NM_006157.5:c.1301-76404C>T

Variant names:

• chr11-21037185-C-T
• rs4569005
• NM_006157.5:c.1301-76404C>T

Variant summary

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

The NM_006157.5(NELL1):​c.1301-76404C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.195 in 151,934 control chromosomes in the GnomAD database, including 3,361 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 0.19 (3361 hom., cov: 32)
• Consequence: NELL1 NM_006157.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.535

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

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.97).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.313 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
NELL1	NM_006157.5	c.1301-76404C>T		intron_variant	Intron 12 of 19	ENST00000357134.10	NP_006148.2
NELL1	NM_001288713.1	c.1385-76404C>T		intron_variant	Intron 13 of 20		NP_001275642.1
NELL1	NM_201551.2	c.1301-76404C>T		intron_variant	Intron 12 of 18		NP_963845.1
NELL1	NM_001288714.1	c.1130-76404C>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.1301-76404C>T		intron_variant	Intron 12 of 19	1	NM_006157.5	ENSP00000349654.5

Frequencies

GnomAD3 genomes AF: 0.194 AC: 29524 AN: 151816 Hom.: 3354 Cov.: 32

Gnomad AFR AF: 0.317

Gnomad AMI AF: 0.124

Gnomad AMR AF: 0.140

Gnomad ASJ AF: 0.129

Gnomad EAS AF: 0.0427

Gnomad SAS AF: 0.190

Gnomad FIN AF: 0.187

Gnomad MID AF: 0.136

Gnomad NFE AF: 0.151

Gnomad OTH AF: 0.163

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

GnomAD4 genome AF: 0.195 AC: 29555 AN: 151934 Hom.: 3361 Cov.: 32 AF XY: 0.196 AC XY: 14531 AN XY: 74244

Gnomad4 AFR AF: 0.318

Gnomad4 AMR AF: 0.140

Gnomad4 ASJ AF: 0.129

Gnomad4 EAS AF: 0.0426

Gnomad4 SAS AF: 0.189

Gnomad4 FIN AF: 0.187

Gnomad4 NFE AF: 0.151

Gnomad4 OTH AF: 0.161

Alfa AF: 0.160 Hom.: 1829

Bravo AF: 0.193

Asia WGS AF: 0.139 AC: 483 AN: 3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.97
CADD	Benign	5.6
DANN	Benign	0.49

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

Publications

LitVar

Other links and lift over

dbSNP: rs4569005; hg19: chr11-21058731;