Variant #0000687236 (NC_000007.13:g.92147479_92147493delinsTTGC, PEX1(NM_000466.2):c.434_448delinsGCAA)
Individual ID |
00310507 |
Chromosome |
7 |
Allele |
Parent #2 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic (recessive) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.92147479_92147493delinsTTGC |
DNA change (hg38) |
g.92518165_92518179delinsTTGC |
Published as |
- |
ISCN |
- |
DB-ID |
PEX1_000027 |
Variant remarks |
- |
Reference |
PubMed: Walter 2001 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
Nancy Braverman |

Variant on transcripts
Screenings
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