Name: rs11400833
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.

rs11400833

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:206639466-206639485 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₇ / del(T)₆ / del(T)₅ / del(…
del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / ins(T)₂₇ / ins(T)₃₆C(T)₂₄
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.14132 (1431/10126, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DYRK3 : 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	10126	TTTTTTTTTTTTTTTTTTTT=0.85404	TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.14132, TTTTTTTTTTTTTTTTTTTTTT=0.00395, TTTTTTTTTTTTTTTTTTTTTTT=0.00049, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT=0.00010, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00010	0.791476	0.072894	0.13563	32
European	Sub	9098	TTTTTTTTTTTTTTTTTTTT=0.8378	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.1571, TTTTTTTTTTTTTTTTTTTTTT=0.0044, TTTTTTTTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT=0.0001, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0001	0.767917	0.080985	0.151098	32
African	Sub	562	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	34	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	528	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	44	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	36	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	30	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	164	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	54	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	174	TTTTTTTTTTTTTTTTTTTT=0.989	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.011, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.988506	0.011494	0.0	32

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
Allele Frequency Aggregator	Total	Global	10126	(T)₂₀=0.85404	del(T)₇=0.00000, del(T)₆=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.14132, dupTT=0.00395, dupTTT=0.00049, ins(T)₂₇=0.00010, ins(T)₃₆C(T)₂₄=0.00010
Allele Frequency Aggregator	European	Sub	9098	(T)₂₀=0.8378	del(T)₇=0.0000, del(T)₆=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1571, dupTT=0.0044, dupTTT=0.0005, ins(T)₂₇=0.0001, ins(T)₃₆C(T)₂₄=0.0001
Allele Frequency Aggregator	African	Sub	562	(T)₂₀=1.000	del(T)₇=0.000, del(T)₆=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, ins(T)₂₇=0.000, ins(T)₃₆C(T)₂₄=0.000
Allele Frequency Aggregator	Other	Sub	174	(T)₂₀=0.989	del(T)₇=0.000, del(T)₆=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.011, dupTT=0.000, dupTTT=0.000, ins(T)₂₇=0.000, ins(T)₃₆C(T)₂₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	164	(T)₂₀=1.000	del(T)₇=0.000, del(T)₆=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, ins(T)₂₇=0.000, ins(T)₃₆C(T)₂₄=0.000
Allele Frequency Aggregator	South Asian	Sub	54	(T)₂₀=1.00	del(T)₇=0.00, del(T)₆=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, ins(T)₂₇=0.00, ins(T)₃₆C(T)₂₄=0.00
Allele Frequency Aggregator	Asian	Sub	44	(T)₂₀=1.00	del(T)₇=0.00, del(T)₆=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, ins(T)₂₇=0.00, ins(T)₃₆C(T)₂₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	30	(T)₂₀=1.00	del(T)₇=0.00, del(T)₆=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, ins(T)₂₇=0.00, ins(T)₃₆C(T)₂₄=0.00

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 1	NC_000001.11:g.206639479_206639485del
GRCh38.p14 chr 1	NC_000001.11:g.206639480_206639485del
GRCh38.p14 chr 1	NC_000001.11:g.206639481_206639485del
GRCh38.p14 chr 1	NC_000001.11:g.206639482_206639485del
GRCh38.p14 chr 1	NC_000001.11:g.206639483_206639485del
GRCh38.p14 chr 1	NC_000001.11:g.206639484_206639485del
GRCh38.p14 chr 1	NC_000001.11:g.206639485del
GRCh38.p14 chr 1	NC_000001.11:g.206639485dup
GRCh38.p14 chr 1	NC_000001.11:g.206639484_206639485dup
GRCh38.p14 chr 1	NC_000001.11:g.206639483_206639485dup
GRCh38.p14 chr 1	NC_000001.11:g.206639482_206639485dup
GRCh38.p14 chr 1	NC_000001.11:g.206639481_206639485dup
GRCh38.p14 chr 1	NC_000001.11:g.206639480_206639485dup
GRCh38.p14 chr 1	NC_000001.11:g.206639479_206639485dup
GRCh38.p14 chr 1	NC_000001.11:g.206639485_206639486insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.206639466_206639485T[56]CTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 1	NC_000001.10:g.206812824_206812830del
GRCh37.p13 chr 1	NC_000001.10:g.206812825_206812830del
GRCh37.p13 chr 1	NC_000001.10:g.206812826_206812830del
GRCh37.p13 chr 1	NC_000001.10:g.206812827_206812830del
GRCh37.p13 chr 1	NC_000001.10:g.206812828_206812830del
GRCh37.p13 chr 1	NC_000001.10:g.206812829_206812830del
GRCh37.p13 chr 1	NC_000001.10:g.206812830del
GRCh37.p13 chr 1	NC_000001.10:g.206812830dup
GRCh37.p13 chr 1	NC_000001.10:g.206812829_206812830dup
GRCh37.p13 chr 1	NC_000001.10:g.206812828_206812830dup
GRCh37.p13 chr 1	NC_000001.10:g.206812827_206812830dup
GRCh37.p13 chr 1	NC_000001.10:g.206812826_206812830dup
GRCh37.p13 chr 1	NC_000001.10:g.206812825_206812830dup
GRCh37.p13 chr 1	NC_000001.10:g.206812824_206812830dup
GRCh37.p13 chr 1	NC_000001.10:g.206812830_206812831insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.206812811_206812830T[56]CTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630333_630339del
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630334_630339del
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630335_630339del
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630336_630339del
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630337_630339del
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630338_630339del
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630339del
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630339dup
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630338_630339dup
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630337_630339dup
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630336_630339dup
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630335_630339dup
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630334_630339dup
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630333_630339dup
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630339_630340insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630320_630339T[56]CTTTTTTTTTTTTTTTTTTTTTTTT[1]

Gene: DYRK3, dual specificity tyrosine phosphorylation regulated kinase 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DYRK3 transcript variant 2	NM_001004023.3:c.129+1718… NM_001004023.3:c.129+1718_129+1724del	N/A	Intron Variant
DYRK3 transcript variant 1	NM_003582.4:c.189+1718_18… NM_003582.4:c.189+1718_189+1724del	N/A	Intron Variant
DYRK3 transcript variant X1	XM_005273315.5:c.129+1718… XM_005273315.5:c.129+1718_129+1724del	N/A	Intron Variant
DYRK3 transcript variant X4	XM_011510061.3:c.84+1718_… XM_011510061.3:c.84+1718_84+1724del	N/A	Intron Variant
DYRK3 transcript variant X2	XM_047432114.1:c.129+1718… XM_047432114.1:c.129+1718_129+1724del	N/A	Intron Variant
DYRK3 transcript variant X3	XM_047432115.1:c.129+1718… XM_047432115.1:c.129+1718_129+1724del	N/A	Intron Variant
DYRK3 transcript variant X5	XM_047432118.1:c.84+1718_… XM_047432118.1:c.84+1718_84+1724del	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₀=	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	ins(T)₂₇	ins(T)₃₆C(T)₂₄
GRCh38.p14 chr 1	NC_000001.11:g.206639466_206639485=	NC_000001.11:g.206639479_206639485del	NC_000001.11:g.206639480_206639485del	NC_000001.11:g.206639481_206639485del	NC_000001.11:g.206639482_206639485del	NC_000001.11:g.206639483_206639485del	NC_000001.11:g.206639484_206639485del	NC_000001.11:g.206639485del	NC_000001.11:g.206639485dup	NC_000001.11:g.206639484_206639485dup	NC_000001.11:g.206639483_206639485dup	NC_000001.11:g.206639482_206639485dup	NC_000001.11:g.206639481_206639485dup	NC_000001.11:g.206639480_206639485dup	NC_000001.11:g.206639479_206639485dup	NC_000001.11:g.206639485_206639486insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.206639466_206639485T[56]CTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 1	NC_000001.10:g.206812811_206812830=	NC_000001.10:g.206812824_206812830del	NC_000001.10:g.206812825_206812830del	NC_000001.10:g.206812826_206812830del	NC_000001.10:g.206812827_206812830del	NC_000001.10:g.206812828_206812830del	NC_000001.10:g.206812829_206812830del	NC_000001.10:g.206812830del	NC_000001.10:g.206812830dup	NC_000001.10:g.206812829_206812830dup	NC_000001.10:g.206812828_206812830dup	NC_000001.10:g.206812827_206812830dup	NC_000001.10:g.206812826_206812830dup	NC_000001.10:g.206812825_206812830dup	NC_000001.10:g.206812824_206812830dup	NC_000001.10:g.206812830_206812831insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.206812811_206812830T[56]CTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 1 fix patch HG1293_PATCH	NW_003871057.1:g.630320_630339=	NW_003871057.1:g.630333_630339del	NW_003871057.1:g.630334_630339del	NW_003871057.1:g.630335_630339del	NW_003871057.1:g.630336_630339del	NW_003871057.1:g.630337_630339del	NW_003871057.1:g.630338_630339del	NW_003871057.1:g.630339del	NW_003871057.1:g.630339dup	NW_003871057.1:g.630338_630339dup	NW_003871057.1:g.630337_630339dup	NW_003871057.1:g.630336_630339dup	NW_003871057.1:g.630335_630339dup	NW_003871057.1:g.630334_630339dup	NW_003871057.1:g.630333_630339dup	NW_003871057.1:g.630339_630340insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NW_003871057.1:g.630320_630339T[56]CTTTTTTTTTTTTTTTTTTTTTTTT[1]
DYRK3 transcript variant 2	NM_001004023.1:c.129+1705=	NM_001004023.1:c.129+1718_129+1724del	NM_001004023.1:c.129+1719_129+1724del	NM_001004023.1:c.129+1720_129+1724del	NM_001004023.1:c.129+1721_129+1724del	NM_001004023.1:c.129+1722_129+1724del	NM_001004023.1:c.129+1723_129+1724del	NM_001004023.1:c.129+1724del	NM_001004023.1:c.129+1724dup	NM_001004023.1:c.129+1723_129+1724dup	NM_001004023.1:c.129+1722_129+1724dup	NM_001004023.1:c.129+1721_129+1724dup	NM_001004023.1:c.129+1720_129+1724dup	NM_001004023.1:c.129+1719_129+1724dup	NM_001004023.1:c.129+1718_129+1724dup	NM_001004023.1:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001004023.1:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT
DYRK3 transcript variant 2	NM_001004023.3:c.129+1705=	NM_001004023.3:c.129+1718_129+1724del	NM_001004023.3:c.129+1719_129+1724del	NM_001004023.3:c.129+1720_129+1724del	NM_001004023.3:c.129+1721_129+1724del	NM_001004023.3:c.129+1722_129+1724del	NM_001004023.3:c.129+1723_129+1724del	NM_001004023.3:c.129+1724del	NM_001004023.3:c.129+1724dup	NM_001004023.3:c.129+1723_129+1724dup	NM_001004023.3:c.129+1722_129+1724dup	NM_001004023.3:c.129+1721_129+1724dup	NM_001004023.3:c.129+1720_129+1724dup	NM_001004023.3:c.129+1719_129+1724dup	NM_001004023.3:c.129+1718_129+1724dup	NM_001004023.3:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001004023.3:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT
DYRK3 transcript variant 1	NM_003582.2:c.189+1705=	NM_003582.2:c.189+1718_189+1724del	NM_003582.2:c.189+1719_189+1724del	NM_003582.2:c.189+1720_189+1724del	NM_003582.2:c.189+1721_189+1724del	NM_003582.2:c.189+1722_189+1724del	NM_003582.2:c.189+1723_189+1724del	NM_003582.2:c.189+1724del	NM_003582.2:c.189+1724dup	NM_003582.2:c.189+1723_189+1724dup	NM_003582.2:c.189+1722_189+1724dup	NM_003582.2:c.189+1721_189+1724dup	NM_003582.2:c.189+1720_189+1724dup	NM_003582.2:c.189+1719_189+1724dup	NM_003582.2:c.189+1718_189+1724dup	NM_003582.2:c.189+1724_189+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_003582.2:c.189+1724_189+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT
DYRK3 transcript variant 1	NM_003582.4:c.189+1705=	NM_003582.4:c.189+1718_189+1724del	NM_003582.4:c.189+1719_189+1724del	NM_003582.4:c.189+1720_189+1724del	NM_003582.4:c.189+1721_189+1724del	NM_003582.4:c.189+1722_189+1724del	NM_003582.4:c.189+1723_189+1724del	NM_003582.4:c.189+1724del	NM_003582.4:c.189+1724dup	NM_003582.4:c.189+1723_189+1724dup	NM_003582.4:c.189+1722_189+1724dup	NM_003582.4:c.189+1721_189+1724dup	NM_003582.4:c.189+1720_189+1724dup	NM_003582.4:c.189+1719_189+1724dup	NM_003582.4:c.189+1718_189+1724dup	NM_003582.4:c.189+1724_189+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_003582.4:c.189+1724_189+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT
DYRK3 transcript variant X1	XM_005273315.1:c.129+1705=	XM_005273315.1:c.129+1718_129+1724del	XM_005273315.1:c.129+1719_129+1724del	XM_005273315.1:c.129+1720_129+1724del	XM_005273315.1:c.129+1721_129+1724del	XM_005273315.1:c.129+1722_129+1724del	XM_005273315.1:c.129+1723_129+1724del	XM_005273315.1:c.129+1724del	XM_005273315.1:c.129+1724dup	XM_005273315.1:c.129+1723_129+1724dup	XM_005273315.1:c.129+1722_129+1724dup	XM_005273315.1:c.129+1721_129+1724dup	XM_005273315.1:c.129+1720_129+1724dup	XM_005273315.1:c.129+1719_129+1724dup	XM_005273315.1:c.129+1718_129+1724dup	XM_005273315.1:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005273315.1:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT
DYRK3 transcript variant X1	XM_005273315.5:c.129+1705=	XM_005273315.5:c.129+1718_129+1724del	XM_005273315.5:c.129+1719_129+1724del	XM_005273315.5:c.129+1720_129+1724del	XM_005273315.5:c.129+1721_129+1724del	XM_005273315.5:c.129+1722_129+1724del	XM_005273315.5:c.129+1723_129+1724del	XM_005273315.5:c.129+1724del	XM_005273315.5:c.129+1724dup	XM_005273315.5:c.129+1723_129+1724dup	XM_005273315.5:c.129+1722_129+1724dup	XM_005273315.5:c.129+1721_129+1724dup	XM_005273315.5:c.129+1720_129+1724dup	XM_005273315.5:c.129+1719_129+1724dup	XM_005273315.5:c.129+1718_129+1724dup	XM_005273315.5:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005273315.5:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT
DYRK3 transcript variant X2	XM_005273316.1:c.129+1705=	XM_005273316.1:c.129+1718_129+1724del	XM_005273316.1:c.129+1719_129+1724del	XM_005273316.1:c.129+1720_129+1724del	XM_005273316.1:c.129+1721_129+1724del	XM_005273316.1:c.129+1722_129+1724del	XM_005273316.1:c.129+1723_129+1724del	XM_005273316.1:c.129+1724del	XM_005273316.1:c.129+1724dup	XM_005273316.1:c.129+1723_129+1724dup	XM_005273316.1:c.129+1722_129+1724dup	XM_005273316.1:c.129+1721_129+1724dup	XM_005273316.1:c.129+1720_129+1724dup	XM_005273316.1:c.129+1719_129+1724dup	XM_005273316.1:c.129+1718_129+1724dup	XM_005273316.1:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005273316.1:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT
DYRK3 transcript variant X1	XM_005277518.1:c.129+1705=	XM_005277518.1:c.129+1718_129+1724del	XM_005277518.1:c.129+1719_129+1724del	XM_005277518.1:c.129+1720_129+1724del	XM_005277518.1:c.129+1721_129+1724del	XM_005277518.1:c.129+1722_129+1724del	XM_005277518.1:c.129+1723_129+1724del	XM_005277518.1:c.129+1724del	XM_005277518.1:c.129+1724dup	XM_005277518.1:c.129+1723_129+1724dup	XM_005277518.1:c.129+1722_129+1724dup	XM_005277518.1:c.129+1721_129+1724dup	XM_005277518.1:c.129+1720_129+1724dup	XM_005277518.1:c.129+1719_129+1724dup	XM_005277518.1:c.129+1718_129+1724dup	XM_005277518.1:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005277518.1:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT
DYRK3 transcript variant X2	XM_005277519.1:c.129+1705=	XM_005277519.1:c.129+1718_129+1724del	XM_005277519.1:c.129+1719_129+1724del	XM_005277519.1:c.129+1720_129+1724del	XM_005277519.1:c.129+1721_129+1724del	XM_005277519.1:c.129+1722_129+1724del	XM_005277519.1:c.129+1723_129+1724del	XM_005277519.1:c.129+1724del	XM_005277519.1:c.129+1724dup	XM_005277519.1:c.129+1723_129+1724dup	XM_005277519.1:c.129+1722_129+1724dup	XM_005277519.1:c.129+1721_129+1724dup	XM_005277519.1:c.129+1720_129+1724dup	XM_005277519.1:c.129+1719_129+1724dup	XM_005277519.1:c.129+1718_129+1724dup	XM_005277519.1:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005277519.1:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT
DYRK3 transcript variant X4	XM_011510061.3:c.84+1705=	XM_011510061.3:c.84+1718_84+1724del	XM_011510061.3:c.84+1719_84+1724del	XM_011510061.3:c.84+1720_84+1724del	XM_011510061.3:c.84+1721_84+1724del	XM_011510061.3:c.84+1722_84+1724del	XM_011510061.3:c.84+1723_84+1724del	XM_011510061.3:c.84+1724del	XM_011510061.3:c.84+1724dup	XM_011510061.3:c.84+1723_84+1724dup	XM_011510061.3:c.84+1722_84+1724dup	XM_011510061.3:c.84+1721_84+1724dup	XM_011510061.3:c.84+1720_84+1724dup	XM_011510061.3:c.84+1719_84+1724dup	XM_011510061.3:c.84+1718_84+1724dup	XM_011510061.3:c.84+1724_84+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_011510061.3:c.84+1724_84+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT
DYRK3 transcript variant X2	XM_047432114.1:c.129+1705=	XM_047432114.1:c.129+1718_129+1724del	XM_047432114.1:c.129+1719_129+1724del	XM_047432114.1:c.129+1720_129+1724del	XM_047432114.1:c.129+1721_129+1724del	XM_047432114.1:c.129+1722_129+1724del	XM_047432114.1:c.129+1723_129+1724del	XM_047432114.1:c.129+1724del	XM_047432114.1:c.129+1724dup	XM_047432114.1:c.129+1723_129+1724dup	XM_047432114.1:c.129+1722_129+1724dup	XM_047432114.1:c.129+1721_129+1724dup	XM_047432114.1:c.129+1720_129+1724dup	XM_047432114.1:c.129+1719_129+1724dup	XM_047432114.1:c.129+1718_129+1724dup	XM_047432114.1:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047432114.1:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT
DYRK3 transcript variant X3	XM_047432115.1:c.129+1705=	XM_047432115.1:c.129+1718_129+1724del	XM_047432115.1:c.129+1719_129+1724del	XM_047432115.1:c.129+1720_129+1724del	XM_047432115.1:c.129+1721_129+1724del	XM_047432115.1:c.129+1722_129+1724del	XM_047432115.1:c.129+1723_129+1724del	XM_047432115.1:c.129+1724del	XM_047432115.1:c.129+1724dup	XM_047432115.1:c.129+1723_129+1724dup	XM_047432115.1:c.129+1722_129+1724dup	XM_047432115.1:c.129+1721_129+1724dup	XM_047432115.1:c.129+1720_129+1724dup	XM_047432115.1:c.129+1719_129+1724dup	XM_047432115.1:c.129+1718_129+1724dup	XM_047432115.1:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047432115.1:c.129+1724_129+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT
DYRK3 transcript variant X5	XM_047432118.1:c.84+1705=	XM_047432118.1:c.84+1718_84+1724del	XM_047432118.1:c.84+1719_84+1724del	XM_047432118.1:c.84+1720_84+1724del	XM_047432118.1:c.84+1721_84+1724del	XM_047432118.1:c.84+1722_84+1724del	XM_047432118.1:c.84+1723_84+1724del	XM_047432118.1:c.84+1724del	XM_047432118.1:c.84+1724dup	XM_047432118.1:c.84+1723_84+1724dup	XM_047432118.1:c.84+1722_84+1724dup	XM_047432118.1:c.84+1721_84+1724dup	XM_047432118.1:c.84+1720_84+1724dup	XM_047432118.1:c.84+1719_84+1724dup	XM_047432118.1:c.84+1718_84+1724dup	XM_047432118.1:c.84+1724_84+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047432118.1:c.84+1724_84+1725insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT

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#.

43 SubSNP, 27 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PJP	ss294622071	May 09, 2011 (138)
2	SSMP	ss663151589	Apr 09, 2015 (144)
3	SWEGEN	ss2988335094	Oct 11, 2018 (152)
4	MCHAISSO	ss3064440742	Nov 08, 2017 (151)
5	MCHAISSO	ss3065346817	Nov 08, 2017 (151)
6	EVA	ss3826607502	Apr 25, 2020 (154)
7	KOGIC	ss3946354696	Apr 25, 2020 (154)
8	KOGIC	ss3946354697	Apr 25, 2020 (154)
9	KOGIC	ss3946354698	Apr 25, 2020 (154)
10	KOGIC	ss3946354699	Apr 25, 2020 (154)
11	GNOMAD	ss4010081780	Apr 25, 2021 (155)
12	GNOMAD	ss4010081781	Apr 25, 2021 (155)
13	GNOMAD	ss4010081782	Apr 25, 2021 (155)
14	GNOMAD	ss4010081783	Apr 25, 2021 (155)
15	GNOMAD	ss4010081784	Apr 25, 2021 (155)
16	GNOMAD	ss4010081785	Apr 25, 2021 (155)
17	GNOMAD	ss4010081786	Apr 25, 2021 (155)
18	GNOMAD	ss4010081788	Apr 25, 2021 (155)
19	GNOMAD	ss4010081789	Apr 25, 2021 (155)
20	GNOMAD	ss4010081790	Apr 25, 2021 (155)
21	GNOMAD	ss4010081791	Apr 25, 2021 (155)
22	GNOMAD	ss4010081792	Apr 25, 2021 (155)
23	TOMMO_GENOMICS	ss5148116754	Apr 25, 2021 (155)
24	TOMMO_GENOMICS	ss5148116755	Apr 25, 2021 (155)
25	TOMMO_GENOMICS	ss5148116756	Apr 25, 2021 (155)
26	TOMMO_GENOMICS	ss5148116757	Apr 25, 2021 (155)
27	TOMMO_GENOMICS	ss5148116758	Apr 25, 2021 (155)
28	1000G_HIGH_COVERAGE	ss5245553193	Oct 12, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5245553194	Oct 12, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5245553195	Oct 12, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5245553196	Oct 12, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5245553197	Oct 12, 2022 (156)
33	HUGCELL_USP	ss5446012856	Oct 12, 2022 (156)
34	HUGCELL_USP	ss5446012857	Oct 12, 2022 (156)
35	HUGCELL_USP	ss5446012858	Oct 12, 2022 (156)
36	HUGCELL_USP	ss5446012859	Oct 12, 2022 (156)
37	HUGCELL_USP	ss5446012860	Oct 12, 2022 (156)
38	TOMMO_GENOMICS	ss5675788011	Oct 12, 2022 (156)
39	TOMMO_GENOMICS	ss5675788012	Oct 12, 2022 (156)
40	TOMMO_GENOMICS	ss5675788013	Oct 12, 2022 (156)
41	TOMMO_GENOMICS	ss5675788014	Oct 12, 2022 (156)
42	TOMMO_GENOMICS	ss5675788015	Oct 12, 2022 (156)
43	EVA	ss5849254182	Oct 12, 2022 (156)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37556443 (NC_000001.11:206639465::T 45698/108586) Row 37556444 (NC_000001.11:206639465::TT 4575/108548) Row 37556445 (NC_000001.11:206639465::TTT 102/108576)...	-	Apr 25, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37556443 (NC_000001.11:206639465::T 45698/108586) Row 37556444 (NC_000001.11:206639465::TT 4575/108548) Row 37556445 (NC_000001.11:206639465::TTT 102/108576)...	-	Apr 25, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37556443 (NC_000001.11:206639465::T 45698/108586) Row 37556444 (NC_000001.11:206639465::TT 4575/108548) Row 37556445 (NC_000001.11:206639465::TTT 102/108576)...	-	Apr 25, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37556443 (NC_000001.11:206639465::T 45698/108586) Row 37556444 (NC_000001.11:206639465::TT 4575/108548) Row 37556445 (NC_000001.11:206639465::TTT 102/108576)...	-	Apr 25, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37556443 (NC_000001.11:206639465::T 45698/108586) Row 37556444 (NC_000001.11:206639465::TT 4575/108548) Row 37556445 (NC_000001.11:206639465::TTT 102/108576)...	-	Apr 25, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37556443 (NC_000001.11:206639465::T 45698/108586) Row 37556444 (NC_000001.11:206639465::TT 4575/108548) Row 37556445 (NC_000001.11:206639465::TTT 102/108576)...	-	Apr 25, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37556443 (NC_000001.11:206639465::T 45698/108586) Row 37556444 (NC_000001.11:206639465::TT 4575/108548) Row 37556445 (NC_000001.11:206639465::TTT 102/108576)...	-	Apr 25, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37556443 (NC_000001.11:206639465::T 45698/108586) Row 37556444 (NC_000001.11:206639465::TT 4575/108548) Row 37556445 (NC_000001.11:206639465::TTT 102/108576)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37556443 (NC_000001.11:206639465::T 45698/108586) Row 37556444 (NC_000001.11:206639465::TT 4575/108548) Row 37556445 (NC_000001.11:206639465::TTT 102/108576)...	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37556443 (NC_000001.11:206639465::T 45698/108586) Row 37556444 (NC_000001.11:206639465::TT 4575/108548) Row 37556445 (NC_000001.11:206639465::TTT 102/108576)...	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37556443 (NC_000001.11:206639465::T 45698/108586) Row 37556444 (NC_000001.11:206639465::TT 4575/108548) Row 37556445 (NC_000001.11:206639465::TTT 102/108576)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 37556443 (NC_000001.11:206639465::T 45698/108586) Row 37556444 (NC_000001.11:206639465::TT 4575/108548) Row 37556445 (NC_000001.11:206639465::TTT 102/108576)...	-	Apr 25, 2021 (155)
56	Korean Genome Project Submission ignored due to conflicting rows: Row 2732697 (NC_000001.11:206639466::T 417/1830) Row 2732698 (NC_000001.11:206639465:T: 175/1830) Row 2732699 (NC_000001.11:206639466::TTT 28/1830)...	-	Apr 25, 2020 (154)
57	Korean Genome Project Submission ignored due to conflicting rows: Row 2732697 (NC_000001.11:206639466::T 417/1830) Row 2732698 (NC_000001.11:206639465:T: 175/1830) Row 2732699 (NC_000001.11:206639466::TTT 28/1830)...	-	Apr 25, 2020 (154)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 2732697 (NC_000001.11:206639466::T 417/1830) Row 2732698 (NC_000001.11:206639465:T: 175/1830) Row 2732699 (NC_000001.11:206639466::TTT 28/1830)...	-	Apr 25, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 2732697 (NC_000001.11:206639466::T 417/1830) Row 2732698 (NC_000001.11:206639465:T: 175/1830) Row 2732699 (NC_000001.11:206639466::TTT 28/1830)...	-	Apr 25, 2020 (154)
60	8.3KJPN Submission ignored due to conflicting rows: Row 6086061 (NC_000001.10:206812810::T 4061/16578) Row 6086062 (NC_000001.10:206812810::TT 1613/16578) Row 6086063 (NC_000001.10:206812810:T: 18/16578)...	-	Apr 25, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 6086061 (NC_000001.10:206812810::T 4061/16578) Row 6086062 (NC_000001.10:206812810::TT 1613/16578) Row 6086063 (NC_000001.10:206812810:T: 18/16578)...	-	Apr 25, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 6086061 (NC_000001.10:206812810::T 4061/16578) Row 6086062 (NC_000001.10:206812810::TT 1613/16578) Row 6086063 (NC_000001.10:206812810:T: 18/16578)...	-	Apr 25, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 6086061 (NC_000001.10:206812810::T 4061/16578) Row 6086062 (NC_000001.10:206812810::TT 1613/16578) Row 6086063 (NC_000001.10:206812810:T: 18/16578)...	-	Apr 25, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 6086061 (NC_000001.10:206812810::T 4061/16578) Row 6086062 (NC_000001.10:206812810::TT 1613/16578) Row 6086063 (NC_000001.10:206812810:T: 18/16578)...	-	Apr 25, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 9625115 (NC_000001.11:206639465::TT 2710/28154) Row 9625116 (NC_000001.11:206639465::T 7091/28154) Row 9625117 (NC_000001.11:206639465:T: 27/28154)...	-	Oct 12, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 9625115 (NC_000001.11:206639465::TT 2710/28154) Row 9625116 (NC_000001.11:206639465::T 7091/28154) Row 9625117 (NC_000001.11:206639465:T: 27/28154)...	-	Oct 12, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 9625115 (NC_000001.11:206639465::TT 2710/28154) Row 9625116 (NC_000001.11:206639465::T 7091/28154) Row 9625117 (NC_000001.11:206639465:T: 27/28154)...	-	Oct 12, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 9625115 (NC_000001.11:206639465::TT 2710/28154) Row 9625116 (NC_000001.11:206639465::T 7091/28154) Row 9625117 (NC_000001.11:206639465:T: 27/28154)...	-	Oct 12, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 9625115 (NC_000001.11:206639465::TT 2710/28154) Row 9625116 (NC_000001.11:206639465::T 7091/28154) Row 9625117 (NC_000001.11:206639465:T: 27/28154)...	-	Oct 12, 2022 (156)
70	ALFA	NC_000001.11 - 206639466	Apr 25, 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)
rs147963432	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
6622997917	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
6622997917	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4010081792	NC_000001.11:206639465:TTTTT:	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4010081791	NC_000001.11:206639465:TTTT:	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4010081790	NC_000001.11:206639465:TTT:	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
6622997917	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4010081789, ss5245553197, ss5446012860	NC_000001.11:206639465:TT:	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
6622997917	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss2988335094, ss5148116756	NC_000001.10:206812810:T:	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3946354697, ss4010081788, ss5245553195, ss5446012857, ss5675788013	NC_000001.11:206639465:T:	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
6622997917	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss294622071	NC_000001.9:204879434::T	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3826607502, ss5148116754	NC_000001.10:206812810::T	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3064440742, ss3065346817, ss4010081780, ss5245553193, ss5446012856, ss5675788012	NC_000001.11:206639465::T	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
6622997917	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3946354696	NC_000001.11:206639466::T	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss663151589, ss5148116755	NC_000001.10:206812810::TT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010081781, ss5245553194, ss5446012858, ss5675788011, ss5849254182	NC_000001.11:206639465::TT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
6622997917	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3946354699	NC_000001.11:206639466::TT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5148116757	NC_000001.10:206812810::TTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010081782, ss5245553196, ss5446012859, ss5675788014	NC_000001.11:206639465::TTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
6622997917	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3946354698	NC_000001.11:206639466::TTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5148116758	NC_000001.10:206812810::TTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010081783, ss5675788015	NC_000001.11:206639465::TTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010081784	NC_000001.11:206639465::TTTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010081785	NC_000001.11:206639465::TTTTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4010081786	NC_000001.11:206639465::TTTTTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6622997917	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6622997917	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2332109969	NC_000001.10:206812810:TTTTTTT:	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT
28088552, ss3101587740	NC_000001.11:206639465:TTTTTTT:	NC_000001.11:206639465:TTTTTTTTTTT… NC_000001.11:206639465:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT

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

No publications for rs11400833

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

rs11400833