Name: rs3073356
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.

rs3073356

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:34061970-34061987 (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)₇ / del(A)₆ / del(A)₅ / del(…
del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₆ / dup(A)₈
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₈=0.4595 (2301/5008, 1000G)
del(A)₇=0.0 (0/2, ALFA)
del(A)₆=0.0 (0/2, ALFA) (+ 9 more)
del(A)₅=0.0 (0/2, ALFA)
del(A)₄=0.0 (0/2, ALFA)
delAAA=0.0 (0/2, ALFA)
delAA=0.0 (0/2, ALFA)
delA=0.0 (0/2, ALFA)
dupA=0.0 (0/2, ALFA)
dupAA=0.0 (0/2, ALFA)
dupAAA=0.0 (0/2, ALFA)
dup(A)₄=0.0 (0/2, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CAPRIN1 : Intron Variant
LOC124902660 : 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	2	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
European	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
African	Sub	2	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African Others	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	2	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 2	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	0	AAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupAA=0.5405
1000Genomes	African	Sub	1322	- No frequency provided	dupAA=0.5484
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupAA=0.5347
1000Genomes	Europe	Sub	1006	- No frequency provided	dupAA=0.5517
1000Genomes	South Asian	Sub	978	- No frequency provided	dupAA=0.545
1000Genomes	American	Sub	694	- No frequency provided	dupAA=0.512
Allele Frequency Aggregator	Total	Global	2	(A)₁₈=1.0	del(A)₇=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, dup(A)₄=0.0
Allele Frequency Aggregator	African	Sub	2	(A)₁₈=1.0	del(A)₇=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, dup(A)₄=0.0
Allele Frequency Aggregator	European	Sub	0	(A)₁₈=0	del(A)₇=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, dup(A)₄=0
Allele Frequency Aggregator	Latin American 1	Sub	0	(A)₁₈=0	del(A)₇=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, dup(A)₄=0
Allele Frequency Aggregator	Latin American 2	Sub	0	(A)₁₈=0	del(A)₇=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, dup(A)₄=0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₁₈=0	del(A)₇=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, dup(A)₄=0
Allele Frequency Aggregator	Other	Sub	0	(A)₁₈=0	del(A)₇=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, dup(A)₄=0
Allele Frequency Aggregator	Asian	Sub	0	(A)₁₈=0	del(A)₇=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, dup(A)₄=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.34061981_34061987del
GRCh38.p14 chr 11	NC_000011.10:g.34061982_34061987del
GRCh38.p14 chr 11	NC_000011.10:g.34061983_34061987del
GRCh38.p14 chr 11	NC_000011.10:g.34061984_34061987del
GRCh38.p14 chr 11	NC_000011.10:g.34061985_34061987del
GRCh38.p14 chr 11	NC_000011.10:g.34061986_34061987del
GRCh38.p14 chr 11	NC_000011.10:g.34061987del
GRCh38.p14 chr 11	NC_000011.10:g.34061987dup
GRCh38.p14 chr 11	NC_000011.10:g.34061986_34061987dup
GRCh38.p14 chr 11	NC_000011.10:g.34061985_34061987dup
GRCh38.p14 chr 11	NC_000011.10:g.34061984_34061987dup
GRCh38.p14 chr 11	NC_000011.10:g.34061982_34061987dup
GRCh38.p14 chr 11	NC_000011.10:g.34061980_34061987dup
GRCh37.p13 chr 11	NC_000011.9:g.34083528_34083534del
GRCh37.p13 chr 11	NC_000011.9:g.34083529_34083534del
GRCh37.p13 chr 11	NC_000011.9:g.34083530_34083534del
GRCh37.p13 chr 11	NC_000011.9:g.34083531_34083534del
GRCh37.p13 chr 11	NC_000011.9:g.34083532_34083534del
GRCh37.p13 chr 11	NC_000011.9:g.34083533_34083534del
GRCh37.p13 chr 11	NC_000011.9:g.34083534del
GRCh37.p13 chr 11	NC_000011.9:g.34083534dup
GRCh37.p13 chr 11	NC_000011.9:g.34083533_34083534dup
GRCh37.p13 chr 11	NC_000011.9:g.34083532_34083534dup
GRCh37.p13 chr 11	NC_000011.9:g.34083531_34083534dup
GRCh37.p13 chr 11	NC_000011.9:g.34083529_34083534dup
GRCh37.p13 chr 11	NC_000011.9:g.34083527_34083534dup

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.216+9345_21… NM_005898.5:c.216+9345_216+9351del	N/A	Intron Variant
CAPRIN1 transcript variant 2	NM_203364.3:c.216+9345_21… NM_203364.3:c.216+9345_216+9351del	N/A	Intron Variant
CAPRIN1 transcript variant X2	XM_047426959.1:c.216+9345… XM_047426959.1:c.216+9345_216+9351del	N/A	Intron Variant
CAPRIN1 transcript variant X1	XM_047426960.1:c.216+9345… XM_047426960.1:c.216+9345_216+9351del	N/A	Intron Variant
CAPRIN1 transcript variant X3	XM_047426961.1:c.216+9345… XM_047426961.1:c.216+9345_216+9351del	N/A	Intron Variant

Gene: LOC124902660, uncharacterized LOC124902660 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124902660 transcript variant X1	XR_007062651.1: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	(A)₁₈=	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₆	dup(A)₈
GRCh38.p14 chr 11	NC_000011.10:g.34061970_34061987=	NC_000011.10:g.34061981_34061987del	NC_000011.10:g.34061982_34061987del	NC_000011.10:g.34061983_34061987del	NC_000011.10:g.34061984_34061987del	NC_000011.10:g.34061985_34061987del	NC_000011.10:g.34061986_34061987del	NC_000011.10:g.34061987del	NC_000011.10:g.34061987dup	NC_000011.10:g.34061986_34061987dup	NC_000011.10:g.34061985_34061987dup	NC_000011.10:g.34061984_34061987dup	NC_000011.10:g.34061982_34061987dup	NC_000011.10:g.34061980_34061987dup
GRCh37.p13 chr 11	NC_000011.9:g.34083517_34083534=	NC_000011.9:g.34083528_34083534del	NC_000011.9:g.34083529_34083534del	NC_000011.9:g.34083530_34083534del	NC_000011.9:g.34083531_34083534del	NC_000011.9:g.34083532_34083534del	NC_000011.9:g.34083533_34083534del	NC_000011.9:g.34083534del	NC_000011.9:g.34083534dup	NC_000011.9:g.34083533_34083534dup	NC_000011.9:g.34083532_34083534dup	NC_000011.9:g.34083531_34083534dup	NC_000011.9:g.34083529_34083534dup	NC_000011.9:g.34083527_34083534dup
CAPRIN1 transcript variant 1	NM_005898.4:c.216+9334=	NM_005898.4:c.216+9345_216+9351del	NM_005898.4:c.216+9346_216+9351del	NM_005898.4:c.216+9347_216+9351del	NM_005898.4:c.216+9348_216+9351del	NM_005898.4:c.216+9349_216+9351del	NM_005898.4:c.216+9350_216+9351del	NM_005898.4:c.216+9351del	NM_005898.4:c.216+9351dup	NM_005898.4:c.216+9350_216+9351dup	NM_005898.4:c.216+9349_216+9351dup	NM_005898.4:c.216+9348_216+9351dup	NM_005898.4:c.216+9346_216+9351dup	NM_005898.4:c.216+9344_216+9351dup
CAPRIN1 transcript variant 1	NM_005898.5:c.216+9334=	NM_005898.5:c.216+9345_216+9351del	NM_005898.5:c.216+9346_216+9351del	NM_005898.5:c.216+9347_216+9351del	NM_005898.5:c.216+9348_216+9351del	NM_005898.5:c.216+9349_216+9351del	NM_005898.5:c.216+9350_216+9351del	NM_005898.5:c.216+9351del	NM_005898.5:c.216+9351dup	NM_005898.5:c.216+9350_216+9351dup	NM_005898.5:c.216+9349_216+9351dup	NM_005898.5:c.216+9348_216+9351dup	NM_005898.5:c.216+9346_216+9351dup	NM_005898.5:c.216+9344_216+9351dup
CAPRIN1 transcript variant 2	NM_203364.2:c.216+9334=	NM_203364.2:c.216+9345_216+9351del	NM_203364.2:c.216+9346_216+9351del	NM_203364.2:c.216+9347_216+9351del	NM_203364.2:c.216+9348_216+9351del	NM_203364.2:c.216+9349_216+9351del	NM_203364.2:c.216+9350_216+9351del	NM_203364.2:c.216+9351del	NM_203364.2:c.216+9351dup	NM_203364.2:c.216+9350_216+9351dup	NM_203364.2:c.216+9349_216+9351dup	NM_203364.2:c.216+9348_216+9351dup	NM_203364.2:c.216+9346_216+9351dup	NM_203364.2:c.216+9344_216+9351dup
CAPRIN1 transcript variant 2	NM_203364.3:c.216+9334=	NM_203364.3:c.216+9345_216+9351del	NM_203364.3:c.216+9346_216+9351del	NM_203364.3:c.216+9347_216+9351del	NM_203364.3:c.216+9348_216+9351del	NM_203364.3:c.216+9349_216+9351del	NM_203364.3:c.216+9350_216+9351del	NM_203364.3:c.216+9351del	NM_203364.3:c.216+9351dup	NM_203364.3:c.216+9350_216+9351dup	NM_203364.3:c.216+9349_216+9351dup	NM_203364.3:c.216+9348_216+9351dup	NM_203364.3:c.216+9346_216+9351dup	NM_203364.3:c.216+9344_216+9351dup
CAPRIN1 transcript variant X1	XM_005252931.1:c.216+9334=	XM_005252931.1:c.216+9345_216+9351del	XM_005252931.1:c.216+9346_216+9351del	XM_005252931.1:c.216+9347_216+9351del	XM_005252931.1:c.216+9348_216+9351del	XM_005252931.1:c.216+9349_216+9351del	XM_005252931.1:c.216+9350_216+9351del	XM_005252931.1:c.216+9351del	XM_005252931.1:c.216+9351dup	XM_005252931.1:c.216+9350_216+9351dup	XM_005252931.1:c.216+9349_216+9351dup	XM_005252931.1:c.216+9348_216+9351dup	XM_005252931.1:c.216+9346_216+9351dup	XM_005252931.1:c.216+9344_216+9351dup
CAPRIN1 transcript variant X2	XM_005252932.1:c.-28+8785=	XM_005252932.1:c.-28+8796_-28+8802del	XM_005252932.1:c.-28+8797_-28+8802del	XM_005252932.1:c.-28+8798_-28+8802del	XM_005252932.1:c.-28+8799_-28+8802del	XM_005252932.1:c.-28+8800_-28+8802del	XM_005252932.1:c.-28+8801_-28+8802del	XM_005252932.1:c.-28+8802del	XM_005252932.1:c.-28+8802dup	XM_005252932.1:c.-28+8801_-28+8802dup	XM_005252932.1:c.-28+8800_-28+8802dup	XM_005252932.1:c.-28+8799_-28+8802dup	XM_005252932.1:c.-28+8797_-28+8802dup	XM_005252932.1:c.-28+8795_-28+8802dup
CAPRIN1 transcript variant X2	XM_047426959.1:c.216+9334=	XM_047426959.1:c.216+9345_216+9351del	XM_047426959.1:c.216+9346_216+9351del	XM_047426959.1:c.216+9347_216+9351del	XM_047426959.1:c.216+9348_216+9351del	XM_047426959.1:c.216+9349_216+9351del	XM_047426959.1:c.216+9350_216+9351del	XM_047426959.1:c.216+9351del	XM_047426959.1:c.216+9351dup	XM_047426959.1:c.216+9350_216+9351dup	XM_047426959.1:c.216+9349_216+9351dup	XM_047426959.1:c.216+9348_216+9351dup	XM_047426959.1:c.216+9346_216+9351dup	XM_047426959.1:c.216+9344_216+9351dup
CAPRIN1 transcript variant X1	XM_047426960.1:c.216+9334=	XM_047426960.1:c.216+9345_216+9351del	XM_047426960.1:c.216+9346_216+9351del	XM_047426960.1:c.216+9347_216+9351del	XM_047426960.1:c.216+9348_216+9351del	XM_047426960.1:c.216+9349_216+9351del	XM_047426960.1:c.216+9350_216+9351del	XM_047426960.1:c.216+9351del	XM_047426960.1:c.216+9351dup	XM_047426960.1:c.216+9350_216+9351dup	XM_047426960.1:c.216+9349_216+9351dup	XM_047426960.1:c.216+9348_216+9351dup	XM_047426960.1:c.216+9346_216+9351dup	XM_047426960.1:c.216+9344_216+9351dup
CAPRIN1 transcript variant X3	XM_047426961.1:c.216+9334=	XM_047426961.1:c.216+9345_216+9351del	XM_047426961.1:c.216+9346_216+9351del	XM_047426961.1:c.216+9347_216+9351del	XM_047426961.1:c.216+9348_216+9351del	XM_047426961.1:c.216+9349_216+9351del	XM_047426961.1:c.216+9350_216+9351del	XM_047426961.1:c.216+9351del	XM_047426961.1:c.216+9351dup	XM_047426961.1:c.216+9350_216+9351dup	XM_047426961.1:c.216+9349_216+9351dup	XM_047426961.1:c.216+9348_216+9351dup	XM_047426961.1:c.216+9346_216+9351dup	XM_047426961.1:c.216+9344_216+9351dup

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#.

56 SubSNP, 27 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4304752	Jan 05, 2002 (102)
2	ABI	ss39920684	Mar 13, 2006 (126)
3	HGSV	ss77995558	Dec 07, 2007 (129)
4	HGSV	ss80505992	Dec 15, 2007 (130)
5	HUMANGENOME_JCVI	ss95565417	Feb 06, 2009 (130)
6	PJP	ss294697653	May 31, 2013 (138)
7	PJP	ss294697654	May 31, 2013 (138)
8	BILGI_BIOE	ss666531028	Apr 25, 2013 (138)
9	1000GENOMES	ss1370758193	Aug 21, 2014 (142)
10	DDI	ss1536686366	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1707060959	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1707060960	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1707061259	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1707061260	Apr 01, 2015 (144)
15	SWEGEN	ss3007867707	Nov 08, 2017 (151)
16	SWEGEN	ss3007867708	Nov 08, 2017 (151)
17	SWEGEN	ss3007867709	Nov 08, 2017 (151)
18	URBANLAB	ss3649577408	Oct 12, 2018 (152)
19	EVA_DECODE	ss3691543889	Jul 13, 2019 (153)
20	EVA_DECODE	ss3691543890	Jul 13, 2019 (153)
21	EVA_DECODE	ss3691543891	Jul 13, 2019 (153)
22	EVA_DECODE	ss3691543892	Jul 13, 2019 (153)
23	EVA_DECODE	ss3691543893	Jul 13, 2019 (153)
24	ACPOP	ss3738071961	Jul 13, 2019 (153)
25	ACPOP	ss3738071962	Jul 13, 2019 (153)
26	PACBIO	ss3792066687	Jul 13, 2019 (153)
27	PACBIO	ss3796948841	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3814495981	Jul 13, 2019 (153)
29	EVA	ss3832568437	Apr 26, 2020 (154)
30	GNOMAD	ss4232950424	Apr 26, 2021 (155)
31	GNOMAD	ss4232950425	Apr 26, 2021 (155)
32	GNOMAD	ss4232950426	Apr 26, 2021 (155)
33	GNOMAD	ss4232950427	Apr 26, 2021 (155)
34	GNOMAD	ss4232950428	Apr 26, 2021 (155)
35	GNOMAD	ss4232950429	Apr 26, 2021 (155)
36	GNOMAD	ss4232950431	Apr 26, 2021 (155)
37	GNOMAD	ss4232950432	Apr 26, 2021 (155)
38	GNOMAD	ss4232950433	Apr 26, 2021 (155)
39	GNOMAD	ss4232950434	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5201425837	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5201425838	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5201425839	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5201425840	Apr 26, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5286979639	Oct 16, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5286979640	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5286979642	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5482223354	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5482223355	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5482223356	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5748390430	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5748390431	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5748390433	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5748390434	Oct 16, 2022 (156)
54	EVA	ss5836490661	Oct 16, 2022 (156)
55	EVA	ss5836490662	Oct 16, 2022 (156)
56	EVA	ss5919493992	Oct 16, 2022 (156)
57	1000Genomes	NC_000011.9 - 34083517	Oct 12, 2018 (152)
58	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 29602843 (NC_000011.9:34083516::AAA 657/3854) Row 29602844 (NC_000011.9:34083516::AA 3197/3854)	-	Oct 12, 2018 (152)
59	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 29602843 (NC_000011.9:34083516::AAA 657/3854) Row 29602844 (NC_000011.9:34083516::AA 3197/3854)	-	Oct 12, 2018 (152)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376153134 (NC_000011.10:34061969::A 1676/108182) Row 376153135 (NC_000011.10:34061969::AA 101869/108188) Row 376153136 (NC_000011.10:34061969::AAA 3287/107864)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376153134 (NC_000011.10:34061969::A 1676/108182) Row 376153135 (NC_000011.10:34061969::AA 101869/108188) Row 376153136 (NC_000011.10:34061969::AAA 3287/107864)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376153134 (NC_000011.10:34061969::A 1676/108182) Row 376153135 (NC_000011.10:34061969::AA 101869/108188) Row 376153136 (NC_000011.10:34061969::AAA 3287/107864)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376153134 (NC_000011.10:34061969::A 1676/108182) Row 376153135 (NC_000011.10:34061969::AA 101869/108188) Row 376153136 (NC_000011.10:34061969::AAA 3287/107864)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376153134 (NC_000011.10:34061969::A 1676/108182) Row 376153135 (NC_000011.10:34061969::AA 101869/108188) Row 376153136 (NC_000011.10:34061969::AAA 3287/107864)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376153134 (NC_000011.10:34061969::A 1676/108182) Row 376153135 (NC_000011.10:34061969::AA 101869/108188) Row 376153136 (NC_000011.10:34061969::AAA 3287/107864)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376153134 (NC_000011.10:34061969::A 1676/108182) Row 376153135 (NC_000011.10:34061969::AA 101869/108188) Row 376153136 (NC_000011.10:34061969::AAA 3287/107864)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376153134 (NC_000011.10:34061969::A 1676/108182) Row 376153135 (NC_000011.10:34061969::AA 101869/108188) Row 376153136 (NC_000011.10:34061969::AAA 3287/107864)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376153134 (NC_000011.10:34061969::A 1676/108182) Row 376153135 (NC_000011.10:34061969::AA 101869/108188) Row 376153136 (NC_000011.10:34061969::AAA 3287/107864)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376153134 (NC_000011.10:34061969::A 1676/108182) Row 376153135 (NC_000011.10:34061969::AA 101869/108188) Row 376153136 (NC_000011.10:34061969::AAA 3287/107864)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 376153134 (NC_000011.10:34061969::A 1676/108182) Row 376153135 (NC_000011.10:34061969::AA 101869/108188) Row 376153136 (NC_000011.10:34061969::AAA 3287/107864)...	-	Apr 26, 2021 (155)
71	Northern Sweden Submission ignored due to conflicting rows: Row 11356826 (NC_000011.9:34083516::AA 558/570) Row 11356827 (NC_000011.9:34083516::AAA 10/570)	-	Jul 13, 2019 (153)
72	Northern Sweden Submission ignored due to conflicting rows: Row 11356826 (NC_000011.9:34083516::AA 558/570) Row 11356827 (NC_000011.9:34083516::AAA 10/570)	-	Jul 13, 2019 (153)
73	8.3KJPN Submission ignored due to conflicting rows: Row 59395144 (NC_000011.9:34083516::AA 14244/15362) Row 59395145 (NC_000011.9:34083516::A 347/15362) Row 59395146 (NC_000011.9:34083516::AAA 182/15362)...	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 59395144 (NC_000011.9:34083516::AA 14244/15362) Row 59395145 (NC_000011.9:34083516::A 347/15362) Row 59395146 (NC_000011.9:34083516::AAA 182/15362)...	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 59395144 (NC_000011.9:34083516::AA 14244/15362) Row 59395145 (NC_000011.9:34083516::A 347/15362) Row 59395146 (NC_000011.9:34083516::AAA 182/15362)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 59395144 (NC_000011.9:34083516::AA 14244/15362) Row 59395145 (NC_000011.9:34083516::A 347/15362) Row 59395146 (NC_000011.9:34083516::AAA 182/15362)...	-	Apr 26, 2021 (155)
77	14KJPN Submission ignored due to conflicting rows: Row 82227534 (NC_000011.10:34061969::AA 25652/28076) Row 82227535 (NC_000011.10:34061969::A 577/28076) Row 82227537 (NC_000011.10:34061969::AAA 343/28076)...	-	Oct 16, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 82227534 (NC_000011.10:34061969::AA 25652/28076) Row 82227535 (NC_000011.10:34061969::A 577/28076) Row 82227537 (NC_000011.10:34061969::AAA 343/28076)...	-	Oct 16, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 82227534 (NC_000011.10:34061969::AA 25652/28076) Row 82227535 (NC_000011.10:34061969::A 577/28076) Row 82227537 (NC_000011.10:34061969::AAA 343/28076)...	-	Oct 16, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 82227534 (NC_000011.10:34061969::AA 25652/28076) Row 82227535 (NC_000011.10:34061969::A 577/28076) Row 82227537 (NC_000011.10:34061969::AAA 343/28076)...	-	Oct 16, 2022 (156)
81	UK 10K study - Twins Submission ignored due to conflicting rows: Row 29602843 (NC_000011.9:34083516::AAA 608/3708) Row 29602844 (NC_000011.9:34083516::AA 3100/3708)	-	Oct 12, 2018 (152)
82	UK 10K study - Twins Submission ignored due to conflicting rows: Row 29602843 (NC_000011.9:34083516::AAA 608/3708) Row 29602844 (NC_000011.9:34083516::AA 3100/3708)	-	Oct 12, 2018 (152)
83	ALFA	NC_000011.10 - 34061970	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)
rs58326968	May 27, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
5920604805	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4232950434	NC_000011.10:34061969:AAAAAA:	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
5920604805	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
5920604805	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4232950433	NC_000011.10:34061969:AAAA:	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
5920604805	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4232950432	NC_000011.10:34061969:AAA:	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
5920604805	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3691543893, ss4232950431	NC_000011.10:34061969:AA:	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
5920604805	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
	NC_000011.10:34061969:A:	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
5920604805	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3691543892	NC_000011.10:34061970:A:	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3007867708, ss5201425838	NC_000011.9:34083516::A	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4232950424, ss5286979639, ss5482223354, ss5748390431	NC_000011.10:34061969::A	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
5920604805	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3691543891	NC_000011.10:34061971::A	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss294697653	NC_000011.8:34040093::AA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss294697654	NC_000011.8:34040109::AA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
53287332, ss1370758193, ss1536686366, ss1707060960, ss1707061260, ss3007867707, ss3738071961, ss3792066687, ss3796948841, ss3832568437, ss5201425837, ss5836490661	NC_000011.9:34083516::AA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3649577408, ss3814495981, ss4232950425, ss5286979640, ss5482223355, ss5748390430, ss5919493992	NC_000011.10:34061969::AA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
5920604805	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3691543890	NC_000011.10:34061971::AA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4304752, ss39920684, ss77995558, ss80505992, ss95565417	NT_009237.18:34023534::AA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss666531028, ss1707060959, ss1707061259, ss3007867709, ss3738071962, ss5201425839, ss5836490662	NC_000011.9:34083516::AAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4232950426, ss5286979642, ss5482223356, ss5748390433	NC_000011.10:34061969::AAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
5920604805	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3691543889	NC_000011.10:34061971::AAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5201425840	NC_000011.9:34083516::AAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4232950427, ss5748390434	NC_000011.10:34061969::AAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
5920604805	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4232950428	NC_000011.10:34061969::AAAAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4232950429	NC_000011.10:34061969::AAAAAAAA	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3141372223	NC_000011.10:34061969:AAAAA:	NC_000011.10:34061969:AAAAAAAAAAAA… NC_000011.10:34061969:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA

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

No publications for rs3073356

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

rs3073356