NM_000193.4(SHH):c.93G>T (p.Gly31=) AND Holoprosencephaly 3
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002625922.3
Allele description [Variation Report for NM_000193.4(SHH):c.93G>T (p.Gly31=)]
NM_000193.4(SHH):c.93G>T (p.Gly31=)
Condition(s)
-
AGENCOURT_13045247 NICHD_XGC_Te1 Xenopus laevis cDNA clone IMAGE:6928663 5', mRN...
AGENCOURT_13045247 NICHD_XGC_Te1 Xenopus laevis cDNA clone IMAGE:6928663 5', mRNA sequencegi|29509735|gnl|dbEST|17327951|gb|C 79.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024