rs9266196

Variant names:

• chr6-31357052-G-A
• rs9266196
• NM_005514.8:c.73+34C>T

Your query was ambiguous. Multiple possible variants found:

• chr6-31357052-G-A
• chr6-31357052-G-C
• chr6-31357052-G-T

Variant summary

Our verdict is Likely benign. The variant received -4 ACMG points: 0P and 4B. BP4_Strong

The NM_005514.8(HLA-B):​c.73+34C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. 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 0.0 (0 hom., cov: 3)
  • Exomes 𝑓: 0.0000039 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: HLA-B NM_005514.8 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.231
• Publications: 10 publications found

Genes affected

HLA-B (HGNC:4932): (major histocompatibility complex, class I, B) HLA-B belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exon 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. Hundreds of HLA-B alleles have been described. [provided by RefSeq, Jul 2008]

ENSG00000271581 (HGNC:):

ACMG classification

Our verdict: Likely_benign. The variant received -4 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
HLA-B	NM_005514.8	c.73+34C>T		intron_variant	Intron 1 of 7	ENST00000412585.7	NP_005505.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
HLA-B	ENST00000412585.7	c.73+34C>T		intron_variant	Intron 1 of 7	6	NM_005514.8	ENSP00000399168.2

Frequencies

GnomAD3 genomes AF: 0.00 AC: 0 AN: 48004 Hom.: 0 Cov.: 3

Gnomad AFR AF: 0.00

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.00

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.00

Gnomad OTH AF: 0.00

GnomAD4 exome Data not reliable, filtered out with message: AS_VQSR AF: 0.00000393 AC: 3 AN: 762860 Hom.: 0 Cov.: 16 AF XY: 0.00000264 AC XY: 1 AN XY: 379418

⚠️ The allele balance in gnomAD version 4 Exomes is significantly skewed from the expected value of 0.5.

African (AFR) AF: 0.00 AC: 0 AN: 14432

American (AMR) AF: 0.00 AC: 0 AN: 22978

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 16272

East Asian (EAS) AF: 0.00 AC: 0 AN: 16538

South Asian (SAS) AF: 0.0000496 AC: 2 AN: 40328

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 24354

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 1860

European-Non Finnish (NFE) AF: 0.00000168 AC: 1 AN: 594350

Other (OTH) AF: 0.00 AC: 0 AN: 31748

⚠️ The allele balance in gnomAD4 Exomes is highly skewed from 0.5 (p-value = 0), which strongly suggests a high chance of mosaicism in these individuals.

GnomAD4 genome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 48004 Hom.: 0 Cov.: 3 AF XY: 0.00 AC XY: 0 AN XY: 22486

African (AFR) AF: 0.00 AC: 0 AN: 10884

American (AMR) AF: 0.00 AC: 0 AN: 4438

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 1590

East Asian (EAS) AF: 0.00 AC: 0 AN: 826

South Asian (SAS) AF: 0.00 AC: 0 AN: 686

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 3164

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 74

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 25448

Other (OTH) AF: 0.00 AC: 0 AN: 596

Alfa AF: 0.00 Hom.: 943

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	6.9
DANN	Benign	0.86
PhyloP100		-0.23
PromoterAI		-0.10	Neutral

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: rs9266196; hg19: chr6-31324829;