rs11070192
Variant summary
Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_StrongBA1
The ENST00000560484.1(ENSG00000259345):n.67+84707C>T 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 0.799 in 152,186 control chromosomes in the GnomAD database, including 49,029 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
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 |
---|---|---|---|---|---|---|---|
LOC105370777 | XR_007064588.1 | n.517+84342C>T | intron_variant, non_coding_transcript_variant |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
ENST00000560484.1 | n.67+84707C>T | intron_variant, non_coding_transcript_variant | 4 | ||||||
ENST00000558209.1 | n.451+23587C>T | intron_variant, non_coding_transcript_variant | 3 | ||||||
ENST00000559318.1 | n.409-36720C>T | intron_variant, non_coding_transcript_variant | 4 |
Frequencies
GnomAD3 genomes ? AF: 0.799 AC: 121563AN: 152068Hom.: 48997 Cov.: 32
GnomAD4 genome ? AF: 0.799 AC: 121643AN: 152186Hom.: 49029 Cov.: 32 AF XY: 0.794 AC XY: 59118AN XY: 74412
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at