Variant #0000886457 (NC_000004.11:g.980932G>A, IDUA(NM_000203.3):c.60G>A)
Chromosome |
4 |
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.980932G>A |
DNA change (hg38) |
- |
Published as |
IDUA(NM_000203.5):c.60G>A (p.A20=), SLC26A1(NM_134425.3):c.576+3984C>T, SLC26A1(NM_134425.4):c.576+3984C>T |
ISCN |
- |
DB-ID |
IDUA_000086 See all 6 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) |
0.50252 View details |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2022-11-01 13:01:21 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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