NM_001031710.3(KLHL7):c.1165G>A (p.Gly389Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 14, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002752584.2
Allele description [Variation Report for NM_001031710.3(KLHL7):c.1165G>A (p.Gly389Ser)]
NM_001031710.3(KLHL7):c.1165G>A (p.Gly389Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Xiphophorus maculatus strain JP 163 A isolate XMAC-090115_JP163A Contig34.78, wh...
Xiphophorus maculatus strain JP 163 A isolate XMAC-090115_JP163A Contig34.78, whole genome shotgun sequencegi|367137694|gb|AGAJ01007371.1||gnl AGAJ01|Contig34.78Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024