rs2092427

Positions:

• chr6-35654430-G-A

Variant summary

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

The NM_004117.4(FKBP5):​c.-19-11587C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0884 in 152,102 control chromosomes in the GnomAD database, including 1,213 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 0.088 (1213 hom., cov: 32)
• Consequence: FKBP5 NM_004117.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.147

Genes affected

FKBP5 (HGNC:3721): (FKBP prolyl isomerase 5) The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. This encoded protein is a cis-trans prolyl isomerase that binds to the immunosuppressants FK506 and rapamycin. It is thought to mediate calcineurin inhibition. It also interacts functionally with mature hetero-oligomeric progesterone receptor complexes along with the 90 kDa heat shock protein and P23 protein. This gene has been found to have multiple polyadenylation sites. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Mar 2009]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.233 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
FKBP5	NM_004117.4	c.-19-11587C>T		intron_variant		ENST00000357266.9
FKBP5	NM_001145775.3	c.-19-11587C>T		intron_variant
FKBP5	NM_001145776.2	c.-19-11587C>T		intron_variant
FKBP5	NM_001145777.2	c.-19-11587C>T		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
FKBP5	ENST00000357266.9	c.-19-11587C>T		intron_variant		1	NM_004117.4	P1
FKBP5	ENST00000536438.5	c.-19-11587C>T		intron_variant		1		P1
FKBP5	ENST00000539068.5	c.-19-11587C>T		intron_variant		1		P1
FKBP5	ENST00000542713.1	c.-19-11587C>T		intron_variant		2

Frequencies

GnomAD3 genomes AF: 0.0881 AC: 13387 AN: 151984 Hom.: 1199 Cov.: 32

Gnomad AFR AF: 0.237

Gnomad AMI AF: 0.0482

Gnomad AMR AF: 0.0664

Gnomad ASJ AF: 0.0606

Gnomad EAS AF: 0.0554

Gnomad SAS AF: 0.00890

Gnomad FIN AF: 0.0136

Gnomad MID AF: 0.0633

Gnomad NFE AF: 0.0248

Gnomad OTH AF: 0.0803

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

GnomAD4 genome AF: 0.0884 AC: 13440 AN: 152102 Hom.: 1213 Cov.: 32 AF XY: 0.0870 AC XY: 6469 AN XY: 74364

Gnomad4 AFR AF: 0.237

Gnomad4 AMR AF: 0.0664

Gnomad4 ASJ AF: 0.0606

Gnomad4 EAS AF: 0.0555

Gnomad4 SAS AF: 0.00850

Gnomad4 FIN AF: 0.0136

Gnomad4 NFE AF: 0.0248

Gnomad4 OTH AF: 0.0799

Alfa AF: 0.0588 Hom.: 86

Bravo AF: 0.0991

Asia WGS AF: 0.0400 AC: 140 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	6.3
DANN	Benign	0.47

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: rs2092427; hg19: chr6-35622207;