chrX-44178493-C-T
Variant summary
Our verdict is Likely benign. Variant got -6 ACMG points: 0P and 6B. BP4_ModerateBS2
The NM_025184.4(EFHC2):c.1823G>A(p.Arg608His) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000914 in 1,204,024 control chromosomes in the GnomAD database, with no homozygous occurrence. There are 2 hemizygotes in GnomAD. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. R608C) has been classified as Uncertain significance.
Frequency
Consequence
NM_025184.4 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Likely_benign. Variant got -6 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
EFHC2 | NM_025184.4 | c.1823G>A | p.Arg608His | missense_variant | 12/15 | ENST00000420999.2 | |
EFHC2 | XM_047442535.1 | c.1823G>A | p.Arg608His | missense_variant | 12/14 | ||
EFHC2 | XM_047442536.1 | c.1823G>A | p.Arg608His | missense_variant | 12/15 | ||
EFHC2 | XM_006724562.3 | c.1235G>A | p.Arg412His | missense_variant | 11/14 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
EFHC2 | ENST00000420999.2 | c.1823G>A | p.Arg608His | missense_variant | 12/15 | 1 | NM_025184.4 | P1 | |
EFHC2 | ENST00000343571.3 | n.144G>A | non_coding_transcript_exon_variant | 2/5 | 2 |
Frequencies
GnomAD3 genomes AF: 0.0000355 AC: 4AN: 112540Hom.: 0 Cov.: 24 AF XY: 0.00 AC XY: 0AN XY: 34706
GnomAD3 exomes AF: 0.0000174 AC: 3AN: 172828Hom.: 0 AF XY: 0.0000168 AC XY: 1AN XY: 59670
GnomAD4 exome AF: 0.00000641 AC: 7AN: 1091484Hom.: 0 Cov.: 29 AF XY: 0.00000560 AC XY: 2AN XY: 357444
GnomAD4 genome AF: 0.0000355 AC: 4AN: 112540Hom.: 0 Cov.: 24 AF XY: 0.00 AC XY: 0AN XY: 34706
ClinVar
Submissions by phenotype
not specified Uncertain:1
Uncertain significance, criteria provided, single submitter | clinical testing | Ambry Genetics | Jan 04, 2024 | The c.1823G>A (p.R608H) alteration is located in exon 12 (coding exon 12) of the EFHC2 gene. This alteration results from a G to A substitution at nucleotide position 1823, causing the arginine (R) at amino acid position 608 to be replaced by a histidine (H). 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