9-133664010-G-A
Variant summary
Our verdict is Uncertain significance. Variant got 1 ACMG points: 2P and 1B. PM2BP4
The NM_001134707.2(SARDH):c.2636C>T(p.Ser879Leu) variant causes a missense change. The variant allele was found at a frequency of 0.0000223 in 1,614,044 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_001134707.2 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Uncertain_significance. Variant got 1 ACMG points.
Transcripts
RefSeq
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | Exon rank | TSL | MANE | Protein | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|---|
SARDH | ENST00000439388.6 | c.2636C>T | p.Ser879Leu | missense_variant | Exon 21 of 21 | 2 | NM_001134707.2 | ENSP00000403084.1 | ||
SARDH | ENST00000371872.8 | c.2636C>T | p.Ser879Leu | missense_variant | Exon 21 of 21 | 1 | ENSP00000360938.4 | |||
SARDH | ENST00000371868.5 | c.986C>T | p.Ser329Leu | missense_variant | Exon 9 of 9 | 2 | ENSP00000360934.1 | |||
SARDH | ENST00000469828.1 | n.394C>T | non_coding_transcript_exon_variant | Exon 2 of 2 | 2 |
Frequencies
GnomAD3 genomes AF: 0.0000394 AC: 6AN: 152230Hom.: 0 Cov.: 33
GnomAD3 exomes AF: 0.0000319 AC: 8AN: 250878Hom.: 0 AF XY: 0.0000369 AC XY: 5AN XY: 135544
GnomAD4 exome AF: 0.0000205 AC: 30AN: 1461696Hom.: 0 Cov.: 31 AF XY: 0.0000248 AC XY: 18AN XY: 727136
GnomAD4 genome AF: 0.0000394 AC: 6AN: 152348Hom.: 0 Cov.: 33 AF XY: 0.0000805 AC XY: 6AN XY: 74506
ClinVar
Submissions by phenotype
not specified Uncertain:1
The c.2636C>T (p.S879L) alteration is located in exon 21 (coding exon 20) of the SARDH gene. This alteration results from a C to T substitution at nucleotide position 2636, causing the serine (S) at amino acid position 879 to be replaced by a leucine (L). 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