Variant #0000856344 (NC_000023.10:g.130419821T>C, NM_001170961.1:c.299A>G (IGSF1))
| Chromosome |
X |
| 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.130419821T>C |
| DNA change (hg38) |
- |
| Published as |
IGSF1(NM_001170961.1):c.299A>G (p.N100S, p.(Asn100Ser)), IGSF1(NM_001170961.2):c.299A>G (p.N100S) |
| ISCN |
- |
| DB-ID |
IGSF1_000090 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) |
0.0002 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2022-05-09 15:47:41 +02:00 (CEST) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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