Name: rs533794156
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.

rs533794156

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:44833097-44833114 (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)₉ / del(T)₈ / del(T)₇ / del(…
del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₄ / dup(T)₁₅ / ins(T)₂₃
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₉=0.00000 (0/10694, ALFA)
del(T)₈=0.00000 (0/10694, ALFA)
del(T)₇=0.00000 (0/10694, ALFA) (+ 12 more)
del(T)₆=0.00000 (0/10694, ALFA)
del(T)₅=0.00000 (0/10694, ALFA)
delTTT=0.00000 (0/10694, ALFA)
delTT=0.00000 (0/10694, ALFA)
delT=0.00000 (0/10694, ALFA)
dupT=0.00000 (0/10694, ALFA)
dupTT=0.00000 (0/10694, ALFA)
dup(T)₄=0.00000 (0/10694, ALFA)
delT=0.1941 (972/5008, 1000G)
dup(T)₁₀=0.2449 (944/3854, ALSPAC)
dup(T)₁₀=0.2309 (856/3708, TWINSUK)
delT=0.07 (3/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ARHGAP8 : Intron Variant
PRR5-ARHGAP8 : 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	HWEP
Total	Global	10694	TTTTTTTTTTTTTTTTTT=1.00000	TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	7588	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2264	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	86	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	2178	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	22	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	18	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	N/A
Latin American 1	Sub	120	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	320	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	62	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	318	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	10694	(T)₁₈=1.00000	del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00000, dupTT=0.00000, dup(T)₄=0.00000
Allele Frequency Aggregator	European	Sub	7588	(T)₁₈=1.0000	del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	2264	(T)₁₈=1.0000	del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	320	(T)₁₈=1.000	del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	318	(T)₁₈=1.000	del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	120	(T)₁₈=1.000	del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	South Asian	Sub	62	(T)₁₈=1.00	del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	22	(T)₁₈=1.00	del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)₄=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₈=0.8059	delT=0.1941
1000Genomes	African	Sub	1322	(T)₁₈=0.8782	delT=0.1218
1000Genomes	East Asian	Sub	1008	(T)₁₈=0.5952	delT=0.4048
1000Genomes	Europe	Sub	1006	(T)₁₈=0.8797	delT=0.1203
1000Genomes	South Asian	Sub	978	(T)₁₈=0.834	delT=0.166
1000Genomes	American	Sub	694	(T)₁₈=0.827	delT=0.173
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dup(T)₁₀=0.2449
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dup(T)₁₀=0.2309
The Danish reference pan genome	Danish	Study-wide	40	(T)₁₈=0.93	delT=0.07

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 22	NC_000022.11:g.44833106_44833114del
GRCh38.p14 chr 22	NC_000022.11:g.44833107_44833114del
GRCh38.p14 chr 22	NC_000022.11:g.44833108_44833114del
GRCh38.p14 chr 22	NC_000022.11:g.44833109_44833114del
GRCh38.p14 chr 22	NC_000022.11:g.44833110_44833114del
GRCh38.p14 chr 22	NC_000022.11:g.44833112_44833114del
GRCh38.p14 chr 22	NC_000022.11:g.44833113_44833114del
GRCh38.p14 chr 22	NC_000022.11:g.44833114del
GRCh38.p14 chr 22	NC_000022.11:g.44833114dup
GRCh38.p14 chr 22	NC_000022.11:g.44833113_44833114dup
GRCh38.p14 chr 22	NC_000022.11:g.44833112_44833114dup
GRCh38.p14 chr 22	NC_000022.11:g.44833111_44833114dup
GRCh38.p14 chr 22	NC_000022.11:g.44833109_44833114dup
GRCh38.p14 chr 22	NC_000022.11:g.44833108_44833114dup
GRCh38.p14 chr 22	NC_000022.11:g.44833107_44833114dup
GRCh38.p14 chr 22	NC_000022.11:g.44833106_44833114dup
GRCh38.p14 chr 22	NC_000022.11:g.44833105_44833114dup
GRCh38.p14 chr 22	NC_000022.11:g.44833104_44833114dup
GRCh38.p14 chr 22	NC_000022.11:g.44833101_44833114dup
GRCh38.p14 chr 22	NC_000022.11:g.44833100_44833114dup
GRCh38.p14 chr 22	NC_000022.11:g.44833114_44833115insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 22	NC_000022.10:g.45228986_45228994del
GRCh37.p13 chr 22	NC_000022.10:g.45228987_45228994del
GRCh37.p13 chr 22	NC_000022.10:g.45228988_45228994del
GRCh37.p13 chr 22	NC_000022.10:g.45228989_45228994del
GRCh37.p13 chr 22	NC_000022.10:g.45228990_45228994del
GRCh37.p13 chr 22	NC_000022.10:g.45228992_45228994del
GRCh37.p13 chr 22	NC_000022.10:g.45228993_45228994del
GRCh37.p13 chr 22	NC_000022.10:g.45228994del
GRCh37.p13 chr 22	NC_000022.10:g.45228994dup
GRCh37.p13 chr 22	NC_000022.10:g.45228993_45228994dup
GRCh37.p13 chr 22	NC_000022.10:g.45228992_45228994dup
GRCh37.p13 chr 22	NC_000022.10:g.45228991_45228994dup
GRCh37.p13 chr 22	NC_000022.10:g.45228989_45228994dup
GRCh37.p13 chr 22	NC_000022.10:g.45228988_45228994dup
GRCh37.p13 chr 22	NC_000022.10:g.45228987_45228994dup
GRCh37.p13 chr 22	NC_000022.10:g.45228986_45228994dup
GRCh37.p13 chr 22	NC_000022.10:g.45228985_45228994dup
GRCh37.p13 chr 22	NC_000022.10:g.45228984_45228994dup
GRCh37.p13 chr 22	NC_000022.10:g.45228981_45228994dup
GRCh37.p13 chr 22	NC_000022.10:g.45228980_45228994dup
GRCh37.p13 chr 22	NC_000022.10:g.45228994_45228995insTTTTTTTTTTTTTTTTTTTTTTT
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135909_135917del
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135910_135917del
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135911_135917del
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135912_135917del
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135913_135917del
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135915_135917del
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135916_135917del
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135917del
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135917dup
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135916_135917dup
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135915_135917dup
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135914_135917dup
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135912_135917dup
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135911_135917dup
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135910_135917dup
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135909_135917dup
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135908_135917dup
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135907_135917dup
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135904_135917dup
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135903_135917dup
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135917_135918insTTTTTTTTTTTTTTTTTTTTTTT

Gene: ARHGAP8, Rho GTPase activating protein 8 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ARHGAP8 transcript variant 1	NM_001017526.2:c.689+7513… NM_001017526.2:c.689+7513_689+7521del	N/A	Intron Variant
ARHGAP8 transcript variant 3	NM_001198726.2:c.596+7513… NM_001198726.2:c.596+7513_596+7521del	N/A	Intron Variant
ARHGAP8 transcript variant 2	NM_181335.3:c.596+7513_59… NM_181335.3:c.596+7513_596+7521del	N/A	Intron Variant

Gene: PRR5-ARHGAP8, PRR5-ARHGAP8 readthrough (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PRR5-ARHGAP8 transcript	NM_181334.6:c.989+7513_98… NM_181334.6:c.989+7513_989+7521del	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(T)₁₈=	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₄	dup(T)₁₅	ins(T)₂₃
GRCh38.p14 chr 22	NC_000022.11:g.44833097_44833114=	NC_000022.11:g.44833106_44833114del	NC_000022.11:g.44833107_44833114del	NC_000022.11:g.44833108_44833114del	NC_000022.11:g.44833109_44833114del	NC_000022.11:g.44833110_44833114del	NC_000022.11:g.44833112_44833114del	NC_000022.11:g.44833113_44833114del	NC_000022.11:g.44833114del	NC_000022.11:g.44833114dup	NC_000022.11:g.44833113_44833114dup	NC_000022.11:g.44833112_44833114dup	NC_000022.11:g.44833111_44833114dup	NC_000022.11:g.44833109_44833114dup	NC_000022.11:g.44833108_44833114dup	NC_000022.11:g.44833107_44833114dup	NC_000022.11:g.44833106_44833114dup	NC_000022.11:g.44833105_44833114dup	NC_000022.11:g.44833104_44833114dup	NC_000022.11:g.44833101_44833114dup	NC_000022.11:g.44833100_44833114dup	NC_000022.11:g.44833114_44833115insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 22	NC_000022.10:g.45228977_45228994=	NC_000022.10:g.45228986_45228994del	NC_000022.10:g.45228987_45228994del	NC_000022.10:g.45228988_45228994del	NC_000022.10:g.45228989_45228994del	NC_000022.10:g.45228990_45228994del	NC_000022.10:g.45228992_45228994del	NC_000022.10:g.45228993_45228994del	NC_000022.10:g.45228994del	NC_000022.10:g.45228994dup	NC_000022.10:g.45228993_45228994dup	NC_000022.10:g.45228992_45228994dup	NC_000022.10:g.45228991_45228994dup	NC_000022.10:g.45228989_45228994dup	NC_000022.10:g.45228988_45228994dup	NC_000022.10:g.45228987_45228994dup	NC_000022.10:g.45228986_45228994dup	NC_000022.10:g.45228985_45228994dup	NC_000022.10:g.45228984_45228994dup	NC_000022.10:g.45228981_45228994dup	NC_000022.10:g.45228980_45228994dup	NC_000022.10:g.45228994_45228995insTTTTTTTTTTTTTTTTTTTTTTT
PRR5-ARHGAP8 RefSeqGene	NG_046967.1:g.135900_135917=	NG_046967.1:g.135909_135917del	NG_046967.1:g.135910_135917del	NG_046967.1:g.135911_135917del	NG_046967.1:g.135912_135917del	NG_046967.1:g.135913_135917del	NG_046967.1:g.135915_135917del	NG_046967.1:g.135916_135917del	NG_046967.1:g.135917del	NG_046967.1:g.135917dup	NG_046967.1:g.135916_135917dup	NG_046967.1:g.135915_135917dup	NG_046967.1:g.135914_135917dup	NG_046967.1:g.135912_135917dup	NG_046967.1:g.135911_135917dup	NG_046967.1:g.135910_135917dup	NG_046967.1:g.135909_135917dup	NG_046967.1:g.135908_135917dup	NG_046967.1:g.135907_135917dup	NG_046967.1:g.135904_135917dup	NG_046967.1:g.135903_135917dup	NG_046967.1:g.135917_135918insTTTTTTTTTTTTTTTTTTTTTTT
ARHGAP8 transcript variant 1	NM_001017526.1:c.689+7504=	NM_001017526.1:c.689+7513_689+7521del	NM_001017526.1:c.689+7514_689+7521del	NM_001017526.1:c.689+7515_689+7521del	NM_001017526.1:c.689+7516_689+7521del	NM_001017526.1:c.689+7517_689+7521del	NM_001017526.1:c.689+7519_689+7521del	NM_001017526.1:c.689+7520_689+7521del	NM_001017526.1:c.689+7521del	NM_001017526.1:c.689+7521dup	NM_001017526.1:c.689+7520_689+7521dup	NM_001017526.1:c.689+7519_689+7521dup	NM_001017526.1:c.689+7518_689+7521dup	NM_001017526.1:c.689+7516_689+7521dup	NM_001017526.1:c.689+7515_689+7521dup	NM_001017526.1:c.689+7514_689+7521dup	NM_001017526.1:c.689+7513_689+7521dup	NM_001017526.1:c.689+7512_689+7521dup	NM_001017526.1:c.689+7511_689+7521dup	NM_001017526.1:c.689+7508_689+7521dup	NM_001017526.1:c.689+7507_689+7521dup	NM_001017526.1:c.689+7521_689+7522insTTTTTTTTTTTTTTTTTTTTTTT
ARHGAP8 transcript variant 1	NM_001017526.2:c.689+7504=	NM_001017526.2:c.689+7513_689+7521del	NM_001017526.2:c.689+7514_689+7521del	NM_001017526.2:c.689+7515_689+7521del	NM_001017526.2:c.689+7516_689+7521del	NM_001017526.2:c.689+7517_689+7521del	NM_001017526.2:c.689+7519_689+7521del	NM_001017526.2:c.689+7520_689+7521del	NM_001017526.2:c.689+7521del	NM_001017526.2:c.689+7521dup	NM_001017526.2:c.689+7520_689+7521dup	NM_001017526.2:c.689+7519_689+7521dup	NM_001017526.2:c.689+7518_689+7521dup	NM_001017526.2:c.689+7516_689+7521dup	NM_001017526.2:c.689+7515_689+7521dup	NM_001017526.2:c.689+7514_689+7521dup	NM_001017526.2:c.689+7513_689+7521dup	NM_001017526.2:c.689+7512_689+7521dup	NM_001017526.2:c.689+7511_689+7521dup	NM_001017526.2:c.689+7508_689+7521dup	NM_001017526.2:c.689+7507_689+7521dup	NM_001017526.2:c.689+7521_689+7522insTTTTTTTTTTTTTTTTTTTTTTT
ARHGAP8 transcript variant 3	NM_001198726.1:c.596+7504=	NM_001198726.1:c.596+7513_596+7521del	NM_001198726.1:c.596+7514_596+7521del	NM_001198726.1:c.596+7515_596+7521del	NM_001198726.1:c.596+7516_596+7521del	NM_001198726.1:c.596+7517_596+7521del	NM_001198726.1:c.596+7519_596+7521del	NM_001198726.1:c.596+7520_596+7521del	NM_001198726.1:c.596+7521del	NM_001198726.1:c.596+7521dup	NM_001198726.1:c.596+7520_596+7521dup	NM_001198726.1:c.596+7519_596+7521dup	NM_001198726.1:c.596+7518_596+7521dup	NM_001198726.1:c.596+7516_596+7521dup	NM_001198726.1:c.596+7515_596+7521dup	NM_001198726.1:c.596+7514_596+7521dup	NM_001198726.1:c.596+7513_596+7521dup	NM_001198726.1:c.596+7512_596+7521dup	NM_001198726.1:c.596+7511_596+7521dup	NM_001198726.1:c.596+7508_596+7521dup	NM_001198726.1:c.596+7507_596+7521dup	NM_001198726.1:c.596+7521_596+7522insTTTTTTTTTTTTTTTTTTTTTTT
ARHGAP8 transcript variant 3	NM_001198726.2:c.596+7504=	NM_001198726.2:c.596+7513_596+7521del	NM_001198726.2:c.596+7514_596+7521del	NM_001198726.2:c.596+7515_596+7521del	NM_001198726.2:c.596+7516_596+7521del	NM_001198726.2:c.596+7517_596+7521del	NM_001198726.2:c.596+7519_596+7521del	NM_001198726.2:c.596+7520_596+7521del	NM_001198726.2:c.596+7521del	NM_001198726.2:c.596+7521dup	NM_001198726.2:c.596+7520_596+7521dup	NM_001198726.2:c.596+7519_596+7521dup	NM_001198726.2:c.596+7518_596+7521dup	NM_001198726.2:c.596+7516_596+7521dup	NM_001198726.2:c.596+7515_596+7521dup	NM_001198726.2:c.596+7514_596+7521dup	NM_001198726.2:c.596+7513_596+7521dup	NM_001198726.2:c.596+7512_596+7521dup	NM_001198726.2:c.596+7511_596+7521dup	NM_001198726.2:c.596+7508_596+7521dup	NM_001198726.2:c.596+7507_596+7521dup	NM_001198726.2:c.596+7521_596+7522insTTTTTTTTTTTTTTTTTTTTTTT
PRR5-ARHGAP8 transcript	NM_181334.4:c.962+7504=	NM_181334.4:c.962+7513_962+7521del	NM_181334.4:c.962+7514_962+7521del	NM_181334.4:c.962+7515_962+7521del	NM_181334.4:c.962+7516_962+7521del	NM_181334.4:c.962+7517_962+7521del	NM_181334.4:c.962+7519_962+7521del	NM_181334.4:c.962+7520_962+7521del	NM_181334.4:c.962+7521del	NM_181334.4:c.962+7521dup	NM_181334.4:c.962+7520_962+7521dup	NM_181334.4:c.962+7519_962+7521dup	NM_181334.4:c.962+7518_962+7521dup	NM_181334.4:c.962+7516_962+7521dup	NM_181334.4:c.962+7515_962+7521dup	NM_181334.4:c.962+7514_962+7521dup	NM_181334.4:c.962+7513_962+7521dup	NM_181334.4:c.962+7512_962+7521dup	NM_181334.4:c.962+7511_962+7521dup	NM_181334.4:c.962+7508_962+7521dup	NM_181334.4:c.962+7507_962+7521dup	NM_181334.4:c.962+7521_962+7522insTTTTTTTTTTTTTTTTTTTTTTT
PRR5-ARHGAP8 transcript	NM_181334.6:c.989+7504=	NM_181334.6:c.989+7513_989+7521del	NM_181334.6:c.989+7514_989+7521del	NM_181334.6:c.989+7515_989+7521del	NM_181334.6:c.989+7516_989+7521del	NM_181334.6:c.989+7517_989+7521del	NM_181334.6:c.989+7519_989+7521del	NM_181334.6:c.989+7520_989+7521del	NM_181334.6:c.989+7521del	NM_181334.6:c.989+7521dup	NM_181334.6:c.989+7520_989+7521dup	NM_181334.6:c.989+7519_989+7521dup	NM_181334.6:c.989+7518_989+7521dup	NM_181334.6:c.989+7516_989+7521dup	NM_181334.6:c.989+7515_989+7521dup	NM_181334.6:c.989+7514_989+7521dup	NM_181334.6:c.989+7513_989+7521dup	NM_181334.6:c.989+7512_989+7521dup	NM_181334.6:c.989+7511_989+7521dup	NM_181334.6:c.989+7508_989+7521dup	NM_181334.6:c.989+7507_989+7521dup	NM_181334.6:c.989+7521_989+7522insTTTTTTTTTTTTTTTTTTTTTTT
ARHGAP8 transcript variant 2	NM_181335.2:c.596+7504=	NM_181335.2:c.596+7513_596+7521del	NM_181335.2:c.596+7514_596+7521del	NM_181335.2:c.596+7515_596+7521del	NM_181335.2:c.596+7516_596+7521del	NM_181335.2:c.596+7517_596+7521del	NM_181335.2:c.596+7519_596+7521del	NM_181335.2:c.596+7520_596+7521del	NM_181335.2:c.596+7521del	NM_181335.2:c.596+7521dup	NM_181335.2:c.596+7520_596+7521dup	NM_181335.2:c.596+7519_596+7521dup	NM_181335.2:c.596+7518_596+7521dup	NM_181335.2:c.596+7516_596+7521dup	NM_181335.2:c.596+7515_596+7521dup	NM_181335.2:c.596+7514_596+7521dup	NM_181335.2:c.596+7513_596+7521dup	NM_181335.2:c.596+7512_596+7521dup	NM_181335.2:c.596+7511_596+7521dup	NM_181335.2:c.596+7508_596+7521dup	NM_181335.2:c.596+7507_596+7521dup	NM_181335.2:c.596+7521_596+7522insTTTTTTTTTTTTTTTTTTTTTTT
ARHGAP8 transcript variant 2	NM_181335.3:c.596+7504=	NM_181335.3:c.596+7513_596+7521del	NM_181335.3:c.596+7514_596+7521del	NM_181335.3:c.596+7515_596+7521del	NM_181335.3:c.596+7516_596+7521del	NM_181335.3:c.596+7517_596+7521del	NM_181335.3:c.596+7519_596+7521del	NM_181335.3:c.596+7520_596+7521del	NM_181335.3:c.596+7521del	NM_181335.3:c.596+7521dup	NM_181335.3:c.596+7520_596+7521dup	NM_181335.3:c.596+7519_596+7521dup	NM_181335.3:c.596+7518_596+7521dup	NM_181335.3:c.596+7516_596+7521dup	NM_181335.3:c.596+7515_596+7521dup	NM_181335.3:c.596+7514_596+7521dup	NM_181335.3:c.596+7513_596+7521dup	NM_181335.3:c.596+7512_596+7521dup	NM_181335.3:c.596+7511_596+7521dup	NM_181335.3:c.596+7508_596+7521dup	NM_181335.3:c.596+7507_596+7521dup	NM_181335.3:c.596+7521_596+7522insTTTTTTTTTTTTTTTTTTTTTTT

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#.

33 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss96111402	Oct 12, 2018 (152)
2	1000GENOMES	ss1379104622	Aug 21, 2014 (142)
3	EVA_GENOME_DK	ss1575849932	Apr 01, 2015 (144)
4	EVA_UK10K_ALSPAC	ss1709615190	Apr 01, 2015 (144)
5	EVA_UK10K_TWINSUK	ss1709615451	Apr 01, 2015 (144)
6	SWEGEN	ss3019413601	Nov 08, 2017 (151)
7	URBANLAB	ss3651192908	Oct 12, 2018 (152)
8	EVA_DECODE	ss3708333875	Jul 13, 2019 (153)
9	EVA_DECODE	ss3708333881	Jul 13, 2019 (153)
10	KHV_HUMAN_GENOMES	ss3822621641	Jul 13, 2019 (153)
11	GNOMAD	ss4365736222	Apr 26, 2021 (155)
12	GNOMAD	ss4365736223	Apr 26, 2021 (155)
13	GNOMAD	ss4365736224	Apr 26, 2021 (155)
14	GNOMAD	ss4365736225	Apr 26, 2021 (155)
15	GNOMAD	ss4365736260	Apr 26, 2021 (155)
16	GNOMAD	ss4365736261	Apr 26, 2021 (155)
17	GNOMAD	ss4365736262	Apr 26, 2021 (155)
18	GNOMAD	ss4365736263	Apr 26, 2021 (155)
19	GNOMAD	ss4365736264	Apr 26, 2021 (155)
20	GNOMAD	ss4365736265	Apr 26, 2021 (155)
21	GNOMAD	ss4365736266	Apr 26, 2021 (155)
22	GNOMAD	ss4365736267	Apr 26, 2021 (155)
23	GNOMAD	ss4365736268	Apr 26, 2021 (155)
24	GNOMAD	ss4365736270	Apr 26, 2021 (155)
25	GNOMAD	ss4365736271	Apr 26, 2021 (155)
26	GNOMAD	ss4365736272	Apr 26, 2021 (155)
27	GNOMAD	ss4365736273	Apr 26, 2021 (155)
28	GNOMAD	ss4365736274	Apr 26, 2021 (155)
29	GNOMAD	ss4365736275	Apr 26, 2021 (155)
30	TOPMED	ss5111530050	Apr 26, 2021 (155)
31	TOPMED	ss5111530051	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5794172014	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5794172015	Oct 16, 2022 (156)
34	1000Genomes	NC_000022.10 - 45228977	Oct 12, 2018 (152)
35	The Avon Longitudinal Study of Parents and Children	NC_000022.10 - 45228978	Oct 12, 2018 (152)
36	The Danish reference pan genome	NC_000022.10 - 45228977	Apr 27, 2020 (154)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571901339 (NC_000022.11:44833096::T 1273/110880) Row 571901340 (NC_000022.11:44833096::TT 11/110868) Row 571901341 (NC_000022.11:44833096::TTT 3/110870)...	-	Apr 26, 2021 (155)
56	14KJPN Submission ignored due to conflicting rows: Row 128009118 (NC_000022.11:44833096:T: 8967/27662) Row 128009119 (NC_000022.11:44833096::T 472/27662)	-	Oct 16, 2022 (156)
57	14KJPN Submission ignored due to conflicting rows: Row 128009118 (NC_000022.11:44833096:T: 8967/27662) Row 128009119 (NC_000022.11:44833096::T 472/27662)	-	Oct 16, 2022 (156)
58	TopMed Submission ignored due to conflicting rows: Row 386638997 (NC_000022.11:44833096:TTTTT: 52/264690) Row 386638998 (NC_000022.11:44833096:TTTTTTTTT: 15/264690)	-	Apr 26, 2021 (155)
59	TopMed Submission ignored due to conflicting rows: Row 386638997 (NC_000022.11:44833096:TTTTT: 52/264690) Row 386638998 (NC_000022.11:44833096:TTTTTTTTT: 15/264690)	-	Apr 26, 2021 (155)
60	UK 10K study - Twins	NC_000022.10 - 45228978	Oct 12, 2018 (152)
61	ALFA	NC_000022.11 - 44833097	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
ss4365736275, ss5111530051	NC_000022.11:44833096:TTTTTTTTT:	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
12015358176	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
12015358176	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
12015358176	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4365736274	NC_000022.11:44833096:TTTTTT:	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
12015358176	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4365736273, ss5111530050	NC_000022.11:44833096:TTTTT:	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
12015358176	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4365736272	NC_000022.11:44833096:TTT:	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
12015358176	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4365736271	NC_000022.11:44833096:TT:	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
12015358176	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
80987196, 799605, ss1379104622, ss1575849932, ss3019413601	NC_000022.10:45228976:T:	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3822621641, ss4365736270, ss5794172014	NC_000022.11:44833096:T:	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
12015358176	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3651192908, ss4365736222, ss5794172015	NC_000022.11:44833096::T	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
12015358176	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss96111402	NT_011520.12:24619563::T	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4365736223	NC_000022.11:44833096::TT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
12015358176	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4365736224	NC_000022.11:44833096::TTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4365736225	NC_000022.11:44833096::TTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
12015358176	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365736260	NC_000022.11:44833096::TTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365736261	NC_000022.11:44833096::TTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3708333881	NC_000022.11:44833099::TTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365736262	NC_000022.11:44833096::TTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365736263	NC_000022.11:44833096::TTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3708333875	NC_000022.11:44833097::TTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
44798884, 44798884, ss1709615190, ss1709615451	NC_000022.10:45228977::TTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365736264	NC_000022.11:44833096::TTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365736265	NC_000022.11:44833096::TTTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365736266	NC_000022.11:44833096::TTTTTTTTTTT… NC_000022.11:44833096::TTTTTTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365736267	NC_000022.11:44833096::TTTTTTTTTTT… NC_000022.11:44833096::TTTTTTTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4365736268	NC_000022.11:44833096::TTTTTTTTTTT… NC_000022.11:44833096::TTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:44833096:TTTTTTTTTTTT… NC_000022.11:44833096:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs533794156

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs533794156