Name: rs1168662549
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.

rs1168662549

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:73540088-73540111 (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)₁₄ / del(A)₁₃ / del(A)₁₀ / d…
del(A)₁₄ / del(A)₁₃ / del(A)₁₀ / del(A)₉ / 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 / dup(A)₁₅ / ins(A)₆T(A)₂₅ / ins(A)₅T(A)₂₇ / ins(AAATAAAAAA)₂AAAAAAAAAAAAAAAAAAAAA / insAAATTAT(A)₂₅
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₄=0.0000 (0/1810, ALFA)
del(A)₁₃=0.0000 (0/1810, ALFA)
del(A)₁₀=0.0000 (0/1810, ALFA) (+ 11 more)
del(A)₉=0.0000 (0/1810, ALFA)
del(A)₈=0.0000 (0/1810, ALFA)
del(A)₇=0.0000 (0/1810, ALFA)
del(A)₆=0.0000 (0/1810, ALFA)
del(A)₅=0.0000 (0/1810, ALFA)
del(A)₄=0.0000 (0/1810, ALFA)
delAAA=0.0000 (0/1810, ALFA)
delAA=0.0000 (0/1810, ALFA)
delA=0.0000 (0/1810, ALFA)
dupA=0.0000 (0/1810, ALFA)
dupAA=0.0000 (0/1810, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PDZRN3 : Intron Variant
LOC101927296 : 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	1810	AAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	1528	AAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African	Sub	136	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	10	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	126	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	10	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	66	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	8	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	58	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=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, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	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	1810	(A)₂₄=1.0000	del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	1528	(A)₂₄=1.0000	del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	136	(A)₂₄=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₀=0.000, del(A)₉=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
Allele Frequency Aggregator	Latin American 2	Sub	66	(A)₂₄=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₀=0.00, del(A)₉=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
Allele Frequency Aggregator	Other	Sub	58	(A)₂₄=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₀=0.00, del(A)₉=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
Allele Frequency Aggregator	Latin American 1	Sub	10	(A)₂₄=1.0	del(A)₁₄=0.0, del(A)₁₃=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	South Asian	Sub	8	(A)₂₄=1.0	del(A)₁₄=0.0, del(A)₁₃=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	Asian	Sub	4	(A)₂₄=1.0	del(A)₁₄=0.0, del(A)₁₃=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0

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 3	NC_000003.12:g.73540098_73540111del
GRCh38.p14 chr 3	NC_000003.12:g.73540099_73540111del
GRCh38.p14 chr 3	NC_000003.12:g.73540102_73540111del
GRCh38.p14 chr 3	NC_000003.12:g.73540103_73540111del
GRCh38.p14 chr 3	NC_000003.12:g.73540104_73540111del
GRCh38.p14 chr 3	NC_000003.12:g.73540105_73540111del
GRCh38.p14 chr 3	NC_000003.12:g.73540106_73540111del
GRCh38.p14 chr 3	NC_000003.12:g.73540107_73540111del
GRCh38.p14 chr 3	NC_000003.12:g.73540108_73540111del
GRCh38.p14 chr 3	NC_000003.12:g.73540109_73540111del
GRCh38.p14 chr 3	NC_000003.12:g.73540110_73540111del
GRCh38.p14 chr 3	NC_000003.12:g.73540111del
GRCh38.p14 chr 3	NC_000003.12:g.73540111dup
GRCh38.p14 chr 3	NC_000003.12:g.73540110_73540111dup
GRCh38.p14 chr 3	NC_000003.12:g.73540109_73540111dup
GRCh38.p14 chr 3	NC_000003.12:g.73540108_73540111dup
GRCh38.p14 chr 3	NC_000003.12:g.73540107_73540111dup
GRCh38.p14 chr 3	NC_000003.12:g.73540106_73540111dup
GRCh38.p14 chr 3	NC_000003.12:g.73540105_73540111dup
GRCh38.p14 chr 3	NC_000003.12:g.73540097_73540111dup
GRCh38.p14 chr 3	NC_000003.12:g.73540088_73540111A[30]TAAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh38.p14 chr 3	NC_000003.12:g.73540088_73540111A[29]TAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh38.p14 chr 3	NC_000003.12:g.73540088_73540111A[27]TAAAAAAAAA[2]A[18]
GRCh38.p14 chr 3	NC_000003.12:g.73540088_73540111A[27]TTATAAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 3	NC_000003.11:g.73589249_73589262del
GRCh37.p13 chr 3	NC_000003.11:g.73589250_73589262del
GRCh37.p13 chr 3	NC_000003.11:g.73589253_73589262del
GRCh37.p13 chr 3	NC_000003.11:g.73589254_73589262del
GRCh37.p13 chr 3	NC_000003.11:g.73589255_73589262del
GRCh37.p13 chr 3	NC_000003.11:g.73589256_73589262del
GRCh37.p13 chr 3	NC_000003.11:g.73589257_73589262del
GRCh37.p13 chr 3	NC_000003.11:g.73589258_73589262del
GRCh37.p13 chr 3	NC_000003.11:g.73589259_73589262del
GRCh37.p13 chr 3	NC_000003.11:g.73589260_73589262del
GRCh37.p13 chr 3	NC_000003.11:g.73589261_73589262del
GRCh37.p13 chr 3	NC_000003.11:g.73589262del
GRCh37.p13 chr 3	NC_000003.11:g.73589262dup
GRCh37.p13 chr 3	NC_000003.11:g.73589261_73589262dup
GRCh37.p13 chr 3	NC_000003.11:g.73589260_73589262dup
GRCh37.p13 chr 3	NC_000003.11:g.73589259_73589262dup
GRCh37.p13 chr 3	NC_000003.11:g.73589258_73589262dup
GRCh37.p13 chr 3	NC_000003.11:g.73589257_73589262dup
GRCh37.p13 chr 3	NC_000003.11:g.73589256_73589262dup
GRCh37.p13 chr 3	NC_000003.11:g.73589248_73589262dup
GRCh37.p13 chr 3	NC_000003.11:g.73589239_73589262A[30]TAAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 3	NC_000003.11:g.73589239_73589262A[29]TAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 3	NC_000003.11:g.73589239_73589262A[27]TAAAAAAAAA[2]A[18]
GRCh37.p13 chr 3	NC_000003.11:g.73589239_73589262A[27]TTATAAAAAAAAAAAAAAAAAAAAAAAAA[1]
PDZRN3 RefSeqGene	NG_047128.1:g.89821_89834del
PDZRN3 RefSeqGene	NG_047128.1:g.89822_89834del
PDZRN3 RefSeqGene	NG_047128.1:g.89825_89834del
PDZRN3 RefSeqGene	NG_047128.1:g.89826_89834del
PDZRN3 RefSeqGene	NG_047128.1:g.89827_89834del
PDZRN3 RefSeqGene	NG_047128.1:g.89828_89834del
PDZRN3 RefSeqGene	NG_047128.1:g.89829_89834del
PDZRN3 RefSeqGene	NG_047128.1:g.89830_89834del
PDZRN3 RefSeqGene	NG_047128.1:g.89831_89834del
PDZRN3 RefSeqGene	NG_047128.1:g.89832_89834del
PDZRN3 RefSeqGene	NG_047128.1:g.89833_89834del
PDZRN3 RefSeqGene	NG_047128.1:g.89834del
PDZRN3 RefSeqGene	NG_047128.1:g.89834dup
PDZRN3 RefSeqGene	NG_047128.1:g.89833_89834dup
PDZRN3 RefSeqGene	NG_047128.1:g.89832_89834dup
PDZRN3 RefSeqGene	NG_047128.1:g.89831_89834dup
PDZRN3 RefSeqGene	NG_047128.1:g.89830_89834dup
PDZRN3 RefSeqGene	NG_047128.1:g.89829_89834dup
PDZRN3 RefSeqGene	NG_047128.1:g.89828_89834dup
PDZRN3 RefSeqGene	NG_047128.1:g.89820_89834dup
PDZRN3 RefSeqGene	NG_047128.1:g.89811_89834T[25]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
PDZRN3 RefSeqGene	NG_047128.1:g.89811_89834T[27]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
PDZRN3 RefSeqGene	NG_047128.1:g.89811_89834T[27]ATTTTTTTTT[2]T[18]
PDZRN3 RefSeqGene	NG_047128.1:g.89811_89834T[25]ATAATTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

Gene: PDZRN3, PDZ domain containing ring finger 3 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PDZRN3 transcript variant 2	NM_001303139.2:c.12+29050… NM_001303139.2:c.12+29050_12+29063del	N/A	Intron Variant
PDZRN3 transcript variant 3	NM_001303140.2:c.-112+213… NM_001303140.2:c.-112+21350_-112+21363del	N/A	Intron Variant
PDZRN3 transcript variant 1	NM_015009.3:c.918+62253_9… NM_015009.3:c.918+62253_918+62266del	N/A	Intron Variant
PDZRN3 transcript variant 4	NM_001303141.2:c.	N/A	Genic Upstream Transcript Variant
PDZRN3 transcript variant 5	NM_001303142.2:c.	N/A	Genic Upstream Transcript Variant
PDZRN3 transcript variant X1	XM_017005942.3:c.831+6225… XM_017005942.3:c.831+62253_831+62266del	N/A	Intron Variant

Gene: LOC101927296, uncharacterized LOC101927296 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC101927296 transcript	NR_121660.1:n.	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)₂₄=	del(A)₁₄	del(A)₁₃	del(A)₁₀	del(A)₉	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	dup(A)₁₅	ins(A)₆T(A)₂₅	ins(A)₅T(A)₂₇	ins(AAATAAAAAA)₂AAAAAAAAAAAAAAAAAAAAA	insAAATTAT(A)₂₅
GRCh38.p14 chr 3	NC_000003.12:g.73540088_73540111=	NC_000003.12:g.73540098_73540111del	NC_000003.12:g.73540099_73540111del	NC_000003.12:g.73540102_73540111del	NC_000003.12:g.73540103_73540111del	NC_000003.12:g.73540104_73540111del	NC_000003.12:g.73540105_73540111del	NC_000003.12:g.73540106_73540111del	NC_000003.12:g.73540107_73540111del	NC_000003.12:g.73540108_73540111del	NC_000003.12:g.73540109_73540111del	NC_000003.12:g.73540110_73540111del	NC_000003.12:g.73540111del	NC_000003.12:g.73540111dup	NC_000003.12:g.73540110_73540111dup	NC_000003.12:g.73540109_73540111dup	NC_000003.12:g.73540108_73540111dup	NC_000003.12:g.73540107_73540111dup	NC_000003.12:g.73540106_73540111dup	NC_000003.12:g.73540105_73540111dup	NC_000003.12:g.73540097_73540111dup	NC_000003.12:g.73540088_73540111A[30]TAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NC_000003.12:g.73540088_73540111A[29]TAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NC_000003.12:g.73540088_73540111A[27]TAAAAAAAAA[2]A[18]	NC_000003.12:g.73540088_73540111A[27]TTATAAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 3	NC_000003.11:g.73589239_73589262=	NC_000003.11:g.73589249_73589262del	NC_000003.11:g.73589250_73589262del	NC_000003.11:g.73589253_73589262del	NC_000003.11:g.73589254_73589262del	NC_000003.11:g.73589255_73589262del	NC_000003.11:g.73589256_73589262del	NC_000003.11:g.73589257_73589262del	NC_000003.11:g.73589258_73589262del	NC_000003.11:g.73589259_73589262del	NC_000003.11:g.73589260_73589262del	NC_000003.11:g.73589261_73589262del	NC_000003.11:g.73589262del	NC_000003.11:g.73589262dup	NC_000003.11:g.73589261_73589262dup	NC_000003.11:g.73589260_73589262dup	NC_000003.11:g.73589259_73589262dup	NC_000003.11:g.73589258_73589262dup	NC_000003.11:g.73589257_73589262dup	NC_000003.11:g.73589256_73589262dup	NC_000003.11:g.73589248_73589262dup	NC_000003.11:g.73589239_73589262A[30]TAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NC_000003.11:g.73589239_73589262A[29]TAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NC_000003.11:g.73589239_73589262A[27]TAAAAAAAAA[2]A[18]	NC_000003.11:g.73589239_73589262A[27]TTATAAAAAAAAAAAAAAAAAAAAAAAAA[1]
PDZRN3 RefSeqGene	NG_047128.1:g.89811_89834=	NG_047128.1:g.89821_89834del	NG_047128.1:g.89822_89834del	NG_047128.1:g.89825_89834del	NG_047128.1:g.89826_89834del	NG_047128.1:g.89827_89834del	NG_047128.1:g.89828_89834del	NG_047128.1:g.89829_89834del	NG_047128.1:g.89830_89834del	NG_047128.1:g.89831_89834del	NG_047128.1:g.89832_89834del	NG_047128.1:g.89833_89834del	NG_047128.1:g.89834del	NG_047128.1:g.89834dup	NG_047128.1:g.89833_89834dup	NG_047128.1:g.89832_89834dup	NG_047128.1:g.89831_89834dup	NG_047128.1:g.89830_89834dup	NG_047128.1:g.89829_89834dup	NG_047128.1:g.89828_89834dup	NG_047128.1:g.89820_89834dup	NG_047128.1:g.89811_89834T[25]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NG_047128.1:g.89811_89834T[27]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NG_047128.1:g.89811_89834T[27]ATTTTTTTTT[2]T[18]	NG_047128.1:g.89811_89834T[25]ATAATTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
PDZRN3 transcript variant 2	NM_001303139.2:c.12+29063=	NM_001303139.2:c.12+29050_12+29063del	NM_001303139.2:c.12+29051_12+29063del	NM_001303139.2:c.12+29054_12+29063del	NM_001303139.2:c.12+29055_12+29063del	NM_001303139.2:c.12+29056_12+29063del	NM_001303139.2:c.12+29057_12+29063del	NM_001303139.2:c.12+29058_12+29063del	NM_001303139.2:c.12+29059_12+29063del	NM_001303139.2:c.12+29060_12+29063del	NM_001303139.2:c.12+29061_12+29063del	NM_001303139.2:c.12+29062_12+29063del	NM_001303139.2:c.12+29063del	NM_001303139.2:c.12+29063dup	NM_001303139.2:c.12+29062_12+29063dup	NM_001303139.2:c.12+29061_12+29063dup	NM_001303139.2:c.12+29060_12+29063dup	NM_001303139.2:c.12+29059_12+29063dup	NM_001303139.2:c.12+29058_12+29063dup	NM_001303139.2:c.12+29057_12+29063dup	NM_001303139.2:c.12+29049_12+29063dup	NM_001303139.2:c.12+29063_12+29064insTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTT	NM_001303139.2:c.12+29063_12+29064insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTT	NM_001303139.2:c.12+29063_12+29064insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTATTT	NM_001303139.2:c.12+29063_12+29064insTTTTTTTTTTTTTTTTTTTTTTTTTATAATTT
PDZRN3 transcript variant 3	NM_001303140.2:c.-112+21363=	NM_001303140.2:c.-112+21350_-112+21363del	NM_001303140.2:c.-112+21351_-112+21363del	NM_001303140.2:c.-112+21354_-112+21363del	NM_001303140.2:c.-112+21355_-112+21363del	NM_001303140.2:c.-112+21356_-112+21363del	NM_001303140.2:c.-112+21357_-112+21363del	NM_001303140.2:c.-112+21358_-112+21363del	NM_001303140.2:c.-112+21359_-112+21363del	NM_001303140.2:c.-112+21360_-112+21363del	NM_001303140.2:c.-112+21361_-112+21363del	NM_001303140.2:c.-112+21362_-112+21363del	NM_001303140.2:c.-112+21363del	NM_001303140.2:c.-112+21363dup	NM_001303140.2:c.-112+21362_-112+21363dup	NM_001303140.2:c.-112+21361_-112+21363dup	NM_001303140.2:c.-112+21360_-112+21363dup	NM_001303140.2:c.-112+21359_-112+21363dup	NM_001303140.2:c.-112+21358_-112+21363dup	NM_001303140.2:c.-112+21357_-112+21363dup	NM_001303140.2:c.-112+21349_-112+21363dup	NM_001303140.2:c.-112+21363_-112+21364insTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTT	NM_001303140.2:c.-112+21363_-112+21364insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTT	NM_001303140.2:c.-112+21363_-112+21364insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTATTT	NM_001303140.2:c.-112+21363_-112+21364insTTTTTTTTTTTTTTTTTTTTTTTTTATAATTT
PDZRN3 transcript	NM_015009.1:c.918+62266=	NM_015009.1:c.918+62253_918+62266del	NM_015009.1:c.918+62254_918+62266del	NM_015009.1:c.918+62257_918+62266del	NM_015009.1:c.918+62258_918+62266del	NM_015009.1:c.918+62259_918+62266del	NM_015009.1:c.918+62260_918+62266del	NM_015009.1:c.918+62261_918+62266del	NM_015009.1:c.918+62262_918+62266del	NM_015009.1:c.918+62263_918+62266del	NM_015009.1:c.918+62264_918+62266del	NM_015009.1:c.918+62265_918+62266del	NM_015009.1:c.918+62266del	NM_015009.1:c.918+62266dup	NM_015009.1:c.918+62265_918+62266dup	NM_015009.1:c.918+62264_918+62266dup	NM_015009.1:c.918+62263_918+62266dup	NM_015009.1:c.918+62262_918+62266dup	NM_015009.1:c.918+62261_918+62266dup	NM_015009.1:c.918+62260_918+62266dup	NM_015009.1:c.918+62252_918+62266dup	NM_015009.1:c.918+62266_918+62267insTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTT	NM_015009.1:c.918+62266_918+62267insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTT	NM_015009.1:c.918+62266_918+62267insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTATTT	NM_015009.1:c.918+62266_918+62267insTTTTTTTTTTTTTTTTTTTTTTTTTATAATTT
PDZRN3 transcript variant 1	NM_015009.3:c.918+62266=	NM_015009.3:c.918+62253_918+62266del	NM_015009.3:c.918+62254_918+62266del	NM_015009.3:c.918+62257_918+62266del	NM_015009.3:c.918+62258_918+62266del	NM_015009.3:c.918+62259_918+62266del	NM_015009.3:c.918+62260_918+62266del	NM_015009.3:c.918+62261_918+62266del	NM_015009.3:c.918+62262_918+62266del	NM_015009.3:c.918+62263_918+62266del	NM_015009.3:c.918+62264_918+62266del	NM_015009.3:c.918+62265_918+62266del	NM_015009.3:c.918+62266del	NM_015009.3:c.918+62266dup	NM_015009.3:c.918+62265_918+62266dup	NM_015009.3:c.918+62264_918+62266dup	NM_015009.3:c.918+62263_918+62266dup	NM_015009.3:c.918+62262_918+62266dup	NM_015009.3:c.918+62261_918+62266dup	NM_015009.3:c.918+62260_918+62266dup	NM_015009.3:c.918+62252_918+62266dup	NM_015009.3:c.918+62266_918+62267insTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTT	NM_015009.3:c.918+62266_918+62267insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTT	NM_015009.3:c.918+62266_918+62267insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTATTT	NM_015009.3:c.918+62266_918+62267insTTTTTTTTTTTTTTTTTTTTTTTTTATAATTT
PDZRN3 transcript variant X3	XM_005264719.1:c.12+29063=	XM_005264719.1:c.12+29050_12+29063del	XM_005264719.1:c.12+29051_12+29063del	XM_005264719.1:c.12+29054_12+29063del	XM_005264719.1:c.12+29055_12+29063del	XM_005264719.1:c.12+29056_12+29063del	XM_005264719.1:c.12+29057_12+29063del	XM_005264719.1:c.12+29058_12+29063del	XM_005264719.1:c.12+29059_12+29063del	XM_005264719.1:c.12+29060_12+29063del	XM_005264719.1:c.12+29061_12+29063del	XM_005264719.1:c.12+29062_12+29063del	XM_005264719.1:c.12+29063del	XM_005264719.1:c.12+29063dup	XM_005264719.1:c.12+29062_12+29063dup	XM_005264719.1:c.12+29061_12+29063dup	XM_005264719.1:c.12+29060_12+29063dup	XM_005264719.1:c.12+29059_12+29063dup	XM_005264719.1:c.12+29058_12+29063dup	XM_005264719.1:c.12+29057_12+29063dup	XM_005264719.1:c.12+29049_12+29063dup	XM_005264719.1:c.12+29063_12+29064insTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTT	XM_005264719.1:c.12+29063_12+29064insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTT	XM_005264719.1:c.12+29063_12+29064insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTATTT	XM_005264719.1:c.12+29063_12+29064insTTTTTTTTTTTTTTTTTTTTTTTTTATAATTT
PDZRN3 transcript variant X1	XM_017005942.3:c.831+62266=	XM_017005942.3:c.831+62253_831+62266del	XM_017005942.3:c.831+62254_831+62266del	XM_017005942.3:c.831+62257_831+62266del	XM_017005942.3:c.831+62258_831+62266del	XM_017005942.3:c.831+62259_831+62266del	XM_017005942.3:c.831+62260_831+62266del	XM_017005942.3:c.831+62261_831+62266del	XM_017005942.3:c.831+62262_831+62266del	XM_017005942.3:c.831+62263_831+62266del	XM_017005942.3:c.831+62264_831+62266del	XM_017005942.3:c.831+62265_831+62266del	XM_017005942.3:c.831+62266del	XM_017005942.3:c.831+62266dup	XM_017005942.3:c.831+62265_831+62266dup	XM_017005942.3:c.831+62264_831+62266dup	XM_017005942.3:c.831+62263_831+62266dup	XM_017005942.3:c.831+62262_831+62266dup	XM_017005942.3:c.831+62261_831+62266dup	XM_017005942.3:c.831+62260_831+62266dup	XM_017005942.3:c.831+62252_831+62266dup	XM_017005942.3:c.831+62266_831+62267insTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTT	XM_017005942.3:c.831+62266_831+62267insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTT	XM_017005942.3:c.831+62266_831+62267insTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTATTT	XM_017005942.3:c.831+62266_831+62267insTTTTTTTTTTTTTTTTTTTTTTTTTATAATTT

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#.

55 SubSNP, 36 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss2992554023	Jan 10, 2018 (151)
2	EVA_DECODE	ss3709527857	Jul 13, 2019 (153)
3	EVA_DECODE	ss3709527858	Jul 13, 2019 (153)
4	EVA_DECODE	ss3709527859	Jul 13, 2019 (153)
5	EVA_DECODE	ss3709527860	Jul 13, 2019 (153)
6	EVA_DECODE	ss3709527861	Jul 13, 2019 (153)
7	EVA_DECODE	ss3709527862	Jul 13, 2019 (153)
8	PACBIO	ss3789864527	Jul 13, 2019 (153)
9	PACBIO	ss3789864528	Jul 13, 2019 (153)
10	PACBIO	ss3794738597	Jul 13, 2019 (153)
11	EVA	ss3827884320	Apr 25, 2020 (154)
12	GNOMAD	ss4073809085	Apr 26, 2021 (155)
13	GNOMAD	ss4073809086	Apr 26, 2021 (155)
14	GNOMAD	ss4073809087	Apr 26, 2021 (155)
15	GNOMAD	ss4073809088	Apr 26, 2021 (155)
16	GNOMAD	ss4073809089	Apr 26, 2021 (155)
17	GNOMAD	ss4073809090	Apr 26, 2021 (155)
18	GNOMAD	ss4073809091	Apr 26, 2021 (155)
19	GNOMAD	ss4073809092	Apr 26, 2021 (155)
20	GNOMAD	ss4073809093	Apr 26, 2021 (155)
21	GNOMAD	ss4073809094	Apr 26, 2021 (155)
22	GNOMAD	ss4073809095	Apr 26, 2021 (155)
23	GNOMAD	ss4073809096	Apr 26, 2021 (155)
24	GNOMAD	ss4073809097	Apr 26, 2021 (155)
25	GNOMAD	ss4073809098	Apr 26, 2021 (155)
26	GNOMAD	ss4073809099	Apr 26, 2021 (155)
27	GNOMAD	ss4073809100	Apr 26, 2021 (155)
28	GNOMAD	ss4073809101	Apr 26, 2021 (155)
29	GNOMAD	ss4073809102	Apr 26, 2021 (155)
30	GNOMAD	ss4073809103	Apr 26, 2021 (155)
31	GNOMAD	ss4073809104	Apr 26, 2021 (155)
32	GNOMAD	ss4073809105	Apr 26, 2021 (155)
33	GNOMAD	ss4073809106	Apr 26, 2021 (155)
34	GNOMAD	ss4073809107	Apr 26, 2021 (155)
35	GNOMAD	ss4073809108	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5159836721	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5159836722	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5159836723	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5159836724	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5159836725	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5159836726	Apr 26, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5254609248	Oct 12, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5254609249	Oct 12, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5254609250	Oct 12, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5254609251	Oct 12, 2022 (156)
46	HUGCELL_USP	ss5453946967	Oct 12, 2022 (156)
47	HUGCELL_USP	ss5453946968	Oct 12, 2022 (156)
48	HUGCELL_USP	ss5453946969	Oct 12, 2022 (156)
49	HUGCELL_USP	ss5453946970	Oct 12, 2022 (156)
50	TOMMO_GENOMICS	ss5691697481	Oct 12, 2022 (156)
51	TOMMO_GENOMICS	ss5691697482	Oct 12, 2022 (156)
52	TOMMO_GENOMICS	ss5691697483	Oct 12, 2022 (156)
53	TOMMO_GENOMICS	ss5691697484	Oct 12, 2022 (156)
54	TOMMO_GENOMICS	ss5691697485	Oct 12, 2022 (156)
55	EVA	ss5853674854	Oct 12, 2022 (156)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 112223902 (NC_000003.12:73540087::A 1097/47490) Row 112223903 (NC_000003.12:73540087::AA 236/47448) Row 112223904 (NC_000003.12:73540087::AAA 254/47388)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 17806028 (NC_000003.11:73589238:A: 5938/16578) Row 17806029 (NC_000003.11:73589238:AA: 2333/16578) Row 17806030 (NC_000003.11:73589238:AAAAAAAAAA: 139/16578)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 17806028 (NC_000003.11:73589238:A: 5938/16578) Row 17806029 (NC_000003.11:73589238:AA: 2333/16578) Row 17806030 (NC_000003.11:73589238:AAAAAAAAAA: 139/16578)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 17806028 (NC_000003.11:73589238:A: 5938/16578) Row 17806029 (NC_000003.11:73589238:AA: 2333/16578) Row 17806030 (NC_000003.11:73589238:AAAAAAAAAA: 139/16578)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 17806028 (NC_000003.11:73589238:A: 5938/16578) Row 17806029 (NC_000003.11:73589238:AA: 2333/16578) Row 17806030 (NC_000003.11:73589238:AAAAAAAAAA: 139/16578)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 17806028 (NC_000003.11:73589238:A: 5938/16578) Row 17806029 (NC_000003.11:73589238:AA: 2333/16578) Row 17806030 (NC_000003.11:73589238:AAAAAAAAAA: 139/16578)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 17806028 (NC_000003.11:73589238:A: 5938/16578) Row 17806029 (NC_000003.11:73589238:AA: 2333/16578) Row 17806030 (NC_000003.11:73589238:AAAAAAAAAA: 139/16578)...	-	Apr 26, 2021 (155)
86	14KJPN Submission ignored due to conflicting rows: Row 25534585 (NC_000003.12:73540087:A: 10167/26548) Row 25534586 (NC_000003.12:73540087:AA: 4070/26548) Row 25534587 (NC_000003.12:73540087:AAAAAAAAAA: 267/26548)...	-	Oct 12, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 25534585 (NC_000003.12:73540087:A: 10167/26548) Row 25534586 (NC_000003.12:73540087:AA: 4070/26548) Row 25534587 (NC_000003.12:73540087:AAAAAAAAAA: 267/26548)...	-	Oct 12, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 25534585 (NC_000003.12:73540087:A: 10167/26548) Row 25534586 (NC_000003.12:73540087:AA: 4070/26548) Row 25534587 (NC_000003.12:73540087:AAAAAAAAAA: 267/26548)...	-	Oct 12, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 25534585 (NC_000003.12:73540087:A: 10167/26548) Row 25534586 (NC_000003.12:73540087:AA: 4070/26548) Row 25534587 (NC_000003.12:73540087:AAAAAAAAAA: 267/26548)...	-	Oct 12, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 25534585 (NC_000003.12:73540087:A: 10167/26548) Row 25534586 (NC_000003.12:73540087:AA: 4070/26548) Row 25534587 (NC_000003.12:73540087:AAAAAAAAAA: 267/26548)...	-	Oct 12, 2022 (156)
91	ALFA	NC_000003.12 - 73540088	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
ss4073809108	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
4635589418	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4073809107	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
4635589418	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss5159836723	NC_000003.11:73589238:AAAAAAAAAA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4073809106, ss5691697483	NC_000003.12:73540087:AAAAAAAAAA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
4635589418	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4073809105	NC_000003.12:73540087:AAAAAAAAA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
4635589418	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4073809104	NC_000003.12:73540087:AAAAAAAA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
4635589418	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4073809103	NC_000003.12:73540087:AAAAAAA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
4635589418	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4073809102, ss5254609251	NC_000003.12:73540087:AAAAAA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
4635589418	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4073809101	NC_000003.12:73540087:AAAAA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
4635589418	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3709527862, ss4073809100, ss5254609249, ss5853674854	NC_000003.12:73540087:AAAA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
4635589418	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5159836724	NC_000003.11:73589238:AAA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809099, ss5254609250, ss5453946970, ss5691697484	NC_000003.12:73540087:AAA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
4635589418	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3709527861	NC_000003.12:73540088:AAA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss2992554023, ss3789864527, ss5159836722	NC_000003.11:73589238:AA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809098, ss5453946969, ss5691697482	NC_000003.12:73540087:AA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
4635589418	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3709527860	NC_000003.12:73540089:AA:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3789864528, ss3794738597, ss3827884320, ss5159836721	NC_000003.11:73589238:A:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809097, ss5453946967, ss5691697481	NC_000003.12:73540087:A:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
4635589418	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3709527859	NC_000003.12:73540090:A:	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5159836725	NC_000003.11:73589238::A	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809085, ss5254609248, ss5691697485	NC_000003.12:73540087::A	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4635589418	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3709527858	NC_000003.12:73540091::A	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809086	NC_000003.12:73540087::AA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4635589418	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5159836726	NC_000003.11:73589238::AAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809087, ss5453946968	NC_000003.12:73540087::AAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809088	NC_000003.12:73540087::AAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3709527857	NC_000003.12:73540091::AAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809089	NC_000003.12:73540087::AAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809090	NC_000003.12:73540087::AAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809091	NC_000003.12:73540087::AAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809092	NC_000003.12:73540087::AAAAAAAAAAA… NC_000003.12:73540087::AAAAAAAAAAAAAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809093	NC_000003.12:73540087::AAAAAAAAAAA… NC_000003.12:73540087::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAATA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809094	NC_000003.12:73540087::AAAAAAAAAAA… NC_000003.12:73540087::AAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809095	NC_000003.12:73540087::AAAAAAAAAAA… NC_000003.12:73540087::AAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAATAAA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4073809096	NC_000003.12:73540087::AAAAAAAAAAA… NC_000003.12:73540087::AAAAAAAAAAAAAAAAAAAAAAAAAAATTATA	NC_000003.12:73540087:AAAAAAAAAAAA… NC_000003.12:73540087:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAATTATAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs1168662549

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

rs1168662549