rs863225091
Variant summary
Our verdict is Pathogenic. Variant got 11 ACMG points: 11P and 0B. PVS1PM2PP5
The NM_005060.4(RORC):c.985C>T(p.Gln329Ter) variant causes a stop gained change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. Variant has been reported in ClinVar as Pathogenic (no stars). Synonymous variant affecting the same amino acid position (i.e. Q329Q) has been classified as Likely benign. Variant results in nonsense mediated mRNA decay.
Frequency
Consequence
NM_005060.4 stop_gained
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Pathogenic. Variant got 11 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
RORC | NM_005060.4 | c.985C>T | p.Gln329Ter | stop_gained | 7/11 | ENST00000318247.7 | |
RORC | NM_001001523.2 | c.922C>T | p.Gln308Ter | stop_gained | 6/10 | ||
RORC | XM_006711484.5 | c.1147C>T | p.Gln383Ter | stop_gained | 8/12 | ||
RORC | XM_047427201.1 | c.1004C>T | p.Ser335Leu | missense_variant | 6/6 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
RORC | ENST00000318247.7 | c.985C>T | p.Gln329Ter | stop_gained | 7/11 | 1 | NM_005060.4 | P4 |
Frequencies
GnomAD3 genomes ? Cov.: 32
GnomAD4 exome Cov.: 31
GnomAD4 genome ? Cov.: 32
ClinVar
Submissions by phenotype
Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency Pathogenic:1
Pathogenic, no assertion criteria provided | literature only | OMIM | Aug 07, 2015 | - - |
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at