NM_003002.4(SDHD):c.268G>T (p.Ala90Ser) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 24, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002453184.2
Allele description [Variation Report for NM_003002.4(SDHD):c.268G>T (p.Ala90Ser)]
NM_003002.4(SDHD):c.268G>T (p.Ala90Ser)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
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Planaltina kaingang voucher LBP18902 75270 cytochrome b (CytB) gene, partial cds...
Planaltina kaingang voucher LBP18902 75270 cytochrome b (CytB) gene, partial cds; mitochondrialgi|1356589254|gb|KY671263.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024