NM_138691.3(TMC1):c.885-11T>C AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Oct 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002260728.4
Allele description [Variation Report for NM_138691.3(TMC1):c.885-11T>C]
NM_138691.3(TMC1):c.885-11T>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
602375 (1)
OMIM
-
Human DNA sequence from clone RP1-202O8 on chromosome 1p36.11-36.31, complete se...
Human DNA sequence from clone RP1-202O8 on chromosome 1p36.11-36.31, complete sequencegi|4914512|emb|AL031848.11|Nucleotide
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Last Updated: Sep 29, 2024