ENST00000512519.2:n.165+362_165+364delTTT

Variant names:

• chr5-38845303-CAAA-C
• rs5867434
• ENST00000512519.2:n.165+362_165+364delTTT

Variant summary

Our verdict is Uncertain significance. The variant received 0 ACMG points: 0P and 0B.

The ENST00000512519.2(OSMR-DT):​n.165+362_165+364delTTT variant causes a intron change involving the alteration of a non-conserved nucleotide. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: 𝑓 0.0 (0 hom., cov: 0)
  • Failed GnomAD Quality Control
• Consequence: OSMR-DT ENST00000512519.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0280
• Publications: 0 publications found

Genes affected

OSMR-DT (HGNC:50296): (OSMR divergent transcript)

ACMG classification

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
OSMR-DT	NR_109951.1	n.162+362_162+364delTTT		intron_variant	Intron 1 of 3
OSMR-DT	NR_171676.1	n.102+362_102+364delTTT		intron_variant	Intron 1 of 2
OSMR-DT	NR_171677.1	n.102+362_102+364delTTT		intron_variant	Intron 1 of 2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
OSMR-DT	ENST00000512519.2	n.165+362_165+364delTTT		intron_variant	Intron 1 of 1	2
OSMR-DT	ENST00000513480.2	n.107+362_107+364delTTT		intron_variant	Intron 1 of 3	4
OSMR-DT	ENST00000636516.3	n.151+362_151+364delTTT		intron_variant	Intron 1 of 5	5

Frequencies

GnomAD3 genomes AF: 0.00 AC: 0 AN: 89692 Hom.: 0 Cov.: 0

Gnomad AFR AF: 0.00

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.00

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.00

Gnomad OTH AF: 0.00

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 89692 Hom.: 0 Cov.: 0 AF XY: 0.00 AC XY: 0 AN XY: 41168

African (AFR) AF: 0.00 AC: 0 AN: 21944

American (AMR) AF: 0.00 AC: 0 AN: 7534

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 2542

East Asian (EAS) AF: 0.00 AC: 0 AN: 3534

South Asian (SAS) AF: 0.00 AC: 0 AN: 2440

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 2704

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 166

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 46992

Other (OTH) AF: 0.00 AC: 0 AN: 1158

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
PhyloP100		-0.028

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs5867434; hg19: chr5-38845405;