Variant #0000966196 (NC_000011.9:g.118898437del, NM_001164277.1:c.525_527= (SLC37A4))
Chromosome |
11 |
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.118898437del |
DNA change (hg38) |
- |
Published as |
SLC37A4(NM_001164277.1):c.527delG (p.C176Lfs*36), SLC37A4(NM_001164278.2):c.528delG (p.C176Wfs*36) |
ISCN |
- |
DB-ID |
SLC37A4_000045 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) |
Retrieve |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2024-02-26 20:06:56 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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