rs722910

Variant names:

• chr5-53485767-A-C
• rs722910
• NM_013409.3:c.953-184A>C

Your query was ambiguous. Multiple possible variants found:

• chr5-53485767-A-C
• chr5-53485767-A-G
• chr5-53485767-A-T

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_013409.3(FST):​c.953-184A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000279 in 1,432,296 control chromosomes in the GnomAD database, with no homozygous occurrence. 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: not found (cov: 29)
  • Exomes 𝑓: 0.0000028 (0 hom.)
• Consequence: FST NM_013409.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.70
• Publications: 13 publications found

Genes affected

FST (HGNC:3971): (follistatin) Follistatin is a single-chain gonadal protein that specifically inhibits follicle-stimulating hormone release. The single FST gene encodes two isoforms, FST317 and FST344 containing 317 and 344 amino acids respectively, resulting from alternative splicing of the precursor mRNA. In a study in which 37 candidate genes were tested for linkage and association with polycystic ovary syndrome (PCOS) or hyperandrogenemia in 150 families, evidence was found for linkage between PCOS and follistatin. [provided by RefSeq, Jul 2008]

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.96).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
FST	NM_013409.3	c.953-184A>C		intron_variant	Intron 5 of 5	ENST00000256759.8	NP_037541.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
FST	ENST00000256759.8	c.953-184A>C		intron_variant	Intron 5 of 5	1	NM_013409.3	ENSP00000256759.3
FST	ENST00000396947.7	c.*79A>C		3_prime_UTR_variant	Exon 6 of 6	5		ENSP00000380151.2
FST	ENST00000497789.2	c.*79A>C		3_prime_UTR_variant	Exon 3 of 3	2		ENSP00000426971.1
FST	ENST00000504226.5	c.566-184A>C		intron_variant	Intron 3 of 3	3		ENSP00000426315.1

Frequencies

GnomAD3 genomes Cov.: 29

GnomAD4 exome AF: 0.00000279 AC: 4 AN: 1432296 Hom.: 0 Cov.: 30 AF XY: 0.00000140 AC XY: 1 AN XY: 712630

African (AFR) AF: 0.00 AC: 0 AN: 31336

American (AMR) AF: 0.00 AC: 0 AN: 37278

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 25080

East Asian (EAS) AF: 0.00 AC: 0 AN: 39560

South Asian (SAS) AF: 0.00 AC: 0 AN: 81078

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 53128

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 5634

European-Non Finnish (NFE) AF: 0.00000364 AC: 4 AN: 1100022

Other (OTH) AF: 0.00 AC: 0 AN: 59180

GnomAD4 genome Cov.: 29

Alfa AF: 0.00 Hom.: 802

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
CADD	Benign	0.011
DANN	Benign	0.17
PhyloP100		-1.7

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs722910; hg19: chr5-52781597;