NM_144499.3(GNAT1):c.762C>T (p.Tyr254=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 7, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000915168.3
Allele description [Variation Report for NM_144499.3(GNAT1):c.762C>T (p.Tyr254=)]
NM_144499.3(GNAT1):c.762C>T (p.Tyr254=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
Rattus norvegicus strain mixed contig_59166.1, whole genome shotgun sequence
Rattus norvegicus strain mixed contig_59166.1, whole genome shotgun sequencegi|661372541|gb|AABR07058089.1||gnl AABR07|contig_59166.1Nucleotide
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D003233 (1)
MeSH
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Homo sapiens cDNA clone IMAGE:4026267, containing frame-shift errors
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602708743F1 NIH_MGC_43 Homo sapiens cDNA clone IMAGE:4845299 5', mRNA sequence
602708743F1 NIH_MGC_43 Homo sapiens cDNA clone IMAGE:4845299 5', mRNA sequencegi|14060643|gnl|dbEST|8509934|gb|BG 0.1|Nucleotide
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Last Updated: Aug 23, 2022