Variant #0000611302 (NC_000007.13:g.92132486dup, NM_000466.2:c.2097dup (PEX1))
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.92132486dup |
| DNA change (hg38) |
g.92503172dup |
| Published as |
PEX1(NM_000466.3):c.2097dup (p.(Ile700TyrfsTer42)), PEX1(NM_000466.3):c.2097dupT (p.I700Yfs*42), PEX1(NM_001282678.1):c.1473dupT (p.I492Yfs*42), PE... |
| ISCN |
- |
| DB-ID |
PEX1_000002 See all 163 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) |
Retrieve |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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