NM_001007237.3(IGSF3):c.711G>C (p.Gln237His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004350099.1
Allele description [Variation Report for NM_001007237.3(IGSF3):c.711G>C (p.Gln237His)]
NM_001007237.3(IGSF3):c.711G>C (p.Gln237His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Rattus norvegicus strain BN/NHsdMcwi chromosome X, GRCr8, whole genome shotgun s...
Rattus norvegicus strain BN/NHsdMcwi chromosome X, GRCr8, whole genome shotgun sequencegi|2671914584|gnl|ASM:GCF_036323745 |ref|NC_086039.1||gpp|GPC_000020864.1||gnl|NCBI_GENOMES|157510Nucleotide
-
GSE93998[Accession] (13)
GEO DataSets
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Last Updated: May 26, 2024