rs610315

Variant names:

• chr10-114372156-T-A
• rs610315
• NM_001001936.3:c.17-31425A>T

Variant summary

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

The NM_001001936.3(AFAP1L2):​c.17-31425A>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.169 in 152,172 control chromosomes in the GnomAD database, including 2,747 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 0.17 (2747 hom., cov: 32)
• Consequence: AFAP1L2 NM_001001936.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.107
• Publications: 1 publications found

Genes affected

AFAP1L2 (HGNC:25901): (actin filament associated protein 1 like 2) Enables SH2 domain binding activity; SH3 domain binding activity; and protein tyrosine kinase activator activity. Involved in several processes, including positive regulation of epidermal growth factor receptor signaling pathway; regulation of gene expression; and regulation of mitotic cell cycle. Located in cytosol and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.81).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.237 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
AFAP1L2	NM_001001936.3	c.17-31425A>T		intron_variant	Intron 1 of 18	ENST00000304129.9	NP_001001936.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
AFAP1L2	ENST00000304129.9	c.17-31425A>T		intron_variant	Intron 1 of 18	1	NM_001001936.3	ENSP00000303042.4

Frequencies

GnomAD3 genomes AF: 0.169 AC: 25706 AN: 152054 Hom.: 2748 Cov.: 32

Gnomad AFR AF: 0.0487

Gnomad AMI AF: 0.389

Gnomad AMR AF: 0.139

Gnomad ASJ AF: 0.165

Gnomad EAS AF: 0.169

Gnomad SAS AF: 0.175

Gnomad FIN AF: 0.210

Gnomad MID AF: 0.206

Gnomad NFE AF: 0.240

Gnomad OTH AF: 0.156

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

GnomAD4 genome AF: 0.169 AC: 25705 AN: 152172 Hom.: 2747 Cov.: 32 AF XY: 0.168 AC XY: 12480 AN XY: 74404

African (AFR) AF: 0.0486 AC: 2018 AN: 41554

American (AMR) AF: 0.139 AC: 2122 AN: 15296

Ashkenazi Jewish (ASJ) AF: 0.165 AC: 573 AN: 3464

East Asian (EAS) AF: 0.170 AC: 878 AN: 5172

South Asian (SAS) AF: 0.175 AC: 842 AN: 4816

European-Finnish (FIN) AF: 0.210 AC: 2227 AN: 10584

Middle Eastern (MID) AF: 0.211 AC: 62 AN: 294

European-Non Finnish (NFE) AF: 0.240 AC: 16298 AN: 67972

Other (OTH) AF: 0.157 AC: 332 AN: 2112

Alfa AF: 0.192 Hom.: 430

Bravo AF: 0.156

Asia WGS AF: 0.203 AC: 705 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
CADD	Benign	3.9
DANN	Benign	0.81
PhyloP100		0.11
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: rs610315; hg19: chr10-116131915;