Name: rs200200146
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.

rs200200146

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:94379371-94379387 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₁₆ / del(A)₁₃ / del(A)₁₂ / d…
del(A)₁₆ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₁₁ / dup(A)₁₂ / ins(A)₁₈
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₆=0.0000 (0/9984, ALFA)
del(A)₁₃=0.0000 (0/9984, ALFA)
del(A)₁₂=0.0000 (0/9984, ALFA) (+ 10 more)
del(A)₁₁=0.0000 (0/9984, ALFA)
del(A)₈=0.0000 (0/9984, ALFA)
del(A)₇=0.0000 (0/9984, ALFA)
del(A)₆=0.0000 (0/9984, ALFA)
delAAA=0.0000 (0/9984, ALFA)
delAA=0.0000 (0/9984, ALFA)
delA=0.0000 (0/9984, ALFA)
dupA=0.0000 (0/9984, ALFA)
dupAA=0.0000 (0/9984, ALFA)
dup(A)₄=0.0000 (0/9984, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GPR83 : 3 Prime UTR 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	HWEP
Total	Global	9984	AAAAAAAAAAAAAAAAA=1.0000	A=0.0000, AAAA=0.0000, AAAAA=0.0000, AAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	6278	AAAAAAAAAAAAAAAAA=1.0000	A=0.0000, AAAA=0.0000, AAAAA=0.0000, AAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	2490	AAAAAAAAAAAAAAAAA=1.0000	A=0.0000, AAAA=0.0000, AAAAA=0.0000, AAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	92	AAAAAAAAAAAAAAAAA=1.00	A=0.00, AAAA=0.00, AAAAA=0.00, AAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	2398	AAAAAAAAAAAAAAAAA=1.0000	A=0.0000, AAAA=0.0000, AAAAA=0.0000, AAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	84	AAAAAAAAAAAAAAAAA=1.00	A=0.00, AAAA=0.00, AAAAA=0.00, AAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	60	AAAAAAAAAAAAAAAAA=1.00	A=0.00, AAAA=0.00, AAAAA=0.00, AAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	24	AAAAAAAAAAAAAAAAA=1.00	A=0.00, AAAA=0.00, AAAAA=0.00, AAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	116	AAAAAAAAAAAAAAAAA=1.000	A=0.000, AAAA=0.000, AAAAA=0.000, AAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Latin American 2	Sub	530	AAAAAAAAAAAAAAAAA=1.000	A=0.000, AAAA=0.000, AAAAA=0.000, AAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	84	AAAAAAAAAAAAAAAAA=1.00	A=0.00, AAAA=0.00, AAAAA=0.00, AAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	402	AAAAAAAAAAAAAAAAA=1.000	A=0.000, AAAA=0.000, AAAAA=0.000, AAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	9984	(A)₁₇=1.0000	del(A)₁₆=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	6278	(A)₁₇=1.0000	del(A)₁₆=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	2490	(A)₁₇=1.0000	del(A)₁₆=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	530	(A)₁₇=1.000	del(A)₁₆=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	402	(A)₁₇=1.000	del(A)₁₆=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	116	(A)₁₇=1.000	del(A)₁₆=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	South Asian	Sub	84	(A)₁₇=1.00	del(A)₁₆=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Asian	Sub	84	(A)₁₇=1.00	del(A)₁₆=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)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 11	NC_000011.10:g.94379372_94379387del
GRCh38.p14 chr 11	NC_000011.10:g.94379375_94379387del
GRCh38.p14 chr 11	NC_000011.10:g.94379376_94379387del
GRCh38.p14 chr 11	NC_000011.10:g.94379377_94379387del
GRCh38.p14 chr 11	NC_000011.10:g.94379380_94379387del
GRCh38.p14 chr 11	NC_000011.10:g.94379381_94379387del
GRCh38.p14 chr 11	NC_000011.10:g.94379382_94379387del
GRCh38.p14 chr 11	NC_000011.10:g.94379384_94379387del
GRCh38.p14 chr 11	NC_000011.10:g.94379385_94379387del
GRCh38.p14 chr 11	NC_000011.10:g.94379386_94379387del
GRCh38.p14 chr 11	NC_000011.10:g.94379387del
GRCh38.p14 chr 11	NC_000011.10:g.94379387dup
GRCh38.p14 chr 11	NC_000011.10:g.94379386_94379387dup
GRCh38.p14 chr 11	NC_000011.10:g.94379385_94379387dup
GRCh38.p14 chr 11	NC_000011.10:g.94379384_94379387dup
GRCh38.p14 chr 11	NC_000011.10:g.94379383_94379387dup
GRCh38.p14 chr 11	NC_000011.10:g.94379382_94379387dup
GRCh38.p14 chr 11	NC_000011.10:g.94379377_94379387dup
GRCh38.p14 chr 11	NC_000011.10:g.94379376_94379387dup
GRCh38.p14 chr 11	NC_000011.10:g.94379387_94379388insAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 11	NC_000011.9:g.94112538_94112553del
GRCh37.p13 chr 11	NC_000011.9:g.94112541_94112553del
GRCh37.p13 chr 11	NC_000011.9:g.94112542_94112553del
GRCh37.p13 chr 11	NC_000011.9:g.94112543_94112553del
GRCh37.p13 chr 11	NC_000011.9:g.94112546_94112553del
GRCh37.p13 chr 11	NC_000011.9:g.94112547_94112553del
GRCh37.p13 chr 11	NC_000011.9:g.94112548_94112553del
GRCh37.p13 chr 11	NC_000011.9:g.94112550_94112553del
GRCh37.p13 chr 11	NC_000011.9:g.94112551_94112553del
GRCh37.p13 chr 11	NC_000011.9:g.94112552_94112553del
GRCh37.p13 chr 11	NC_000011.9:g.94112553del
GRCh37.p13 chr 11	NC_000011.9:g.94112553dup
GRCh37.p13 chr 11	NC_000011.9:g.94112552_94112553dup
GRCh37.p13 chr 11	NC_000011.9:g.94112551_94112553dup
GRCh37.p13 chr 11	NC_000011.9:g.94112550_94112553dup
GRCh37.p13 chr 11	NC_000011.9:g.94112549_94112553dup
GRCh37.p13 chr 11	NC_000011.9:g.94112548_94112553dup
GRCh37.p13 chr 11	NC_000011.9:g.94112543_94112553dup
GRCh37.p13 chr 11	NC_000011.9:g.94112542_94112553dup
GRCh37.p13 chr 11	NC_000011.9:g.94112553_94112554insAAAAAAAAAAAAAAAAAA

Gene: GPR83, G protein-coupled receptor 83 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GPR83 transcript variant 1	NM_016540.4:c.762_778=	N/A	3 Prime UTR Variant
GPR83 transcript variant 2	NM_001330345.2:c.762_77… NM_001330345.2:c.762_778=	N/A	3 Prime UTR Variant

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

Not Reported in ClinVar

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

Placement	(A)₁₇=	del(A)₁₆	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₈	del(A)₇	del(A)₆	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₁₁	dup(A)₁₂	ins(A)₁₈
GRCh38.p14 chr 11	NC_000011.10:g.94379371_94379387=	NC_000011.10:g.94379372_94379387del	NC_000011.10:g.94379375_94379387del	NC_000011.10:g.94379376_94379387del	NC_000011.10:g.94379377_94379387del	NC_000011.10:g.94379380_94379387del	NC_000011.10:g.94379381_94379387del	NC_000011.10:g.94379382_94379387del	NC_000011.10:g.94379384_94379387del	NC_000011.10:g.94379385_94379387del	NC_000011.10:g.94379386_94379387del	NC_000011.10:g.94379387del	NC_000011.10:g.94379387dup	NC_000011.10:g.94379386_94379387dup	NC_000011.10:g.94379385_94379387dup	NC_000011.10:g.94379384_94379387dup	NC_000011.10:g.94379383_94379387dup	NC_000011.10:g.94379382_94379387dup	NC_000011.10:g.94379377_94379387dup	NC_000011.10:g.94379376_94379387dup	NC_000011.10:g.94379387_94379388insAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 11	NC_000011.9:g.94112537_94112553=	NC_000011.9:g.94112538_94112553del	NC_000011.9:g.94112541_94112553del	NC_000011.9:g.94112542_94112553del	NC_000011.9:g.94112543_94112553del	NC_000011.9:g.94112546_94112553del	NC_000011.9:g.94112547_94112553del	NC_000011.9:g.94112548_94112553del	NC_000011.9:g.94112550_94112553del	NC_000011.9:g.94112551_94112553del	NC_000011.9:g.94112552_94112553del	NC_000011.9:g.94112553del	NC_000011.9:g.94112553dup	NC_000011.9:g.94112552_94112553dup	NC_000011.9:g.94112551_94112553dup	NC_000011.9:g.94112550_94112553dup	NC_000011.9:g.94112549_94112553dup	NC_000011.9:g.94112548_94112553dup	NC_000011.9:g.94112543_94112553dup	NC_000011.9:g.94112542_94112553dup	NC_000011.9:g.94112553_94112554insAAAAAAAAAAAAAAAAAA
GPR83 transcript variant 1	NM_016540.4:c.762_778=	NM_016540.4:c.763_778del	NM_016540.4:c.766_778del	NM_016540.4:c.767_778del	NM_016540.4:c.768_778del	NM_016540.4:c.771_778del	NM_016540.4:c.772_778del	NM_016540.4:c.773_778del	NM_016540.4:c.775_778del	NM_016540.4:c.776_778del	NM_016540.4:c.777_778del	NM_016540.4:c.*778del	NM_016540.4:c.*778dup	NM_016540.4:c.777_778dup	NM_016540.4:c.776_778dup	NM_016540.4:c.775_778dup	NM_016540.4:c.774_778dup	NM_016540.4:c.773_778dup	NM_016540.4:c.768_778dup	NM_016540.4:c.767_778dup	NM_016540.4:c.778_779insTTTTTTTTTTTTTTTTTT
GPR83 transcript variant 1	NM_016540.3:c.762_778=	NM_016540.3:c.763_778del	NM_016540.3:c.766_778del	NM_016540.3:c.767_778del	NM_016540.3:c.768_778del	NM_016540.3:c.771_778del	NM_016540.3:c.772_778del	NM_016540.3:c.773_778del	NM_016540.3:c.775_778del	NM_016540.3:c.776_778del	NM_016540.3:c.777_778del	NM_016540.3:c.*778del	NM_016540.3:c.*778dup	NM_016540.3:c.777_778dup	NM_016540.3:c.776_778dup	NM_016540.3:c.775_778dup	NM_016540.3:c.774_778dup	NM_016540.3:c.773_778dup	NM_016540.3:c.768_778dup	NM_016540.3:c.767_778dup	NM_016540.3:c.778_779insTTTTTTTTTTTTTTTTTT
GPR83 transcript variant 2	NM_001330345.2:c.762_778=	NM_001330345.2:c.763_778del	NM_001330345.2:c.766_778del	NM_001330345.2:c.767_778del	NM_001330345.2:c.768_778del	NM_001330345.2:c.771_778del	NM_001330345.2:c.772_778del	NM_001330345.2:c.773_778del	NM_001330345.2:c.775_778del	NM_001330345.2:c.776_778del	NM_001330345.2:c.777_778del	NM_001330345.2:c.*778del	NM_001330345.2:c.*778dup	NM_001330345.2:c.777_778dup	NM_001330345.2:c.776_778dup	NM_001330345.2:c.775_778dup	NM_001330345.2:c.774_778dup	NM_001330345.2:c.773_778dup	NM_001330345.2:c.768_778dup	NM_001330345.2:c.767_778dup	NM_001330345.2:c.778_779insTTTTTTTTTTTTTTTTTT
GPR83 transcript variant 2	NM_001330345.1:c.762_778=	NM_001330345.1:c.763_778del	NM_001330345.1:c.766_778del	NM_001330345.1:c.767_778del	NM_001330345.1:c.768_778del	NM_001330345.1:c.771_778del	NM_001330345.1:c.772_778del	NM_001330345.1:c.773_778del	NM_001330345.1:c.775_778del	NM_001330345.1:c.776_778del	NM_001330345.1:c.777_778del	NM_001330345.1:c.*778del	NM_001330345.1:c.*778dup	NM_001330345.1:c.777_778dup	NM_001330345.1:c.776_778dup	NM_001330345.1:c.775_778dup	NM_001330345.1:c.774_778dup	NM_001330345.1:c.773_778dup	NM_001330345.1:c.768_778dup	NM_001330345.1:c.767_778dup	NM_001330345.1:c.778_779insTTTTTTTTTTTTTTTTTT

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#.

50 SubSNP, 27 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GMI	ss289088557	May 04, 2012 (137)
2	SSMP	ss664079703	Apr 01, 2015 (144)
3	DDI	ss1536701015	Apr 01, 2015 (144)
4	MCHAISSO	ss3063702648	Nov 08, 2017 (151)
5	EVA_DECODE	ss3692363617	Jul 13, 2019 (153)
6	EVA_DECODE	ss3692363618	Jul 13, 2019 (153)
7	EVA_DECODE	ss3692363619	Jul 13, 2019 (153)
8	EVA_DECODE	ss3692363620	Jul 13, 2019 (153)
9	EVA_DECODE	ss3692363621	Jul 13, 2019 (153)
10	ACPOP	ss3738431405	Jul 13, 2019 (153)
11	ACPOP	ss3738431406	Jul 13, 2019 (153)
12	ACPOP	ss3738431407	Jul 13, 2019 (153)
13	PACBIO	ss3787031428	Jul 13, 2019 (153)
14	EVA	ss3832773664	Apr 26, 2020 (154)
15	EVA	ss3839946722	Apr 26, 2020 (154)
16	EVA	ss3845427446	Apr 26, 2020 (154)
17	FSA-LAB	ss3984011367	Apr 26, 2021 (155)
18	GNOMAD	ss4240364506	Apr 26, 2021 (155)
19	GNOMAD	ss4240364507	Apr 26, 2021 (155)
20	GNOMAD	ss4240364508	Apr 26, 2021 (155)
21	GNOMAD	ss4240364509	Apr 26, 2021 (155)
22	GNOMAD	ss4240364510	Apr 26, 2021 (155)
23	GNOMAD	ss4240364511	Apr 26, 2021 (155)
24	GNOMAD	ss4240364512	Apr 26, 2021 (155)
25	GNOMAD	ss4240364513	Apr 26, 2021 (155)
26	GNOMAD	ss4240364514	Apr 26, 2021 (155)
27	GNOMAD	ss4240364515	Apr 26, 2021 (155)
28	GNOMAD	ss4240364516	Apr 26, 2021 (155)
29	GNOMAD	ss4240364517	Apr 26, 2021 (155)
30	GNOMAD	ss4240364518	Apr 26, 2021 (155)
31	GNOMAD	ss4240364519	Apr 26, 2021 (155)
32	GNOMAD	ss4240364520	Apr 26, 2021 (155)
33	TOPMED	ss4895677871	Apr 26, 2021 (155)
34	TOPMED	ss4895677872	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5203349775	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5203349776	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5203349777	Apr 26, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5288474315	Oct 16, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5288474316	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5288474317	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5288474318	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5483509887	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5483509888	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5483509890	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5483509891	Oct 16, 2022 (156)
46	SANFORD_IMAGENETICS	ss5651824052	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5751643303	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5751643304	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5751643305	Oct 16, 2022 (156)
50	EVA	ss5837059191	Oct 16, 2022 (156)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 388427762 (NC_000011.10:94379370::A 1203/47338) Row 388427763 (NC_000011.10:94379370::AA 14/48498) Row 388427764 (NC_000011.10:94379370::AAA 5/48626)...	-	Apr 26, 2021 (155)
66	Northern Sweden Submission ignored due to conflicting rows: Row 11716270 (NC_000011.9:94112536:AAAAAAA: 31/556) Row 11716271 (NC_000011.9:94112536::AAAAAAAAAAAA 12/556) Row 11716272 (NC_000011.9:94112536::AAAAAAAAAAA 11/556)	-	Jul 13, 2019 (153)
67	Northern Sweden Submission ignored due to conflicting rows: Row 11716270 (NC_000011.9:94112536:AAAAAAA: 31/556) Row 11716271 (NC_000011.9:94112536::AAAAAAAAAAAA 12/556) Row 11716272 (NC_000011.9:94112536::AAAAAAAAAAA 11/556)	-	Jul 13, 2019 (153)
68	Northern Sweden Submission ignored due to conflicting rows: Row 11716270 (NC_000011.9:94112536:AAAAAAA: 31/556) Row 11716271 (NC_000011.9:94112536::AAAAAAAAAAAA 12/556) Row 11716272 (NC_000011.9:94112536::AAAAAAAAAAA 11/556)	-	Jul 13, 2019 (153)
69	8.3KJPN Submission ignored due to conflicting rows: Row 61319082 (NC_000011.9:94112536:AAAAAAA: 2292/16748) Row 61319083 (NC_000011.9:94112536::A 64/16748) Row 61319084 (NC_000011.9:94112536:A: 23/16748)	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 61319082 (NC_000011.9:94112536:AAAAAAA: 2292/16748) Row 61319083 (NC_000011.9:94112536::A 64/16748) Row 61319084 (NC_000011.9:94112536:A: 23/16748)	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 61319082 (NC_000011.9:94112536:AAAAAAA: 2292/16748) Row 61319083 (NC_000011.9:94112536::A 64/16748) Row 61319084 (NC_000011.9:94112536:A: 23/16748)	-	Apr 26, 2021 (155)
72	14KJPN Submission ignored due to conflicting rows: Row 85480407 (NC_000011.10:94379370:AAAAAAA: 3957/28250) Row 85480408 (NC_000011.10:94379370::A 133/28250) Row 85480409 (NC_000011.10:94379370:A: 36/28250)	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 85480407 (NC_000011.10:94379370:AAAAAAA: 3957/28250) Row 85480408 (NC_000011.10:94379370::A 133/28250) Row 85480409 (NC_000011.10:94379370:A: 36/28250)	-	Oct 16, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 85480407 (NC_000011.10:94379370:AAAAAAA: 3957/28250) Row 85480408 (NC_000011.10:94379370::A 133/28250) Row 85480409 (NC_000011.10:94379370:A: 36/28250)	-	Oct 16, 2022 (156)
75	TopMed Submission ignored due to conflicting rows: Row 111223527 (NC_000011.10:94379370::AAAA 1/264690) Row 111223528 (NC_000011.10:94379370:AAAAAAAAAAAAAAAA: 1/264690)	-	Apr 26, 2021 (155)
76	TopMed Submission ignored due to conflicting rows: Row 111223527 (NC_000011.10:94379370::AAAA 1/264690) Row 111223528 (NC_000011.10:94379370:AAAAAAAAAAAAAAAA: 1/264690)	-	Apr 26, 2021 (155)
77	ALFA	NC_000011.10 - 94379371	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4895677872	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAA:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:A	(self)
10868062089	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:A	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:A	(self)
ss4240364520	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAA:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAA	(self)
10868062089	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAA	(self)
10868062089	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAA	(self)
10868062089	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAA	(self)
10868062089	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss289088557	NC_000011.8:93752184:AAAAAAA:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss664079703, ss1536701015, ss3738431405, ss3832773664, ss3839946722, ss5203349775, ss5651824052, ss5837059191	NC_000011.9:94112536:AAAAAAA:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss3063702648, ss3692363621, ss3845427446, ss4240364519, ss5288474316, ss5483509888, ss5751643303	NC_000011.10:94379370:AAAAAAA:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
10868062089	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4240364518	NC_000011.10:94379370:AAAAAA:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
10868062089	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4240364517	NC_000011.10:94379370:AAAA:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3692363620	NC_000011.10:94379373:AAAA:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4240364516	NC_000011.10:94379370:AAA:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
10868062089	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3984011367	NC_000011.9:94112536:AA:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4240364515, ss5288474318, ss5483509891	NC_000011.10:94379370:AA:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
10868062089	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3692363619	NC_000011.10:94379375:AA:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3787031428, ss5203349777	NC_000011.9:94112536:A:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4240364514, ss5288474317, ss5483509887, ss5751643305	NC_000011.10:94379370:A:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
10868062089	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3692363618	NC_000011.10:94379376:A:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5203349776	NC_000011.9:94112536::A	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4240364506, ss5288474315, ss5483509890, ss5751643304	NC_000011.10:94379370::A	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
10868062089	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3692363617	NC_000011.10:94379377::A	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4240364507	NC_000011.10:94379370::AA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
10868062089	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4240364508	NC_000011.10:94379370::AAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4240364509, ss4895677871	NC_000011.10:94379370::AAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
10868062089	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4240364510	NC_000011.10:94379370::AAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4240364511	NC_000011.10:94379370::AAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3738431407	NC_000011.9:94112536::AAAAAAAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4240364512	NC_000011.10:94379370::AAAAAAAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3738431406	NC_000011.9:94112536::AAAAAAAAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4240364513	NC_000011.10:94379370::AAAAAAAAAAA… NC_000011.10:94379370::AAAAAAAAAAAAAAAAAA	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3153218398	NC_000011.10:94379370:AAAAAAAA:	NC_000011.10:94379370:AAAAAAAAAAAA… NC_000011.10:94379370:AAAAAAAAAAAAAAAAA:AAAAAAAAA

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

No publications for rs200200146

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

rs200200146