NM_203446.3(SYNJ1):c.1868A>G (p.Asn623Ser) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004036479.1
Allele description [Variation Report for NM_203446.3(SYNJ1):c.1868A>G (p.Asn623Ser)]
NM_203446.3(SYNJ1):c.1868A>G (p.Asn623Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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50S ribosomal protein L1 [Chlamydia trachomatis]
50S ribosomal protein L1 [Chlamydia trachomatis]gi|497557481|ref|WP_009871665.1|Protein
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Homo sapiens Wolf-Hirschhorn syndrome candidate 1-like 1 (FLJ20353), mRNA
Homo sapiens Wolf-Hirschhorn syndrome candidate 1-like 1 (FLJ20353), mRNAgi|8923325|ref|NM_017778.1|Nucleotide
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solute carrier family 2, facilitated glucose transporter member 8 isoform 1 prec...
solute carrier family 2, facilitated glucose transporter member 8 isoform 1 precursor [Mus musculus]gi|9506735|ref|NP_062361.1|Protein
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Homologene neighbors for GEO Profiles (Select 77902383) (0)
GEO Profiles
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Homologene neighbors for GEO Profiles (Select 69905569) (0)
GEO Profiles
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024