chr1-173946576-T-C
Variant summary
Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2BP4_Moderate
The NM_172071.4(RC3H1):c.2861A>G(p.His954Arg) variant causes a missense change. The variant allele was found at a frequency of 0.000000684 in 1,461,802 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).
Frequency
Consequence
NM_172071.4 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Uncertain_significance. Variant got 0 ACMG points.
Transcripts
RefSeq
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | Exon rank | TSL | MANE | Protein | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|---|
RC3H1 | ENST00000367696.7 | c.2861A>G | p.His954Arg | missense_variant | Exon 17 of 20 | 5 | NM_172071.4 | ENSP00000356669.2 | ||
RC3H1 | ENST00000258349.8 | c.2861A>G | p.His954Arg | missense_variant | Exon 16 of 19 | 1 | ||||
RC3H1 | ENST00000367694.2 | c.2861A>G | p.His954Arg | missense_variant | Exon 16 of 19 | 2 | ENSP00000356667.2 |
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD3 exomes AF: 0.00000398 AC: 1AN: 251290Hom.: 0 AF XY: 0.00000736 AC XY: 1AN XY: 135822
GnomAD4 exome AF: 6.84e-7 AC: 1AN: 1461802Hom.: 0 Cov.: 31 AF XY: 0.00000138 AC XY: 1AN XY: 727208
GnomAD4 genome Cov.: 32
ClinVar
Submissions by phenotype
not specified Uncertain:1
The c.2861A>G (p.H954R) alteration is located in exon 16 (coding exon 16) of the RC3H1 gene. This alteration results from a A to G substitution at nucleotide position 2861, causing the histidine (H) at amino acid position 954 to be replaced by an arginine (R). 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