NM_002968.3(SALL1):c.1144A>G (p.Ser382Gly) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 9, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000175743.4
Allele description [Variation Report for NM_002968.3(SALL1):c.1144A>G (p.Ser382Gly)]
NM_002968.3(SALL1):c.1144A>G (p.Ser382Gly)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
Homo sapiens peroxisomal biogenesis factor 26 (PEX26), transcript variant 3, mRN...
Homo sapiens peroxisomal biogenesis factor 26 (PEX26), transcript variant 3, mRNAgi|1756309444|ref|NM_001199319.2|Nucleotide
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Last Updated: Apr 1, 2023