NM_001845.6(COL4A1):c.2705C>T (p.Pro902Leu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 15, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002551089.2
Allele description [Variation Report for NM_001845.6(COL4A1):c.2705C>T (p.Pro902Leu)]
NM_001845.6(COL4A1):c.2705C>T (p.Pro902Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Human DNA sequence from clone RP11-231P20 on chromosome 1, complete sequence
Human DNA sequence from clone RP11-231P20 on chromosome 1, complete sequencegi|16972866|emb|AL355877.25|Nucleotide
-
CBST1126.fwd NICHD_XGC_tropThy1 Xenopus tropicalis cDNA clone IMAGE:8923364 5', ...
CBST1126.fwd NICHD_XGC_tropThy1 Xenopus tropicalis cDNA clone IMAGE:8923364 5', mRNA sequencegi|126545533|gnl|dbEST|45059404|gb| 045.1|Nucleotide
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Last Updated: Oct 8, 2024