Name: rs59107049
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.

rs59107049

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:34069908-34069925 (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(A)₁₀ / del(A)₈ / del(A)₆ / del…
del(A)₁₀ / del(A)₈ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / ins(A)₂₇
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₈=0.4868 (2438/5008, 1000G)
(A)₁₈=0.271 (141/520, NorthernSweden)
del(A)₁₀=0.000 (0/194, ALFA) (+ 10 more)
del(A)₈=0.000 (0/194, ALFA)
del(A)₆=0.000 (0/194, ALFA)
del(A)₅=0.000 (0/194, ALFA)
del(A)₄=0.000 (0/194, ALFA)
delAAA=0.000 (0/194, ALFA)
delAA=0.000 (0/194, ALFA)
delA=0.000 (0/194, ALFA)
dupA=0.000 (0/194, ALFA)
dupAA=0.000 (0/194, ALFA)
dupAAA=0.000 (0/194, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CAPRIN1 : 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	Alt HMOZ	HTRZ	HWEP
Total	Global	194	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	68	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African	Sub	114	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	6	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	108	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	4	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	8	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(A)₁₈=0.4868	delAA=0.5132
1000Genomes	African	Sub	1322	(A)₁₈=0.5756	delAA=0.4244
1000Genomes	East Asian	Sub	1008	(A)₁₈=0.3958	delAA=0.6042
1000Genomes	Europe	Sub	1006	(A)₁₈=0.4871	delAA=0.5129
1000Genomes	South Asian	Sub	978	(A)₁₈=0.487	delAA=0.513
1000Genomes	American	Sub	694	(A)₁₈=0.450	delAA=0.550
Northern Sweden	ACPOP	Study-wide	520	(A)₁₈=0.271	delAA=0.729
Allele Frequency Aggregator	Total	Global	194	(A)₁₈=1.000	del(A)₁₀=0.000, del(A)₈=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	African	Sub	114	(A)₁₈=1.000	del(A)₁₀=0.000, del(A)₈=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	European	Sub	68	(A)₁₈=1.00	del(A)₁₀=0.00, del(A)₈=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Other	Sub	8	(A)₁₈=1.0	del(A)₁₀=0.0, del(A)₈=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0
Allele Frequency Aggregator	Latin American 1	Sub	4	(A)₁₈=1.0	del(A)₁₀=0.0, del(A)₈=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0
Allele Frequency Aggregator	Latin American 2	Sub	0	(A)₁₈=0	del(A)₁₀=0, del(A)₈=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₁₈=0	del(A)₁₀=0, del(A)₈=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0
Allele Frequency Aggregator	Asian	Sub	0	(A)₁₈=0	del(A)₁₀=0, del(A)₈=0, del(A)₆=0, del(A)₅=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=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.34069916_34069925del
GRCh38.p14 chr 11	NC_000011.10:g.34069918_34069925del
GRCh38.p14 chr 11	NC_000011.10:g.34069920_34069925del
GRCh38.p14 chr 11	NC_000011.10:g.34069921_34069925del
GRCh38.p14 chr 11	NC_000011.10:g.34069922_34069925del
GRCh38.p14 chr 11	NC_000011.10:g.34069923_34069925del
GRCh38.p14 chr 11	NC_000011.10:g.34069924_34069925del
GRCh38.p14 chr 11	NC_000011.10:g.34069925del
GRCh38.p14 chr 11	NC_000011.10:g.34069925dup
GRCh38.p14 chr 11	NC_000011.10:g.34069924_34069925dup
GRCh38.p14 chr 11	NC_000011.10:g.34069923_34069925dup
GRCh38.p14 chr 11	NC_000011.10:g.34069922_34069925dup
GRCh38.p14 chr 11	NC_000011.10:g.34069925_34069926insAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 11	NC_000011.9:g.34091463_34091472del
GRCh37.p13 chr 11	NC_000011.9:g.34091465_34091472del
GRCh37.p13 chr 11	NC_000011.9:g.34091467_34091472del
GRCh37.p13 chr 11	NC_000011.9:g.34091468_34091472del
GRCh37.p13 chr 11	NC_000011.9:g.34091469_34091472del
GRCh37.p13 chr 11	NC_000011.9:g.34091470_34091472del
GRCh37.p13 chr 11	NC_000011.9:g.34091471_34091472del
GRCh37.p13 chr 11	NC_000011.9:g.34091472del
GRCh37.p13 chr 11	NC_000011.9:g.34091472dup
GRCh37.p13 chr 11	NC_000011.9:g.34091471_34091472dup
GRCh37.p13 chr 11	NC_000011.9:g.34091470_34091472dup
GRCh37.p13 chr 11	NC_000011.9:g.34091469_34091472dup
GRCh37.p13 chr 11	NC_000011.9:g.34091472_34091473insAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: CAPRIN1, cell cycle associated protein 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CAPRIN1 transcript variant 1	NM_005898.5:c.217-1810_21… NM_005898.5:c.217-1810_217-1801del	N/A	Intron Variant
CAPRIN1 transcript variant 2	NM_203364.3:c.217-1810_21… NM_203364.3:c.217-1810_217-1801del	N/A	Intron Variant
CAPRIN1 transcript variant X2	XM_047426959.1:c.217-1810… XM_047426959.1:c.217-1810_217-1801del	N/A	Intron Variant
CAPRIN1 transcript variant X1	XM_047426960.1:c.217-1810… XM_047426960.1:c.217-1810_217-1801del	N/A	Intron Variant
CAPRIN1 transcript variant X3	XM_047426961.1:c.217-1810… XM_047426961.1:c.217-1810_217-1801del	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	(A)₁₈=	del(A)₁₀	del(A)₈	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	ins(A)₂₇
GRCh38.p14 chr 11	NC_000011.10:g.34069908_34069925=	NC_000011.10:g.34069916_34069925del	NC_000011.10:g.34069918_34069925del	NC_000011.10:g.34069920_34069925del	NC_000011.10:g.34069921_34069925del	NC_000011.10:g.34069922_34069925del	NC_000011.10:g.34069923_34069925del	NC_000011.10:g.34069924_34069925del	NC_000011.10:g.34069925del	NC_000011.10:g.34069925dup	NC_000011.10:g.34069924_34069925dup	NC_000011.10:g.34069923_34069925dup	NC_000011.10:g.34069922_34069925dup	NC_000011.10:g.34069925_34069926insAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 11	NC_000011.9:g.34091455_34091472=	NC_000011.9:g.34091463_34091472del	NC_000011.9:g.34091465_34091472del	NC_000011.9:g.34091467_34091472del	NC_000011.9:g.34091468_34091472del	NC_000011.9:g.34091469_34091472del	NC_000011.9:g.34091470_34091472del	NC_000011.9:g.34091471_34091472del	NC_000011.9:g.34091472del	NC_000011.9:g.34091472dup	NC_000011.9:g.34091471_34091472dup	NC_000011.9:g.34091470_34091472dup	NC_000011.9:g.34091469_34091472dup	NC_000011.9:g.34091472_34091473insAAAAAAAAAAAAAAAAAAAAAAAAAAA
CAPRIN1 transcript variant 1	NM_005898.4:c.217-1818=	NM_005898.4:c.217-1810_217-1801del	NM_005898.4:c.217-1808_217-1801del	NM_005898.4:c.217-1806_217-1801del	NM_005898.4:c.217-1805_217-1801del	NM_005898.4:c.217-1804_217-1801del	NM_005898.4:c.217-1803_217-1801del	NM_005898.4:c.217-1802_217-1801del	NM_005898.4:c.217-1801del	NM_005898.4:c.217-1801dup	NM_005898.4:c.217-1802_217-1801dup	NM_005898.4:c.217-1803_217-1801dup	NM_005898.4:c.217-1804_217-1801dup	NM_005898.4:c.217-1801_217-1800insAAAAAAAAAAAAAAAAAAAAAAAAAAA
CAPRIN1 transcript variant 1	NM_005898.5:c.217-1818=	NM_005898.5:c.217-1810_217-1801del	NM_005898.5:c.217-1808_217-1801del	NM_005898.5:c.217-1806_217-1801del	NM_005898.5:c.217-1805_217-1801del	NM_005898.5:c.217-1804_217-1801del	NM_005898.5:c.217-1803_217-1801del	NM_005898.5:c.217-1802_217-1801del	NM_005898.5:c.217-1801del	NM_005898.5:c.217-1801dup	NM_005898.5:c.217-1802_217-1801dup	NM_005898.5:c.217-1803_217-1801dup	NM_005898.5:c.217-1804_217-1801dup	NM_005898.5:c.217-1801_217-1800insAAAAAAAAAAAAAAAAAAAAAAAAAAA
CAPRIN1 transcript variant 2	NM_203364.2:c.217-1818=	NM_203364.2:c.217-1810_217-1801del	NM_203364.2:c.217-1808_217-1801del	NM_203364.2:c.217-1806_217-1801del	NM_203364.2:c.217-1805_217-1801del	NM_203364.2:c.217-1804_217-1801del	NM_203364.2:c.217-1803_217-1801del	NM_203364.2:c.217-1802_217-1801del	NM_203364.2:c.217-1801del	NM_203364.2:c.217-1801dup	NM_203364.2:c.217-1802_217-1801dup	NM_203364.2:c.217-1803_217-1801dup	NM_203364.2:c.217-1804_217-1801dup	NM_203364.2:c.217-1801_217-1800insAAAAAAAAAAAAAAAAAAAAAAAAAAA
CAPRIN1 transcript variant 2	NM_203364.3:c.217-1818=	NM_203364.3:c.217-1810_217-1801del	NM_203364.3:c.217-1808_217-1801del	NM_203364.3:c.217-1806_217-1801del	NM_203364.3:c.217-1805_217-1801del	NM_203364.3:c.217-1804_217-1801del	NM_203364.3:c.217-1803_217-1801del	NM_203364.3:c.217-1802_217-1801del	NM_203364.3:c.217-1801del	NM_203364.3:c.217-1801dup	NM_203364.3:c.217-1802_217-1801dup	NM_203364.3:c.217-1803_217-1801dup	NM_203364.3:c.217-1804_217-1801dup	NM_203364.3:c.217-1801_217-1800insAAAAAAAAAAAAAAAAAAAAAAAAAAA
CAPRIN1 transcript variant X1	XM_005252931.1:c.217-1818=	XM_005252931.1:c.217-1810_217-1801del	XM_005252931.1:c.217-1808_217-1801del	XM_005252931.1:c.217-1806_217-1801del	XM_005252931.1:c.217-1805_217-1801del	XM_005252931.1:c.217-1804_217-1801del	XM_005252931.1:c.217-1803_217-1801del	XM_005252931.1:c.217-1802_217-1801del	XM_005252931.1:c.217-1801del	XM_005252931.1:c.217-1801dup	XM_005252931.1:c.217-1802_217-1801dup	XM_005252931.1:c.217-1803_217-1801dup	XM_005252931.1:c.217-1804_217-1801dup	XM_005252931.1:c.217-1801_217-1800insAAAAAAAAAAAAAAAAAAAAAAAAAAA
CAPRIN1 transcript variant X2	XM_005252932.1:c.-27-1818=	XM_005252932.1:c.-27-1810_-27-1801del	XM_005252932.1:c.-27-1808_-27-1801del	XM_005252932.1:c.-27-1806_-27-1801del	XM_005252932.1:c.-27-1805_-27-1801del	XM_005252932.1:c.-27-1804_-27-1801del	XM_005252932.1:c.-27-1803_-27-1801del	XM_005252932.1:c.-27-1802_-27-1801del	XM_005252932.1:c.-27-1801del	XM_005252932.1:c.-27-1801dup	XM_005252932.1:c.-27-1802_-27-1801dup	XM_005252932.1:c.-27-1803_-27-1801dup	XM_005252932.1:c.-27-1804_-27-1801dup	XM_005252932.1:c.-27-1801_-27-1800insAAAAAAAAAAAAAAAAAAAAAAAAAAA
CAPRIN1 transcript variant X2	XM_047426959.1:c.217-1818=	XM_047426959.1:c.217-1810_217-1801del	XM_047426959.1:c.217-1808_217-1801del	XM_047426959.1:c.217-1806_217-1801del	XM_047426959.1:c.217-1805_217-1801del	XM_047426959.1:c.217-1804_217-1801del	XM_047426959.1:c.217-1803_217-1801del	XM_047426959.1:c.217-1802_217-1801del	XM_047426959.1:c.217-1801del	XM_047426959.1:c.217-1801dup	XM_047426959.1:c.217-1802_217-1801dup	XM_047426959.1:c.217-1803_217-1801dup	XM_047426959.1:c.217-1804_217-1801dup	XM_047426959.1:c.217-1801_217-1800insAAAAAAAAAAAAAAAAAAAAAAAAAAA
CAPRIN1 transcript variant X1	XM_047426960.1:c.217-1818=	XM_047426960.1:c.217-1810_217-1801del	XM_047426960.1:c.217-1808_217-1801del	XM_047426960.1:c.217-1806_217-1801del	XM_047426960.1:c.217-1805_217-1801del	XM_047426960.1:c.217-1804_217-1801del	XM_047426960.1:c.217-1803_217-1801del	XM_047426960.1:c.217-1802_217-1801del	XM_047426960.1:c.217-1801del	XM_047426960.1:c.217-1801dup	XM_047426960.1:c.217-1802_217-1801dup	XM_047426960.1:c.217-1803_217-1801dup	XM_047426960.1:c.217-1804_217-1801dup	XM_047426960.1:c.217-1801_217-1800insAAAAAAAAAAAAAAAAAAAAAAAAAAA
CAPRIN1 transcript variant X3	XM_047426961.1:c.217-1818=	XM_047426961.1:c.217-1810_217-1801del	XM_047426961.1:c.217-1808_217-1801del	XM_047426961.1:c.217-1806_217-1801del	XM_047426961.1:c.217-1805_217-1801del	XM_047426961.1:c.217-1804_217-1801del	XM_047426961.1:c.217-1803_217-1801del	XM_047426961.1:c.217-1802_217-1801del	XM_047426961.1:c.217-1801del	XM_047426961.1:c.217-1801dup	XM_047426961.1:c.217-1802_217-1801dup	XM_047426961.1:c.217-1803_217-1801dup	XM_047426961.1:c.217-1804_217-1801dup	XM_047426961.1:c.217-1801_217-1800insAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

66 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss79727528	Sep 08, 2015 (146)
2	HGSV	ss80123020	Sep 08, 2015 (146)
3	HGSV	ss80204620	Sep 08, 2015 (146)
4	HGSV	ss81800422	Sep 08, 2015 (146)
5	HGSV	ss82047965	Sep 08, 2015 (146)
6	HGSV	ss82564862	Sep 08, 2015 (146)
7	HUMANGENOME_JCVI	ss95565421	Dec 05, 2013 (138)
8	BCMHGSC_JDW	ss103523276	Dec 01, 2009 (131)
9	GMI	ss289062817	May 04, 2012 (137)
10	PJP	ss294697659	Aug 21, 2014 (142)
11	PJP	ss294697660	May 09, 2011 (135)
12	SSMP	ss664047634	Apr 01, 2015 (144)
13	BILGI_BIOE	ss666531030	Apr 25, 2013 (138)
14	SSIP	ss947275060	Aug 21, 2014 (142)
15	1000GENOMES	ss1370758217	Aug 21, 2014 (142)
16	EVA_UK10K_ALSPAC	ss1707060983	Apr 01, 2015 (144)
17	EVA_UK10K_TWINSUK	ss1707061275	Apr 01, 2015 (144)
18	EVA_UK10K_TWINSUK	ss1710508584	Apr 01, 2015 (144)
19	EVA_UK10K_ALSPAC	ss1710508596	Apr 01, 2015 (144)
20	SYSTEMSBIOZJU	ss2627784469	Nov 08, 2017 (151)
21	SWEGEN	ss3007867809	Nov 08, 2017 (151)
22	MCHAISSO	ss3063687411	Nov 08, 2017 (151)
23	MCHAISSO	ss3064511924	Nov 08, 2017 (151)
24	MCHAISSO	ss3065424083	Nov 08, 2017 (151)
25	BIOINF_KMB_FNS_UNIBA	ss3645189069	Oct 12, 2018 (152)
26	URBANLAB	ss3649577414	Oct 12, 2018 (152)
27	EVA_DECODE	ss3691544024	Jul 13, 2019 (153)
28	EVA_DECODE	ss3691544025	Jul 13, 2019 (153)
29	EVA_DECODE	ss3691544026	Jul 13, 2019 (153)
30	EVA_DECODE	ss3691544027	Jul 13, 2019 (153)
31	EVA_DECODE	ss3691544028	Jul 13, 2019 (153)
32	ACPOP	ss3738072019	Jul 13, 2019 (153)
33	PACBIO	ss3786919749	Jul 13, 2019 (153)
34	PACBIO	ss3786919750	Jul 13, 2019 (153)
35	PACBIO	ss3792066695	Jul 13, 2019 (153)
36	PACBIO	ss3796948849	Jul 13, 2019 (153)
37	KHV_HUMAN_GENOMES	ss3814496056	Jul 13, 2019 (153)
38	EVA	ss3832568479	Apr 26, 2020 (154)
39	GNOMAD	ss4232951598	Apr 26, 2021 (155)
40	GNOMAD	ss4232951599	Apr 26, 2021 (155)
41	GNOMAD	ss4232951600	Apr 26, 2021 (155)
42	GNOMAD	ss4232951601	Apr 26, 2021 (155)
43	GNOMAD	ss4232951603	Apr 26, 2021 (155)
44	GNOMAD	ss4232951604	Apr 26, 2021 (155)
45	GNOMAD	ss4232951605	Apr 26, 2021 (155)
46	GNOMAD	ss4232951606	Apr 26, 2021 (155)
47	GNOMAD	ss4232951607	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5201426124	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5201426125	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5201426126	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5201426127	Apr 26, 2021 (155)
52	1000G_HIGH_COVERAGE	ss5286979887	Oct 16, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5286979888	Oct 16, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5286979889	Oct 16, 2022 (156)
55	HUGCELL_USP	ss5482223574	Oct 16, 2022 (156)
56	HUGCELL_USP	ss5482223575	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5482223576	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5748390808	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5748390809	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5748390810	Oct 16, 2022 (156)
61	TOMMO_GENOMICS	ss5748390811	Oct 16, 2022 (156)
62	TOMMO_GENOMICS	ss5748390812	Oct 16, 2022 (156)
63	EVA	ss5836490752	Oct 16, 2022 (156)
64	EVA	ss5836490753	Oct 16, 2022 (156)
65	EVA	ss5836490754	Oct 16, 2022 (156)
66	EVA	ss5919494250	Oct 16, 2022 (156)
67	1000Genomes	NC_000011.9 - 34091455	Oct 12, 2018 (152)
68	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 29602990 (NC_000011.9:34091455:A: 3287/3854) Row 29602991 (NC_000011.9:34091454:AAA: 566/3854)	-	Oct 12, 2018 (152)
69	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 29602990 (NC_000011.9:34091455:A: 3287/3854) Row 29602991 (NC_000011.9:34091454:AAA: 566/3854)	-	Oct 12, 2018 (152)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376155052 (NC_000011.10:34069907::A 41/126658) Row 376155053 (NC_000011.10:34069907::AAA 2/126660) Row 376155054 (NC_000011.10:34069907::AAAA 1/126660)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376155052 (NC_000011.10:34069907::A 41/126658) Row 376155053 (NC_000011.10:34069907::AAA 2/126660) Row 376155054 (NC_000011.10:34069907::AAAA 1/126660)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376155052 (NC_000011.10:34069907::A 41/126658) Row 376155053 (NC_000011.10:34069907::AAA 2/126660) Row 376155054 (NC_000011.10:34069907::AAAA 1/126660)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376155052 (NC_000011.10:34069907::A 41/126658) Row 376155053 (NC_000011.10:34069907::AAA 2/126660) Row 376155054 (NC_000011.10:34069907::AAAA 1/126660)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376155052 (NC_000011.10:34069907::A 41/126658) Row 376155053 (NC_000011.10:34069907::AAA 2/126660) Row 376155054 (NC_000011.10:34069907::AAAA 1/126660)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376155052 (NC_000011.10:34069907::A 41/126658) Row 376155053 (NC_000011.10:34069907::AAA 2/126660) Row 376155054 (NC_000011.10:34069907::AAAA 1/126660)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376155052 (NC_000011.10:34069907::A 41/126658) Row 376155053 (NC_000011.10:34069907::AAA 2/126660) Row 376155054 (NC_000011.10:34069907::AAAA 1/126660)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376155052 (NC_000011.10:34069907::A 41/126658) Row 376155053 (NC_000011.10:34069907::AAA 2/126660) Row 376155054 (NC_000011.10:34069907::AAAA 1/126660)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376155052 (NC_000011.10:34069907::A 41/126658) Row 376155053 (NC_000011.10:34069907::AAA 2/126660) Row 376155054 (NC_000011.10:34069907::AAAA 1/126660)...	-	Apr 26, 2021 (155)
79	Northern Sweden	NC_000011.9 - 34091455	Jul 13, 2019 (153)
80	8.3KJPN Submission ignored due to conflicting rows: Row 59395431 (NC_000011.9:34091454:AA: 16410/16738) Row 59395432 (NC_000011.9:34091454:A: 58/16738) Row 59395433 (NC_000011.9:34091454:AAA: 107/16738)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 59395431 (NC_000011.9:34091454:AA: 16410/16738) Row 59395432 (NC_000011.9:34091454:A: 58/16738) Row 59395433 (NC_000011.9:34091454:AAA: 107/16738)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 59395431 (NC_000011.9:34091454:AA: 16410/16738) Row 59395432 (NC_000011.9:34091454:A: 58/16738) Row 59395433 (NC_000011.9:34091454:AAA: 107/16738)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 59395431 (NC_000011.9:34091454:AA: 16410/16738) Row 59395432 (NC_000011.9:34091454:A: 58/16738) Row 59395433 (NC_000011.9:34091454:AAA: 107/16738)...	-	Apr 26, 2021 (155)
84	14KJPN Submission ignored due to conflicting rows: Row 82227912 (NC_000011.10:34069907:AA: 27830/28250) Row 82227913 (NC_000011.10:34069907:AAA: 127/28250) Row 82227914 (NC_000011.10:34069907:A: 97/28250)...	-	Oct 16, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 82227912 (NC_000011.10:34069907:AA: 27830/28250) Row 82227913 (NC_000011.10:34069907:AAA: 127/28250) Row 82227914 (NC_000011.10:34069907:A: 97/28250)...	-	Oct 16, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 82227912 (NC_000011.10:34069907:AA: 27830/28250) Row 82227913 (NC_000011.10:34069907:AAA: 127/28250) Row 82227914 (NC_000011.10:34069907:A: 97/28250)...	-	Oct 16, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 82227912 (NC_000011.10:34069907:AA: 27830/28250) Row 82227913 (NC_000011.10:34069907:AAA: 127/28250) Row 82227914 (NC_000011.10:34069907:A: 97/28250)...	-	Oct 16, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 82227912 (NC_000011.10:34069907:AA: 27830/28250) Row 82227913 (NC_000011.10:34069907:AAA: 127/28250) Row 82227914 (NC_000011.10:34069907:A: 97/28250)...	-	Oct 16, 2022 (156)
89	UK 10K study - Twins Submission ignored due to conflicting rows: Row 29602990 (NC_000011.9:34091455:A: 3267/3708) Row 29602991 (NC_000011.9:34091454:AAA: 441/3708)	-	Oct 12, 2018 (152)
90	UK 10K study - Twins Submission ignored due to conflicting rows: Row 29602990 (NC_000011.9:34091455:A: 3267/3708) Row 29602991 (NC_000011.9:34091454:AAA: 441/3708)	-	Oct 12, 2018 (152)
91	ALFA	NC_000011.10 - 34069908	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)
rs71873228	May 11, 2012 (137)
rs147727832	Sep 17, 2011 (135)
rs199823170	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
5365114701	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
5365114701	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss5748390812	NC_000011.10:34069907:AAAAAA:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA
5365114701	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4232951607	NC_000011.10:34069907:AAAAA:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
5365114701	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss103523276	NT_009237.18:34031467:AAAAA:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5201426127, ss5836490754	NC_000011.9:34091454:AAAA:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3691544028, ss4232951606, ss5748390811	NC_000011.10:34069907:AAAA:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
5365114701	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss1707060983, ss1707061275, ss3007867809, ss3786919749, ss5201426126, ss5836490753	NC_000011.9:34091454:AAA:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4232951605, ss5286979889, ss5482223574, ss5748390809	NC_000011.10:34069907:AAA:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
5365114701	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3691544027	NC_000011.10:34069908:AAA:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss289062817, ss294697659	NC_000011.8:34048030:AA:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss79727528, ss80123020, ss80204620, ss81800422, ss82047965, ss82564862, ss294697660	NC_000011.8:34048046:AA:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
53287603, 11356884, ss664047634, ss666531030, ss1370758217, ss2627784469, ss3738072019, ss3786919750, ss3792066695, ss3796948849, ss3832568479, ss5201426124, ss5836490752	NC_000011.9:34091454:AA:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss947275060, ss1710508584, ss1710508596	NC_000011.9:34091455:AA:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3063687411, ss3064511924, ss3065424083, ss3645189069, ss3649577414, ss3814496056, ss4232951604, ss5286979887, ss5482223575, ss5748390808, ss5919494250	NC_000011.10:34069907:AA:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
5365114701	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3691544026	NC_000011.10:34069909:AA:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5201426125	NC_000011.9:34091454:A:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
	NC_000011.9:34091455:A:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4232951603, ss5286979888, ss5482223576, ss5748390810	NC_000011.10:34069907:A:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
5365114701	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3691544025	NC_000011.10:34069910:A:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss95565421	NT_009237.18:34031471:A:	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4232951598	NC_000011.10:34069907::A	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
5365114701	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss95565421	NT_009237.18:34031471:A:AA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
5365114701	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4232951599	NC_000011.10:34069907::AAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
5365114701	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3691544024	NC_000011.10:34069911::AAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4232951600	NC_000011.10:34069907::AAAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4232951601	NC_000011.10:34069907::AAAAAAAAAAA… NC_000011.10:34069907::AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3141373974	NC_000011.10:34069907::AA	NC_000011.10:34069907:AAAAAAAAAAAA… NC_000011.10:34069907:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

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

No publications for rs59107049

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

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs59107049