Name: rs1185726609
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.

rs1185726609

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:38852748-38852768 (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)₁₁ / del(T)₁₀ / del(T)₈ / de…
del(T)₁₁ / del(T)₁₀ / del(T)₈ / 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)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1204 (844/7012, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PPP1R16B : 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	7012	TTTTTTTTTTTTTTTTTTTTT=0.8577	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0053, TTTTTTTTTTTTTTTTTTTTTT=0.1204, TTTTTTTTTTTTTTTTTTTTTTT=0.0097, TTTTTTTTTTTTTTTTTTTTTTTT=0.0040, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0016, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0014	0.859246	0.100707	0.040047	32
European	Sub	6292	TTTTTTTTTTTTTTTTTTTTT=0.8415	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0059, TTTTTTTTTTTTTTTTTTTTTT=0.1340, TTTTTTTTTTTTTTTTTTTTTTT=0.0108, TTTTTTTTTTTTTTTTTTTTTTTT=0.0045, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0017, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0016	0.842885	0.112648	0.044466	32
African	Sub	456	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	22	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	434	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	10	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	8	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	22	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	126	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	12	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	94	TTTTTTTTTTTTTTTTTTTTT=0.99	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.978723	0.0	0.021277	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	7012	(T)₂₁=0.8577	del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTT=0.0000, delT=0.0053, dupT=0.1204, dupTT=0.0097, dupTTT=0.0040, dup(T)₄=0.0016, dup(T)₁₀=0.0014
Allele Frequency Aggregator	European	Sub	6292	(T)₂₁=0.8415	del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTT=0.0000, delT=0.0059, dupT=0.1340, dupTT=0.0108, dupTTT=0.0045, dup(T)₄=0.0017, dup(T)₁₀=0.0016
Allele Frequency Aggregator	African	Sub	456	(T)₂₁=1.000	del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₁₀=0.000
Allele Frequency Aggregator	Latin American 2	Sub	126	(T)₂₁=1.000	del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₁₀=0.000
Allele Frequency Aggregator	Other	Sub	94	(T)₂₁=0.99	del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.01, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₁₀=0.00
Allele Frequency Aggregator	Latin American 1	Sub	22	(T)₂₁=1.00	del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₁₀=0.00
Allele Frequency Aggregator	South Asian	Sub	12	(T)₂₁=1.00	del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₁₀=0.00
Allele Frequency Aggregator	Asian	Sub	10	(T)₂₁=1.0	del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₁₀=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 20	NC_000020.11:g.38852758_38852768del
GRCh38.p14 chr 20	NC_000020.11:g.38852759_38852768del
GRCh38.p14 chr 20	NC_000020.11:g.38852761_38852768del
GRCh38.p14 chr 20	NC_000020.11:g.38852762_38852768del
GRCh38.p14 chr 20	NC_000020.11:g.38852763_38852768del
GRCh38.p14 chr 20	NC_000020.11:g.38852764_38852768del
GRCh38.p14 chr 20	NC_000020.11:g.38852765_38852768del
GRCh38.p14 chr 20	NC_000020.11:g.38852766_38852768del
GRCh38.p14 chr 20	NC_000020.11:g.38852767_38852768del
GRCh38.p14 chr 20	NC_000020.11:g.38852768del
GRCh38.p14 chr 20	NC_000020.11:g.38852768dup
GRCh38.p14 chr 20	NC_000020.11:g.38852767_38852768dup
GRCh38.p14 chr 20	NC_000020.11:g.38852766_38852768dup
GRCh38.p14 chr 20	NC_000020.11:g.38852765_38852768dup
GRCh38.p14 chr 20	NC_000020.11:g.38852764_38852768dup
GRCh38.p14 chr 20	NC_000020.11:g.38852763_38852768dup
GRCh38.p14 chr 20	NC_000020.11:g.38852761_38852768dup
GRCh38.p14 chr 20	NC_000020.11:g.38852760_38852768dup
GRCh38.p14 chr 20	NC_000020.11:g.38852759_38852768dup
GRCh38.p14 chr 20	NC_000020.11:g.38852758_38852768dup
GRCh37.p13 chr 20	NC_000020.10:g.37481401_37481411del
GRCh37.p13 chr 20	NC_000020.10:g.37481402_37481411del
GRCh37.p13 chr 20	NC_000020.10:g.37481404_37481411del
GRCh37.p13 chr 20	NC_000020.10:g.37481405_37481411del
GRCh37.p13 chr 20	NC_000020.10:g.37481406_37481411del
GRCh37.p13 chr 20	NC_000020.10:g.37481407_37481411del
GRCh37.p13 chr 20	NC_000020.10:g.37481408_37481411del
GRCh37.p13 chr 20	NC_000020.10:g.37481409_37481411del
GRCh37.p13 chr 20	NC_000020.10:g.37481410_37481411del
GRCh37.p13 chr 20	NC_000020.10:g.37481411del
GRCh37.p13 chr 20	NC_000020.10:g.37481411dup
GRCh37.p13 chr 20	NC_000020.10:g.37481410_37481411dup
GRCh37.p13 chr 20	NC_000020.10:g.37481409_37481411dup
GRCh37.p13 chr 20	NC_000020.10:g.37481408_37481411dup
GRCh37.p13 chr 20	NC_000020.10:g.37481407_37481411dup
GRCh37.p13 chr 20	NC_000020.10:g.37481406_37481411dup
GRCh37.p13 chr 20	NC_000020.10:g.37481404_37481411dup
GRCh37.p13 chr 20	NC_000020.10:g.37481403_37481411dup
GRCh37.p13 chr 20	NC_000020.10:g.37481402_37481411dup
GRCh37.p13 chr 20	NC_000020.10:g.37481401_37481411dup

Gene: PPP1R16B, protein phosphatase 1 regulatory subunit 16B (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PPP1R16B transcript variant 2	NM_001172735.3:c.250+1658… NM_001172735.3:c.250+16583_250+16593del	N/A	Intron Variant
PPP1R16B transcript variant 1	NM_015568.4:c.250+16583_2… NM_015568.4:c.250+16583_250+16593del	N/A	Intron Variant
PPP1R16B transcript variant X1	XM_011528768.4:c.	N/A	Genic Upstream Transcript Variant
PPP1R16B transcript variant X2	XM_047440086.1:c.	N/A	Genic Upstream Transcript 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)₂₁=	del(T)₁₁	del(T)₁₀	del(T)₈	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)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁
GRCh38.p14 chr 20	NC_000020.11:g.38852748_38852768=	NC_000020.11:g.38852758_38852768del	NC_000020.11:g.38852759_38852768del	NC_000020.11:g.38852761_38852768del	NC_000020.11:g.38852762_38852768del	NC_000020.11:g.38852763_38852768del	NC_000020.11:g.38852764_38852768del	NC_000020.11:g.38852765_38852768del	NC_000020.11:g.38852766_38852768del	NC_000020.11:g.38852767_38852768del	NC_000020.11:g.38852768del	NC_000020.11:g.38852768dup	NC_000020.11:g.38852767_38852768dup	NC_000020.11:g.38852766_38852768dup	NC_000020.11:g.38852765_38852768dup	NC_000020.11:g.38852764_38852768dup	NC_000020.11:g.38852763_38852768dup	NC_000020.11:g.38852761_38852768dup	NC_000020.11:g.38852760_38852768dup	NC_000020.11:g.38852759_38852768dup	NC_000020.11:g.38852758_38852768dup
GRCh37.p13 chr 20	NC_000020.10:g.37481391_37481411=	NC_000020.10:g.37481401_37481411del	NC_000020.10:g.37481402_37481411del	NC_000020.10:g.37481404_37481411del	NC_000020.10:g.37481405_37481411del	NC_000020.10:g.37481406_37481411del	NC_000020.10:g.37481407_37481411del	NC_000020.10:g.37481408_37481411del	NC_000020.10:g.37481409_37481411del	NC_000020.10:g.37481410_37481411del	NC_000020.10:g.37481411del	NC_000020.10:g.37481411dup	NC_000020.10:g.37481410_37481411dup	NC_000020.10:g.37481409_37481411dup	NC_000020.10:g.37481408_37481411dup	NC_000020.10:g.37481407_37481411dup	NC_000020.10:g.37481406_37481411dup	NC_000020.10:g.37481404_37481411dup	NC_000020.10:g.37481403_37481411dup	NC_000020.10:g.37481402_37481411dup	NC_000020.10:g.37481401_37481411dup
PPP1R16B transcript variant 2	NM_001172735.1:c.250+16573=	NM_001172735.1:c.250+16583_250+16593del	NM_001172735.1:c.250+16584_250+16593del	NM_001172735.1:c.250+16586_250+16593del	NM_001172735.1:c.250+16587_250+16593del	NM_001172735.1:c.250+16588_250+16593del	NM_001172735.1:c.250+16589_250+16593del	NM_001172735.1:c.250+16590_250+16593del	NM_001172735.1:c.250+16591_250+16593del	NM_001172735.1:c.250+16592_250+16593del	NM_001172735.1:c.250+16593del	NM_001172735.1:c.250+16593dup	NM_001172735.1:c.250+16592_250+16593dup	NM_001172735.1:c.250+16591_250+16593dup	NM_001172735.1:c.250+16590_250+16593dup	NM_001172735.1:c.250+16589_250+16593dup	NM_001172735.1:c.250+16588_250+16593dup	NM_001172735.1:c.250+16586_250+16593dup	NM_001172735.1:c.250+16585_250+16593dup	NM_001172735.1:c.250+16584_250+16593dup	NM_001172735.1:c.250+16583_250+16593dup
PPP1R16B transcript variant 2	NM_001172735.3:c.250+16573=	NM_001172735.3:c.250+16583_250+16593del	NM_001172735.3:c.250+16584_250+16593del	NM_001172735.3:c.250+16586_250+16593del	NM_001172735.3:c.250+16587_250+16593del	NM_001172735.3:c.250+16588_250+16593del	NM_001172735.3:c.250+16589_250+16593del	NM_001172735.3:c.250+16590_250+16593del	NM_001172735.3:c.250+16591_250+16593del	NM_001172735.3:c.250+16592_250+16593del	NM_001172735.3:c.250+16593del	NM_001172735.3:c.250+16593dup	NM_001172735.3:c.250+16592_250+16593dup	NM_001172735.3:c.250+16591_250+16593dup	NM_001172735.3:c.250+16590_250+16593dup	NM_001172735.3:c.250+16589_250+16593dup	NM_001172735.3:c.250+16588_250+16593dup	NM_001172735.3:c.250+16586_250+16593dup	NM_001172735.3:c.250+16585_250+16593dup	NM_001172735.3:c.250+16584_250+16593dup	NM_001172735.3:c.250+16583_250+16593dup
PPP1R16B transcript variant 1	NM_015568.2:c.250+16573=	NM_015568.2:c.250+16583_250+16593del	NM_015568.2:c.250+16584_250+16593del	NM_015568.2:c.250+16586_250+16593del	NM_015568.2:c.250+16587_250+16593del	NM_015568.2:c.250+16588_250+16593del	NM_015568.2:c.250+16589_250+16593del	NM_015568.2:c.250+16590_250+16593del	NM_015568.2:c.250+16591_250+16593del	NM_015568.2:c.250+16592_250+16593del	NM_015568.2:c.250+16593del	NM_015568.2:c.250+16593dup	NM_015568.2:c.250+16592_250+16593dup	NM_015568.2:c.250+16591_250+16593dup	NM_015568.2:c.250+16590_250+16593dup	NM_015568.2:c.250+16589_250+16593dup	NM_015568.2:c.250+16588_250+16593dup	NM_015568.2:c.250+16586_250+16593dup	NM_015568.2:c.250+16585_250+16593dup	NM_015568.2:c.250+16584_250+16593dup	NM_015568.2:c.250+16583_250+16593dup
PPP1R16B transcript variant 1	NM_015568.4:c.250+16573=	NM_015568.4:c.250+16583_250+16593del	NM_015568.4:c.250+16584_250+16593del	NM_015568.4:c.250+16586_250+16593del	NM_015568.4:c.250+16587_250+16593del	NM_015568.4:c.250+16588_250+16593del	NM_015568.4:c.250+16589_250+16593del	NM_015568.4:c.250+16590_250+16593del	NM_015568.4:c.250+16591_250+16593del	NM_015568.4:c.250+16592_250+16593del	NM_015568.4:c.250+16593del	NM_015568.4:c.250+16593dup	NM_015568.4:c.250+16592_250+16593dup	NM_015568.4:c.250+16591_250+16593dup	NM_015568.4:c.250+16590_250+16593dup	NM_015568.4:c.250+16589_250+16593dup	NM_015568.4:c.250+16588_250+16593dup	NM_015568.4:c.250+16586_250+16593dup	NM_015568.4:c.250+16585_250+16593dup	NM_015568.4:c.250+16584_250+16593dup	NM_015568.4:c.250+16583_250+16593dup

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#.

42 SubSNP, 34 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41367981	Oct 12, 2018 (152)
2	PJP	ss295047914	Oct 12, 2018 (152)
3	SWEGEN	ss3018175157	Nov 08, 2017 (151)
4	MCHAISSO	ss3064855506	Nov 08, 2017 (151)
5	EVA	ss3835669009	Apr 27, 2020 (154)
6	KOGIC	ss3982271408	Apr 27, 2020 (154)
7	KOGIC	ss3982271409	Apr 27, 2020 (154)
8	KOGIC	ss3982271410	Apr 27, 2020 (154)
9	KOGIC	ss3982271411	Apr 27, 2020 (154)
10	GNOMAD	ss4353317517	Apr 27, 2021 (155)
11	GNOMAD	ss4353317518	Apr 27, 2021 (155)
12	GNOMAD	ss4353317519	Apr 27, 2021 (155)
13	GNOMAD	ss4353317520	Apr 27, 2021 (155)
14	GNOMAD	ss4353317521	Apr 27, 2021 (155)
15	GNOMAD	ss4353317522	Apr 27, 2021 (155)
16	GNOMAD	ss4353317523	Apr 27, 2021 (155)
17	GNOMAD	ss4353317524	Apr 27, 2021 (155)
18	GNOMAD	ss4353317525	Apr 27, 2021 (155)
19	GNOMAD	ss4353317526	Apr 27, 2021 (155)
20	GNOMAD	ss4353317528	Apr 27, 2021 (155)
21	GNOMAD	ss4353317529	Apr 27, 2021 (155)
22	GNOMAD	ss4353317530	Apr 27, 2021 (155)
23	GNOMAD	ss4353317531	Apr 27, 2021 (155)
24	GNOMAD	ss4353317532	Apr 27, 2021 (155)
25	GNOMAD	ss4353317533	Apr 27, 2021 (155)
26	GNOMAD	ss4353317534	Apr 27, 2021 (155)
27	GNOMAD	ss4353317535	Apr 27, 2021 (155)
28	TOMMO_GENOMICS	ss5229626196	Apr 27, 2021 (155)
29	TOMMO_GENOMICS	ss5229626197	Apr 27, 2021 (155)
30	TOMMO_GENOMICS	ss5229626198	Apr 27, 2021 (155)
31	TOMMO_GENOMICS	ss5229626199	Apr 27, 2021 (155)
32	TOMMO_GENOMICS	ss5229626200	Apr 27, 2021 (155)
33	1000G_HIGH_COVERAGE	ss5308780394	Oct 16, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5308780395	Oct 16, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5308780396	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5501059182	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5501059183	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5789422444	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5789422445	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5789422446	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5789422447	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5789422448	Oct 16, 2022 (156)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551710419 (NC_000020.11:38852747::T 15561/29502) Row 551710420 (NC_000020.11:38852747::TT 906/29502) Row 551710421 (NC_000020.11:38852747::TTT 148/29490)...	-	Apr 27, 2021 (155)
62	Korean Genome Project Submission ignored due to conflicting rows: Row 38649409 (NC_000020.11:38852748::T 309/1694) Row 38649410 (NC_000020.11:38852748::TT 62/1694) Row 38649411 (NC_000020.11:38852747:T: 58/1694)...	-	Apr 27, 2020 (154)
63	Korean Genome Project Submission ignored due to conflicting rows: Row 38649409 (NC_000020.11:38852748::T 309/1694) Row 38649410 (NC_000020.11:38852748::TT 62/1694) Row 38649411 (NC_000020.11:38852747:T: 58/1694)...	-	Apr 27, 2020 (154)
64	Korean Genome Project Submission ignored due to conflicting rows: Row 38649409 (NC_000020.11:38852748::T 309/1694) Row 38649410 (NC_000020.11:38852748::TT 62/1694) Row 38649411 (NC_000020.11:38852747:T: 58/1694)...	-	Apr 27, 2020 (154)
65	Korean Genome Project Submission ignored due to conflicting rows: Row 38649409 (NC_000020.11:38852748::T 309/1694) Row 38649410 (NC_000020.11:38852748::TT 62/1694) Row 38649411 (NC_000020.11:38852747:T: 58/1694)...	-	Apr 27, 2020 (154)
66	8.3KJPN Submission ignored due to conflicting rows: Row 87595503 (NC_000020.10:37481390::T 7300/16002) Row 87595504 (NC_000020.10:37481390:T: 481/16002) Row 87595505 (NC_000020.10:37481390::TT 148/16002)...	-	Apr 27, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 87595503 (NC_000020.10:37481390::T 7300/16002) Row 87595504 (NC_000020.10:37481390:T: 481/16002) Row 87595505 (NC_000020.10:37481390::TT 148/16002)...	-	Apr 27, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 87595503 (NC_000020.10:37481390::T 7300/16002) Row 87595504 (NC_000020.10:37481390:T: 481/16002) Row 87595505 (NC_000020.10:37481390::TT 148/16002)...	-	Apr 27, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 87595503 (NC_000020.10:37481390::T 7300/16002) Row 87595504 (NC_000020.10:37481390:T: 481/16002) Row 87595505 (NC_000020.10:37481390::TT 148/16002)...	-	Apr 27, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 87595503 (NC_000020.10:37481390::T 7300/16002) Row 87595504 (NC_000020.10:37481390:T: 481/16002) Row 87595505 (NC_000020.10:37481390::TT 148/16002)...	-	Apr 27, 2021 (155)
71	14KJPN Submission ignored due to conflicting rows: Row 123259548 (NC_000020.11:38852747::T 12618/27134) Row 123259549 (NC_000020.11:38852747:T: 902/27134) Row 123259550 (NC_000020.11:38852747::TT 236/27134)...	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 123259548 (NC_000020.11:38852747::T 12618/27134) Row 123259549 (NC_000020.11:38852747:T: 902/27134) Row 123259550 (NC_000020.11:38852747::TT 236/27134)...	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 123259548 (NC_000020.11:38852747::T 12618/27134) Row 123259549 (NC_000020.11:38852747:T: 902/27134) Row 123259550 (NC_000020.11:38852747::TT 236/27134)...	-	Oct 16, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 123259548 (NC_000020.11:38852747::T 12618/27134) Row 123259549 (NC_000020.11:38852747:T: 902/27134) Row 123259550 (NC_000020.11:38852747::TT 236/27134)...	-	Oct 16, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 123259548 (NC_000020.11:38852747::T 12618/27134) Row 123259549 (NC_000020.11:38852747:T: 902/27134) Row 123259550 (NC_000020.11:38852747::TT 236/27134)...	-	Oct 16, 2022 (156)
76	ALFA	NC_000020.11 - 38852748	Apr 27, 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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5229626200	NC_000020.10:37481390:TTTTTTTTTTT:	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4353317535, ss5789422447	NC_000020.11:38852747:TTTTTTTTTTT:	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
3177548395	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
3177548395	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4353317534	NC_000020.11:38852747:TTTTTTTT:	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
3177548395	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4353317533	NC_000020.11:38852747:TTTTTTT:	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
3177548395	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4353317532	NC_000020.11:38852747:TTTTTT:	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
3177548395	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4353317531	NC_000020.11:38852747:TTTTT:	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
3177548395	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4353317530	NC_000020.11:38852747:TTTT:	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
3177548395	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4353317529	NC_000020.11:38852747:TTT:	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4353317528	NC_000020.11:38852747:TT:	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
3177548395	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3018175157, ss5229626197	NC_000020.10:37481390:T:	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3982271410, ss5308780396, ss5501059183, ss5789422445	NC_000020.11:38852747:T:	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
3177548395	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss295047914	NC_000020.9:36914805::T	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5229626196	NC_000020.10:37481390::T	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3064855506, ss4353317517, ss5501059182, ss5789422444	NC_000020.11:38852747::T	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
3177548395	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3982271408	NC_000020.11:38852748::T	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss41367981	NT_011362.10:7677503::T	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3835669009, ss5229626198	NC_000020.10:37481390::TT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353317518, ss5308780394, ss5789422446	NC_000020.11:38852747::TT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
3177548395	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3982271409	NC_000020.11:38852748::TT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353317519, ss5308780395	NC_000020.11:38852747::TTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
3177548395	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3982271411	NC_000020.11:38852748::TTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5229626199	NC_000020.10:37481390::TTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353317520, ss5789422448	NC_000020.11:38852747::TTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3177548395	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353317521	NC_000020.11:38852747::TTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353317522	NC_000020.11:38852747::TTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353317523	NC_000020.11:38852747::TTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353317524	NC_000020.11:38852747::TTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353317525	NC_000020.11:38852747::TTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3177548395	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353317526	NC_000020.11:38852747::TTTTTTTTTTT	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3360316771	NC_000020.11:38852747:TTTTTTTTTT:	NC_000020.11:38852747:TTTTTTTTTTTT… NC_000020.11:38852747:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT

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

No publications for rs1185726609

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

rs1185726609