NM_001360.3(DHCR7):c.89G>C (p.Gly30Ala) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (3 submissions)
- Last evaluated:
- May 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000728279.32
Allele description [Variation Report for NM_001360.3(DHCR7):c.89G>C (p.Gly30Ala)]
NM_001360.3(DHCR7):c.89G>C (p.Gly30Ala)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PM1-HT0350-070100-006-b02 HT0350 Homo sapiens cDNA, mRNA sequence
PM1-HT0350-070100-006-b02 HT0350 Homo sapiens cDNA, mRNA sequencegi|7254879|gnl|dbEST|4012352|gb|AW5 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 1, 2024