NM_001200.4(BMP2):c.787T>A (p.Leu263Met) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003214393.2
Allele description [Variation Report for NM_001200.4(BMP2):c.787T>A (p.Leu263Met)]
NM_001200.4(BMP2):c.787T>A (p.Leu263Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens clone HTL-T-99 testicular tissue protein Li 99 mRNA, complete cds
Homo sapiens clone HTL-T-99 testicular tissue protein Li 99 mRNA, complete cdsgi|332367637|gb|HM005412.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024