NM_000388.4(CASR):c.2349G>A (p.Leu783=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001242556.8
Allele description [Variation Report for NM_000388.4(CASR):c.2349G>A (p.Leu783=)]
NM_000388.4(CASR):c.2349G>A (p.Leu783=)
Condition(s)
-
Glycos_transf_1, partial [uncultured Candidatus Desulforudis sp.]
Glycos_transf_1, partial [uncultured Candidatus Desulforudis sp.]gi|643017809|gb|AIA85489.1|Protein
-
CAZy families GT2 protein, partial [uncultured Candidatus Desulforudis sp.]
CAZy families GT2 protein, partial [uncultured Candidatus Desulforudis sp.]gi|643035154|gb|AIA94201.1|Protein
-
CAZy families GT51 protein, partial [uncultured Candidatus Desulforudis sp.]
CAZy families GT51 protein, partial [uncultured Candidatus Desulforudis sp.]gi|643024905|gb|AIA89052.1|Protein
-
uncharacterized protein C2orf92 isoform X7 [Homo sapiens]
uncharacterized protein C2orf92 isoform X7 [Homo sapiens]gi|2462496681|ref|XP_054188970.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024