NM_000392.5(ABCC2):c.3873G>A (p.Pro1291=) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Aug 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000593239.5
Allele description [Variation Report for NM_000392.5(ABCC2):c.3873G>A (p.Pro1291=)]
NM_000392.5(ABCC2):c.3873G>A (p.Pro1291=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens limb development membrane protein 1 (LMBR1), transcript variant 6, ...
Homo sapiens limb development membrane protein 1 (LMBR1), transcript variant 6, mRNAgi|1676317084|ref|NM_001350957.2|Nucleotide
-
Homo sapiens cytochrome P450 family 4 subfamily B member 1 (CYP4B1), transcript ...
Homo sapiens cytochrome P450 family 4 subfamily B member 1 (CYP4B1), transcript variant 2, mRNAgi|153218659|ref|NM_000779.3|Nucleotide
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Last Updated: Mar 5, 2024