dbSNP rs10761741: JMJD1C:c.334-41662C>A (chr10-63306426-G-T) – ACMG Classification: Benign (-12 pts)

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_StrongBA1

The NM_032776.3(JMJD1C):c.334-41662C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.384 in 151,964 control chromosomes in the GnomAD database, including 11,589 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 0.38 ( 11589 hom., cov: 32)

Consequence

JMJD1C
NM_032776.3 intron

Scores

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 0.221

Publications

51 publications found

Variant links:

Genes affected

JMJD1C (HGNC:12313): (jumonji domain containing 1C) The protein encoded by this gene interacts with thyroid hormone receptors and contains a jumonji domain. It is a candidate histone demethylase and is thought to be a coactivator for key transcription factors. It plays a role in the DNA-damage response pathway by demethylating the mediator of DNA damage checkpoint 1 (MDC1) protein, and is required for the survival of acute myeloid leukemia. Mutations in this gene are associated with Rett syndrome and intellectual disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]

JMJD1C Gene-Disease associations (from GenCC):

22q11.2 deletion syndrome
Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
complex neurodevelopmental disorder
Inheritance: AD Classification: LIMITED Submitted by: Illumina
neurodevelopmental disorder
Inheritance: AD Classification: LIMITED Submitted by: G2P

JMJD1C links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

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

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.95).

BA1

GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.485 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
JMJD1C	NM_032776.3 link	c.334-41662C>A		intron_variant	Intron 2 of 25	ENST00000399262.7	NP_116165.1	Q15652-1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
JMJD1C	ENST00000399262.7 link	c.334-41662C>A		intron_variant	Intron 2 of 25	5	NM_032776.3	ENSP00000382204.2		Q15652-1
JMJD1C	ENST00000633035.1 link	n.279-41662C>A		intron_variant	Intron 2 of 3	3

Frequencies

GnomAD3 genomes

AF:

0.385

AC:

58419

AN:

151846

Hom.:

11597

Cov.:

show subpopulations

Gnomad AFR

AF:

0.318

Gnomad AMI

AF:

0.481

Gnomad AMR

AF:

0.318

Gnomad ASJ

AF:

0.560

Gnomad EAS

AF:

0.333

Gnomad SAS

AF:

0.504

Gnomad FIN

AF:

0.383

Gnomad MID

AF:

0.421

Gnomad NFE

AF:

0.425

Gnomad OTH

AF:

0.392

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

GnomAD4 genome

AF:

0.384

AC:

58397

AN:

151964

Hom.:

11589

Cov.:

AF XY:

0.384

AC XY:

28497

AN XY:

74290

show subpopulations

African (AFR)

AF:

0.317

AC:

13146

AN:

41442

American (AMR)

AF:

0.317

AC:

4849

AN:

15276

Ashkenazi Jewish (ASJ)

AF:

0.560

AC:

1943

AN:

3470

East Asian (EAS)

AF:

0.332

AC:

1716

AN:

5176

South Asian (SAS)

AF:

0.502

AC:

2415

AN:

4810

European-Finnish (FIN)

AF:

0.383

AC:

4045

AN:

10552

Middle Eastern (MID)

AF:

0.415

AC:

122

AN:

294

European-Non Finnish (NFE)

AF:

0.425

AC:

28902

AN:

67928

Other (OTH)

AF:

0.390

AC:

821

AN:

2106

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.505

Heterozygous variant carriers

1843

3686

5528

7371

9214

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Alfa

AF:

0.396

Hom.:

5562

Bravo

AF:

0.370

Asia WGS

AF:

0.397

AC:

1382

AN:

3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.95

CADD

Benign

4.6

(source)

DANN

Benign

0.71

PhyloP100

0.22

Mutation Taster

=100/0

polymorphism (auto)

(source)

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

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rs10761741

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

ClinVar

Computational scores

Splicing

Publications

Other links and lift over