NM_001184.4(ATR):c.438A>G (p.Thr146=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003283376.2
Allele description [Variation Report for NM_001184.4(ATR):c.438A>G (p.Thr146=)]
NM_001184.4(ATR):c.438A>G (p.Thr146=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens lipase F, gastric type (LIPF), transcript variant 4, mRNA
Homo sapiens lipase F, gastric type (LIPF), transcript variant 4, mRNAgi|1677498528|ref|NM_001198830.2|Nucleotide
-
hypothetical protein SDJN03_07793, partial [Cucurbita argyrosperma subsp. sorori...
hypothetical protein SDJN03_07793, partial [Cucurbita argyrosperma subsp. sororia]gi|2047932218|gb|KAG6602560.1||gnl| AGKQH|SDJN03_07793Protein
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See more...Assertion and evidence details
Last Updated: May 1, 2024