Name: rs752596283
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.

rs752596283

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chrX:140753769-140753793 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / d…
del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₁ / dup(T)₁₃ / dup(T)₁₄ / dup(T)₁₅ / dup(T)₁₆ / dup(T)₁₈ / dup(T)₁₉ / dup(T)₂₀ / dup(T)₂₁ / dup(T)₂₃ / dup(T)₂₄ / dup(T)₂₅ / ins(T)₂₉ / ins(T)₃₀ / ins(T)₃₁ / ins(T)₃₂ / ins(T)₃₃
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.01736 (232/13366, ALFA)
(T)₂₅=0.40 (16/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC00632 : 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	13366	TTTTTTTTTTTTTTTTTTTTTTTTT=0.95631	TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.01736, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00688, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00382, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00965, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00224, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00374	0.979412	0.012258	0.008329	32
European	Sub	10880	TTTTTTTTTTTTTTTTTTTTTTTTT=0.94632	TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.02132, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00846, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00469, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.01186, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00276, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00460	0.974414	0.015234	0.010352	32
African	Sub	1408	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	46	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1362	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	90	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	70	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	20	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	122	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	456	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	76	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	334	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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	13366	(T)₂₅=0.95631	del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.01736, dupTT=0.00688, dupTTT=0.00382, dup(T)₄=0.00965, dup(T)₅=0.00224, dup(T)₈=0.00374
Allele Frequency Aggregator	European	Sub	10880	(T)₂₅=0.94632	del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.02132, dupTT=0.00846, dupTTT=0.00469, dup(T)₄=0.01186, dup(T)₅=0.00276, dup(T)₈=0.00460
Allele Frequency Aggregator	African	Sub	1408	(T)₂₅=1.0000	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₈=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	456	(T)₂₅=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	Other	Sub	334	(T)₂₅=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	Latin American 1	Sub	122	(T)₂₅=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	Asian	Sub	90	(T)₂₅=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	South Asian	Sub	76	(T)₂₅=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₈=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.60

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 X	NC_000023.11:g.140753781_140753793del
GRCh38.p14 chr X	NC_000023.11:g.140753782_140753793del
GRCh38.p14 chr X	NC_000023.11:g.140753783_140753793del
GRCh38.p14 chr X	NC_000023.11:g.140753784_140753793del
GRCh38.p14 chr X	NC_000023.11:g.140753785_140753793del
GRCh38.p14 chr X	NC_000023.11:g.140753786_140753793del
GRCh38.p14 chr X	NC_000023.11:g.140753787_140753793del
GRCh38.p14 chr X	NC_000023.11:g.140753788_140753793del
GRCh38.p14 chr X	NC_000023.11:g.140753789_140753793del
GRCh38.p14 chr X	NC_000023.11:g.140753790_140753793del
GRCh38.p14 chr X	NC_000023.11:g.140753791_140753793del
GRCh38.p14 chr X	NC_000023.11:g.140753792_140753793del
GRCh38.p14 chr X	NC_000023.11:g.140753793del
GRCh38.p14 chr X	NC_000023.11:g.140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753792_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753791_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753790_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753789_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753788_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753787_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753786_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753785_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753783_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753781_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753780_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753779_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753778_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753776_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753775_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753774_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753773_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753771_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753770_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753769_140753793dup
GRCh38.p14 chr X	NC_000023.11:g.140753793_140753794insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr X	NC_000023.11:g.140753793_140753794insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr X	NC_000023.11:g.140753793_140753794insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr X	NC_000023.11:g.140753793_140753794insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr X	NC_000023.11:g.140753793_140753794insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr X	NC_000023.10:g.139835946_139835958del
GRCh37.p13 chr X	NC_000023.10:g.139835947_139835958del
GRCh37.p13 chr X	NC_000023.10:g.139835948_139835958del
GRCh37.p13 chr X	NC_000023.10:g.139835949_139835958del
GRCh37.p13 chr X	NC_000023.10:g.139835950_139835958del
GRCh37.p13 chr X	NC_000023.10:g.139835951_139835958del
GRCh37.p13 chr X	NC_000023.10:g.139835952_139835958del
GRCh37.p13 chr X	NC_000023.10:g.139835953_139835958del
GRCh37.p13 chr X	NC_000023.10:g.139835954_139835958del
GRCh37.p13 chr X	NC_000023.10:g.139835955_139835958del
GRCh37.p13 chr X	NC_000023.10:g.139835956_139835958del
GRCh37.p13 chr X	NC_000023.10:g.139835957_139835958del
GRCh37.p13 chr X	NC_000023.10:g.139835958del
GRCh37.p13 chr X	NC_000023.10:g.139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835957_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835956_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835955_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835954_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835953_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835952_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835951_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835950_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835948_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835946_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835945_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835944_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835943_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835941_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835940_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835939_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835938_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835936_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835935_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835934_139835958dup
GRCh37.p13 chr X	NC_000023.10:g.139835958_139835959insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr X	NC_000023.10:g.139835958_139835959insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr X	NC_000023.10:g.139835958_139835959insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr X	NC_000023.10:g.139835958_139835959insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr X	NC_000023.10:g.139835958_139835959insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: LINC00632, long intergenic non-protein coding RNA 632 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC00632 transcript variant 3	NR_104228.1:n.	N/A	Intron Variant
LINC00632 transcript variant 4	NR_173139.1:n.	N/A	Intron Variant
LINC00632 transcript variant 5	NR_173140.1:n.	N/A	Intron Variant
LINC00632 transcript variant 6	NR_173141.1:n.	N/A	Intron Variant
LINC00632 transcript variant 9	NR_173144.1:n.	N/A	Intron Variant
LINC00632 transcript variant 7	NR_173142.1:n.	N/A	Genic Upstream Transcript Variant
LINC00632 transcript variant 8	NR_173143.1:n.	N/A	Genic Upstream Transcript Variant
LINC00632 transcript variant 1	NR_028344.1:n.	N/A	Genic Downstream Transcript Variant
LINC00632 transcript variant 2	NR_028345.2:n.	N/A	Genic Downstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₅=	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₁	dup(T)₁₃	dup(T)₁₄	dup(T)₁₅	dup(T)₁₆	dup(T)₁₈	dup(T)₁₉	dup(T)₂₀	dup(T)₂₁	dup(T)₂₃	dup(T)₂₄	dup(T)₂₅	ins(T)₂₉	ins(T)₃₀	ins(T)₃₁	ins(T)₃₂	ins(T)₃₃
GRCh38.p14 chr X	NC_000023.11:g.140753769_140753793=	NC_000023.11:g.140753781_140753793del	NC_000023.11:g.140753782_140753793del	NC_000023.11:g.140753783_140753793del	NC_000023.11:g.140753784_140753793del	NC_000023.11:g.140753785_140753793del	NC_000023.11:g.140753786_140753793del	NC_000023.11:g.140753787_140753793del	NC_000023.11:g.140753788_140753793del	NC_000023.11:g.140753789_140753793del	NC_000023.11:g.140753790_140753793del	NC_000023.11:g.140753791_140753793del	NC_000023.11:g.140753792_140753793del	NC_000023.11:g.140753793del	NC_000023.11:g.140753793dup	NC_000023.11:g.140753792_140753793dup	NC_000023.11:g.140753791_140753793dup	NC_000023.11:g.140753790_140753793dup	NC_000023.11:g.140753789_140753793dup	NC_000023.11:g.140753788_140753793dup	NC_000023.11:g.140753787_140753793dup	NC_000023.11:g.140753786_140753793dup	NC_000023.11:g.140753785_140753793dup	NC_000023.11:g.140753783_140753793dup	NC_000023.11:g.140753781_140753793dup	NC_000023.11:g.140753780_140753793dup	NC_000023.11:g.140753779_140753793dup	NC_000023.11:g.140753778_140753793dup	NC_000023.11:g.140753776_140753793dup	NC_000023.11:g.140753775_140753793dup	NC_000023.11:g.140753774_140753793dup	NC_000023.11:g.140753773_140753793dup	NC_000023.11:g.140753771_140753793dup	NC_000023.11:g.140753770_140753793dup	NC_000023.11:g.140753769_140753793dup	NC_000023.11:g.140753793_140753794insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:g.140753793_140753794insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:g.140753793_140753794insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:g.140753793_140753794insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:g.140753793_140753794insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr X	NC_000023.10:g.139835934_139835958=	NC_000023.10:g.139835946_139835958del	NC_000023.10:g.139835947_139835958del	NC_000023.10:g.139835948_139835958del	NC_000023.10:g.139835949_139835958del	NC_000023.10:g.139835950_139835958del	NC_000023.10:g.139835951_139835958del	NC_000023.10:g.139835952_139835958del	NC_000023.10:g.139835953_139835958del	NC_000023.10:g.139835954_139835958del	NC_000023.10:g.139835955_139835958del	NC_000023.10:g.139835956_139835958del	NC_000023.10:g.139835957_139835958del	NC_000023.10:g.139835958del	NC_000023.10:g.139835958dup	NC_000023.10:g.139835957_139835958dup	NC_000023.10:g.139835956_139835958dup	NC_000023.10:g.139835955_139835958dup	NC_000023.10:g.139835954_139835958dup	NC_000023.10:g.139835953_139835958dup	NC_000023.10:g.139835952_139835958dup	NC_000023.10:g.139835951_139835958dup	NC_000023.10:g.139835950_139835958dup	NC_000023.10:g.139835948_139835958dup	NC_000023.10:g.139835946_139835958dup	NC_000023.10:g.139835945_139835958dup	NC_000023.10:g.139835944_139835958dup	NC_000023.10:g.139835943_139835958dup	NC_000023.10:g.139835941_139835958dup	NC_000023.10:g.139835940_139835958dup	NC_000023.10:g.139835939_139835958dup	NC_000023.10:g.139835938_139835958dup	NC_000023.10:g.139835936_139835958dup	NC_000023.10:g.139835935_139835958dup	NC_000023.10:g.139835934_139835958dup	NC_000023.10:g.139835958_139835959insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.10:g.139835958_139835959insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.10:g.139835958_139835959insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.10:g.139835958_139835959insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.10:g.139835958_139835959insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

62 SubSNP, 48 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PJP	ss295465997	Oct 12, 2018 (152)
2	EVA_GENOME_DK	ss1577650208	Apr 01, 2015 (144)
3	SWEGEN	ss3020705355	Nov 08, 2017 (151)
4	SWEGEN	ss3020705356	Nov 08, 2017 (151)
5	SWEGEN	ss3020705357	Nov 08, 2017 (151)
6	SWEGEN	ss3020705358	Nov 08, 2017 (151)
7	SWEGEN	ss3020705359	Nov 08, 2017 (151)
8	SWEGEN	ss3020705360	Nov 08, 2017 (151)
9	EVA	ss3836335018	Apr 27, 2020 (154)
10	GNOMAD	ss4379539458	Apr 26, 2021 (155)
11	GNOMAD	ss4379539459	Apr 26, 2021 (155)
12	GNOMAD	ss4379539460	Apr 26, 2021 (155)
13	GNOMAD	ss4379539461	Apr 26, 2021 (155)
14	GNOMAD	ss4379539462	Apr 26, 2021 (155)
15	GNOMAD	ss4379539463	Apr 26, 2021 (155)
16	GNOMAD	ss4379539464	Apr 26, 2021 (155)
17	GNOMAD	ss4379539465	Apr 26, 2021 (155)
18	GNOMAD	ss4379539466	Apr 26, 2021 (155)
19	GNOMAD	ss4379539467	Apr 26, 2021 (155)
20	GNOMAD	ss4379539468	Apr 26, 2021 (155)
21	GNOMAD	ss4379539469	Apr 26, 2021 (155)
22	GNOMAD	ss4379539470	Apr 26, 2021 (155)
23	GNOMAD	ss4379539471	Apr 26, 2021 (155)
24	GNOMAD	ss4379539472	Apr 26, 2021 (155)
25	GNOMAD	ss4379539473	Apr 26, 2021 (155)
26	GNOMAD	ss4379539474	Apr 26, 2021 (155)
27	GNOMAD	ss4379539475	Apr 26, 2021 (155)
28	GNOMAD	ss4379539476	Apr 26, 2021 (155)
29	GNOMAD	ss4379539478	Apr 26, 2021 (155)
30	GNOMAD	ss4379539479	Apr 26, 2021 (155)
31	GNOMAD	ss4379539480	Apr 26, 2021 (155)
32	GNOMAD	ss4379539481	Apr 26, 2021 (155)
33	GNOMAD	ss4379539482	Apr 26, 2021 (155)
34	GNOMAD	ss4379539483	Apr 26, 2021 (155)
35	GNOMAD	ss4379539484	Apr 26, 2021 (155)
36	GNOMAD	ss4379539485	Apr 26, 2021 (155)
37	GNOMAD	ss4379539486	Apr 26, 2021 (155)
38	GNOMAD	ss4379539487	Apr 26, 2021 (155)
39	GNOMAD	ss4379539488	Apr 26, 2021 (155)
40	GNOMAD	ss4379539489	Apr 26, 2021 (155)
41	TOPMED	ss5139200302	Apr 26, 2021 (155)
42	TOPMED	ss5139200303	Apr 26, 2021 (155)
43	TOPMED	ss5139200304	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5236498302	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5236498303	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5236498304	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5236498305	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5236498306	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5236498307	Apr 26, 2021 (155)
50	1000G_HIGH_COVERAGE	ss5314109707	Oct 17, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5314109708	Oct 17, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5314109709	Oct 17, 2022 (156)
53	HUGCELL_USP	ss5505493230	Oct 17, 2022 (156)
54	HUGCELL_USP	ss5505493231	Oct 17, 2022 (156)
55	HUGCELL_USP	ss5505493232	Oct 17, 2022 (156)
56	HUGCELL_USP	ss5505493233	Oct 17, 2022 (156)
57	TOMMO_GENOMICS	ss5798940822	Oct 17, 2022 (156)
58	TOMMO_GENOMICS	ss5798940823	Oct 17, 2022 (156)
59	TOMMO_GENOMICS	ss5798940824	Oct 17, 2022 (156)
60	TOMMO_GENOMICS	ss5798940825	Oct 17, 2022 (156)
61	TOMMO_GENOMICS	ss5798940826	Oct 17, 2022 (156)
62	TOMMO_GENOMICS	ss5798940827	Oct 17, 2022 (156)
63	The Danish reference pan genome	NC_000023.10 - 139835934	Apr 27, 2020 (154)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 592730317 (NC_000023.11:140753768::TTTTTTT 175/47518) Row 592730318 (NC_000023.11:140753768::TTTTTTTTT 208/47533) Row 592730319 (NC_000023.11:140753768::TTTTTTTTTTT 37/47536)...	-	Apr 26, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 94467609 (NC_000023.10:139835933::T 752/12655) Row 94467610 (NC_000023.10:139835933:T: 43/12655) Row 94467611 (NC_000023.10:139835933::TTTT 52/12655)...	-	Apr 26, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 94467609 (NC_000023.10:139835933::T 752/12655) Row 94467610 (NC_000023.10:139835933:T: 43/12655) Row 94467611 (NC_000023.10:139835933::TTTT 52/12655)...	-	Apr 26, 2021 (155)
97	8.3KJPN Submission ignored due to conflicting rows: Row 94467609 (NC_000023.10:139835933::T 752/12655) Row 94467610 (NC_000023.10:139835933:T: 43/12655) Row 94467611 (NC_000023.10:139835933::TTTT 52/12655)...	-	Apr 26, 2021 (155)
98	8.3KJPN Submission ignored due to conflicting rows: Row 94467609 (NC_000023.10:139835933::T 752/12655) Row 94467610 (NC_000023.10:139835933:T: 43/12655) Row 94467611 (NC_000023.10:139835933::TTTT 52/12655)...	-	Apr 26, 2021 (155)
99	8.3KJPN Submission ignored due to conflicting rows: Row 94467609 (NC_000023.10:139835933::T 752/12655) Row 94467610 (NC_000023.10:139835933:T: 43/12655) Row 94467611 (NC_000023.10:139835933::TTTT 52/12655)...	-	Apr 26, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 94467609 (NC_000023.10:139835933::T 752/12655) Row 94467610 (NC_000023.10:139835933:T: 43/12655) Row 94467611 (NC_000023.10:139835933::TTTT 52/12655)...	-	Apr 26, 2021 (155)
101	14KJPN Submission ignored due to conflicting rows: Row 132777926 (NC_000023.11:140753768::T 1152/19288) Row 132777927 (NC_000023.11:140753768:T: 66/19288) Row 132777928 (NC_000023.11:140753768::TTTT 53/19288)...	-	Oct 17, 2022 (156)
102	14KJPN Submission ignored due to conflicting rows: Row 132777926 (NC_000023.11:140753768::T 1152/19288) Row 132777927 (NC_000023.11:140753768:T: 66/19288) Row 132777928 (NC_000023.11:140753768::TTTT 53/19288)...	-	Oct 17, 2022 (156)
103	14KJPN Submission ignored due to conflicting rows: Row 132777926 (NC_000023.11:140753768::T 1152/19288) Row 132777927 (NC_000023.11:140753768:T: 66/19288) Row 132777928 (NC_000023.11:140753768::TTTT 53/19288)...	-	Oct 17, 2022 (156)
104	14KJPN Submission ignored due to conflicting rows: Row 132777926 (NC_000023.11:140753768::T 1152/19288) Row 132777927 (NC_000023.11:140753768:T: 66/19288) Row 132777928 (NC_000023.11:140753768::TTTT 53/19288)...	-	Oct 17, 2022 (156)
105	14KJPN Submission ignored due to conflicting rows: Row 132777926 (NC_000023.11:140753768::T 1152/19288) Row 132777927 (NC_000023.11:140753768:T: 66/19288) Row 132777928 (NC_000023.11:140753768::TTTT 53/19288)...	-	Oct 17, 2022 (156)
106	14KJPN Submission ignored due to conflicting rows: Row 132777926 (NC_000023.11:140753768::T 1152/19288) Row 132777927 (NC_000023.11:140753768:T: 66/19288) Row 132777928 (NC_000023.11:140753768::TTTT 53/19288)...	-	Oct 17, 2022 (156)
107	TopMed Submission ignored due to conflicting rows: Row 702806659 (NC_000023.11:140753768:TTTTTTTTTTT: 7/264690) Row 702806660 (NC_000023.11:140753768:TTTTTTTTTTTT: 5/264690) Row 702806661 (NC_000023.11:140753768:TTTTTTTTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
108	TopMed Submission ignored due to conflicting rows: Row 702806659 (NC_000023.11:140753768:TTTTTTTTTTT: 7/264690) Row 702806660 (NC_000023.11:140753768:TTTTTTTTTTTT: 5/264690) Row 702806661 (NC_000023.11:140753768:TTTTTTTTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
109	TopMed Submission ignored due to conflicting rows: Row 702806659 (NC_000023.11:140753768:TTTTTTTTTTT: 7/264690) Row 702806660 (NC_000023.11:140753768:TTTTTTTTTTTT: 5/264690) Row 702806661 (NC_000023.11:140753768:TTTTTTTTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
110	ALFA	NC_000023.11 - 140753769	Apr 26, 2021 (155)

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

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5139200304	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTT:	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4379539489, ss5139200303	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTT:	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4379539488, ss5139200302	NC_000023.11:140753768:TTTTTTTTTTT:	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4379539487	NC_000023.11:140753768:TTTTTTTTTT:	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4379539486, ss5314109709	NC_000023.11:140753768:TTTTTTTTT:	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4379539485	NC_000023.11:140753768:TTTTTTTT:	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4379539484	NC_000023.11:140753768:TTTTTTT:	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4379539483	NC_000023.11:140753768:TTTTTT:	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4379539482	NC_000023.11:140753768:TTTTT:	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4379539481	NC_000023.11:140753768:TTTT:	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539480	NC_000023.11:140753768:TTT:	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539479	NC_000023.11:140753768:TT:	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5236498303	NC_000023.10:139835933:T:	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539478, ss5314109708, ss5505493230, ss5798940823	NC_000023.11:140753768:T:	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss295465997	NC_000023.9:139663600::T	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1350609, ss1577650208, ss3020705355, ss5236498302	NC_000023.10:139835933::T	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5505493231, ss5798940822	NC_000023.11:140753768::T	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3020705356, ss5236498305	NC_000023.10:139835933::TT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5505493232, ss5798940826	NC_000023.11:140753768::TT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3020705357, ss5236498307	NC_000023.10:139835933::TTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5314109707, ss5798940825	NC_000023.11:140753768::TTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3020705359, ss5236498304	NC_000023.10:139835933::TTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5798940824	NC_000023.11:140753768::TTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3020705360	NC_000023.10:139835933::TTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5505493233, ss5798940827	NC_000023.11:140753768::TTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3020705358, ss3836335018	NC_000023.10:139835933::TTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539458	NC_000023.11:140753768::TTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5236498306	NC_000023.10:139835933::TTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1502839844	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539459	NC_000023.11:140753768::TTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539460	NC_000023.11:140753768::TTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539461	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539462	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539463	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539464	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539465	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539466	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539467	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539468	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539469	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539470	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539471	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539472	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539473	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539474	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539475	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4379539476	NC_000023.11:140753768::TTTTTTTTTT… NC_000023.11:140753768::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000023.11:140753768:TTTTTTTTTTT… NC_000023.11:140753768:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs752596283

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

rs752596283