Variant #0000277682 (NC_000021.8:g.38137321C>T, NM_000411.6:c.1672G>A (HLCS))
Chromosome |
21 |
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.38137321C>T |
DNA change (hg38) |
g.36765020C>T |
Published as |
HLCS(NM_000411.6):c.1672G>A (p.(Glu558Lys)), HLCS(NM_001242784.2):c.1672G>A (p.E558K), HLCS(NM_001242784.3):c.1672G>A (p.E558K) |
ISCN |
- |
DB-ID |
HLCS_000004 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) |
0.00266 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2019-12-04 15:24:38 +01:00 (CET) |

Variant on transcripts
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