NM_020335.3(VANGL2):c.215C>T (p.Thr72Met) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 25, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004480054.1
Allele description [Variation Report for NM_020335.3(VANGL2):c.215C>T (p.Thr72Met)]
NM_020335.3(VANGL2):c.215C>T (p.Thr72Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Hypothetical protein
Hypothetical proteingi|122396861|sp|Q1G849|Q1G849_LACDAProtein
-
MIR6798[gene] (3)
ClinVar
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Limosilactobacillus reuteri strain PTA4_C1 NODE_78_length_2706_cov_88.2963, whol...
Limosilactobacillus reuteri strain PTA4_C1 NODE_78_length_2706_cov_88.2963, whole genome shotgun sequencegi|1771426394|ref|NZ_QKQH01000078.1 |WGS:NZ_QKQH01|NODE_78_length_2706_cov_88.2963Nucleotide
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Limosilactobacillus reuteri strain PTA2_C2 NODE_81_length_2598_cov_133.783, whol...
Limosilactobacillus reuteri strain PTA2_C2 NODE_81_length_2598_cov_133.783, whole genome shotgun sequencegi|1771405795|ref|NZ_QKQI01000081.1 |WGS:NZ_QKQI01|NODE_81_length_2598_cov_133.783Nucleotide
-
PREDICTED: Homo sapiens uncharacterized lncRNA (LOC105372432), transcript varian...
PREDICTED: Homo sapiens uncharacterized lncRNA (LOC105372432), transcript variant X3, ncRNAgi|2217502164|ref|XR_007089194.1|Nucleotide
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Last Updated: May 7, 2024