NM_173628.4(DNAH17):c.13216A>G (p.Ile4406Val) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004376511.1
Allele description [Variation Report for NM_173628.4(DNAH17):c.13216A>G (p.Ile4406Val)]
NM_173628.4(DNAH17):c.13216A>G (p.Ile4406Val)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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PREDICTED: Homo sapiens uncharacterized lncRNA (LOC124904755), transcript varian...
PREDICTED: Homo sapiens uncharacterized lncRNA (LOC124904755), transcript variant X3, ncRNAgi|2217324654|ref|XR_007067323.1|Nucleotide
-
PREDICTED: Rattus norvegicus sodium voltage-gated channel alpha subunit 7 (Scn7a...
PREDICTED: Rattus norvegicus sodium voltage-gated channel alpha subunit 7 (Scn7a), transcript variant X2, mRNAgi|2678931815|ref|XM_039105778.2|Nucleotide
-
urea transporter 1 [Rattus norvegicus]
urea transporter 1 [Rattus norvegicus]gi|1937903927|ref|NP_062219.3|Protein
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Alosa alosa isolate M-15738 ecotype Scorff River chromosome 8, whole genome shot...
Alosa alosa isolate M-15738 ecotype Scorff River chromosome 8, whole genome shotgun sequencegi|2019796132|gb|CM030053.1||gnl|WG WDJ|AALO_1.0_LG8Nucleotide
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Hemicentrotus pulcherrimus genome isolated from sperm of 3 males
Hemicentrotus pulcherrimus genome isolated from sperm of 3 malesbiosample
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Last Updated: Sep 1, 2024