NM_001184.4(ATR):c.2719G>A (p.Ala907Thr) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 8, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002431248.2
Allele description [Variation Report for NM_001184.4(ATR):c.2719G>A (p.Ala907Thr)]
NM_001184.4(ATR):c.2719G>A (p.Ala907Thr)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
carboxy terminal-processing peptidase [Pseudomonas alvandae]
carboxy terminal-processing peptidase [Pseudomonas alvandae]gi|2063538736|gnl|PRJNA639797|KSS97 5|gb|QXI56079.1|Protein
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See more...Assertion and evidence details
Last Updated: May 1, 2024