NM_001387025.1(GRAMD1B):c.1397A>G (p.Asn466Ser) AND GRAMD1B-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 24, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003924590.2
Allele description [Variation Report for NM_001387025.1(GRAMD1B):c.1397A>G (p.Asn466Ser)]
NM_001387025.1(GRAMD1B):c.1397A>G (p.Asn466Ser)
Condition(s)
- Name:
- GRAMD1B-related disorder
- Synonyms:
- GRAMD1B-related condition
- Identifiers:
-
MAG: Nitrospira sp. AMX-MBFR-67 DNA, sequence001, whole genome shotgun sequence
MAG: Nitrospira sp. AMX-MBFR-67 DNA, sequence001, whole genome shotgun sequencegi|2804189585|dbj|BTVL01000001.1||g S:BTVL01|sequence001Nucleotide
-
DB551809 RIKEN full-length enriched human cDNA library, hippocampus Homo sapiens...
DB551809 RIKEN full-length enriched human cDNA library, hippocampus Homo sapiens cDNA clone H023095J15 3', mRNA sequencegi|90943068|gnl|dbEST|37977425|dbj| 809.1|Nucleotide
-
RecName: Full=DNA mismatch repair protein MutS 1
RecName: Full=DNA mismatch repair protein MutS 1gi|115299204|sp|Q5UZG9.2|MUTS1_HALMProtein
-
H.sapiens mRNA for amphiglycan
H.sapiens mRNA for amphiglycangi|28679|emb|X67016.1|Nucleotide
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Last Updated: Oct 13, 2024