NM_001195553.2(DCX):c.27C>T (p.Asp9=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003731769.2
Allele description [Variation Report for NM_001195553.2(DCX):c.27C>T (p.Asp9=)]
NM_001195553.2(DCX):c.27C>T (p.Asp9=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Human DNA sequence from clone RP11-439N12 on chromosome 9, complete sequence
Human DNA sequence from clone RP11-439N12 on chromosome 9, complete sequencegi|14031103|emb|AL390732.10|Nucleotide
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Oenococcus oeni strain NXH82 16S ribosomal RNA gene, partial sequence
Oenococcus oeni strain NXH82 16S ribosomal RNA gene, partial sequencegi|2811561117|gb|PQ394697.1|Nucleotide
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Oenococcus oeni strain NXL76 16S ribosomal RNA gene, partial sequence
Oenococcus oeni strain NXL76 16S ribosomal RNA gene, partial sequencegi|2811561112|gb|PQ394692.1|Nucleotide
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Oenococcus oeni strain NXH76 16S ribosomal RNA gene, partial sequence
Oenococcus oeni strain NXH76 16S ribosomal RNA gene, partial sequencegi|2811561102|gb|PQ394682.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024