NM_005199.5(CHRNG):c.921-68del AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 2, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001683705.1
Allele description [Variation Report for NM_005199.5(CHRNG):c.921-68del]
NM_005199.5(CHRNG):c.921-68del
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
Homo sapiens serum amyloid A1 (SAA1), transcript variant 2, mRNA
Homo sapiens serum amyloid A1 (SAA1), transcript variant 2, mRNAgi|1519315675|ref|NM_199161.5|Nucleotide
-
unnamed protein product [Homo sapiens]
unnamed protein product [Homo sapiens]gi|21750235|dbj|BAC03746.1|Protein
-
Ikappa B-zeta variant 3 [Homo sapiens]
Ikappa B-zeta variant 3 [Homo sapiens]gi|77744977|gb|ABB02425.1|Protein
-
acetyl-CoA carboxylase 1 isoform 3 [Homo sapiens]
acetyl-CoA carboxylase 1 isoform 3 [Homo sapiens]gi|38679971|ref|NP_942134.1|Protein
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See more...Assertion and evidence details
Last Updated: Apr 23, 2022