NM_000190.4(HMBS):c.33+18G>A AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 11, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004526203.2
Allele description [Variation Report for NM_000190.4(HMBS):c.33+18G>A]
NM_000190.4(HMBS):c.33+18G>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens prolylcarboxypeptidase (PRCP), transcript variant 2, mRNA
Homo sapiens prolylcarboxypeptidase (PRCP), transcript variant 2, mRNAgi|1889462748|ref|NM_199418.4|Nucleotide
-
cytochrome b (mitochondrion) [Acosmetura nigrogeniculata]
cytochrome b (mitochondrion) [Acosmetura nigrogeniculata]gi|1778128417|ref|YP_009711023.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024