7-50214301-G-A

Variant names:

• chr7-50214301-G-A
• rs17664743
• ENST00000639870.1:n.215-10235C>T

Variant summary

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

The ENST00000639870.1(ENSG00000231681):​n.215-10235C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.239 in 152,184 control chromosomes in the GnomAD database, including 5,063 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 0.24 (5063 hom., cov: 33)
• Consequence: ENSG00000231681 ENST00000639870.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.259
• Publications: 17 publications found

Genes affected

ENSG00000231681 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.641 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000639870.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
There are no transcript annotations for this variant.

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000231681	ENST00000639870.1	TSL:5	n.215-10235C>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.239 AC: 36381 AN: 152066 Hom.: 5064 Cov.: 33

Gnomad AFR AF: 0.280

Gnomad AMI AF: 0.276

Gnomad AMR AF: 0.199

Gnomad ASJ AF: 0.325

Gnomad EAS AF: 0.660

Gnomad SAS AF: 0.165

Gnomad FIN AF: 0.133

Gnomad MID AF: 0.287

Gnomad NFE AF: 0.207

Gnomad OTH AF: 0.284

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

GnomAD4 genome AF: 0.239 AC: 36406 AN: 152184 Hom.: 5063 Cov.: 33 AF XY: 0.239 AC XY: 17777 AN XY: 74406

African (AFR) AF: 0.280 AC: 11614 AN: 41498

American (AMR) AF: 0.198 AC: 3034 AN: 15292

Ashkenazi Jewish (ASJ) AF: 0.325 AC: 1129 AN: 3470

East Asian (EAS) AF: 0.660 AC: 3404 AN: 5160

South Asian (SAS) AF: 0.163 AC: 786 AN: 4822

European-Finnish (FIN) AF: 0.133 AC: 1410 AN: 10618

Middle Eastern (MID) AF: 0.281 AC: 82 AN: 292

European-Non Finnish (NFE) AF: 0.207 AC: 14095 AN: 68006

Other (OTH) AF: 0.284 AC: 600 AN: 2114

Alfa AF: 0.221 Hom.: 1056

Bravo AF: 0.253

Asia WGS AF: 0.317 AC: 1102 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.62
DANN	Benign	0.36
PhyloP100		-0.26

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs17664743; hg19: chr7-50253897;