chr9-134544368-G-C
Variant summary
Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_StrongBA1
The ENST00000435284.2(ENSG00000228877):n.104-552G>C 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 0.297 in 152,154 control chromosomes in the GnomAD database, including 6,983 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 |
---|---|---|---|---|---|---|---|
LOC100506532 | XR_930417.3 | n.352-552G>C | intron_variant, non_coding_transcript_variant | ||||
LOC100506532 | XR_109854.6 | n.2233-552G>C | intron_variant, non_coding_transcript_variant | ||||
LOC100506532 | XR_930416.3 | n.181-552G>C | intron_variant, non_coding_transcript_variant |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
ENST00000435284.2 | n.104-552G>C | intron_variant, non_coding_transcript_variant | 3 |
Frequencies
GnomAD3 genomes AF: 0.297 AC: 45144AN: 152036Hom.: 6981 Cov.: 33
GnomAD4 genome AF: 0.297 AC: 45165AN: 152154Hom.: 6983 Cov.: 33 AF XY: 0.296 AC XY: 22053AN XY: 74390
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at