chr6-26463408-G-A
Variant summary
Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2BP4_Moderate
The NM_007049.5(BTN2A1):c.595G>A(p.Gly199Ser) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000113 in 1,614,118 control chromosomes in the GnomAD database, including 1 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).
Frequency
Genomes: 𝑓 0.000059 ( 0 hom., cov: 31)
Exomes 𝑓: 0.00012 ( 1 hom. )
Consequence
BTN2A1
NM_007049.5 missense
NM_007049.5 missense
Scores
1
3
13
Clinical Significance
Conservation
PhyloP100: 2.43
Genes affected
BTN2A1 (HGNC:1136): (butyrophilin subfamily 2 member A1) This gene encodes a member of the immunoglobulin superfamily. The gene is located in a cluster of butyrophilin-like genes in the juxta-telomeric region of the major histocompatibility complex on chromosome 6. A pseudogene of this gene has been identified in this cluster. The encoded protein is an integral plasma membrane protein involved in lipid, fatty-acid, and sterol metabolism. Alterations in this gene may be associated with several disease states including metabolic syndrome. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2013]
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ACMG classification
Classification made for transcript
Verdict is Uncertain_significance. Variant got 0 ACMG points.
PM2
?
Very rare variant in population databases, with high coverage;
BP4
?
Computational evidence support a benign effect (MetaRNN=0.12674662).
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
BTN2A1 | NM_007049.5 | c.595G>A | p.Gly199Ser | missense_variant | 4/8 | ENST00000312541.10 | |
BTN2A1 | NM_001197233.3 | c.412G>A | p.Gly138Ser | missense_variant | 3/7 | ||
BTN2A1 | NM_078476.4 | c.595G>A | p.Gly199Ser | missense_variant | 4/8 | ||
BTN2A1 | NM_001197234.3 | c.595G>A | p.Gly199Ser | missense_variant | 4/8 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
BTN2A1 | ENST00000312541.10 | c.595G>A | p.Gly199Ser | missense_variant | 4/8 | 1 | NM_007049.5 | P1 | |
ENST00000707189.1 | n.1000-89779G>A | intron_variant, non_coding_transcript_variant | |||||||
ENST00000707191.1 | n.1001-69297G>A | intron_variant, non_coding_transcript_variant |
Frequencies
GnomAD3 genomes ? AF: 0.0000592 AC: 9AN: 152108Hom.: 0 Cov.: 31
GnomAD3 genomes
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GnomAD3 exomes AF: 0.0000915 AC: 23AN: 251480Hom.: 0 AF XY: 0.000125 AC XY: 17AN XY: 135914
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GnomAD4 exome AF: 0.000118 AC: 173AN: 1461892Hom.: 1 Cov.: 31 AF XY: 0.000129 AC XY: 94AN XY: 727246
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GnomAD4 genome ? AF: 0.0000591 AC: 9AN: 152226Hom.: 0 Cov.: 31 AF XY: 0.0000806 AC XY: 6AN XY: 74426
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ClinVar
Significance: Uncertain significance
Submissions summary: Uncertain:1
Revision: criteria provided, single submitter
LINK: link
Submissions by phenotype
not specified Uncertain:1
Uncertain significance, criteria provided, single submitter | clinical testing | Ambry Genetics | Jun 11, 2021 | The c.595G>A (p.G199S) alteration is located in exon 4 (coding exon 3) of the BTN2A1 gene. This alteration results from a G to A substitution at nucleotide position 595, causing the glycine (G) at amino acid position 199 to be replaced by a serine (S). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. - |
Computational scores
Source:
Name
Calibrated prediction
Score
Prediction
AlphaMissense
Benign
BayesDel_addAF
Benign
T
BayesDel_noAF
Benign
Cadd
Uncertain
Dann
Uncertain
Eigen
Benign
Eigen_PC
Benign
FATHMM_MKL
Uncertain
D
LIST_S2
Benign
T;T;T;T
M_CAP
Benign
T
MetaRNN
Benign
T;T;T;T
MetaSVM
Benign
T
MutationTaster
Benign
N;N;N;N
PrimateAI
Benign
T
PROVEAN
Pathogenic
D;D;D;D
REVEL
Benign
Sift
Benign
D;D;D;D
Sift4G
Uncertain
D;D;T;T
Polyphen
0.98
.;D;.;.
Vest4
MVP
MPC
0.34
ClinPred
D
GERP RS
Varity_R
gMVP
Splicing
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SpliceAI score (max)
Details are displayed if max score is > 0.2
Find out detailed SpliceAI scores and Pangolin per-transcript scores at