NM_000428.3(LTBP2):c.4693C>T (p.Arg1565Cys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 3, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004245948.1
Allele description [Variation Report for NM_000428.3(LTBP2):c.4693C>T (p.Arg1565Cys)]
NM_000428.3(LTBP2):c.4693C>T (p.Arg1565Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
TSA: Tetralonia malvae s7977_L_20383_0_a_3_4_l_1159 transcribed RNA sequence
TSA: Tetralonia malvae s7977_L_20383_0_a_3_4_l_1159 transcribed RNA sequencegi|1163964569|gb|GBNI01029739.1||gn :GBNI01|s7977_L_20383_0_a_3_4_l_1159Nucleotide
-
TSA: Tetralonia malvae s7979_L_20388_0_a_8_9_l_1010 transcribed RNA sequence
TSA: Tetralonia malvae s7979_L_20388_0_a_8_9_l_1010 transcribed RNA sequencegi|1163964567|gb|GBNI01029741.1||gn :GBNI01|s7979_L_20388_0_a_8_9_l_1010Nucleotide
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Last Updated: Sep 29, 2024