NM_080680.3(COL11A2):c.3174G>A (p.Pro1058=) AND Autosomal dominant nonsyndromic hearing loss 13
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001582527.2
Allele description [Variation Report for NM_080680.3(COL11A2):c.3174G>A (p.Pro1058=)]
NM_080680.3(COL11A2):c.3174G>A (p.Pro1058=)
Condition(s)
-
Homo sapiens small nucleolar RNA host gene 17 (SNHG17), transcript variant 16, l...
Homo sapiens small nucleolar RNA host gene 17 (SNHG17), transcript variant 16, long non-coding RNAgi|2515437341|ref|NR_185921.1|Nucleotide
-
Homo sapiens small nucleolar RNA host gene 17 (SNHG17), transcript variant 21, l...
Homo sapiens small nucleolar RNA host gene 17 (SNHG17), transcript variant 21, long non-coding RNAgi|2515430451|ref|NR_185926.1|Nucleotide
-
Homo sapiens small nucleolar RNA host gene 17 (SNHG17), transcript variant 4, lo...
Homo sapiens small nucleolar RNA host gene 17 (SNHG17), transcript variant 4, long non-coding RNAgi|2515429207|ref|NR_152754.2|Nucleotide
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Last Updated: Sep 29, 2024