rs10510474

Variant names:

• chr3-17376004-T-G
• rs10510474
• NM_001349074.2:c.701+521A>C

Variant summary

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

The NM_001349074.2(TBC1D5):​c.701+521A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0901 in 152,104 control chromosomes in the GnomAD database, including 1,419 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 0.090 (1419 hom., cov: 32)
• Consequence: TBC1D5 NM_001349074.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0880
• Publications: 0 publications found

Genes affected

TBC1D5 (HGNC:19166): (TBC1 domain family member 5) Enables AP-2 adaptor complex binding activity and retromer complex binding activity. Involved in several processes, including macroautophagy; positive regulation of receptor internalization; and retrograde transport, endosome to Golgi. Located in Golgi apparatus; autophagosome; and endosome membrane. Part of retromer complex. Colocalizes with AP-2 adaptor complex and Atg1/ULK1 kinase complex. [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=-0.88).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.251 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TBC1D5	NM_001349074.2	c.701+521A>C		intron_variant	Intron 10 of 22	ENST00000696125.1	NP_001336003.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TBC1D5	ENST00000696125.1	c.701+521A>C		intron_variant	Intron 10 of 22		NM_001349074.2	ENSP00000512418.1

Frequencies

GnomAD3 genomes AF: 0.0897 AC: 13635 AN: 151986 Hom.: 1401 Cov.: 32

Gnomad AFR AF: 0.254

Gnomad AMI AF: 0.00110

Gnomad AMR AF: 0.0428

Gnomad ASJ AF: 0.00808

Gnomad EAS AF: 0.0316

Gnomad SAS AF: 0.0487

Gnomad FIN AF: 0.0660

Gnomad MID AF: 0.0316

Gnomad NFE AF: 0.0175

Gnomad OTH AF: 0.0636

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

GnomAD4 genome AF: 0.0901 AC: 13698 AN: 152104 Hom.: 1419 Cov.: 32 AF XY: 0.0904 AC XY: 6719 AN XY: 74342

African (AFR) AF: 0.255 AC: 10584 AN: 41482

American (AMR) AF: 0.0427 AC: 651 AN: 15254

Ashkenazi Jewish (ASJ) AF: 0.00808 AC: 28 AN: 3466

East Asian (EAS) AF: 0.0321 AC: 166 AN: 5170

South Asian (SAS) AF: 0.0483 AC: 233 AN: 4820

European-Finnish (FIN) AF: 0.0660 AC: 700 AN: 10602

Middle Eastern (MID) AF: 0.0306 AC: 9 AN: 294

European-Non Finnish (NFE) AF: 0.0175 AC: 1190 AN: 67992

Other (OTH) AF: 0.0644 AC: 136 AN: 2112

Alfa AF: 0.0745 Hom.: 180

Bravo AF: 0.0957

Asia WGS AF: 0.0610 AC: 211 AN: 3474

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	6.4
DANN	Benign	0.58
PhyloP100		-0.088
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: rs10510474; hg19: chr3-17417496;