NM_004174.4(SLC9A3):c.1795C>A (p.Gln599Lys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002884013.2
Allele description [Variation Report for NM_004174.4(SLC9A3):c.1795C>A (p.Gln599Lys)]
NM_004174.4(SLC9A3):c.1795C>A (p.Gln599Lys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
GSE8002[Accession] (5)
GEO DataSets
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Osmia ferruginea voucher BBSLID115538 ATP synthase F0 subunit 6 (ATP6) gene, par...
Osmia ferruginea voucher BBSLID115538 ATP synthase F0 subunit 6 (ATP6) gene, partial cds; mitochondrialgi|2294228359|gb|MW043092.1|Nucleotide
-
Prionochilus maculatus Brahma protein (BRM) gene, partial cds
Prionochilus maculatus Brahma protein (BRM) gene, partial cdsgi|1835272055|gb|MT235555.1|Nucleotide
-
Prionochilus maculatus voucher LSUMZ B36382 NADH dehydrogenase subunit II (ND2) ...
Prionochilus maculatus voucher LSUMZ B36382 NADH dehydrogenase subunit II (ND2) gene, complete cds; mitochondrialgi|1827950253|gb|MN897917.1|Nucleotide
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Last Updated: May 1, 2024