rs73043345

Variant names:

• chr2-201055337-G-A
• rs73043345
• NM_001321623.1:c.-128-9744C>T

Your query was ambiguous. Multiple possible variants found:

• chr2-201055337-G-A
• chr2-201055337-G-C

Variant summary

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

The NM_001321623.1(HYCC2):​c.-128-9744C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.216 in 148,278 control chromosomes in the GnomAD database, including 4,223 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 0.22 (4223 hom., cov: 28)
• Consequence: HYCC2 NM_001321623.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.06
• Publications: 6 publications found

Genes affected

HYCC2 (HGNC:28593): (hyccin PI4KA lipid kinase complex subunit 2) Predicted to be involved in phosphatidylinositol phosphate biosynthetic process and protein localization to plasma membrane. Predicted to be located in cytosol. Predicted to be active 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=-0.8).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.363 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001321623.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	HYCC2	NM_001321623.1	MANE Select	c.-128-9744C>T		intron	N/A	NP_001308552.1	A0A804HIT6
	HYCC2	NM_001321624.1		c.-31+16273C>T		intron	N/A	NP_001308553.1	A0A804HIT6
	HYCC2	NM_001321625.2		c.-128-9744C>T		intron	N/A	NP_001308554.1	A0A804HIT6

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	HYCC2	ENST00000681958.1	MANE Select	c.-128-9744C>T		intron	N/A	ENSP00000507218.1	A0A804HIT6
	HYCC2	ENST00000418596.7	TSL:1	c.-128-9744C>T		intron	N/A	ENSP00000393667.2	Q8IXS8
	HYCC2	ENST00000286181.7	TSL:1	n.-128-9744C>T		intron	N/A	ENSP00000286181.3	F8W7X4

Frequencies

GnomAD3 genomes AF: 0.216 AC: 31987 AN: 148192 Hom.: 4216 Cov.: 28

Gnomad AFR AF: 0.368

Gnomad AMI AF: 0.139

Gnomad AMR AF: 0.165

Gnomad ASJ AF: 0.215

Gnomad EAS AF: 0.00868

Gnomad SAS AF: 0.0693

Gnomad FIN AF: 0.173

Gnomad MID AF: 0.129

Gnomad NFE AF: 0.170

Gnomad OTH AF: 0.207

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

GnomAD4 genome AF: 0.216 AC: 32024 AN: 148278 Hom.: 4223 Cov.: 28 AF XY: 0.212 AC XY: 15270 AN XY: 72006

African (AFR) AF: 0.368 AC: 14746 AN: 40044

American (AMR) AF: 0.165 AC: 2440 AN: 14798

Ashkenazi Jewish (ASJ) AF: 0.215 AC: 741 AN: 3452

East Asian (EAS) AF: 0.00871 AC: 44 AN: 5054

South Asian (SAS) AF: 0.0694 AC: 324 AN: 4670

European-Finnish (FIN) AF: 0.173 AC: 1655 AN: 9586

Middle Eastern (MID) AF: 0.125 AC: 36 AN: 288

European-Non Finnish (NFE) AF: 0.170 AC: 11493 AN: 67440

Other (OTH) AF: 0.206 AC: 419 AN: 2038

Alfa AF: 0.0807 Hom.: 100

Bravo AF: 0.224

Asia WGS AF: 0.0660 AC: 231 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.80
CADD	Benign	0.48
DANN	Benign	0.94
PhyloP100		-2.1
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: rs73043345; hg19: chr2-201920060;