Name: rs11284510
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.

rs11284510

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:190544931-190544953 (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)₇ / del…
del(A)₁₀ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₆
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.1928 (1099/5700, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NEMP2 : Intron Variant
NEMP2-DT : 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	5700	AAAAAAAAAAAAAAAAAAAAAAA=0.6133	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0002, AAAAAAAAAAAAAAAAAAAAA=0.1928, AAAAAAAAAAAAAAAAAAAAAA=0.1553, AAAAAAAAAAAAAAAAAAAAAAAA=0.0339, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0046, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.644351	0.084205	0.271444	32
European	Sub	5070	AAAAAAAAAAAAAAAAAAAAAAA=0.5659	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0002, AAAAAAAAAAAAAAAAAAAAA=0.2166, AAAAAAAAAAAAAAAAAAAAAA=0.1744, AAAAAAAAAAAAAAAAAAAAAAAA=0.0379, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0051, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.57536	0.100688	0.323952	23
African	Sub	258	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	6	AAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	252	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	26	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	16	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	AAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	10	AAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	246	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	6	AAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	84	AAAAAAAAAAAAAAAAAAAAAAA=0.96	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.01, AAAAAAAAAAAAAAAAAAAAAA=0.01, AAAAAAAAAAAAAAAAAAAAAAAA=0.01, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	0.975	0.0	0.025	0

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	5700	(A)₂₃=0.6133	del(A)₁₀=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0002, delAA=0.1928, delA=0.1553, dupA=0.0339, dupAA=0.0046, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	5070	(A)₂₃=0.5659	del(A)₁₀=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0002, delAA=0.2166, delA=0.1744, dupA=0.0379, dupAA=0.0051, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	258	(A)₂₃=1.000	del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=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, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	246	(A)₂₃=1.000	del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=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, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	84	(A)₂₃=0.96	del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.01, delA=0.01, dupA=0.01, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Asian	Sub	26	(A)₂₃=1.00	del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=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, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	10	(A)₂₃=1.0	del(A)₁₀=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=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	South Asian	Sub	6	(A)₂₃=1.0	del(A)₁₀=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=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

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 2	NC_000002.12:g.190544944_190544953del
GRCh38.p14 chr 2	NC_000002.12:g.190544946_190544953del
GRCh38.p14 chr 2	NC_000002.12:g.190544947_190544953del
GRCh38.p14 chr 2	NC_000002.12:g.190544948_190544953del
GRCh38.p14 chr 2	NC_000002.12:g.190544949_190544953del
GRCh38.p14 chr 2	NC_000002.12:g.190544950_190544953del
GRCh38.p14 chr 2	NC_000002.12:g.190544951_190544953del
GRCh38.p14 chr 2	NC_000002.12:g.190544952_190544953del
GRCh38.p14 chr 2	NC_000002.12:g.190544953del
GRCh38.p14 chr 2	NC_000002.12:g.190544953dup
GRCh38.p14 chr 2	NC_000002.12:g.190544952_190544953dup
GRCh38.p14 chr 2	NC_000002.12:g.190544951_190544953dup
GRCh38.p14 chr 2	NC_000002.12:g.190544950_190544953dup
GRCh38.p14 chr 2	NC_000002.12:g.190544948_190544953dup
GRCh37.p13 chr 2	NC_000002.11:g.191409670_191409679del
GRCh37.p13 chr 2	NC_000002.11:g.191409672_191409679del
GRCh37.p13 chr 2	NC_000002.11:g.191409673_191409679del
GRCh37.p13 chr 2	NC_000002.11:g.191409674_191409679del
GRCh37.p13 chr 2	NC_000002.11:g.191409675_191409679del
GRCh37.p13 chr 2	NC_000002.11:g.191409676_191409679del
GRCh37.p13 chr 2	NC_000002.11:g.191409677_191409679del
GRCh37.p13 chr 2	NC_000002.11:g.191409678_191409679del
GRCh37.p13 chr 2	NC_000002.11:g.191409679del
GRCh37.p13 chr 2	NC_000002.11:g.191409679dup
GRCh37.p13 chr 2	NC_000002.11:g.191409678_191409679dup
GRCh37.p13 chr 2	NC_000002.11:g.191409677_191409679dup
GRCh37.p13 chr 2	NC_000002.11:g.191409676_191409679dup
GRCh37.p13 chr 2	NC_000002.11:g.191409674_191409679dup

Gene: NEMP2, nuclear envelope integral membrane protein 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NEMP2 transcript variant 1	NM_001142645.2:c.	N/A	Genic Upstream Transcript Variant
NEMP2 transcript variant 2	NR_136298.2:n.	N/A	Genic Upstream Transcript Variant
NEMP2 transcript variant X1	XM_017003098.2:c.128-1956… XM_017003098.2:c.128-19562_128-19553del	N/A	Intron Variant
NEMP2 transcript variant X2	XM_017003099.1:c.128-1956… XM_017003099.1:c.128-19562_128-19553del	N/A	Intron Variant
NEMP2 transcript variant X3	XM_017003100.2:c.128-1956… XM_017003100.2:c.128-19562_128-19553del	N/A	Intron Variant
NEMP2 transcript variant X10	XM_047441958.1:c.-110-195… XM_047441958.1:c.-110-19562_-110-19553del	N/A	Intron Variant
NEMP2 transcript variant X8	XM_005246212.4:c.	N/A	Genic Upstream Transcript Variant
NEMP2 transcript variant X7	XM_011510458.4:c.	N/A	Genic Upstream Transcript Variant
NEMP2 transcript variant X9	XM_011510459.4:c.	N/A	Genic Upstream Transcript Variant
NEMP2 transcript variant X5	XM_047441941.1:c.	N/A	Genic Upstream Transcript Variant
NEMP2 transcript variant X6	XM_047441946.1:c.	N/A	Genic Upstream Transcript Variant
NEMP2 transcript variant X11	XM_047441961.1:c.	N/A	Genic Upstream Transcript Variant
NEMP2 transcript variant X4	XR_007068185.1:n.	N/A	Genic Upstream Transcript Variant

Gene: NEMP2-DT, uncharacterized NEMP2-DT (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NEMP2-DT transcript variant X4	XR_001739154.3:n.	N/A	Intron Variant
NEMP2-DT transcript variant X1	XR_001739155.3:n.	N/A	Intron Variant
NEMP2-DT transcript variant X3	XR_001739157.2:n.	N/A	Intron Variant
NEMP2-DT transcript variant X5	XR_001739158.3:n.	N/A	Intron Variant
NEMP2-DT transcript variant X2	XR_001739159.3:n.	N/A	Intron Variant
NEMP2-DT transcript variant X6	XR_007087764.1: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)₂₃=	del(A)₁₀	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₆
GRCh38.p14 chr 2	NC_000002.12:g.190544931_190544953=	NC_000002.12:g.190544944_190544953del	NC_000002.12:g.190544946_190544953del	NC_000002.12:g.190544947_190544953del	NC_000002.12:g.190544948_190544953del	NC_000002.12:g.190544949_190544953del	NC_000002.12:g.190544950_190544953del	NC_000002.12:g.190544951_190544953del	NC_000002.12:g.190544952_190544953del	NC_000002.12:g.190544953del	NC_000002.12:g.190544953dup	NC_000002.12:g.190544952_190544953dup	NC_000002.12:g.190544951_190544953dup	NC_000002.12:g.190544950_190544953dup	NC_000002.12:g.190544948_190544953dup
GRCh37.p13 chr 2	NC_000002.11:g.191409657_191409679=	NC_000002.11:g.191409670_191409679del	NC_000002.11:g.191409672_191409679del	NC_000002.11:g.191409673_191409679del	NC_000002.11:g.191409674_191409679del	NC_000002.11:g.191409675_191409679del	NC_000002.11:g.191409676_191409679del	NC_000002.11:g.191409677_191409679del	NC_000002.11:g.191409678_191409679del	NC_000002.11:g.191409679del	NC_000002.11:g.191409679dup	NC_000002.11:g.191409678_191409679dup	NC_000002.11:g.191409677_191409679dup	NC_000002.11:g.191409676_191409679dup	NC_000002.11:g.191409674_191409679dup
NEMP2 transcript variant X1	XM_017003098.2:c.128-19553=	XM_017003098.2:c.128-19562_128-19553del	XM_017003098.2:c.128-19560_128-19553del	XM_017003098.2:c.128-19559_128-19553del	XM_017003098.2:c.128-19558_128-19553del	XM_017003098.2:c.128-19557_128-19553del	XM_017003098.2:c.128-19556_128-19553del	XM_017003098.2:c.128-19555_128-19553del	XM_017003098.2:c.128-19554_128-19553del	XM_017003098.2:c.128-19553del	XM_017003098.2:c.128-19553dup	XM_017003098.2:c.128-19554_128-19553dup	XM_017003098.2:c.128-19555_128-19553dup	XM_017003098.2:c.128-19556_128-19553dup	XM_017003098.2:c.128-19558_128-19553dup
NEMP2 transcript variant X2	XM_017003099.1:c.128-19553=	XM_017003099.1:c.128-19562_128-19553del	XM_017003099.1:c.128-19560_128-19553del	XM_017003099.1:c.128-19559_128-19553del	XM_017003099.1:c.128-19558_128-19553del	XM_017003099.1:c.128-19557_128-19553del	XM_017003099.1:c.128-19556_128-19553del	XM_017003099.1:c.128-19555_128-19553del	XM_017003099.1:c.128-19554_128-19553del	XM_017003099.1:c.128-19553del	XM_017003099.1:c.128-19553dup	XM_017003099.1:c.128-19554_128-19553dup	XM_017003099.1:c.128-19555_128-19553dup	XM_017003099.1:c.128-19556_128-19553dup	XM_017003099.1:c.128-19558_128-19553dup
NEMP2 transcript variant X3	XM_017003100.2:c.128-19553=	XM_017003100.2:c.128-19562_128-19553del	XM_017003100.2:c.128-19560_128-19553del	XM_017003100.2:c.128-19559_128-19553del	XM_017003100.2:c.128-19558_128-19553del	XM_017003100.2:c.128-19557_128-19553del	XM_017003100.2:c.128-19556_128-19553del	XM_017003100.2:c.128-19555_128-19553del	XM_017003100.2:c.128-19554_128-19553del	XM_017003100.2:c.128-19553del	XM_017003100.2:c.128-19553dup	XM_017003100.2:c.128-19554_128-19553dup	XM_017003100.2:c.128-19555_128-19553dup	XM_017003100.2:c.128-19556_128-19553dup	XM_017003100.2:c.128-19558_128-19553dup
NEMP2 transcript variant X10	XM_047441958.1:c.-110-19553=	XM_047441958.1:c.-110-19562_-110-19553del	XM_047441958.1:c.-110-19560_-110-19553del	XM_047441958.1:c.-110-19559_-110-19553del	XM_047441958.1:c.-110-19558_-110-19553del	XM_047441958.1:c.-110-19557_-110-19553del	XM_047441958.1:c.-110-19556_-110-19553del	XM_047441958.1:c.-110-19555_-110-19553del	XM_047441958.1:c.-110-19554_-110-19553del	XM_047441958.1:c.-110-19553del	XM_047441958.1:c.-110-19553dup	XM_047441958.1:c.-110-19554_-110-19553dup	XM_047441958.1:c.-110-19555_-110-19553dup	XM_047441958.1:c.-110-19556_-110-19553dup	XM_047441958.1:c.-110-19558_-110-19553dup

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#.

55 SubSNP, 31 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41615384	Mar 14, 2006 (126)
2	HGSV	ss82060810	Aug 21, 2014 (142)
3	HUMANGENOME_JCVI	ss95296977	Feb 06, 2009 (130)
4	HUMANGENOME_JCVI	ss96734487	Feb 06, 2009 (137)
5	PJP	ss295019620	May 09, 2011 (137)
6	PJP	ss295019621	May 09, 2011 (134)
7	EVA_UK10K_TWINSUK	ss1703334422	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1703334425	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1710044433	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1710044434	Apr 01, 2015 (144)
11	SWEGEN	ss2991075432	Nov 08, 2017 (151)
12	EVA_DECODE	ss3705678204	Jul 13, 2019 (153)
13	EVA_DECODE	ss3705678205	Jul 13, 2019 (153)
14	EVA_DECODE	ss3705678206	Jul 13, 2019 (153)
15	EVA_DECODE	ss3705678207	Jul 13, 2019 (153)
16	EVA_DECODE	ss3705678208	Jul 13, 2019 (153)
17	ACPOP	ss3729222492	Jul 13, 2019 (153)
18	ACPOP	ss3729222493	Jul 13, 2019 (153)
19	EVA	ss3827419204	Apr 25, 2020 (154)
20	GNOMAD	ss4057911724	Apr 26, 2021 (155)
21	GNOMAD	ss4057911725	Apr 26, 2021 (155)
22	GNOMAD	ss4057911726	Apr 26, 2021 (155)
23	GNOMAD	ss4057911727	Apr 26, 2021 (155)
24	GNOMAD	ss4057911728	Apr 26, 2021 (155)
25	GNOMAD	ss4057911729	Apr 26, 2021 (155)
26	GNOMAD	ss4057911730	Apr 26, 2021 (155)
27	GNOMAD	ss4057911731	Apr 26, 2021 (155)
28	GNOMAD	ss4057911732	Apr 26, 2021 (155)
29	GNOMAD	ss4057911733	Apr 26, 2021 (155)
30	GNOMAD	ss4057911734	Apr 26, 2021 (155)
31	GNOMAD	ss4057911735	Apr 26, 2021 (155)
32	GNOMAD	ss4057911736	Apr 26, 2021 (155)
33	GNOMAD	ss4057911737	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5155697747	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5155697748	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5155697749	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5155697750	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5155697751	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5251416393	Oct 13, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5251416394	Oct 13, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5251416395	Oct 13, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5251416396	Oct 13, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5251416397	Oct 13, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5251416398	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5451093581	Oct 13, 2022 (156)
46	HUGCELL_USP	ss5451093582	Oct 13, 2022 (156)
47	HUGCELL_USP	ss5451093583	Oct 13, 2022 (156)
48	HUGCELL_USP	ss5451093584	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5686346259	Oct 13, 2022 (156)
50	TOMMO_GENOMICS	ss5686346260	Oct 13, 2022 (156)
51	TOMMO_GENOMICS	ss5686346261	Oct 13, 2022 (156)
52	TOMMO_GENOMICS	ss5686346262	Oct 13, 2022 (156)
53	TOMMO_GENOMICS	ss5686346263	Oct 13, 2022 (156)
54	EVA	ss5821355128	Oct 13, 2022 (156)
55	EVA	ss5821355129	Oct 13, 2022 (156)
56	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 6642222 (NC_000002.11:191409657:A: 2798/3854) Row 6642223 (NC_000002.11:191409656:AAA: 842/3854)	-	Oct 11, 2018 (152)
57	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 6642222 (NC_000002.11:191409657:A: 2798/3854) Row 6642223 (NC_000002.11:191409656:AAA: 842/3854)	-	Oct 11, 2018 (152)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 85671774 (NC_000002.12:190544930::A 2463/82442) Row 85671775 (NC_000002.12:190544930::AA 214/82518) Row 85671776 (NC_000002.12:190544930::AAA 57/82552)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 85671774 (NC_000002.12:190544930::A 2463/82442) Row 85671775 (NC_000002.12:190544930::AA 214/82518) Row 85671776 (NC_000002.12:190544930::AAA 57/82552)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 85671774 (NC_000002.12:190544930::A 2463/82442) Row 85671775 (NC_000002.12:190544930::AA 214/82518) Row 85671776 (NC_000002.12:190544930::AAA 57/82552)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 85671774 (NC_000002.12:190544930::A 2463/82442) Row 85671775 (NC_000002.12:190544930::AA 214/82518) Row 85671776 (NC_000002.12:190544930::AAA 57/82552)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 85671774 (NC_000002.12:190544930::A 2463/82442) Row 85671775 (NC_000002.12:190544930::AA 214/82518) Row 85671776 (NC_000002.12:190544930::AAA 57/82552)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 85671774 (NC_000002.12:190544930::A 2463/82442) Row 85671775 (NC_000002.12:190544930::AA 214/82518) Row 85671776 (NC_000002.12:190544930::AAA 57/82552)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 85671774 (NC_000002.12:190544930::A 2463/82442) Row 85671775 (NC_000002.12:190544930::AA 214/82518) Row 85671776 (NC_000002.12:190544930::AAA 57/82552)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 85671774 (NC_000002.12:190544930::A 2463/82442) Row 85671775 (NC_000002.12:190544930::AA 214/82518) Row 85671776 (NC_000002.12:190544930::AAA 57/82552)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 85671774 (NC_000002.12:190544930::A 2463/82442) Row 85671775 (NC_000002.12:190544930::AA 214/82518) Row 85671776 (NC_000002.12:190544930::AAA 57/82552)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 85671774 (NC_000002.12:190544930::A 2463/82442) Row 85671775 (NC_000002.12:190544930::AA 214/82518) Row 85671776 (NC_000002.12:190544930::AAA 57/82552)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 85671774 (NC_000002.12:190544930::A 2463/82442) Row 85671775 (NC_000002.12:190544930::AA 214/82518) Row 85671776 (NC_000002.12:190544930::AAA 57/82552)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 85671774 (NC_000002.12:190544930::A 2463/82442) Row 85671775 (NC_000002.12:190544930::AA 214/82518) Row 85671776 (NC_000002.12:190544930::AAA 57/82552)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 85671774 (NC_000002.12:190544930::A 2463/82442) Row 85671775 (NC_000002.12:190544930::AA 214/82518) Row 85671776 (NC_000002.12:190544930::AAA 57/82552)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 85671774 (NC_000002.12:190544930::A 2463/82442) Row 85671775 (NC_000002.12:190544930::AA 214/82518) Row 85671776 (NC_000002.12:190544930::AAA 57/82552)...	-	Apr 26, 2021 (155)
72	Northern Sweden Submission ignored due to conflicting rows: Row 2507357 (NC_000002.11:191409656:A: 101/584) Row 2507358 (NC_000002.11:191409656:AA: 95/584)	-	Jul 13, 2019 (153)
73	Northern Sweden Submission ignored due to conflicting rows: Row 2507357 (NC_000002.11:191409656:A: 101/584) Row 2507358 (NC_000002.11:191409656:AA: 95/584)	-	Jul 13, 2019 (153)
74	8.3KJPN Submission ignored due to conflicting rows: Row 13667054 (NC_000002.11:191409656:A: 4827/16662) Row 13667055 (NC_000002.11:191409656:AA: 4192/16662) Row 13667056 (NC_000002.11:191409656::A 308/16662)...	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 13667054 (NC_000002.11:191409656:A: 4827/16662) Row 13667055 (NC_000002.11:191409656:AA: 4192/16662) Row 13667056 (NC_000002.11:191409656::A 308/16662)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 13667054 (NC_000002.11:191409656:A: 4827/16662) Row 13667055 (NC_000002.11:191409656:AA: 4192/16662) Row 13667056 (NC_000002.11:191409656::A 308/16662)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 13667054 (NC_000002.11:191409656:A: 4827/16662) Row 13667055 (NC_000002.11:191409656:AA: 4192/16662) Row 13667056 (NC_000002.11:191409656::A 308/16662)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 13667054 (NC_000002.11:191409656:A: 4827/16662) Row 13667055 (NC_000002.11:191409656:AA: 4192/16662) Row 13667056 (NC_000002.11:191409656::A 308/16662)...	-	Apr 26, 2021 (155)
79	14KJPN Submission ignored due to conflicting rows: Row 20183363 (NC_000002.12:190544930:AA: 7538/28066) Row 20183364 (NC_000002.12:190544930:A: 8351/28066) Row 20183365 (NC_000002.12:190544930::A 493/28066)...	-	Oct 13, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 20183363 (NC_000002.12:190544930:AA: 7538/28066) Row 20183364 (NC_000002.12:190544930:A: 8351/28066) Row 20183365 (NC_000002.12:190544930::A 493/28066)...	-	Oct 13, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 20183363 (NC_000002.12:190544930:AA: 7538/28066) Row 20183364 (NC_000002.12:190544930:A: 8351/28066) Row 20183365 (NC_000002.12:190544930::A 493/28066)...	-	Oct 13, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 20183363 (NC_000002.12:190544930:AA: 7538/28066) Row 20183364 (NC_000002.12:190544930:A: 8351/28066) Row 20183365 (NC_000002.12:190544930::A 493/28066)...	-	Oct 13, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 20183363 (NC_000002.12:190544930:AA: 7538/28066) Row 20183364 (NC_000002.12:190544930:A: 8351/28066) Row 20183365 (NC_000002.12:190544930::A 493/28066)...	-	Oct 13, 2022 (156)
84	UK 10K study - Twins Submission ignored due to conflicting rows: Row 6642222 (NC_000002.11:191409657:A: 2645/3708) Row 6642223 (NC_000002.11:191409656:AAA: 851/3708)	-	Oct 11, 2018 (152)
85	UK 10K study - Twins Submission ignored due to conflicting rows: Row 6642222 (NC_000002.11:191409657:A: 2645/3708) Row 6642223 (NC_000002.11:191409656:AAA: 851/3708)	-	Oct 11, 2018 (152)
86	ALFA	NC_000002.12 - 190544931	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)
rs57498245	Oct 12, 2011 (135)
rs67817858	May 11, 2012 (137)
rs67817859	Feb 27, 2009 (130)
rs67817860	Feb 27, 2009 (130)
rs71902306	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4057911737	NC_000002.12:190544930:AAAAAAAAAA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
2975620598	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5155697751	NC_000002.11:191409656:AAAAAAAA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4057911736, ss5686346263	NC_000002.12:190544930:AAAAAAAA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
2975620598	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4057911735	NC_000002.12:190544930:AAAAAAA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
2975620598	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4057911734	NC_000002.12:190544930:AAAAAA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
2975620598	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3705678208, ss4057911733	NC_000002.12:190544930:AAAAA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4057911732	NC_000002.12:190544930:AAAA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
2975620598	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss1703334422, ss1703334425, ss5155697750, ss5821355129	NC_000002.11:191409656:AAA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4057911731, ss5251416398, ss5451093584, ss5686346262	NC_000002.12:190544930:AAA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
2975620598	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3705678207	NC_000002.12:190544932:AAA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss82060810	NC_000002.9:191235183:AA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss2991075432, ss3729222493, ss3827419204, ss5155697748, ss5821355128	NC_000002.11:191409656:AA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss1710044433, ss1710044434	NC_000002.11:191409657:AA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4057911730, ss5251416393, ss5451093583, ss5686346259	NC_000002.12:190544930:AA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
2975620598	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3705678206	NC_000002.12:190544933:AA:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss295019620	NC_000002.10:191117901:A:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss295019621	NC_000002.10:191117923:A:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3729222492, ss5155697747	NC_000002.11:191409656:A:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
	NC_000002.11:191409657:A:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4057911729, ss5251416394, ss5451093581, ss5686346260	NC_000002.12:190544930:A:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
2975620598	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3705678205	NC_000002.12:190544934:A:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss96734487	NT_005403.17:41619074:A:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss41615384, ss95296977	NT_005403.17:41619096:A:	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5155697749	NC_000002.11:191409656::A	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4057911724, ss5251416395, ss5451093582, ss5686346261	NC_000002.12:190544930::A	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
2975620598	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3705678204	NC_000002.12:190544935::A	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4057911725, ss5251416396	NC_000002.12:190544930::AA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2975620598	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4057911726, ss5251416397	NC_000002.12:190544930::AAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2975620598	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4057911727	NC_000002.12:190544930::AAAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2975620598	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4057911728	NC_000002.12:190544930::AAAAAA	NC_000002.12:190544930:AAAAAAAAAAA… NC_000002.12:190544930:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs11284510

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

rs11284510