17-7583790-A-T

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2BP4_Strong

The NM_001330073.1(MPDU1):​c.-73A>T variant causes a 5 prime UTR change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 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: not found (cov: 34)

Consequence

MPDU1
NM_001330073.1 5_prime_UTR

Scores

2

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: -0.244

Publications

37 publications found
Variant links:
Genes affected
MPDU1 (HGNC:7207): (mannose-P-dolichol utilization defect 1) This gene encodes an endoplasmic reticulum membrane protein that is required for utilization of the mannose donor mannose-P-dolichol in the synthesis of lipid-linked oligosaccharides and glycosylphosphatidylinositols. Mutations in this gene result in congenital disorder of glycosylation type If. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]
MPDU1-AS1 (HGNC:40379): (MPDU1 antisense RNA 1)

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ACMG classification

Classification was made for transcript

Our verdict: Likely_benign. The variant received -2 ACMG points.

PM2
Very rare variant in population databases, with high coverage;
BP4
Computational evidence support a benign effect (BayesDel_noAF=-0.77).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001330073.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.
GeneTranscriptTagsHGVScHGVSpEffectExon RankProteinUniProt
MPDU1
NM_001330073.1
c.-73A>T
5_prime_UTR
Exon 1 of 6NP_001317002.1
MPDU1
NR_024603.1
n.144A>T
non_coding_transcript_exon
Exon 1 of 7
MPDU1-AS1
NR_136401.2
n.175+128T>A
intron
N/A

Ensembl Transcripts

Sel.
GeneTranscriptTagsHGVScHGVSpEffectExon RankProteinUniProt
MPDU1
ENST00000582151.1
TSL:6
c.-73A>T
5_prime_UTR
Exon 1 of 1ENSP00000462500.1
MPDU1
ENST00000572936.5
TSL:5
n.-73A>T
non_coding_transcript_exon
Exon 1 of 7ENSP00000459306.1
MPDU1-AS1
ENST00000687005.2
n.309T>A
non_coding_transcript_exon
Exon 1 of 1

Frequencies

GnomAD3 genomes
Cov.:
34
GnomAD4 exome
Cov.:
20
GnomAD4 genome
Cov.:
34

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name
Calibrated prediction
Score
Prediction
BayesDel_noAF
Benign
-0.77
CADD
Benign
2.0
DANN
Benign
0.85
PhyloP100
-0.24
PromoterAI
-0.16
Neutral

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

Publications

Other links and lift over

dbSNP: rs2075230; hg19: chr17-7487108; API