NM_001184.4(ATR):c.1024C>G (p.Leu342Val) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002383267.2
Allele description [Variation Report for NM_001184.4(ATR):c.1024C>G (p.Leu342Val)]
NM_001184.4(ATR):c.1024C>G (p.Leu342Val)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Mus musculus a disintegrin and metallopeptidase domain 32 (Adam32), transcript v...
Mus musculus a disintegrin and metallopeptidase domain 32 (Adam32), transcript variant 2, mRNAgi|2633575875|ref|NM_001293693.2|Nucleotide
-
UI-M-DJ1-bub-e-03-0-UI.s1 NIH_BMAP_DJ1 Mus musculus cDNA clone UI-M-DJ1-bub-e-03...
UI-M-DJ1-bub-e-03-0-UI.s1 NIH_BMAP_DJ1 Mus musculus cDNA clone UI-M-DJ1-bub-e-03-0-UI 3', mRNA sequencegi|19382258|gnl|dbEST|11626838|gb|B 70.1|Nucleotide
-
KL [Nomascus leucogenys]
KL [Nomascus leucogenys]Gene ID:100597454Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024