9-34411028-T-C

Variant names:

• chr9-34411028-T-C
• rs10738927
• NM_001184940.2:c.61-5064A>G

Variant summary

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

The NM_001184940.2(FAM219A):​c.61-5064A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.984 in 152,330 control chromosomes in the GnomAD database, including 73,871 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 0.98 (73871 hom., cov: 31)
• Consequence: FAM219A NM_001184940.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.670
• Publications: 0 publications found

Genes affected

FAM219A (HGNC:19920): (family with sequence similarity 219 member A) The protein encoded by this gene has homologs that have been identified in mouse, macaque, etc organisms. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Dec 2010]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.0).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.993 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001184940.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FAM219A	NM_001184940.2	MANE Select	c.61-5064A>G		intron	N/A	NP_001171869.1
	FAM219A	NM_001184941.2		c.61-5064A>G		intron	N/A	NP_001171870.1
	FAM219A	NM_001184942.2		c.28-5064A>G		intron	N/A	NP_001171871.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FAM219A	ENST00000651358.1	MANE Select	c.61-5064A>G		intron	N/A	ENSP00000499069.1
	FAM219A	ENST00000445726.5	TSL:2	c.61-5064A>G		intron	N/A	ENSP00000392452.1
	FAM219A	ENST00000379089.5	TSL:3	c.58-5064A>G		intron	N/A	ENSP00000368382.1

Frequencies

GnomAD3 genomes AF: 0.985 AC: 149864 AN: 152212 Hom.: 73825 Cov.: 31

Gnomad AFR AF: 0.950

Gnomad AMI AF: 1.00

Gnomad AMR AF: 0.994

Gnomad ASJ AF: 0.965

Gnomad EAS AF: 1.00

Gnomad SAS AF: 1.00

Gnomad FIN AF: 1.00

Gnomad MID AF: 1.00

Gnomad NFE AF: 0.999

Gnomad OTH AF: 0.986

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

GnomAD4 genome AF: 0.984 AC: 149968 AN: 152330 Hom.: 73871 Cov.: 31 AF XY: 0.986 AC XY: 73450 AN XY: 74498

African (AFR) AF: 0.950 AC: 39489 AN: 41554

American (AMR) AF: 0.994 AC: 15208 AN: 15306

Ashkenazi Jewish (ASJ) AF: 0.965 AC: 3352 AN: 3472

East Asian (EAS) AF: 1.00 AC: 5178 AN: 5178

South Asian (SAS) AF: 1.00 AC: 4828 AN: 4830

European-Finnish (FIN) AF: 1.00 AC: 10632 AN: 10632

Middle Eastern (MID) AF: 1.00 AC: 294 AN: 294

European-Non Finnish (NFE) AF: 0.999 AC: 67997 AN: 68044

Other (OTH) AF: 0.986 AC: 2078 AN: 2108

Alfa AF: 0.989 Hom.: 10968

Bravo AF: 0.983

Asia WGS AF: 0.997 AC: 3467 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	5.7
DANN	Benign	0.69
PhyloP100		-0.67
Mutation Taster		=100/0	polymorphism (auto)

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: rs10738927; hg19: chr9-34411026;