Name: rs56973202
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.

rs56973202

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:21774715-21774739 (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)₂₂ / del(A)₁₆ / del(A)₁₄ / d…
del(A)₂₂ / del(A)₁₆ / del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / 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 / dup(A)₈ / dup(A)₁₈ / ins(A)₃₁
Variation Type: Indel Insertion and Deletion
Frequency: delAAA=0.0778 (557/7160, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MAPK1 : 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	7160	AAAAAAAAAAAAAAAAAAAAAAAAA=0.8265	AAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0778, AAAAAAAAAAAAAAAAAAAAAAA=0.0518, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0289, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0087, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0031, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0032, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.854704	0.005022	0.140275	0
European	Sub	6290	AAAAAAAAAAAAAAAAAAAAAAAAA=0.8032	AAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0886, AAAAAAAAAAAAAAAAAAAAAAA=0.0585, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0329, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0097, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0035, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0037, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.830137	0.005871	0.163992	1
African	Sub	592	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	26	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	566	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	38	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	34	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	30	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	72	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	20	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	118	AAAAAAAAAAAAAAAAAAAAAAAAA=0.966	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.025, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.008, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA=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	7160	(A)₂₅=0.8265	del(A)₁₆=0.0000, del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0778, delAA=0.0518, delA=0.0000, dupA=0.0289, dupAA=0.0087, dupAAA=0.0032, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0031
Allele Frequency Aggregator	European	Sub	6290	(A)₂₅=0.8032	del(A)₁₆=0.0000, del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0886, delAA=0.0585, delA=0.0000, dupA=0.0329, dupAA=0.0097, dupAAA=0.0037, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0035
Allele Frequency Aggregator	African	Sub	592	(A)₂₅=1.000	del(A)₁₆=0.000, del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, 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)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	118	(A)₂₅=0.966	del(A)₁₆=0.000, del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, 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)₄=0.000, delAAA=0.000, delAA=0.025, delA=0.000, dupA=0.000, dupAA=0.008, 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	72	(A)₂₅=1.00	del(A)₁₆=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, 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)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	Asian	Sub	38	(A)₂₅=1.00	del(A)₁₆=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, 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)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	30	(A)₂₅=1.00	del(A)₁₆=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, 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)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	20	(A)₂₅=1.00	del(A)₁₆=0.00, del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, 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)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

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.21774718_21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774724_21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774726_21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774727_21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774728_21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774729_21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774730_21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774732_21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774733_21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774734_21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774735_21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774736_21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774737_21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774738_21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774739del
GRCh38.p14 chr 22	NC_000022.11:g.21774739dup
GRCh38.p14 chr 22	NC_000022.11:g.21774738_21774739dup
GRCh38.p14 chr 22	NC_000022.11:g.21774737_21774739dup
GRCh38.p14 chr 22	NC_000022.11:g.21774736_21774739dup
GRCh38.p14 chr 22	NC_000022.11:g.21774735_21774739dup
GRCh38.p14 chr 22	NC_000022.11:g.21774734_21774739dup
GRCh38.p14 chr 22	NC_000022.11:g.21774733_21774739dup
GRCh38.p14 chr 22	NC_000022.11:g.21774732_21774739dup
GRCh38.p14 chr 22	NC_000022.11:g.21774722_21774739dup
GRCh38.p14 chr 22	NC_000022.11:g.21774739_21774740insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 22	NC_000022.10:g.22129007_22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129013_22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129015_22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129016_22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129017_22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129018_22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129019_22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129021_22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129022_22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129023_22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129024_22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129025_22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129026_22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129027_22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129028del
GRCh37.p13 chr 22	NC_000022.10:g.22129028dup
GRCh37.p13 chr 22	NC_000022.10:g.22129027_22129028dup
GRCh37.p13 chr 22	NC_000022.10:g.22129026_22129028dup
GRCh37.p13 chr 22	NC_000022.10:g.22129025_22129028dup
GRCh37.p13 chr 22	NC_000022.10:g.22129024_22129028dup
GRCh37.p13 chr 22	NC_000022.10:g.22129023_22129028dup
GRCh37.p13 chr 22	NC_000022.10:g.22129022_22129028dup
GRCh37.p13 chr 22	NC_000022.10:g.22129021_22129028dup
GRCh37.p13 chr 22	NC_000022.10:g.22129011_22129028dup
GRCh37.p13 chr 22	NC_000022.10:g.22129028_22129029insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97945_97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97951_97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97953_97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97954_97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97955_97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97956_97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97957_97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97959_97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97960_97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97961_97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97962_97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97963_97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97964_97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97965_97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97966del
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97966dup
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97965_97966dup
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97964_97966dup
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97963_97966dup
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97962_97966dup
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97961_97966dup
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97960_97966dup
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97959_97966dup
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97949_97966dup
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97966_97967insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: MAPK1, mitogen-activated protein kinase 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MAPK1 transcript variant 1	NM_002745.5:c.857-1754_85… NM_002745.5:c.857-1754_857-1733del	N/A	Intron Variant
MAPK1 transcript variant 2	NM_138957.3:c.857-1754_85… NM_138957.3:c.857-1754_857-1733del	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)₂₅=	del(A)₂₂	del(A)₁₆	del(A)₁₄	del(A)₁₃	del(A)₁₂	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	dup(A)₈	dup(A)₁₈	ins(A)₃₁
GRCh38.p14 chr 22	NC_000022.11:g.21774715_21774739=	NC_000022.11:g.21774718_21774739del	NC_000022.11:g.21774724_21774739del	NC_000022.11:g.21774726_21774739del	NC_000022.11:g.21774727_21774739del	NC_000022.11:g.21774728_21774739del	NC_000022.11:g.21774729_21774739del	NC_000022.11:g.21774730_21774739del	NC_000022.11:g.21774732_21774739del	NC_000022.11:g.21774733_21774739del	NC_000022.11:g.21774734_21774739del	NC_000022.11:g.21774735_21774739del	NC_000022.11:g.21774736_21774739del	NC_000022.11:g.21774737_21774739del	NC_000022.11:g.21774738_21774739del	NC_000022.11:g.21774739del	NC_000022.11:g.21774739dup	NC_000022.11:g.21774738_21774739dup	NC_000022.11:g.21774737_21774739dup	NC_000022.11:g.21774736_21774739dup	NC_000022.11:g.21774735_21774739dup	NC_000022.11:g.21774734_21774739dup	NC_000022.11:g.21774733_21774739dup	NC_000022.11:g.21774732_21774739dup	NC_000022.11:g.21774722_21774739dup	NC_000022.11:g.21774739_21774740insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 22	NC_000022.10:g.22129004_22129028=	NC_000022.10:g.22129007_22129028del	NC_000022.10:g.22129013_22129028del	NC_000022.10:g.22129015_22129028del	NC_000022.10:g.22129016_22129028del	NC_000022.10:g.22129017_22129028del	NC_000022.10:g.22129018_22129028del	NC_000022.10:g.22129019_22129028del	NC_000022.10:g.22129021_22129028del	NC_000022.10:g.22129022_22129028del	NC_000022.10:g.22129023_22129028del	NC_000022.10:g.22129024_22129028del	NC_000022.10:g.22129025_22129028del	NC_000022.10:g.22129026_22129028del	NC_000022.10:g.22129027_22129028del	NC_000022.10:g.22129028del	NC_000022.10:g.22129028dup	NC_000022.10:g.22129027_22129028dup	NC_000022.10:g.22129026_22129028dup	NC_000022.10:g.22129025_22129028dup	NC_000022.10:g.22129024_22129028dup	NC_000022.10:g.22129023_22129028dup	NC_000022.10:g.22129022_22129028dup	NC_000022.10:g.22129021_22129028dup	NC_000022.10:g.22129011_22129028dup	NC_000022.10:g.22129028_22129029insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
MAPK1 RefSeqGene (LRG_786)	NG_023054.2:g.97942_97966=	NG_023054.2:g.97945_97966del	NG_023054.2:g.97951_97966del	NG_023054.2:g.97953_97966del	NG_023054.2:g.97954_97966del	NG_023054.2:g.97955_97966del	NG_023054.2:g.97956_97966del	NG_023054.2:g.97957_97966del	NG_023054.2:g.97959_97966del	NG_023054.2:g.97960_97966del	NG_023054.2:g.97961_97966del	NG_023054.2:g.97962_97966del	NG_023054.2:g.97963_97966del	NG_023054.2:g.97964_97966del	NG_023054.2:g.97965_97966del	NG_023054.2:g.97966del	NG_023054.2:g.97966dup	NG_023054.2:g.97965_97966dup	NG_023054.2:g.97964_97966dup	NG_023054.2:g.97963_97966dup	NG_023054.2:g.97962_97966dup	NG_023054.2:g.97961_97966dup	NG_023054.2:g.97960_97966dup	NG_023054.2:g.97959_97966dup	NG_023054.2:g.97949_97966dup	NG_023054.2:g.97966_97967insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MAPK1 transcript variant 1	NM_002745.4:c.857-1733=	NM_002745.4:c.857-1754_857-1733del	NM_002745.4:c.857-1748_857-1733del	NM_002745.4:c.857-1746_857-1733del	NM_002745.4:c.857-1745_857-1733del	NM_002745.4:c.857-1744_857-1733del	NM_002745.4:c.857-1743_857-1733del	NM_002745.4:c.857-1742_857-1733del	NM_002745.4:c.857-1740_857-1733del	NM_002745.4:c.857-1739_857-1733del	NM_002745.4:c.857-1738_857-1733del	NM_002745.4:c.857-1737_857-1733del	NM_002745.4:c.857-1736_857-1733del	NM_002745.4:c.857-1735_857-1733del	NM_002745.4:c.857-1734_857-1733del	NM_002745.4:c.857-1733del	NM_002745.4:c.857-1733dup	NM_002745.4:c.857-1734_857-1733dup	NM_002745.4:c.857-1735_857-1733dup	NM_002745.4:c.857-1736_857-1733dup	NM_002745.4:c.857-1737_857-1733dup	NM_002745.4:c.857-1738_857-1733dup	NM_002745.4:c.857-1739_857-1733dup	NM_002745.4:c.857-1740_857-1733dup	NM_002745.4:c.857-1750_857-1733dup	NM_002745.4:c.857-1733_857-1732insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MAPK1 transcript variant 1	NM_002745.5:c.857-1733=	NM_002745.5:c.857-1754_857-1733del	NM_002745.5:c.857-1748_857-1733del	NM_002745.5:c.857-1746_857-1733del	NM_002745.5:c.857-1745_857-1733del	NM_002745.5:c.857-1744_857-1733del	NM_002745.5:c.857-1743_857-1733del	NM_002745.5:c.857-1742_857-1733del	NM_002745.5:c.857-1740_857-1733del	NM_002745.5:c.857-1739_857-1733del	NM_002745.5:c.857-1738_857-1733del	NM_002745.5:c.857-1737_857-1733del	NM_002745.5:c.857-1736_857-1733del	NM_002745.5:c.857-1735_857-1733del	NM_002745.5:c.857-1734_857-1733del	NM_002745.5:c.857-1733del	NM_002745.5:c.857-1733dup	NM_002745.5:c.857-1734_857-1733dup	NM_002745.5:c.857-1735_857-1733dup	NM_002745.5:c.857-1736_857-1733dup	NM_002745.5:c.857-1737_857-1733dup	NM_002745.5:c.857-1738_857-1733dup	NM_002745.5:c.857-1739_857-1733dup	NM_002745.5:c.857-1740_857-1733dup	NM_002745.5:c.857-1750_857-1733dup	NM_002745.5:c.857-1733_857-1732insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MAPK1 transcript variant 2	NM_138957.2:c.857-1733=	NM_138957.2:c.857-1754_857-1733del	NM_138957.2:c.857-1748_857-1733del	NM_138957.2:c.857-1746_857-1733del	NM_138957.2:c.857-1745_857-1733del	NM_138957.2:c.857-1744_857-1733del	NM_138957.2:c.857-1743_857-1733del	NM_138957.2:c.857-1742_857-1733del	NM_138957.2:c.857-1740_857-1733del	NM_138957.2:c.857-1739_857-1733del	NM_138957.2:c.857-1738_857-1733del	NM_138957.2:c.857-1737_857-1733del	NM_138957.2:c.857-1736_857-1733del	NM_138957.2:c.857-1735_857-1733del	NM_138957.2:c.857-1734_857-1733del	NM_138957.2:c.857-1733del	NM_138957.2:c.857-1733dup	NM_138957.2:c.857-1734_857-1733dup	NM_138957.2:c.857-1735_857-1733dup	NM_138957.2:c.857-1736_857-1733dup	NM_138957.2:c.857-1737_857-1733dup	NM_138957.2:c.857-1738_857-1733dup	NM_138957.2:c.857-1739_857-1733dup	NM_138957.2:c.857-1740_857-1733dup	NM_138957.2:c.857-1750_857-1733dup	NM_138957.2:c.857-1733_857-1732insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
MAPK1 transcript variant 2	NM_138957.3:c.857-1733=	NM_138957.3:c.857-1754_857-1733del	NM_138957.3:c.857-1748_857-1733del	NM_138957.3:c.857-1746_857-1733del	NM_138957.3:c.857-1745_857-1733del	NM_138957.3:c.857-1744_857-1733del	NM_138957.3:c.857-1743_857-1733del	NM_138957.3:c.857-1742_857-1733del	NM_138957.3:c.857-1740_857-1733del	NM_138957.3:c.857-1739_857-1733del	NM_138957.3:c.857-1738_857-1733del	NM_138957.3:c.857-1737_857-1733del	NM_138957.3:c.857-1736_857-1733del	NM_138957.3:c.857-1735_857-1733del	NM_138957.3:c.857-1734_857-1733del	NM_138957.3:c.857-1733del	NM_138957.3:c.857-1733dup	NM_138957.3:c.857-1734_857-1733dup	NM_138957.3:c.857-1735_857-1733dup	NM_138957.3:c.857-1736_857-1733dup	NM_138957.3:c.857-1737_857-1733dup	NM_138957.3:c.857-1738_857-1733dup	NM_138957.3:c.857-1739_857-1733dup	NM_138957.3:c.857-1740_857-1733dup	NM_138957.3:c.857-1750_857-1733dup	NM_138957.3:c.857-1733_857-1732insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

66 SubSNP, 43 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4283952	Mar 15, 2016 (147)
2	HGSV	ss82880150	Dec 14, 2007 (129)
3	HUMANGENOME_JCVI	ss95754433	Feb 13, 2009 (130)
4	HUMANGENOME_JCVI	ss96108706	Mar 15, 2016 (147)
5	EVA_GENOME_DK	ss1575811357	Apr 01, 2015 (144)
6	EVA_GENOME_DK	ss1577948862	Apr 01, 2015 (144)
7	SWEGEN	ss3019117873	Nov 08, 2017 (151)
8	MCHAISSO	ss3064882313	Nov 08, 2017 (151)
9	EVA_DECODE	ss3707977972	Jul 13, 2019 (153)
10	EVA_DECODE	ss3707977973	Jul 13, 2019 (153)
11	EVA_DECODE	ss3707977974	Jul 13, 2019 (153)
12	EVA_DECODE	ss3707977975	Jul 13, 2019 (153)
13	EVA_DECODE	ss3707977976	Jul 13, 2019 (153)
14	PACBIO	ss3793668022	Jul 13, 2019 (153)
15	PACBIO	ss3798554359	Jul 13, 2019 (153)
16	PACBIO	ss3798554360	Jul 13, 2019 (153)
17	EVA	ss3835933094	Apr 27, 2020 (154)
18	KOGIC	ss3983422078	Apr 27, 2020 (154)
19	KOGIC	ss3983422079	Apr 27, 2020 (154)
20	KOGIC	ss3983422080	Apr 27, 2020 (154)
21	KOGIC	ss3983422081	Apr 27, 2020 (154)
22	KOGIC	ss3983422082	Apr 27, 2020 (154)
23	KOGIC	ss3983422083	Apr 27, 2020 (154)
24	GNOMAD	ss4362770911	Apr 27, 2021 (155)
25	GNOMAD	ss4362770912	Apr 27, 2021 (155)
26	GNOMAD	ss4362770913	Apr 27, 2021 (155)
27	GNOMAD	ss4362770914	Apr 27, 2021 (155)
28	GNOMAD	ss4362770915	Apr 27, 2021 (155)
29	GNOMAD	ss4362770916	Apr 27, 2021 (155)
30	GNOMAD	ss4362770917	Apr 27, 2021 (155)
31	GNOMAD	ss4362770918	Apr 27, 2021 (155)
32	GNOMAD	ss4362770919	Apr 27, 2021 (155)
33	GNOMAD	ss4362770920	Apr 27, 2021 (155)
34	GNOMAD	ss4362770921	Apr 27, 2021 (155)
35	GNOMAD	ss4362770922	Apr 27, 2021 (155)
36	GNOMAD	ss4362770923	Apr 27, 2021 (155)
37	GNOMAD	ss4362770924	Apr 27, 2021 (155)
38	GNOMAD	ss4362770925	Apr 27, 2021 (155)
39	GNOMAD	ss4362770926	Apr 27, 2021 (155)
40	GNOMAD	ss4362770927	Apr 27, 2021 (155)
41	GNOMAD	ss4362770928	Apr 27, 2021 (155)
42	GNOMAD	ss4362770929	Apr 27, 2021 (155)
43	GNOMAD	ss4362770930	Apr 27, 2021 (155)
44	TOPMED	ss5105505260	Apr 27, 2021 (155)
45	TOPMED	ss5105505261	Apr 27, 2021 (155)
46	TOPMED	ss5105505262	Apr 27, 2021 (155)
47	TOMMO_GENOMICS	ss5232122927	Apr 27, 2021 (155)
48	TOMMO_GENOMICS	ss5232122928	Apr 27, 2021 (155)
49	TOMMO_GENOMICS	ss5232122929	Apr 27, 2021 (155)
50	TOMMO_GENOMICS	ss5232122930	Apr 27, 2021 (155)
51	TOMMO_GENOMICS	ss5232122931	Apr 27, 2021 (155)
52	1000G_HIGH_COVERAGE	ss5310705529	Oct 16, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5310705530	Oct 16, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5310705532	Oct 16, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5310705533	Oct 16, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5310705534	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5502602550	Oct 16, 2022 (156)
58	HUGCELL_USP	ss5502602551	Oct 16, 2022 (156)
59	HUGCELL_USP	ss5502602552	Oct 16, 2022 (156)
60	HUGCELL_USP	ss5502602553	Oct 16, 2022 (156)
61	HUGCELL_USP	ss5502602554	Oct 16, 2022 (156)
62	TOMMO_GENOMICS	ss5793086420	Oct 16, 2022 (156)
63	TOMMO_GENOMICS	ss5793086421	Oct 16, 2022 (156)
64	TOMMO_GENOMICS	ss5793086422	Oct 16, 2022 (156)
65	TOMMO_GENOMICS	ss5793086423	Oct 16, 2022 (156)
66	TOMMO_GENOMICS	ss5793086425	Oct 16, 2022 (156)
67	The Danish reference pan genome Submission ignored due to conflicting rows: Row 67088 (NC_000022.10:22129003:AAAAAAAAAAAAAAAAAAAAAA: 40/40) Row 788937 (NC_000022.10:22129003:A: 14/40)	-	Apr 27, 2020 (154)
68	The Danish reference pan genome Submission ignored due to conflicting rows: Row 67088 (NC_000022.10:22129003:AAAAAAAAAAAAAAAAAAAAAA: 40/40) Row 788937 (NC_000022.10:22129003:A: 14/40)	-	Apr 27, 2020 (154)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 566900273 (NC_000022.11:21774714::A 5516/67256) Row 566900274 (NC_000022.11:21774714::AA 1104/67214) Row 566900275 (NC_000022.11:21774714::AAA 92/67412)...	-	Apr 27, 2021 (155)
90	Korean Genome Project Submission ignored due to conflicting rows: Row 39800079 (NC_000022.11:21774714:AAAA: 25/1742) Row 39800080 (NC_000022.11:21774715:AAA: 130/1742) Row 39800081 (NC_000022.11:21774717:A: 144/1742)...	-	Apr 27, 2020 (154)
91	Korean Genome Project Submission ignored due to conflicting rows: Row 39800079 (NC_000022.11:21774714:AAAA: 25/1742) Row 39800080 (NC_000022.11:21774715:AAA: 130/1742) Row 39800081 (NC_000022.11:21774717:A: 144/1742)...	-	Apr 27, 2020 (154)
92	Korean Genome Project Submission ignored due to conflicting rows: Row 39800079 (NC_000022.11:21774714:AAAA: 25/1742) Row 39800080 (NC_000022.11:21774715:AAA: 130/1742) Row 39800081 (NC_000022.11:21774717:A: 144/1742)...	-	Apr 27, 2020 (154)
93	Korean Genome Project Submission ignored due to conflicting rows: Row 39800079 (NC_000022.11:21774714:AAAA: 25/1742) Row 39800080 (NC_000022.11:21774715:AAA: 130/1742) Row 39800081 (NC_000022.11:21774717:A: 144/1742)...	-	Apr 27, 2020 (154)
94	Korean Genome Project Submission ignored due to conflicting rows: Row 39800079 (NC_000022.11:21774714:AAAA: 25/1742) Row 39800080 (NC_000022.11:21774715:AAA: 130/1742) Row 39800081 (NC_000022.11:21774717:A: 144/1742)...	-	Apr 27, 2020 (154)
95	Korean Genome Project Submission ignored due to conflicting rows: Row 39800079 (NC_000022.11:21774714:AAAA: 25/1742) Row 39800080 (NC_000022.11:21774715:AAA: 130/1742) Row 39800081 (NC_000022.11:21774717:A: 144/1742)...	-	Apr 27, 2020 (154)
96	8.3KJPN Submission ignored due to conflicting rows: Row 90092234 (NC_000022.10:22129003::A 2302/16268) Row 90092235 (NC_000022.10:22129003:AAA: 790/16268) Row 90092236 (NC_000022.10:22129003::AA 166/16268)...	-	Apr 27, 2021 (155)
97	8.3KJPN Submission ignored due to conflicting rows: Row 90092234 (NC_000022.10:22129003::A 2302/16268) Row 90092235 (NC_000022.10:22129003:AAA: 790/16268) Row 90092236 (NC_000022.10:22129003::AA 166/16268)...	-	Apr 27, 2021 (155)
98	8.3KJPN Submission ignored due to conflicting rows: Row 90092234 (NC_000022.10:22129003::A 2302/16268) Row 90092235 (NC_000022.10:22129003:AAA: 790/16268) Row 90092236 (NC_000022.10:22129003::AA 166/16268)...	-	Apr 27, 2021 (155)
99	8.3KJPN Submission ignored due to conflicting rows: Row 90092234 (NC_000022.10:22129003::A 2302/16268) Row 90092235 (NC_000022.10:22129003:AAA: 790/16268) Row 90092236 (NC_000022.10:22129003::AA 166/16268)...	-	Apr 27, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 90092234 (NC_000022.10:22129003::A 2302/16268) Row 90092235 (NC_000022.10:22129003:AAA: 790/16268) Row 90092236 (NC_000022.10:22129003::AA 166/16268)...	-	Apr 27, 2021 (155)
101	14KJPN Submission ignored due to conflicting rows: Row 126923524 (NC_000022.11:21774714:AAA: 1556/26030) Row 126923525 (NC_000022.11:21774714::A 3840/26030) Row 126923526 (NC_000022.11:21774714:AA: 1608/26030)...	-	Oct 16, 2022 (156)
102	14KJPN Submission ignored due to conflicting rows: Row 126923524 (NC_000022.11:21774714:AAA: 1556/26030) Row 126923525 (NC_000022.11:21774714::A 3840/26030) Row 126923526 (NC_000022.11:21774714:AA: 1608/26030)...	-	Oct 16, 2022 (156)
103	14KJPN Submission ignored due to conflicting rows: Row 126923524 (NC_000022.11:21774714:AAA: 1556/26030) Row 126923525 (NC_000022.11:21774714::A 3840/26030) Row 126923526 (NC_000022.11:21774714:AA: 1608/26030)...	-	Oct 16, 2022 (156)
104	14KJPN Submission ignored due to conflicting rows: Row 126923524 (NC_000022.11:21774714:AAA: 1556/26030) Row 126923525 (NC_000022.11:21774714::A 3840/26030) Row 126923526 (NC_000022.11:21774714:AA: 1608/26030)...	-	Oct 16, 2022 (156)
105	14KJPN Submission ignored due to conflicting rows: Row 126923524 (NC_000022.11:21774714:AAA: 1556/26030) Row 126923525 (NC_000022.11:21774714::A 3840/26030) Row 126923526 (NC_000022.11:21774714:AA: 1608/26030)...	-	Oct 16, 2022 (156)
106	TopMed Submission ignored due to conflicting rows: Row 380614207 (NC_000022.11:21774714:AAAAAAAAAAA: 2/264690) Row 380614208 (NC_000022.11:21774714:AAAAAAAAAAAA: 4/264690) Row 380614209 (NC_000022.11:21774714:AAAAAAAAAAAAAA: 1/264690)	-	Apr 27, 2021 (155)
107	TopMed Submission ignored due to conflicting rows: Row 380614207 (NC_000022.11:21774714:AAAAAAAAAAA: 2/264690) Row 380614208 (NC_000022.11:21774714:AAAAAAAAAAAA: 4/264690) Row 380614209 (NC_000022.11:21774714:AAAAAAAAAAAAAA: 1/264690)	-	Apr 27, 2021 (155)
108	TopMed Submission ignored due to conflicting rows: Row 380614207 (NC_000022.11:21774714:AAAAAAAAAAA: 2/264690) Row 380614208 (NC_000022.11:21774714:AAAAAAAAAAAA: 4/264690) Row 380614209 (NC_000022.11:21774714:AAAAAAAAAAAAAA: 1/264690)	-	Apr 27, 2021 (155)
109	ALFA	NC_000022.11 - 21774715	Apr 27, 2021 (155)

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

Associated ID	History Updated (Build)
rs869196390	Jul 19, 2016 (147)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss1577948862	NC_000022.10:22129003:AAAAAAAAAAAA… NC_000022.10:22129003:AAAAAAAAAAAAAAAAAAAAAA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4362770930, ss5105505262	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4362770929	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4362770928, ss5105505261	NC_000022.11:21774714:AAAAAAAAAAAA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4362770927, ss5105505260	NC_000022.11:21774714:AAAAAAAAAAA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4362770926	NC_000022.11:21774714:AAAAAAAAAA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4362770925	NC_000022.11:21774714:AAAAAAAA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4362770924	NC_000022.11:21774714:AAAAAAA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4362770923	NC_000022.11:21774714:AAAAA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3707977976, ss3983422078	NC_000022.11:21774714:AAAA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3019117873, ss3798554359, ss3835933094, ss5232122928	NC_000022.10:22129003:AAA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4362770922, ss5310705534, ss5502602553, ss5793086420	NC_000022.11:21774714:AAA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3707977975, ss3983422079	NC_000022.11:21774715:AAA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss82880150	NC_000022.8:20453580:AA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3793668022, ss3798554360, ss5232122930	NC_000022.10:22129003:AA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3064882313, ss4362770921, ss5310705529, ss5502602554, ss5793086422	NC_000022.11:21774714:AA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3707977974, ss3983422082	NC_000022.11:21774716:AA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4283952	NT_011520.12:1519594:AA:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss1575811357	NC_000022.10:22129003:A:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5310705530, ss5502602550	NC_000022.11:21774714:A:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3707977973, ss3983422080	NC_000022.11:21774717:A:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss96108706	NT_011520.12:1519572:A:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss95754433	NT_011520.12:1519596:A:	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5232122927	NC_000022.10:22129003::A	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4362770911, ss5310705532, ss5502602551, ss5793086421	NC_000022.11:21774714::A	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3707977972, ss3983422081	NC_000022.11:21774718::A	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5232122929	NC_000022.10:22129003::AA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4362770912, ss5310705533, ss5502602552, ss5793086423	NC_000022.11:21774714::AA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3983422083	NC_000022.11:21774718::AA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5232122931	NC_000022.10:22129003::AAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4362770913, ss5793086425	NC_000022.11:21774714::AAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4362770914	NC_000022.11:21774714::AAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4362770915	NC_000022.11:21774714::AAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4362770916	NC_000022.11:21774714::AAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4843284591	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4362770917	NC_000022.11:21774714::AAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4362770918	NC_000022.11:21774714::AAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4362770919	NC_000022.11:21774714::AAAAAAAAAAA… NC_000022.11:21774714::AAAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4362770920	NC_000022.11:21774714::AAAAAAAAAAA… NC_000022.11:21774714::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:21774714:AAAAAAAAAAAA… NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs56973202

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

rs56973202