13-50843511-C-T
Variant summary
Our verdict is Likely benign. Variant got -2 ACMG points: 0P and 2B. BP4_Moderate
The NM_001306135.2(DLEU7):c.136G>A(p.Val46Met) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0000184 in 1,409,790 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. 12/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).
Frequency
Consequence
NM_001306135.2 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Likely_benign. Variant got -2 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
DLEU7 | NM_001306135.2 | c.136G>A | p.Val46Met | missense_variant | 1/2 | ENST00000504404.2 | |
DLEU7-AS1 | NR_046551.1 | n.438+3417C>T | intron_variant, non_coding_transcript_variant | ||||
DLEU7 | NM_198989.3 | c.136G>A | p.Val46Met | missense_variant | 1/2 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
DLEU7 | ENST00000504404.2 | c.136G>A | p.Val46Met | missense_variant | 1/2 | 1 | NM_001306135.2 | P1 |
Frequencies
GnomAD3 genomes ? AF: 0.00000659 AC: 1AN: 151650Hom.: 0 Cov.: 32
GnomAD4 exome AF: 0.0000199 AC: 25AN: 1258140Hom.: 0 Cov.: 31 AF XY: 0.0000261 AC XY: 16AN XY: 613976
GnomAD4 genome ? AF: 0.00000659 AC: 1AN: 151650Hom.: 0 Cov.: 32 AF XY: 0.0000135 AC XY: 1AN XY: 74050
ClinVar
Submissions by phenotype
not specified Uncertain:1
Uncertain significance, criteria provided, single submitter | clinical testing | Ambry Genetics | Nov 22, 2021 | The c.136G>A (p.V46M) alteration is located in exon 1 (coding exon 1) of the DLEU7 gene. This alteration results from a G to A substitution at nucleotide position 136, causing the valine (V) at amino acid position 46 to be replaced by a methionine (M). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. - |
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at