NM_006988.5(ADAMTS1):c.1840C>T (p.Pro614Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 8, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004615137.1
Allele description [Variation Report for NM_006988.5(ADAMTS1):c.1840C>T (p.Pro614Ser)]
NM_006988.5(ADAMTS1):c.1840C>T (p.Pro614Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Human DNA sequence from clone RP11-231K24 on chromosome 9, complete sequence
Human DNA sequence from clone RP11-231K24 on chromosome 9, complete sequencegi|20068404|emb|AL357073.19|Nucleotide
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See more...Assertion and evidence details
Last Updated: Aug 11, 2024