rs6483747

Variant names:

• chr11-21159431-G-A
• rs6483747
• NM_006157.5:c.1426+45717G>A

Variant summary

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

The NM_006157.5(NELL1):​c.1426+45717G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.268 in 152,122 control chromosomes in the GnomAD database, including 5,716 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 0.27 (5716 hom., cov: 32)
• Consequence: NELL1 NM_006157.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.348
• Publications: 1 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=-0.88).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.304 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
NELL1	NM_006157.5	c.1426+45717G>A		intron_variant	Intron 13 of 19	ENST00000357134.10	NP_006148.2
NELL1	NM_001288713.1	c.1510+45717G>A		intron_variant	Intron 14 of 20		NP_001275642.1
NELL1	NM_201551.2	c.1426+45717G>A		intron_variant	Intron 13 of 18		NP_963845.1
NELL1	NM_001288714.1	c.1255+45717G>A		intron_variant	Intron 12 of 18		NP_001275643.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
NELL1	ENST00000357134.10	c.1426+45717G>A		intron_variant	Intron 13 of 19	1	NM_006157.5	ENSP00000349654.5

Frequencies

GnomAD3 genomes AF: 0.268 AC: 40732 AN: 152004 Hom.: 5710 Cov.: 32

Gnomad AFR AF: 0.210

Gnomad AMI AF: 0.357

Gnomad AMR AF: 0.302

Gnomad ASJ AF: 0.326

Gnomad EAS AF: 0.124

Gnomad SAS AF: 0.238

Gnomad FIN AF: 0.237

Gnomad MID AF: 0.367

Gnomad NFE AF: 0.307

Gnomad OTH AF: 0.313

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

GnomAD4 genome AF: 0.268 AC: 40756 AN: 152122 Hom.: 5716 Cov.: 32 AF XY: 0.265 AC XY: 19735 AN XY: 74372

African (AFR) AF: 0.210 AC: 8716 AN: 41504

American (AMR) AF: 0.302 AC: 4613 AN: 15288

Ashkenazi Jewish (ASJ) AF: 0.326 AC: 1130 AN: 3470

East Asian (EAS) AF: 0.125 AC: 646 AN: 5180

South Asian (SAS) AF: 0.237 AC: 1143 AN: 4822

European-Finnish (FIN) AF: 0.237 AC: 2506 AN: 10586

Middle Eastern (MID) AF: 0.364 AC: 107 AN: 294

European-Non Finnish (NFE) AF: 0.308 AC: 20901 AN: 67962

Other (OTH) AF: 0.317 AC: 668 AN: 2104

Alfa AF: 0.286 Hom.: 1000

Bravo AF: 0.272

Asia WGS AF: 0.189 AC: 658 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	4.3
DANN	Benign	0.58
PhyloP100		0.35
Mutation Taster		=100/0	polymorphism (auto)

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: rs6483747; hg19: chr11-21180977;