Name: rs34406812
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.

rs34406812

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:190445574-190445596 (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(AC)₄ / del(AC)₃ / delACAC / de…
del(AC)₄ / del(AC)₃ / delACAC / delAC / dupAC / dupACAC / dup(AC)₃ / dup(AC)₄
Variation Type: Indel Insertion and Deletion
Frequency: dupAC=0.09189 (925/10066, ALFA)
dupAC=0.1172 (587/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BRINP3 : 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	10066	CACACACACACACACACACACAC=0.82356	CACACACACACACAC=0.00000, CACACACACACACACAC=0.00000, CACACACACACACACACAC=0.00040, CACACACACACACACACACAC=0.08355, CACACACACACACACACACACACAC=0.09189, CACACACACACACACACACACACACAC=0.00060, CACACACACACACACACACACACACACAC=0.00000, CACACACACACACACACACACACACACACAC=0.00000	0.846442	0.023642	0.129916	32
European	Sub	8004	CACACACACACACACACACACAC=0.7785	CACACACACACACAC=0.0000, CACACACACACACACAC=0.0000, CACACACACACACACACAC=0.0005, CACACACACACACACACACAC=0.1049, CACACACACACACACACACACACAC=0.1153, CACACACACACACACACACACACACAC=0.0007, CACACACACACACACACACACACACACAC=0.0000, CACACACACACACACACACACACACACACAC=0.0000	0.798273	0.031154	0.170574	32
African	Sub	1326	CACACACACACACACACACACAC=1.0000	CACACACACACACAC=0.0000, CACACACACACACACAC=0.0000, CACACACACACACACACAC=0.0000, CACACACACACACACACACAC=0.0000, CACACACACACACACACACACACAC=0.0000, CACACACACACACACACACACACACAC=0.0000, CACACACACACACACACACACACACACAC=0.0000, CACACACACACACACACACACACACACACAC=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	50	CACACACACACACACACACACAC=1.00	CACACACACACACAC=0.00, CACACACACACACACAC=0.00, CACACACACACACACACAC=0.00, CACACACACACACACACACAC=0.00, CACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACAC=0.00	1.0	0.0	0.0	N/A
African American	Sub	1276	CACACACACACACACACACACAC=1.0000	CACACACACACACAC=0.0000, CACACACACACACACAC=0.0000, CACACACACACACACACAC=0.0000, CACACACACACACACACACAC=0.0000, CACACACACACACACACACACACAC=0.0000, CACACACACACACACACACACACACAC=0.0000, CACACACACACACACACACACACACACAC=0.0000, CACACACACACACACACACACACACACACAC=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	82	CACACACACACACACACACACAC=1.00	CACACACACACACAC=0.00, CACACACACACACACAC=0.00, CACACACACACACACACAC=0.00, CACACACACACACACACACAC=0.00, CACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACAC=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	66	CACACACACACACACACACACAC=1.00	CACACACACACACAC=0.00, CACACACACACACACAC=0.00, CACACACACACACACACAC=0.00, CACACACACACACACACACAC=0.00, CACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACAC=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	CACACACACACACACACACACAC=1.00	CACACACACACACAC=0.00, CACACACACACACACAC=0.00, CACACACACACACACACAC=0.00, CACACACACACACACACACAC=0.00, CACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACAC=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	78	CACACACACACACACACACACAC=1.00	CACACACACACACAC=0.00, CACACACACACACACAC=0.00, CACACACACACACACACAC=0.00, CACACACACACACACACACAC=0.00, CACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACAC=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	308	CACACACACACACACACACACAC=1.000	CACACACACACACAC=0.000, CACACACACACACACAC=0.000, CACACACACACACACACAC=0.000, CACACACACACACACACACAC=0.000, CACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACACAC=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	38	CACACACACACACACACACACAC=1.00	CACACACACACACAC=0.00, CACACACACACACACAC=0.00, CACACACACACACACACAC=0.00, CACACACACACACACACACAC=0.00, CACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACAC=0.00	1.0	0.0	0.0	N/A
Other	Sub	230	CACACACACACACACACACACAC=0.987	CACACACACACACAC=0.000, CACACACACACACACAC=0.000, CACACACACACACACACAC=0.000, CACACACACACACACACACAC=0.004, CACACACACACACACACACACACAC=0.009, CACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACACAC=0.000	0.982456	0.0	0.017544	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	10066	(CA)₁₁C=0.82356	del(AC)₄=0.00000, del(AC)₃=0.00000, delACAC=0.00040, delAC=0.08355, dupAC=0.09189, dupACAC=0.00060, dup(AC)₃=0.00000, dup(AC)₄=0.00000
Allele Frequency Aggregator	European	Sub	8004	(CA)₁₁C=0.7785	del(AC)₄=0.0000, del(AC)₃=0.0000, delACAC=0.0005, delAC=0.1049, dupAC=0.1153, dupACAC=0.0007, dup(AC)₃=0.0000, dup(AC)₄=0.0000
Allele Frequency Aggregator	African	Sub	1326	(CA)₁₁C=1.0000	del(AC)₄=0.0000, del(AC)₃=0.0000, delACAC=0.0000, delAC=0.0000, dupAC=0.0000, dupACAC=0.0000, dup(AC)₃=0.0000, dup(AC)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	308	(CA)₁₁C=1.000	del(AC)₄=0.000, del(AC)₃=0.000, delACAC=0.000, delAC=0.000, dupAC=0.000, dupACAC=0.000, dup(AC)₃=0.000, dup(AC)₄=0.000
Allele Frequency Aggregator	Other	Sub	230	(CA)₁₁C=0.987	del(AC)₄=0.000, del(AC)₃=0.000, delACAC=0.000, delAC=0.004, dupAC=0.009, dupACAC=0.000, dup(AC)₃=0.000, dup(AC)₄=0.000
Allele Frequency Aggregator	Asian	Sub	82	(CA)₁₁C=1.00	del(AC)₄=0.00, del(AC)₃=0.00, delACAC=0.00, delAC=0.00, dupAC=0.00, dupACAC=0.00, dup(AC)₃=0.00, dup(AC)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	78	(CA)₁₁C=1.00	del(AC)₄=0.00, del(AC)₃=0.00, delACAC=0.00, delAC=0.00, dupAC=0.00, dupACAC=0.00, dup(AC)₃=0.00, dup(AC)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	38	(CA)₁₁C=1.00	del(AC)₄=0.00, del(AC)₃=0.00, delACAC=0.00, delAC=0.00, dupAC=0.00, dupACAC=0.00, dup(AC)₃=0.00, dup(AC)₄=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupAC=0.1172
1000Genomes	African	Sub	1322	- No frequency provided	dupAC=0.0378
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupAC=0.1518
1000Genomes	Europe	Sub	1006	- No frequency provided	dupAC=0.1252
1000Genomes	South Asian	Sub	978	- No frequency provided	dupAC=0.187
1000Genomes	American	Sub	694	- No frequency provided	dupAC=0.108

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 1	NC_000001.11:g.190445575AC[7]
GRCh38.p14 chr 1	NC_000001.11:g.190445575AC[8]
GRCh38.p14 chr 1	NC_000001.11:g.190445575AC[9]
GRCh38.p14 chr 1	NC_000001.11:g.190445575AC[10]
GRCh38.p14 chr 1	NC_000001.11:g.190445575AC[12]
GRCh38.p14 chr 1	NC_000001.11:g.190445575AC[13]
GRCh38.p14 chr 1	NC_000001.11:g.190445575AC[14]
GRCh38.p14 chr 1	NC_000001.11:g.190445575AC[15]
GRCh37.p13 chr 1	NC_000001.10:g.190414705AC[7]
GRCh37.p13 chr 1	NC_000001.10:g.190414705AC[8]
GRCh37.p13 chr 1	NC_000001.10:g.190414705AC[9]
GRCh37.p13 chr 1	NC_000001.10:g.190414705AC[10]
GRCh37.p13 chr 1	NC_000001.10:g.190414705AC[12]
GRCh37.p13 chr 1	NC_000001.10:g.190414705AC[13]
GRCh37.p13 chr 1	NC_000001.10:g.190414705AC[14]
GRCh37.p13 chr 1	NC_000001.10:g.190414705AC[15]

Gene: BRINP3, BMP/retinoic acid inducible neural specific 3 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BRINP3 transcript variant 2	NM_001317188.2:c.121+9060… NM_001317188.2:c.121+9060TG[7]	N/A	Intron Variant
BRINP3 transcript variant 1	NM_199051.3:c.236+9060TG[… NM_199051.3:c.236+9060TG[7]	N/A	Intron Variant
BRINP3 transcript variant X5	XM_011509472.3:c.122-6384… XM_011509472.3:c.122-6384TG[7]	N/A	Intron Variant
BRINP3 transcript variant X9	XM_011509476.3:c.121+9060… XM_011509476.3:c.121+9060TG[7]	N/A	Intron Variant
BRINP3 transcript variant X4	XM_017001125.2:c.236+9060… XM_017001125.2:c.236+9060TG[7]	N/A	Intron Variant
BRINP3 transcript variant X2	XM_017001126.2:c.236+9060… XM_017001126.2:c.236+9060TG[7]	N/A	Intron Variant
BRINP3 transcript variant X6	XM_017001127.2:c.122-6384… XM_017001127.2:c.122-6384TG[7]	N/A	Intron Variant
BRINP3 transcript variant X7	XM_017001128.2:c.122-6384… XM_017001128.2:c.122-6384TG[7]	N/A	Intron Variant
BRINP3 transcript variant X10	XM_017001129.2:c.121+9060… XM_017001129.2:c.121+9060TG[7]	N/A	Intron Variant
BRINP3 transcript variant X11	XM_017001132.2:c.236+9060… XM_017001132.2:c.236+9060TG[7]	N/A	Intron Variant
BRINP3 transcript variant X12	XM_017001133.2:c.236+9060… XM_017001133.2:c.236+9060TG[7]	N/A	Intron Variant
BRINP3 transcript variant X1	XM_047419245.1:c.236+9060… XM_047419245.1:c.236+9060TG[7]	N/A	Intron Variant
BRINP3 transcript variant X3	XM_047419250.1:c.236+9060… XM_047419250.1:c.236+9060TG[7]	N/A	Intron Variant
BRINP3 transcript variant X8	XM_011509475.3: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	(CA)₁₁C=	del(AC)₄	del(AC)₃	delACAC	delAC	dupAC	dupACAC	dup(AC)₃	dup(AC)₄
GRCh38.p14 chr 1	NC_000001.11:g.190445574_190445596=	NC_000001.11:g.190445575AC[7]	NC_000001.11:g.190445575AC[8]	NC_000001.11:g.190445575AC[9]	NC_000001.11:g.190445575AC[10]	NC_000001.11:g.190445575AC[12]	NC_000001.11:g.190445575AC[13]	NC_000001.11:g.190445575AC[14]	NC_000001.11:g.190445575AC[15]
GRCh37.p13 chr 1	NC_000001.10:g.190414704_190414726=	NC_000001.10:g.190414705AC[7]	NC_000001.10:g.190414705AC[8]	NC_000001.10:g.190414705AC[9]	NC_000001.10:g.190414705AC[10]	NC_000001.10:g.190414705AC[12]	NC_000001.10:g.190414705AC[13]	NC_000001.10:g.190414705AC[14]	NC_000001.10:g.190414705AC[15]
BRINP3 transcript variant 2	NM_001317188.2:c.121+9081=	NM_001317188.2:c.121+9060TG[7]	NM_001317188.2:c.121+9060TG[8]	NM_001317188.2:c.121+9060TG[9]	NM_001317188.2:c.121+9060TG[10]	NM_001317188.2:c.121+9060TG[12]	NM_001317188.2:c.121+9060TG[13]	NM_001317188.2:c.121+9060TG[14]	NM_001317188.2:c.121+9060TG[15]
BRINP3 transcript	NM_199051.1:c.236+9081=	NM_199051.1:c.236+9060TG[7]	NM_199051.1:c.236+9060TG[8]	NM_199051.1:c.236+9060TG[9]	NM_199051.1:c.236+9060TG[10]	NM_199051.1:c.236+9060TG[12]	NM_199051.1:c.236+9060TG[13]	NM_199051.1:c.236+9060TG[14]	NM_199051.1:c.236+9060TG[15]
BRINP3 transcript variant 1	NM_199051.3:c.236+9081=	NM_199051.3:c.236+9060TG[7]	NM_199051.3:c.236+9060TG[8]	NM_199051.3:c.236+9060TG[9]	NM_199051.3:c.236+9060TG[10]	NM_199051.3:c.236+9060TG[12]	NM_199051.3:c.236+9060TG[13]	NM_199051.3:c.236+9060TG[14]	NM_199051.3:c.236+9060TG[15]
BRINP3 transcript variant X2	XM_005245117.1:c.236+9081=	XM_005245117.1:c.236+9060TG[7]	XM_005245117.1:c.236+9060TG[8]	XM_005245117.1:c.236+9060TG[9]	XM_005245117.1:c.236+9060TG[10]	XM_005245117.1:c.236+9060TG[12]	XM_005245117.1:c.236+9060TG[13]	XM_005245117.1:c.236+9060TG[14]	XM_005245117.1:c.236+9060TG[15]
FAM5C transcript variant X2	XM_005245118.1:c.236+9081=	XM_005245118.1:c.236+9060TG[7]	XM_005245118.1:c.236+9060TG[8]	XM_005245118.1:c.236+9060TG[9]	XM_005245118.1:c.236+9060TG[10]	XM_005245118.1:c.236+9060TG[12]	XM_005245118.1:c.236+9060TG[13]	XM_005245118.1:c.236+9060TG[14]	XM_005245118.1:c.236+9060TG[15]
BRINP3 transcript variant X3	XM_005245119.1:c.236+9081=	XM_005245119.1:c.236+9060TG[7]	XM_005245119.1:c.236+9060TG[8]	XM_005245119.1:c.236+9060TG[9]	XM_005245119.1:c.236+9060TG[10]	XM_005245119.1:c.236+9060TG[12]	XM_005245119.1:c.236+9060TG[13]	XM_005245119.1:c.236+9060TG[14]	XM_005245119.1:c.236+9060TG[15]
BRINP3 transcript variant X4	XM_005245120.1:c.236+9081=	XM_005245120.1:c.236+9060TG[7]	XM_005245120.1:c.236+9060TG[8]	XM_005245120.1:c.236+9060TG[9]	XM_005245120.1:c.236+9060TG[10]	XM_005245120.1:c.236+9060TG[12]	XM_005245120.1:c.236+9060TG[13]	XM_005245120.1:c.236+9060TG[14]	XM_005245120.1:c.236+9060TG[15]
FAM5C transcript variant X5	XM_005245121.1:c.121+9081=	XM_005245121.1:c.121+9060TG[7]	XM_005245121.1:c.121+9060TG[8]	XM_005245121.1:c.121+9060TG[9]	XM_005245121.1:c.121+9060TG[10]	XM_005245121.1:c.121+9060TG[12]	XM_005245121.1:c.121+9060TG[13]	XM_005245121.1:c.121+9060TG[14]	XM_005245121.1:c.121+9060TG[15]
FAM5C transcript variant X6	XM_005245122.1:c.121+9081=	XM_005245122.1:c.121+9060TG[7]	XM_005245122.1:c.121+9060TG[8]	XM_005245122.1:c.121+9060TG[9]	XM_005245122.1:c.121+9060TG[10]	XM_005245122.1:c.121+9060TG[12]	XM_005245122.1:c.121+9060TG[13]	XM_005245122.1:c.121+9060TG[14]	XM_005245122.1:c.121+9060TG[15]
BRINP3 transcript variant X7	XM_005245123.1:c.236+9081=	XM_005245123.1:c.236+9060TG[7]	XM_005245123.1:c.236+9060TG[8]	XM_005245123.1:c.236+9060TG[9]	XM_005245123.1:c.236+9060TG[10]	XM_005245123.1:c.236+9060TG[12]	XM_005245123.1:c.236+9060TG[13]	XM_005245123.1:c.236+9060TG[14]	XM_005245123.1:c.236+9060TG[15]
BRINP3 transcript variant X5	XM_011509472.3:c.122-6363=	XM_011509472.3:c.122-6384TG[7]	XM_011509472.3:c.122-6384TG[8]	XM_011509472.3:c.122-6384TG[9]	XM_011509472.3:c.122-6384TG[10]	XM_011509472.3:c.122-6384TG[12]	XM_011509472.3:c.122-6384TG[13]	XM_011509472.3:c.122-6384TG[14]	XM_011509472.3:c.122-6384TG[15]
BRINP3 transcript variant X9	XM_011509476.3:c.121+9081=	XM_011509476.3:c.121+9060TG[7]	XM_011509476.3:c.121+9060TG[8]	XM_011509476.3:c.121+9060TG[9]	XM_011509476.3:c.121+9060TG[10]	XM_011509476.3:c.121+9060TG[12]	XM_011509476.3:c.121+9060TG[13]	XM_011509476.3:c.121+9060TG[14]	XM_011509476.3:c.121+9060TG[15]
BRINP3 transcript variant X4	XM_017001125.2:c.236+9081=	XM_017001125.2:c.236+9060TG[7]	XM_017001125.2:c.236+9060TG[8]	XM_017001125.2:c.236+9060TG[9]	XM_017001125.2:c.236+9060TG[10]	XM_017001125.2:c.236+9060TG[12]	XM_017001125.2:c.236+9060TG[13]	XM_017001125.2:c.236+9060TG[14]	XM_017001125.2:c.236+9060TG[15]
BRINP3 transcript variant X2	XM_017001126.2:c.236+9081=	XM_017001126.2:c.236+9060TG[7]	XM_017001126.2:c.236+9060TG[8]	XM_017001126.2:c.236+9060TG[9]	XM_017001126.2:c.236+9060TG[10]	XM_017001126.2:c.236+9060TG[12]	XM_017001126.2:c.236+9060TG[13]	XM_017001126.2:c.236+9060TG[14]	XM_017001126.2:c.236+9060TG[15]
BRINP3 transcript variant X6	XM_017001127.2:c.122-6363=	XM_017001127.2:c.122-6384TG[7]	XM_017001127.2:c.122-6384TG[8]	XM_017001127.2:c.122-6384TG[9]	XM_017001127.2:c.122-6384TG[10]	XM_017001127.2:c.122-6384TG[12]	XM_017001127.2:c.122-6384TG[13]	XM_017001127.2:c.122-6384TG[14]	XM_017001127.2:c.122-6384TG[15]
BRINP3 transcript variant X7	XM_017001128.2:c.122-6363=	XM_017001128.2:c.122-6384TG[7]	XM_017001128.2:c.122-6384TG[8]	XM_017001128.2:c.122-6384TG[9]	XM_017001128.2:c.122-6384TG[10]	XM_017001128.2:c.122-6384TG[12]	XM_017001128.2:c.122-6384TG[13]	XM_017001128.2:c.122-6384TG[14]	XM_017001128.2:c.122-6384TG[15]
BRINP3 transcript variant X10	XM_017001129.2:c.121+9081=	XM_017001129.2:c.121+9060TG[7]	XM_017001129.2:c.121+9060TG[8]	XM_017001129.2:c.121+9060TG[9]	XM_017001129.2:c.121+9060TG[10]	XM_017001129.2:c.121+9060TG[12]	XM_017001129.2:c.121+9060TG[13]	XM_017001129.2:c.121+9060TG[14]	XM_017001129.2:c.121+9060TG[15]
BRINP3 transcript variant X11	XM_017001132.2:c.236+9081=	XM_017001132.2:c.236+9060TG[7]	XM_017001132.2:c.236+9060TG[8]	XM_017001132.2:c.236+9060TG[9]	XM_017001132.2:c.236+9060TG[10]	XM_017001132.2:c.236+9060TG[12]	XM_017001132.2:c.236+9060TG[13]	XM_017001132.2:c.236+9060TG[14]	XM_017001132.2:c.236+9060TG[15]
BRINP3 transcript variant X12	XM_017001133.2:c.236+9081=	XM_017001133.2:c.236+9060TG[7]	XM_017001133.2:c.236+9060TG[8]	XM_017001133.2:c.236+9060TG[9]	XM_017001133.2:c.236+9060TG[10]	XM_017001133.2:c.236+9060TG[12]	XM_017001133.2:c.236+9060TG[13]	XM_017001133.2:c.236+9060TG[14]	XM_017001133.2:c.236+9060TG[15]
BRINP3 transcript variant X1	XM_047419245.1:c.236+9081=	XM_047419245.1:c.236+9060TG[7]	XM_047419245.1:c.236+9060TG[8]	XM_047419245.1:c.236+9060TG[9]	XM_047419245.1:c.236+9060TG[10]	XM_047419245.1:c.236+9060TG[12]	XM_047419245.1:c.236+9060TG[13]	XM_047419245.1:c.236+9060TG[14]	XM_047419245.1:c.236+9060TG[15]
BRINP3 transcript variant X3	XM_047419250.1:c.236+9081=	XM_047419250.1:c.236+9060TG[7]	XM_047419250.1:c.236+9060TG[8]	XM_047419250.1:c.236+9060TG[9]	XM_047419250.1:c.236+9060TG[10]	XM_047419250.1:c.236+9060TG[12]	XM_047419250.1:c.236+9060TG[13]	XM_047419250.1:c.236+9060TG[14]	XM_047419250.1:c.236+9060TG[15]

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#.

66 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41197572	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss95951389	Oct 11, 2018 (152)
3	BL	ss255959252	May 09, 2011 (135)
4	GMI	ss287685181	Dec 06, 2013 (144)
5	GMI	ss288069998	Jan 10, 2018 (151)
6	GMI	ss288070000	May 04, 2012 (137)
7	1000GENOMES	ss326113328	May 09, 2011 (135)
8	1000GENOMES	ss326117844	Jan 10, 2018 (151)
9	1000GENOMES	ss326154909	Jan 10, 2018 (151)
10	LUNTER	ss551004101	Jan 10, 2018 (151)
11	LUNTER	ss551029924	Jan 10, 2018 (151)
12	LUNTER	ss552828313	Apr 25, 2013 (138)
13	SSMP	ss663142326	Apr 01, 2015 (144)
14	BILGI_BIOE	ss666120375	Apr 25, 2013 (138)
15	1000GENOMES	ss1367935534	Aug 21, 2014 (142)
16	EVA_UK10K_ALSPAC	ss1701558943	Jan 10, 2018 (151)
17	EVA_UK10K_ALSPAC	ss1701558947	Apr 01, 2015 (144)
18	EVA_UK10K_TWINSUK	ss1701559065	Jan 10, 2018 (151)
19	EVA_UK10K_TWINSUK	ss1701559071	Apr 01, 2015 (144)
20	EVA_UK10K_TWINSUK	ss1709962557	Apr 01, 2015 (144)
21	EVA_UK10K_ALSPAC	ss1709962571	Apr 01, 2015 (144)
22	SWEGEN	ss2988151928	Jan 10, 2018 (151)
23	MCHAISSO	ss3064435497	Jan 10, 2018 (151)
24	URBANLAB	ss3646846391	Oct 11, 2018 (152)
25	EVA_DECODE	ss3688266567	Jul 12, 2019 (153)
26	EVA_DECODE	ss3688266568	Jul 12, 2019 (153)
27	EVA_DECODE	ss3688266569	Jul 12, 2019 (153)
28	EVA_DECODE	ss3688266570	Jul 12, 2019 (153)
29	EVA_DECODE	ss3688266571	Jul 12, 2019 (153)
30	ACPOP	ss3727700865	Jul 12, 2019 (153)
31	ACPOP	ss3727700866	Jul 12, 2019 (153)
32	KHV_HUMAN_GENOMES	ss3800116130	Jul 12, 2019 (153)
33	EVA	ss3826552778	Apr 25, 2020 (154)
34	EVA	ss3842084355	Apr 25, 2020 (154)
35	KOGIC	ss3946134421	Apr 25, 2020 (154)
36	KOGIC	ss3946134422	Apr 25, 2020 (154)
37	KOGIC	ss3946134423	Apr 25, 2020 (154)
38	KOGIC	ss3946134424	Apr 25, 2020 (154)
39	GNOMAD	ss4008044706	Apr 25, 2021 (155)
40	GNOMAD	ss4008044707	Apr 25, 2021 (155)
41	GNOMAD	ss4008044708	Apr 25, 2021 (155)
42	GNOMAD	ss4008044709	Apr 25, 2021 (155)
43	GNOMAD	ss4008044710	Apr 25, 2021 (155)
44	GNOMAD	ss4008044711	Apr 25, 2021 (155)
45	GNOMAD	ss4008044712	Apr 25, 2021 (155)
46	TOMMO_GENOMICS	ss5147601799	Apr 25, 2021 (155)
47	TOMMO_GENOMICS	ss5147601800	Apr 25, 2021 (155)
48	TOMMO_GENOMICS	ss5147601801	Apr 25, 2021 (155)
49	TOMMO_GENOMICS	ss5147601802	Apr 25, 2021 (155)
50	1000G_HIGH_COVERAGE	ss5245158413	Oct 12, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5245158414	Oct 12, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5245158415	Oct 12, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5245158416	Oct 12, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5245158417	Oct 12, 2022 (156)
55	HUGCELL_USP	ss5445657093	Oct 12, 2022 (156)
56	HUGCELL_USP	ss5445657094	Oct 12, 2022 (156)
57	HUGCELL_USP	ss5445657095	Oct 12, 2022 (156)
58	HUGCELL_USP	ss5445657096	Oct 12, 2022 (156)
59	TOMMO_GENOMICS	ss5675121913	Oct 12, 2022 (156)
60	TOMMO_GENOMICS	ss5675121914	Oct 12, 2022 (156)
61	TOMMO_GENOMICS	ss5675121916	Oct 12, 2022 (156)
62	TOMMO_GENOMICS	ss5675121917	Oct 12, 2022 (156)
63	EVA	ss5833006026	Oct 12, 2022 (156)
64	EVA	ss5833006027	Oct 12, 2022 (156)
65	EVA	ss5938905279	Oct 12, 2022 (156)
66	EVA	ss5938905280	Oct 12, 2022 (156)
67	1000Genomes	NC_000001.10 - 190414704	Oct 11, 2018 (152)
68	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 2605295 (NC_000001.10:190414703:CA: 630/3854) Row 2605296 (NC_000001.10:190414703::CA 685/3854) Row 2605297 (NC_000001.10:190414704::AC 710/3854)	-	Oct 11, 2018 (152)
69	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 2605295 (NC_000001.10:190414703:CA: 630/3854) Row 2605296 (NC_000001.10:190414703::CA 685/3854) Row 2605297 (NC_000001.10:190414704::AC 710/3854)	-	Oct 11, 2018 (152)
70	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 2605295 (NC_000001.10:190414703:CA: 630/3854) Row 2605296 (NC_000001.10:190414703::CA 685/3854) Row 2605297 (NC_000001.10:190414704::AC 710/3854)	-	Oct 11, 2018 (152)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 34246939 (NC_000001.11:190445573::CA 20277/136992) Row 34246940 (NC_000001.11:190445573::CACA 781/137068) Row 34246941 (NC_000001.11:190445573::CACACA 5/137072)...	-	Apr 25, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 34246939 (NC_000001.11:190445573::CA 20277/136992) Row 34246940 (NC_000001.11:190445573::CACA 781/137068) Row 34246941 (NC_000001.11:190445573::CACACA 5/137072)...	-	Apr 25, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 34246939 (NC_000001.11:190445573::CA 20277/136992) Row 34246940 (NC_000001.11:190445573::CACA 781/137068) Row 34246941 (NC_000001.11:190445573::CACACA 5/137072)...	-	Apr 25, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 34246939 (NC_000001.11:190445573::CA 20277/136992) Row 34246940 (NC_000001.11:190445573::CACA 781/137068) Row 34246941 (NC_000001.11:190445573::CACACA 5/137072)...	-	Apr 25, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 34246939 (NC_000001.11:190445573::CA 20277/136992) Row 34246940 (NC_000001.11:190445573::CACA 781/137068) Row 34246941 (NC_000001.11:190445573::CACACA 5/137072)...	-	Apr 25, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 34246939 (NC_000001.11:190445573::CA 20277/136992) Row 34246940 (NC_000001.11:190445573::CACA 781/137068) Row 34246941 (NC_000001.11:190445573::CACACA 5/137072)...	-	Apr 25, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 34246939 (NC_000001.11:190445573::CA 20277/136992) Row 34246940 (NC_000001.11:190445573::CACA 781/137068) Row 34246941 (NC_000001.11:190445573::CACACA 5/137072)...	-	Apr 25, 2021 (155)
78	Korean Genome Project Submission ignored due to conflicting rows: Row 2512422 (NC_000001.11:190445575:CA: 105/1832) Row 2512423 (NC_000001.11:190445577::CA 282/1832) Row 2512424 (NC_000001.11:190445577::CACA 2/1832)...	-	Apr 25, 2020 (154)
79	Korean Genome Project Submission ignored due to conflicting rows: Row 2512422 (NC_000001.11:190445575:CA: 105/1832) Row 2512423 (NC_000001.11:190445577::CA 282/1832) Row 2512424 (NC_000001.11:190445577::CACA 2/1832)...	-	Apr 25, 2020 (154)
80	Korean Genome Project Submission ignored due to conflicting rows: Row 2512422 (NC_000001.11:190445575:CA: 105/1832) Row 2512423 (NC_000001.11:190445577::CA 282/1832) Row 2512424 (NC_000001.11:190445577::CACA 2/1832)...	-	Apr 25, 2020 (154)
81	Korean Genome Project Submission ignored due to conflicting rows: Row 2512422 (NC_000001.11:190445575:CA: 105/1832) Row 2512423 (NC_000001.11:190445577::CA 282/1832) Row 2512424 (NC_000001.11:190445577::CACA 2/1832)...	-	Apr 25, 2020 (154)
82	Northern Sweden Submission ignored due to conflicting rows: Row 985730 (NC_000001.10:190414703::CA 135/600) Row 985731 (NC_000001.10:190414703:CA: 96/600)	-	Jul 12, 2019 (153)
83	Northern Sweden Submission ignored due to conflicting rows: Row 985730 (NC_000001.10:190414703::CA 135/600) Row 985731 (NC_000001.10:190414703:CA: 96/600)	-	Jul 12, 2019 (153)
84	8.3KJPN Submission ignored due to conflicting rows: Row 5571106 (NC_000001.10:190414703:CA: 636/16760) Row 5571107 (NC_000001.10:190414703::CA 1865/16760) Row 5571108 (NC_000001.10:190414703::CACA 11/16760)...	-	Apr 25, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 5571106 (NC_000001.10:190414703:CA: 636/16760) Row 5571107 (NC_000001.10:190414703::CA 1865/16760) Row 5571108 (NC_000001.10:190414703::CACA 11/16760)...	-	Apr 25, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 5571106 (NC_000001.10:190414703:CA: 636/16760) Row 5571107 (NC_000001.10:190414703::CA 1865/16760) Row 5571108 (NC_000001.10:190414703::CACA 11/16760)...	-	Apr 25, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 5571106 (NC_000001.10:190414703:CA: 636/16760) Row 5571107 (NC_000001.10:190414703::CA 1865/16760) Row 5571108 (NC_000001.10:190414703::CACA 11/16760)...	-	Apr 25, 2021 (155)
88	14KJPN Submission ignored due to conflicting rows: Row 8959017 (NC_000001.11:190445573:CA: 1095/28256) Row 8959018 (NC_000001.11:190445573::CA 3184/28256) Row 8959020 (NC_000001.11:190445573:CACA: 4/28256)...	-	Oct 12, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 8959017 (NC_000001.11:190445573:CA: 1095/28256) Row 8959018 (NC_000001.11:190445573::CA 3184/28256) Row 8959020 (NC_000001.11:190445573:CACA: 4/28256)...	-	Oct 12, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 8959017 (NC_000001.11:190445573:CA: 1095/28256) Row 8959018 (NC_000001.11:190445573::CA 3184/28256) Row 8959020 (NC_000001.11:190445573:CACA: 4/28256)...	-	Oct 12, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 8959017 (NC_000001.11:190445573:CA: 1095/28256) Row 8959018 (NC_000001.11:190445573::CA 3184/28256) Row 8959020 (NC_000001.11:190445573:CACA: 4/28256)...	-	Oct 12, 2022 (156)
92	UK 10K study - Twins Submission ignored due to conflicting rows: Row 2605295 (NC_000001.10:190414703:CA: 681/3708) Row 2605296 (NC_000001.10:190414703::CA 622/3708) Row 2605297 (NC_000001.10:190414704::AC 653/3708)	-	Oct 11, 2018 (152)
93	UK 10K study - Twins Submission ignored due to conflicting rows: Row 2605295 (NC_000001.10:190414703:CA: 681/3708) Row 2605296 (NC_000001.10:190414703::CA 622/3708) Row 2605297 (NC_000001.10:190414704::AC 653/3708)	-	Oct 11, 2018 (152)
94	UK 10K study - Twins Submission ignored due to conflicting rows: Row 2605295 (NC_000001.10:190414703:CA: 681/3708) Row 2605296 (NC_000001.10:190414703::CA 622/3708) Row 2605297 (NC_000001.10:190414704::AC 653/3708)	-	Oct 11, 2018 (152)
95	ALFA	NC_000001.11 - 190445574	Apr 25, 2021 (155)

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

Associated ID	History Updated (Build)
rs148327909	Sep 17, 2011 (135)
rs72080749	May 15, 2013 (138)
rs143025476	May 11, 2012 (137)
rs144354268	May 11, 2012 (137)
rs375959082	May 13, 2013 (138)
rs398103498	Apr 01, 2015 (144)
rs796962155	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4008044712	NC_000001.11:190445573:CACACACA:	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACAC	(self)
13904723921	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACAC	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACAC	(self)
ss3688266571, ss4008044711, ss5245158416	NC_000001.11:190445573:CACACA:	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACAC	(self)
13904723921	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACAC	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACAC	(self)
ss5147601802	NC_000001.10:190414703:CACA:	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACAC	(self)
ss3946134424, ss4008044710, ss5245158417, ss5445657095, ss5675121916	NC_000001.11:190445573:CACA:	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACAC	(self)
13904723921	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACAC	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACAC	(self)
ss3688266570	NC_000001.11:190445575:CACA:	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACAC	(self)
ss288069998, ss326117844, ss326154909, ss551004101, ss551029924	NC_000001.9:188681326:CA:	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACAC	(self)
ss1701558943, ss1701559065, ss2988151928, ss3727700866, ss3826552778, ss5147601799, ss5833006027	NC_000001.10:190414703:CA:	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACAC	(self)
ss3064435497, ss4008044709, ss5245158413, ss5445657093, ss5675121913	NC_000001.11:190445573:CA:	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACAC	(self)
13904723921	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACAC	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACAC	(self)
ss3946134421	NC_000001.11:190445575:CA:	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACAC	(self)
ss3688266569	NC_000001.11:190445577:CA:	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACAC	(self)
ss287685181	NT_004487.19:41903345:CA:	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACAC	(self)
ss255959252, ss326113328, ss552828313	NC_000001.9:188681326::CA	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACAC	(self)
ss288070000	NC_000001.9:188681349::AC	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACAC	(self)
4749814, ss663142326, ss666120375, ss1367935534, ss3727700865, ss5147601800, ss5833006026, ss5938905279	NC_000001.10:190414703::CA	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACAC	(self)
ss1701558947, ss1701559071, ss5938905280	NC_000001.10:190414704::AC	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACAC	(self)
ss1709962557, ss1709962571	NC_000001.10:190414705::CA	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACAC	(self)
ss3646846391, ss3800116130, ss3842084355, ss4008044706, ss5245158415, ss5445657094, ss5675121914	NC_000001.11:190445573::CA	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACAC	(self)
13904723921	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACAC	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACAC	(self)
ss3946134422	NC_000001.11:190445577::CA	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACAC	(self)
ss3688266568	NC_000001.11:190445579::CA	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACAC	(self)
ss41197572	NT_004487.19:41903345::CA	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACAC	(self)
ss95951389	NT_004487.19:41903368::AC	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACAC	(self)
ss5147601801	NC_000001.10:190414703::CACA	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACACAC	(self)
ss4008044707, ss5245158414, ss5445657096, ss5675121917	NC_000001.11:190445573::CACA	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACACAC	(self)
13904723921	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACACAC	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACACAC	(self)
ss3946134423	NC_000001.11:190445577::CACA	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACACAC	(self)
ss3688266567	NC_000001.11:190445579::CACA	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACACAC	(self)
ss4008044708	NC_000001.11:190445573::CACACA	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACACACAC	(self)
13904723921	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACACACAC	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACACACAC	(self)
13904723921	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI
ss2331153494	NC_000001.10:190414703::CACACACA	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC
ss2331153495	NC_000001.10:190414703:CACACACA:	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACAC
ss3098613169	NC_000001.11:190445573::CACACACA	NC_000001.11:190445573:CACACACACAC… NC_000001.11:190445573:CACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC

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

No publications for rs34406812

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

rs34406812