Variant #0000249008 (NC_000002.11:g.48948856A>G, NC_000002.11(NM_000233.3):c.536+1739T>C (LHCGR))
| Chromosome |
2 |
| 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.48948856A>G |
| DNA change (hg38) |
g.48721717A>G |
| Published as |
LHCGR(NM_000233.4):c.536+1739T>C, STON1-GTF2A1L(NM_001198593.2):c.3441+50037A>G |
| ISCN |
- |
| DB-ID |
LHCGR_000005 |
| 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 |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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