Variant #0001013659 (NC_000002.11:g.219924998G>C, NM_002181.3:c.192C>G (IHH))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.219924998G>C |
DNA change (hg38) |
- |
Published as |
IHH(NM_002181.4):c.192C>G (p.S64R) |
ISCN |
- |
DB-ID |
IHH_000092 |
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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2024-10-29 20:49:11 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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