NM_003900.5(SQSTM1):c.183C>T (p.Gly61=) AND Paget disease of bone 3
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000372389.6
Allele description [Variation Report for NM_003900.5(SQSTM1):c.183C>T (p.Gly61=)]
NM_003900.5(SQSTM1):c.183C>T (p.Gly61=)
Condition(s)
-
ATP-binding cassette sub-family C member 3 isoform X1 [Rattus norvegicus]
ATP-binding cassette sub-family C member 3 isoform X1 [Rattus norvegicus]gi|1958656202|ref|XP_038941015.1|Protein
-
Homo sapiens protocadherin alpha subfamily C, 1 (PCDHAC1), transcript variant 1,...
Homo sapiens protocadherin alpha subfamily C, 1 (PCDHAC1), transcript variant 1, mRNAgi|1788703473|ref|NM_018898.5|Nucleotide
-
Vibrio tapetis subsp. tapetis isolate Vibrio tapetis CECT4600 genome assembly, c...
Vibrio tapetis subsp. tapetis isolate Vibrio tapetis CECT4600 genome assembly, chromosome: Agi|1325783819|emb|LT960611.1|Nucleotide
-
ribosomal protein S4, partial (chloroplast) [Oleolophozia perssonii]
ribosomal protein S4, partial (chloroplast) [Oleolophozia perssonii]gi|1878849016|gb|QLP88691.1|Protein
-
CG46510 uncharacterized protein [Drosophila melanogaster]
CG46510 uncharacterized protein [Drosophila melanogaster]Gene ID:76382441Gene
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Last Updated: Oct 20, 2024