Name: rs35188952
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.

rs35188952

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:2984167-2984189 (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)₁₅ / del(A)₁₃ / del(A)₁₂ / d…
del(A)₁₅ / del(A)₁₃ / del(A)₁₂ / del(A)₁₀ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₁₂
Variation Type: Indel Insertion and Deletion
Frequency: delAAA=0.1232 (807/6549, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NAP1L4 : 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	6549	AAAAAAAAAAAAAAAAAAAAAAA=0.8325	AAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.1232, AAAAAAAAAAAAAAAAAAAAA=0.0250, AAAAAAAAAAAAAAAAAAAAAAAA=0.0101, AAAAAAAAAAAAAAAAAAAAAA=0.0037, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0055, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.795477	0.044563	0.15996	32
European	Sub	5977	AAAAAAAAAAAAAAAAAAAAAAA=0.8171	AAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.1343, AAAAAAAAAAAAAAAAAAAAA=0.0274, AAAAAAAAAAAAAAAAAAAAAAAA=0.0110, AAAAAAAAAAAAAAAAAAAAAA=0.0040, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0060, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.775083	0.048879	0.176038	32
African	Sub	342	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	12	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	330	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	8	AAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	6	AAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	2	AAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	34	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	80	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	20	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	88	AAAAAAAAAAAAAAAAAAAAAAA=0.95	AAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.05, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	0.931818	0.022727	0.045455	6

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	6549	(A)₂₃=0.8325	del(A)₁₅=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₀=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.1232, delAA=0.0250, delA=0.0037, dupA=0.0101, dupAA=0.0055, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	5977	(A)₂₃=0.8171	del(A)₁₅=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₀=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.1343, delAA=0.0274, delA=0.0040, dupA=0.0110, dupAA=0.0060, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	342	(A)₂₃=1.000	del(A)₁₅=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	88	(A)₂₃=0.95	del(A)₁₅=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₀=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.05, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 2	Sub	80	(A)₂₃=1.00	del(A)₁₅=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₀=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	34	(A)₂₃=1.00	del(A)₁₅=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₀=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	20	(A)₂₃=1.00	del(A)₁₅=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₀=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Asian	Sub	8	(A)₂₃=1.0	del(A)₁₅=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₀=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, dupAAA=0.0, dup(A)₄=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 11	NC_000011.10:g.2984175_2984189del
GRCh38.p14 chr 11	NC_000011.10:g.2984177_2984189del
GRCh38.p14 chr 11	NC_000011.10:g.2984178_2984189del
GRCh38.p14 chr 11	NC_000011.10:g.2984180_2984189del
GRCh38.p14 chr 11	NC_000011.10:g.2984185_2984189del
GRCh38.p14 chr 11	NC_000011.10:g.2984186_2984189del
GRCh38.p14 chr 11	NC_000011.10:g.2984187_2984189del
GRCh38.p14 chr 11	NC_000011.10:g.2984188_2984189del
GRCh38.p14 chr 11	NC_000011.10:g.2984189del
GRCh38.p14 chr 11	NC_000011.10:g.2984189dup
GRCh38.p14 chr 11	NC_000011.10:g.2984188_2984189dup
GRCh38.p14 chr 11	NC_000011.10:g.2984187_2984189dup
GRCh38.p14 chr 11	NC_000011.10:g.2984186_2984189dup
GRCh38.p14 chr 11	NC_000011.10:g.2984185_2984189dup
GRCh38.p14 chr 11	NC_000011.10:g.2984178_2984189dup
GRCh37.p13 chr 11	NC_000011.9:g.3005405_3005419del
GRCh37.p13 chr 11	NC_000011.9:g.3005407_3005419del
GRCh37.p13 chr 11	NC_000011.9:g.3005408_3005419del
GRCh37.p13 chr 11	NC_000011.9:g.3005410_3005419del
GRCh37.p13 chr 11	NC_000011.9:g.3005415_3005419del
GRCh37.p13 chr 11	NC_000011.9:g.3005416_3005419del
GRCh37.p13 chr 11	NC_000011.9:g.3005417_3005419del
GRCh37.p13 chr 11	NC_000011.9:g.3005418_3005419del
GRCh37.p13 chr 11	NC_000011.9:g.3005419del
GRCh37.p13 chr 11	NC_000011.9:g.3005419dup
GRCh37.p13 chr 11	NC_000011.9:g.3005418_3005419dup
GRCh37.p13 chr 11	NC_000011.9:g.3005417_3005419dup
GRCh37.p13 chr 11	NC_000011.9:g.3005416_3005419dup
GRCh37.p13 chr 11	NC_000011.9:g.3005415_3005419dup
GRCh37.p13 chr 11	NC_000011.9:g.3005408_3005419dup
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215261_215263dup
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215252_215263del
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215254_215263del
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215255_215263del
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215257_215263del
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215262_215263del
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215263del
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215263dup
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215262_215263dup
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215260_215263dup
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215259_215263dup
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215258_215263dup
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215257_215263dup
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215256_215263dup
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215249_215263dup

Gene: NAP1L4, nucleosome assembly protein 1 like 4 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NAP1L4 transcript variant 2	NM_001369375.1:c.-18+3896… NM_001369375.1:c.-18+3896_-18+3910del	N/A	Intron Variant
NAP1L4 transcript variant 3	NM_001369376.1:c.-17-4944… NM_001369376.1:c.-17-4944_-17-4930del	N/A	Intron Variant
NAP1L4 transcript variant 4	NM_001369377.1:c.-18+3896… NM_001369377.1:c.-18+3896_-18+3910del	N/A	Intron Variant
NAP1L4 transcript variant 5	NM_001369378.1:c.-17-4944… NM_001369378.1:c.-17-4944_-17-4930del	N/A	Intron Variant
NAP1L4 transcript variant 6	NM_001369379.1:c.-17-4944… NM_001369379.1:c.-17-4944_-17-4930del	N/A	Intron Variant
NAP1L4 transcript variant 7	NM_001369380.1:c.-17-4944… NM_001369380.1:c.-17-4944_-17-4930del	N/A	Intron Variant
NAP1L4 transcript variant 8	NM_001369381.1:c.-17-4944… NM_001369381.1:c.-17-4944_-17-4930del	N/A	Intron Variant
NAP1L4 transcript variant 9	NM_001369382.1:c.-17-4944… NM_001369382.1:c.-17-4944_-17-4930del	N/A	Intron Variant
NAP1L4 transcript variant 10	NM_001369383.1:c.-17-4944… NM_001369383.1:c.-17-4944_-17-4930del	N/A	Intron Variant
NAP1L4 transcript variant 11	NM_001369384.1:c.-17-4944… NM_001369384.1:c.-17-4944_-17-4930del	N/A	Intron Variant
NAP1L4 transcript variant 12	NM_001369385.1:c.-17-4944… NM_001369385.1:c.-17-4944_-17-4930del	N/A	Intron Variant
NAP1L4 transcript variant 13	NM_001369386.1:c.-18+3896… NM_001369386.1:c.-18+3896_-18+3910del	N/A	Intron Variant
NAP1L4 transcript variant 14	NM_001369388.1:c.-17-4944… NM_001369388.1:c.-17-4944_-17-4930del	N/A	Intron Variant
NAP1L4 transcript variant 1	NM_005969.4:c.-17-4944_-1… NM_005969.4:c.-17-4944_-17-4930del	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)₂₃=	del(A)₁₅	del(A)₁₃	del(A)₁₂	del(A)₁₀	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₁₂
GRCh38.p14 chr 11	NC_000011.10:g.2984167_2984189=	NC_000011.10:g.2984175_2984189del	NC_000011.10:g.2984177_2984189del	NC_000011.10:g.2984178_2984189del	NC_000011.10:g.2984180_2984189del	NC_000011.10:g.2984185_2984189del	NC_000011.10:g.2984186_2984189del	NC_000011.10:g.2984187_2984189del	NC_000011.10:g.2984188_2984189del	NC_000011.10:g.2984189del	NC_000011.10:g.2984189dup	NC_000011.10:g.2984188_2984189dup	NC_000011.10:g.2984187_2984189dup	NC_000011.10:g.2984186_2984189dup	NC_000011.10:g.2984185_2984189dup	NC_000011.10:g.2984178_2984189dup
GRCh37.p13 chr 11	NC_000011.9:g.3005397_3005419=	NC_000011.9:g.3005405_3005419del	NC_000011.9:g.3005407_3005419del	NC_000011.9:g.3005408_3005419del	NC_000011.9:g.3005410_3005419del	NC_000011.9:g.3005415_3005419del	NC_000011.9:g.3005416_3005419del	NC_000011.9:g.3005417_3005419del	NC_000011.9:g.3005418_3005419del	NC_000011.9:g.3005419del	NC_000011.9:g.3005419dup	NC_000011.9:g.3005418_3005419dup	NC_000011.9:g.3005417_3005419dup	NC_000011.9:g.3005416_3005419dup	NC_000011.9:g.3005415_3005419dup	NC_000011.9:g.3005408_3005419dup
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.215261_215263dup	NT_187585.1:g.215252_215263del	NT_187585.1:g.215254_215263del	NT_187585.1:g.215255_215263del	NT_187585.1:g.215257_215263del	NT_187585.1:g.215262_215263del	NT_187585.1:g.215263del	NT_187585.1:g.215244_215263=	NT_187585.1:g.215263dup	NT_187585.1:g.215262_215263dup	NT_187585.1:g.215260_215263dup	NT_187585.1:g.215259_215263dup	NT_187585.1:g.215258_215263dup	NT_187585.1:g.215257_215263dup	NT_187585.1:g.215256_215263dup	NT_187585.1:g.215249_215263dup
NAP1L4 transcript variant 2	NM_001369375.1:c.-18+3910=	NM_001369375.1:c.-18+3896_-18+3910del	NM_001369375.1:c.-18+3898_-18+3910del	NM_001369375.1:c.-18+3899_-18+3910del	NM_001369375.1:c.-18+3901_-18+3910del	NM_001369375.1:c.-18+3906_-18+3910del	NM_001369375.1:c.-18+3907_-18+3910del	NM_001369375.1:c.-18+3908_-18+3910del	NM_001369375.1:c.-18+3909_-18+3910del	NM_001369375.1:c.-18+3910del	NM_001369375.1:c.-18+3910dup	NM_001369375.1:c.-18+3909_-18+3910dup	NM_001369375.1:c.-18+3908_-18+3910dup	NM_001369375.1:c.-18+3907_-18+3910dup	NM_001369375.1:c.-18+3906_-18+3910dup	NM_001369375.1:c.-18+3899_-18+3910dup
NAP1L4 transcript variant 3	NM_001369376.1:c.-17-4930=	NM_001369376.1:c.-17-4944_-17-4930del	NM_001369376.1:c.-17-4942_-17-4930del	NM_001369376.1:c.-17-4941_-17-4930del	NM_001369376.1:c.-17-4939_-17-4930del	NM_001369376.1:c.-17-4934_-17-4930del	NM_001369376.1:c.-17-4933_-17-4930del	NM_001369376.1:c.-17-4932_-17-4930del	NM_001369376.1:c.-17-4931_-17-4930del	NM_001369376.1:c.-17-4930del	NM_001369376.1:c.-17-4930dup	NM_001369376.1:c.-17-4931_-17-4930dup	NM_001369376.1:c.-17-4932_-17-4930dup	NM_001369376.1:c.-17-4933_-17-4930dup	NM_001369376.1:c.-17-4934_-17-4930dup	NM_001369376.1:c.-17-4941_-17-4930dup
NAP1L4 transcript variant 4	NM_001369377.1:c.-18+3910=	NM_001369377.1:c.-18+3896_-18+3910del	NM_001369377.1:c.-18+3898_-18+3910del	NM_001369377.1:c.-18+3899_-18+3910del	NM_001369377.1:c.-18+3901_-18+3910del	NM_001369377.1:c.-18+3906_-18+3910del	NM_001369377.1:c.-18+3907_-18+3910del	NM_001369377.1:c.-18+3908_-18+3910del	NM_001369377.1:c.-18+3909_-18+3910del	NM_001369377.1:c.-18+3910del	NM_001369377.1:c.-18+3910dup	NM_001369377.1:c.-18+3909_-18+3910dup	NM_001369377.1:c.-18+3908_-18+3910dup	NM_001369377.1:c.-18+3907_-18+3910dup	NM_001369377.1:c.-18+3906_-18+3910dup	NM_001369377.1:c.-18+3899_-18+3910dup
NAP1L4 transcript variant 5	NM_001369378.1:c.-17-4930=	NM_001369378.1:c.-17-4944_-17-4930del	NM_001369378.1:c.-17-4942_-17-4930del	NM_001369378.1:c.-17-4941_-17-4930del	NM_001369378.1:c.-17-4939_-17-4930del	NM_001369378.1:c.-17-4934_-17-4930del	NM_001369378.1:c.-17-4933_-17-4930del	NM_001369378.1:c.-17-4932_-17-4930del	NM_001369378.1:c.-17-4931_-17-4930del	NM_001369378.1:c.-17-4930del	NM_001369378.1:c.-17-4930dup	NM_001369378.1:c.-17-4931_-17-4930dup	NM_001369378.1:c.-17-4932_-17-4930dup	NM_001369378.1:c.-17-4933_-17-4930dup	NM_001369378.1:c.-17-4934_-17-4930dup	NM_001369378.1:c.-17-4941_-17-4930dup
NAP1L4 transcript variant 6	NM_001369379.1:c.-17-4930=	NM_001369379.1:c.-17-4944_-17-4930del	NM_001369379.1:c.-17-4942_-17-4930del	NM_001369379.1:c.-17-4941_-17-4930del	NM_001369379.1:c.-17-4939_-17-4930del	NM_001369379.1:c.-17-4934_-17-4930del	NM_001369379.1:c.-17-4933_-17-4930del	NM_001369379.1:c.-17-4932_-17-4930del	NM_001369379.1:c.-17-4931_-17-4930del	NM_001369379.1:c.-17-4930del	NM_001369379.1:c.-17-4930dup	NM_001369379.1:c.-17-4931_-17-4930dup	NM_001369379.1:c.-17-4932_-17-4930dup	NM_001369379.1:c.-17-4933_-17-4930dup	NM_001369379.1:c.-17-4934_-17-4930dup	NM_001369379.1:c.-17-4941_-17-4930dup
NAP1L4 transcript variant 7	NM_001369380.1:c.-17-4930=	NM_001369380.1:c.-17-4944_-17-4930del	NM_001369380.1:c.-17-4942_-17-4930del	NM_001369380.1:c.-17-4941_-17-4930del	NM_001369380.1:c.-17-4939_-17-4930del	NM_001369380.1:c.-17-4934_-17-4930del	NM_001369380.1:c.-17-4933_-17-4930del	NM_001369380.1:c.-17-4932_-17-4930del	NM_001369380.1:c.-17-4931_-17-4930del	NM_001369380.1:c.-17-4930del	NM_001369380.1:c.-17-4930dup	NM_001369380.1:c.-17-4931_-17-4930dup	NM_001369380.1:c.-17-4932_-17-4930dup	NM_001369380.1:c.-17-4933_-17-4930dup	NM_001369380.1:c.-17-4934_-17-4930dup	NM_001369380.1:c.-17-4941_-17-4930dup
NAP1L4 transcript variant 8	NM_001369381.1:c.-17-4930=	NM_001369381.1:c.-17-4944_-17-4930del	NM_001369381.1:c.-17-4942_-17-4930del	NM_001369381.1:c.-17-4941_-17-4930del	NM_001369381.1:c.-17-4939_-17-4930del	NM_001369381.1:c.-17-4934_-17-4930del	NM_001369381.1:c.-17-4933_-17-4930del	NM_001369381.1:c.-17-4932_-17-4930del	NM_001369381.1:c.-17-4931_-17-4930del	NM_001369381.1:c.-17-4930del	NM_001369381.1:c.-17-4930dup	NM_001369381.1:c.-17-4931_-17-4930dup	NM_001369381.1:c.-17-4932_-17-4930dup	NM_001369381.1:c.-17-4933_-17-4930dup	NM_001369381.1:c.-17-4934_-17-4930dup	NM_001369381.1:c.-17-4941_-17-4930dup
NAP1L4 transcript variant 9	NM_001369382.1:c.-17-4930=	NM_001369382.1:c.-17-4944_-17-4930del	NM_001369382.1:c.-17-4942_-17-4930del	NM_001369382.1:c.-17-4941_-17-4930del	NM_001369382.1:c.-17-4939_-17-4930del	NM_001369382.1:c.-17-4934_-17-4930del	NM_001369382.1:c.-17-4933_-17-4930del	NM_001369382.1:c.-17-4932_-17-4930del	NM_001369382.1:c.-17-4931_-17-4930del	NM_001369382.1:c.-17-4930del	NM_001369382.1:c.-17-4930dup	NM_001369382.1:c.-17-4931_-17-4930dup	NM_001369382.1:c.-17-4932_-17-4930dup	NM_001369382.1:c.-17-4933_-17-4930dup	NM_001369382.1:c.-17-4934_-17-4930dup	NM_001369382.1:c.-17-4941_-17-4930dup
NAP1L4 transcript variant 10	NM_001369383.1:c.-17-4930=	NM_001369383.1:c.-17-4944_-17-4930del	NM_001369383.1:c.-17-4942_-17-4930del	NM_001369383.1:c.-17-4941_-17-4930del	NM_001369383.1:c.-17-4939_-17-4930del	NM_001369383.1:c.-17-4934_-17-4930del	NM_001369383.1:c.-17-4933_-17-4930del	NM_001369383.1:c.-17-4932_-17-4930del	NM_001369383.1:c.-17-4931_-17-4930del	NM_001369383.1:c.-17-4930del	NM_001369383.1:c.-17-4930dup	NM_001369383.1:c.-17-4931_-17-4930dup	NM_001369383.1:c.-17-4932_-17-4930dup	NM_001369383.1:c.-17-4933_-17-4930dup	NM_001369383.1:c.-17-4934_-17-4930dup	NM_001369383.1:c.-17-4941_-17-4930dup
NAP1L4 transcript variant 11	NM_001369384.1:c.-17-4930=	NM_001369384.1:c.-17-4944_-17-4930del	NM_001369384.1:c.-17-4942_-17-4930del	NM_001369384.1:c.-17-4941_-17-4930del	NM_001369384.1:c.-17-4939_-17-4930del	NM_001369384.1:c.-17-4934_-17-4930del	NM_001369384.1:c.-17-4933_-17-4930del	NM_001369384.1:c.-17-4932_-17-4930del	NM_001369384.1:c.-17-4931_-17-4930del	NM_001369384.1:c.-17-4930del	NM_001369384.1:c.-17-4930dup	NM_001369384.1:c.-17-4931_-17-4930dup	NM_001369384.1:c.-17-4932_-17-4930dup	NM_001369384.1:c.-17-4933_-17-4930dup	NM_001369384.1:c.-17-4934_-17-4930dup	NM_001369384.1:c.-17-4941_-17-4930dup
NAP1L4 transcript variant 12	NM_001369385.1:c.-17-4930=	NM_001369385.1:c.-17-4944_-17-4930del	NM_001369385.1:c.-17-4942_-17-4930del	NM_001369385.1:c.-17-4941_-17-4930del	NM_001369385.1:c.-17-4939_-17-4930del	NM_001369385.1:c.-17-4934_-17-4930del	NM_001369385.1:c.-17-4933_-17-4930del	NM_001369385.1:c.-17-4932_-17-4930del	NM_001369385.1:c.-17-4931_-17-4930del	NM_001369385.1:c.-17-4930del	NM_001369385.1:c.-17-4930dup	NM_001369385.1:c.-17-4931_-17-4930dup	NM_001369385.1:c.-17-4932_-17-4930dup	NM_001369385.1:c.-17-4933_-17-4930dup	NM_001369385.1:c.-17-4934_-17-4930dup	NM_001369385.1:c.-17-4941_-17-4930dup
NAP1L4 transcript variant 13	NM_001369386.1:c.-18+3910=	NM_001369386.1:c.-18+3896_-18+3910del	NM_001369386.1:c.-18+3898_-18+3910del	NM_001369386.1:c.-18+3899_-18+3910del	NM_001369386.1:c.-18+3901_-18+3910del	NM_001369386.1:c.-18+3906_-18+3910del	NM_001369386.1:c.-18+3907_-18+3910del	NM_001369386.1:c.-18+3908_-18+3910del	NM_001369386.1:c.-18+3909_-18+3910del	NM_001369386.1:c.-18+3910del	NM_001369386.1:c.-18+3910dup	NM_001369386.1:c.-18+3909_-18+3910dup	NM_001369386.1:c.-18+3908_-18+3910dup	NM_001369386.1:c.-18+3907_-18+3910dup	NM_001369386.1:c.-18+3906_-18+3910dup	NM_001369386.1:c.-18+3899_-18+3910dup
NAP1L4 transcript variant 14	NM_001369388.1:c.-17-4930=	NM_001369388.1:c.-17-4944_-17-4930del	NM_001369388.1:c.-17-4942_-17-4930del	NM_001369388.1:c.-17-4941_-17-4930del	NM_001369388.1:c.-17-4939_-17-4930del	NM_001369388.1:c.-17-4934_-17-4930del	NM_001369388.1:c.-17-4933_-17-4930del	NM_001369388.1:c.-17-4932_-17-4930del	NM_001369388.1:c.-17-4931_-17-4930del	NM_001369388.1:c.-17-4930del	NM_001369388.1:c.-17-4930dup	NM_001369388.1:c.-17-4931_-17-4930dup	NM_001369388.1:c.-17-4932_-17-4930dup	NM_001369388.1:c.-17-4933_-17-4930dup	NM_001369388.1:c.-17-4934_-17-4930dup	NM_001369388.1:c.-17-4941_-17-4930dup
NAP1L4 transcript	NM_005969.3:c.-17-4930=	NM_005969.3:c.-17-4944_-17-4930del	NM_005969.3:c.-17-4942_-17-4930del	NM_005969.3:c.-17-4941_-17-4930del	NM_005969.3:c.-17-4939_-17-4930del	NM_005969.3:c.-17-4934_-17-4930del	NM_005969.3:c.-17-4933_-17-4930del	NM_005969.3:c.-17-4932_-17-4930del	NM_005969.3:c.-17-4931_-17-4930del	NM_005969.3:c.-17-4930del	NM_005969.3:c.-17-4930dup	NM_005969.3:c.-17-4931_-17-4930dup	NM_005969.3:c.-17-4932_-17-4930dup	NM_005969.3:c.-17-4933_-17-4930dup	NM_005969.3:c.-17-4934_-17-4930dup	NM_005969.3:c.-17-4941_-17-4930dup
NAP1L4 transcript variant 1	NM_005969.4:c.-17-4930=	NM_005969.4:c.-17-4944_-17-4930del	NM_005969.4:c.-17-4942_-17-4930del	NM_005969.4:c.-17-4941_-17-4930del	NM_005969.4:c.-17-4939_-17-4930del	NM_005969.4:c.-17-4934_-17-4930del	NM_005969.4:c.-17-4933_-17-4930del	NM_005969.4:c.-17-4932_-17-4930del	NM_005969.4:c.-17-4931_-17-4930del	NM_005969.4:c.-17-4930del	NM_005969.4:c.-17-4930dup	NM_005969.4:c.-17-4931_-17-4930dup	NM_005969.4:c.-17-4932_-17-4930dup	NM_005969.4:c.-17-4933_-17-4930dup	NM_005969.4:c.-17-4934_-17-4930dup	NM_005969.4:c.-17-4941_-17-4930dup
NAP1L4 transcript variant X1	XM_005252935.1:c.-17-4930=	XM_005252935.1:c.-17-4944_-17-4930del	XM_005252935.1:c.-17-4942_-17-4930del	XM_005252935.1:c.-17-4941_-17-4930del	XM_005252935.1:c.-17-4939_-17-4930del	XM_005252935.1:c.-17-4934_-17-4930del	XM_005252935.1:c.-17-4933_-17-4930del	XM_005252935.1:c.-17-4932_-17-4930del	XM_005252935.1:c.-17-4931_-17-4930del	XM_005252935.1:c.-17-4930del	XM_005252935.1:c.-17-4930dup	XM_005252935.1:c.-17-4931_-17-4930dup	XM_005252935.1:c.-17-4932_-17-4930dup	XM_005252935.1:c.-17-4933_-17-4930dup	XM_005252935.1:c.-17-4934_-17-4930dup	XM_005252935.1:c.-17-4941_-17-4930dup
NAP1L4 transcript variant X2	XM_005252936.1:c.-17-4930=	XM_005252936.1:c.-17-4944_-17-4930del	XM_005252936.1:c.-17-4942_-17-4930del	XM_005252936.1:c.-17-4941_-17-4930del	XM_005252936.1:c.-17-4939_-17-4930del	XM_005252936.1:c.-17-4934_-17-4930del	XM_005252936.1:c.-17-4933_-17-4930del	XM_005252936.1:c.-17-4932_-17-4930del	XM_005252936.1:c.-17-4931_-17-4930del	XM_005252936.1:c.-17-4930del	XM_005252936.1:c.-17-4930dup	XM_005252936.1:c.-17-4931_-17-4930dup	XM_005252936.1:c.-17-4932_-17-4930dup	XM_005252936.1:c.-17-4933_-17-4930dup	XM_005252936.1:c.-17-4934_-17-4930dup	XM_005252936.1:c.-17-4941_-17-4930dup
NAP1L4 transcript variant X3	XM_005252937.1:c.-17-4930=	XM_005252937.1:c.-17-4944_-17-4930del	XM_005252937.1:c.-17-4942_-17-4930del	XM_005252937.1:c.-17-4941_-17-4930del	XM_005252937.1:c.-17-4939_-17-4930del	XM_005252937.1:c.-17-4934_-17-4930del	XM_005252937.1:c.-17-4933_-17-4930del	XM_005252937.1:c.-17-4932_-17-4930del	XM_005252937.1:c.-17-4931_-17-4930del	XM_005252937.1:c.-17-4930del	XM_005252937.1:c.-17-4930dup	XM_005252937.1:c.-17-4931_-17-4930dup	XM_005252937.1:c.-17-4932_-17-4930dup	XM_005252937.1:c.-17-4933_-17-4930dup	XM_005252937.1:c.-17-4934_-17-4930dup	XM_005252937.1:c.-17-4941_-17-4930dup
NAP1L4 transcript variant X4	XM_005252938.1:c.-17-4930=	XM_005252938.1:c.-17-4944_-17-4930del	XM_005252938.1:c.-17-4942_-17-4930del	XM_005252938.1:c.-17-4941_-17-4930del	XM_005252938.1:c.-17-4939_-17-4930del	XM_005252938.1:c.-17-4934_-17-4930del	XM_005252938.1:c.-17-4933_-17-4930del	XM_005252938.1:c.-17-4932_-17-4930del	XM_005252938.1:c.-17-4931_-17-4930del	XM_005252938.1:c.-17-4930del	XM_005252938.1:c.-17-4930dup	XM_005252938.1:c.-17-4931_-17-4930dup	XM_005252938.1:c.-17-4932_-17-4930dup	XM_005252938.1:c.-17-4933_-17-4930dup	XM_005252938.1:c.-17-4934_-17-4930dup	XM_005252938.1:c.-17-4941_-17-4930dup

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#.

49 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss39991404	Mar 14, 2006 (126)
2	HGSV	ss81181899	Dec 15, 2007 (129)
3	HUMANGENOME_JCVI	ss95558606	Feb 06, 2009 (130)
4	PJP	ss294685784	May 09, 2011 (142)
5	SWEGEN	ss3007486409	Nov 08, 2017 (151)
6	URBANLAB	ss3649515226	Oct 12, 2018 (152)
7	EVA_DECODE	ss3691090368	Jul 13, 2019 (153)
8	EVA_DECODE	ss3691090369	Jul 13, 2019 (153)
9	EVA_DECODE	ss3691090370	Jul 13, 2019 (153)
10	EVA_DECODE	ss3691090371	Jul 13, 2019 (153)
11	EVA_DECODE	ss3691090372	Jul 13, 2019 (153)
12	PACBIO	ss3786845012	Jul 13, 2019 (153)
13	PACBIO	ss3792001212	Jul 13, 2019 (153)
14	PACBIO	ss3796883387	Jul 13, 2019 (153)
15	EVA	ss3832440930	Apr 26, 2020 (154)
16	GNOMAD	ss4229005922	Apr 26, 2021 (155)
17	GNOMAD	ss4229005923	Apr 26, 2021 (155)
18	GNOMAD	ss4229005924	Apr 26, 2021 (155)
19	GNOMAD	ss4229005925	Apr 26, 2021 (155)
20	GNOMAD	ss4229005926	Apr 26, 2021 (155)
21	GNOMAD	ss4229005927	Apr 26, 2021 (155)
22	GNOMAD	ss4229005928	Apr 26, 2021 (155)
23	GNOMAD	ss4229005929	Apr 26, 2021 (155)
24	GNOMAD	ss4229005930	Apr 26, 2021 (155)
25	GNOMAD	ss4229005931	Apr 26, 2021 (155)
26	GNOMAD	ss4229005932	Apr 26, 2021 (155)
27	GNOMAD	ss4229005933	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5200398594	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5200398595	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5200398596	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5200398597	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5200398598	Apr 26, 2021 (155)
33	1000G_HIGH_COVERAGE	ss5286177113	Oct 16, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5286177114	Oct 16, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5286177115	Oct 16, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5286177116	Oct 16, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5286177117	Oct 16, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5286177118	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5481516229	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5481516230	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5481516231	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5481516232	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5481516233	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5481516234	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5747073151	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5747073152	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5747073153	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5747073154	Oct 16, 2022 (156)
49	EVA	ss5849830543	Oct 16, 2022 (156)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369589441 (NC_000011.10:2984166::A 1523/73368) Row 369589442 (NC_000011.10:2984166::AA 49/73498) Row 369589443 (NC_000011.10:2984166::AAA 9/73580)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369589441 (NC_000011.10:2984166::A 1523/73368) Row 369589442 (NC_000011.10:2984166::AA 49/73498) Row 369589443 (NC_000011.10:2984166::AAA 9/73580)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369589441 (NC_000011.10:2984166::A 1523/73368) Row 369589442 (NC_000011.10:2984166::AA 49/73498) Row 369589443 (NC_000011.10:2984166::AAA 9/73580)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369589441 (NC_000011.10:2984166::A 1523/73368) Row 369589442 (NC_000011.10:2984166::AA 49/73498) Row 369589443 (NC_000011.10:2984166::AAA 9/73580)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369589441 (NC_000011.10:2984166::A 1523/73368) Row 369589442 (NC_000011.10:2984166::AA 49/73498) Row 369589443 (NC_000011.10:2984166::AAA 9/73580)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369589441 (NC_000011.10:2984166::A 1523/73368) Row 369589442 (NC_000011.10:2984166::AA 49/73498) Row 369589443 (NC_000011.10:2984166::AAA 9/73580)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369589441 (NC_000011.10:2984166::A 1523/73368) Row 369589442 (NC_000011.10:2984166::AA 49/73498) Row 369589443 (NC_000011.10:2984166::AAA 9/73580)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369589441 (NC_000011.10:2984166::A 1523/73368) Row 369589442 (NC_000011.10:2984166::AA 49/73498) Row 369589443 (NC_000011.10:2984166::AAA 9/73580)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369589441 (NC_000011.10:2984166::A 1523/73368) Row 369589442 (NC_000011.10:2984166::AA 49/73498) Row 369589443 (NC_000011.10:2984166::AAA 9/73580)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369589441 (NC_000011.10:2984166::A 1523/73368) Row 369589442 (NC_000011.10:2984166::AA 49/73498) Row 369589443 (NC_000011.10:2984166::AAA 9/73580)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369589441 (NC_000011.10:2984166::A 1523/73368) Row 369589442 (NC_000011.10:2984166::AA 49/73498) Row 369589443 (NC_000011.10:2984166::AAA 9/73580)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369589441 (NC_000011.10:2984166::A 1523/73368) Row 369589442 (NC_000011.10:2984166::AA 49/73498) Row 369589443 (NC_000011.10:2984166::AAA 9/73580)...	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 58367901 (NC_000011.9:3005396::A 617/16478) Row 58367902 (NC_000011.9:3005396:AAA: 7402/16478) Row 58367903 (NC_000011.9:3005396:AAAA: 332/16478)...	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 58367901 (NC_000011.9:3005396::A 617/16478) Row 58367902 (NC_000011.9:3005396:AAA: 7402/16478) Row 58367903 (NC_000011.9:3005396:AAAA: 332/16478)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 58367901 (NC_000011.9:3005396::A 617/16478) Row 58367902 (NC_000011.9:3005396:AAA: 7402/16478) Row 58367903 (NC_000011.9:3005396:AAAA: 332/16478)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 58367901 (NC_000011.9:3005396::A 617/16478) Row 58367902 (NC_000011.9:3005396:AAA: 7402/16478) Row 58367903 (NC_000011.9:3005396:AAAA: 332/16478)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 58367901 (NC_000011.9:3005396::A 617/16478) Row 58367902 (NC_000011.9:3005396:AAA: 7402/16478) Row 58367903 (NC_000011.9:3005396:AAAA: 332/16478)...	-	Apr 26, 2021 (155)
67	14KJPN Submission ignored due to conflicting rows: Row 80910255 (NC_000011.10:2984166:AAA: 12612/25820) Row 80910256 (NC_000011.10:2984166:AAAA: 582/25820) Row 80910257 (NC_000011.10:2984166:AA: 400/25820)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 80910255 (NC_000011.10:2984166:AAA: 12612/25820) Row 80910256 (NC_000011.10:2984166:AAAA: 582/25820) Row 80910257 (NC_000011.10:2984166:AA: 400/25820)...	-	Oct 16, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 80910255 (NC_000011.10:2984166:AAA: 12612/25820) Row 80910256 (NC_000011.10:2984166:AAAA: 582/25820) Row 80910257 (NC_000011.10:2984166:AA: 400/25820)...	-	Oct 16, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 80910255 (NC_000011.10:2984166:AAA: 12612/25820) Row 80910256 (NC_000011.10:2984166:AAAA: 582/25820) Row 80910257 (NC_000011.10:2984166:AA: 400/25820)...	-	Oct 16, 2022 (156)
71	ALFA	NC_000011.10 - 2984167	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).

Associated ID	History Updated (Build)
rs148053694	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
6340880027	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
6340880027	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4229005933	NC_000011.10:2984166:AAAAAAAAAAAA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
6340880027	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
6340880027	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3691090372, ss4229005932, ss5286177117, ss5481516234	NC_000011.10:2984166:AAAAA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
6340880027	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3007486409, ss5200398596	NC_000011.9:3005396:AAAA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4229005931, ss5286177118, ss5481516231, ss5747073152	NC_000011.10:2984166:AAAA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
6340880027	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3691090371	NC_000011.10:2984167:AAAA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss81181899, ss294685784	NC_000011.8:2961992:AAA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3786845012, ss3792001212, ss3796883387, ss3832440930, ss5200398595	NC_000011.9:3005396:AAA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3649515226, ss4229005930, ss5286177113, ss5481516229, ss5747073151, ss5849830543	NC_000011.10:2984166:AAA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
6340880027	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3691090370	NC_000011.10:2984168:AAA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss95558606	NT_009237.18:2945416:AAA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5200398597	NC_000011.9:3005396:AA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4229005929, ss5286177115, ss5481516232, ss5747073153	NC_000011.10:2984166:AA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
6340880027	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3691090369	NC_000011.10:2984169:AA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4229005928, ss5286177114, ss5481516233	NC_000011.10:2984166:A:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
6340880027	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3691090368	NC_000011.10:2984170:A:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss39991404	NT_009237.18:2945396:A:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5200398594	NC_000011.9:3005396::A	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4229005922, ss5286177116, ss5481516230, ss5747073154	NC_000011.10:2984166::A	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
6340880027	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5200398598	NC_000011.9:3005396::AA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4229005923	NC_000011.10:2984166::AA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
6340880027	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4229005924	NC_000011.10:2984166::AAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
6340880027	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4229005925	NC_000011.10:2984166::AAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
6340880027	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4229005926	NC_000011.10:2984166::AAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4229005927	NC_000011.10:2984166::AAAAAAAAAAAA	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3135481032	NC_000011.10:2984166:AAAAAAAAAAAAA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA
ss3135481033	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAA:	NC_000011.10:2984166:AAAAAAAAAAAAA… NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA

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

No publications for rs35188952

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

rs35188952