rs1360780

Variant names:

• chr6-35639794-T-C
• rs1360780
• NM_004117.4:c.106-2636A>G

Your query was ambiguous. Multiple possible variants found:

• chr6-35639794-T-C
• chr6-35639794-T-A

Variant summary

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

The ENST00000539068.5(FKBP5):​c.106-2636A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.672 in 152,130 control chromosomes in the GnomAD database, including 34,608 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely risk allele (no stars).

• Frequency: Genomes: 𝑓 0.67 (34608 hom., cov: 32)
• Consequence: FKBP5 ENST00000539068.5 intron
• Clinical Significance: Likely risk allele no assertion criteria provided P:1
• Conservation: PhyloP100: -0.0870
• Publications: 453 publications found

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

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.718 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000539068.5. 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
	FKBP5	NM_004117.4	MANE Select	c.106-2636A>G		intron	N/A	NP_004108.1	Q13451-1
	FKBP5	NM_001145775.3		c.106-2636A>G		intron	N/A	NP_001139247.1	Q13451-1
	FKBP5	NM_001145776.2		c.106-2636A>G		intron	N/A	NP_001139248.1	Q13451-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FKBP5	ENST00000357266.9	TSL:1 MANE Select	c.106-2636A>G		intron	N/A	ENSP00000349811.3	Q13451-1
	FKBP5	ENST00000536438.5	TSL:1	c.106-2636A>G		intron	N/A	ENSP00000444810.1	Q13451-1
	FKBP5	ENST00000539068.5	TSL:1	c.106-2636A>G		intron	N/A	ENSP00000441205.1	Q13451-1

Frequencies

GnomAD3 genomes AF: 0.673 AC: 102235 AN: 152012 Hom.: 34588 Cov.: 32

Gnomad AFR AF: 0.587

Gnomad AMI AF: 0.740

Gnomad AMR AF: 0.674

Gnomad ASJ AF: 0.729

Gnomad EAS AF: 0.737

Gnomad SAS AF: 0.657

Gnomad FIN AF: 0.803

Gnomad MID AF: 0.652

Gnomad NFE AF: 0.697

Gnomad OTH AF: 0.659

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

GnomAD4 genome AF: 0.672 AC: 102294 AN: 152130 Hom.: 34608 Cov.: 32 AF XY: 0.677 AC XY: 50377 AN XY: 74368

African (AFR) AF: 0.587 AC: 24351 AN: 41486

American (AMR) AF: 0.675 AC: 10309 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.729 AC: 2528 AN: 3468

East Asian (EAS) AF: 0.738 AC: 3825 AN: 5184

South Asian (SAS) AF: 0.658 AC: 3177 AN: 4826

European-Finnish (FIN) AF: 0.803 AC: 8502 AN: 10584

Middle Eastern (MID) AF: 0.643 AC: 189 AN: 294

European-Non Finnish (NFE) AF: 0.697 AC: 47356 AN: 67986

Other (OTH) AF: 0.655 AC: 1382 AN: 2110

Alfa AF: 0.682 Hom.: 71524

Bravo AF: 0.660

Asia WGS AF: 0.686 AC: 2381 AN: 3476

ClinVar

ClinVar submissions

Significance: Likely risk allele

Revision: no assertion criteria provided

Pathogenic	VUS	Benign	Condition
-	-	-	Post-traumatic stress disorder (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	4.8
DANN	Benign	0.70
PhyloP100		-0.087
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs1360780; hg19: chr6-35607571;