rs13434995

Variant names:

• chr4-55601047-A-G
• rs13434995
• NM_006681.4:c.436-472T>C

Variant summary

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

The NM_006681.4(NMU):​c.436-472T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.174 in 152,078 control chromosomes in the GnomAD database, including 2,434 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 0.17 (2434 hom., cov: 32)
• Consequence: NMU NM_006681.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.753
• Publications: 14 publications found

Genes affected

NMU (HGNC:7859): (neuromedin U) This gene encodes a member of the neuromedin family of neuropeptides. The encoded protein is a precursor that is proteolytically processed to generate a biologically active neuropeptide that plays a role in pain, stress, immune-mediated inflammatory diseases and feeding regulation. Increased expression of this gene was observed in renal, pancreatic and lung cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. Some of these isoforms may undergo similar processing to generate the mature peptide. [provided by RefSeq, Jul 2015]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.23 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_006681.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NMU	NM_006681.4	MANE Select	c.436-472T>C		intron	N/A	NP_006672.1
	NMU	NM_001292045.2		c.388-472T>C		intron	N/A	NP_001278974.1
	NMU	NM_001292046.2		c.361-472T>C		intron	N/A	NP_001278975.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NMU	ENST00000264218.7	TSL:1 MANE Select	c.436-472T>C		intron	N/A	ENSP00000264218.3
	NMU	ENST00000509371.1	TSL:1	n.200-472T>C		intron	N/A
	NMU	ENST00000920357.1		c.436-472T>C		intron	N/A	ENSP00000590416.1

Frequencies

GnomAD3 genomes AF: 0.174 AC: 26379 AN: 151962 Hom.: 2430 Cov.: 32

Gnomad AFR AF: 0.134

Gnomad AMI AF: 0.196

Gnomad AMR AF: 0.165

Gnomad ASJ AF: 0.153

Gnomad EAS AF: 0.0924

Gnomad SAS AF: 0.241

Gnomad FIN AF: 0.253

Gnomad MID AF: 0.142

Gnomad NFE AF: 0.190

Gnomad OTH AF: 0.160

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

GnomAD4 genome AF: 0.174 AC: 26398 AN: 152078 Hom.: 2434 Cov.: 32 AF XY: 0.176 AC XY: 13067 AN XY: 74336

African (AFR) AF: 0.134 AC: 5552 AN: 41522

American (AMR) AF: 0.165 AC: 2527 AN: 15286

Ashkenazi Jewish (ASJ) AF: 0.153 AC: 530 AN: 3470

East Asian (EAS) AF: 0.0923 AC: 478 AN: 5180

South Asian (SAS) AF: 0.242 AC: 1163 AN: 4814

European-Finnish (FIN) AF: 0.253 AC: 2667 AN: 10560

Middle Eastern (MID) AF: 0.143 AC: 42 AN: 294

European-Non Finnish (NFE) AF: 0.190 AC: 12917 AN: 67930

Other (OTH) AF: 0.163 AC: 344 AN: 2112

Alfa AF: 0.179 Hom.: 1753

Bravo AF: 0.160

Asia WGS AF: 0.198 AC: 680 AN: 3446

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	0.69
DANN	Benign	0.47
PhyloP100		-0.75
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: rs13434995; hg19: chr4-56467214;