rs55645543

Variant names:

• chr4-121686023-T-C
• rs55645543
• NM_001154.4:c.94+265A>G

Your query was ambiguous. Multiple possible variants found:

• chr4-121686023-T-C
• chr4-121686023-T-G

Variant summary

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

The NM_001154.4(ANXA5):​c.94+265A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0943 in 75,416 control chromosomes in the GnomAD database, including 202 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 0.094 (202 hom., cov: 31)
• Consequence: ANXA5 NM_001154.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.649
• Publications: 5 publications found

Genes affected

ANXA5 (HGNC:543): (annexin A5) The Annexin 5 gene spans 29 kb containing 13 exons, and encodes a single transcript of approximately 1.6 kb and a protein product with a molecular weight of about 35 kDa.The protein encoded by this gene belongs to the annexin family of calcium-dependent phospholipid binding proteins some of which have been implicated in membrane-related events along exocytotic and endocytotic pathways. Annexin 5 is a phospholipase A2 and protein kinase C inhibitory protein with calcium channel activity and a potential role in cellular signal transduction, inflammation, growth and differentiation. Annexin 5 has also been described as placental anticoagulant protein I, vascular anticoagulant-alpha, endonexin II, lipocortin V, placental protein 4 and anchorin CII. Polymorphisms in this gene have been implicated in various obstetric complications. [provided by RefSeq, Dec 2019]

ANXA5 Gene-Disease associations (from GenCC):

• pregnancy loss, recurrent, susceptibility to, 3

  Inheritance: Unknown Classification: NO_KNOWN Submitted by: Ambry Genetics

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.3 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ANXA5	NM_001154.4	c.94+265A>G		intron_variant	Intron 3 of 12	ENST00000296511.10	NP_001145.1
ANXA5	XM_017008141.3	c.94+265A>G		intron_variant	Intron 3 of 6		XP_016863630.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ANXA5	ENST00000296511.10	c.94+265A>G		intron_variant	Intron 3 of 12	1	NM_001154.4	ENSP00000296511.5

Frequencies

GnomAD3 genomes AF: 0.0945 AC: 7117 AN: 75310 Hom.: 203 Cov.: 31

Gnomad AFR AF: 0.0699

Gnomad AMI AF: 0.0504

Gnomad AMR AF: 0.127

Gnomad ASJ AF: 0.111

Gnomad EAS AF: 0.00361

Gnomad SAS AF: 0.324

Gnomad FIN AF: 0.0651

Gnomad MID AF: 0.191

Gnomad NFE AF: 0.102

Gnomad OTH AF: 0.120

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

GnomAD4 genome AF: 0.0943 AC: 7114 AN: 75416 Hom.: 202 Cov.: 31 AF XY: 0.0980 AC XY: 3427 AN XY: 34978

African (AFR) AF: 0.0700 AC: 1799 AN: 25686

American (AMR) AF: 0.127 AC: 591 AN: 4670

Ashkenazi Jewish (ASJ) AF: 0.111 AC: 210 AN: 1890

East Asian (EAS) AF: 0.00361 AC: 6 AN: 1664

South Asian (SAS) AF: 0.322 AC: 567 AN: 1760

European-Finnish (FIN) AF: 0.0651 AC: 171 AN: 2626

Middle Eastern (MID) AF: 0.167 AC: 22 AN: 132

European-Non Finnish (NFE) AF: 0.102 AC: 3625 AN: 35656

Other (OTH) AF: 0.117 AC: 98 AN: 836

Alfa AF: 0.0161 Hom.: 2

Bravo AF: 0.0470

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	1.3
DANN	Benign	0.44
PhyloP100		-0.65
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: rs55645543; hg19: chr4-122607178;