dbSNP
Genome
hg38
Position
chr8:24,956,248-24,956,248
Variant Type
snv
Reference Allele
C
Alternative Allele
T
Genome browser