NM_021170.4(HES4):c.559C>T (p.Pro187Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004253647.1
Allele description [Variation Report for NM_021170.4(HES4):c.559C>T (p.Pro187Ser)]
NM_021170.4(HES4):c.559C>T (p.Pro187Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
TMEM169 transmembrane protein 169 [Homo sapiens]
TMEM169 transmembrane protein 169 [Homo sapiens]Gene ID:92691Gene
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Gene Links for GEO Profiles (Select 59294528) (1)
Gene
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RPL37A ribosomal protein L37a [Homo sapiens]
RPL37A ribosomal protein L37a [Homo sapiens]Gene ID:6168Gene
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Gene Links for GEO Profiles (Select 82274741) (1)
Gene
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Related DataSets for GEO Profiles (Select 59294528) (1)
GEO DataSets
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024