NM_000094.4(COL7A1):c.7983+10G>A AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 4, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001410263.6
Allele description [Variation Report for NM_000094.4(COL7A1):c.7983+10G>A]
NM_000094.4(COL7A1):c.7983+10G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
UI-CF-EN1-adh-e-12-0-UI.s1 UI-CF-EN1 Homo sapiens cDNA clone UI-CF-EN1-adh-e-12-...
UI-CF-EN1-adh-e-12-0-UI.s1 UI-CF-EN1 Homo sapiens cDNA clone UI-CF-EN1-adh-e-12-0-UI 3', mRNA sequencegi|19603663|gnl|dbEST|11799607|gb|B 09.1|Nucleotide
-
Homo sapiens golgi autoantigen, golgin subfamily a, 3, mRNA (cDNA clone MGC:1648...
Homo sapiens golgi autoantigen, golgin subfamily a, 3, mRNA (cDNA clone MGC:164894 IMAGE:40148073), complete cdsgi|148744348|gb|BC142658.1|Nucleotide
-
UI-1-BB1-aib-e-02-0-UI.s1 NCI_CGAP_Pl5 Homo sapiens cDNA clone UI-1-BB1-aib-e-02...
UI-1-BB1-aib-e-02-0-UI.s1 NCI_CGAP_Pl5 Homo sapiens cDNA clone UI-1-BB1-aib-e-02-0-UI 3', mRNA sequencegi|23710546|gnl|dbEST|14217476|gb|B 79.1|Nucleotide
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Last Updated: Sep 29, 2024