Name: rs149124193
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.

rs149124193

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:63385107-63385127 (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: del(T)₁₀ / del(T)₉ / del(T)₈ / del…
del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₉ / dup(T)₂₀ / ins(T)₂₇A(T)₂₉ / ins(T)₄₀
Variation Type: Indel Insertion and Deletion
Frequency: dupTTT=0.2992 (1687/5638, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC22A9 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	5638	(T)₂₁=0.5302	del(T)₉=0.0369, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0669, dupT=0.0137, dupTT=0.0000, dupTTT=0.2992, dup(T)₄=0.0475, dup(T)₅=0.0000, dup(T)₆=0.0057
Allele Frequency Aggregator	European	Sub	5092	(T)₂₁=0.4806	del(T)₉=0.0408, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0734, dupT=0.0151, dupTT=0.0000, dupTTT=0.3311, dup(T)₄=0.0526, dup(T)₅=0.0000, dup(T)₆=0.0063
Allele Frequency Aggregator	African	Sub	438	(T)₂₁=1.000	del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Other	Sub	62	(T)₂₁=0.94	del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.05, dupT=0.00, dupTT=0.00, dupTTT=0.02, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	16	(T)₂₁=1.00	del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Asian	Sub	14	(T)₂₁=1.00	del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Latin American 2	Sub	12	(T)₂₁=1.00	del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	4	(T)₂₁=1.0	del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0

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 11	NC_000011.10:g.63385118_63385127del
GRCh38.p14 chr 11	NC_000011.10:g.63385119_63385127del
GRCh38.p14 chr 11	NC_000011.10:g.63385120_63385127del
GRCh38.p14 chr 11	NC_000011.10:g.63385121_63385127del
GRCh38.p14 chr 11	NC_000011.10:g.63385123_63385127del
GRCh38.p14 chr 11	NC_000011.10:g.63385124_63385127del
GRCh38.p14 chr 11	NC_000011.10:g.63385125_63385127del
GRCh38.p14 chr 11	NC_000011.10:g.63385126_63385127del
GRCh38.p14 chr 11	NC_000011.10:g.63385127del
GRCh38.p14 chr 11	NC_000011.10:g.63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385126_63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385125_63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385124_63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385123_63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385122_63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385121_63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385120_63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385119_63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385118_63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385117_63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385116_63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385115_63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385109_63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385108_63385127dup
GRCh38.p14 chr 11	NC_000011.10:g.63385107_63385127T[48]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 11	NC_000011.10:g.63385127_63385128insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 11	NC_000011.9:g.63152590_63152599del
GRCh37.p13 chr 11	NC_000011.9:g.63152591_63152599del
GRCh37.p13 chr 11	NC_000011.9:g.63152592_63152599del
GRCh37.p13 chr 11	NC_000011.9:g.63152593_63152599del
GRCh37.p13 chr 11	NC_000011.9:g.63152595_63152599del
GRCh37.p13 chr 11	NC_000011.9:g.63152596_63152599del
GRCh37.p13 chr 11	NC_000011.9:g.63152597_63152599del
GRCh37.p13 chr 11	NC_000011.9:g.63152598_63152599del
GRCh37.p13 chr 11	NC_000011.9:g.63152599del
GRCh37.p13 chr 11	NC_000011.9:g.63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152598_63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152597_63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152596_63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152595_63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152594_63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152593_63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152592_63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152591_63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152590_63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152589_63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152588_63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152587_63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152581_63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152580_63152599dup
GRCh37.p13 chr 11	NC_000011.9:g.63152579_63152599T[48]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 11	NC_000011.9:g.63152599_63152600insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: SLC22A9, solute carrier family 22 member 9 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC22A9 transcript	NM_080866.3:c.1073+2841_1… NM_080866.3:c.1073+2841_1073+2850del	N/A	Intron Variant
SLC22A9 transcript variant X1	XM_017017159.3:c.1073+284… XM_017017159.3:c.1073+2841_1073+2850del	N/A	Intron Variant
SLC22A9 transcript variant X2	XM_047426335.1:c.380+2841… XM_047426335.1:c.380+2841_380+2850del	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	(T)₂₁=	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₉	dup(T)₂₀	ins(T)₂₇A(T)₂₉	ins(T)₄₀
GRCh38.p14 chr 11	NC_000011.10:g.63385107_63385127=	NC_000011.10:g.63385118_63385127del	NC_000011.10:g.63385119_63385127del	NC_000011.10:g.63385120_63385127del	NC_000011.10:g.63385121_63385127del	NC_000011.10:g.63385123_63385127del	NC_000011.10:g.63385124_63385127del	NC_000011.10:g.63385125_63385127del	NC_000011.10:g.63385126_63385127del	NC_000011.10:g.63385127del	NC_000011.10:g.63385127dup	NC_000011.10:g.63385126_63385127dup	NC_000011.10:g.63385125_63385127dup	NC_000011.10:g.63385124_63385127dup	NC_000011.10:g.63385123_63385127dup	NC_000011.10:g.63385122_63385127dup	NC_000011.10:g.63385121_63385127dup	NC_000011.10:g.63385120_63385127dup	NC_000011.10:g.63385119_63385127dup	NC_000011.10:g.63385118_63385127dup	NC_000011.10:g.63385117_63385127dup	NC_000011.10:g.63385116_63385127dup	NC_000011.10:g.63385115_63385127dup	NC_000011.10:g.63385109_63385127dup	NC_000011.10:g.63385108_63385127dup	NC_000011.10:g.63385107_63385127T[48]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000011.10:g.63385127_63385128insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 11	NC_000011.9:g.63152579_63152599=	NC_000011.9:g.63152590_63152599del	NC_000011.9:g.63152591_63152599del	NC_000011.9:g.63152592_63152599del	NC_000011.9:g.63152593_63152599del	NC_000011.9:g.63152595_63152599del	NC_000011.9:g.63152596_63152599del	NC_000011.9:g.63152597_63152599del	NC_000011.9:g.63152598_63152599del	NC_000011.9:g.63152599del	NC_000011.9:g.63152599dup	NC_000011.9:g.63152598_63152599dup	NC_000011.9:g.63152597_63152599dup	NC_000011.9:g.63152596_63152599dup	NC_000011.9:g.63152595_63152599dup	NC_000011.9:g.63152594_63152599dup	NC_000011.9:g.63152593_63152599dup	NC_000011.9:g.63152592_63152599dup	NC_000011.9:g.63152591_63152599dup	NC_000011.9:g.63152590_63152599dup	NC_000011.9:g.63152589_63152599dup	NC_000011.9:g.63152588_63152599dup	NC_000011.9:g.63152587_63152599dup	NC_000011.9:g.63152581_63152599dup	NC_000011.9:g.63152580_63152599dup	NC_000011.9:g.63152579_63152599T[48]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000011.9:g.63152599_63152600insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC22A9 transcript	NM_080866.2:c.1073+2830=	NM_080866.2:c.1073+2841_1073+2850del	NM_080866.2:c.1073+2842_1073+2850del	NM_080866.2:c.1073+2843_1073+2850del	NM_080866.2:c.1073+2844_1073+2850del	NM_080866.2:c.1073+2846_1073+2850del	NM_080866.2:c.1073+2847_1073+2850del	NM_080866.2:c.1073+2848_1073+2850del	NM_080866.2:c.1073+2849_1073+2850del	NM_080866.2:c.1073+2850del	NM_080866.2:c.1073+2850dup	NM_080866.2:c.1073+2849_1073+2850dup	NM_080866.2:c.1073+2848_1073+2850dup	NM_080866.2:c.1073+2847_1073+2850dup	NM_080866.2:c.1073+2846_1073+2850dup	NM_080866.2:c.1073+2845_1073+2850dup	NM_080866.2:c.1073+2844_1073+2850dup	NM_080866.2:c.1073+2843_1073+2850dup	NM_080866.2:c.1073+2842_1073+2850dup	NM_080866.2:c.1073+2841_1073+2850dup	NM_080866.2:c.1073+2840_1073+2850dup	NM_080866.2:c.1073+2839_1073+2850dup	NM_080866.2:c.1073+2838_1073+2850dup	NM_080866.2:c.1073+2832_1073+2850dup	NM_080866.2:c.1073+2831_1073+2850dup	NM_080866.2:c.1073+2850_1073+2851insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_080866.2:c.1073+2850_1073+2851insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC22A9 transcript	NM_080866.3:c.1073+2830=	NM_080866.3:c.1073+2841_1073+2850del	NM_080866.3:c.1073+2842_1073+2850del	NM_080866.3:c.1073+2843_1073+2850del	NM_080866.3:c.1073+2844_1073+2850del	NM_080866.3:c.1073+2846_1073+2850del	NM_080866.3:c.1073+2847_1073+2850del	NM_080866.3:c.1073+2848_1073+2850del	NM_080866.3:c.1073+2849_1073+2850del	NM_080866.3:c.1073+2850del	NM_080866.3:c.1073+2850dup	NM_080866.3:c.1073+2849_1073+2850dup	NM_080866.3:c.1073+2848_1073+2850dup	NM_080866.3:c.1073+2847_1073+2850dup	NM_080866.3:c.1073+2846_1073+2850dup	NM_080866.3:c.1073+2845_1073+2850dup	NM_080866.3:c.1073+2844_1073+2850dup	NM_080866.3:c.1073+2843_1073+2850dup	NM_080866.3:c.1073+2842_1073+2850dup	NM_080866.3:c.1073+2841_1073+2850dup	NM_080866.3:c.1073+2840_1073+2850dup	NM_080866.3:c.1073+2839_1073+2850dup	NM_080866.3:c.1073+2838_1073+2850dup	NM_080866.3:c.1073+2832_1073+2850dup	NM_080866.3:c.1073+2831_1073+2850dup	NM_080866.3:c.1073+2850_1073+2851insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_080866.3:c.1073+2850_1073+2851insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC22A9 transcript variant X1	XM_005273736.1:c.1073+2830=	XM_005273736.1:c.1073+2841_1073+2850del	XM_005273736.1:c.1073+2842_1073+2850del	XM_005273736.1:c.1073+2843_1073+2850del	XM_005273736.1:c.1073+2844_1073+2850del	XM_005273736.1:c.1073+2846_1073+2850del	XM_005273736.1:c.1073+2847_1073+2850del	XM_005273736.1:c.1073+2848_1073+2850del	XM_005273736.1:c.1073+2849_1073+2850del	XM_005273736.1:c.1073+2850del	XM_005273736.1:c.1073+2850dup	XM_005273736.1:c.1073+2849_1073+2850dup	XM_005273736.1:c.1073+2848_1073+2850dup	XM_005273736.1:c.1073+2847_1073+2850dup	XM_005273736.1:c.1073+2846_1073+2850dup	XM_005273736.1:c.1073+2845_1073+2850dup	XM_005273736.1:c.1073+2844_1073+2850dup	XM_005273736.1:c.1073+2843_1073+2850dup	XM_005273736.1:c.1073+2842_1073+2850dup	XM_005273736.1:c.1073+2841_1073+2850dup	XM_005273736.1:c.1073+2840_1073+2850dup	XM_005273736.1:c.1073+2839_1073+2850dup	XM_005273736.1:c.1073+2838_1073+2850dup	XM_005273736.1:c.1073+2832_1073+2850dup	XM_005273736.1:c.1073+2831_1073+2850dup	XM_005273736.1:c.1073+2850_1073+2851insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005273736.1:c.1073+2850_1073+2851insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC22A9 transcript variant X1	XM_017017159.3:c.1073+2830=	XM_017017159.3:c.1073+2841_1073+2850del	XM_017017159.3:c.1073+2842_1073+2850del	XM_017017159.3:c.1073+2843_1073+2850del	XM_017017159.3:c.1073+2844_1073+2850del	XM_017017159.3:c.1073+2846_1073+2850del	XM_017017159.3:c.1073+2847_1073+2850del	XM_017017159.3:c.1073+2848_1073+2850del	XM_017017159.3:c.1073+2849_1073+2850del	XM_017017159.3:c.1073+2850del	XM_017017159.3:c.1073+2850dup	XM_017017159.3:c.1073+2849_1073+2850dup	XM_017017159.3:c.1073+2848_1073+2850dup	XM_017017159.3:c.1073+2847_1073+2850dup	XM_017017159.3:c.1073+2846_1073+2850dup	XM_017017159.3:c.1073+2845_1073+2850dup	XM_017017159.3:c.1073+2844_1073+2850dup	XM_017017159.3:c.1073+2843_1073+2850dup	XM_017017159.3:c.1073+2842_1073+2850dup	XM_017017159.3:c.1073+2841_1073+2850dup	XM_017017159.3:c.1073+2840_1073+2850dup	XM_017017159.3:c.1073+2839_1073+2850dup	XM_017017159.3:c.1073+2838_1073+2850dup	XM_017017159.3:c.1073+2832_1073+2850dup	XM_017017159.3:c.1073+2831_1073+2850dup	XM_017017159.3:c.1073+2850_1073+2851insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_017017159.3:c.1073+2850_1073+2851insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC22A9 transcript variant X2	XM_047426335.1:c.380+2830=	XM_047426335.1:c.380+2841_380+2850del	XM_047426335.1:c.380+2842_380+2850del	XM_047426335.1:c.380+2843_380+2850del	XM_047426335.1:c.380+2844_380+2850del	XM_047426335.1:c.380+2846_380+2850del	XM_047426335.1:c.380+2847_380+2850del	XM_047426335.1:c.380+2848_380+2850del	XM_047426335.1:c.380+2849_380+2850del	XM_047426335.1:c.380+2850del	XM_047426335.1:c.380+2850dup	XM_047426335.1:c.380+2849_380+2850dup	XM_047426335.1:c.380+2848_380+2850dup	XM_047426335.1:c.380+2847_380+2850dup	XM_047426335.1:c.380+2846_380+2850dup	XM_047426335.1:c.380+2845_380+2850dup	XM_047426335.1:c.380+2844_380+2850dup	XM_047426335.1:c.380+2843_380+2850dup	XM_047426335.1:c.380+2842_380+2850dup	XM_047426335.1:c.380+2841_380+2850dup	XM_047426335.1:c.380+2840_380+2850dup	XM_047426335.1:c.380+2839_380+2850dup	XM_047426335.1:c.380+2838_380+2850dup	XM_047426335.1:c.380+2832_380+2850dup	XM_047426335.1:c.380+2831_380+2850dup	XM_047426335.1:c.380+2850_380+2851insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047426335.1:c.380+2850_380+2851insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

71 SubSNP, 45 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss82815809	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss95570585	Apr 25, 2013 (138)
3	PJP	ss294706504	May 31, 2013 (142)
4	PJP	ss294706505	May 31, 2013 (138)
5	PJP	ss294706506	May 09, 2011 (134)
6	SSMP	ss664062612	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1707129297	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1707129395	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1710517182	Oct 12, 2018 (152)
10	EVA_UK10K_TWINSUK	ss1710517184	Oct 12, 2018 (152)
11	EVA_UK10K_ALSPAC	ss1710517194	Oct 12, 2018 (152)
12	EVA_UK10K_ALSPAC	ss1710517196	Oct 12, 2018 (152)
13	SWEGEN	ss3008216843	Nov 08, 2017 (151)
14	EVA_DECODE	ss3691929177	Jul 13, 2019 (153)
15	EVA_DECODE	ss3691929178	Jul 13, 2019 (153)
16	EVA_DECODE	ss3691929179	Jul 13, 2019 (153)
17	EVA_DECODE	ss3691929180	Jul 13, 2019 (153)
18	EVA_DECODE	ss3691929181	Jul 13, 2019 (153)
19	EVA_DECODE	ss3691929182	Jul 13, 2019 (153)
20	PACBIO	ss3792111925	Jul 13, 2019 (153)
21	PACBIO	ss3792111926	Jul 13, 2019 (153)
22	PACBIO	ss3796994269	Jul 13, 2019 (153)
23	PACBIO	ss3796994270	Jul 13, 2019 (153)
24	EVA	ss3832665995	Apr 26, 2020 (154)
25	GNOMAD	ss4236356113	Apr 26, 2021 (155)
26	GNOMAD	ss4236356114	Apr 26, 2021 (155)
27	GNOMAD	ss4236356115	Apr 26, 2021 (155)
28	GNOMAD	ss4236356116	Apr 26, 2021 (155)
29	GNOMAD	ss4236356129	Apr 26, 2021 (155)
30	GNOMAD	ss4236356130	Apr 26, 2021 (155)
31	GNOMAD	ss4236356131	Apr 26, 2021 (155)
32	GNOMAD	ss4236356132	Apr 26, 2021 (155)
33	GNOMAD	ss4236356133	Apr 26, 2021 (155)
34	GNOMAD	ss4236356134	Apr 26, 2021 (155)
35	GNOMAD	ss4236356135	Apr 26, 2021 (155)
36	GNOMAD	ss4236356136	Apr 26, 2021 (155)
37	GNOMAD	ss4236356137	Apr 26, 2021 (155)
38	GNOMAD	ss4236356138	Apr 26, 2021 (155)
39	GNOMAD	ss4236356139	Apr 26, 2021 (155)
40	GNOMAD	ss4236356140	Apr 26, 2021 (155)
41	GNOMAD	ss4236356142	Apr 26, 2021 (155)
42	GNOMAD	ss4236356143	Apr 26, 2021 (155)
43	GNOMAD	ss4236356144	Apr 26, 2021 (155)
44	GNOMAD	ss4236356145	Apr 26, 2021 (155)
45	GNOMAD	ss4236356146	Apr 26, 2021 (155)
46	GNOMAD	ss4236356147	Apr 26, 2021 (155)
47	GNOMAD	ss4236356148	Apr 26, 2021 (155)
48	GNOMAD	ss4236356149	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5202313891	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5202313892	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5202313893	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5202313894	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5202313895	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5202313896	Apr 26, 2021 (155)
55	1000G_HIGH_COVERAGE	ss5287677846	Oct 13, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5287677847	Oct 13, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5287677848	Oct 13, 2022 (156)
58	HUGCELL_USP	ss5482826885	Oct 13, 2022 (156)
59	HUGCELL_USP	ss5482826886	Oct 13, 2022 (156)
60	HUGCELL_USP	ss5482826887	Oct 13, 2022 (156)
61	HUGCELL_USP	ss5482826888	Oct 13, 2022 (156)
62	HUGCELL_USP	ss5482826889	Oct 13, 2022 (156)
63	TOMMO_GENOMICS	ss5750291380	Oct 13, 2022 (156)
64	TOMMO_GENOMICS	ss5750291381	Oct 13, 2022 (156)
65	TOMMO_GENOMICS	ss5750291382	Oct 13, 2022 (156)
66	TOMMO_GENOMICS	ss5750291383	Oct 13, 2022 (156)
67	TOMMO_GENOMICS	ss5750291384	Oct 13, 2022 (156)
68	TOMMO_GENOMICS	ss5750291385	Oct 13, 2022 (156)
69	EVA	ss5836761681	Oct 13, 2022 (156)
70	EVA	ss5836761682	Oct 13, 2022 (156)
71	EVA	ss5836761683	Oct 13, 2022 (156)
72	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 30043295 (NC_000011.9:63152578::TTT 1786/3854) Row 30043296 (NC_000011.9:63152578:TTTTTTTTT: 340/3854) Row 30043297 (NC_000011.9:63152578::TT 1614/3854)	-	Oct 12, 2018 (152)
73	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 30043295 (NC_000011.9:63152578::TTT 1786/3854) Row 30043296 (NC_000011.9:63152578:TTTTTTTTT: 340/3854) Row 30043297 (NC_000011.9:63152578::TT 1614/3854)	-	Oct 12, 2018 (152)
74	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 30043295 (NC_000011.9:63152578::TTT 1786/3854) Row 30043296 (NC_000011.9:63152578:TTTTTTTTT: 340/3854) Row 30043297 (NC_000011.9:63152578::TT 1614/3854)	-	Oct 12, 2018 (152)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 381876339 (NC_000011.10:63385106::T 2890/71880) Row 381876340 (NC_000011.10:63385106::TT 2168/71948) Row 381876341 (NC_000011.10:63385106::TTT 27214/71192)...	-	Apr 26, 2021 (155)
101	8.3KJPN Submission ignored due to conflicting rows: Row 60283198 (NC_000011.9:63152578:T: 5571/16322) Row 60283199 (NC_000011.9:63152578::TTT 3974/16322) Row 60283200 (NC_000011.9:63152578::TT 28/16322)...	-	Apr 26, 2021 (155)
102	8.3KJPN Submission ignored due to conflicting rows: Row 60283198 (NC_000011.9:63152578:T: 5571/16322) Row 60283199 (NC_000011.9:63152578::TTT 3974/16322) Row 60283200 (NC_000011.9:63152578::TT 28/16322)...	-	Apr 26, 2021 (155)
103	8.3KJPN Submission ignored due to conflicting rows: Row 60283198 (NC_000011.9:63152578:T: 5571/16322) Row 60283199 (NC_000011.9:63152578::TTT 3974/16322) Row 60283200 (NC_000011.9:63152578::TT 28/16322)...	-	Apr 26, 2021 (155)
104	8.3KJPN Submission ignored due to conflicting rows: Row 60283198 (NC_000011.9:63152578:T: 5571/16322) Row 60283199 (NC_000011.9:63152578::TTT 3974/16322) Row 60283200 (NC_000011.9:63152578::TT 28/16322)...	-	Apr 26, 2021 (155)
105	8.3KJPN Submission ignored due to conflicting rows: Row 60283198 (NC_000011.9:63152578:T: 5571/16322) Row 60283199 (NC_000011.9:63152578::TTT 3974/16322) Row 60283200 (NC_000011.9:63152578::TT 28/16322)...	-	Apr 26, 2021 (155)
106	8.3KJPN Submission ignored due to conflicting rows: Row 60283198 (NC_000011.9:63152578:T: 5571/16322) Row 60283199 (NC_000011.9:63152578::TTT 3974/16322) Row 60283200 (NC_000011.9:63152578::TT 28/16322)...	-	Apr 26, 2021 (155)
107	14KJPN Submission ignored due to conflicting rows: Row 84128484 (NC_000011.10:63385106::TTT 5617/26834) Row 84128485 (NC_000011.10:63385106:T: 9701/26834) Row 84128486 (NC_000011.10:63385106::TTTT 1629/26834)...	-	Oct 13, 2022 (156)
108	14KJPN Submission ignored due to conflicting rows: Row 84128484 (NC_000011.10:63385106::TTT 5617/26834) Row 84128485 (NC_000011.10:63385106:T: 9701/26834) Row 84128486 (NC_000011.10:63385106::TTTT 1629/26834)...	-	Oct 13, 2022 (156)
109	14KJPN Submission ignored due to conflicting rows: Row 84128484 (NC_000011.10:63385106::TTT 5617/26834) Row 84128485 (NC_000011.10:63385106:T: 9701/26834) Row 84128486 (NC_000011.10:63385106::TTTT 1629/26834)...	-	Oct 13, 2022 (156)
110	14KJPN Submission ignored due to conflicting rows: Row 84128484 (NC_000011.10:63385106::TTT 5617/26834) Row 84128485 (NC_000011.10:63385106:T: 9701/26834) Row 84128486 (NC_000011.10:63385106::TTTT 1629/26834)...	-	Oct 13, 2022 (156)
111	14KJPN Submission ignored due to conflicting rows: Row 84128484 (NC_000011.10:63385106::TTT 5617/26834) Row 84128485 (NC_000011.10:63385106:T: 9701/26834) Row 84128486 (NC_000011.10:63385106::TTTT 1629/26834)...	-	Oct 13, 2022 (156)
112	14KJPN Submission ignored due to conflicting rows: Row 84128484 (NC_000011.10:63385106::TTT 5617/26834) Row 84128485 (NC_000011.10:63385106:T: 9701/26834) Row 84128486 (NC_000011.10:63385106::TTTT 1629/26834)...	-	Oct 13, 2022 (156)
113	UK 10K study - Twins Submission ignored due to conflicting rows: Row 30043295 (NC_000011.9:63152578::TTT 1723/3708) Row 30043296 (NC_000011.9:63152578:TTTTTTTTT: 288/3708) Row 30043297 (NC_000011.9:63152578::TT 1571/3708)	-	Oct 12, 2018 (152)
114	UK 10K study - Twins Submission ignored due to conflicting rows: Row 30043295 (NC_000011.9:63152578::TTT 1723/3708) Row 30043296 (NC_000011.9:63152578:TTTTTTTTT: 288/3708) Row 30043297 (NC_000011.9:63152578::TT 1571/3708)	-	Oct 12, 2018 (152)
115	UK 10K study - Twins Submission ignored due to conflicting rows: Row 30043295 (NC_000011.9:63152578::TTT 1723/3708) Row 30043296 (NC_000011.9:63152578:TTTTTTTTT: 288/3708) Row 30043297 (NC_000011.9:63152578::TT 1571/3708)	-	Oct 12, 2018 (152)
116	ALFA	NC_000011.10 - 63385107	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).

Associated ID	History Updated (Build)
rs386373968	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4236356149	NC_000011.10:63385106:TTTTTTTTTT:	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss1707129297, ss1707129395, ss3008216843, ss5836761683	NC_000011.9:63152578:TTTTTTTTT:	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3691929177, ss4236356148, ss5482826889	NC_000011.10:63385106:TTTTTTTTT:	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
1046102433	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4236356147	NC_000011.10:63385106:TTTTTTTT:	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
1046102433	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4236356146	NC_000011.10:63385106:TTTTTTT:	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
1046102433	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4236356145	NC_000011.10:63385106:TTTTT:	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
1046102433	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4236356144	NC_000011.10:63385106:TTTT:	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
1046102433	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4236356143	NC_000011.10:63385106:TTT:	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
1046102433	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4236356142	NC_000011.10:63385106:TT:	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
1046102433	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss294706506	NC_000011.8:62909174:T:	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5202313891	NC_000011.9:63152578:T:	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5287677846, ss5482826888, ss5750291381	NC_000011.10:63385106:T:	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
1046102433	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3691929178	NC_000011.10:63385114:T:	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5202313895	NC_000011.9:63152578::T	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356113, ss5482826885, ss5750291383	NC_000011.10:63385106::T	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
1046102433	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3691929179	NC_000011.10:63385115::T	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3792111925, ss3796994269, ss5202313893	NC_000011.9:63152578::TT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1710517184, ss1710517196	NC_000011.9:63152587::TT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356114, ss5287677848, ss5750291384	NC_000011.10:63385106::TT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
1046102433	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3691929180	NC_000011.10:63385115::TT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss82815809	NT_167190.1:8458394::TT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294706504	NC_000011.8:62909155::TTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294706505	NC_000011.8:62909173::TTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss664062612, ss3792111926, ss3796994270, ss5202313892, ss5836761681	NC_000011.9:63152578::TTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1710517182, ss1710517194	NC_000011.9:63152587::TTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356115, ss5482826886, ss5750291380	NC_000011.10:63385106::TTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
1046102433	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3691929181	NC_000011.10:63385115::TTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95570585	NT_167190.1:8458393::TTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5202313894, ss5836761682	NC_000011.9:63152578::TTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356116, ss5287677847, ss5482826887, ss5750291382	NC_000011.10:63385106::TTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1046102433	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3691929182	NC_000011.10:63385115::TTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3832665995, ss5202313896	NC_000011.9:63152578::TTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356129, ss5750291385	NC_000011.10:63385106::TTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1046102433	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356130	NC_000011.10:63385106::TTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1046102433	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356131	NC_000011.10:63385106::TTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356132	NC_000011.10:63385106::TTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356133	NC_000011.10:63385106::TTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356134	NC_000011.10:63385106::TTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356135	NC_000011.10:63385106::TTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356136	NC_000011.10:63385106::TTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356137	NC_000011.10:63385106::TTTTTTTTTTT… NC_000011.10:63385106::TTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356138	NC_000011.10:63385106::TTTTTTTTTTT… NC_000011.10:63385106::TTTTTTTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356139	NC_000011.10:63385106::TTTTTTTTTTT… NC_000011.10:63385106::TTTTTTTTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000011.10:63385106::TTTTTTTTTTT… NC_000011.10:63385106::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4236356140	NC_000011.10:63385106::TTTTTTTTTTT… NC_000011.10:63385106::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:63385106:TTTTTTTTTTTT… NC_000011.10:63385106:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs149124193

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
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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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs149124193