NM_020848.4(JCAD):c.731C>T (p.Thr244Met) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 20, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004635748.1
Allele description [Variation Report for NM_020848.4(JCAD):c.731C>T (p.Thr244Met)]
NM_020848.4(JCAD):c.731C>T (p.Thr244Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens lymphocyte antigen 9 (LY9), transcript variant X11, mRNA
PREDICTED: Homo sapiens lymphocyte antigen 9 (LY9), transcript variant X11, mRNAgi|2462509259|ref|XM_054336635.1|Nucleotide
-
PF3D7_1416700 [Plasmodium falciparum 3D7]
PF3D7_1416700 [Plasmodium falciparum 3D7]Gene ID:8445028Gene
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See more...Assertion and evidence details
Last Updated: Aug 11, 2024