NM_001160148.2(DDHD1):c.2432C>G (p.Ser811Cys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003168807.3
Allele description [Variation Report for NM_001160148.2(DDHD1):c.2432C>G (p.Ser811Cys)]
NM_001160148.2(DDHD1):c.2432C>G (p.Ser811Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
PREDICTED: Oncorhynchus keta dnaJ homolog subfamily B member 6-like (LOC11840207...
PREDICTED: Oncorhynchus keta dnaJ homolog subfamily B member 6-like (LOC118402075), mRNAgi|2401579271|ref|XM_035799946.2|Nucleotide
-
zt78c01.r1 Soares_testis_NHT Homo sapiens cDNA clone IMAGE:728448 5', mRNA seque...
zt78c01.r1 Soares_testis_NHT Homo sapiens cDNA clone IMAGE:728448 5', mRNA sequencegi|2046933|gnl|dbEST|1035297|gb|AA3 .1|Nucleotide
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Last Updated: Sep 29, 2024