NM_000550.3(TYRP1):c.1082-8G>A AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 8, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001821116.4
Allele description [Variation Report for NM_000550.3(TYRP1):c.1082-8G>A]
NM_000550.3(TYRP1):c.1082-8G>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens chromosome 16 open reading frame 74 (C16orf74), transcript variant ...
Homo sapiens chromosome 16 open reading frame 74 (C16orf74), transcript variant 2, non-coding RNAgi|1614232066|ref|NR_161452.1|Nucleotide
-
Homo sapiens chromosome 16 open reading frame 74 (C16orf74), transcript variant ...
Homo sapiens chromosome 16 open reading frame 74 (C16orf74), transcript variant 3, non-coding RNAgi|1614232109|ref|NR_161453.1|Nucleotide
-
RecName: Full=Actin-11; Flags: Precursor
RecName: Full=Actin-11; Flags: Precursorgi|728798|sp|P41341.1|ACTY_LIMPOProtein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024