NM_198129.4(LAMA3):c.856-5T>C AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 16, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000976217.15
Allele description [Variation Report for NM_198129.4(LAMA3):c.856-5T>C]
NM_198129.4(LAMA3):c.856-5T>C
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens chromosome 18, clone RP11-666O22, complete sequence
Homo sapiens chromosome 18, clone RP11-666O22, complete sequencegi|18370004|gnl|WIBR|L12657|gb|AC09 8|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024