NM_015527.4(TBC1D10B):c.2041C>T (p.Pro681Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004471767.1
Allele description [Variation Report for NM_015527.4(TBC1D10B):c.2041C>T (p.Pro681Ser)]
NM_015527.4(TBC1D10B):c.2041C>T (p.Pro681Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
xd80c12.x1 Soares_NFL_T_GBC_S1 Homo sapiens cDNA clone IMAGE:2603926 3', mRNA se...
xd80c12.x1 Soares_NFL_T_GBC_S1 Homo sapiens cDNA clone IMAGE:2603926 3', mRNA sequencegi|6086759|gnl|dbEST|3263477|gb|AW1 .1|Nucleotide
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Last Updated: May 7, 2024