NM_000243.3(MEFV):c.2090A>T (p.Asn697Ile) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 8, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001755257.2
Allele description [Variation Report for NM_000243.3(MEFV):c.2090A>T (p.Asn697Ile)]
NM_000243.3(MEFV):c.2090A>T (p.Asn697Ile)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens SH2 domain containing 4A (SH2D4A), transcript variant 1, mRNA
Homo sapiens SH2 domain containing 4A (SH2D4A), transcript variant 1, mRNAgi|1519313784|ref|NM_022071.4|Nucleotide
-
Synthetic construct Homo sapiens clone IMAGE:100015698, MGC:183153 bone morphoge...
Synthetic construct Homo sapiens clone IMAGE:100015698, MGC:183153 bone morphogenetic protein 2 (BMP2) mRNA, encodes complete proteingi|151555118|gb|BC148689.1|Nucleotide
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Last Updated: Dec 24, 2023