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 International |
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) |

Variant on transcripts
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