NM_001101662.2(NRDC):c.2869A>G (p.Thr957Ala) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 12, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004143170.1
Allele description [Variation Report for NM_001101662.2(NRDC):c.2869A>G (p.Thr957Ala)]
NM_001101662.2(NRDC):c.2869A>G (p.Thr957Ala)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Gossypium raimondii isolate D5-3 chromosome 3
Gossypium raimondii isolate D5-3 chromosome 3gi|2748524284|gb|CP156733.1|Nucleotide
-
Gossypium raimondii isolate D5-3 chromosome 2
Gossypium raimondii isolate D5-3 chromosome 2gi|2748524209|gb|CP156732.1|Nucleotide
-
RC-BT017-311298-002 BT017 Homo sapiens cDNA, mRNA sequence
RC-BT017-311298-002 BT017 Homo sapiens cDNA, mRNA sequencegi|6493210|gnl|dbEST|3024788|gb|AI9 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024