NM_024669.3:c.484-4284G>A

Variant names:

• chr5-56148213-C-T
• rs10214316
• NM_024669.3:c.484-4284G>A

Variant summary

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

The NM_024669.3(ANKRD55):​c.484-4284G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.694 in 152,084 control chromosomes in the GnomAD database, including 36,941 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 0.69 (36941 hom., cov: 32)
• Consequence: ANKRD55 NM_024669.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.706
• Publications: 5 publications found

Genes affected

ANKRD55 (HGNC:25681): (ankyrin repeat domain 55)

ENSG00000296884 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.722 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_024669.3. 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
	ANKRD55	NM_024669.3	MANE Select	c.484-4284G>A		intron	N/A	NP_078945.2	Q3KP44-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ANKRD55	ENST00000341048.9	TSL:2 MANE Select	c.484-4284G>A		intron	N/A	ENSP00000342295.4	Q3KP44-1
	ANKRD55	ENST00000504958.6	TSL:5	c.483+11620G>A		intron	N/A	ENSP00000424230.1	D6RBD3
	ANKRD55	ENST00000513241.2	TSL:5	c.397-4284G>A		intron	N/A	ENSP00000423507.2	D6R9N4

Frequencies

GnomAD3 genomes AF: 0.694 AC: 105466 AN: 151966 Hom.: 36918 Cov.: 32

Gnomad AFR AF: 0.729

Gnomad AMI AF: 0.743

Gnomad AMR AF: 0.582

Gnomad ASJ AF: 0.778

Gnomad EAS AF: 0.454

Gnomad SAS AF: 0.608

Gnomad FIN AF: 0.672

Gnomad MID AF: 0.823

Gnomad NFE AF: 0.720

Gnomad OTH AF: 0.698

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

GnomAD4 genome AF: 0.694 AC: 105534 AN: 152084 Hom.: 36941 Cov.: 32 AF XY: 0.687 AC XY: 51099 AN XY: 74362

African (AFR) AF: 0.729 AC: 30240 AN: 41476

American (AMR) AF: 0.581 AC: 8874 AN: 15268

Ashkenazi Jewish (ASJ) AF: 0.778 AC: 2701 AN: 3472

East Asian (EAS) AF: 0.454 AC: 2348 AN: 5174

South Asian (SAS) AF: 0.610 AC: 2936 AN: 4816

European-Finnish (FIN) AF: 0.672 AC: 7097 AN: 10562

Middle Eastern (MID) AF: 0.823 AC: 242 AN: 294

European-Non Finnish (NFE) AF: 0.720 AC: 48954 AN: 68002

Other (OTH) AF: 0.694 AC: 1464 AN: 2108

Alfa AF: 0.712 Hom.: 73071

Bravo AF: 0.691

Asia WGS AF: 0.534 AC: 1861 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	6.4
DANN	Benign	0.54
PhyloP100		0.71
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: rs10214316; hg19: chr5-55444040;