Variant #0000571737 (NC_000022.10:g.29885576_29885593dup, NM_021076.3:c.1947_1964dup (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.29885576_29885593dup
DNA change (hg38) g.29489587_29489604dup
Published as NEFH(NM_021076.3):c.1947_1964dupTGAGAAGGCCAAGTCCCC (p.A652_K657dup), NEFH(NM_021076.4):c.1947_1964dupTGAGAAGGCCAAGTCCCC (p.A652_K657dup)
ISCN -
DB-ID NEFH_000018 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +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.1947_1964dup r.(?) p.(Ala652_Lys657dup)


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