NM_006662.3(SRCAP):c.546G>C (p.Arg182=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 6, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002766785.2
Allele description
NM_006662.3(SRCAP):c.546G>C (p.Arg182=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens retinitis pigmentosa GTPase regulator (RPGR), transcript variant E,...
Homo sapiens retinitis pigmentosa GTPase regulator (RPGR), transcript variant E, mRNAgi|1512432668|ref|NM_001367246.1|Nucleotide
-
X-linked retinitis pigmentosa GTPase regulator isoform J [Homo sapiens]
X-linked retinitis pigmentosa GTPase regulator isoform J [Homo sapiens]gi|1512432630|ref|NP_001354180.1|Protein
-
JGI_XZG45939.rev NIH_XGC_tropGas7 Xenopus tropicalis cDNA clone IMAGE:7560568 3'...
JGI_XZG45939.rev NIH_XGC_tropGas7 Xenopus tropicalis cDNA clone IMAGE:7560568 3', mRNA sequencegi|71977670|gnl|dbEST|30630437|gb|C 29.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Feb 28, 2024