NM_173593.4(B4GALNT3):c.2306C>T (p.Ala769Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004357753.1
Allele description [Variation Report for NM_173593.4(B4GALNT3):c.2306C>T (p.Ala769Val)]
NM_173593.4(B4GALNT3):c.2306C>T (p.Ala769Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens galactose-3-O-sulfotransferase 1 (GAL3ST1), transcript variant 7, m...
Homo sapiens galactose-3-O-sulfotransferase 1 (GAL3ST1), transcript variant 7, mRNAgi|1676317178|ref|NM_001318111.2|Nucleotide
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Last Updated: Oct 13, 2024