NM_033656.4(BRWD1):c.4601A>G (p.Asp1534Gly) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004299063.1
Allele description [Variation Report for NM_033656.4(BRWD1):c.4601A>G (p.Asp1534Gly)]
NM_033656.4(BRWD1):c.4601A>G (p.Asp1534Gly)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens coronin 6 (CORO6), transcript variant X7, mRNA
PREDICTED: Homo sapiens coronin 6 (CORO6), transcript variant X7, mRNAgi|2217314420|ref|XM_011525391.4|Nucleotide
-
coronin-6 isoform X1 [Homo sapiens]
coronin-6 isoform X1 [Homo sapiens]gi|2462558340|ref|XP_054173558.1|Protein
-
Homo sapiens coronin 6 (CORO6), transcript variant 11, non-coding RNA
Homo sapiens coronin 6 (CORO6), transcript variant 11, non-coding RNAgi|1926856118|ref|NR_170977.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024