Name: rs11413210
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.

rs11413210

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:120850493-120850513 (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)₅ / del(A)₄ / delAAA / delAA…
del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₈ / dup(A)₉ / dup(A)₁₀ / dup(A)₁₁ / dup(A)₁₃ / dup(A)₁₄ / dup(A)₁₆ / dup(A)₁₉ / ins(A)₃₆ / ins(A)₃₈ / ins(A)₃₉
Variation Type: Indel Insertion and Deletion
Frequency: (A)₂₁=0.0521 (261/5008, 1000G)
(A)₂₁=0.3586 (1590/4434, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SPPL3 : 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	4434	AAAAAAAAAAAAAAAAAAAAA=0.3586	AAAAAAAAAAAAAAAAAA=0.0016, AAAAAAAAAAAAAAAAAAA=0.4023, AAAAAAAAAAAAAAAAAAAAAA=0.1910, AAAAAAAAAAAAAAAAAAAAAAA=0.0171, AAAAAAAAAAAAAAAAAAAA=0.0117, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0176, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.384226	0.304631	0.311143	32
European	Sub	4386	AAAAAAAAAAAAAAAAAAAAA=0.3527	AAAAAAAAAAAAAAAAAA=0.0016, AAAAAAAAAAAAAAAAAAA=0.4058, AAAAAAAAAAAAAAAAAAAAAA=0.1931, AAAAAAAAAAAAAAAAAAAAAAA=0.0173, AAAAAAAAAAAAAAAAAAAA=0.0116, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0178, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.375276	0.308315	0.316409	32
African	Sub	32	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	2	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	30	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
East Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 2	Sub	4	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	8	AAAAAAAAAAAAAAAAAAAAA=0.4	AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.5, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.1, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	0.333333	0.666667	0.0	2

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)₂₁=0.0521	delAA=0.9479
1000Genomes	African	Sub	1322	(A)₂₁=0.0900	delAA=0.9100
1000Genomes	East Asian	Sub	1008	(A)₂₁=0.0198	delAA=0.9802
1000Genomes	Europe	Sub	1006	(A)₂₁=0.0507	delAA=0.9493
1000Genomes	South Asian	Sub	978	(A)₂₁=0.051	delAA=0.949
1000Genomes	American	Sub	694	(A)₂₁=0.030	delAA=0.970
Allele Frequency Aggregator	Total	Global	4434	(A)₂₁=0.3586	delAAA=0.0016, delAA=0.4023, delA=0.0117, dupA=0.1910, dupAA=0.0171, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₈=0.0176
Allele Frequency Aggregator	European	Sub	4386	(A)₂₁=0.3527	delAAA=0.0016, delAA=0.4058, delA=0.0116, dupA=0.1931, dupAA=0.0173, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₈=0.0178
Allele Frequency Aggregator	African	Sub	32	(A)₂₁=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₈=0.00
Allele Frequency Aggregator	Other	Sub	8	(A)₂₁=0.4	delAAA=0.0, delAA=0.5, delA=0.1, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₈=0.0
Allele Frequency Aggregator	Latin American 2	Sub	4	(A)₂₁=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₈=0.0
Allele Frequency Aggregator	South Asian	Sub	4	(A)₂₁=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₈=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(A)₂₁=0	delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0, dup(A)₈=0
Allele Frequency Aggregator	Asian	Sub	0	(A)₂₁=0	delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0, dup(A)₄=0, dup(A)₈=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 12	NC_000012.12:g.120850509_120850513del
GRCh38.p14 chr 12	NC_000012.12:g.120850510_120850513del
GRCh38.p14 chr 12	NC_000012.12:g.120850511_120850513del
GRCh38.p14 chr 12	NC_000012.12:g.120850512_120850513del
GRCh38.p14 chr 12	NC_000012.12:g.120850513del
GRCh38.p14 chr 12	NC_000012.12:g.120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850512_120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850511_120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850510_120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850509_120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850508_120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850507_120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850506_120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850505_120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850504_120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850503_120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850501_120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850500_120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850498_120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850495_120850513dup
GRCh38.p14 chr 12	NC_000012.12:g.120850513_120850514insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 12	NC_000012.12:g.120850513_120850514insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 12	NC_000012.12:g.120850513_120850514insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 12	NC_000012.11:g.121288312_121288316del
GRCh37.p13 chr 12	NC_000012.11:g.121288313_121288316del
GRCh37.p13 chr 12	NC_000012.11:g.121288314_121288316del
GRCh37.p13 chr 12	NC_000012.11:g.121288315_121288316del
GRCh37.p13 chr 12	NC_000012.11:g.121288316del
GRCh37.p13 chr 12	NC_000012.11:g.121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288315_121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288314_121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288313_121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288312_121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288311_121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288310_121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288309_121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288308_121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288307_121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288306_121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288304_121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288303_121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288301_121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288298_121288316dup
GRCh37.p13 chr 12	NC_000012.11:g.121288316_121288317insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 12	NC_000012.11:g.121288316_121288317insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 12	NC_000012.11:g.121288316_121288317insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: SPPL3, signal peptide peptidase like 3 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SPPL3 transcript	NM_139015.5:c.24-39611_24… NM_139015.5:c.24-39611_24-39607del	N/A	Intron Variant
SPPL3 transcript variant X1	XM_011537925.3:c.23+16022… XM_011537925.3:c.23+16022_23+16026del	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)₂₁=	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₈	dup(A)₉	dup(A)₁₀	dup(A)₁₁	dup(A)₁₃	dup(A)₁₄	dup(A)₁₆	dup(A)₁₉	ins(A)₃₆	ins(A)₃₈	ins(A)₃₉
GRCh38.p14 chr 12	NC_000012.12:g.120850493_120850513=	NC_000012.12:g.120850509_120850513del	NC_000012.12:g.120850510_120850513del	NC_000012.12:g.120850511_120850513del	NC_000012.12:g.120850512_120850513del	NC_000012.12:g.120850513del	NC_000012.12:g.120850513dup	NC_000012.12:g.120850512_120850513dup	NC_000012.12:g.120850511_120850513dup	NC_000012.12:g.120850510_120850513dup	NC_000012.12:g.120850509_120850513dup	NC_000012.12:g.120850508_120850513dup	NC_000012.12:g.120850507_120850513dup	NC_000012.12:g.120850506_120850513dup	NC_000012.12:g.120850505_120850513dup	NC_000012.12:g.120850504_120850513dup	NC_000012.12:g.120850503_120850513dup	NC_000012.12:g.120850501_120850513dup	NC_000012.12:g.120850500_120850513dup	NC_000012.12:g.120850498_120850513dup	NC_000012.12:g.120850495_120850513dup	NC_000012.12:g.120850513_120850514insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:g.120850513_120850514insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:g.120850513_120850514insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 12	NC_000012.11:g.121288296_121288316=	NC_000012.11:g.121288312_121288316del	NC_000012.11:g.121288313_121288316del	NC_000012.11:g.121288314_121288316del	NC_000012.11:g.121288315_121288316del	NC_000012.11:g.121288316del	NC_000012.11:g.121288316dup	NC_000012.11:g.121288315_121288316dup	NC_000012.11:g.121288314_121288316dup	NC_000012.11:g.121288313_121288316dup	NC_000012.11:g.121288312_121288316dup	NC_000012.11:g.121288311_121288316dup	NC_000012.11:g.121288310_121288316dup	NC_000012.11:g.121288309_121288316dup	NC_000012.11:g.121288308_121288316dup	NC_000012.11:g.121288307_121288316dup	NC_000012.11:g.121288306_121288316dup	NC_000012.11:g.121288304_121288316dup	NC_000012.11:g.121288303_121288316dup	NC_000012.11:g.121288301_121288316dup	NC_000012.11:g.121288298_121288316dup	NC_000012.11:g.121288316_121288317insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000012.11:g.121288316_121288317insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000012.11:g.121288316_121288317insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SPPL3 transcript	NM_139015.4:c.24-39607=	NM_139015.4:c.24-39611_24-39607del	NM_139015.4:c.24-39610_24-39607del	NM_139015.4:c.24-39609_24-39607del	NM_139015.4:c.24-39608_24-39607del	NM_139015.4:c.24-39607del	NM_139015.4:c.24-39607dup	NM_139015.4:c.24-39608_24-39607dup	NM_139015.4:c.24-39609_24-39607dup	NM_139015.4:c.24-39610_24-39607dup	NM_139015.4:c.24-39611_24-39607dup	NM_139015.4:c.24-39612_24-39607dup	NM_139015.4:c.24-39613_24-39607dup	NM_139015.4:c.24-39614_24-39607dup	NM_139015.4:c.24-39615_24-39607dup	NM_139015.4:c.24-39616_24-39607dup	NM_139015.4:c.24-39617_24-39607dup	NM_139015.4:c.24-39619_24-39607dup	NM_139015.4:c.24-39620_24-39607dup	NM_139015.4:c.24-39622_24-39607dup	NM_139015.4:c.24-39625_24-39607dup	NM_139015.4:c.24-39607_24-39606insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_139015.4:c.24-39607_24-39606insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_139015.4:c.24-39607_24-39606insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SPPL3 transcript	NM_139015.5:c.24-39607=	NM_139015.5:c.24-39611_24-39607del	NM_139015.5:c.24-39610_24-39607del	NM_139015.5:c.24-39609_24-39607del	NM_139015.5:c.24-39608_24-39607del	NM_139015.5:c.24-39607del	NM_139015.5:c.24-39607dup	NM_139015.5:c.24-39608_24-39607dup	NM_139015.5:c.24-39609_24-39607dup	NM_139015.5:c.24-39610_24-39607dup	NM_139015.5:c.24-39611_24-39607dup	NM_139015.5:c.24-39612_24-39607dup	NM_139015.5:c.24-39613_24-39607dup	NM_139015.5:c.24-39614_24-39607dup	NM_139015.5:c.24-39615_24-39607dup	NM_139015.5:c.24-39616_24-39607dup	NM_139015.5:c.24-39617_24-39607dup	NM_139015.5:c.24-39619_24-39607dup	NM_139015.5:c.24-39620_24-39607dup	NM_139015.5:c.24-39622_24-39607dup	NM_139015.5:c.24-39625_24-39607dup	NM_139015.5:c.24-39607_24-39606insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_139015.5:c.24-39607_24-39606insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_139015.5:c.24-39607_24-39606insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SPPL3 transcript variant X1	XM_005253841.1:c.-88-39607=	XM_005253841.1:c.-88-39611_-88-39607del	XM_005253841.1:c.-88-39610_-88-39607del	XM_005253841.1:c.-88-39609_-88-39607del	XM_005253841.1:c.-88-39608_-88-39607del	XM_005253841.1:c.-88-39607del	XM_005253841.1:c.-88-39607dup	XM_005253841.1:c.-88-39608_-88-39607dup	XM_005253841.1:c.-88-39609_-88-39607dup	XM_005253841.1:c.-88-39610_-88-39607dup	XM_005253841.1:c.-88-39611_-88-39607dup	XM_005253841.1:c.-88-39612_-88-39607dup	XM_005253841.1:c.-88-39613_-88-39607dup	XM_005253841.1:c.-88-39614_-88-39607dup	XM_005253841.1:c.-88-39615_-88-39607dup	XM_005253841.1:c.-88-39616_-88-39607dup	XM_005253841.1:c.-88-39617_-88-39607dup	XM_005253841.1:c.-88-39619_-88-39607dup	XM_005253841.1:c.-88-39620_-88-39607dup	XM_005253841.1:c.-88-39622_-88-39607dup	XM_005253841.1:c.-88-39625_-88-39607dup	XM_005253841.1:c.-88-39607_-88-39606insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005253841.1:c.-88-39607_-88-39606insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005253841.1:c.-88-39607_-88-39606insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SPPL3 transcript variant X1	XM_011537925.3:c.23+16026=	XM_011537925.3:c.23+16022_23+16026del	XM_011537925.3:c.23+16023_23+16026del	XM_011537925.3:c.23+16024_23+16026del	XM_011537925.3:c.23+16025_23+16026del	XM_011537925.3:c.23+16026del	XM_011537925.3:c.23+16026dup	XM_011537925.3:c.23+16025_23+16026dup	XM_011537925.3:c.23+16024_23+16026dup	XM_011537925.3:c.23+16023_23+16026dup	XM_011537925.3:c.23+16022_23+16026dup	XM_011537925.3:c.23+16021_23+16026dup	XM_011537925.3:c.23+16020_23+16026dup	XM_011537925.3:c.23+16019_23+16026dup	XM_011537925.3:c.23+16018_23+16026dup	XM_011537925.3:c.23+16017_23+16026dup	XM_011537925.3:c.23+16016_23+16026dup	XM_011537925.3:c.23+16014_23+16026dup	XM_011537925.3:c.23+16013_23+16026dup	XM_011537925.3:c.23+16011_23+16026dup	XM_011537925.3:c.23+16008_23+16026dup	XM_011537925.3:c.23+16026_23+16027insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_011537925.3:c.23+16026_23+16027insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_011537925.3:c.23+16026_23+16027insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

75 SubSNP, 44 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	DEVINE_LAB	ss8061443	Mar 15, 2016 (147)
2	HGSV	ss82395200	Aug 21, 2014 (142)
3	HUMANGENOME_JCVI	ss95609397	Mar 15, 2016 (147)
4	PJP	ss294778289	Aug 21, 2014 (142)
5	PJP	ss294778290	May 09, 2011 (137)
6	BILGI_BIOE	ss666585945	Apr 25, 2013 (138)
7	1000GENOMES	ss1372711507	Aug 21, 2014 (142)
8	EVA_UK10K_ALSPAC	ss1707652585	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1707652632	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1710584031	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710584032	Apr 01, 2015 (144)
12	SWEGEN	ss3010462891	Nov 08, 2017 (151)
13	MCHAISSO	ss3063748852	Nov 08, 2017 (151)
14	MCHAISSO	ss3065501291	Nov 08, 2017 (151)
15	URBANLAB	ss3649935686	Oct 12, 2018 (152)
16	EVA_DECODE	ss3694609341	Jul 13, 2019 (153)
17	EVA_DECODE	ss3694609342	Jul 13, 2019 (153)
18	EVA_DECODE	ss3694609343	Jul 13, 2019 (153)
19	EVA_DECODE	ss3694609344	Jul 13, 2019 (153)
20	EVA_DECODE	ss3694609345	Jul 13, 2019 (153)
21	EVA_DECODE	ss3694609346	Jul 13, 2019 (153)
22	ACPOP	ss3739443761	Jul 13, 2019 (153)
23	ACPOP	ss3739443762	Jul 13, 2019 (153)
24	ACPOP	ss3739443763	Jul 13, 2019 (153)
25	ACPOP	ss3739443764	Jul 13, 2019 (153)
26	ACPOP	ss3739443765	Jul 13, 2019 (153)
27	PACBIO	ss3792434006	Jul 13, 2019 (153)
28	PACBIO	ss3797317161	Jul 13, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3816380023	Jul 13, 2019 (153)
30	EVA	ss3833362314	Apr 27, 2020 (154)
31	GNOMAD	ss4260232606	Apr 26, 2021 (155)
32	GNOMAD	ss4260232607	Apr 26, 2021 (155)
33	GNOMAD	ss4260232608	Apr 26, 2021 (155)
34	GNOMAD	ss4260232609	Apr 26, 2021 (155)
35	GNOMAD	ss4260232610	Apr 26, 2021 (155)
36	GNOMAD	ss4260232611	Apr 26, 2021 (155)
37	GNOMAD	ss4260232612	Apr 26, 2021 (155)
38	GNOMAD	ss4260232613	Apr 26, 2021 (155)
39	GNOMAD	ss4260232614	Apr 26, 2021 (155)
40	GNOMAD	ss4260232615	Apr 26, 2021 (155)
41	GNOMAD	ss4260232616	Apr 26, 2021 (155)
42	GNOMAD	ss4260232617	Apr 26, 2021 (155)
43	GNOMAD	ss4260232618	Apr 26, 2021 (155)
44	GNOMAD	ss4260232619	Apr 26, 2021 (155)
45	GNOMAD	ss4260232620	Apr 26, 2021 (155)
46	GNOMAD	ss4260232621	Apr 26, 2021 (155)
47	GNOMAD	ss4260232622	Apr 26, 2021 (155)
48	GNOMAD	ss4260232623	Apr 26, 2021 (155)
49	GNOMAD	ss4260232626	Apr 26, 2021 (155)
50	GNOMAD	ss4260232627	Apr 26, 2021 (155)
51	GNOMAD	ss4260232628	Apr 26, 2021 (155)
52	GNOMAD	ss4260232629	Apr 26, 2021 (155)
53	GNOMAD	ss4260232630	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5208490731	Apr 26, 2021 (155)
55	TOMMO_GENOMICS	ss5208490732	Apr 26, 2021 (155)
56	TOMMO_GENOMICS	ss5208490733	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5208490734	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5208490735	Apr 26, 2021 (155)
59	1000G_HIGH_COVERAGE	ss5292480990	Oct 16, 2022 (156)
60	1000G_HIGH_COVERAGE	ss5292480991	Oct 16, 2022 (156)
61	1000G_HIGH_COVERAGE	ss5292480992	Oct 16, 2022 (156)
62	1000G_HIGH_COVERAGE	ss5292480993	Oct 16, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5292480994	Oct 16, 2022 (156)
64	HUGCELL_USP	ss5487061255	Oct 16, 2022 (156)
65	HUGCELL_USP	ss5487061256	Oct 16, 2022 (156)
66	HUGCELL_USP	ss5487061257	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5758913441	Oct 16, 2022 (156)
68	TOMMO_GENOMICS	ss5758913442	Oct 16, 2022 (156)
69	TOMMO_GENOMICS	ss5758913443	Oct 16, 2022 (156)
70	TOMMO_GENOMICS	ss5758913444	Oct 16, 2022 (156)
71	TOMMO_GENOMICS	ss5758913445	Oct 16, 2022 (156)
72	EVA	ss5838610075	Oct 16, 2022 (156)
73	EVA	ss5838610076	Oct 16, 2022 (156)
74	EVA	ss5838610077	Oct 16, 2022 (156)
75	EVA	ss5850577588	Oct 16, 2022 (156)
76	1000Genomes	NC_000012.11 - 121288296	Oct 12, 2018 (152)
77	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 33182470 (NC_000012.11:121288296:A: 3150/3854) Row 33182471 (NC_000012.11:121288295:AAA: 699/3854)	-	Oct 12, 2018 (152)
78	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 33182470 (NC_000012.11:121288296:A: 3150/3854) Row 33182471 (NC_000012.11:121288295:AAA: 699/3854)	-	Oct 12, 2018 (152)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421361988 (NC_000012.12:120850492::A 21710/108544) Row 421361989 (NC_000012.12:120850492::AA 770/109712) Row 421361990 (NC_000012.12:120850492::AAA 46/109916)...	-	Apr 26, 2021 (155)
102	Northern Sweden Submission ignored due to conflicting rows: Row 12728626 (NC_000012.11:121288295:AA: 216/580) Row 12728627 (NC_000012.11:121288295::AAAAAAAAAA 20/580) Row 12728628 (NC_000012.11:121288295::AAAAAAAA 28/580)...	-	Jul 13, 2019 (153)
103	Northern Sweden Submission ignored due to conflicting rows: Row 12728626 (NC_000012.11:121288295:AA: 216/580) Row 12728627 (NC_000012.11:121288295::AAAAAAAAAA 20/580) Row 12728628 (NC_000012.11:121288295::AAAAAAAA 28/580)...	-	Jul 13, 2019 (153)
104	Northern Sweden Submission ignored due to conflicting rows: Row 12728626 (NC_000012.11:121288295:AA: 216/580) Row 12728627 (NC_000012.11:121288295::AAAAAAAAAA 20/580) Row 12728628 (NC_000012.11:121288295::AAAAAAAA 28/580)...	-	Jul 13, 2019 (153)
105	Northern Sweden Submission ignored due to conflicting rows: Row 12728626 (NC_000012.11:121288295:AA: 216/580) Row 12728627 (NC_000012.11:121288295::AAAAAAAAAA 20/580) Row 12728628 (NC_000012.11:121288295::AAAAAAAA 28/580)...	-	Jul 13, 2019 (153)
106	Northern Sweden Submission ignored due to conflicting rows: Row 12728626 (NC_000012.11:121288295:AA: 216/580) Row 12728627 (NC_000012.11:121288295::AAAAAAAAAA 20/580) Row 12728628 (NC_000012.11:121288295::AAAAAAAA 28/580)...	-	Jul 13, 2019 (153)
107	8.3KJPN Submission ignored due to conflicting rows: Row 66460038 (NC_000012.11:121288295:AA: 12800/16686) Row 66460039 (NC_000012.11:121288295::A 2337/16686) Row 66460040 (NC_000012.11:121288295::AA 231/16686)...	-	Apr 26, 2021 (155)
108	8.3KJPN Submission ignored due to conflicting rows: Row 66460038 (NC_000012.11:121288295:AA: 12800/16686) Row 66460039 (NC_000012.11:121288295::A 2337/16686) Row 66460040 (NC_000012.11:121288295::AA 231/16686)...	-	Apr 26, 2021 (155)
109	8.3KJPN Submission ignored due to conflicting rows: Row 66460038 (NC_000012.11:121288295:AA: 12800/16686) Row 66460039 (NC_000012.11:121288295::A 2337/16686) Row 66460040 (NC_000012.11:121288295::AA 231/16686)...	-	Apr 26, 2021 (155)
110	8.3KJPN Submission ignored due to conflicting rows: Row 66460038 (NC_000012.11:121288295:AA: 12800/16686) Row 66460039 (NC_000012.11:121288295::A 2337/16686) Row 66460040 (NC_000012.11:121288295::AA 231/16686)...	-	Apr 26, 2021 (155)
111	8.3KJPN Submission ignored due to conflicting rows: Row 66460038 (NC_000012.11:121288295:AA: 12800/16686) Row 66460039 (NC_000012.11:121288295::A 2337/16686) Row 66460040 (NC_000012.11:121288295::AA 231/16686)...	-	Apr 26, 2021 (155)
112	14KJPN Submission ignored due to conflicting rows: Row 92750545 (NC_000012.12:120850492:AA: 22003/28228) Row 92750546 (NC_000012.12:120850492:A: 165/28228) Row 92750547 (NC_000012.12:120850492::A 4318/28228)...	-	Oct 16, 2022 (156)
113	14KJPN Submission ignored due to conflicting rows: Row 92750545 (NC_000012.12:120850492:AA: 22003/28228) Row 92750546 (NC_000012.12:120850492:A: 165/28228) Row 92750547 (NC_000012.12:120850492::A 4318/28228)...	-	Oct 16, 2022 (156)
114	14KJPN Submission ignored due to conflicting rows: Row 92750545 (NC_000012.12:120850492:AA: 22003/28228) Row 92750546 (NC_000012.12:120850492:A: 165/28228) Row 92750547 (NC_000012.12:120850492::A 4318/28228)...	-	Oct 16, 2022 (156)
115	14KJPN Submission ignored due to conflicting rows: Row 92750545 (NC_000012.12:120850492:AA: 22003/28228) Row 92750546 (NC_000012.12:120850492:A: 165/28228) Row 92750547 (NC_000012.12:120850492::A 4318/28228)...	-	Oct 16, 2022 (156)
116	14KJPN Submission ignored due to conflicting rows: Row 92750545 (NC_000012.12:120850492:AA: 22003/28228) Row 92750546 (NC_000012.12:120850492:A: 165/28228) Row 92750547 (NC_000012.12:120850492::A 4318/28228)...	-	Oct 16, 2022 (156)
117	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33182470 (NC_000012.11:121288296:A: 3111/3708) Row 33182471 (NC_000012.11:121288295:AAA: 595/3708)	-	Oct 12, 2018 (152)
118	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33182470 (NC_000012.11:121288296:A: 3111/3708) Row 33182471 (NC_000012.11:121288295:AAA: 595/3708)	-	Oct 12, 2018 (152)
119	ALFA	NC_000012.12 - 120850493	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)
rs139298197	May 11, 2012 (137)
rs374743510	May 13, 2013 (138)
rs59181367	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4260232630	NC_000012.12:120850492:AAAAA:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4260232629	NC_000012.12:120850492:AAAA:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss1707652585, ss1707652632, ss5208490734, ss5838610076	NC_000012.11:121288295:AAA:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3694609346, ss4260232628, ss5292480993, ss5758913445	NC_000012.12:120850492:AAA:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
8664447173	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss82395200	NC_000012.9:119751034:AA:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss294778289	NC_000012.10:119772678:AA:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss294778290	NC_000012.10:119772697:AA:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
59737544, ss666585945, ss1372711507, ss3010462891, ss3739443761, ss3792434006, ss3797317161, ss3833362314, ss5208490731, ss5838610075	NC_000012.11:121288295:AA:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss1710584031, ss1710584032	NC_000012.11:121288296:AA:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3063748852, ss3065501291, ss3649935686, ss3816380023, ss4260232627, ss5292480990, ss5487061255, ss5758913441, ss5850577588	NC_000012.12:120850492:AA:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
8664447173	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3694609345	NC_000012.12:120850493:AA:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss8061443	NT_009775.17:11864825:AA:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss95609397	NT_009775.17:11864844:AA:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5208490735	NC_000012.11:121288295:A:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
	NC_000012.11:121288296:A:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4260232626, ss5292480992, ss5487061256, ss5758913442	NC_000012.12:120850492:A:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
8664447173	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3694609344	NC_000012.12:120850494:A:	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3739443764, ss5208490732	NC_000012.11:121288295::A	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232606, ss5292480991, ss5487061257, ss5758913443	NC_000012.12:120850492::A	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
8664447173	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3694609343	NC_000012.12:120850495::A	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5208490733	NC_000012.11:121288295::AA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232607, ss5292480994, ss5758913444	NC_000012.12:120850492::AA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
8664447173	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3694609342	NC_000012.12:120850495::AA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232608	NC_000012.12:120850492::AAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
8664447173	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232609	NC_000012.12:120850492::AAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
8664447173	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3694609341	NC_000012.12:120850495::AAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232610	NC_000012.12:120850492::AAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232611	NC_000012.12:120850492::AAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5838610077	NC_000012.11:121288295::AAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA
ss4260232612	NC_000012.12:120850492::AAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3739443763	NC_000012.11:121288295::AAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232613	NC_000012.12:120850492::AAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
8664447173	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232614	NC_000012.12:120850492::AAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3739443762	NC_000012.11:121288295::AAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232615	NC_000012.12:120850492::AAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3739443765	NC_000012.11:121288295::AAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232616	NC_000012.12:120850492::AAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232617	NC_000012.12:120850492::AAAAAAAAAA… NC_000012.12:120850492::AAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232618	NC_000012.12:120850492::AAAAAAAAAA… NC_000012.12:120850492::AAAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232619	NC_000012.12:120850492::AAAAAAAAAA… NC_000012.12:120850492::AAAAAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232620	NC_000012.12:120850492::AAAAAAAAAA… NC_000012.12:120850492::AAAAAAAAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232621	NC_000012.12:120850492::AAAAAAAAAA… NC_000012.12:120850492::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232622	NC_000012.12:120850492::AAAAAAAAAA… NC_000012.12:120850492::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4260232623	NC_000012.12:120850492::AAAAAAAAAA… NC_000012.12:120850492::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000012.12:120850492:AAAAAAAAAAA… NC_000012.12:120850492:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs11413210

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

rs11413210