Variant #0000614640 (NC_000013.10:g.36239272G>T, NM_005584.4:c.-188997C>A (MAB21L1))
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.36239272G>T |
DNA change (hg38) |
g.35665135G>T |
Published as |
NBEA(NM_015678.4):c.8350G>T (p.V2784F), NBEA(NM_015678.5):c.8350G>T (p.V2784F) |
ISCN |
- |
DB-ID |
NBEA_000032 See all 2 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) |
0.00252 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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