rs4151664

Variant names:

• chr6-31953096-C-T
• rs4151664
• NM_002904.6:c.1045+633G>A

Variant summary

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

The NM_002904.6(NELFE):​c.1045+633G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0872 in 152,280 control chromosomes in the GnomAD database, including 809 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 0.087 (809 hom., cov: 32)
• Consequence: NELFE NM_002904.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.393
• Publications: 31 publications found

Genes affected

NELFE (HGNC:13974): (negative elongation factor complex member E) The protein encoded by this gene is part of a complex termed negative elongation factor (NELF) which represses RNA polymerase II transcript elongation. This protein bears similarity to nuclear RNA-binding proteins; however, it has not been demonstrated that this protein binds RNA. The protein contains a tract of alternating basic and acidic residues, largely arginine (R) and aspartic acid (D). The gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.8).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.153 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_002904.6. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NELFE	NM_002904.6	MANE Select	c.1045+633G>A		intron	N/A	NP_002895.3

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NELFE	ENST00000375429.8	TSL:1 MANE Select	c.1045+633G>A		intron	N/A	ENSP00000364578.3	P18615-1
	NELFE	ENST00000375425.9	TSL:2	c.1066+633G>A		intron	N/A	ENSP00000364574.5	P18615-3
	NELFE	ENST00000948308.1		c.1063+633G>A		intron	N/A	ENSP00000618367.1

Frequencies

GnomAD3 genomes AF: 0.0872 AC: 13264 AN: 152162 Hom.: 812 Cov.: 32

Gnomad AFR AF: 0.156

Gnomad AMI AF: 0.154

Gnomad AMR AF: 0.0631

Gnomad ASJ AF: 0.0490

Gnomad EAS AF: 0.0589

Gnomad SAS AF: 0.159

Gnomad FIN AF: 0.0201

Gnomad MID AF: 0.101

Gnomad NFE AF: 0.0588

Gnomad OTH AF: 0.0928

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

GnomAD4 genome AF: 0.0872 AC: 13272 AN: 152280 Hom.: 809 Cov.: 32 AF XY: 0.0865 AC XY: 6442 AN XY: 74476

African (AFR) AF: 0.156 AC: 6485 AN: 41536

American (AMR) AF: 0.0630 AC: 964 AN: 15302

Ashkenazi Jewish (ASJ) AF: 0.0490 AC: 170 AN: 3472

East Asian (EAS) AF: 0.0594 AC: 308 AN: 5184

South Asian (SAS) AF: 0.158 AC: 764 AN: 4822

European-Finnish (FIN) AF: 0.0201 AC: 213 AN: 10618

Middle Eastern (MID) AF: 0.102 AC: 30 AN: 294

European-Non Finnish (NFE) AF: 0.0589 AC: 4004 AN: 68030

Other (OTH) AF: 0.0919 AC: 194 AN: 2112

Alfa AF: 0.0645 Hom.: 1482

Bravo AF: 0.0909

Asia WGS AF: 0.0860 AC: 299 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.80
CADD	Benign	8.9
DANN	Benign	0.73
PhyloP100		0.39
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: rs4151664; hg19: chr6-31920873;