rs7544568
Variant summary
Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_StrongBA1
The XR_001737985.1(LOC105378654):n.62-19469G>A variant causes a intron, non coding transcript change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.198 in 152,118 control chromosomes in the GnomAD database, including 3,337 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.
Frequency
Consequence
XR_001737985.1 intron, non_coding_transcript
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Benign. Variant got -12 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
LOC105378654 | XR_001737985.1 | n.62-19469G>A | intron_variant, non_coding_transcript_variant | ||||
LOC105378654 | XR_001737986.1 | n.175+11713G>A | intron_variant, non_coding_transcript_variant | ||||
LOC105378654 | XR_001737987.2 | n.175+11713G>A | intron_variant, non_coding_transcript_variant |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|
Frequencies
GnomAD3 genomes AF: 0.198 AC: 30078AN: 152000Hom.: 3334 Cov.: 32
GnomAD4 genome AF: 0.198 AC: 30094AN: 152118Hom.: 3337 Cov.: 32 AF XY: 0.197 AC XY: 14678AN XY: 74340
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at