Name: rs148405512
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.

rs148405512

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:138389783-138389813 (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(GT)₇ / del(GT)₆ / del(GT)₅ / d…
del(GT)₇ / del(GT)₆ / del(GT)₅ / del(GT)₄ / del(GT)₃ / delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃ / dup(GT)₄ / dup(GT)₅ / dup(GT)₆ / dup(GT)₇ / dup(GT)₈ / dup(GT)₉ / dup(GT)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: dupGT=0.2408 (1319/5477, ALFA)
dupGT=0.1869 (936/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: KDM3B : 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	5477	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.5720	TGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.2408, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0137, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.1596, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0113, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0026, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.701475	0.126844	0.171681	32
European	Sub	4698	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.5015	TGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.2808, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0160, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.1856, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0132, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0030, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.612854	0.164499	0.222647	32
African	Sub	604	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	26	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
African American	Sub	578	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	4	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	TGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	TGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	TGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	20	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	56	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	12	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other	Sub	83	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.98	TGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.02, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A

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

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	5477	(TG)₁₅T=0.5720	del(GT)₇=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0000, delGT=0.0000, dupGT=0.2408, dupGTGT=0.0137, dup(GT)₃=0.1596, dup(GT)₄=0.0113, dup(GT)₅=0.0026, dup(GT)₆=0.0000, dup(GT)₇=0.0000, dup(GT)₈=0.0000, dup(GT)₉=0.0000, dup(GT)₁₀=0.0000
Allele Frequency Aggregator	European	Sub	4698	(TG)₁₅T=0.5015	del(GT)₇=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0000, delGT=0.0000, dupGT=0.2808, dupGTGT=0.0160, dup(GT)₃=0.1856, dup(GT)₄=0.0132, dup(GT)₅=0.0030, dup(GT)₆=0.0000, dup(GT)₇=0.0000, dup(GT)₈=0.0000, dup(GT)₉=0.0000, dup(GT)₁₀=0.0000
Allele Frequency Aggregator	African	Sub	604	(TG)₁₅T=1.000	del(GT)₇=0.000, del(GT)₆=0.000, del(GT)₅=0.000, del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, dup(GT)₉=0.000, dup(GT)₁₀=0.000
Allele Frequency Aggregator	Other	Sub	83	(TG)₁₅T=0.98	del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.02, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00, dup(GT)₁₀=0.00
Allele Frequency Aggregator	Latin American 2	Sub	56	(TG)₁₅T=1.00	del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00, dup(GT)₁₀=0.00
Allele Frequency Aggregator	Latin American 1	Sub	20	(TG)₁₅T=1.00	del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00, dup(GT)₁₀=0.00
Allele Frequency Aggregator	South Asian	Sub	12	(TG)₁₅T=1.00	del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00, dup(GT)₁₀=0.00
Allele Frequency Aggregator	Asian	Sub	4	(TG)₁₅T=1.0	del(GT)₇=0.0, del(GT)₆=0.0, del(GT)₅=0.0, del(GT)₄=0.0, del(GT)₃=0.0, delGTGT=0.0, delGT=0.0, dupGT=0.0, dupGTGT=0.0, dup(GT)₃=0.0, dup(GT)₄=0.0, dup(GT)₅=0.0, dup(GT)₆=0.0, dup(GT)₇=0.0, dup(GT)₈=0.0, dup(GT)₉=0.0, dup(GT)₁₀=0.0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupGT=0.1869
1000Genomes	African	Sub	1322	- No frequency provided	dupGT=0.1014
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupGT=0.1548
1000Genomes	Europe	Sub	1006	- No frequency provided	dupGT=0.2247
1000Genomes	South Asian	Sub	978	- No frequency provided	dupGT=0.253
1000Genomes	American	Sub	694	- No frequency provided	dupGT=0.249

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 5	NC_000005.10:g.138389784GT[8]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[9]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[10]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[11]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[12]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[13]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[14]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[16]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[17]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[18]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[19]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[20]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[21]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[22]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[23]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[24]
GRCh38.p14 chr 5	NC_000005.10:g.138389784GT[25]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[8]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[9]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[10]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[11]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[12]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[13]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[14]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[16]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[17]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[18]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[19]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[20]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[21]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[22]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[23]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[24]
GRCh37.p13 chr 5	NC_000005.9:g.137725473GT[25]

Gene: KDM3B, lysine demethylase 3B (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
KDM3B transcript	NM_016604.4:c.1381-1230TG… NM_016604.4:c.1381-1230TG[8]	N/A	Intron Variant
KDM3B transcript variant X4	XM_005272018.5:c.781-1230… XM_005272018.5:c.781-1230TG[8]	N/A	Intron Variant
KDM3B transcript variant X1	XM_011543488.3:c.1249-123… XM_011543488.3:c.1249-1230TG[8]	N/A	Intron Variant
KDM3B transcript variant X2	XM_011543489.3:c.1237-123… XM_011543489.3:c.1237-1230TG[8]	N/A	Intron Variant
KDM3B transcript variant X5	XM_017009584.2:c.634-1230… XM_017009584.2:c.634-1230TG[8]	N/A	Intron Variant
KDM3B transcript variant X3	XM_047417313.1:c.1237-123… XM_047417313.1:c.1237-1230TG[8]	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	(TG)₁₅T=	del(GT)₇	del(GT)₆	del(GT)₅	del(GT)₄	del(GT)₃	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃	dup(GT)₄	dup(GT)₅	dup(GT)₆	dup(GT)₇	dup(GT)₈	dup(GT)₉	dup(GT)₁₀
GRCh38.p14 chr 5	NC_000005.10:g.138389783_138389813=	NC_000005.10:g.138389784GT[8]	NC_000005.10:g.138389784GT[9]	NC_000005.10:g.138389784GT[10]	NC_000005.10:g.138389784GT[11]	NC_000005.10:g.138389784GT[12]	NC_000005.10:g.138389784GT[13]	NC_000005.10:g.138389784GT[14]	NC_000005.10:g.138389784GT[16]	NC_000005.10:g.138389784GT[17]	NC_000005.10:g.138389784GT[18]	NC_000005.10:g.138389784GT[19]	NC_000005.10:g.138389784GT[20]	NC_000005.10:g.138389784GT[21]	NC_000005.10:g.138389784GT[22]	NC_000005.10:g.138389784GT[23]	NC_000005.10:g.138389784GT[24]	NC_000005.10:g.138389784GT[25]
GRCh37.p13 chr 5	NC_000005.9:g.137725472_137725502=	NC_000005.9:g.137725473GT[8]	NC_000005.9:g.137725473GT[9]	NC_000005.9:g.137725473GT[10]	NC_000005.9:g.137725473GT[11]	NC_000005.9:g.137725473GT[12]	NC_000005.9:g.137725473GT[13]	NC_000005.9:g.137725473GT[14]	NC_000005.9:g.137725473GT[16]	NC_000005.9:g.137725473GT[17]	NC_000005.9:g.137725473GT[18]	NC_000005.9:g.137725473GT[19]	NC_000005.9:g.137725473GT[20]	NC_000005.9:g.137725473GT[21]	NC_000005.9:g.137725473GT[22]	NC_000005.9:g.137725473GT[23]	NC_000005.9:g.137725473GT[24]	NC_000005.9:g.137725473GT[25]
KDM3B transcript	NM_016604.3:c.1381-1230=	NM_016604.3:c.1381-1230TG[8]	NM_016604.3:c.1381-1230TG[9]	NM_016604.3:c.1381-1230TG[10]	NM_016604.3:c.1381-1230TG[11]	NM_016604.3:c.1381-1230TG[12]	NM_016604.3:c.1381-1230TG[13]	NM_016604.3:c.1381-1230TG[14]	NM_016604.3:c.1381-1230TG[16]	NM_016604.3:c.1381-1230TG[17]	NM_016604.3:c.1381-1230TG[18]	NM_016604.3:c.1381-1230TG[19]	NM_016604.3:c.1381-1230TG[20]	NM_016604.3:c.1381-1230TG[21]	NM_016604.3:c.1381-1230TG[22]	NM_016604.3:c.1381-1230TG[23]	NM_016604.3:c.1381-1230TG[24]	NM_016604.3:c.1381-1230TG[25]
KDM3B transcript	NM_016604.4:c.1381-1230=	NM_016604.4:c.1381-1230TG[8]	NM_016604.4:c.1381-1230TG[9]	NM_016604.4:c.1381-1230TG[10]	NM_016604.4:c.1381-1230TG[11]	NM_016604.4:c.1381-1230TG[12]	NM_016604.4:c.1381-1230TG[13]	NM_016604.4:c.1381-1230TG[14]	NM_016604.4:c.1381-1230TG[16]	NM_016604.4:c.1381-1230TG[17]	NM_016604.4:c.1381-1230TG[18]	NM_016604.4:c.1381-1230TG[19]	NM_016604.4:c.1381-1230TG[20]	NM_016604.4:c.1381-1230TG[21]	NM_016604.4:c.1381-1230TG[22]	NM_016604.4:c.1381-1230TG[23]	NM_016604.4:c.1381-1230TG[24]	NM_016604.4:c.1381-1230TG[25]
KDM3B transcript variant X1	XM_005272018.1:c.781-1230=	XM_005272018.1:c.781-1230TG[8]	XM_005272018.1:c.781-1230TG[9]	XM_005272018.1:c.781-1230TG[10]	XM_005272018.1:c.781-1230TG[11]	XM_005272018.1:c.781-1230TG[12]	XM_005272018.1:c.781-1230TG[13]	XM_005272018.1:c.781-1230TG[14]	XM_005272018.1:c.781-1230TG[16]	XM_005272018.1:c.781-1230TG[17]	XM_005272018.1:c.781-1230TG[18]	XM_005272018.1:c.781-1230TG[19]	XM_005272018.1:c.781-1230TG[20]	XM_005272018.1:c.781-1230TG[21]	XM_005272018.1:c.781-1230TG[22]	XM_005272018.1:c.781-1230TG[23]	XM_005272018.1:c.781-1230TG[24]	XM_005272018.1:c.781-1230TG[25]
KDM3B transcript variant X4	XM_005272018.5:c.781-1230=	XM_005272018.5:c.781-1230TG[8]	XM_005272018.5:c.781-1230TG[9]	XM_005272018.5:c.781-1230TG[10]	XM_005272018.5:c.781-1230TG[11]	XM_005272018.5:c.781-1230TG[12]	XM_005272018.5:c.781-1230TG[13]	XM_005272018.5:c.781-1230TG[14]	XM_005272018.5:c.781-1230TG[16]	XM_005272018.5:c.781-1230TG[17]	XM_005272018.5:c.781-1230TG[18]	XM_005272018.5:c.781-1230TG[19]	XM_005272018.5:c.781-1230TG[20]	XM_005272018.5:c.781-1230TG[21]	XM_005272018.5:c.781-1230TG[22]	XM_005272018.5:c.781-1230TG[23]	XM_005272018.5:c.781-1230TG[24]	XM_005272018.5:c.781-1230TG[25]
KDM3B transcript variant X2	XM_005272019.1:c.349-1230=	XM_005272019.1:c.349-1230TG[8]	XM_005272019.1:c.349-1230TG[9]	XM_005272019.1:c.349-1230TG[10]	XM_005272019.1:c.349-1230TG[11]	XM_005272019.1:c.349-1230TG[12]	XM_005272019.1:c.349-1230TG[13]	XM_005272019.1:c.349-1230TG[14]	XM_005272019.1:c.349-1230TG[16]	XM_005272019.1:c.349-1230TG[17]	XM_005272019.1:c.349-1230TG[18]	XM_005272019.1:c.349-1230TG[19]	XM_005272019.1:c.349-1230TG[20]	XM_005272019.1:c.349-1230TG[21]	XM_005272019.1:c.349-1230TG[22]	XM_005272019.1:c.349-1230TG[23]	XM_005272019.1:c.349-1230TG[24]	XM_005272019.1:c.349-1230TG[25]
KDM3B transcript variant X1	XM_011543488.3:c.1249-1230=	XM_011543488.3:c.1249-1230TG[8]	XM_011543488.3:c.1249-1230TG[9]	XM_011543488.3:c.1249-1230TG[10]	XM_011543488.3:c.1249-1230TG[11]	XM_011543488.3:c.1249-1230TG[12]	XM_011543488.3:c.1249-1230TG[13]	XM_011543488.3:c.1249-1230TG[14]	XM_011543488.3:c.1249-1230TG[16]	XM_011543488.3:c.1249-1230TG[17]	XM_011543488.3:c.1249-1230TG[18]	XM_011543488.3:c.1249-1230TG[19]	XM_011543488.3:c.1249-1230TG[20]	XM_011543488.3:c.1249-1230TG[21]	XM_011543488.3:c.1249-1230TG[22]	XM_011543488.3:c.1249-1230TG[23]	XM_011543488.3:c.1249-1230TG[24]	XM_011543488.3:c.1249-1230TG[25]
KDM3B transcript variant X2	XM_011543489.3:c.1237-1230=	XM_011543489.3:c.1237-1230TG[8]	XM_011543489.3:c.1237-1230TG[9]	XM_011543489.3:c.1237-1230TG[10]	XM_011543489.3:c.1237-1230TG[11]	XM_011543489.3:c.1237-1230TG[12]	XM_011543489.3:c.1237-1230TG[13]	XM_011543489.3:c.1237-1230TG[14]	XM_011543489.3:c.1237-1230TG[16]	XM_011543489.3:c.1237-1230TG[17]	XM_011543489.3:c.1237-1230TG[18]	XM_011543489.3:c.1237-1230TG[19]	XM_011543489.3:c.1237-1230TG[20]	XM_011543489.3:c.1237-1230TG[21]	XM_011543489.3:c.1237-1230TG[22]	XM_011543489.3:c.1237-1230TG[23]	XM_011543489.3:c.1237-1230TG[24]	XM_011543489.3:c.1237-1230TG[25]
KDM3B transcript variant X5	XM_017009584.2:c.634-1230=	XM_017009584.2:c.634-1230TG[8]	XM_017009584.2:c.634-1230TG[9]	XM_017009584.2:c.634-1230TG[10]	XM_017009584.2:c.634-1230TG[11]	XM_017009584.2:c.634-1230TG[12]	XM_017009584.2:c.634-1230TG[13]	XM_017009584.2:c.634-1230TG[14]	XM_017009584.2:c.634-1230TG[16]	XM_017009584.2:c.634-1230TG[17]	XM_017009584.2:c.634-1230TG[18]	XM_017009584.2:c.634-1230TG[19]	XM_017009584.2:c.634-1230TG[20]	XM_017009584.2:c.634-1230TG[21]	XM_017009584.2:c.634-1230TG[22]	XM_017009584.2:c.634-1230TG[23]	XM_017009584.2:c.634-1230TG[24]	XM_017009584.2:c.634-1230TG[25]
KDM3B transcript variant X3	XM_047417313.1:c.1237-1230=	XM_047417313.1:c.1237-1230TG[8]	XM_047417313.1:c.1237-1230TG[9]	XM_047417313.1:c.1237-1230TG[10]	XM_047417313.1:c.1237-1230TG[11]	XM_047417313.1:c.1237-1230TG[12]	XM_047417313.1:c.1237-1230TG[13]	XM_047417313.1:c.1237-1230TG[14]	XM_047417313.1:c.1237-1230TG[16]	XM_047417313.1:c.1237-1230TG[17]	XM_047417313.1:c.1237-1230TG[18]	XM_047417313.1:c.1237-1230TG[19]	XM_047417313.1:c.1237-1230TG[20]	XM_047417313.1:c.1237-1230TG[21]	XM_047417313.1:c.1237-1230TG[22]	XM_047417313.1:c.1237-1230TG[23]	XM_047417313.1:c.1237-1230TG[24]	XM_047417313.1:c.1237-1230TG[25]

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#.

61 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4272414	Oct 12, 2018 (152)
2	HGSV	ss80766413	Oct 12, 2018 (152)
3	HUMANGENOME_JCVI	ss95976141	Oct 12, 2018 (152)
4	GMI	ss288661116	Oct 12, 2018 (152)
5	1000GENOMES	ss326724620	May 09, 2011 (134)
6	1000GENOMES	ss326997129	May 09, 2011 (134)
7	LUNTER	ss551718859	Apr 25, 2013 (138)
8	LUNTER	ss553218886	Apr 25, 2013 (138)
9	1000GENOMES	ss1374570449	Aug 21, 2014 (142)
10	SWEGEN	ss2997868824	Nov 08, 2017 (151)
11	SWEGEN	ss2997868825	Nov 08, 2017 (151)
12	SWEGEN	ss2997868827	Nov 08, 2017 (151)
13	SWEGEN	ss2997868828	Nov 08, 2017 (151)
14	MCHAISSO	ss3064176785	Nov 08, 2017 (151)
15	MCHAISSO	ss3065053004	Nov 08, 2017 (151)
16	MCHAISSO	ss3065053005	Nov 08, 2017 (151)
17	MCHAISSO	ss3066044726	Nov 08, 2017 (151)
18	PACBIO	ss3785262999	Jul 13, 2019 (153)
19	PACBIO	ss3790644465	Jul 13, 2019 (153)
20	PACBIO	ss3795521421	Jul 13, 2019 (153)
21	KHV_HUMAN_GENOMES	ss3807292742	Jul 13, 2019 (153)
22	KHV_HUMAN_GENOMES	ss3807292743	Jul 13, 2019 (153)
23	EVA	ss3838238679	Apr 26, 2020 (154)
24	KOGIC	ss3957736244	Apr 26, 2020 (154)
25	KOGIC	ss3957736245	Apr 26, 2020 (154)
26	KOGIC	ss3957736246	Apr 26, 2020 (154)
27	KOGIC	ss3957736248	Apr 26, 2020 (154)
28	GNOMAD	ss4130159118	Apr 26, 2021 (155)
29	GNOMAD	ss4130159119	Apr 26, 2021 (155)
30	GNOMAD	ss4130159120	Apr 26, 2021 (155)
31	GNOMAD	ss4130159121	Apr 26, 2021 (155)
32	GNOMAD	ss4130159122	Apr 26, 2021 (155)
33	GNOMAD	ss4130159123	Apr 26, 2021 (155)
34	GNOMAD	ss4130159124	Apr 26, 2021 (155)
35	GNOMAD	ss4130159125	Apr 26, 2021 (155)
36	GNOMAD	ss4130159126	Apr 26, 2021 (155)
37	GNOMAD	ss4130159127	Apr 26, 2021 (155)
38	GNOMAD	ss4130159129	Apr 26, 2021 (155)
39	GNOMAD	ss4130159130	Apr 26, 2021 (155)
40	GNOMAD	ss4130159131	Apr 26, 2021 (155)
41	GNOMAD	ss4130159132	Apr 26, 2021 (155)
42	GNOMAD	ss4130159133	Apr 26, 2021 (155)
43	GNOMAD	ss4130159134	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5174355403	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5174355404	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5174355405	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5174355406	Apr 26, 2021 (155)
48	1000G_HIGH_COVERAGE	ss5266011194	Oct 13, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5266011195	Oct 13, 2022 (156)
50	HUGCELL_USP	ss5463960962	Oct 13, 2022 (156)
51	HUGCELL_USP	ss5463960963	Oct 13, 2022 (156)
52	HUGCELL_USP	ss5463960964	Oct 13, 2022 (156)
53	HUGCELL_USP	ss5463960965	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5463960966	Oct 13, 2022 (156)
55	TOMMO_GENOMICS	ss5711495562	Oct 13, 2022 (156)
56	TOMMO_GENOMICS	ss5711495563	Oct 13, 2022 (156)
57	TOMMO_GENOMICS	ss5711495564	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5711495565	Oct 13, 2022 (156)
59	EVA	ss5835707125	Oct 13, 2022 (156)
60	EVA	ss5835707126	Oct 13, 2022 (156)
61	EVA	ss5835707127	Oct 13, 2022 (156)
62	1000Genomes	NC_000005.9 - 137725472	Oct 12, 2018 (152)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 205776990 (NC_000005.10:138389782::TG 39521/131998) Row 205776991 (NC_000005.10:138389782::TGTG 2691/132192) Row 205776992 (NC_000005.10:138389782::TGTGTG 28333/131992)...	-	Apr 26, 2021 (155)
79	Korean Genome Project Submission ignored due to conflicting rows: Row 14114245 (NC_000005.10:138389782::TG 444/1832) Row 14114246 (NC_000005.10:138389782::TGTG 124/1832) Row 14114247 (NC_000005.10:138389782::TGTGTG 775/1832)...	-	Apr 26, 2020 (154)
80	Korean Genome Project Submission ignored due to conflicting rows: Row 14114245 (NC_000005.10:138389782::TG 444/1832) Row 14114246 (NC_000005.10:138389782::TGTG 124/1832) Row 14114247 (NC_000005.10:138389782::TGTGTG 775/1832)...	-	Apr 26, 2020 (154)
81	Korean Genome Project Submission ignored due to conflicting rows: Row 14114245 (NC_000005.10:138389782::TG 444/1832) Row 14114246 (NC_000005.10:138389782::TGTG 124/1832) Row 14114247 (NC_000005.10:138389782::TGTGTG 775/1832)...	-	Apr 26, 2020 (154)
82	Korean Genome Project Submission ignored due to conflicting rows: Row 14114245 (NC_000005.10:138389782::TG 444/1832) Row 14114246 (NC_000005.10:138389782::TGTG 124/1832) Row 14114247 (NC_000005.10:138389782::TGTGTG 775/1832)...	-	Apr 26, 2020 (154)
83	8.3KJPN Submission ignored due to conflicting rows: Row 32324710 (NC_000005.9:137725471::TGTGTG 7149/16758) Row 32324711 (NC_000005.9:137725471::TG 5358/16758) Row 32324712 (NC_000005.9:137725471::TGTG 968/16758)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 32324710 (NC_000005.9:137725471::TGTGTG 7149/16758) Row 32324711 (NC_000005.9:137725471::TG 5358/16758) Row 32324712 (NC_000005.9:137725471::TGTG 968/16758)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 32324710 (NC_000005.9:137725471::TGTGTG 7149/16758) Row 32324711 (NC_000005.9:137725471::TG 5358/16758) Row 32324712 (NC_000005.9:137725471::TGTG 968/16758)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 32324710 (NC_000005.9:137725471::TGTGTG 7149/16758) Row 32324711 (NC_000005.9:137725471::TG 5358/16758) Row 32324712 (NC_000005.9:137725471::TGTG 968/16758)...	-	Apr 26, 2021 (155)
87	14KJPN Submission ignored due to conflicting rows: Row 45332666 (NC_000005.10:138389782::TG 9005/28258) Row 45332667 (NC_000005.10:138389782::TGTGTG 12091/28258) Row 45332668 (NC_000005.10:138389782::TGTGTGTG 939/28258)...	-	Oct 13, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 45332666 (NC_000005.10:138389782::TG 9005/28258) Row 45332667 (NC_000005.10:138389782::TGTGTG 12091/28258) Row 45332668 (NC_000005.10:138389782::TGTGTGTG 939/28258)...	-	Oct 13, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 45332666 (NC_000005.10:138389782::TG 9005/28258) Row 45332667 (NC_000005.10:138389782::TGTGTG 12091/28258) Row 45332668 (NC_000005.10:138389782::TGTGTGTG 939/28258)...	-	Oct 13, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 45332666 (NC_000005.10:138389782::TG 9005/28258) Row 45332667 (NC_000005.10:138389782::TGTGTG 12091/28258) Row 45332668 (NC_000005.10:138389782::TGTGTGTG 939/28258)...	-	Oct 13, 2022 (156)
91	ALFA	NC_000005.10 - 138389783	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
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT	(self)
ss4130159134	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTG:	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
ss4130159133	NC_000005.10:138389782:TGTGTGTGTG:	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss4130159132	NC_000005.10:138389782:TGTGTGTG:	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4130159131	NC_000005.10:138389782:TGTGTG:	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4130159130	NC_000005.10:138389782:TGTG:	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4130159129	NC_000005.10:138389782:TG:	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
29094521, ss1374570449, ss2997868824, ss5174355404, ss5835707126	NC_000005.9:137725471::TG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3065053004, ss3807292742, ss3957736244, ss4130159118, ss5266011194, ss5463960964, ss5711495562	NC_000005.10:138389782::TG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss95976141	NT_034772.6:46039374::GT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss2997868828, ss5174355405, ss5835707125	NC_000005.9:137725471::TGTG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3957736245, ss4130159119, ss5463960965, ss5711495565	NC_000005.10:138389782::TGTG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4272414, ss80766413	NT_034772.6:46039374::GTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss326724620, ss326997129, ss551718859, ss553218886	NC_000005.8:137753370::TGTGTG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss288661116	NC_000005.8:137753401::GTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss2997868825, ss3785262999, ss3790644465, ss3795521421, ss3838238679, ss5174355403, ss5835707127	NC_000005.9:137725471::TGTGTG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3064176785, ss3065053005, ss3066044726, ss3807292743, ss3957736246, ss4130159120, ss5266011195, ss5463960962, ss5711495563	NC_000005.10:138389782::TGTGTG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss2997868827, ss5174355406	NC_000005.9:137725471::TGTGTGTG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3957736248, ss4130159121, ss5463960963, ss5711495564	NC_000005.10:138389782::TGTGTGTG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4130159122	NC_000005.10:138389782::TGTGTGTGTG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4130159123	NC_000005.10:138389782::TGTGTGTGTG… NC_000005.10:138389782::TGTGTGTGTGTG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4130159124, ss5463960966	NC_000005.10:138389782::TGTGTGTGTG… NC_000005.10:138389782::TGTGTGTGTGTGTG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4130159125	NC_000005.10:138389782::TGTGTGTGTG… NC_000005.10:138389782::TGTGTGTGTGTGTGTG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4130159126	NC_000005.10:138389782::TGTGTGTGTG… NC_000005.10:138389782::TGTGTGTGTGTGTGTGTG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4130159127	NC_000005.10:138389782::TGTGTGTGTG… NC_000005.10:138389782::TGTGTGTGTGTGTGTGTGTG	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
1826335727	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:138389782:TGTGTGTGTGT… NC_000005.10:138389782:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(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 rs148405512

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
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs148405512