rs17479589

Positions:

• chr15-49461335-T-C

Variant summary

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

The NM_152647.3(FAM227B):​c.1012+46876A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.254 in 152,202 control chromosomes in the GnomAD database, including 5,774 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 0.25 (5774 hom., cov: 32)
• Consequence: FAM227B NM_152647.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.826

Genes affected

FGF7 (HGNC:3685): (fibroblast growth factor 7) The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein is a potent epithelial cell-specific growth factor, whose mitogenic activity is predominantly exhibited in keratinocytes but not in fibroblasts and endothelial cells. Studies of mouse and rat homologs of this gene implicated roles in morphogenesis of epithelium, reepithelialization of wounds, hair development and early lung organogenesis. [provided by RefSeq, Jul 2008]

FAM227B (HGNC:26543): (family with sequence similarity 227 member B)

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 = 0.343 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
FGF7	NM_002009.4	c.287-21816T>C		intron_variant		ENST00000267843.9
FAM227B	NM_152647.3	c.1012+46876A>G		intron_variant		ENST00000299338.11

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
FGF7	ENST00000267843.9	c.287-21816T>C		intron_variant		1	NM_002009.4	P1
FAM227B	ENST00000299338.11	c.1012+46876A>G		intron_variant		2	NM_152647.3	P1

Frequencies

GnomAD3 genomes AF: 0.254 AC: 38678 AN: 152084 Hom.: 5773 Cov.: 32

Gnomad AFR AF: 0.0998

Gnomad AMI AF: 0.444

Gnomad AMR AF: 0.247

Gnomad ASJ AF: 0.355

Gnomad EAS AF: 0.182

Gnomad SAS AF: 0.200

Gnomad FIN AF: 0.284

Gnomad MID AF: 0.239

Gnomad NFE AF: 0.347

Gnomad OTH AF: 0.273

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

GnomAD4 genome AF: 0.254 AC: 38665 AN: 152202 Hom.: 5774 Cov.: 32 AF XY: 0.251 AC XY: 18670 AN XY: 74412

Gnomad4 AFR AF: 0.0997

Gnomad4 AMR AF: 0.246

Gnomad4 ASJ AF: 0.355

Gnomad4 EAS AF: 0.183

Gnomad4 SAS AF: 0.200

Gnomad4 FIN AF: 0.284

Gnomad4 NFE AF: 0.347

Gnomad4 OTH AF: 0.268

Alfa AF: 0.289 Hom.: 889

Bravo AF: 0.244

Asia WGS AF: 0.176 AC: 613 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	1.7
DANN	Benign	0.58

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: rs17479589; hg19: chr15-49753532;