Name: rs72473603
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.

rs72473603

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:147548980-147548996 (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)₁₁ / del(T)₁₀ / del(T)₈ / de…
del(T)₁₁ / del(T)₁₀ / del(T)₈ / del(T)₇ / del(T)₆ / 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)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₄ / dup(T)₁₅ / ins(T)₁₅G(T)₁₈ / dup(T)₁₆ / dup(T)₁₇ / ins(T)₁₈ / ins(T)₁₉ / ins(T)₂₀ / ins(T)₂₂(CTTT)₃TTTTTTTTTTTTTTTTT / ins(T)₂₉ / ins(T)₃₂ / ins(T)₃₄ / ins(T)₃₆ / ins(T)₄₃
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₀=0.000004 (1/264690, TOPMED)
(T)₁₇=0.0800 (84/1050, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BCL9 : 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	1050	TTTTTTTTTTTTTTTTT=0.0800	TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.9200, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.08	0.92	0.0	32
European	Sub	1048	TTTTTTTTTTTTTTTTT=0.0782	TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.9218, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.078244	0.921756	0.0	32
African	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTT=0, TTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
African Others	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTT=0, TTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
African American	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTT=0, TTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTT=0, TTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTT=0, TTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTT=0, TTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTT=0, TTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 2	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTT=0, TTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
South Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTT=0, TTTTTTT=0, TTTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	2	TTTTTTTTTTTTTTTTT=1.0	TTTTTT=0.0, TTTTTTT=0.0, TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	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
TopMed	Global	Study-wide	264690	(T)₁₇=0.999996	del(T)₁₀=0.000004
Allele Frequency Aggregator	Total	Global	1050	(T)₁₇=0.0800	del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.9200, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000, dup(T)₈=0.0000
Allele Frequency Aggregator	European	Sub	1048	(T)₁₇=0.0782	del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.9218, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000, dup(T)₈=0.0000
Allele Frequency Aggregator	Other	Sub	2	(T)₁₇=1.0	del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0, dup(T)₈=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(T)₁₇=0	del(T)₁₁=0, del(T)₁₀=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0, dup(T)₆=0, dup(T)₇=0, dup(T)₈=0
Allele Frequency Aggregator	Latin American 2	Sub	0	(T)₁₇=0	del(T)₁₁=0, del(T)₁₀=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0, dup(T)₆=0, dup(T)₇=0, dup(T)₈=0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₁₇=0	del(T)₁₁=0, del(T)₁₀=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0, dup(T)₆=0, dup(T)₇=0, dup(T)₈=0
Allele Frequency Aggregator	African	Sub	0	(T)₁₇=0	del(T)₁₁=0, del(T)₁₀=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0, dup(T)₆=0, dup(T)₇=0, dup(T)₈=0
Allele Frequency Aggregator	Asian	Sub	0	(T)₁₇=0	del(T)₁₁=0, del(T)₁₀=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0, dup(T)₆=0, dup(T)₇=0, dup(T)₈=0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 1	NC_000001.11:g.147548986_147548996del
GRCh38.p14 chr 1	NC_000001.11:g.147548987_147548996del
GRCh38.p14 chr 1	NC_000001.11:g.147548989_147548996del
GRCh38.p14 chr 1	NC_000001.11:g.147548990_147548996del
GRCh38.p14 chr 1	NC_000001.11:g.147548991_147548996del
GRCh38.p14 chr 1	NC_000001.11:g.147548993_147548996del
GRCh38.p14 chr 1	NC_000001.11:g.147548994_147548996del
GRCh38.p14 chr 1	NC_000001.11:g.147548995_147548996del
GRCh38.p14 chr 1	NC_000001.11:g.147548996del
GRCh38.p14 chr 1	NC_000001.11:g.147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548995_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548994_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548993_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548992_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548991_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548990_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548989_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548988_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548987_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548986_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548985_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548984_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548983_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548982_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548980_147548996T[32]GTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 1	NC_000001.11:g.147548981_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548980_147548996dup
GRCh38.p14 chr 1	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.147548980_147548996T[39]CTTT[3]T[17]
GRCh38.p14 chr 1	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364399_4364409del
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364400_4364409del
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364402_4364409del
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364403_4364409del
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364404_4364409del
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364406_4364409del
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364407_4364409del
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364408_4364409del
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364409del
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364408_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364407_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364406_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364405_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364404_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364403_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364402_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364401_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364400_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364399_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364398_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364397_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364396_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364395_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364393_4364409T[32]GTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364394_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364393_4364409dup
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364393_4364409T[39]CTTT[3]T[17]
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.147020759_147020769del
GRCh37.p13 chr 1	NC_000001.10:g.147020760_147020769del
GRCh37.p13 chr 1	NC_000001.10:g.147020762_147020769del
GRCh37.p13 chr 1	NC_000001.10:g.147020763_147020769del
GRCh37.p13 chr 1	NC_000001.10:g.147020764_147020769del
GRCh37.p13 chr 1	NC_000001.10:g.147020766_147020769del
GRCh37.p13 chr 1	NC_000001.10:g.147020767_147020769del
GRCh37.p13 chr 1	NC_000001.10:g.147020768_147020769del
GRCh37.p13 chr 1	NC_000001.10:g.147020769del
GRCh37.p13 chr 1	NC_000001.10:g.147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020768_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020767_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020766_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020765_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020764_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020763_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020762_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020761_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020760_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020759_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020758_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020757_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020756_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020755_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020752_147020769T[33]GTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 1	NC_000001.10:g.147020754_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020753_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020752_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020751_147020769dup
GRCh37.p13 chr 1	NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.147020751_147020769T[41]CTTT[3]T[17]
GRCh37.p13 chr 1	NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: BCL9, BCL9 transcription coactivator (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BCL9 transcript	NM_004326.4:c.-478+7312_-… NM_004326.4:c.-478+7312_-478+7322del	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	(T)₁₇=	del(T)₁₁	del(T)₁₀	del(T)₈	del(T)₇	del(T)₆	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)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₄	dup(T)₁₅	ins(T)₁₅G(T)₁₈	dup(T)₁₆	dup(T)₁₇	ins(T)₁₈	ins(T)₁₉	ins(T)₂₀	ins(T)₂₂(CTTT)₃TTTTTTTTTTTTTTTTT	ins(T)₂₉	ins(T)₃₂	ins(T)₃₄	ins(T)₃₆	ins(T)₄₃
GRCh38.p14 chr 1	NC_000001.11:g.147548980_147548996=	NC_000001.11:g.147548986_147548996del	NC_000001.11:g.147548987_147548996del	NC_000001.11:g.147548989_147548996del	NC_000001.11:g.147548990_147548996del	NC_000001.11:g.147548991_147548996del	NC_000001.11:g.147548993_147548996del	NC_000001.11:g.147548994_147548996del	NC_000001.11:g.147548995_147548996del	NC_000001.11:g.147548996del	NC_000001.11:g.147548996dup	NC_000001.11:g.147548995_147548996dup	NC_000001.11:g.147548994_147548996dup	NC_000001.11:g.147548993_147548996dup	NC_000001.11:g.147548992_147548996dup	NC_000001.11:g.147548991_147548996dup	NC_000001.11:g.147548990_147548996dup	NC_000001.11:g.147548989_147548996dup	NC_000001.11:g.147548988_147548996dup	NC_000001.11:g.147548987_147548996dup	NC_000001.11:g.147548986_147548996dup	NC_000001.11:g.147548985_147548996dup	NC_000001.11:g.147548984_147548996dup	NC_000001.11:g.147548983_147548996dup	NC_000001.11:g.147548982_147548996dup	NC_000001.11:g.147548980_147548996T[32]GTTTTTTTTTTTTTTTTTT[1]	NC_000001.11:g.147548981_147548996dup	NC_000001.11:g.147548980_147548996dup	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTT	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.147548980_147548996T[39]CTTT[3]T[17]	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.147548996_147548997insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.4364393_4364409=	NW_003871055.3:g.4364399_4364409del	NW_003871055.3:g.4364400_4364409del	NW_003871055.3:g.4364402_4364409del	NW_003871055.3:g.4364403_4364409del	NW_003871055.3:g.4364404_4364409del	NW_003871055.3:g.4364406_4364409del	NW_003871055.3:g.4364407_4364409del	NW_003871055.3:g.4364408_4364409del	NW_003871055.3:g.4364409del	NW_003871055.3:g.4364409dup	NW_003871055.3:g.4364408_4364409dup	NW_003871055.3:g.4364407_4364409dup	NW_003871055.3:g.4364406_4364409dup	NW_003871055.3:g.4364405_4364409dup	NW_003871055.3:g.4364404_4364409dup	NW_003871055.3:g.4364403_4364409dup	NW_003871055.3:g.4364402_4364409dup	NW_003871055.3:g.4364401_4364409dup	NW_003871055.3:g.4364400_4364409dup	NW_003871055.3:g.4364399_4364409dup	NW_003871055.3:g.4364398_4364409dup	NW_003871055.3:g.4364397_4364409dup	NW_003871055.3:g.4364396_4364409dup	NW_003871055.3:g.4364395_4364409dup	NW_003871055.3:g.4364393_4364409T[32]GTTTTTTTTTTTTTTTTTT[1]	NW_003871055.3:g.4364394_4364409dup	NW_003871055.3:g.4364393_4364409dup	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTT	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTT	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTT	NW_003871055.3:g.4364393_4364409T[39]CTTT[3]T[17]	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NW_003871055.3:g.4364409_4364410insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.147020751_147020769=	NC_000001.10:g.147020759_147020769del	NC_000001.10:g.147020760_147020769del	NC_000001.10:g.147020762_147020769del	NC_000001.10:g.147020763_147020769del	NC_000001.10:g.147020764_147020769del	NC_000001.10:g.147020766_147020769del	NC_000001.10:g.147020767_147020769del	NC_000001.10:g.147020768_147020769del	NC_000001.10:g.147020769del	NC_000001.10:g.147020769dup	NC_000001.10:g.147020768_147020769dup	NC_000001.10:g.147020767_147020769dup	NC_000001.10:g.147020766_147020769dup	NC_000001.10:g.147020765_147020769dup	NC_000001.10:g.147020764_147020769dup	NC_000001.10:g.147020763_147020769dup	NC_000001.10:g.147020762_147020769dup	NC_000001.10:g.147020761_147020769dup	NC_000001.10:g.147020760_147020769dup	NC_000001.10:g.147020759_147020769dup	NC_000001.10:g.147020758_147020769dup	NC_000001.10:g.147020757_147020769dup	NC_000001.10:g.147020756_147020769dup	NC_000001.10:g.147020755_147020769dup	NC_000001.10:g.147020752_147020769T[33]GTTTTTTTTTTTTTTTTTT[1]	NC_000001.10:g.147020754_147020769dup	NC_000001.10:g.147020753_147020769dup	NC_000001.10:g.147020752_147020769dup	NC_000001.10:g.147020751_147020769dup	NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.147020751_147020769T[41]CTTT[3]T[17]	NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.147020769_147020770insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
BCL9 transcript	NM_004326.3:c.-478+7307=	NM_004326.3:c.-478+7315_-478+7325del	NM_004326.3:c.-478+7316_-478+7325del	NM_004326.3:c.-478+7318_-478+7325del	NM_004326.3:c.-478+7319_-478+7325del	NM_004326.3:c.-478+7320_-478+7325del	NM_004326.3:c.-478+7322_-478+7325del	NM_004326.3:c.-478+7323_-478+7325del	NM_004326.3:c.-478+7324_-478+7325del	NM_004326.3:c.-478+7325del	NM_004326.3:c.-478+7325dup	NM_004326.3:c.-478+7324_-478+7325dup	NM_004326.3:c.-478+7323_-478+7325dup	NM_004326.3:c.-478+7322_-478+7325dup	NM_004326.3:c.-478+7321_-478+7325dup	NM_004326.3:c.-478+7320_-478+7325dup	NM_004326.3:c.-478+7319_-478+7325dup	NM_004326.3:c.-478+7318_-478+7325dup	NM_004326.3:c.-478+7317_-478+7325dup	NM_004326.3:c.-478+7316_-478+7325dup	NM_004326.3:c.-478+7315_-478+7325dup	NM_004326.3:c.-478+7314_-478+7325dup	NM_004326.3:c.-478+7313_-478+7325dup	NM_004326.3:c.-478+7312_-478+7325dup	NM_004326.3:c.-478+7311_-478+7325dup	NM_004326.3:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT	NM_004326.3:c.-478+7310_-478+7325dup	NM_004326.3:c.-478+7309_-478+7325dup	NM_004326.3:c.-478+7308_-478+7325dup	NM_004326.3:c.-478+7307_-478+7325dup	NM_004326.3:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTT	NM_004326.3:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTT	NM_004326.3:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004326.3:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004326.3:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004326.3:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004326.3:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
BCL9 transcript	NM_004326.4:c.-478+7306=	NM_004326.4:c.-478+7312_-478+7322del	NM_004326.4:c.-478+7313_-478+7322del	NM_004326.4:c.-478+7315_-478+7322del	NM_004326.4:c.-478+7316_-478+7322del	NM_004326.4:c.-478+7317_-478+7322del	NM_004326.4:c.-478+7319_-478+7322del	NM_004326.4:c.-478+7320_-478+7322del	NM_004326.4:c.-478+7321_-478+7322del	NM_004326.4:c.-478+7322del	NM_004326.4:c.-478+7322dup	NM_004326.4:c.-478+7321_-478+7322dup	NM_004326.4:c.-478+7320_-478+7322dup	NM_004326.4:c.-478+7319_-478+7322dup	NM_004326.4:c.-478+7318_-478+7322dup	NM_004326.4:c.-478+7317_-478+7322dup	NM_004326.4:c.-478+7316_-478+7322dup	NM_004326.4:c.-478+7315_-478+7322dup	NM_004326.4:c.-478+7314_-478+7322dup	NM_004326.4:c.-478+7313_-478+7322dup	NM_004326.4:c.-478+7312_-478+7322dup	NM_004326.4:c.-478+7311_-478+7322dup	NM_004326.4:c.-478+7310_-478+7322dup	NM_004326.4:c.-478+7309_-478+7322dup	NM_004326.4:c.-478+7308_-478+7322dup	NM_004326.4:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT	NM_004326.4:c.-478+7307_-478+7322dup	NM_004326.4:c.-478+7306_-478+7322dup	NM_004326.4:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTT	NM_004326.4:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTT	NM_004326.4:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTT	NM_004326.4:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTT	NM_004326.4:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004326.4:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004326.4:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004326.4:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004326.4:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
BCL9 transcript variant X2	XM_005272972.1:c.-478+7307=	XM_005272972.1:c.-478+7315_-478+7325del	XM_005272972.1:c.-478+7316_-478+7325del	XM_005272972.1:c.-478+7318_-478+7325del	XM_005272972.1:c.-478+7319_-478+7325del	XM_005272972.1:c.-478+7320_-478+7325del	XM_005272972.1:c.-478+7322_-478+7325del	XM_005272972.1:c.-478+7323_-478+7325del	XM_005272972.1:c.-478+7324_-478+7325del	XM_005272972.1:c.-478+7325del	XM_005272972.1:c.-478+7325dup	XM_005272972.1:c.-478+7324_-478+7325dup	XM_005272972.1:c.-478+7323_-478+7325dup	XM_005272972.1:c.-478+7322_-478+7325dup	XM_005272972.1:c.-478+7321_-478+7325dup	XM_005272972.1:c.-478+7320_-478+7325dup	XM_005272972.1:c.-478+7319_-478+7325dup	XM_005272972.1:c.-478+7318_-478+7325dup	XM_005272972.1:c.-478+7317_-478+7325dup	XM_005272972.1:c.-478+7316_-478+7325dup	XM_005272972.1:c.-478+7315_-478+7325dup	XM_005272972.1:c.-478+7314_-478+7325dup	XM_005272972.1:c.-478+7313_-478+7325dup	XM_005272972.1:c.-478+7312_-478+7325dup	XM_005272972.1:c.-478+7311_-478+7325dup	XM_005272972.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT	XM_005272972.1:c.-478+7310_-478+7325dup	XM_005272972.1:c.-478+7309_-478+7325dup	XM_005272972.1:c.-478+7308_-478+7325dup	XM_005272972.1:c.-478+7307_-478+7325dup	XM_005272972.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTT	XM_005272972.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTT	XM_005272972.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005272972.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005272972.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005272972.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005272972.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
BCL9 transcript variant X3	XM_005272973.1:c.-478+7307=	XM_005272973.1:c.-478+7315_-478+7325del	XM_005272973.1:c.-478+7316_-478+7325del	XM_005272973.1:c.-478+7318_-478+7325del	XM_005272973.1:c.-478+7319_-478+7325del	XM_005272973.1:c.-478+7320_-478+7325del	XM_005272973.1:c.-478+7322_-478+7325del	XM_005272973.1:c.-478+7323_-478+7325del	XM_005272973.1:c.-478+7324_-478+7325del	XM_005272973.1:c.-478+7325del	XM_005272973.1:c.-478+7325dup	XM_005272973.1:c.-478+7324_-478+7325dup	XM_005272973.1:c.-478+7323_-478+7325dup	XM_005272973.1:c.-478+7322_-478+7325dup	XM_005272973.1:c.-478+7321_-478+7325dup	XM_005272973.1:c.-478+7320_-478+7325dup	XM_005272973.1:c.-478+7319_-478+7325dup	XM_005272973.1:c.-478+7318_-478+7325dup	XM_005272973.1:c.-478+7317_-478+7325dup	XM_005272973.1:c.-478+7316_-478+7325dup	XM_005272973.1:c.-478+7315_-478+7325dup	XM_005272973.1:c.-478+7314_-478+7325dup	XM_005272973.1:c.-478+7313_-478+7325dup	XM_005272973.1:c.-478+7312_-478+7325dup	XM_005272973.1:c.-478+7311_-478+7325dup	XM_005272973.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT	XM_005272973.1:c.-478+7310_-478+7325dup	XM_005272973.1:c.-478+7309_-478+7325dup	XM_005272973.1:c.-478+7308_-478+7325dup	XM_005272973.1:c.-478+7307_-478+7325dup	XM_005272973.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTT	XM_005272973.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTT	XM_005272973.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005272973.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005272973.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005272973.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005272973.1:c.-478+7325_-478+7326insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
BCL9 transcript variant X2	XM_005277417.1:c.-478+7306=	XM_005277417.1:c.-478+7312_-478+7322del	XM_005277417.1:c.-478+7313_-478+7322del	XM_005277417.1:c.-478+7315_-478+7322del	XM_005277417.1:c.-478+7316_-478+7322del	XM_005277417.1:c.-478+7317_-478+7322del	XM_005277417.1:c.-478+7319_-478+7322del	XM_005277417.1:c.-478+7320_-478+7322del	XM_005277417.1:c.-478+7321_-478+7322del	XM_005277417.1:c.-478+7322del	XM_005277417.1:c.-478+7322dup	XM_005277417.1:c.-478+7321_-478+7322dup	XM_005277417.1:c.-478+7320_-478+7322dup	XM_005277417.1:c.-478+7319_-478+7322dup	XM_005277417.1:c.-478+7318_-478+7322dup	XM_005277417.1:c.-478+7317_-478+7322dup	XM_005277417.1:c.-478+7316_-478+7322dup	XM_005277417.1:c.-478+7315_-478+7322dup	XM_005277417.1:c.-478+7314_-478+7322dup	XM_005277417.1:c.-478+7313_-478+7322dup	XM_005277417.1:c.-478+7312_-478+7322dup	XM_005277417.1:c.-478+7311_-478+7322dup	XM_005277417.1:c.-478+7310_-478+7322dup	XM_005277417.1:c.-478+7309_-478+7322dup	XM_005277417.1:c.-478+7308_-478+7322dup	XM_005277417.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT	XM_005277417.1:c.-478+7307_-478+7322dup	XM_005277417.1:c.-478+7306_-478+7322dup	XM_005277417.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTT	XM_005277417.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTT	XM_005277417.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTT	XM_005277417.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTT	XM_005277417.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005277417.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005277417.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005277417.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005277417.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
BCL9 transcript variant X3	XM_005277418.1:c.-478+7306=	XM_005277418.1:c.-478+7312_-478+7322del	XM_005277418.1:c.-478+7313_-478+7322del	XM_005277418.1:c.-478+7315_-478+7322del	XM_005277418.1:c.-478+7316_-478+7322del	XM_005277418.1:c.-478+7317_-478+7322del	XM_005277418.1:c.-478+7319_-478+7322del	XM_005277418.1:c.-478+7320_-478+7322del	XM_005277418.1:c.-478+7321_-478+7322del	XM_005277418.1:c.-478+7322del	XM_005277418.1:c.-478+7322dup	XM_005277418.1:c.-478+7321_-478+7322dup	XM_005277418.1:c.-478+7320_-478+7322dup	XM_005277418.1:c.-478+7319_-478+7322dup	XM_005277418.1:c.-478+7318_-478+7322dup	XM_005277418.1:c.-478+7317_-478+7322dup	XM_005277418.1:c.-478+7316_-478+7322dup	XM_005277418.1:c.-478+7315_-478+7322dup	XM_005277418.1:c.-478+7314_-478+7322dup	XM_005277418.1:c.-478+7313_-478+7322dup	XM_005277418.1:c.-478+7312_-478+7322dup	XM_005277418.1:c.-478+7311_-478+7322dup	XM_005277418.1:c.-478+7310_-478+7322dup	XM_005277418.1:c.-478+7309_-478+7322dup	XM_005277418.1:c.-478+7308_-478+7322dup	XM_005277418.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT	XM_005277418.1:c.-478+7307_-478+7322dup	XM_005277418.1:c.-478+7306_-478+7322dup	XM_005277418.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTT	XM_005277418.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTT	XM_005277418.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTT	XM_005277418.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTT	XM_005277418.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005277418.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005277418.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005277418.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005277418.1:c.-478+7322_-478+7323insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

84 SubSNP, 50 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77905917	Oct 11, 2018 (152)
2	HGSV	ss77924153	Oct 11, 2018 (152)
3	HGSV	ss81968851	Oct 11, 2018 (152)
4	HGSV	ss82104209	Oct 11, 2018 (152)
5	HGSV	ss82971157	Oct 11, 2018 (152)
6	HUMANGENOME_JCVI	ss95242334	Oct 11, 2018 (152)
7	PJP	ss294602728	May 09, 2011 (136)
8	PJP	ss294602729	May 31, 2013 (138)
9	BILGI_BIOE	ss666109955	Apr 25, 2013 (138)
10	DDI	ss1536246834	Apr 09, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1701202994	Apr 09, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1701202996	Apr 09, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1701202998	Apr 09, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1701203000	Apr 09, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1701203002	Apr 09, 2015 (144)
16	EVA_UK10K_ALSPAC	ss1701203004	Apr 09, 2015 (144)
17	HAMMER_LAB	ss1795039797	Sep 11, 2015 (146)
18	SWEGEN	ss2987658371	Oct 11, 2018 (152)
19	MCHAISSO	ss3064423183	Nov 08, 2017 (151)
20	EVA_DECODE	ss3687703518	Jul 12, 2019 (153)
21	EVA_DECODE	ss3687703519	Jul 12, 2019 (153)
22	EVA_DECODE	ss3687703520	Jul 12, 2019 (153)
23	EVA_DECODE	ss3687703521	Jul 12, 2019 (153)
24	EVA_DECODE	ss3687703522	Jul 12, 2019 (153)
25	EVA_DECODE	ss3687703523	Jul 12, 2019 (153)
26	PACBIO	ss3783552289	Jul 12, 2019 (153)
27	PACBIO	ss3789187857	Jul 12, 2019 (153)
28	PACBIO	ss3789187858	Jul 12, 2019 (153)
29	PACBIO	ss3794059843	Jul 12, 2019 (153)
30	PACBIO	ss3794059844	Jul 12, 2019 (153)
31	EVA	ss3826406684	Apr 25, 2020 (154)
32	GNOMAD	ss4002733550	Apr 25, 2021 (155)
33	GNOMAD	ss4002733551	Apr 25, 2021 (155)
34	GNOMAD	ss4002733554	Apr 25, 2021 (155)
35	GNOMAD	ss4002733555	Apr 25, 2021 (155)
36	GNOMAD	ss4002733556	Apr 25, 2021 (155)
37	GNOMAD	ss4002733557	Apr 25, 2021 (155)
38	GNOMAD	ss4002733558	Apr 25, 2021 (155)
39	GNOMAD	ss4002733559	Apr 25, 2021 (155)
40	GNOMAD	ss4002733560	Apr 25, 2021 (155)
41	GNOMAD	ss4002733561	Apr 25, 2021 (155)
42	GNOMAD	ss4002733562	Apr 25, 2021 (155)
43	GNOMAD	ss4002733563	Apr 25, 2021 (155)
44	GNOMAD	ss4002733564	Apr 25, 2021 (155)
45	GNOMAD	ss4002733565	Apr 25, 2021 (155)
46	GNOMAD	ss4002733566	Apr 25, 2021 (155)
47	GNOMAD	ss4002733567	Apr 25, 2021 (155)
48	GNOMAD	ss4002733568	Apr 25, 2021 (155)
49	GNOMAD	ss4002733569	Apr 25, 2021 (155)
50	GNOMAD	ss4002733570	Apr 25, 2021 (155)
51	GNOMAD	ss4002733571	Apr 25, 2021 (155)
52	GNOMAD	ss4002733572	Apr 25, 2021 (155)
53	GNOMAD	ss4002733573	Apr 25, 2021 (155)
54	GNOMAD	ss4002733574	Apr 25, 2021 (155)
55	GNOMAD	ss4002733575	Apr 25, 2021 (155)
56	GNOMAD	ss4002733576	Apr 25, 2021 (155)
57	GNOMAD	ss4002733577	Apr 25, 2021 (155)
58	GNOMAD	ss4002733578	Apr 25, 2021 (155)
59	GNOMAD	ss4002733579	Apr 25, 2021 (155)
60	GNOMAD	ss4002733580	Apr 25, 2021 (155)
61	GNOMAD	ss4002733581	Apr 25, 2021 (155)
62	TOPMED	ss4466770917	Apr 25, 2021 (155)
63	TOMMO_GENOMICS	ss5146225084	Apr 25, 2021 (155)
64	TOMMO_GENOMICS	ss5146225085	Apr 25, 2021 (155)
65	TOMMO_GENOMICS	ss5146225086	Apr 25, 2021 (155)
66	TOMMO_GENOMICS	ss5146225087	Apr 25, 2021 (155)
67	TOMMO_GENOMICS	ss5146225088	Apr 25, 2021 (155)
68	TOMMO_GENOMICS	ss5146225089	Apr 25, 2021 (155)
69	1000G_HIGH_COVERAGE	ss5244131299	Oct 12, 2022 (156)
70	1000G_HIGH_COVERAGE	ss5244131300	Oct 12, 2022 (156)
71	1000G_HIGH_COVERAGE	ss5244131301	Oct 12, 2022 (156)
72	HUGCELL_USP	ss5444772100	Oct 12, 2022 (156)
73	HUGCELL_USP	ss5444772101	Oct 12, 2022 (156)
74	HUGCELL_USP	ss5444772102	Oct 12, 2022 (156)
75	HUGCELL_USP	ss5444772103	Oct 12, 2022 (156)
76	HUGCELL_USP	ss5444772104	Oct 12, 2022 (156)
77	TOMMO_GENOMICS	ss5673368007	Oct 12, 2022 (156)
78	TOMMO_GENOMICS	ss5673368008	Oct 12, 2022 (156)
79	TOMMO_GENOMICS	ss5673368009	Oct 12, 2022 (156)
80	TOMMO_GENOMICS	ss5673368010	Oct 12, 2022 (156)
81	TOMMO_GENOMICS	ss5673368012	Oct 12, 2022 (156)
82	EVA	ss5832604808	Oct 12, 2022 (156)
83	EVA	ss5832604809	Oct 12, 2022 (156)
84	EVA	ss5832604810	Oct 12, 2022 (156)
85	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 1936123 (NC_000001.10:147020750::T 884/3854) Row 1936124 (NC_000001.10:147020750::TT 2215/3854) Row 1936125 (NC_000001.10:147020750::TTTTT 647/3854)	-	Oct 11, 2018 (152)
86	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 1936123 (NC_000001.10:147020750::T 884/3854) Row 1936124 (NC_000001.10:147020750::TT 2215/3854) Row 1936125 (NC_000001.10:147020750::TTTTT 647/3854)	-	Oct 11, 2018 (152)
87	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 1936123 (NC_000001.10:147020750::T 884/3854) Row 1936124 (NC_000001.10:147020750::TT 2215/3854) Row 1936125 (NC_000001.10:147020750::TTTTT 647/3854)	-	Oct 11, 2018 (152)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
102	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
103	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
104	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
105	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
106	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
107	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
108	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
109	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
110	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
111	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
112	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
113	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
114	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
115	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
116	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
117	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
118	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25713808 (NC_000001.11:147548979::T 6187/103158) Row 25713809 (NC_000001.11:147548979::TTT 47909/103272) Row 25713812 (NC_000001.11:147548979::TTTT 34502/103272)...	-	Apr 25, 2021 (155)
119	8.3KJPN Submission ignored due to conflicting rows: Row 4194391 (NC_000001.10:147020750::TT 8908/15874) Row 4194392 (NC_000001.10:147020750:T: 3184/15874) Row 4194393 (NC_000001.10:147020750::T 1576/15874)...	-	Apr 25, 2021 (155)
120	8.3KJPN Submission ignored due to conflicting rows: Row 4194391 (NC_000001.10:147020750::TT 8908/15874) Row 4194392 (NC_000001.10:147020750:T: 3184/15874) Row 4194393 (NC_000001.10:147020750::T 1576/15874)...	-	Apr 25, 2021 (155)
121	8.3KJPN Submission ignored due to conflicting rows: Row 4194391 (NC_000001.10:147020750::TT 8908/15874) Row 4194392 (NC_000001.10:147020750:T: 3184/15874) Row 4194393 (NC_000001.10:147020750::T 1576/15874)...	-	Apr 25, 2021 (155)
122	8.3KJPN Submission ignored due to conflicting rows: Row 4194391 (NC_000001.10:147020750::TT 8908/15874) Row 4194392 (NC_000001.10:147020750:T: 3184/15874) Row 4194393 (NC_000001.10:147020750::T 1576/15874)...	-	Apr 25, 2021 (155)
123	8.3KJPN Submission ignored due to conflicting rows: Row 4194391 (NC_000001.10:147020750::TT 8908/15874) Row 4194392 (NC_000001.10:147020750:T: 3184/15874) Row 4194393 (NC_000001.10:147020750::T 1576/15874)...	-	Apr 25, 2021 (155)
124	8.3KJPN Submission ignored due to conflicting rows: Row 4194391 (NC_000001.10:147020750::TT 8908/15874) Row 4194392 (NC_000001.10:147020750:T: 3184/15874) Row 4194393 (NC_000001.10:147020750::T 1576/15874)...	-	Apr 25, 2021 (155)
125	14KJPN Submission ignored due to conflicting rows: Row 7205111 (NC_000001.11:147548979::TTTT 16736/28164) Row 7205112 (NC_000001.11:147548979::T 6039/28164) Row 7205113 (NC_000001.11:147548979::TTT 3045/28164)...	-	Oct 12, 2022 (156)
126	14KJPN Submission ignored due to conflicting rows: Row 7205111 (NC_000001.11:147548979::TTTT 16736/28164) Row 7205112 (NC_000001.11:147548979::T 6039/28164) Row 7205113 (NC_000001.11:147548979::TTT 3045/28164)...	-	Oct 12, 2022 (156)
127	14KJPN Submission ignored due to conflicting rows: Row 7205111 (NC_000001.11:147548979::TTTT 16736/28164) Row 7205112 (NC_000001.11:147548979::T 6039/28164) Row 7205113 (NC_000001.11:147548979::TTT 3045/28164)...	-	Oct 12, 2022 (156)
128	14KJPN Submission ignored due to conflicting rows: Row 7205111 (NC_000001.11:147548979::TTTT 16736/28164) Row 7205112 (NC_000001.11:147548979::T 6039/28164) Row 7205113 (NC_000001.11:147548979::TTT 3045/28164)...	-	Oct 12, 2022 (156)
129	14KJPN Submission ignored due to conflicting rows: Row 7205111 (NC_000001.11:147548979::TTTT 16736/28164) Row 7205112 (NC_000001.11:147548979::T 6039/28164) Row 7205113 (NC_000001.11:147548979::TTT 3045/28164)...	-	Oct 12, 2022 (156)
130	TopMed	NC_000001.11 - 147548980	Apr 25, 2021 (155)
131	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1936123 (NC_000001.10:147020750::T 835/3708) Row 1936124 (NC_000001.10:147020750::TT 2155/3708) Row 1936125 (NC_000001.10:147020750::TTTTT 628/3708)	-	Oct 11, 2018 (152)
132	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1936123 (NC_000001.10:147020750::T 835/3708) Row 1936124 (NC_000001.10:147020750::TT 2155/3708) Row 1936125 (NC_000001.10:147020750::TTTTT 628/3708)	-	Oct 11, 2018 (152)
133	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1936123 (NC_000001.10:147020750::T 835/3708) Row 1936124 (NC_000001.10:147020750::TT 2155/3708) Row 1936125 (NC_000001.10:147020750::TTTTT 628/3708)	-	Oct 11, 2018 (152)
134	ALFA	NC_000001.11 - 147548980	Apr 25, 2021 (155)

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

Associated ID	History Updated (Build)
rs141494837	Oct 18, 2011 (136)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4002733581	NC_000001.11:147548979:TTTTTTTTTTT:	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTT	(self)
30377252, ss4466770917	NC_000001.11:147548979:TTTTTTTTTT:	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTT	(self)
ss4002733580	NC_000001.11:147548979:TTTTTTTT:	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4002733579	NC_000001.11:147548979:TTTTTTT:	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4002733578	NC_000001.11:147548979:TTTTTT:	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4002733577	NC_000001.11:147548979:TTTT:	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4002733576	NC_000001.11:147548979:TTT:	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss1795039797, ss2987658371, ss3826406684	NC_000001.10:147020750:TTTT:	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3687703518, ss4002733575, ss5444772104	NC_000001.11:147548979:TT:	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4002733574	NC_000001.11:147548979:T:	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5146225085	NC_000001.10:147020750:T:	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4002733550, ss5244131300, ss5444772103, ss5673368008	NC_000001.11:147548979::T	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3687703519	NC_000001.11:147548981::T	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss1795039797, ss2987658371, ss3826406684	NC_000001.10:147020750:TTTT:TTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3064423183, ss5444772101	NC_000001.11:147548979::TT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3687703520	NC_000001.11:147548981::TT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss294602728	NC_000001.9:145487375::T	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss666109955, ss1701202994, ss1701202996, ss3789187857, ss3794059843, ss5146225086	NC_000001.10:147020750::T	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4002733551, ss5244131301, ss5444772102, ss5673368009	NC_000001.11:147548979::TTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3687703521	NC_000001.11:147548981::TTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss77905917, ss77924153, ss82971157, ss95242334	NT_167185.1:2348356::T	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss294602729	NC_000001.9:145487392::TT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss1536246834, ss1701202998, ss1701203000, ss3783552289, ss3789187858, ss3794059844, ss5146225084, ss5832604808	NC_000001.10:147020750::TT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733554, ss5244131299, ss5444772100, ss5673368007	NC_000001.11:147548979::TTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3687703522	NC_000001.11:147548981::TTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss81968851, ss82104209	NT_167185.1:2348356::TT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5146225088, ss5832604809	NC_000001.10:147020750::TTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5673368012	NC_000001.11:147548979::TTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733555	NC_000001.11:147548979::TTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1701203002, ss1701203004, ss5832604810	NC_000001.10:147020750::TTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5146225087	NC_000001.10:147020750::TTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5673368010	NC_000001.11:147548979::TTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
11326409188	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733556	NC_000001.11:147548979::TTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733557	NC_000001.11:147548979::TTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3687703523	NC_000001.11:147548981::TTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733558	NC_000001.11:147548979::TTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5146225089	NC_000001.10:147020750::TTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733559	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733560	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733561	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733562	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733570	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT	(self)
ss4002733563	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733564	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733565	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733566	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733567	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTCTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733568	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733569	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733571	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733572	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4002733573	NC_000001.11:147548979::TTTTTTTTTT… NC_000001.11:147548979::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:147548979:TTTTTTTTTTT… NC_000001.11:147548979:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs72473603

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

rs72473603