chr10-14670444-A-G

Variant names:

• chr10-14670444-A-G
• rs1459019
• NM_031453.4:c.412-2753T>C

Variant summary

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

The NM_031453.4(FAM107B):​c.412-2753T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.358 in 152,088 control chromosomes in the GnomAD database, including 9,872 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 0.36 (9872 hom., cov: 33)
• Consequence: FAM107B NM_031453.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.623
• Publications: 0 publications found

Genes affected

FAM107B (HGNC:23726): (family with sequence similarity 107 member B) Predicted to act upstream of or within sensory perception of sound. [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=-0.84).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.397 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_031453.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FAM107B	NM_031453.4	MANE Select	c.412-2753T>C		intron	N/A	NP_113641.2
	FAM107B	NM_001282695.2		c.-180-2753T>C		intron	N/A	NP_001269624.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FAM107B	ENST00000181796.7	TSL:2 MANE Select	c.412-2753T>C		intron	N/A	ENSP00000181796.2
	FAM107B	ENST00000487335.5	TSL:1	n.412-2753T>C		intron	N/A	ENSP00000420273.1

Frequencies

GnomAD3 genomes AF: 0.357 AC: 54329 AN: 151970 Hom.: 9858 Cov.: 33

Gnomad AFR AF: 0.336

Gnomad AMI AF: 0.478

Gnomad AMR AF: 0.379

Gnomad ASJ AF: 0.480

Gnomad EAS AF: 0.411

Gnomad SAS AF: 0.334

Gnomad FIN AF: 0.271

Gnomad MID AF: 0.437

Gnomad NFE AF: 0.367

Gnomad OTH AF: 0.413

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

GnomAD4 genome AF: 0.358 AC: 54372 AN: 152088 Hom.: 9872 Cov.: 33 AF XY: 0.353 AC XY: 26247 AN XY: 74340

African (AFR) AF: 0.336 AC: 13927 AN: 41466

American (AMR) AF: 0.379 AC: 5795 AN: 15278

Ashkenazi Jewish (ASJ) AF: 0.480 AC: 1662 AN: 3466

East Asian (EAS) AF: 0.411 AC: 2126 AN: 5172

South Asian (SAS) AF: 0.334 AC: 1614 AN: 4832

European-Finnish (FIN) AF: 0.271 AC: 2862 AN: 10572

Middle Eastern (MID) AF: 0.429 AC: 126 AN: 294

European-Non Finnish (NFE) AF: 0.367 AC: 24954 AN: 67982

Other (OTH) AF: 0.412 AC: 870 AN: 2114

Alfa AF: 0.368 Hom.: 5459

Bravo AF: 0.368

Asia WGS AF: 0.354 AC: 1232 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
CADD	Benign	4.4
DANN	Benign	0.75
PhyloP100		0.62
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs1459019; hg19: chr10-14712443;