NM_000112.4(SLC26A2):c.1838G>T (p.Trp613Leu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 26, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004456658.1
Allele description [Variation Report for NM_000112.4(SLC26A2):c.1838G>T (p.Trp613Leu)]
NM_000112.4(SLC26A2):c.1838G>T (p.Trp613Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
IZUMO1R [Mustela putorius furo]
IZUMO1R [Mustela putorius furo]Gene ID:101678569Gene
-
PIP4K2A [Odobenus rosmarus divergens]
PIP4K2A [Odobenus rosmarus divergens]Gene ID:101366625Gene
-
B4GALT7 [Leptosomus discolor]
B4GALT7 [Leptosomus discolor]Gene ID:104341468Gene
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Last Updated: May 7, 2024