NM_017581.4(CHRNA9):c.298G>C (p.Asp100His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 9, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004441500.1
Allele description [Variation Report for NM_017581.4(CHRNA9):c.298G>C (p.Asp100His)]
NM_017581.4(CHRNA9):c.298G>C (p.Asp100His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens cDNA FLJ32542 fis, clone SMINT2000537
Homo sapiens cDNA FLJ32542 fis, clone SMINT2000537gi|16552690|dbj|AK057104.1|Nucleotide
-
UI-H-BI2-agy-e-08-0-UI.s1 NCI_CGAP_Sub4 Homo sapiens cDNA clone IMAGE:2726102 3'...
UI-H-BI2-agy-e-08-0-UI.s1 NCI_CGAP_Sub4 Homo sapiens cDNA clone IMAGE:2726102 3', mRNA sequencegi|6698939|gnl|dbEST|3675411|gb|AW2 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024