9-123787676-T-G

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP4_ModerateBA1

The NM_001352964.2(DENND1A):​c.132+4911A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0685 in 152,188 control chromosomes in the GnomAD database, including 482 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 0.069 ( 482 hom., cov: 32)

Consequence

DENND1A
NM_001352964.2 intron

Scores

2

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 2.02
Variant links:
Genes affected
DENND1A (HGNC:29324): (DENN domain containing 1A) Clathrin (see MIM 118955)-mediated endocytosis is a major mechanism for internalization of proteins and lipids. Members of the connecdenn family, such as DENND1A, function as guanine nucleotide exchange factors (GEFs) for the early endosomal small GTPase RAB35 (MIM 604199) and bind to clathrin and clathrin adaptor protein-2 (AP2; see MIM 601024). Thus, connecdenns link RAB35 activation with the clathrin machinery (Marat and McPherson, 2010 [PubMed 20154091]).[supplied by OMIM, Nov 2010]

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -10 ACMG points.

BP4
Computational evidence support a benign effect (BayesDel_noAF=-0.25).
BA1
GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.129 is higher than 0.05.

Transcripts

RefSeq

Gene Transcript HGVSc HGVSp Effect #exon/exons MANE Protein UniProt
DENND1ANM_001352964.2 linkuse as main transcriptc.132+4911A>C intron_variant ENST00000394215.7 NP_001339893.1

Ensembl

Gene Transcript HGVSc HGVSp Effect #exon/exons TSL MANE Protein Appris UniProt
DENND1AENST00000394215.7 linkuse as main transcriptc.132+4911A>C intron_variant 5 NM_001352964.2 ENSP00000377763 A2

Frequencies

GnomAD3 genomes
AF:
0.0686
AC:
10425
AN:
152070
Hom.:
482
Cov.:
32
show subpopulations
Gnomad AFR
AF:
0.132
Gnomad AMI
AF:
0.0518
Gnomad AMR
AF:
0.0569
Gnomad ASJ
AF:
0.0623
Gnomad EAS
AF:
0.0537
Gnomad SAS
AF:
0.0669
Gnomad FIN
AF:
0.0560
Gnomad MID
AF:
0.0475
Gnomad NFE
AF:
0.0363
Gnomad OTH
AF:
0.0713
We have no GnomAD4 exomes data on this position. Probably position not covered by the project.
GnomAD4 genome
AF:
0.0685
AC:
10426
AN:
152188
Hom.:
482
Cov.:
32
AF XY:
0.0699
AC XY:
5202
AN XY:
74426
show subpopulations
Gnomad4 AFR
AF:
0.132
Gnomad4 AMR
AF:
0.0567
Gnomad4 ASJ
AF:
0.0623
Gnomad4 EAS
AF:
0.0538
Gnomad4 SAS
AF:
0.0671
Gnomad4 FIN
AF:
0.0560
Gnomad4 NFE
AF:
0.0363
Gnomad4 OTH
AF:
0.0705
Alfa
AF:
0.0559
Hom.:
51
Bravo
AF:
0.0726
Asia WGS
AF:
0.0480
AC:
167
AN:
3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name
Calibrated prediction
Score
Prediction
BayesDel_noAF
Benign
-0.25
CADD
Benign
17
DANN
Benign
0.85

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

Below is the list of publications found by LitVar. It may be empty.

Other links and lift over

dbSNP: rs10986105; hg19: chr9-126549955; API