NM_001276700.2(NLRP6):c.2632G>C (p.Asp878His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004304264.1
Allele description [Variation Report for NM_001276700.2(NLRP6):c.2632G>C (p.Asp878His)]
NM_001276700.2(NLRP6):c.2632G>C (p.Asp878His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
zw03h12.r1 Soares_NhHMPu_S1 Homo sapiens cDNA clone IMAGE:768263 5', mRNA sequen...
zw03h12.r1 Soares_NhHMPu_S1 Homo sapiens cDNA clone IMAGE:768263 5', mRNA sequencegi|2107061|gnl|dbEST|1070075|gb|AA4 .1|Nucleotide
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Last Updated: Oct 8, 2024