NM_000343.4(SLC5A1):c.1725G>A (p.Ala575=) AND Congenital glucose-galactose malabsorption
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Nov 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000358722.12
Allele description [Variation Report for NM_000343.4(SLC5A1):c.1725G>A (p.Ala575=)]
NM_000343.4(SLC5A1):c.1725G>A (p.Ala575=)
Condition(s)
- Name:
- Congenital glucose-galactose malabsorption (GGM)
- Synonyms:
- Glucose galactose malabsorption deficiency; Carbohydrate intolerance of glucose galactose; Complex carbohydrate intolerance; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0011731; MedGen: C0268186; Orphanet: 35710; OMIM: 606824
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RNA binding protein fox-1 homolog 3 isoform X1 [Homo sapiens]
RNA binding protein fox-1 homolog 3 isoform X1 [Homo sapiens]gi|1370470216|ref|XP_024306363.1|Protein
-
RNA binding protein fox-1 homolog 3 isoform 1 [Homo sapiens]
RNA binding protein fox-1 homolog 3 isoform 1 [Homo sapiens]gi|1882652652|ref|NP_001372761.1|Protein
-
Mus musculus two pore segment channel 2 (Tpcn2), transcript variant 2, non-codin...
Mus musculus two pore segment channel 2 (Tpcn2), transcript variant 2, non-coding RNAgi|2174214091|ref|NR_132642.2|Nucleotide
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Last Updated: Sep 29, 2024