NM_000504.4(F10):c.1216G>A (p.Gly406Ser) AND Hereditary factor X deficiency disease
- Germline classification:
- Pathogenic (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001834560.2
Allele description [Variation Report for NM_000504.4(F10):c.1216G>A (p.Gly406Ser)]
NM_000504.4(F10):c.1216G>A (p.Gly406Ser)
Condition(s)
-
Osmia ferruginea voucher BBSLID115538 NADH dehydrogenase subunit 5 (ND5) gene, p...
Osmia ferruginea voucher BBSLID115538 NADH dehydrogenase subunit 5 (ND5) gene, partial cds; mitochondrialgi|2294229775|gb|MW043344.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024