rs4656701

Variant names:

• chr1-169718762-G-C
• rs4656701
• ENST00000498289.5:n.851+34830G>C

Variant summary

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

The ENST00000498289.5(FIRRM):​n.851+34830G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.309 in 151,800 control chromosomes in the GnomAD database, including 7,528 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 0.31 (7528 hom., cov: 31)
• Consequence: FIRRM ENST00000498289.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0100
• Publications: 6 publications found

Genes affected

FIRRM (HGNC:25565): (FIGNL1 interacting regulator of recombination and mitosis)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.99).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.397 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000498289.5. 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
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FIRRM	ENST00000498289.5	TSL:2	n.851+34830G>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.309 AC: 46828 AN: 151682 Hom.: 7495 Cov.: 31

Gnomad AFR AF: 0.380

Gnomad AMI AF: 0.276

Gnomad AMR AF: 0.332

Gnomad ASJ AF: 0.342

Gnomad EAS AF: 0.331

Gnomad SAS AF: 0.411

Gnomad FIN AF: 0.269

Gnomad MID AF: 0.380

Gnomad NFE AF: 0.255

Gnomad OTH AF: 0.330

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

GnomAD4 genome AF: 0.309 AC: 46919 AN: 151800 Hom.: 7528 Cov.: 31 AF XY: 0.311 AC XY: 23086 AN XY: 74172

African (AFR) AF: 0.381 AC: 15766 AN: 41372

American (AMR) AF: 0.332 AC: 5056 AN: 15220

Ashkenazi Jewish (ASJ) AF: 0.342 AC: 1184 AN: 3464

East Asian (EAS) AF: 0.332 AC: 1713 AN: 5164

South Asian (SAS) AF: 0.412 AC: 1986 AN: 4818

European-Finnish (FIN) AF: 0.269 AC: 2833 AN: 10530

Middle Eastern (MID) AF: 0.388 AC: 114 AN: 294

European-Non Finnish (NFE) AF: 0.255 AC: 17317 AN: 67920

Other (OTH) AF: 0.332 AC: 699 AN: 2108

Alfa AF: 0.279 Hom.: 755

Bravo AF: 0.317

Asia WGS AF: 0.381 AC: 1328 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.99
CADD	Benign	1.8
DANN	Benign	0.32
PhyloP100		0.010

Splicing

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

Other links and lift over

dbSNP: rs4656701; hg19: chr1-169687903;