3-186538897-G-T
Variant summary
Our verdict is Likely benign. Variant got -3 ACMG points: 2P and 5B. PM2BP4_StrongBP7
The NM_017541.4(CRYGS):c.336C>A(p.Thr112Thr) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000205 in 1,461,832 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Synonymous variant affecting the same amino acid position (i.e. T112T) has been classified as Likely benign.
Frequency
Consequence
NM_017541.4 synonymous
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Likely_benign. Variant got -3 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | Exon rank | MANE | Protein | UniProt |
---|---|---|---|---|---|---|---|---|
CRYGS | NM_017541.4 | c.336C>A | p.Thr112Thr | synonymous_variant | Exon 3 of 3 | ENST00000307944.6 | NP_060011.1 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | Exon rank | TSL | MANE | Protein | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|---|
CRYGS | ENST00000307944.6 | c.336C>A | p.Thr112Thr | synonymous_variant | Exon 3 of 3 | 1 | NM_017541.4 | ENSP00000312099.5 | ||
CRYGS | ENST00000460288.1 | n.1238C>A | non_coding_transcript_exon_variant | Exon 2 of 2 | 1 | |||||
CRYGS | ENST00000392499.6 | c.336C>A | p.Thr112Thr | synonymous_variant | Exon 4 of 4 | 2 | ENSP00000376287.2 |
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD4 exome AF: 0.00000205 AC: 3AN: 1461832Hom.: 0 Cov.: 31 AF XY: 0.00000138 AC XY: 1AN XY: 727214
GnomAD4 genome Cov.: 32
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at
Publications
No publications associated with this variant yet.