Variant #0000618548 (NC_000022.10:g.29885861_29885878del, NM_021076.3:c.2232_2249del (NEFH))

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.29885861_29885878del
DNA change (hg38) g.29489872_29489889del
Published as NEFH(NM_021076.4):c.2232_2249delTAAGTCCCCAGAGAAGGC (p.S752_K757del)
ISCN -
DB-ID NEFH_000008 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NEFH NM_021076.3 -/. - c.2232_2249del r.(?) p.(Ser752_Lys757del)


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