NM_021646.4(ZNF500):c.1346G>A (p.Gly449Asp) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004315201.1
Allele description [Variation Report for NM_021646.4(ZNF500):c.1346G>A (p.Gly449Asp)]
NM_021646.4(ZNF500):c.1346G>A (p.Gly449Asp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Sequence 133 from Patent WO2004058805
Sequence 133 from Patent WO2004058805gi|50833799|emb|CQ834262.1||pat|WO| 58805|133Nucleotide
-
Homo sapiens chromosome 19 open reading frame 56, mRNA (cDNA clone MGC:70730 IMA...
Homo sapiens chromosome 19 open reading frame 56, mRNA (cDNA clone MGC:70730 IMAGE:4444565), complete cdsgi|38541369|gb|BC061912.1|Nucleotide
-
602779943F2 NCI_CGAP_Brn67 Homo sapiens cDNA clone IMAGE:4915570 5', mRNA sequen...
602779943F2 NCI_CGAP_Brn67 Homo sapiens cDNA clone IMAGE:4915570 5', mRNA sequencegi|14165986|gnl|dbEST|8557721|gb|BG 9.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 8, 2024