dbSNP rs782640388: SLC9A6:p.Met1? (chrX-135985503-A-C) – ACMG Classification: Uncertain_significance (4 pts)

Variant summary

Our verdict is Uncertain significance. The variant received 4 ACMG points: 4P and 0B. PVS1_ModeratePM2

The NM_001438742.1(SLC9A6):c.1A>C(p.Met1?) variant causes a initiator codon change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000102 in 982,421 control chromosomes in the GnomAD database, with no homozygous occurrence. There are 1 hemizygotes in GnomAD. In-silico tool predicts a pathogenic outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

Frequency

Genomes: not found (cov: 22)

Exomes 𝑓: 0.0000010 ( 0 hom. 1 hem. )

Consequence

SLC9A6
NM_001438742.1 initiator_codon

Scores

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 3.06

Publications

0 publications found

Variant links:

Genes affected

SLC9A6 (HGNC:11079): (solute carrier family 9 member A6) This gene encodes a sodium-hydrogen exchanger that is amember of the solute carrier family 9. The encoded protein localizes to early and recycling endosomes and may be involved in regulating endosomal pH and volume. Defects in this gene are associated with X-linked syndromic cognitive disability, Christianson type. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010]

SLC9A6 Gene-Disease associations (from GenCC):

Christianson syndrome
Inheritance: XL Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Orphanet, PanelApp Australia, G2P, ClinGen

SLC9A6 links:

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ACMG classification

Classification was made for transcript

Our verdict: Uncertain_significance. The variant received 4 ACMG points.

PVS1

Start lost variant, next in-frame start position is after 1 pathogenic variants. Next in-frame start position is after 25 codons. Genomic position: 135985575. Lost 0.033 part of the original CDS.

PM2

Very rare variant in population databases, with high coverage;

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001438742.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
SLC9A6	NM_001379110.1	MANE Select	c.-57+26A>C		intron	N/A	NP_001366039.1	A0A0D9SGH0
SLC9A6	NM_001438742.1		c.1A>C	p.Met1?	initiator_codon	Exon 1 of 17	NP_001425671.1
SLC9A6	NM_001042537.2		c.1A>C	p.Met1?	initiator_codon	Exon 1 of 16	NP_001036002.1	Q92581-2

Ensembl Transcripts

Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
SLC9A6	ENST00000370695.8	TSL:1	c.1A>C	p.Met1?	initiator_codon	Exon 1 of 16	ENSP00000359729.4	Q92581-2
SLC9A6	ENST00000370698.7	TSL:1	c.1A>C	p.Met1?	initiator_codon	Exon 1 of 16	ENSP00000359732.3	Q92581-1
SLC9A6	ENST00000630721.3	TSL:4 MANE Select	c.-57+26A>C		intron	N/A	ENSP00000487486.2	A0A0D9SGH0

Frequencies

GnomAD3 genomes

Cov.:

GnomAD4 exome

AF:

0.00000102

AC:

AN:

982421

Hom.:

Cov.:

AF XY:

0.00000324

AC XY:

AN XY:

308303

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

22085

American (AMR)

AF:

0.00

AC:

AN:

19318

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

14540

East Asian (EAS)

AF:

0.0000391

AC:

AN:

25599

South Asian (SAS)

AF:

0.00

AC:

AN:

41270

European-Finnish (FIN)

AF:

0.00

AC:

AN:

25116

Middle Eastern (MID)

AF:

0.00

AC:

AN:

2697

European-Non Finnish (NFE)

AF:

0.00

AC:

AN:

790307

Other (OTH)

AF:

0.00

AC:

AN:

41489

Age Distribution

Exome Hom

Variant carriers

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

Cov.:

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name

Calibrated prediction

Score

Prediction

BayesDel_addAF

Pathogenic

0.26

BayesDel_noAF

Uncertain

0.13

CADD

Benign

(source)

DANN

Benign

0.86

DEOGEN2

Benign

0.091

FATHMM_MKL

Benign

0.62

LIST_S2

Uncertain

0.90

M_CAP

Pathogenic

0.92

MetaRNN

Pathogenic

0.98

MetaSVM

Benign

-1.0

PhyloP100

3.1

PROVEAN

Benign

-0.15

REVEL

Benign

0.27

Sift

Benign

0.11

Sift4G

Pathogenic

0.0

Polyphen

0.0040

Vest4

0.86

MutPred

0.83

Gain of stability (P = 0.1523)

MVP

0.96

ClinPred

0.90

GERP RS

4.9

PromoterAI

-0.29

Neutral

(source)

RBP_binding_hub_radar

0.0

RBP_regulation_power_radar

1.6

Varity_R

0.33

gMVP

0.60

Mutation Taster

=80/120

disease causing

(source)

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

Publications

You must be logged in to view publications. This limit was set because tens of millions (!) of queries from AI bots are generated daily.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Variant Effect in Transcripts

RefSeq Transcripts

Ensembl Transcripts

Frequencies

Age Distribution

ClinVar

Computational scores

Splicing

Publications

Other links and lift over