rs10492246

Variant names:

• chr12-13058782-A-G
• rs10492246
• NM_020853.2:c.532+233A>G

Variant summary

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

The NM_020853.2(FAM234B):​c.532+233A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0635 in 152,238 control chromosomes in the GnomAD database, including 642 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as (no stars).

• Frequency: Genomes: 𝑓 0.063 (642 hom., cov: 32)
• Consequence: FAM234B NM_020853.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.191
• Publications: 1 publications found

Genes affected

FAM234B (HGNC:29288): (family with sequence similarity 234 member B) Predicted to be located in Golgi apparatus and cytoskeleton. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.258 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_020853.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FAM234B	NM_020853.2	MANE Select	c.532+233A>G		intron	N/A	NP_065904.1	A2RU67

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FAM234B	ENST00000197268.13	TSL:1 MANE Select	c.532+233A>G		intron	N/A	ENSP00000197268.8	A2RU67
	FAM234B	ENST00000893327.1		c.434-2793A>G		intron	N/A	ENSP00000563386.1
	FAM234B	ENST00000416494.6	TSL:2	n.532+233A>G		intron	N/A	ENSP00000394063.2	A2RU67

Frequencies

GnomAD3 genomes AF: 0.0634 AC: 9647 AN: 152120 Hom.: 642 Cov.: 32

Gnomad AFR AF: 0.122

Gnomad AMI AF: 0.0197

Gnomad AMR AF: 0.0227

Gnomad ASJ AF: 0.0395

Gnomad EAS AF: 0.269

Gnomad SAS AF: 0.144

Gnomad FIN AF: 0.0874

Gnomad MID AF: 0.0253

Gnomad NFE AF: 0.0141

Gnomad OTH AF: 0.0502

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

GnomAD4 genome AF: 0.0635 AC: 9660 AN: 152238 Hom.: 642 Cov.: 32 AF XY: 0.0681 AC XY: 5070 AN XY: 74446

African (AFR) AF: 0.122 AC: 5069 AN: 41510

American (AMR) AF: 0.0226 AC: 346 AN: 15306

Ashkenazi Jewish (ASJ) AF: 0.0395 AC: 137 AN: 3470

East Asian (EAS) AF: 0.270 AC: 1396 AN: 5172

South Asian (SAS) AF: 0.144 AC: 693 AN: 4826

European-Finnish (FIN) AF: 0.0874 AC: 928 AN: 10618

Middle Eastern (MID) AF: 0.0272 AC: 8 AN: 294

European-Non Finnish (NFE) AF: 0.0141 AC: 959 AN: 68016

Other (OTH) AF: 0.0501 AC: 106 AN: 2114

Alfa AF: 0.0360 Hom.: 71

Bravo AF: 0.0609

Asia WGS AF: 0.211 AC: 733 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.50
DANN	Benign	0.64
PhyloP100		-0.19
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: rs10492246; hg19: chr12-13211716;