rs1362621

Positions:

• chr16-55654572-G-A

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The XR_007065075.1(LOC124903693):​n.516-633C>T variant causes a intron, non coding transcript change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.748 in 152,122 control chromosomes in the GnomAD database, including 42,783 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.75 (42783 hom., cov: 32)
• Consequence: LOC124903693 XR_007065075.1 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.451

Genes affected

LOC124903693 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.8 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
LOC124903693	XR_007065075.1	n.516-633C>T		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt

Frequencies

GnomAD3 genomes AF: 0.748 AC: 113717 AN: 152004 Hom.: 42746 Cov.: 32

Gnomad AFR AF: 0.807

Gnomad AMI AF: 0.651

Gnomad AMR AF: 0.782

Gnomad ASJ AF: 0.707

Gnomad EAS AF: 0.712

Gnomad SAS AF: 0.728

Gnomad FIN AF: 0.737

Gnomad MID AF: 0.630

Gnomad NFE AF: 0.715

Gnomad OTH AF: 0.730

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

GnomAD4 genome AF: 0.748 AC: 113818 AN: 152122 Hom.: 42783 Cov.: 32 AF XY: 0.752 AC XY: 55925 AN XY: 74384

Gnomad4 AFR AF: 0.807

Gnomad4 AMR AF: 0.783

Gnomad4 ASJ AF: 0.707

Gnomad4 EAS AF: 0.711

Gnomad4 SAS AF: 0.728

Gnomad4 FIN AF: 0.737

Gnomad4 NFE AF: 0.715

Gnomad4 OTH AF: 0.734

Alfa AF: 0.734 Hom.: 5102

Bravo AF: 0.755

Asia WGS AF: 0.715 AC: 2485 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	1.0
DANN	Benign	0.56

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs1362621; hg19: chr16-55688484;