NM_001075.6(UGT2B10):c.583G>A (p.Val195Ile) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004344624.1
Allele description [Variation Report for NM_001075.6(UGT2B10):c.583G>A (p.Val195Ile)]
NM_001075.6(UGT2B10):c.583G>A (p.Val195Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Mirafra rufocinnamomea fischeri voucher FMNH 484672 myoglobin gene, intron
Mirafra rufocinnamomea fischeri voucher FMNH 484672 myoglobin gene, introngi|2512549215|gb|OQ551025.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024