rs61883261

Variant names:

• chr11-20962659-A-T
• rs61883261
• NM_006157.5:c.1300+2099A>T

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_006157.5(NELL1):​c.1300+2099A>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0408 in 152,226 control chromosomes in the GnomAD database, including 132 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 0.041 (132 hom., cov: 32)
• Consequence: NELL1 NM_006157.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.258
• Publications: 2 publications found

Genes affected

NELL1 (HGNC:7750): (neural EGFL like 1) This gene encodes a cytoplasmic protein that contains epidermal growth factor (EGF)-like repeats. The encoded heterotrimeric protein may be involved in cell growth regulation and differentiation. A similar protein in rodents is involved in craniosynostosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.0775 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
NELL1	NM_006157.5	c.1300+2099A>T		intron_variant	Intron 12 of 19	ENST00000357134.10	NP_006148.2
NELL1	NM_001288713.1	c.1384+2099A>T		intron_variant	Intron 13 of 20		NP_001275642.1
NELL1	NM_201551.2	c.1300+2099A>T		intron_variant	Intron 12 of 18		NP_963845.1
NELL1	NM_001288714.1	c.1129+2099A>T		intron_variant	Intron 11 of 18		NP_001275643.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
NELL1	ENST00000357134.10	c.1300+2099A>T		intron_variant	Intron 12 of 19	1	NM_006157.5	ENSP00000349654.5

Frequencies

GnomAD3 genomes AF: 0.0409 AC: 6218 AN: 152108 Hom.: 132 Cov.: 32

Gnomad AFR AF: 0.0209

Gnomad AMI AF: 0.0363

Gnomad AMR AF: 0.0376

Gnomad ASJ AF: 0.0715

Gnomad EAS AF: 0.0842

Gnomad SAS AF: 0.0580

Gnomad FIN AF: 0.0412

Gnomad MID AF: 0.0475

Gnomad NFE AF: 0.0472

Gnomad OTH AF: 0.0575

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

GnomAD4 genome AF: 0.0408 AC: 6218 AN: 152226 Hom.: 132 Cov.: 32 AF XY: 0.0414 AC XY: 3080 AN XY: 74426

African (AFR) AF: 0.0209 AC: 868 AN: 41558

American (AMR) AF: 0.0375 AC: 574 AN: 15292

Ashkenazi Jewish (ASJ) AF: 0.0715 AC: 248 AN: 3470

East Asian (EAS) AF: 0.0840 AC: 434 AN: 5168

South Asian (SAS) AF: 0.0587 AC: 283 AN: 4822

European-Finnish (FIN) AF: 0.0412 AC: 437 AN: 10594

Middle Eastern (MID) AF: 0.0476 AC: 14 AN: 294

European-Non Finnish (NFE) AF: 0.0472 AC: 3207 AN: 68010

Other (OTH) AF: 0.0569 AC: 120 AN: 2110

Alfa AF: 0.0426 Hom.: 21

Bravo AF: 0.0400

Asia WGS AF: 0.0660 AC: 228 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	1.3
DANN	Benign	0.48
PhyloP100		-0.26
Mutation Taster		=100/0	polymorphism

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

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

Other links and lift over

dbSNP: rs61883261; hg19: chr11-20984205;