rs10485202

Variant names:

• chr6-156987993-G-C
• rs10485202
• NM_001374828.1:c.2247+52417G>C

Your query was ambiguous. Multiple possible variants found:

• chr6-156987993-G-C
• chr6-156987993-G-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001374828.1(ARID1B):​c.2247+52417G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.266 in 152,118 control chromosomes in the GnomAD database, including 5,829 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 0.27 (5829 hom., cov: 32)
• Consequence: ARID1B NM_001374828.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.417

Genes affected

ARID1B (HGNC:18040): (AT-rich interaction domain 1B) This locus encodes an AT-rich DNA interacting domain-containing protein. The encoded protein is a component of the SWI/SNF chromatin remodeling complex and may play a role in cell-cycle activation. The protein encoded by this locus is similar to AT-rich interactive domain-containing protein 1A. These two proteins function as alternative, mutually exclusive ARID-subunits of the SWI/SNF complex. The associated complexes play opposing roles. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.312 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ARID1B	NM_001374828.1	c.2247+52417G>C		intron_variant	Intron 4 of 19	ENST00000636930.2	NP_001361757.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ARID1B	ENST00000636930.2	c.2247+52417G>C		intron_variant	Intron 4 of 19	2	NM_001374828.1	ENSP00000490491.2

Frequencies

GnomAD3 genomes AF: 0.266 AC: 40374 AN: 152000 Hom.: 5823 Cov.: 32

Gnomad AFR AF: 0.158

Gnomad AMI AF: 0.202

Gnomad AMR AF: 0.299

Gnomad ASJ AF: 0.241

Gnomad EAS AF: 0.258

Gnomad SAS AF: 0.173

Gnomad FIN AF: 0.377

Gnomad MID AF: 0.184

Gnomad NFE AF: 0.316

Gnomad OTH AF: 0.279

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

GnomAD4 genome AF: 0.266 AC: 40391 AN: 152118 Hom.: 5829 Cov.: 32 AF XY: 0.267 AC XY: 19839 AN XY: 74346

Gnomad4 AFR AF: 0.157

Gnomad4 AMR AF: 0.299

Gnomad4 ASJ AF: 0.241

Gnomad4 EAS AF: 0.258

Gnomad4 SAS AF: 0.173

Gnomad4 FIN AF: 0.377

Gnomad4 NFE AF: 0.316

Gnomad4 OTH AF: 0.281

Alfa AF: 0.168 Hom.: 345

Bravo AF: 0.257

Asia WGS AF: 0.246 AC: 852 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	5.0
DANN	Benign	0.63
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1

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

Other links and lift over

dbSNP: rs10485202; hg19: chr6-157309127;