NM_004646.4(NPHS1):c.840+14C>T AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003729399.2
Allele description [Variation Report for NM_004646.4(NPHS1):c.840+14C>T]
NM_004646.4(NPHS1):c.840+14C>T
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Myotis lucifugus cont2.10193, whole genome shotgun sequence
Myotis lucifugus cont2.10193, whole genome shotgun sequencegi|306742830|gnl|WGS:AAPE02|cont2.1 gb|AAPE02010194.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024