Name: rs869187206
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.

rs869187206

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:38861674-38861694 (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)₁₃ / del(T)₁₂ / del(T)₁₁ / d…
del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₈ / del(T)₇ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈
Variation Type: Indel Insertion and Deletion
Frequency: dupTTT=0.00194 (33/17036, 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	17036	TTTTTTTTTTTTTTTTTTTTT=0.99577	TTTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00018, TTTTTTTTTTTTTTTTTTTTTT=0.00164, TTTTTTTTTTTTTTTTTTTTTTT=0.00047, TTTTTTTTTTTTTTTTTTTTTTTT=0.00194, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.996226	0.000118	0.003656	16
European	Sub	14056	TTTTTTTTTTTTTTTTTTTTT=0.99488	TTTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00021, TTTTTTTTTTTTTTTTTTTTTT=0.00199, TTTTTTTTTTTTTTTTTTTTTTT=0.00057, TTTTTTTTTTTTTTTTTTTTTTTT=0.00235, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.995422	0.000143	0.004435	13
African	Sub	1608	TTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	58	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1550	TTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	110	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	84	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	26	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	128	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	584	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	98	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	452	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	17036	(T)₂₁=0.99577	del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00018, dupT=0.00164, dupTT=0.00047, dupTTT=0.00194, dup(T)₄=0.00000
Allele Frequency Aggregator	European	Sub	14056	(T)₂₁=0.99488	del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00021, dupT=0.00199, dupTT=0.00057, dupTTT=0.00235, dup(T)₄=0.00000
Allele Frequency Aggregator	African	Sub	1608	(T)₂₁=1.0000	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	584	(T)₂₁=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	452	(T)₂₁=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	128	(T)₂₁=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Asian	Sub	110	(T)₂₁=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	South Asian	Sub	98	(T)₂₁=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=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 20	NC_000020.11:g.38861682_38861694del
GRCh38.p14 chr 20	NC_000020.11:g.38861683_38861694del
GRCh38.p14 chr 20	NC_000020.11:g.38861684_38861694del
GRCh38.p14 chr 20	NC_000020.11:g.38861685_38861694del
GRCh38.p14 chr 20	NC_000020.11:g.38861687_38861694del
GRCh38.p14 chr 20	NC_000020.11:g.38861688_38861694del
GRCh38.p14 chr 20	NC_000020.11:g.38861691_38861694del
GRCh38.p14 chr 20	NC_000020.11:g.38861692_38861694del
GRCh38.p14 chr 20	NC_000020.11:g.38861693_38861694del
GRCh38.p14 chr 20	NC_000020.11:g.38861694del
GRCh38.p14 chr 20	NC_000020.11:g.38861694dup
GRCh38.p14 chr 20	NC_000020.11:g.38861693_38861694dup
GRCh38.p14 chr 20	NC_000020.11:g.38861692_38861694dup
GRCh38.p14 chr 20	NC_000020.11:g.38861691_38861694dup
GRCh38.p14 chr 20	NC_000020.11:g.38861690_38861694dup
GRCh38.p14 chr 20	NC_000020.11:g.38861689_38861694dup
GRCh38.p14 chr 20	NC_000020.11:g.38861688_38861694dup
GRCh38.p14 chr 20	NC_000020.11:g.38861687_38861694dup
GRCh37.p13 chr 20	NC_000020.10:g.37490325_37490337del
GRCh37.p13 chr 20	NC_000020.10:g.37490326_37490337del
GRCh37.p13 chr 20	NC_000020.10:g.37490327_37490337del
GRCh37.p13 chr 20	NC_000020.10:g.37490328_37490337del
GRCh37.p13 chr 20	NC_000020.10:g.37490330_37490337del
GRCh37.p13 chr 20	NC_000020.10:g.37490331_37490337del
GRCh37.p13 chr 20	NC_000020.10:g.37490334_37490337del
GRCh37.p13 chr 20	NC_000020.10:g.37490335_37490337del
GRCh37.p13 chr 20	NC_000020.10:g.37490336_37490337del
GRCh37.p13 chr 20	NC_000020.10:g.37490337del
GRCh37.p13 chr 20	NC_000020.10:g.37490337dup
GRCh37.p13 chr 20	NC_000020.10:g.37490336_37490337dup
GRCh37.p13 chr 20	NC_000020.10:g.37490335_37490337dup
GRCh37.p13 chr 20	NC_000020.10:g.37490334_37490337dup
GRCh37.p13 chr 20	NC_000020.10:g.37490333_37490337dup
GRCh37.p13 chr 20	NC_000020.10:g.37490332_37490337dup
GRCh37.p13 chr 20	NC_000020.10:g.37490331_37490337dup
GRCh37.p13 chr 20	NC_000020.10:g.37490330_37490337dup

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+2550… NM_001172735.3:c.250+25507_250+25519del	N/A	Intron Variant
PPP1R16B transcript variant 1	NM_015568.4:c.250+25507_2… NM_015568.4:c.250+25507_250+25519del	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)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₈	del(T)₇	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈
GRCh38.p14 chr 20	NC_000020.11:g.38861674_38861694=	NC_000020.11:g.38861682_38861694del	NC_000020.11:g.38861683_38861694del	NC_000020.11:g.38861684_38861694del	NC_000020.11:g.38861685_38861694del	NC_000020.11:g.38861687_38861694del	NC_000020.11:g.38861688_38861694del	NC_000020.11:g.38861691_38861694del	NC_000020.11:g.38861692_38861694del	NC_000020.11:g.38861693_38861694del	NC_000020.11:g.38861694del	NC_000020.11:g.38861694dup	NC_000020.11:g.38861693_38861694dup	NC_000020.11:g.38861692_38861694dup	NC_000020.11:g.38861691_38861694dup	NC_000020.11:g.38861690_38861694dup	NC_000020.11:g.38861689_38861694dup	NC_000020.11:g.38861688_38861694dup	NC_000020.11:g.38861687_38861694dup
GRCh37.p13 chr 20	NC_000020.10:g.37490317_37490337=	NC_000020.10:g.37490325_37490337del	NC_000020.10:g.37490326_37490337del	NC_000020.10:g.37490327_37490337del	NC_000020.10:g.37490328_37490337del	NC_000020.10:g.37490330_37490337del	NC_000020.10:g.37490331_37490337del	NC_000020.10:g.37490334_37490337del	NC_000020.10:g.37490335_37490337del	NC_000020.10:g.37490336_37490337del	NC_000020.10:g.37490337del	NC_000020.10:g.37490337dup	NC_000020.10:g.37490336_37490337dup	NC_000020.10:g.37490335_37490337dup	NC_000020.10:g.37490334_37490337dup	NC_000020.10:g.37490333_37490337dup	NC_000020.10:g.37490332_37490337dup	NC_000020.10:g.37490331_37490337dup	NC_000020.10:g.37490330_37490337dup
PPP1R16B transcript variant 2	NM_001172735.1:c.250+25499=	NM_001172735.1:c.250+25507_250+25519del	NM_001172735.1:c.250+25508_250+25519del	NM_001172735.1:c.250+25509_250+25519del	NM_001172735.1:c.250+25510_250+25519del	NM_001172735.1:c.250+25512_250+25519del	NM_001172735.1:c.250+25513_250+25519del	NM_001172735.1:c.250+25516_250+25519del	NM_001172735.1:c.250+25517_250+25519del	NM_001172735.1:c.250+25518_250+25519del	NM_001172735.1:c.250+25519del	NM_001172735.1:c.250+25519dup	NM_001172735.1:c.250+25518_250+25519dup	NM_001172735.1:c.250+25517_250+25519dup	NM_001172735.1:c.250+25516_250+25519dup	NM_001172735.1:c.250+25515_250+25519dup	NM_001172735.1:c.250+25514_250+25519dup	NM_001172735.1:c.250+25513_250+25519dup	NM_001172735.1:c.250+25512_250+25519dup
PPP1R16B transcript variant 2	NM_001172735.3:c.250+25499=	NM_001172735.3:c.250+25507_250+25519del	NM_001172735.3:c.250+25508_250+25519del	NM_001172735.3:c.250+25509_250+25519del	NM_001172735.3:c.250+25510_250+25519del	NM_001172735.3:c.250+25512_250+25519del	NM_001172735.3:c.250+25513_250+25519del	NM_001172735.3:c.250+25516_250+25519del	NM_001172735.3:c.250+25517_250+25519del	NM_001172735.3:c.250+25518_250+25519del	NM_001172735.3:c.250+25519del	NM_001172735.3:c.250+25519dup	NM_001172735.3:c.250+25518_250+25519dup	NM_001172735.3:c.250+25517_250+25519dup	NM_001172735.3:c.250+25516_250+25519dup	NM_001172735.3:c.250+25515_250+25519dup	NM_001172735.3:c.250+25514_250+25519dup	NM_001172735.3:c.250+25513_250+25519dup	NM_001172735.3:c.250+25512_250+25519dup
PPP1R16B transcript variant 1	NM_015568.2:c.250+25499=	NM_015568.2:c.250+25507_250+25519del	NM_015568.2:c.250+25508_250+25519del	NM_015568.2:c.250+25509_250+25519del	NM_015568.2:c.250+25510_250+25519del	NM_015568.2:c.250+25512_250+25519del	NM_015568.2:c.250+25513_250+25519del	NM_015568.2:c.250+25516_250+25519del	NM_015568.2:c.250+25517_250+25519del	NM_015568.2:c.250+25518_250+25519del	NM_015568.2:c.250+25519del	NM_015568.2:c.250+25519dup	NM_015568.2:c.250+25518_250+25519dup	NM_015568.2:c.250+25517_250+25519dup	NM_015568.2:c.250+25516_250+25519dup	NM_015568.2:c.250+25515_250+25519dup	NM_015568.2:c.250+25514_250+25519dup	NM_015568.2:c.250+25513_250+25519dup	NM_015568.2:c.250+25512_250+25519dup
PPP1R16B transcript variant 1	NM_015568.4:c.250+25499=	NM_015568.4:c.250+25507_250+25519del	NM_015568.4:c.250+25508_250+25519del	NM_015568.4:c.250+25509_250+25519del	NM_015568.4:c.250+25510_250+25519del	NM_015568.4:c.250+25512_250+25519del	NM_015568.4:c.250+25513_250+25519del	NM_015568.4:c.250+25516_250+25519del	NM_015568.4:c.250+25517_250+25519del	NM_015568.4:c.250+25518_250+25519del	NM_015568.4:c.250+25519del	NM_015568.4:c.250+25519dup	NM_015568.4:c.250+25518_250+25519dup	NM_015568.4:c.250+25517_250+25519dup	NM_015568.4:c.250+25516_250+25519dup	NM_015568.4:c.250+25515_250+25519dup	NM_015568.4:c.250+25514_250+25519dup	NM_015568.4:c.250+25513_250+25519dup	NM_015568.4:c.250+25512_250+25519dup

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#.

37 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCMHGSC_JDW	ss103650515	Mar 15, 2016 (147)
2	SWEGEN	ss3018175273	Nov 08, 2017 (151)
3	EVA	ss3835669034	Apr 27, 2020 (154)
4	GNOMAD	ss4353318739	Apr 27, 2021 (155)
5	GNOMAD	ss4353318740	Apr 27, 2021 (155)
6	GNOMAD	ss4353318741	Apr 27, 2021 (155)
7	GNOMAD	ss4353318742	Apr 27, 2021 (155)
8	GNOMAD	ss4353318743	Apr 27, 2021 (155)
9	GNOMAD	ss4353318744	Apr 27, 2021 (155)
10	GNOMAD	ss4353318745	Apr 27, 2021 (155)
11	GNOMAD	ss4353318746	Apr 27, 2021 (155)
12	GNOMAD	ss4353318748	Apr 27, 2021 (155)
13	GNOMAD	ss4353318749	Apr 27, 2021 (155)
14	GNOMAD	ss4353318750	Apr 27, 2021 (155)
15	GNOMAD	ss4353318751	Apr 27, 2021 (155)
16	GNOMAD	ss4353318752	Apr 27, 2021 (155)
17	GNOMAD	ss4353318753	Apr 27, 2021 (155)
18	GNOMAD	ss4353318754	Apr 27, 2021 (155)
19	TOPMED	ss5088417206	Apr 27, 2021 (155)
20	TOPMED	ss5088417207	Apr 27, 2021 (155)
21	TOPMED	ss5088417208	Apr 27, 2021 (155)
22	TOMMO_GENOMICS	ss5229626554	Apr 27, 2021 (155)
23	TOMMO_GENOMICS	ss5229626555	Apr 27, 2021 (155)
24	TOMMO_GENOMICS	ss5229626556	Apr 27, 2021 (155)
25	1000G_HIGH_COVERAGE	ss5308780625	Oct 16, 2022 (156)
26	1000G_HIGH_COVERAGE	ss5308780626	Oct 16, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5308780627	Oct 16, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5308780628	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5501059371	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5501059372	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5501059373	Oct 16, 2022 (156)
32	HUGCELL_USP	ss5501059374	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5501059375	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5501059376	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5789422932	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5789422933	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5789422934	Oct 16, 2022 (156)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 551712333 (NC_000020.11:38861673::T 2329/115084) Row 551712334 (NC_000020.11:38861673::TT 2551/115046) Row 551712335 (NC_000020.11:38861673::TTT 1129/114852)...	-	Apr 27, 2021 (155)
54	8.3KJPN Submission ignored due to conflicting rows: Row 87595861 (NC_000020.10:37490316::T 70/16706) Row 87595862 (NC_000020.10:37490316:TTTTTTTTTTTT: 3/16706) Row 87595863 (NC_000020.10:37490316:T: 15/16706)	-	Apr 27, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 87595861 (NC_000020.10:37490316::T 70/16706) Row 87595862 (NC_000020.10:37490316:TTTTTTTTTTTT: 3/16706) Row 87595863 (NC_000020.10:37490316:T: 15/16706)	-	Apr 27, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 87595861 (NC_000020.10:37490316::T 70/16706) Row 87595862 (NC_000020.10:37490316:TTTTTTTTTTTT: 3/16706) Row 87595863 (NC_000020.10:37490316:T: 15/16706)	-	Apr 27, 2021 (155)
57	14KJPN Submission ignored due to conflicting rows: Row 123260036 (NC_000020.11:38861673:T: 20/28212) Row 123260037 (NC_000020.11:38861673::T 111/28212) Row 123260038 (NC_000020.11:38861673:TTTTTTTTTTTT: 6/28212)	-	Oct 16, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 123260036 (NC_000020.11:38861673:T: 20/28212) Row 123260037 (NC_000020.11:38861673::T 111/28212) Row 123260038 (NC_000020.11:38861673:TTTTTTTTTTTT: 6/28212)	-	Oct 16, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 123260036 (NC_000020.11:38861673:T: 20/28212) Row 123260037 (NC_000020.11:38861673::T 111/28212) Row 123260038 (NC_000020.11:38861673:TTTTTTTTTTTT: 6/28212)	-	Oct 16, 2022 (156)
60	TopMed Submission ignored due to conflicting rows: Row 363526151 (NC_000020.11:38861673:TTTTTTTTTT: 6/264690) Row 363526152 (NC_000020.11:38861673:TTTTTTTTTTT: 5/264690) Row 363526153 (NC_000020.11:38861673:TTTTTTTTTTTTT: 58/264690)	-	Apr 27, 2021 (155)
61	TopMed Submission ignored due to conflicting rows: Row 363526151 (NC_000020.11:38861673:TTTTTTTTTT: 6/264690) Row 363526152 (NC_000020.11:38861673:TTTTTTTTTTT: 5/264690) Row 363526153 (NC_000020.11:38861673:TTTTTTTTTTTTT: 58/264690)	-	Apr 27, 2021 (155)
62	TopMed Submission ignored due to conflicting rows: Row 363526151 (NC_000020.11:38861673:TTTTTTTTTT: 6/264690) Row 363526152 (NC_000020.11:38861673:TTTTTTTTTTT: 5/264690) Row 363526153 (NC_000020.11:38861673:TTTTTTTTTTTTT: 58/264690)	-	Apr 27, 2021 (155)
63	ALFA	NC_000020.11 - 38861674	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
ss4353318754, ss5088417208	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTT:	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
3973518171	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss5229626555	NC_000020.10:37490316:TTTTTTTTTTTT:	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4353318753, ss5789422934	NC_000020.11:38861673:TTTTTTTTTTTT:	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
3973518171	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4353318752, ss5088417207	NC_000020.11:38861673:TTTTTTTTTTT:	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
3973518171	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4353318751, ss5088417206	NC_000020.11:38861673:TTTTTTTTTT:	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
3973518171	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4353318750	NC_000020.11:38861673:TTTTTTTT:	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
3973518171	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
3973518171	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
3973518171	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4353318749, ss5501059375	NC_000020.11:38861673:TTT:	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
3973518171	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4353318748, ss5308780627, ss5501059376	NC_000020.11:38861673:TT:	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
3973518171	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3018175273, ss5229626556	NC_000020.10:37490316:T:	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5501059371, ss5789422932	NC_000020.11:38861673:T:	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
3973518171	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss103650515	NT_011362.10:7686409:T:	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5229626554	NC_000020.10:37490316::T	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353318739, ss5308780625, ss5501059372, ss5789422933	NC_000020.11:38861673::T	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
3973518171	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3835669034	NC_000020.10:37490316::TT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353318740, ss5308780628, ss5501059374	NC_000020.11:38861673::TT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
3973518171	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353318741, ss5308780626, ss5501059373	NC_000020.11:38861673::TTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
3973518171	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353318742	NC_000020.11:38861673::TTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3973518171	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353318743	NC_000020.11:38861673::TTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353318744	NC_000020.11:38861673::TTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353318745	NC_000020.11:38861673::TTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4353318746	NC_000020.11:38861673::TTTTTTTT	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2409234821	NC_000020.10:37490316:TTTTTTTTTTTT… NC_000020.10:37490316:TTTTTTTTTTTTT:	NC_000020.11:38861673:TTTTTTTTTTTT… NC_000020.11:38861673:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT

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

No publications for rs869187206

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

rs869187206