rs10887581

Positions:

• chr10-80177467-T-C
• chr10-80177467-T-G

Variant summary

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

The NM_145868.2(ANXA11):​c.-57-1312A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.347 in 151,954 control chromosomes in the GnomAD database, including 9,458 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 0.35 (9458 hom., cov: 31)
• Consequence: ANXA11 NM_145868.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.00

Genes affected

ANXA11 (HGNC:535): (annexin A11) This gene encodes a member of the annexin family, a group of calcium-dependent phospholipid-binding proteins. Annexins have unique N-terminal domains and conserved C-terminal domains, which contain calcium-dependent phospholipid-binding sites. The encoded protein is a 56-kD antigen recognized by sera from patients with various autoimmune diseases. Several transcript variants encoding two different isoforms have been identified. [provided by RefSeq, Dec 2015]

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 (AFR) allele frequency at 95% confidence interval = 0.398 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
ANXA11	NM_145868.2	c.-57-1312A>G		intron_variant		ENST00000422982.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
ANXA11	ENST00000422982.8	c.-57-1312A>G		intron_variant		1	NM_145868.2	P2
ANXA11	ENST00000372231.7	c.-8-4598A>G		intron_variant		1		P2
ANXA11	ENST00000438331.5	c.-57-1312A>G		intron_variant		1		P2
ANXA11	ENST00000463657.1	n.696-1312A>G		intron_variant, non_coding_transcript_variant		5

Frequencies

GnomAD3 genomes AF: 0.347 AC: 52690 AN: 151836 Hom.: 9430 Cov.: 31

Gnomad AFR AF: 0.403

Gnomad AMI AF: 0.336

Gnomad AMR AF: 0.244

Gnomad ASJ AF: 0.291

Gnomad EAS AF: 0.320

Gnomad SAS AF: 0.345

Gnomad FIN AF: 0.370

Gnomad MID AF: 0.294

Gnomad NFE AF: 0.339

Gnomad OTH AF: 0.334

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

GnomAD4 genome AF: 0.347 AC: 52765 AN: 151954 Hom.: 9458 Cov.: 31 AF XY: 0.345 AC XY: 25649 AN XY: 74268

Gnomad4 AFR AF: 0.403

Gnomad4 AMR AF: 0.244

Gnomad4 ASJ AF: 0.291

Gnomad4 EAS AF: 0.320

Gnomad4 SAS AF: 0.348

Gnomad4 FIN AF: 0.370

Gnomad4 NFE AF: 0.339

Gnomad4 OTH AF: 0.334

Alfa AF: 0.219 Hom.: 636

Bravo AF: 0.341

Asia WGS AF: 0.361 AC: 1259 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.52
DANN	Benign	0.71

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: rs10887581; hg19: chr10-81937223;