NM_000203.5(IDUA):c.1727+4C>T AND Hurler syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 26, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000670259.1
Allele description [Variation Report for NM_000203.5(IDUA):c.1727+4C>T]
NM_000203.5(IDUA):c.1727+4C>T
Condition(s)
-
23S rRNA pseudouridine synthase D [Vibrio vulnificus CMCP6]
23S rRNA pseudouridine synthase D [Vibrio vulnificus CMCP6]gi|27363948|gnl|REF_CMCP6|VV1_0484| P_759476.1|Protein
-
23S rRNA pseudouridine synthase D [Vibrio vulnificus YJ016]
23S rRNA pseudouridine synthase D [Vibrio vulnificus YJ016]gi|37678897|ref|NP_933506.1|Protein
-
Homo sapiens FOSMID clone ABC12-46663800M24 from chromosome unknown, complete se...
Homo sapiens FOSMID clone ABC12-46663800M24 from chromosome unknown, complete sequencegi|256821038|gb|AC234917.3||gnl|wug C12-46663800M24Nucleotide
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See more...Assertion and evidence details
Last Updated: Jul 15, 2024