5-122425766-A-G

Variant names:

• chr5-122425766-A-G
• rs2242223
• NM_005460.4:c.1182+235A>G

Variant summary

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

The NM_005460.4(SNCAIP):​c.1182+235A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.223 in 152,190 control chromosomes in the GnomAD database, including 4,373 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 0.22 (4373 hom., cov: 33)
• Consequence: SNCAIP NM_005460.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.01
• Publications: 2 publications found

Genes affected

SNCAIP (HGNC:11139): (synuclein alpha interacting protein) This gene encodes a protein containing several protein-protein interaction domains, including ankyrin-like repeats, a coiled-coil domain, and an ATP/GTP-binding motif. The encoded protein interacts with alpha-synuclein in neuronal tissue and may play a role in the formation of cytoplasmic inclusions and neurodegeneration. A mutation in this gene has been associated with Parkinson's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]

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 (SAS) allele frequency at 95% confidence interval = 0.309 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_005460.4. 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
	SNCAIP	NM_005460.4	MANE Select	c.1182+235A>G		intron	N/A	NP_005451.2	Q9Y6H5-1
	SNCAIP	NM_001308100.2		c.1323+235A>G		intron	N/A	NP_001295029.1	Q9Y6H5-3
	SNCAIP	NM_001308105.1		c.1002+2027A>G		intron	N/A	NP_001295034.1	B7Z995

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SNCAIP	ENST00000261368.13	TSL:1 MANE Select	c.1182+235A>G		intron	N/A	ENSP00000261368.8	Q9Y6H5-1
	SNCAIP	ENST00000261367.11	TSL:1	c.1323+235A>G		intron	N/A	ENSP00000261367.7	Q9Y6H5-3
	SNCAIP	ENST00000508017.5	TSL:1	n.131-6203A>G		intron	N/A	ENSP00000424338.1	Q6L982

Frequencies

GnomAD3 genomes AF: 0.223 AC: 33982 AN: 152072 Hom.: 4365 Cov.: 33

Gnomad AFR AF: 0.104

Gnomad AMI AF: 0.292

Gnomad AMR AF: 0.288

Gnomad ASJ AF: 0.201

Gnomad EAS AF: 0.301

Gnomad SAS AF: 0.321

Gnomad FIN AF: 0.336

Gnomad MID AF: 0.209

Gnomad NFE AF: 0.252

Gnomad OTH AF: 0.212

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

GnomAD4 genome AF: 0.223 AC: 34004 AN: 152190 Hom.: 4373 Cov.: 33 AF XY: 0.230 AC XY: 17107 AN XY: 74396

African (AFR) AF: 0.104 AC: 4329 AN: 41532

American (AMR) AF: 0.289 AC: 4425 AN: 15286

Ashkenazi Jewish (ASJ) AF: 0.201 AC: 698 AN: 3470

East Asian (EAS) AF: 0.301 AC: 1560 AN: 5176

South Asian (SAS) AF: 0.322 AC: 1553 AN: 4820

European-Finnish (FIN) AF: 0.336 AC: 3555 AN: 10582

Middle Eastern (MID) AF: 0.204 AC: 60 AN: 294

European-Non Finnish (NFE) AF: 0.252 AC: 17111 AN: 68004

Other (OTH) AF: 0.211 AC: 447 AN: 2116

Alfa AF: 0.232 Hom.: 7282

Bravo AF: 0.211

Asia WGS AF: 0.275 AC: 954 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
CADD	Benign	1.9
DANN	Benign	0.82
PhyloP100		-1.0
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: rs2242223; hg19: chr5-121761461;