chr8:24956235:A>G Detail (hg38) (NEFL)

Information

Genome

Assembly Position
hg19 chr8:24,813,749-24,813,749 View the variant detail on this assembly version.
hg38 chr8:24,956,235-24,956,235

HGVS

Type Transcript Protein
RefSeq NM_006158.4:c.281T>C NP_006149.2:p.Leu94Pro
Ensemble ENST00000610854.2:c.281T>C ENST00000610854.2:p.Leu94Pro
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 2007-07-01 no assertion criteria provided Charcot-Marie-Tooth disease type 2E germline Detail
not provided no assertion provided not provided not provided Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.481 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder) NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_006158.5(NEFL):c.281T>C (p.Leu94Pro) AND Charcot-Marie-Tooth disease type 2E ClinVar Detail
NM_006158.5(NEFL):c.281T>C (p.Leu94Pro) AND not provided ClinVar Detail
NA 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
rs62636505 dbSNP
Genome
hg38
Position
chr8:24,956,235-24,956,235
Variant Type
snv
Reference Allele
A
Alternative Allele
G
Genome browser