NM_018109.4(MTPAP):c.500A>T (p.Asn167Ile) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 13, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002900352.2
Allele description [Variation Report for NM_018109.4(MTPAP):c.500A>T (p.Asn167Ile)]
NM_018109.4(MTPAP):c.500A>T (p.Asn167Ile)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens talin mRNA, complete cds
Homo sapiens talin mRNA, complete cdsgi|4235274|gb|AF078828.1|Nucleotide
-
LOC127458870 [Homo sapiens]
LOC127458870 [Homo sapiens]Gene ID:127458870Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024