6-100420845-G-C
Variant summary
Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2BP4_Moderate
The NM_005068.3(SIM1):c.1112C>G(p.Ala371Gly) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 14/21 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. A371V) has been classified as Benign.
Frequency
Consequence
NM_005068.3 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Uncertain_significance. Variant got 0 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
SIM1 | NM_005068.3 | c.1112C>G | p.Ala371Gly | missense_variant | 10/12 | ENST00000369208.8 | |
SIM1-AS1 | XR_942815.4 | n.891-6273G>C | intron_variant, non_coding_transcript_variant | ||||
SIM1 | NM_001374769.1 | c.1112C>G | p.Ala371Gly | missense_variant | 10/12 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
SIM1 | ENST00000369208.8 | c.1112C>G | p.Ala371Gly | missense_variant | 10/12 | 1 | NM_005068.3 | P1 | |
SIM1 | ENST00000262901.4 | c.1112C>G | p.Ala371Gly | missense_variant | 9/11 | 1 | P1 |
Frequencies
GnomAD3 genomes ? Cov.: 32
GnomAD4 exome Cov.: 33
GnomAD4 genome ? Cov.: 32
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at