Variant #0000611805 (NC_000009.11:g.108456979C>G, NM_018112.2:c.38C>G (TMEM38B))
| Chromosome |
9 |
| 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.108456979C>G |
| DNA change (hg38) |
g.105694698C>G |
| Published as |
TMEM38B(NM_018112.1):c.38C>G (p.(Ser13Cys)) |
| ISCN |
- |
| DB-ID |
TMEM38B_000106 |
| 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) |
1.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2021-05-12 09:17:44 +02:00 (CEST) |

Variant on transcripts
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