chr19-38906009-C-T

Variant names:

• chr19-38906009-C-T
• rs3136641
• NM_002503.5:c.619+474C>T

Variant summary

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

The NM_002503.5(NFKBIB):​c.619+474C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.213 in 151,974 control chromosomes in the GnomAD database, including 3,695 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 0.21 (3695 hom., cov: 31)
• Consequence: NFKBIB NM_002503.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.829
• Publications: 14 publications found

Genes affected

NFKBIB (HGNC:7798): (NFKB inhibitor beta) The protein encoded by this gene belongs to the NF-kappa-B inhibitor family, which inhibit NF-kappa-B by complexing with, and trapping it in the cytoplasm. Phosphorylation of serine residues on these proteins by kinases marks them for destruction via the ubiquitination pathway, thereby allowing activation of the NF-kappa-B, which translocates to the nucleus to function as a transcription factor. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Jul 2011]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.355 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_002503.5. 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
	NFKBIB	NM_002503.5	MANE Select	c.619+474C>T		intron	N/A	NP_002494.2
	NFKBIB	NM_001369699.1		c.619+474C>T		intron	N/A	NP_001356628.1	Q15653-2
	NFKBIB	NM_001243116.2		c.361+474C>T		intron	N/A	NP_001230045.1	G5E9C2

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NFKBIB	ENST00000313582.6	TSL:1 MANE Select	c.619+474C>T		intron	N/A	ENSP00000312988.5	Q15653-1
	NFKBIB	ENST00000572515.5	TSL:1	c.619+474C>T		intron	N/A	ENSP00000459728.1	Q15653-2
	NFKBIB	ENST00000392079.7	TSL:5	c.361+474C>T		intron	N/A	ENSP00000375929.4	G5E9C2

Frequencies

GnomAD3 genomes AF: 0.214 AC: 32434 AN: 151856 Hom.: 3697 Cov.: 31

Gnomad AFR AF: 0.154

Gnomad AMI AF: 0.259

Gnomad AMR AF: 0.190

Gnomad ASJ AF: 0.250

Gnomad EAS AF: 0.369

Gnomad SAS AF: 0.246

Gnomad FIN AF: 0.251

Gnomad MID AF: 0.266

Gnomad NFE AF: 0.232

Gnomad OTH AF: 0.220

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

GnomAD4 genome AF: 0.213 AC: 32431 AN: 151974 Hom.: 3695 Cov.: 31 AF XY: 0.216 AC XY: 16046 AN XY: 74288

African (AFR) AF: 0.153 AC: 6358 AN: 41428

American (AMR) AF: 0.190 AC: 2898 AN: 15270

Ashkenazi Jewish (ASJ) AF: 0.250 AC: 866 AN: 3470

East Asian (EAS) AF: 0.369 AC: 1903 AN: 5164

South Asian (SAS) AF: 0.247 AC: 1191 AN: 4824

European-Finnish (FIN) AF: 0.251 AC: 2644 AN: 10540

Middle Eastern (MID) AF: 0.262 AC: 77 AN: 294

European-Non Finnish (NFE) AF: 0.232 AC: 15799 AN: 67964

Other (OTH) AF: 0.218 AC: 459 AN: 2108

Alfa AF: 0.227 Hom.: 6647

Bravo AF: 0.207

Asia WGS AF: 0.250 AC: 867 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	0.80
DANN	Benign	0.41
PhyloP100		-0.83
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs3136641; hg19: chr19-39396649;