ENST00000630472.1:n.540T>C

Variant names:

• chr6-29873244-A-G
• rs3132712
• ENST00000630472.1:n.540T>C

Variant summary

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

The ENST00000630472.1(HCP5B):​n.540T>C variant causes a non coding transcript exon change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.622 in 152,120 control chromosomes in the GnomAD database, including 29,610 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 0.62 (29603 hom., cov: 31)
  • Exomes 𝑓: 0.60 (7 hom.)
• Consequence: HCP5B ENST00000630472.1 non_coding_transcript_exon
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.657
• Publications: 5 publications found

Genes affected

HCP5B (HGNC:30984): (HLA complex P5B)

ENSG00000290870 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.642 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000630472.1. 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
	HCP5B	NR_031762.2		n.540T>C		non_coding_transcript_exon	Exon 1 of 1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	HCP5B	ENST00000630472.1	TSL:6	n.540T>C		non_coding_transcript_exon	Exon 1 of 1
	ENSG00000290870	ENST00000647952.1		n.2062+10310T>C		intron	N/A
	POLR1HASP	ENST00000849679.1		n.587-10418T>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.622 AC: 94552 AN: 151960 Hom.: 29566 Cov.: 31

Gnomad AFR AF: 0.630

Gnomad AMI AF: 0.640

Gnomad AMR AF: 0.618

Gnomad ASJ AF: 0.660

Gnomad EAS AF: 0.463

Gnomad SAS AF: 0.527

Gnomad FIN AF: 0.545

Gnomad MID AF: 0.608

Gnomad NFE AF: 0.647

Gnomad OTH AF: 0.623

GnomAD4 exome AF: 0.595 AC: 25 AN: 42 Hom.: 7 Cov.: 0 AF XY: 0.588 AC XY: 20 AN XY: 34

African (AFR) AF: 0.750 AC: 3 AN: 4

American (AMR) AC: 0 AN: 0

Ashkenazi Jewish (ASJ) AC: 0 AN: 0

East Asian (EAS) AC: 0 AN: 0

South Asian (SAS) AC: 0 AN: 0

European-Finnish (FIN) AF: 1.00 AC: 4 AN: 4

Middle Eastern (MID) AF: 0.500 AC: 1 AN: 2

European-Non Finnish (NFE) AF: 0.538 AC: 14 AN: 26

Other (OTH) AF: 0.500 AC: 3 AN: 6

GnomAD4 genome AF: 0.622 AC: 94638 AN: 152078 Hom.: 29603 Cov.: 31 AF XY: 0.615 AC XY: 45737 AN XY: 74352

African (AFR) AF: 0.631 AC: 26157 AN: 41460

American (AMR) AF: 0.617 AC: 9435 AN: 15286

Ashkenazi Jewish (ASJ) AF: 0.660 AC: 2291 AN: 3470

East Asian (EAS) AF: 0.464 AC: 2407 AN: 5182

South Asian (SAS) AF: 0.527 AC: 2542 AN: 4824

European-Finnish (FIN) AF: 0.545 AC: 5762 AN: 10572

Middle Eastern (MID) AF: 0.599 AC: 176 AN: 294

European-Non Finnish (NFE) AF: 0.647 AC: 43977 AN: 67966

Other (OTH) AF: 0.619 AC: 1307 AN: 2112

Alfa AF: 0.642 Hom.: 8688

Bravo AF: 0.631

Asia WGS AF: 0.458 AC: 1595 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	6.2
DANN	Benign	0.41
PhyloP100		0.66

Splicing

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

Other links and lift over

dbSNP: rs3132712; hg19: chr6-29841021;