chr19-44929300-G-C

Variant names:

• chr19-44929300-G-C
• rs7259004
• ENST00000575148.8:n.404+1370G>C

Variant summary

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

The ENST00000575148.8(APOC1P1):​n.404+1370G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.164 in 151,480 control chromosomes in the GnomAD database, including 2,665 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 0.16 (2665 hom., cov: 30)
• Consequence: APOC1P1 ENST00000575148.8 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.649
• Publications: 25 publications found

Genes affected

APOC1P1 (HGNC:):

APOC1P1 (HGNC:608): (apolipoprotein C1 pseudogene 1)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.01).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.286 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000575148.8. 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
	APOC1P1	NR_028412.1		n.552+1370G>C		intron	N/A
	APOC1P1	NR_028413.1		n.367+1370G>C		intron	N/A
	APOC1P1	NR_028414.1		n.244+1370G>C		intron	N/A

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	APOC1P1	ENST00000575148.8	TSL:1	n.404+1370G>C		intron	N/A
	APOC1P1	ENST00000507983.7	TSL:4	n.243+1370G>C		intron	N/A
	APOC1P1	ENST00000571466.3	TSL:6	n.194+1370G>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.164 AC: 24773 AN: 151364 Hom.: 2656 Cov.: 30

Gnomad AFR AF: 0.290

Gnomad AMI AF: 0.0482

Gnomad AMR AF: 0.169

Gnomad ASJ AF: 0.124

Gnomad EAS AF: 0.252

Gnomad SAS AF: 0.161

Gnomad FIN AF: 0.0394

Gnomad MID AF: 0.120

Gnomad NFE AF: 0.103

Gnomad OTH AF: 0.154

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

GnomAD4 genome AF: 0.164 AC: 24806 AN: 151480 Hom.: 2665 Cov.: 30 AF XY: 0.163 AC XY: 12086 AN XY: 74016

African (AFR) AF: 0.291 AC: 11957 AN: 41150

American (AMR) AF: 0.169 AC: 2561 AN: 15164

Ashkenazi Jewish (ASJ) AF: 0.124 AC: 430 AN: 3468

East Asian (EAS) AF: 0.252 AC: 1289 AN: 5124

South Asian (SAS) AF: 0.160 AC: 766 AN: 4796

European-Finnish (FIN) AF: 0.0394 AC: 415 AN: 10536

Middle Eastern (MID) AF: 0.126 AC: 37 AN: 294

European-Non Finnish (NFE) AF: 0.103 AC: 6975 AN: 67936

Other (OTH) AF: 0.158 AC: 332 AN: 2100

Alfa AF: 0.0428 Hom.: 40

Bravo AF: 0.178

Asia WGS AF: 0.264 AC: 918 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.39
DANN	Benign	0.31
PhyloP100		-0.65

Splicing

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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs7259004;

hg19: chr19-45432557;