NM_000051.4(ATM):c.2036G>A (p.Gly679Asp) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 8, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001804452.2
Allele description [Variation Report for NM_000051.4(ATM):c.2036G>A (p.Gly679Asp)]
NM_000051.4(ATM):c.2036G>A (p.Gly679Asp)
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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Shld2 shieldin complex subunit 2 [Mus musculus]
Shld2 shieldin complex subunit 2 [Mus musculus]Gene ID:75698Gene
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olfactory receptor Olr1682 [Rattus norvegicus]
olfactory receptor Olr1682 [Rattus norvegicus]gi|47576633|ref|NP_001000890.1|Protein
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Homo sapiens amphiphysin II mRNA, complete cds
Homo sapiens amphiphysin II mRNA, complete cdsgi|2160718|gb|U87558.1|HSU87558Nucleotide
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Gene Links for GEO Profiles (Select 61691367) (2)
Gene
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Homo sapiens shieldin complex subunit 2 (SHLD2), transcript variant 12, mRNA
Homo sapiens shieldin complex subunit 2 (SHLD2), transcript variant 12, mRNAgi|1784638736|ref|NM_001377167.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023