rs776954576

Variant names:

• chr10-102862895-C-A
• rs776954576
• NM_001136200.2:c.292C>A

Your query was ambiguous. Multiple possible variants found:

• chr10-102862895-C-A
• chr10-102862895-C-G
• chr10-102862895-C-T

Variant summary

Our verdict is Uncertain significance. The variant received 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_001136200.2(BORCS7):​c.292C>A​(p.Gln98Lys) variant causes a missense change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 12/18 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. Q98E) has been classified as Uncertain significance.

• Frequency: Genomes: not found (cov: 32)
• Consequence: BORCS7 NM_001136200.2 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 4.68
• Publications: 0 publications found

Genes affected

BORCS7 (HGNC:23516): (BLOC-1 related complex subunit 7) Part of BORC complex. [provided by Alliance of Genome Resources, Apr 2022]

BORCS7-ASMT (HGNC:49183): (BORCS7-ASMT readthrough (NMD candidate)) This locus represents naturally occurring read-through transcription between the neighboring C10orf32 (chromosome 10 open reading frame 32) and AS3MT (arsenic, +3 oxidation state, methyltransferase) genes. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is therefore unlikely to produce a protein product. [provided by RefSeq, Dec 2010]

ENSG00000296999 (HGNC:):

ACMG classification

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.12234184).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
BORCS7	NM_001136200.2	c.292C>A	p.Gln98Lys	missense_variant	Exon 5 of 5	ENST00000339834.10	NP_001129672.1
BORCS7	NM_144591.5	c.292C>A	p.Gln98Lys	missense_variant	Exon 5 of 6		NP_653192.2
BORCS7-ASMT	NR_037644.1	n.369C>A		non_coding_transcript_exon_variant	Exon 5 of 15

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
BORCS7	ENST00000339834.10	c.292C>A	p.Gln98Lys	missense_variant	Exon 5 of 5	1	NM_001136200.2	ENSP00000342331.5
BORCS7	ENST00000369883.3	c.292C>A	p.Gln98Lys	missense_variant	Exon 5 of 6	1		ENSP00000358899.3
BORCS7-ASMT	ENST00000299353.6	n.292C>A		non_coding_transcript_exon_variant	Exon 5 of 15	5		ENSP00000299353.5
ENSG00000296999	ENST00000744161.1	n.484-117G>T		intron_variant	Intron 2 of 2

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 29

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.088
BayesDel_addAF	Uncertain	0.060	T
BayesDel_noAF	Benign	-0.15
CADD	Benign	23
DANN	Benign	0.51
Eigen	Benign	-0.26
Eigen_PC	Benign	-0.058
FATHMM_MKL	Pathogenic	0.98	D
LIST_S2	Benign	0.85	.;T
M_CAP	Benign	0.0078	T
MetaRNN	Benign	0.12	T;T
MetaSVM	Benign	-0.92	T
PhyloP100		4.7
PROVEAN	Benign	0.69	N;N
REVEL	Benign	0.20
Sift	Benign	0.80	T;T
Sift4G	Benign	0.80	T;T
Vest4		0.34
MVP		0.25
MPC		0.22
ClinPred		0.54	D
GERP RS		6.1
gMVP		0.60
Mutation Taster		=72/28	polymorphism

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.090		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: rs776954576; hg19: chr10-104622652;