rs11895934

Variant names:

• chr2-189937527-G-C
• rs11895934
• ENST00000478197.1:n.219+57700G>C

Your query was ambiguous. Multiple possible variants found:

• chr2-189937527-G-C
• chr2-189937527-G-T

Variant summary

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

The ENST00000478197.1(C2orf88):​n.219+57700G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.204 in 151,786 control chromosomes in the GnomAD database, including 3,396 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 0.20 (3396 hom., cov: 31)
• Consequence: C2orf88 ENST00000478197.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.806
• Publications: 4 publications found

Genes affected

C2orf88 (HGNC:28191): (chromosome 2 open reading frame 88) Predicted to enable protein kinase A regulatory subunit binding activity. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.97).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.288 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
AKAP19	XM_047446008.1	c.-518+39964G>C		intron_variant	Intron 2 of 6		XP_047301964.1
AKAP19	XM_047446009.1	c.-518+57849G>C		intron_variant	Intron 1 of 5		XP_047301965.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
C2orf88	ENST00000478197.1	n.219+57700G>C		intron_variant	Intron 1 of 1	4
C2orf88	ENST00000495546.1	n.201+57700G>C		intron_variant	Intron 1 of 2	4

Frequencies

GnomAD3 genomes AF: 0.204 AC: 30984 AN: 151666 Hom.: 3392 Cov.: 31

Gnomad AFR AF: 0.292

Gnomad AMI AF: 0.0899

Gnomad AMR AF: 0.150

Gnomad ASJ AF: 0.234

Gnomad EAS AF: 0.107

Gnomad SAS AF: 0.157

Gnomad FIN AF: 0.158

Gnomad MID AF: 0.261

Gnomad NFE AF: 0.181

Gnomad OTH AF: 0.209

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

GnomAD4 genome AF: 0.204 AC: 31020 AN: 151786 Hom.: 3396 Cov.: 31 AF XY: 0.201 AC XY: 14913 AN XY: 74178

African (AFR) AF: 0.292 AC: 12078 AN: 41362

American (AMR) AF: 0.149 AC: 2280 AN: 15256

Ashkenazi Jewish (ASJ) AF: 0.234 AC: 811 AN: 3470

East Asian (EAS) AF: 0.106 AC: 549 AN: 5162

South Asian (SAS) AF: 0.157 AC: 752 AN: 4790

European-Finnish (FIN) AF: 0.158 AC: 1658 AN: 10508

Middle Eastern (MID) AF: 0.264 AC: 77 AN: 292

European-Non Finnish (NFE) AF: 0.181 AC: 12288 AN: 67926

Other (OTH) AF: 0.211 AC: 445 AN: 2108

Alfa AF: 0.0943 Hom.: 144

Bravo AF: 0.208

Asia WGS AF: 0.173 AC: 603 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.97
CADD	Benign	0.79
DANN	Benign	0.53
PhyloP100		-0.81

Splicing

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

Other links and lift over

dbSNP: rs11895934; hg19: chr2-190802253;