Name: rs746640708
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.

rs746640708

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:90475754-90475775 (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)₁₁ / del(A)₁₀ / del(A)₈ / de…
del(A)₁₁ / del(A)₁₀ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.02308 (306/13256, ALFA)
delA=0.33 (13/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IQGAP1 : 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	13256	AAAAAAAAAAAAAAAAAAAAAA=0.95346	AAAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAA=0.02308, AAAAAAAAAAAAAAAAAAAAAAA=0.02173, AAAAAAAAAAAAAAAAAAAAAAAA=0.00174, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000	0.956894	0.003011	0.040095	32
European	Sub	11488	AAAAAAAAAAAAAAAAAAAAAA=0.94647	AAAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAA=0.02655, AAAAAAAAAAAAAAAAAAAAAAA=0.02498, AAAAAAAAAAAAAAAAAAAAAAAA=0.00200, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000	0.94988	0.003501	0.046619	33
African	Sub	758	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	24	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	734	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	96	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	72	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	86	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	438	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	86	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	304	AAAAAAAAAAAAAAAAAAAAAA=0.993	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.003, AAAAAAAAAAAAAAAAAAAAAAA=0.003, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	13256	(A)₂₂=0.95346	del(A)₁₁=0.00000, del(A)₁₀=0.00000, del(A)₈=0.00000, del(A)₇=0.00000, del(A)₆=0.00000, del(A)₅=0.00000, del(A)₄=0.00000, delAAA=0.00000, delAA=0.00000, delA=0.02308, dupA=0.02173, dupAA=0.00174, dupAAA=0.00000, dup(A)₄=0.00000, dup(A)₅=0.00000, dup(A)₆=0.00000
Allele Frequency Aggregator	European	Sub	11488	(A)₂₂=0.94647	del(A)₁₁=0.00000, del(A)₁₀=0.00000, del(A)₈=0.00000, del(A)₇=0.00000, del(A)₆=0.00000, del(A)₅=0.00000, del(A)₄=0.00000, delAAA=0.00000, delAA=0.00000, delA=0.02655, dupA=0.02498, dupAA=0.00200, dupAAA=0.00000, dup(A)₄=0.00000, dup(A)₅=0.00000, dup(A)₆=0.00000
Allele Frequency Aggregator	African	Sub	758	(A)₂₂=1.000	del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	438	(A)₂₂=1.000	del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Other	Sub	304	(A)₂₂=0.993	del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.003, dupA=0.003, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Asian	Sub	96	(A)₂₂=1.00	del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	86	(A)₂₂=1.00	del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	86	(A)₂₂=1.00	del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00
The Danish reference pan genome	Danish	Study-wide	40	(A)₂₂=0.68	delA=0.33

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 15	NC_000015.10:g.90475765_90475775del
GRCh38.p14 chr 15	NC_000015.10:g.90475766_90475775del
GRCh38.p14 chr 15	NC_000015.10:g.90475768_90475775del
GRCh38.p14 chr 15	NC_000015.10:g.90475769_90475775del
GRCh38.p14 chr 15	NC_000015.10:g.90475770_90475775del
GRCh38.p14 chr 15	NC_000015.10:g.90475771_90475775del
GRCh38.p14 chr 15	NC_000015.10:g.90475772_90475775del
GRCh38.p14 chr 15	NC_000015.10:g.90475773_90475775del
GRCh38.p14 chr 15	NC_000015.10:g.90475774_90475775del
GRCh38.p14 chr 15	NC_000015.10:g.90475775del
GRCh38.p14 chr 15	NC_000015.10:g.90475775dup
GRCh38.p14 chr 15	NC_000015.10:g.90475774_90475775dup
GRCh38.p14 chr 15	NC_000015.10:g.90475773_90475775dup
GRCh38.p14 chr 15	NC_000015.10:g.90475772_90475775dup
GRCh38.p14 chr 15	NC_000015.10:g.90475771_90475775dup
GRCh38.p14 chr 15	NC_000015.10:g.90475770_90475775dup
GRCh38.p14 chr 15	NC_000015.10:g.90475769_90475775dup
GRCh37.p13 chr 15	NC_000015.9:g.91018997_91019007del
GRCh37.p13 chr 15	NC_000015.9:g.91018998_91019007del
GRCh37.p13 chr 15	NC_000015.9:g.91019000_91019007del
GRCh37.p13 chr 15	NC_000015.9:g.91019001_91019007del
GRCh37.p13 chr 15	NC_000015.9:g.91019002_91019007del
GRCh37.p13 chr 15	NC_000015.9:g.91019003_91019007del
GRCh37.p13 chr 15	NC_000015.9:g.91019004_91019007del
GRCh37.p13 chr 15	NC_000015.9:g.91019005_91019007del
GRCh37.p13 chr 15	NC_000015.9:g.91019006_91019007del
GRCh37.p13 chr 15	NC_000015.9:g.91019007del
GRCh37.p13 chr 15	NC_000015.9:g.91019007dup
GRCh37.p13 chr 15	NC_000015.9:g.91019006_91019007dup
GRCh37.p13 chr 15	NC_000015.9:g.91019005_91019007dup
GRCh37.p13 chr 15	NC_000015.9:g.91019004_91019007dup
GRCh37.p13 chr 15	NC_000015.9:g.91019003_91019007dup
GRCh37.p13 chr 15	NC_000015.9:g.91019002_91019007dup
GRCh37.p13 chr 15	NC_000015.9:g.91019001_91019007dup
IQGAP1 RefSeqGene	NG_052946.1:g.92525_92535del
IQGAP1 RefSeqGene	NG_052946.1:g.92526_92535del
IQGAP1 RefSeqGene	NG_052946.1:g.92528_92535del
IQGAP1 RefSeqGene	NG_052946.1:g.92529_92535del
IQGAP1 RefSeqGene	NG_052946.1:g.92530_92535del
IQGAP1 RefSeqGene	NG_052946.1:g.92531_92535del
IQGAP1 RefSeqGene	NG_052946.1:g.92532_92535del
IQGAP1 RefSeqGene	NG_052946.1:g.92533_92535del
IQGAP1 RefSeqGene	NG_052946.1:g.92534_92535del
IQGAP1 RefSeqGene	NG_052946.1:g.92535del
IQGAP1 RefSeqGene	NG_052946.1:g.92535dup
IQGAP1 RefSeqGene	NG_052946.1:g.92534_92535dup
IQGAP1 RefSeqGene	NG_052946.1:g.92533_92535dup
IQGAP1 RefSeqGene	NG_052946.1:g.92532_92535dup
IQGAP1 RefSeqGene	NG_052946.1:g.92531_92535dup
IQGAP1 RefSeqGene	NG_052946.1:g.92530_92535dup
IQGAP1 RefSeqGene	NG_052946.1:g.92529_92535dup

Gene: IQGAP1, IQ motif containing GTPase activating protein 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IQGAP1 transcript	NM_003870.4:c.2785-898_27… NM_003870.4:c.2785-898_2785-888del	N/A	Intron Variant
IQGAP1 transcript variant X1	XM_047433204.1:c.2785-898… XM_047433204.1:c.2785-898_2785-888del	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	(A)₂₂=	del(A)₁₁	del(A)₁₀	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇
GRCh38.p14 chr 15	NC_000015.10:g.90475754_90475775=	NC_000015.10:g.90475765_90475775del	NC_000015.10:g.90475766_90475775del	NC_000015.10:g.90475768_90475775del	NC_000015.10:g.90475769_90475775del	NC_000015.10:g.90475770_90475775del	NC_000015.10:g.90475771_90475775del	NC_000015.10:g.90475772_90475775del	NC_000015.10:g.90475773_90475775del	NC_000015.10:g.90475774_90475775del	NC_000015.10:g.90475775del	NC_000015.10:g.90475775dup	NC_000015.10:g.90475774_90475775dup	NC_000015.10:g.90475773_90475775dup	NC_000015.10:g.90475772_90475775dup	NC_000015.10:g.90475771_90475775dup	NC_000015.10:g.90475770_90475775dup	NC_000015.10:g.90475769_90475775dup
GRCh37.p13 chr 15	NC_000015.9:g.91018986_91019007=	NC_000015.9:g.91018997_91019007del	NC_000015.9:g.91018998_91019007del	NC_000015.9:g.91019000_91019007del	NC_000015.9:g.91019001_91019007del	NC_000015.9:g.91019002_91019007del	NC_000015.9:g.91019003_91019007del	NC_000015.9:g.91019004_91019007del	NC_000015.9:g.91019005_91019007del	NC_000015.9:g.91019006_91019007del	NC_000015.9:g.91019007del	NC_000015.9:g.91019007dup	NC_000015.9:g.91019006_91019007dup	NC_000015.9:g.91019005_91019007dup	NC_000015.9:g.91019004_91019007dup	NC_000015.9:g.91019003_91019007dup	NC_000015.9:g.91019002_91019007dup	NC_000015.9:g.91019001_91019007dup
IQGAP1 RefSeqGene	NG_052946.1:g.92514_92535=	NG_052946.1:g.92525_92535del	NG_052946.1:g.92526_92535del	NG_052946.1:g.92528_92535del	NG_052946.1:g.92529_92535del	NG_052946.1:g.92530_92535del	NG_052946.1:g.92531_92535del	NG_052946.1:g.92532_92535del	NG_052946.1:g.92533_92535del	NG_052946.1:g.92534_92535del	NG_052946.1:g.92535del	NG_052946.1:g.92535dup	NG_052946.1:g.92534_92535dup	NG_052946.1:g.92533_92535dup	NG_052946.1:g.92532_92535dup	NG_052946.1:g.92531_92535dup	NG_052946.1:g.92530_92535dup	NG_052946.1:g.92529_92535dup
IQGAP1 transcript	NM_003870.3:c.2785-909=	NM_003870.3:c.2785-898_2785-888del	NM_003870.3:c.2785-897_2785-888del	NM_003870.3:c.2785-895_2785-888del	NM_003870.3:c.2785-894_2785-888del	NM_003870.3:c.2785-893_2785-888del	NM_003870.3:c.2785-892_2785-888del	NM_003870.3:c.2785-891_2785-888del	NM_003870.3:c.2785-890_2785-888del	NM_003870.3:c.2785-889_2785-888del	NM_003870.3:c.2785-888del	NM_003870.3:c.2785-888dup	NM_003870.3:c.2785-889_2785-888dup	NM_003870.3:c.2785-890_2785-888dup	NM_003870.3:c.2785-891_2785-888dup	NM_003870.3:c.2785-892_2785-888dup	NM_003870.3:c.2785-893_2785-888dup	NM_003870.3:c.2785-894_2785-888dup
IQGAP1 transcript	NM_003870.4:c.2785-909=	NM_003870.4:c.2785-898_2785-888del	NM_003870.4:c.2785-897_2785-888del	NM_003870.4:c.2785-895_2785-888del	NM_003870.4:c.2785-894_2785-888del	NM_003870.4:c.2785-893_2785-888del	NM_003870.4:c.2785-892_2785-888del	NM_003870.4:c.2785-891_2785-888del	NM_003870.4:c.2785-890_2785-888del	NM_003870.4:c.2785-889_2785-888del	NM_003870.4:c.2785-888del	NM_003870.4:c.2785-888dup	NM_003870.4:c.2785-889_2785-888dup	NM_003870.4:c.2785-890_2785-888dup	NM_003870.4:c.2785-891_2785-888dup	NM_003870.4:c.2785-892_2785-888dup	NM_003870.4:c.2785-893_2785-888dup	NM_003870.4:c.2785-894_2785-888dup
IQGAP1 transcript variant X1	XM_005254984.1:c.2785-909=	XM_005254984.1:c.2785-898_2785-888del	XM_005254984.1:c.2785-897_2785-888del	XM_005254984.1:c.2785-895_2785-888del	XM_005254984.1:c.2785-894_2785-888del	XM_005254984.1:c.2785-893_2785-888del	XM_005254984.1:c.2785-892_2785-888del	XM_005254984.1:c.2785-891_2785-888del	XM_005254984.1:c.2785-890_2785-888del	XM_005254984.1:c.2785-889_2785-888del	XM_005254984.1:c.2785-888del	XM_005254984.1:c.2785-888dup	XM_005254984.1:c.2785-889_2785-888dup	XM_005254984.1:c.2785-890_2785-888dup	XM_005254984.1:c.2785-891_2785-888dup	XM_005254984.1:c.2785-892_2785-888dup	XM_005254984.1:c.2785-893_2785-888dup	XM_005254984.1:c.2785-894_2785-888dup
IQGAP1 transcript variant X1	XM_047433204.1:c.2785-909=	XM_047433204.1:c.2785-898_2785-888del	XM_047433204.1:c.2785-897_2785-888del	XM_047433204.1:c.2785-895_2785-888del	XM_047433204.1:c.2785-894_2785-888del	XM_047433204.1:c.2785-893_2785-888del	XM_047433204.1:c.2785-892_2785-888del	XM_047433204.1:c.2785-891_2785-888del	XM_047433204.1:c.2785-890_2785-888del	XM_047433204.1:c.2785-889_2785-888del	XM_047433204.1:c.2785-888del	XM_047433204.1:c.2785-888dup	XM_047433204.1:c.2785-889_2785-888dup	XM_047433204.1:c.2785-890_2785-888dup	XM_047433204.1:c.2785-891_2785-888dup	XM_047433204.1:c.2785-892_2785-888dup	XM_047433204.1:c.2785-893_2785-888dup	XM_047433204.1:c.2785-894_2785-888dup

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#.

36 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_GENOME_DK	ss1574897746	Apr 01, 2015 (144)
2	ACPOP	ss3741161767	Jul 13, 2019 (153)
3	ACPOP	ss3741161768	Jul 13, 2019 (153)
4	EVA	ss3834370888	Apr 27, 2020 (154)
5	GNOMAD	ss4293659085	Apr 26, 2021 (155)
6	GNOMAD	ss4293659086	Apr 26, 2021 (155)
7	GNOMAD	ss4293659087	Apr 26, 2021 (155)
8	GNOMAD	ss4293659088	Apr 26, 2021 (155)
9	GNOMAD	ss4293659089	Apr 26, 2021 (155)
10	GNOMAD	ss4293659090	Apr 26, 2021 (155)
11	GNOMAD	ss4293659091	Apr 26, 2021 (155)
12	GNOMAD	ss4293659092	Apr 26, 2021 (155)
13	GNOMAD	ss4293659093	Apr 26, 2021 (155)
14	GNOMAD	ss4293659094	Apr 26, 2021 (155)
15	GNOMAD	ss4293659095	Apr 26, 2021 (155)
16	GNOMAD	ss4293659096	Apr 26, 2021 (155)
17	GNOMAD	ss4293659097	Apr 26, 2021 (155)
18	GNOMAD	ss4293659098	Apr 26, 2021 (155)
19	TOPMED	ss5001172528	Apr 26, 2021 (155)
20	TOPMED	ss5001172529	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5217507583	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5217507584	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5217507585	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5217507586	Apr 26, 2021 (155)
25	1000G_HIGH_COVERAGE	ss5299426996	Oct 17, 2022 (156)
26	1000G_HIGH_COVERAGE	ss5299426997	Oct 17, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5299426998	Oct 17, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5299426999	Oct 17, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5299427000	Oct 17, 2022 (156)
30	HUGCELL_USP	ss5493040638	Oct 17, 2022 (156)
31	HUGCELL_USP	ss5493040639	Oct 17, 2022 (156)
32	HUGCELL_USP	ss5493040640	Oct 17, 2022 (156)
33	TOMMO_GENOMICS	ss5771711223	Oct 17, 2022 (156)
34	TOMMO_GENOMICS	ss5771711224	Oct 17, 2022 (156)
35	TOMMO_GENOMICS	ss5771711225	Oct 17, 2022 (156)
36	TOMMO_GENOMICS	ss5771711227	Oct 17, 2022 (156)
37	The Danish reference pan genome	NC_000015.9 - 91018986	Apr 27, 2020 (154)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477241557 (NC_000015.10:90475753::A 4108/63764) Row 477241558 (NC_000015.10:90475753::AA 246/64934) Row 477241559 (NC_000015.10:90475753::AAA 10/65002)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477241557 (NC_000015.10:90475753::A 4108/63764) Row 477241558 (NC_000015.10:90475753::AA 246/64934) Row 477241559 (NC_000015.10:90475753::AAA 10/65002)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477241557 (NC_000015.10:90475753::A 4108/63764) Row 477241558 (NC_000015.10:90475753::AA 246/64934) Row 477241559 (NC_000015.10:90475753::AAA 10/65002)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477241557 (NC_000015.10:90475753::A 4108/63764) Row 477241558 (NC_000015.10:90475753::AA 246/64934) Row 477241559 (NC_000015.10:90475753::AAA 10/65002)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477241557 (NC_000015.10:90475753::A 4108/63764) Row 477241558 (NC_000015.10:90475753::AA 246/64934) Row 477241559 (NC_000015.10:90475753::AAA 10/65002)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477241557 (NC_000015.10:90475753::A 4108/63764) Row 477241558 (NC_000015.10:90475753::AA 246/64934) Row 477241559 (NC_000015.10:90475753::AAA 10/65002)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477241557 (NC_000015.10:90475753::A 4108/63764) Row 477241558 (NC_000015.10:90475753::AA 246/64934) Row 477241559 (NC_000015.10:90475753::AAA 10/65002)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477241557 (NC_000015.10:90475753::A 4108/63764) Row 477241558 (NC_000015.10:90475753::AA 246/64934) Row 477241559 (NC_000015.10:90475753::AAA 10/65002)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477241557 (NC_000015.10:90475753::A 4108/63764) Row 477241558 (NC_000015.10:90475753::AA 246/64934) Row 477241559 (NC_000015.10:90475753::AAA 10/65002)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477241557 (NC_000015.10:90475753::A 4108/63764) Row 477241558 (NC_000015.10:90475753::AA 246/64934) Row 477241559 (NC_000015.10:90475753::AAA 10/65002)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477241557 (NC_000015.10:90475753::A 4108/63764) Row 477241558 (NC_000015.10:90475753::AA 246/64934) Row 477241559 (NC_000015.10:90475753::AAA 10/65002)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477241557 (NC_000015.10:90475753::A 4108/63764) Row 477241558 (NC_000015.10:90475753::AA 246/64934) Row 477241559 (NC_000015.10:90475753::AAA 10/65002)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477241557 (NC_000015.10:90475753::A 4108/63764) Row 477241558 (NC_000015.10:90475753::AA 246/64934) Row 477241559 (NC_000015.10:90475753::AAA 10/65002)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477241557 (NC_000015.10:90475753::A 4108/63764) Row 477241558 (NC_000015.10:90475753::AA 246/64934) Row 477241559 (NC_000015.10:90475753::AAA 10/65002)...	-	Apr 26, 2021 (155)
52	Northern Sweden Submission ignored due to conflicting rows: Row 14446632 (NC_000015.9:91018985::A 23/578) Row 14446633 (NC_000015.9:91018985:A: 56/578)	-	Jul 13, 2019 (153)
53	Northern Sweden Submission ignored due to conflicting rows: Row 14446632 (NC_000015.9:91018985::A 23/578) Row 14446633 (NC_000015.9:91018985:A: 56/578)	-	Jul 13, 2019 (153)
54	8.3KJPN Submission ignored due to conflicting rows: Row 75476890 (NC_000015.9:91018985:A: 891/16722) Row 75476891 (NC_000015.9:91018985::A 815/16722) Row 75476892 (NC_000015.9:91018985:AA: 1/16722)...	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 75476890 (NC_000015.9:91018985:A: 891/16722) Row 75476891 (NC_000015.9:91018985::A 815/16722) Row 75476892 (NC_000015.9:91018985:AA: 1/16722)...	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 75476890 (NC_000015.9:91018985:A: 891/16722) Row 75476891 (NC_000015.9:91018985::A 815/16722) Row 75476892 (NC_000015.9:91018985:AA: 1/16722)...	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 75476890 (NC_000015.9:91018985:A: 891/16722) Row 75476891 (NC_000015.9:91018985::A 815/16722) Row 75476892 (NC_000015.9:91018985:AA: 1/16722)...	-	Apr 26, 2021 (155)
58	14KJPN Submission ignored due to conflicting rows: Row 105548327 (NC_000015.10:90475753::A 1387/28248) Row 105548328 (NC_000015.10:90475753:A: 1619/28248) Row 105548329 (NC_000015.10:90475753:AA: 1/28248)...	-	Oct 17, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 105548327 (NC_000015.10:90475753::A 1387/28248) Row 105548328 (NC_000015.10:90475753:A: 1619/28248) Row 105548329 (NC_000015.10:90475753:AA: 1/28248)...	-	Oct 17, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 105548327 (NC_000015.10:90475753::A 1387/28248) Row 105548328 (NC_000015.10:90475753:A: 1619/28248) Row 105548329 (NC_000015.10:90475753:AA: 1/28248)...	-	Oct 17, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 105548327 (NC_000015.10:90475753::A 1387/28248) Row 105548328 (NC_000015.10:90475753:A: 1619/28248) Row 105548329 (NC_000015.10:90475753:AA: 1/28248)...	-	Oct 17, 2022 (156)
62	TopMed Submission ignored due to conflicting rows: Row 216718188 (NC_000015.10:90475753:AAAAAAAA: 1/264690) Row 216718189 (NC_000015.10:90475753:AAAAAAAAAAA: 2/264690)	-	Apr 26, 2021 (155)
63	TopMed Submission ignored due to conflicting rows: Row 216718188 (NC_000015.10:90475753:AAAAAAAA: 1/264690) Row 216718189 (NC_000015.10:90475753:AAAAAAAAAAA: 2/264690)	-	Apr 26, 2021 (155)
64	ALFA	NC_000015.10 - 90475754	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
ss4293659098, ss5001172529	NC_000015.10:90475753:AAAAAAAAAAA:	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss5001172528	NC_000015.10:90475753:AAAAAAAA:	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4293659097	NC_000015.10:90475753:AAAAAAA:	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4293659096	NC_000015.10:90475753:AAAAAA:	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4293659095	NC_000015.10:90475753:AAAAA:	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4293659094	NC_000015.10:90475753:AAA:	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5217507585	NC_000015.9:91018985:AA:	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4293659093, ss5299426997, ss5493040639, ss5771711225	NC_000015.10:90475753:AA:	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
505836, ss1574897746, ss3741161768, ss3834370888, ss5217507583	NC_000015.9:91018985:A:	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4293659092, ss5299426996, ss5493040640, ss5771711224	NC_000015.10:90475753:A:	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3741161767, ss5217507584	NC_000015.9:91018985::A	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4293659085, ss5299426998, ss5493040638, ss5771711223	NC_000015.10:90475753::A	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5217507586	NC_000015.9:91018985::AA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4293659086, ss5299426999, ss5771711227	NC_000015.10:90475753::AA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4293659087	NC_000015.10:90475753::AAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4293659088, ss5299427000	NC_000015.10:90475753::AAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4293659089	NC_000015.10:90475753::AAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4293659090	NC_000015.10:90475753::AAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4986001783	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4293659091	NC_000015.10:90475753::AAAAAAA	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2373587090	NC_000015.9:91018985:AAAAAAA:	NC_000015.10:90475753:AAAAAAAAAAAA… NC_000015.10:90475753:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA

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

No publications for rs746640708

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

rs746640708