Name: rs1491295251
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs1491295251

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chrX:46730670-46730671 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: insA / insAA / insAATA / insAATATA…
insA / insAA / insAATA / insAATATA / insAA(TA)₃ / insAA(TA)₄ / insAA(TA)₅ / insAA(TA)₆ / insAA(TA)₇ / insAA(TA)₈ / insAA(TA)₉ / insAA(TA)₁₀ / insAA(TA)₁₁ / insAA(TA)₁₂ / insATA / insATATA / ins(AT)₃A / ins(AT)₄A / ins(AT)₅A / ins(AT)₆A / ins(AT)₇A / ins(AT)₈A / ins(AT)₉A / ins(AT)₁₀A / insC(AT)₄A
Variation Type: Insertion
Frequency: insA=0.00000 (0/11808, ALFA)
insAA=0.00000 (0/11808, ALFA)
insAATA=0.00000 (0/11808, ALFA) (+ 12 more)
insAATATA=0.00000 (0/11808, ALFA)
insAA(TA)₃=0.00000 (0/11808, ALFA)
insAA(TA)₄=0.00000 (0/11808, ALFA)
insAA(TA)₅=0.00000 (0/11808, ALFA)
insAA(TA)₆=0.00000 (0/11808, ALFA)
insAA(TA)₇=0.00000 (0/11808, ALFA)
insATA=0.00000 (0/11808, ALFA)
insATATA=0.00000 (0/11808, ALFA)
ins(AT)₃A=0.00000 (0/11808, ALFA)
ins(AT)₄A=0.00000 (0/11808, ALFA)
ins(AT)₆A=0.00000 (0/11808, ALFA)
insC(AT)₄A=0.00000 (0/11808, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC9A7 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	11808	=1.00000	A=0.00000, AA=0.00000, AATA=0.00000, AATATA=0.00000, AATATATA=0.00000, AATATATATA=0.00000, AATATATATATA=0.00000, AATATATATATATA=0.00000, AATATATATATATATA=0.00000, ATA=0.00000, ATATA=0.00000, ATATATA=0.00000, ATATATATA=0.00000, ATATATATATATA=0.00000, CATATATATA=0.00000	1.0	N/A
European	Sub	7616	=1.0000	A=0.0000, AA=0.0000, AATA=0.0000, AATATA=0.0000, AATATATA=0.0000, AATATATATA=0.0000, AATATATATATA=0.0000, AATATATATATATA=0.0000, AATATATATATATATA=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATATA=0.0000, CATATATATA=0.0000	1.0	N/A
African	Sub	2766	=1.0000	A=0.0000, AA=0.0000, AATA=0.0000, AATATA=0.0000, AATATATA=0.0000, AATATATATA=0.0000, AATATATATATA=0.0000, AATATATATATATA=0.0000, AATATATATATATATA=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATATA=0.0000, CATATATATA=0.0000	1.0	N/A
African Others	Sub	108	=1.000	A=0.000, AA=0.000, AATA=0.000, AATATA=0.000, AATATATA=0.000, AATATATATA=0.000, AATATATATATA=0.000, AATATATATATATA=0.000, AATATATATATATATA=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATATA=0.000, CATATATATA=0.000	1.0	N/A
African American	Sub	2658	=1.0000	A=0.0000, AA=0.0000, AATA=0.0000, AATATA=0.0000, AATATATA=0.0000, AATATATATA=0.0000, AATATATATATA=0.0000, AATATATATATATA=0.0000, AATATATATATATATA=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATATA=0.0000, CATATATATA=0.0000	1.0	N/A
Asian	Sub	108	=1.000	A=0.000, AA=0.000, AATA=0.000, AATATA=0.000, AATATATA=0.000, AATATATATA=0.000, AATATATATATA=0.000, AATATATATATATA=0.000, AATATATATATATATA=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATATA=0.000, CATATATATA=0.000	1.0	N/A
East Asian	Sub	84	=1.00	A=0.00, AA=0.00, AATA=0.00, AATATA=0.00, AATATATA=0.00, AATATATATA=0.00, AATATATATATA=0.00, AATATATATATATA=0.00, AATATATATATATATA=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATATA=0.00, CATATATATA=0.00	1.0	N/A
Other Asian	Sub	24	=1.00	A=0.00, AA=0.00, AATA=0.00, AATATA=0.00, AATATATA=0.00, AATATATATA=0.00, AATATATATATA=0.00, AATATATATATATA=0.00, AATATATATATATATA=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATATA=0.00, CATATATATA=0.00	1.0	N/A
Latin American 1	Sub	144	=1.000	A=0.000, AA=0.000, AATA=0.000, AATATA=0.000, AATATATA=0.000, AATATATATA=0.000, AATATATATATA=0.000, AATATATATATATA=0.000, AATATATATATATATA=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATATA=0.000, CATATATATA=0.000	1.0	N/A
Latin American 2	Sub	610	=1.000	A=0.000, AA=0.000, AATA=0.000, AATATA=0.000, AATATATA=0.000, AATATATATA=0.000, AATATATATATA=0.000, AATATATATATATA=0.000, AATATATATATATATA=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATATA=0.000, CATATATATA=0.000	1.0	N/A
South Asian	Sub	94	=1.00	A=0.00, AA=0.00, AATA=0.00, AATATA=0.00, AATATATA=0.00, AATATATATA=0.00, AATATATATATA=0.00, AATATATATATATA=0.00, AATATATATATATATA=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATATA=0.00, CATATATATA=0.00	1.0	N/A
Other	Sub	470	=1.000	A=0.000, AA=0.000, AATA=0.000, AATATA=0.000, AATATATA=0.000, AATATATATA=0.000, AATATATATATA=0.000, AATATATATATATA=0.000, AATATATATATATATA=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATATA=0.000, CATATATATA=0.000	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	11808	- No frequency provided	insA=0.00000, insAA=0.00000, insAATA=0.00000, insAATATA=0.00000, insAA(TA)₃=0.00000, insAA(TA)₄=0.00000, insAA(TA)₅=0.00000, insAA(TA)₆=0.00000, insAA(TA)₇=0.00000, insATA=0.00000, insATATA=0.00000, ins(AT)₃A=0.00000, ins(AT)₄A=0.00000, ins(AT)₆A=0.00000, insC(AT)₄A=0.00000
Allele Frequency Aggregator	European	Sub	7616	- No frequency provided	insA=0.0000, insAA=0.0000, insAATA=0.0000, insAATATA=0.0000, insAA(TA)₃=0.0000, insAA(TA)₄=0.0000, insAA(TA)₅=0.0000, insAA(TA)₆=0.0000, insAA(TA)₇=0.0000, insATA=0.0000, insATATA=0.0000, ins(AT)₃A=0.0000, ins(AT)₄A=0.0000, ins(AT)₆A=0.0000, insC(AT)₄A=0.0000
Allele Frequency Aggregator	African	Sub	2766	- No frequency provided	insA=0.0000, insAA=0.0000, insAATA=0.0000, insAATATA=0.0000, insAA(TA)₃=0.0000, insAA(TA)₄=0.0000, insAA(TA)₅=0.0000, insAA(TA)₆=0.0000, insAA(TA)₇=0.0000, insATA=0.0000, insATATA=0.0000, ins(AT)₃A=0.0000, ins(AT)₄A=0.0000, ins(AT)₆A=0.0000, insC(AT)₄A=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	- No frequency provided	insA=0.000, insAA=0.000, insAATA=0.000, insAATATA=0.000, insAA(TA)₃=0.000, insAA(TA)₄=0.000, insAA(TA)₅=0.000, insAA(TA)₆=0.000, insAA(TA)₇=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₆A=0.000, insC(AT)₄A=0.000
Allele Frequency Aggregator	Other	Sub	470	- No frequency provided	insA=0.000, insAA=0.000, insAATA=0.000, insAATATA=0.000, insAA(TA)₃=0.000, insAA(TA)₄=0.000, insAA(TA)₅=0.000, insAA(TA)₆=0.000, insAA(TA)₇=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₆A=0.000, insC(AT)₄A=0.000
Allele Frequency Aggregator	Latin American 1	Sub	144	- No frequency provided	insA=0.000, insAA=0.000, insAATA=0.000, insAATATA=0.000, insAA(TA)₃=0.000, insAA(TA)₄=0.000, insAA(TA)₅=0.000, insAA(TA)₆=0.000, insAA(TA)₇=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₆A=0.000, insC(AT)₄A=0.000
Allele Frequency Aggregator	Asian	Sub	108	- No frequency provided	insA=0.000, insAA=0.000, insAATA=0.000, insAATATA=0.000, insAA(TA)₃=0.000, insAA(TA)₄=0.000, insAA(TA)₅=0.000, insAA(TA)₆=0.000, insAA(TA)₇=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₆A=0.000, insC(AT)₄A=0.000
Allele Frequency Aggregator	South Asian	Sub	94	- No frequency provided	insA=0.00, insAA=0.00, insAATA=0.00, insAATATA=0.00, insAA(TA)₃=0.00, insAA(TA)₄=0.00, insAA(TA)₅=0.00, insAA(TA)₆=0.00, insAA(TA)₇=0.00, insATA=0.00, insATATA=0.00, ins(AT)₃A=0.00, ins(AT)₄A=0.00, ins(AT)₆A=0.00, insC(AT)₄A=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insAA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insAATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insAATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insAATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insAATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insAATATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insAATATATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insAATATATATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insAATATATATATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insAATATATATATATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insAATATATATATATATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insAATATATATATATATATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insAATATATATATATATATATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insATATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insATATATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insATATATATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insATATATATATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insATATATATATATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insATATATATATATATATATATA
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671insCATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insAA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insAATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insAATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insAATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insAATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insAATATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insAATATATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insAATATATATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insAATATATATATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insAATATATATATATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insAATATATATATATATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insAATATATATATATATATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insAATATATATATATATATATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insATATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insATATATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insATATATATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insATATATATATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insATATATATATATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insATATATATATATATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106insCATATATATA
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATATT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATATATT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATATATATT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATATATATATT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATATATATATATT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATATATATATATATT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATATATATATATATATT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATATATATATATATATATT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTAT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATAT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATAT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATAT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATAT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATATAT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATATATAT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATATATATAT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATATATATATAT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATATATATATATAT
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368insTATATATATG

Gene: SLC9A7, solute carrier family 9 member A7 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC9A7 transcript variant 1	NM_001257291.2:c.325+2803… NM_001257291.2:c.325+28034_325+28035insT	N/A	Intron Variant
SLC9A7 transcript variant 2	NM_032591.3:c.325+28034_3… NM_032591.3:c.325+28034_325+28035insT	N/A	Intron Variant
SLC9A7 transcript variant X1	XM_005272681.5:c.325+2803… XM_005272681.5:c.325+28034_325+28035insT	N/A	Intron Variant
SLC9A7 transcript variant X2	XM_005272682.5:c.325+2803… XM_005272682.5:c.325+28034_325+28035insT	N/A	Intron Variant
SLC9A7 transcript variant X3	XM_011543990.3:c.325+2803… XM_011543990.3:c.325+28034_325+28035insT	N/A	Intron Variant
SLC9A7 transcript variant X4	XM_017029905.2:c.325+2803… XM_017029905.2:c.325+28034_325+28035insT	N/A	Intron Variant
SLC9A7 transcript variant X6	XM_017029906.3:c.325+2803… XM_017029906.3:c.325+28034_325+28035insT	N/A	Intron Variant
SLC9A7 transcript variant X7	XM_047442581.1:c.325+2803… XM_047442581.1:c.325+28034_325+28035insT	N/A	Intron Variant
SLC9A7 transcript variant X8	XM_047442582.1:c.325+2803… XM_047442582.1:c.325+28034_325+28035insT	N/A	Intron Variant
SLC9A7 transcript variant X5	XR_007068203.1:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	=	insA	insAA	insAATA	insAATATA	insAA(TA)₃	insAA(TA)₄	insAA(TA)₅	insAA(TA)₆	insAA(TA)₇	insAA(TA)₈	insAA(TA)₉	insAA(TA)₁₀	insAA(TA)₁₁	insAA(TA)₁₂	insATA	insATATA	ins(AT)₃A	ins(AT)₄A	ins(AT)₅A	ins(AT)₆A	ins(AT)₇A	ins(AT)₈A	ins(AT)₉A	ins(AT)₁₀A	insC(AT)₄A
GRCh38.p14 chr X	NC_000023.11:g.46730670_46730671=	NC_000023.11:g.46730670_46730671insA	NC_000023.11:g.46730670_46730671insAA	NC_000023.11:g.46730670_46730671insAATA	NC_000023.11:g.46730670_46730671insAATATA	NC_000023.11:g.46730670_46730671insAATATATA	NC_000023.11:g.46730670_46730671insAATATATATA	NC_000023.11:g.46730670_46730671insAATATATATATA	NC_000023.11:g.46730670_46730671insAATATATATATATA	NC_000023.11:g.46730670_46730671insAATATATATATATATA	NC_000023.11:g.46730670_46730671insAATATATATATATATATA	NC_000023.11:g.46730670_46730671insAATATATATATATATATATA	NC_000023.11:g.46730670_46730671insAATATATATATATATATATATA	NC_000023.11:g.46730670_46730671insAATATATATATATATATATATATA	NC_000023.11:g.46730670_46730671insAATATATATATATATATATATATATA	NC_000023.11:g.46730670_46730671insATA	NC_000023.11:g.46730670_46730671insATATA	NC_000023.11:g.46730670_46730671insATATATA	NC_000023.11:g.46730670_46730671insATATATATA	NC_000023.11:g.46730670_46730671insATATATATATA	NC_000023.11:g.46730670_46730671insATATATATATATA	NC_000023.11:g.46730670_46730671insATATATATATATATA	NC_000023.11:g.46730670_46730671insATATATATATATATATA	NC_000023.11:g.46730670_46730671insATATATATATATATATATA	NC_000023.11:g.46730670_46730671insATATATATATATATATATATA	NC_000023.11:g.46730670_46730671insCATATATATA
GRCh37.p13 chr X	NC_000023.10:g.46590105_46590106=	NC_000023.10:g.46590105_46590106insA	NC_000023.10:g.46590105_46590106insAA	NC_000023.10:g.46590105_46590106insAATA	NC_000023.10:g.46590105_46590106insAATATA	NC_000023.10:g.46590105_46590106insAATATATA	NC_000023.10:g.46590105_46590106insAATATATATA	NC_000023.10:g.46590105_46590106insAATATATATATA	NC_000023.10:g.46590105_46590106insAATATATATATATA	NC_000023.10:g.46590105_46590106insAATATATATATATATA	NC_000023.10:g.46590105_46590106insAATATATATATATATATA	NC_000023.10:g.46590105_46590106insAATATATATATATATATATA	NC_000023.10:g.46590105_46590106insAATATATATATATATATATATA	NC_000023.10:g.46590105_46590106insAATATATATATATATATATATATA	NC_000023.10:g.46590105_46590106insAATATATATATATATATATATATATA	NC_000023.10:g.46590105_46590106insATA	NC_000023.10:g.46590105_46590106insATATA	NC_000023.10:g.46590105_46590106insATATATA	NC_000023.10:g.46590105_46590106insATATATATA	NC_000023.10:g.46590105_46590106insATATATATATA	NC_000023.10:g.46590105_46590106insATATATATATATA	NC_000023.10:g.46590105_46590106insATATATATATATATA	NC_000023.10:g.46590105_46590106insATATATATATATATATA	NC_000023.10:g.46590105_46590106insATATATATATATATATATA	NC_000023.10:g.46590105_46590106insATATATATATATATATATATA	NC_000023.10:g.46590105_46590106insCATATATATA
SLC9A7 RefSeqGene	NG_012622.2:g.33367_33368=	NG_012622.2:g.33367_33368insT	NG_012622.2:g.33367_33368insTT	NG_012622.2:g.33367_33368insTATT	NG_012622.2:g.33367_33368insTATATT	NG_012622.2:g.33367_33368insTATATATT	NG_012622.2:g.33367_33368insTATATATATT	NG_012622.2:g.33367_33368insTATATATATATT	NG_012622.2:g.33367_33368insTATATATATATATT	NG_012622.2:g.33367_33368insTATATATATATATATT	NG_012622.2:g.33367_33368insTATATATATATATATATT	NG_012622.2:g.33367_33368insTATATATATATATATATATT	NG_012622.2:g.33367_33368insTATATATATATATATATATATT	NG_012622.2:g.33367_33368insTATATATATATATATATATATATT	NG_012622.2:g.33367_33368insTATATATATATATATATATATATATT	NG_012622.2:g.33367_33368insTAT	NG_012622.2:g.33367_33368insTATAT	NG_012622.2:g.33367_33368insTATATAT	NG_012622.2:g.33367_33368insTATATATAT	NG_012622.2:g.33367_33368insTATATATATAT	NG_012622.2:g.33367_33368insTATATATATATAT	NG_012622.2:g.33367_33368insTATATATATATATAT	NG_012622.2:g.33367_33368insTATATATATATATATAT	NG_012622.2:g.33367_33368insTATATATATATATATATAT	NG_012622.2:g.33367_33368insTATATATATATATATATATAT	NG_012622.2:g.33367_33368insTATATATATG
SLC9A7 transcript variant 1	NM_001257291.1:c.325+28034=	NM_001257291.1:c.325+28034_325+28035insT	NM_001257291.1:c.325+28034_325+28035insTT	NM_001257291.1:c.325+28034_325+28035insTATT	NM_001257291.1:c.325+28034_325+28035insTATATT	NM_001257291.1:c.325+28034_325+28035insTATATATT	NM_001257291.1:c.325+28034_325+28035insTATATATATT	NM_001257291.1:c.325+28034_325+28035insTATATATATATT	NM_001257291.1:c.325+28034_325+28035insTATATATATATATT	NM_001257291.1:c.325+28034_325+28035insTATATATATATATATT	NM_001257291.1:c.325+28034_325+28035insTATATATATATATATATT	NM_001257291.1:c.325+28034_325+28035insTATATATATATATATATATT	NM_001257291.1:c.325+28034_325+28035insTATATATATATATATATATATT	NM_001257291.1:c.325+28034_325+28035insTATATATATATATATATATATATT	NM_001257291.1:c.325+28034_325+28035insTATATATATATATATATATATATATT	NM_001257291.1:c.325+28034_325+28035insTAT	NM_001257291.1:c.325+28034_325+28035insTATAT	NM_001257291.1:c.325+28034_325+28035insTATATAT	NM_001257291.1:c.325+28034_325+28035insTATATATAT	NM_001257291.1:c.325+28034_325+28035insTATATATATAT	NM_001257291.1:c.325+28034_325+28035insTATATATATATAT	NM_001257291.1:c.325+28034_325+28035insTATATATATATATAT	NM_001257291.1:c.325+28034_325+28035insTATATATATATATATAT	NM_001257291.1:c.325+28034_325+28035insTATATATATATATATATAT	NM_001257291.1:c.325+28034_325+28035insTATATATATATATATATATAT	NM_001257291.1:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant 1	NM_001257291.2:c.325+28034=	NM_001257291.2:c.325+28034_325+28035insT	NM_001257291.2:c.325+28034_325+28035insTT	NM_001257291.2:c.325+28034_325+28035insTATT	NM_001257291.2:c.325+28034_325+28035insTATATT	NM_001257291.2:c.325+28034_325+28035insTATATATT	NM_001257291.2:c.325+28034_325+28035insTATATATATT	NM_001257291.2:c.325+28034_325+28035insTATATATATATT	NM_001257291.2:c.325+28034_325+28035insTATATATATATATT	NM_001257291.2:c.325+28034_325+28035insTATATATATATATATT	NM_001257291.2:c.325+28034_325+28035insTATATATATATATATATT	NM_001257291.2:c.325+28034_325+28035insTATATATATATATATATATT	NM_001257291.2:c.325+28034_325+28035insTATATATATATATATATATATT	NM_001257291.2:c.325+28034_325+28035insTATATATATATATATATATATATT	NM_001257291.2:c.325+28034_325+28035insTATATATATATATATATATATATATT	NM_001257291.2:c.325+28034_325+28035insTAT	NM_001257291.2:c.325+28034_325+28035insTATAT	NM_001257291.2:c.325+28034_325+28035insTATATAT	NM_001257291.2:c.325+28034_325+28035insTATATATAT	NM_001257291.2:c.325+28034_325+28035insTATATATATAT	NM_001257291.2:c.325+28034_325+28035insTATATATATATAT	NM_001257291.2:c.325+28034_325+28035insTATATATATATATAT	NM_001257291.2:c.325+28034_325+28035insTATATATATATATATAT	NM_001257291.2:c.325+28034_325+28035insTATATATATATATATATAT	NM_001257291.2:c.325+28034_325+28035insTATATATATATATATATATAT	NM_001257291.2:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant 2	NM_032591.2:c.325+28034=	NM_032591.2:c.325+28034_325+28035insT	NM_032591.2:c.325+28034_325+28035insTT	NM_032591.2:c.325+28034_325+28035insTATT	NM_032591.2:c.325+28034_325+28035insTATATT	NM_032591.2:c.325+28034_325+28035insTATATATT	NM_032591.2:c.325+28034_325+28035insTATATATATT	NM_032591.2:c.325+28034_325+28035insTATATATATATT	NM_032591.2:c.325+28034_325+28035insTATATATATATATT	NM_032591.2:c.325+28034_325+28035insTATATATATATATATT	NM_032591.2:c.325+28034_325+28035insTATATATATATATATATT	NM_032591.2:c.325+28034_325+28035insTATATATATATATATATATT	NM_032591.2:c.325+28034_325+28035insTATATATATATATATATATATT	NM_032591.2:c.325+28034_325+28035insTATATATATATATATATATATATT	NM_032591.2:c.325+28034_325+28035insTATATATATATATATATATATATATT	NM_032591.2:c.325+28034_325+28035insTAT	NM_032591.2:c.325+28034_325+28035insTATAT	NM_032591.2:c.325+28034_325+28035insTATATAT	NM_032591.2:c.325+28034_325+28035insTATATATAT	NM_032591.2:c.325+28034_325+28035insTATATATATAT	NM_032591.2:c.325+28034_325+28035insTATATATATATAT	NM_032591.2:c.325+28034_325+28035insTATATATATATATAT	NM_032591.2:c.325+28034_325+28035insTATATATATATATATAT	NM_032591.2:c.325+28034_325+28035insTATATATATATATATATAT	NM_032591.2:c.325+28034_325+28035insTATATATATATATATATATAT	NM_032591.2:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant 2	NM_032591.3:c.325+28034=	NM_032591.3:c.325+28034_325+28035insT	NM_032591.3:c.325+28034_325+28035insTT	NM_032591.3:c.325+28034_325+28035insTATT	NM_032591.3:c.325+28034_325+28035insTATATT	NM_032591.3:c.325+28034_325+28035insTATATATT	NM_032591.3:c.325+28034_325+28035insTATATATATT	NM_032591.3:c.325+28034_325+28035insTATATATATATT	NM_032591.3:c.325+28034_325+28035insTATATATATATATT	NM_032591.3:c.325+28034_325+28035insTATATATATATATATT	NM_032591.3:c.325+28034_325+28035insTATATATATATATATATT	NM_032591.3:c.325+28034_325+28035insTATATATATATATATATATT	NM_032591.3:c.325+28034_325+28035insTATATATATATATATATATATT	NM_032591.3:c.325+28034_325+28035insTATATATATATATATATATATATT	NM_032591.3:c.325+28034_325+28035insTATATATATATATATATATATATATT	NM_032591.3:c.325+28034_325+28035insTAT	NM_032591.3:c.325+28034_325+28035insTATAT	NM_032591.3:c.325+28034_325+28035insTATATAT	NM_032591.3:c.325+28034_325+28035insTATATATAT	NM_032591.3:c.325+28034_325+28035insTATATATATAT	NM_032591.3:c.325+28034_325+28035insTATATATATATAT	NM_032591.3:c.325+28034_325+28035insTATATATATATATAT	NM_032591.3:c.325+28034_325+28035insTATATATATATATATAT	NM_032591.3:c.325+28034_325+28035insTATATATATATATATATAT	NM_032591.3:c.325+28034_325+28035insTATATATATATATATATATAT	NM_032591.3:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant X1	XM_005272680.1:c.325+28034=	XM_005272680.1:c.325+28034_325+28035insT	XM_005272680.1:c.325+28034_325+28035insTT	XM_005272680.1:c.325+28034_325+28035insTATT	XM_005272680.1:c.325+28034_325+28035insTATATT	XM_005272680.1:c.325+28034_325+28035insTATATATT	XM_005272680.1:c.325+28034_325+28035insTATATATATT	XM_005272680.1:c.325+28034_325+28035insTATATATATATT	XM_005272680.1:c.325+28034_325+28035insTATATATATATATT	XM_005272680.1:c.325+28034_325+28035insTATATATATATATATT	XM_005272680.1:c.325+28034_325+28035insTATATATATATATATATT	XM_005272680.1:c.325+28034_325+28035insTATATATATATATATATATT	XM_005272680.1:c.325+28034_325+28035insTATATATATATATATATATATT	XM_005272680.1:c.325+28034_325+28035insTATATATATATATATATATATATT	XM_005272680.1:c.325+28034_325+28035insTATATATATATATATATATATATATT	XM_005272680.1:c.325+28034_325+28035insTAT	XM_005272680.1:c.325+28034_325+28035insTATAT	XM_005272680.1:c.325+28034_325+28035insTATATAT	XM_005272680.1:c.325+28034_325+28035insTATATATAT	XM_005272680.1:c.325+28034_325+28035insTATATATATAT	XM_005272680.1:c.325+28034_325+28035insTATATATATATAT	XM_005272680.1:c.325+28034_325+28035insTATATATATATATAT	XM_005272680.1:c.325+28034_325+28035insTATATATATATATATAT	XM_005272680.1:c.325+28034_325+28035insTATATATATATATATATAT	XM_005272680.1:c.325+28034_325+28035insTATATATATATATATATATAT	XM_005272680.1:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant X2	XM_005272681.1:c.325+28034=	XM_005272681.1:c.325+28034_325+28035insT	XM_005272681.1:c.325+28034_325+28035insTT	XM_005272681.1:c.325+28034_325+28035insTATT	XM_005272681.1:c.325+28034_325+28035insTATATT	XM_005272681.1:c.325+28034_325+28035insTATATATT	XM_005272681.1:c.325+28034_325+28035insTATATATATT	XM_005272681.1:c.325+28034_325+28035insTATATATATATT	XM_005272681.1:c.325+28034_325+28035insTATATATATATATT	XM_005272681.1:c.325+28034_325+28035insTATATATATATATATT	XM_005272681.1:c.325+28034_325+28035insTATATATATATATATATT	XM_005272681.1:c.325+28034_325+28035insTATATATATATATATATATT	XM_005272681.1:c.325+28034_325+28035insTATATATATATATATATATATT	XM_005272681.1:c.325+28034_325+28035insTATATATATATATATATATATATT	XM_005272681.1:c.325+28034_325+28035insTATATATATATATATATATATATATT	XM_005272681.1:c.325+28034_325+28035insTAT	XM_005272681.1:c.325+28034_325+28035insTATAT	XM_005272681.1:c.325+28034_325+28035insTATATAT	XM_005272681.1:c.325+28034_325+28035insTATATATAT	XM_005272681.1:c.325+28034_325+28035insTATATATATAT	XM_005272681.1:c.325+28034_325+28035insTATATATATATAT	XM_005272681.1:c.325+28034_325+28035insTATATATATATATAT	XM_005272681.1:c.325+28034_325+28035insTATATATATATATATAT	XM_005272681.1:c.325+28034_325+28035insTATATATATATATATATAT	XM_005272681.1:c.325+28034_325+28035insTATATATATATATATATATAT	XM_005272681.1:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant X1	XM_005272681.5:c.325+28034=	XM_005272681.5:c.325+28034_325+28035insT	XM_005272681.5:c.325+28034_325+28035insTT	XM_005272681.5:c.325+28034_325+28035insTATT	XM_005272681.5:c.325+28034_325+28035insTATATT	XM_005272681.5:c.325+28034_325+28035insTATATATT	XM_005272681.5:c.325+28034_325+28035insTATATATATT	XM_005272681.5:c.325+28034_325+28035insTATATATATATT	XM_005272681.5:c.325+28034_325+28035insTATATATATATATT	XM_005272681.5:c.325+28034_325+28035insTATATATATATATATT	XM_005272681.5:c.325+28034_325+28035insTATATATATATATATATT	XM_005272681.5:c.325+28034_325+28035insTATATATATATATATATATT	XM_005272681.5:c.325+28034_325+28035insTATATATATATATATATATATT	XM_005272681.5:c.325+28034_325+28035insTATATATATATATATATATATATT	XM_005272681.5:c.325+28034_325+28035insTATATATATATATATATATATATATT	XM_005272681.5:c.325+28034_325+28035insTAT	XM_005272681.5:c.325+28034_325+28035insTATAT	XM_005272681.5:c.325+28034_325+28035insTATATAT	XM_005272681.5:c.325+28034_325+28035insTATATATAT	XM_005272681.5:c.325+28034_325+28035insTATATATATAT	XM_005272681.5:c.325+28034_325+28035insTATATATATATAT	XM_005272681.5:c.325+28034_325+28035insTATATATATATATAT	XM_005272681.5:c.325+28034_325+28035insTATATATATATATATAT	XM_005272681.5:c.325+28034_325+28035insTATATATATATATATATAT	XM_005272681.5:c.325+28034_325+28035insTATATATATATATATATATAT	XM_005272681.5:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant X3	XM_005272682.1:c.325+28034=	XM_005272682.1:c.325+28034_325+28035insT	XM_005272682.1:c.325+28034_325+28035insTT	XM_005272682.1:c.325+28034_325+28035insTATT	XM_005272682.1:c.325+28034_325+28035insTATATT	XM_005272682.1:c.325+28034_325+28035insTATATATT	XM_005272682.1:c.325+28034_325+28035insTATATATATT	XM_005272682.1:c.325+28034_325+28035insTATATATATATT	XM_005272682.1:c.325+28034_325+28035insTATATATATATATT	XM_005272682.1:c.325+28034_325+28035insTATATATATATATATT	XM_005272682.1:c.325+28034_325+28035insTATATATATATATATATT	XM_005272682.1:c.325+28034_325+28035insTATATATATATATATATATT	XM_005272682.1:c.325+28034_325+28035insTATATATATATATATATATATT	XM_005272682.1:c.325+28034_325+28035insTATATATATATATATATATATATT	XM_005272682.1:c.325+28034_325+28035insTATATATATATATATATATATATATT	XM_005272682.1:c.325+28034_325+28035insTAT	XM_005272682.1:c.325+28034_325+28035insTATAT	XM_005272682.1:c.325+28034_325+28035insTATATAT	XM_005272682.1:c.325+28034_325+28035insTATATATAT	XM_005272682.1:c.325+28034_325+28035insTATATATATAT	XM_005272682.1:c.325+28034_325+28035insTATATATATATAT	XM_005272682.1:c.325+28034_325+28035insTATATATATATATAT	XM_005272682.1:c.325+28034_325+28035insTATATATATATATATAT	XM_005272682.1:c.325+28034_325+28035insTATATATATATATATATAT	XM_005272682.1:c.325+28034_325+28035insTATATATATATATATATATAT	XM_005272682.1:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant X2	XM_005272682.5:c.325+28034=	XM_005272682.5:c.325+28034_325+28035insT	XM_005272682.5:c.325+28034_325+28035insTT	XM_005272682.5:c.325+28034_325+28035insTATT	XM_005272682.5:c.325+28034_325+28035insTATATT	XM_005272682.5:c.325+28034_325+28035insTATATATT	XM_005272682.5:c.325+28034_325+28035insTATATATATT	XM_005272682.5:c.325+28034_325+28035insTATATATATATT	XM_005272682.5:c.325+28034_325+28035insTATATATATATATT	XM_005272682.5:c.325+28034_325+28035insTATATATATATATATT	XM_005272682.5:c.325+28034_325+28035insTATATATATATATATATT	XM_005272682.5:c.325+28034_325+28035insTATATATATATATATATATT	XM_005272682.5:c.325+28034_325+28035insTATATATATATATATATATATT	XM_005272682.5:c.325+28034_325+28035insTATATATATATATATATATATATT	XM_005272682.5:c.325+28034_325+28035insTATATATATATATATATATATATATT	XM_005272682.5:c.325+28034_325+28035insTAT	XM_005272682.5:c.325+28034_325+28035insTATAT	XM_005272682.5:c.325+28034_325+28035insTATATAT	XM_005272682.5:c.325+28034_325+28035insTATATATAT	XM_005272682.5:c.325+28034_325+28035insTATATATATAT	XM_005272682.5:c.325+28034_325+28035insTATATATATATAT	XM_005272682.5:c.325+28034_325+28035insTATATATATATATAT	XM_005272682.5:c.325+28034_325+28035insTATATATATATATATAT	XM_005272682.5:c.325+28034_325+28035insTATATATATATATATATAT	XM_005272682.5:c.325+28034_325+28035insTATATATATATATATATATAT	XM_005272682.5:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant X4	XM_005272683.1:c.325+28034=	XM_005272683.1:c.325+28034_325+28035insT	XM_005272683.1:c.325+28034_325+28035insTT	XM_005272683.1:c.325+28034_325+28035insTATT	XM_005272683.1:c.325+28034_325+28035insTATATT	XM_005272683.1:c.325+28034_325+28035insTATATATT	XM_005272683.1:c.325+28034_325+28035insTATATATATT	XM_005272683.1:c.325+28034_325+28035insTATATATATATT	XM_005272683.1:c.325+28034_325+28035insTATATATATATATT	XM_005272683.1:c.325+28034_325+28035insTATATATATATATATT	XM_005272683.1:c.325+28034_325+28035insTATATATATATATATATT	XM_005272683.1:c.325+28034_325+28035insTATATATATATATATATATT	XM_005272683.1:c.325+28034_325+28035insTATATATATATATATATATATT	XM_005272683.1:c.325+28034_325+28035insTATATATATATATATATATATATT	XM_005272683.1:c.325+28034_325+28035insTATATATATATATATATATATATATT	XM_005272683.1:c.325+28034_325+28035insTAT	XM_005272683.1:c.325+28034_325+28035insTATAT	XM_005272683.1:c.325+28034_325+28035insTATATAT	XM_005272683.1:c.325+28034_325+28035insTATATATAT	XM_005272683.1:c.325+28034_325+28035insTATATATATAT	XM_005272683.1:c.325+28034_325+28035insTATATATATATAT	XM_005272683.1:c.325+28034_325+28035insTATATATATATATAT	XM_005272683.1:c.325+28034_325+28035insTATATATATATATATAT	XM_005272683.1:c.325+28034_325+28035insTATATATATATATATATAT	XM_005272683.1:c.325+28034_325+28035insTATATATATATATATATATAT	XM_005272683.1:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant X5	XM_005272684.1:c.325+28034=	XM_005272684.1:c.325+28034_325+28035insT	XM_005272684.1:c.325+28034_325+28035insTT	XM_005272684.1:c.325+28034_325+28035insTATT	XM_005272684.1:c.325+28034_325+28035insTATATT	XM_005272684.1:c.325+28034_325+28035insTATATATT	XM_005272684.1:c.325+28034_325+28035insTATATATATT	XM_005272684.1:c.325+28034_325+28035insTATATATATATT	XM_005272684.1:c.325+28034_325+28035insTATATATATATATT	XM_005272684.1:c.325+28034_325+28035insTATATATATATATATT	XM_005272684.1:c.325+28034_325+28035insTATATATATATATATATT	XM_005272684.1:c.325+28034_325+28035insTATATATATATATATATATT	XM_005272684.1:c.325+28034_325+28035insTATATATATATATATATATATT	XM_005272684.1:c.325+28034_325+28035insTATATATATATATATATATATATT	XM_005272684.1:c.325+28034_325+28035insTATATATATATATATATATATATATT	XM_005272684.1:c.325+28034_325+28035insTAT	XM_005272684.1:c.325+28034_325+28035insTATAT	XM_005272684.1:c.325+28034_325+28035insTATATAT	XM_005272684.1:c.325+28034_325+28035insTATATATAT	XM_005272684.1:c.325+28034_325+28035insTATATATATAT	XM_005272684.1:c.325+28034_325+28035insTATATATATATAT	XM_005272684.1:c.325+28034_325+28035insTATATATATATATAT	XM_005272684.1:c.325+28034_325+28035insTATATATATATATATAT	XM_005272684.1:c.325+28034_325+28035insTATATATATATATATATAT	XM_005272684.1:c.325+28034_325+28035insTATATATATATATATATATAT	XM_005272684.1:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant X3	XM_011543990.3:c.325+28034=	XM_011543990.3:c.325+28034_325+28035insT	XM_011543990.3:c.325+28034_325+28035insTT	XM_011543990.3:c.325+28034_325+28035insTATT	XM_011543990.3:c.325+28034_325+28035insTATATT	XM_011543990.3:c.325+28034_325+28035insTATATATT	XM_011543990.3:c.325+28034_325+28035insTATATATATT	XM_011543990.3:c.325+28034_325+28035insTATATATATATT	XM_011543990.3:c.325+28034_325+28035insTATATATATATATT	XM_011543990.3:c.325+28034_325+28035insTATATATATATATATT	XM_011543990.3:c.325+28034_325+28035insTATATATATATATATATT	XM_011543990.3:c.325+28034_325+28035insTATATATATATATATATATT	XM_011543990.3:c.325+28034_325+28035insTATATATATATATATATATATT	XM_011543990.3:c.325+28034_325+28035insTATATATATATATATATATATATT	XM_011543990.3:c.325+28034_325+28035insTATATATATATATATATATATATATT	XM_011543990.3:c.325+28034_325+28035insTAT	XM_011543990.3:c.325+28034_325+28035insTATAT	XM_011543990.3:c.325+28034_325+28035insTATATAT	XM_011543990.3:c.325+28034_325+28035insTATATATAT	XM_011543990.3:c.325+28034_325+28035insTATATATATAT	XM_011543990.3:c.325+28034_325+28035insTATATATATATAT	XM_011543990.3:c.325+28034_325+28035insTATATATATATATAT	XM_011543990.3:c.325+28034_325+28035insTATATATATATATATAT	XM_011543990.3:c.325+28034_325+28035insTATATATATATATATATAT	XM_011543990.3:c.325+28034_325+28035insTATATATATATATATATATAT	XM_011543990.3:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant X4	XM_017029905.2:c.325+28034=	XM_017029905.2:c.325+28034_325+28035insT	XM_017029905.2:c.325+28034_325+28035insTT	XM_017029905.2:c.325+28034_325+28035insTATT	XM_017029905.2:c.325+28034_325+28035insTATATT	XM_017029905.2:c.325+28034_325+28035insTATATATT	XM_017029905.2:c.325+28034_325+28035insTATATATATT	XM_017029905.2:c.325+28034_325+28035insTATATATATATT	XM_017029905.2:c.325+28034_325+28035insTATATATATATATT	XM_017029905.2:c.325+28034_325+28035insTATATATATATATATT	XM_017029905.2:c.325+28034_325+28035insTATATATATATATATATT	XM_017029905.2:c.325+28034_325+28035insTATATATATATATATATATT	XM_017029905.2:c.325+28034_325+28035insTATATATATATATATATATATT	XM_017029905.2:c.325+28034_325+28035insTATATATATATATATATATATATT	XM_017029905.2:c.325+28034_325+28035insTATATATATATATATATATATATATT	XM_017029905.2:c.325+28034_325+28035insTAT	XM_017029905.2:c.325+28034_325+28035insTATAT	XM_017029905.2:c.325+28034_325+28035insTATATAT	XM_017029905.2:c.325+28034_325+28035insTATATATAT	XM_017029905.2:c.325+28034_325+28035insTATATATATAT	XM_017029905.2:c.325+28034_325+28035insTATATATATATAT	XM_017029905.2:c.325+28034_325+28035insTATATATATATATAT	XM_017029905.2:c.325+28034_325+28035insTATATATATATATATAT	XM_017029905.2:c.325+28034_325+28035insTATATATATATATATATAT	XM_017029905.2:c.325+28034_325+28035insTATATATATATATATATATAT	XM_017029905.2:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant X6	XM_017029906.3:c.325+28034=	XM_017029906.3:c.325+28034_325+28035insT	XM_017029906.3:c.325+28034_325+28035insTT	XM_017029906.3:c.325+28034_325+28035insTATT	XM_017029906.3:c.325+28034_325+28035insTATATT	XM_017029906.3:c.325+28034_325+28035insTATATATT	XM_017029906.3:c.325+28034_325+28035insTATATATATT	XM_017029906.3:c.325+28034_325+28035insTATATATATATT	XM_017029906.3:c.325+28034_325+28035insTATATATATATATT	XM_017029906.3:c.325+28034_325+28035insTATATATATATATATT	XM_017029906.3:c.325+28034_325+28035insTATATATATATATATATT	XM_017029906.3:c.325+28034_325+28035insTATATATATATATATATATT	XM_017029906.3:c.325+28034_325+28035insTATATATATATATATATATATT	XM_017029906.3:c.325+28034_325+28035insTATATATATATATATATATATATT	XM_017029906.3:c.325+28034_325+28035insTATATATATATATATATATATATATT	XM_017029906.3:c.325+28034_325+28035insTAT	XM_017029906.3:c.325+28034_325+28035insTATAT	XM_017029906.3:c.325+28034_325+28035insTATATAT	XM_017029906.3:c.325+28034_325+28035insTATATATAT	XM_017029906.3:c.325+28034_325+28035insTATATATATAT	XM_017029906.3:c.325+28034_325+28035insTATATATATATAT	XM_017029906.3:c.325+28034_325+28035insTATATATATATATAT	XM_017029906.3:c.325+28034_325+28035insTATATATATATATATAT	XM_017029906.3:c.325+28034_325+28035insTATATATATATATATATAT	XM_017029906.3:c.325+28034_325+28035insTATATATATATATATATATAT	XM_017029906.3:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant X7	XM_047442581.1:c.325+28034=	XM_047442581.1:c.325+28034_325+28035insT	XM_047442581.1:c.325+28034_325+28035insTT	XM_047442581.1:c.325+28034_325+28035insTATT	XM_047442581.1:c.325+28034_325+28035insTATATT	XM_047442581.1:c.325+28034_325+28035insTATATATT	XM_047442581.1:c.325+28034_325+28035insTATATATATT	XM_047442581.1:c.325+28034_325+28035insTATATATATATT	XM_047442581.1:c.325+28034_325+28035insTATATATATATATT	XM_047442581.1:c.325+28034_325+28035insTATATATATATATATT	XM_047442581.1:c.325+28034_325+28035insTATATATATATATATATT	XM_047442581.1:c.325+28034_325+28035insTATATATATATATATATATT	XM_047442581.1:c.325+28034_325+28035insTATATATATATATATATATATT	XM_047442581.1:c.325+28034_325+28035insTATATATATATATATATATATATT	XM_047442581.1:c.325+28034_325+28035insTATATATATATATATATATATATATT	XM_047442581.1:c.325+28034_325+28035insTAT	XM_047442581.1:c.325+28034_325+28035insTATAT	XM_047442581.1:c.325+28034_325+28035insTATATAT	XM_047442581.1:c.325+28034_325+28035insTATATATAT	XM_047442581.1:c.325+28034_325+28035insTATATATATAT	XM_047442581.1:c.325+28034_325+28035insTATATATATATAT	XM_047442581.1:c.325+28034_325+28035insTATATATATATATAT	XM_047442581.1:c.325+28034_325+28035insTATATATATATATATAT	XM_047442581.1:c.325+28034_325+28035insTATATATATATATATATAT	XM_047442581.1:c.325+28034_325+28035insTATATATATATATATATATAT	XM_047442581.1:c.325+28034_325+28035insTATATATATG
SLC9A7 transcript variant X8	XM_047442582.1:c.325+28034=	XM_047442582.1:c.325+28034_325+28035insT	XM_047442582.1:c.325+28034_325+28035insTT	XM_047442582.1:c.325+28034_325+28035insTATT	XM_047442582.1:c.325+28034_325+28035insTATATT	XM_047442582.1:c.325+28034_325+28035insTATATATT	XM_047442582.1:c.325+28034_325+28035insTATATATATT	XM_047442582.1:c.325+28034_325+28035insTATATATATATT	XM_047442582.1:c.325+28034_325+28035insTATATATATATATT	XM_047442582.1:c.325+28034_325+28035insTATATATATATATATT	XM_047442582.1:c.325+28034_325+28035insTATATATATATATATATT	XM_047442582.1:c.325+28034_325+28035insTATATATATATATATATATT	XM_047442582.1:c.325+28034_325+28035insTATATATATATATATATATATT	XM_047442582.1:c.325+28034_325+28035insTATATATATATATATATATATATT	XM_047442582.1:c.325+28034_325+28035insTATATATATATATATATATATATATT	XM_047442582.1:c.325+28034_325+28035insTAT	XM_047442582.1:c.325+28034_325+28035insTATAT	XM_047442582.1:c.325+28034_325+28035insTATATAT	XM_047442582.1:c.325+28034_325+28035insTATATATAT	XM_047442582.1:c.325+28034_325+28035insTATATATATAT	XM_047442582.1:c.325+28034_325+28035insTATATATATATAT	XM_047442582.1:c.325+28034_325+28035insTATATATATATATAT	XM_047442582.1:c.325+28034_325+28035insTATATATATATATATAT	XM_047442582.1:c.325+28034_325+28035insTATATATATATATATATAT	XM_047442582.1:c.325+28034_325+28035insTATATATATATATATATATAT	XM_047442582.1:c.325+28034_325+28035insTATATATATG

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

24 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GNOMAD	ss4370952881	Apr 26, 2021 (155)
2	GNOMAD	ss4370952882	Apr 26, 2021 (155)
3	GNOMAD	ss4370952883	Apr 26, 2021 (155)
4	GNOMAD	ss4370952884	Apr 26, 2021 (155)
5	GNOMAD	ss4370952885	Apr 26, 2021 (155)
6	GNOMAD	ss4370952886	Apr 26, 2021 (155)
7	GNOMAD	ss4370952887	Apr 26, 2021 (155)
8	GNOMAD	ss4370952888	Apr 26, 2021 (155)
9	GNOMAD	ss4370952889	Apr 26, 2021 (155)
10	GNOMAD	ss4370952890	Apr 26, 2021 (155)
11	GNOMAD	ss4370952891	Apr 26, 2021 (155)
12	GNOMAD	ss4370952892	Apr 26, 2021 (155)
13	GNOMAD	ss4370952893	Apr 26, 2021 (155)
14	GNOMAD	ss4370952894	Apr 26, 2021 (155)
15	GNOMAD	ss4370952895	Apr 26, 2021 (155)
16	GNOMAD	ss4370952896	Apr 26, 2021 (155)
17	GNOMAD	ss4370952897	Apr 26, 2021 (155)
18	GNOMAD	ss4370952898	Apr 26, 2021 (155)
19	GNOMAD	ss4370952899	Apr 26, 2021 (155)
20	GNOMAD	ss4370952900	Apr 26, 2021 (155)
21	GNOMAD	ss4370952901	Apr 26, 2021 (155)
22	GNOMAD	ss4370952902	Apr 26, 2021 (155)
23	GNOMAD	ss4370952903	Apr 26, 2021 (155)
24	GNOMAD	ss4370952904	Apr 26, 2021 (155)
25	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 579954550 (NC_000023.11:46730670::A 24/40433) Row 579954551 (NC_000023.11:46730670::AA 48/40435) Row 579954552 (NC_000023.11:46730670::AATA 3/40435)...	-	Apr 26, 2021 (155)
49	ALFA	NC_000023.11 - 46730671	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs1491295251

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
1649636977, ss4370952881	NC_000023.11:46730670::A	NC_000023.11:46730670::A	(self)
1649636977, ss4370952882	NC_000023.11:46730670::AA	NC_000023.11:46730670::AA	(self)
1649636977, ss4370952883	NC_000023.11:46730670::AATA	NC_000023.11:46730670::AATA	(self)
1649636977, ss4370952884	NC_000023.11:46730670::AATATA	NC_000023.11:46730670::AATATA	(self)
1649636977, ss4370952885	NC_000023.11:46730670::AATATATA	NC_000023.11:46730670::AATATATA	(self)
1649636977, ss4370952886	NC_000023.11:46730670::AATATATATA	NC_000023.11:46730670::AATATATATA	(self)
1649636977, ss4370952887	NC_000023.11:46730670::AATATATATATA	NC_000023.11:46730670::AATATATATATA	(self)
1649636977, ss4370952888	NC_000023.11:46730670::AATATATATAT… NC_000023.11:46730670::AATATATATATATA	NC_000023.11:46730670::AATATATATAT… NC_000023.11:46730670::AATATATATATATA	(self)
1649636977, ss4370952889	NC_000023.11:46730670::AATATATATAT… NC_000023.11:46730670::AATATATATATATATA	NC_000023.11:46730670::AATATATATAT… NC_000023.11:46730670::AATATATATATATATA	(self)
ss4370952890	NC_000023.11:46730670::AATATATATAT… NC_000023.11:46730670::AATATATATATATATATA	NC_000023.11:46730670::AATATATATAT… NC_000023.11:46730670::AATATATATATATATATA	(self)
ss4370952891	NC_000023.11:46730670::AATATATATAT… NC_000023.11:46730670::AATATATATATATATATATA	NC_000023.11:46730670::AATATATATAT… NC_000023.11:46730670::AATATATATATATATATATA	(self)
ss4370952892	NC_000023.11:46730670::AATATATATAT… NC_000023.11:46730670::AATATATATATATATATATATA	NC_000023.11:46730670::AATATATATAT… NC_000023.11:46730670::AATATATATATATATATATATA	(self)
ss4370952893	NC_000023.11:46730670::AATATATATAT… NC_000023.11:46730670::AATATATATATATATATATATATA	NC_000023.11:46730670::AATATATATAT… NC_000023.11:46730670::AATATATATATATATATATATATA	(self)
ss4370952894	NC_000023.11:46730670::AATATATATAT… NC_000023.11:46730670::AATATATATATATATATATATATATA	NC_000023.11:46730670::AATATATATAT… NC_000023.11:46730670::AATATATATATATATATATATATATA	(self)
1649636977, ss4370952895	NC_000023.11:46730670::ATA	NC_000023.11:46730670::ATA	(self)
1649636977, ss4370952896	NC_000023.11:46730670::ATATA	NC_000023.11:46730670::ATATA	(self)
1649636977, ss4370952897	NC_000023.11:46730670::ATATATA	NC_000023.11:46730670::ATATATA	(self)
1649636977, ss4370952898	NC_000023.11:46730670::ATATATATA	NC_000023.11:46730670::ATATATATA	(self)
ss4370952899	NC_000023.11:46730670::ATATATATATA	NC_000023.11:46730670::ATATATATATA	(self)
1649636977, ss4370952900	NC_000023.11:46730670::ATATATATATA… NC_000023.11:46730670::ATATATATATATA	NC_000023.11:46730670::ATATATATATA… NC_000023.11:46730670::ATATATATATATA	(self)
ss4370952901	NC_000023.11:46730670::ATATATATATA… NC_000023.11:46730670::ATATATATATATATA	NC_000023.11:46730670::ATATATATATA… NC_000023.11:46730670::ATATATATATATATA	(self)
ss4370952902	NC_000023.11:46730670::ATATATATATA… NC_000023.11:46730670::ATATATATATATATATA	NC_000023.11:46730670::ATATATATATA… NC_000023.11:46730670::ATATATATATATATATA	(self)
ss4370952903	NC_000023.11:46730670::ATATATATATA… NC_000023.11:46730670::ATATATATATATATATATA	NC_000023.11:46730670::ATATATATATA… NC_000023.11:46730670::ATATATATATATATATATA	(self)
ss4370952904	NC_000023.11:46730670::ATATATATATA… NC_000023.11:46730670::ATATATATATATATATATATA	NC_000023.11:46730670::ATATATATATA… NC_000023.11:46730670::ATATATATATATATATATATA	(self)
1649636977	NC_000023.11:46730670::CATATATATA	NC_000023.11:46730670::CATATATATA	(self)

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1491295251