NM_000135.4(FANCA):c.4183C>T (p.Leu1395=) AND Fanconi anemia
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002204843.6
Allele description [Variation Report for NM_000135.4(FANCA):c.4183C>T (p.Leu1395=)]
NM_000135.4(FANCA):c.4183C>T (p.Leu1395=)
Condition(s)
-
AV724901 HTB Homo sapiens cDNA clone HTBCFD07 5', mRNA sequence
AV724901 HTB Homo sapiens cDNA clone HTBCFD07 5', mRNA sequencegi|55949322|gnl|dbEST|26486168|dbj| 901.2|Nucleotide
-
AV724884 HTB Homo sapiens cDNA clone HTBARF11 5', mRNA sequence
AV724884 HTB Homo sapiens cDNA clone HTBARF11 5', mRNA sequencegi|55949321|gnl|dbEST|26486167|dbj| 884.2|Nucleotide
-
AV724931 HTB Homo sapiens cDNA clone HTBCEH04 5', mRNA sequence
AV724931 HTB Homo sapiens cDNA clone HTBCEH04 5', mRNA sequencegi|55949329|gnl|dbEST|26486175|dbj| 931.2|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024