NM_005249.5(FOXG1):c.1235G>A (p.Gly412Asp) AND Rett syndrome, congenital variant
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 23, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002302966.4
Allele description [Variation Report for NM_005249.5(FOXG1):c.1235G>A (p.Gly412Asp)]
NM_005249.5(FOXG1):c.1235G>A (p.Gly412Asp)
Condition(s)
-
AGENCOURT_15065407 NICHD_XGC_Emb7 Xenopus tropicalis cDNA clone IMAGE:6976931 3'...
AGENCOURT_15065407 NICHD_XGC_Emb7 Xenopus tropicalis cDNA clone IMAGE:6976931 3', mRNA sequencegi|33423955|gnl|dbEST|19437092|gb|C 47.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024