Name: rs61245532
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.

rs61245532

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:51582767-51582776 (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: delTT / delT / dupT / dup(T)₅ / du…
delTT / delT / dupT / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / ins(T)₁₁ / ins(T)₁₂ / ins(T)₁₃ / ins(T)₁₇ / ins(T)₁₈ / ins(T)₁₉ / ins(T)₂₀ / ins(T)₂₁ / ins(T)₂₂ / ins(T)₂₃ / ins(T)₂₇
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.000008 (2/264690, TOPMED)
dup(T)₈=0.00363 (61/16820, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RAD54L2 : 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	HTRZ	HWEP
Total	Global	16820	TTTTTTTTTT=0.99625	TTTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00363, TTTTTTTTTTTTTTTTTTT=0.00012, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.992745	0.007255	0
European	Sub	13934	TTTTTTTTTT=0.99548	TTTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00438, TTTTTTTTTTTTTTTTTTT=0.00014, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.991242	0.008758	0
African	Sub	1900	TTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	N/A
African Others	Sub	74	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	N/A
African American	Sub	1826	TTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	N/A
Asian	Sub	52	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	N/A
East Asian	Sub	40	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	N/A
Other Asian	Sub	12	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	N/A
Latin American 1	Sub	126	TTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	N/A
Latin American 2	Sub	304	TTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	N/A
South Asian	Sub	88	TTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	N/A
Other	Sub	416	TTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	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)₁₀=0.999992	delTT=0.000008
Allele Frequency Aggregator	Total	Global	16820	(T)₁₀=0.99625	delTT=0.00000, delT=0.00000, dupT=0.00000, dup(T)₅=0.00000, dup(T)₇=0.00000, dup(T)₈=0.00363, dup(T)₉=0.00012, ins(T)₁₁=0.00000, ins(T)₁₂=0.00000, ins(T)₁₈=0.00000, ins(T)₁₉=0.00000
Allele Frequency Aggregator	European	Sub	13934	(T)₁₀=0.99548	delTT=0.00000, delT=0.00000, dupT=0.00000, dup(T)₅=0.00000, dup(T)₇=0.00000, dup(T)₈=0.00438, dup(T)₉=0.00014, ins(T)₁₁=0.00000, ins(T)₁₂=0.00000, ins(T)₁₈=0.00000, ins(T)₁₉=0.00000
Allele Frequency Aggregator	African	Sub	1900	(T)₁₀=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dup(T)₅=0.0000, dup(T)₇=0.0000, dup(T)₈=0.0000, dup(T)₉=0.0000, ins(T)₁₁=0.0000, ins(T)₁₂=0.0000, ins(T)₁₈=0.0000, ins(T)₁₉=0.0000
Allele Frequency Aggregator	Other	Sub	416	(T)₁₀=1.000	delTT=0.000, delT=0.000, dupT=0.000, dup(T)₅=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, ins(T)₁₁=0.000, ins(T)₁₂=0.000, ins(T)₁₈=0.000, ins(T)₁₉=0.000
Allele Frequency Aggregator	Latin American 2	Sub	304	(T)₁₀=1.000	delTT=0.000, delT=0.000, dupT=0.000, dup(T)₅=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, ins(T)₁₁=0.000, ins(T)₁₂=0.000, ins(T)₁₈=0.000, ins(T)₁₉=0.000
Allele Frequency Aggregator	Latin American 1	Sub	126	(T)₁₀=1.000	delTT=0.000, delT=0.000, dupT=0.000, dup(T)₅=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, ins(T)₁₁=0.000, ins(T)₁₂=0.000, ins(T)₁₈=0.000, ins(T)₁₉=0.000
Allele Frequency Aggregator	South Asian	Sub	88	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00, dup(T)₅=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, ins(T)₁₁=0.00, ins(T)₁₂=0.00, ins(T)₁₈=0.00, ins(T)₁₉=0.00
Allele Frequency Aggregator	Asian	Sub	52	(T)₁₀=1.00	delTT=0.00, delT=0.00, dupT=0.00, dup(T)₅=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, ins(T)₁₁=0.00, ins(T)₁₂=0.00, ins(T)₁₈=0.00, ins(T)₁₉=0.00

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 3	NC_000003.12:g.51582775_51582776del
GRCh38.p14 chr 3	NC_000003.12:g.51582776del
GRCh38.p14 chr 3	NC_000003.12:g.51582776dup
GRCh38.p14 chr 3	NC_000003.12:g.51582772_51582776dup
GRCh38.p14 chr 3	NC_000003.12:g.51582771_51582776dup
GRCh38.p14 chr 3	NC_000003.12:g.51582770_51582776dup
GRCh38.p14 chr 3	NC_000003.12:g.51582769_51582776dup
GRCh38.p14 chr 3	NC_000003.12:g.51582768_51582776dup
GRCh38.p14 chr 3	NC_000003.12:g.51582767_51582776dup
GRCh38.p14 chr 3	NC_000003.12:g.51582776_51582777insTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.51616791_51616792del
GRCh37.p13 chr 3	NC_000003.11:g.51616792del
GRCh37.p13 chr 3	NC_000003.11:g.51616792dup
GRCh37.p13 chr 3	NC_000003.11:g.51616788_51616792dup
GRCh37.p13 chr 3	NC_000003.11:g.51616787_51616792dup
GRCh37.p13 chr 3	NC_000003.11:g.51616786_51616792dup
GRCh37.p13 chr 3	NC_000003.11:g.51616785_51616792dup
GRCh37.p13 chr 3	NC_000003.11:g.51616784_51616792dup
GRCh37.p13 chr 3	NC_000003.11:g.51616783_51616792dup
GRCh37.p13 chr 3	NC_000003.11:g.51616792_51616793insTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: RAD54L2, RAD54 like 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RAD54L2 transcript variant 1	NM_001322253.2:c.-54-7592… NM_001322253.2:c.-54-7592_-54-7591del	N/A	Intron Variant
RAD54L2 transcript variant 3	NM_001322256.2:c.-54-7592… NM_001322256.2:c.-54-7592_-54-7591del	N/A	Intron Variant
RAD54L2 transcript variant 5	NM_001387866.1:c.-54-7592… NM_001387866.1:c.-54-7592_-54-7591del	N/A	Intron Variant
RAD54L2 transcript variant 6	NM_001387867.1:c.-54-7592… NM_001387867.1:c.-54-7592_-54-7591del	N/A	Intron Variant
RAD54L2 transcript variant 7	NM_001387869.1:c.-18+4386… NM_001387869.1:c.-18+43860_-18+43861del	N/A	Intron Variant
RAD54L2 transcript variant 2	NM_015106.4:c.-54-7592_-5… NM_015106.4:c.-54-7592_-54-7591del	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)₁₀=	delTT	delT	dupT	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	ins(T)₁₁	ins(T)₁₂	ins(T)₁₃	ins(T)₁₇	ins(T)₁₈	ins(T)₁₉	ins(T)₂₀	ins(T)₂₁	ins(T)₂₂	ins(T)₂₃	ins(T)₂₇
GRCh38.p14 chr 3	NC_000003.12:g.51582767_51582776=	NC_000003.12:g.51582775_51582776del	NC_000003.12:g.51582776del	NC_000003.12:g.51582776dup	NC_000003.12:g.51582772_51582776dup	NC_000003.12:g.51582771_51582776dup	NC_000003.12:g.51582770_51582776dup	NC_000003.12:g.51582769_51582776dup	NC_000003.12:g.51582768_51582776dup	NC_000003.12:g.51582767_51582776dup	NC_000003.12:g.51582776_51582777insTTTTTTTTTTT	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTT	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTT	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTT	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTT	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTT	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTT	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:g.51582776_51582777insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.51616783_51616792=	NC_000003.11:g.51616791_51616792del	NC_000003.11:g.51616792del	NC_000003.11:g.51616792dup	NC_000003.11:g.51616788_51616792dup	NC_000003.11:g.51616787_51616792dup	NC_000003.11:g.51616786_51616792dup	NC_000003.11:g.51616785_51616792dup	NC_000003.11:g.51616784_51616792dup	NC_000003.11:g.51616783_51616792dup	NC_000003.11:g.51616792_51616793insTTTTTTTTTTT	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTT	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTT	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTT	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTT	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTT	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTT	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTTT	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTTTT	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.11:g.51616792_51616793insTTTTTTTTTTTTTTTTTTTTTTTTTTT
RAD54L2 transcript variant 1	NM_001322253.2:c.-54-7600=	NM_001322253.2:c.-54-7592_-54-7591del	NM_001322253.2:c.-54-7591del	NM_001322253.2:c.-54-7591dup	NM_001322253.2:c.-54-7595_-54-7591dup	NM_001322253.2:c.-54-7596_-54-7591dup	NM_001322253.2:c.-54-7597_-54-7591dup	NM_001322253.2:c.-54-7598_-54-7591dup	NM_001322253.2:c.-54-7599_-54-7591dup	NM_001322253.2:c.-54-7600_-54-7591dup	NM_001322253.2:c.-54-7591_-54-7590insTTTTTTTTTTT	NM_001322253.2:c.-54-7591_-54-7590insTTTTTTTTTTTT	NM_001322253.2:c.-54-7591_-54-7590insTTTTTTTTTTTTT	NM_001322253.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTT	NM_001322253.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTT	NM_001322253.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTT	NM_001322253.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTT	NM_001322253.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTT	NM_001322253.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTT	NM_001322253.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTTT	NM_001322253.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTTTTTTT
RAD54L2 transcript variant 3	NM_001322256.2:c.-54-7600=	NM_001322256.2:c.-54-7592_-54-7591del	NM_001322256.2:c.-54-7591del	NM_001322256.2:c.-54-7591dup	NM_001322256.2:c.-54-7595_-54-7591dup	NM_001322256.2:c.-54-7596_-54-7591dup	NM_001322256.2:c.-54-7597_-54-7591dup	NM_001322256.2:c.-54-7598_-54-7591dup	NM_001322256.2:c.-54-7599_-54-7591dup	NM_001322256.2:c.-54-7600_-54-7591dup	NM_001322256.2:c.-54-7591_-54-7590insTTTTTTTTTTT	NM_001322256.2:c.-54-7591_-54-7590insTTTTTTTTTTTT	NM_001322256.2:c.-54-7591_-54-7590insTTTTTTTTTTTTT	NM_001322256.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTT	NM_001322256.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTT	NM_001322256.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTT	NM_001322256.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTT	NM_001322256.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTT	NM_001322256.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTT	NM_001322256.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTTT	NM_001322256.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTTTTTTT
RAD54L2 transcript variant 5	NM_001387866.1:c.-54-7600=	NM_001387866.1:c.-54-7592_-54-7591del	NM_001387866.1:c.-54-7591del	NM_001387866.1:c.-54-7591dup	NM_001387866.1:c.-54-7595_-54-7591dup	NM_001387866.1:c.-54-7596_-54-7591dup	NM_001387866.1:c.-54-7597_-54-7591dup	NM_001387866.1:c.-54-7598_-54-7591dup	NM_001387866.1:c.-54-7599_-54-7591dup	NM_001387866.1:c.-54-7600_-54-7591dup	NM_001387866.1:c.-54-7591_-54-7590insTTTTTTTTTTT	NM_001387866.1:c.-54-7591_-54-7590insTTTTTTTTTTTT	NM_001387866.1:c.-54-7591_-54-7590insTTTTTTTTTTTTT	NM_001387866.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTT	NM_001387866.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTT	NM_001387866.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTT	NM_001387866.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTT	NM_001387866.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTT	NM_001387866.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTT	NM_001387866.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTTT	NM_001387866.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTTTTTTT
RAD54L2 transcript variant 6	NM_001387867.1:c.-54-7600=	NM_001387867.1:c.-54-7592_-54-7591del	NM_001387867.1:c.-54-7591del	NM_001387867.1:c.-54-7591dup	NM_001387867.1:c.-54-7595_-54-7591dup	NM_001387867.1:c.-54-7596_-54-7591dup	NM_001387867.1:c.-54-7597_-54-7591dup	NM_001387867.1:c.-54-7598_-54-7591dup	NM_001387867.1:c.-54-7599_-54-7591dup	NM_001387867.1:c.-54-7600_-54-7591dup	NM_001387867.1:c.-54-7591_-54-7590insTTTTTTTTTTT	NM_001387867.1:c.-54-7591_-54-7590insTTTTTTTTTTTT	NM_001387867.1:c.-54-7591_-54-7590insTTTTTTTTTTTTT	NM_001387867.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTT	NM_001387867.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTT	NM_001387867.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTT	NM_001387867.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTT	NM_001387867.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTT	NM_001387867.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTT	NM_001387867.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTTT	NM_001387867.1:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTTTTTTT
RAD54L2 transcript variant 7	NM_001387869.1:c.-18+43852=	NM_001387869.1:c.-18+43860_-18+43861del	NM_001387869.1:c.-18+43861del	NM_001387869.1:c.-18+43861dup	NM_001387869.1:c.-18+43857_-18+43861dup	NM_001387869.1:c.-18+43856_-18+43861dup	NM_001387869.1:c.-18+43855_-18+43861dup	NM_001387869.1:c.-18+43854_-18+43861dup	NM_001387869.1:c.-18+43853_-18+43861dup	NM_001387869.1:c.-18+43852_-18+43861dup	NM_001387869.1:c.-18+43861_-18+43862insTTTTTTTTTTT	NM_001387869.1:c.-18+43861_-18+43862insTTTTTTTTTTTT	NM_001387869.1:c.-18+43861_-18+43862insTTTTTTTTTTTTT	NM_001387869.1:c.-18+43861_-18+43862insTTTTTTTTTTTTTTTTT	NM_001387869.1:c.-18+43861_-18+43862insTTTTTTTTTTTTTTTTTT	NM_001387869.1:c.-18+43861_-18+43862insTTTTTTTTTTTTTTTTTTT	NM_001387869.1:c.-18+43861_-18+43862insTTTTTTTTTTTTTTTTTTTT	NM_001387869.1:c.-18+43861_-18+43862insTTTTTTTTTTTTTTTTTTTTT	NM_001387869.1:c.-18+43861_-18+43862insTTTTTTTTTTTTTTTTTTTTTT	NM_001387869.1:c.-18+43861_-18+43862insTTTTTTTTTTTTTTTTTTTTTTT	NM_001387869.1:c.-18+43861_-18+43862insTTTTTTTTTTTTTTTTTTTTTTTTTTT
RAD54L2 transcript	NM_015106.2:c.-54-7600=	NM_015106.2:c.-54-7592_-54-7591del	NM_015106.2:c.-54-7591del	NM_015106.2:c.-54-7591dup	NM_015106.2:c.-54-7595_-54-7591dup	NM_015106.2:c.-54-7596_-54-7591dup	NM_015106.2:c.-54-7597_-54-7591dup	NM_015106.2:c.-54-7598_-54-7591dup	NM_015106.2:c.-54-7599_-54-7591dup	NM_015106.2:c.-54-7600_-54-7591dup	NM_015106.2:c.-54-7591_-54-7590insTTTTTTTTTTT	NM_015106.2:c.-54-7591_-54-7590insTTTTTTTTTTTT	NM_015106.2:c.-54-7591_-54-7590insTTTTTTTTTTTTT	NM_015106.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTT	NM_015106.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTT	NM_015106.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTT	NM_015106.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTT	NM_015106.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTT	NM_015106.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTT	NM_015106.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTTT	NM_015106.2:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTTTTTTT
RAD54L2 transcript variant 2	NM_015106.4:c.-54-7600=	NM_015106.4:c.-54-7592_-54-7591del	NM_015106.4:c.-54-7591del	NM_015106.4:c.-54-7591dup	NM_015106.4:c.-54-7595_-54-7591dup	NM_015106.4:c.-54-7596_-54-7591dup	NM_015106.4:c.-54-7597_-54-7591dup	NM_015106.4:c.-54-7598_-54-7591dup	NM_015106.4:c.-54-7599_-54-7591dup	NM_015106.4:c.-54-7600_-54-7591dup	NM_015106.4:c.-54-7591_-54-7590insTTTTTTTTTTT	NM_015106.4:c.-54-7591_-54-7590insTTTTTTTTTTTT	NM_015106.4:c.-54-7591_-54-7590insTTTTTTTTTTTTT	NM_015106.4:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTT	NM_015106.4:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTT	NM_015106.4:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTT	NM_015106.4:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTT	NM_015106.4:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTT	NM_015106.4:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTT	NM_015106.4:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTTT	NM_015106.4:c.-54-7591_-54-7590insTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

48 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss83179664	Dec 16, 2007 (129)
2	LUNTER	ss553020310	Oct 12, 2018 (152)
3	SSMP	ss663413282	Apr 01, 2015 (144)
4	SWEGEN	ss2992293903	Nov 08, 2017 (151)
5	MCHAISSO	ss3064046969	Nov 08, 2017 (151)
6	MCHAISSO	ss3065879794	Nov 08, 2017 (151)
7	EGCUT_WGS	ss3660214803	Jul 13, 2019 (153)
8	EGCUT_WGS	ss3660214804	Jul 13, 2019 (153)
9	EVA_DECODE	ss3709205269	Jul 13, 2019 (153)
10	EVA_DECODE	ss3709205270	Jul 13, 2019 (153)
11	EVA_DECODE	ss3709205271	Jul 13, 2019 (153)
12	PACBIO	ss3784310740	Jul 13, 2019 (153)
13	GNOMAD	ss4070893012	Apr 26, 2021 (155)
14	GNOMAD	ss4070893014	Apr 26, 2021 (155)
15	GNOMAD	ss4070893015	Apr 26, 2021 (155)
16	GNOMAD	ss4070893016	Apr 26, 2021 (155)
17	GNOMAD	ss4070893017	Apr 26, 2021 (155)
18	GNOMAD	ss4070893018	Apr 26, 2021 (155)
19	GNOMAD	ss4070893019	Apr 26, 2021 (155)
20	GNOMAD	ss4070893020	Apr 26, 2021 (155)
21	GNOMAD	ss4070893021	Apr 26, 2021 (155)
22	GNOMAD	ss4070893022	Apr 26, 2021 (155)
23	GNOMAD	ss4070893023	Apr 26, 2021 (155)
24	GNOMAD	ss4070893024	Apr 26, 2021 (155)
25	GNOMAD	ss4070893025	Apr 26, 2021 (155)
26	GNOMAD	ss4070893026	Apr 26, 2021 (155)
27	GNOMAD	ss4070893027	Apr 26, 2021 (155)
28	GNOMAD	ss4070893028	Apr 26, 2021 (155)
29	GNOMAD	ss4070893029	Apr 26, 2021 (155)
30	GNOMAD	ss4070893031	Apr 26, 2021 (155)
31	GNOMAD	ss4070893032	Apr 26, 2021 (155)
32	TOPMED	ss4564237711	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5159103379	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5159103380	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5159103381	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5159103382	Apr 26, 2021 (155)
37	1000G_HIGH_COVERAGE	ss5254040876	Oct 12, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5254040877	Oct 12, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5254040878	Oct 12, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5254040879	Oct 12, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5254040880	Oct 12, 2022 (156)
42	HUGCELL_USP	ss5453435439	Oct 12, 2022 (156)
43	HUGCELL_USP	ss5453435440	Oct 12, 2022 (156)
44	TOMMO_GENOMICS	ss5690751176	Oct 12, 2022 (156)
45	TOMMO_GENOMICS	ss5690751177	Oct 12, 2022 (156)
46	TOMMO_GENOMICS	ss5690751179	Oct 12, 2022 (156)
47	YY_MCH	ss5803727009	Oct 12, 2022 (156)
48	EVA	ss5825736868	Oct 12, 2022 (156)
49	Genetic variation in the Estonian population Submission ignored due to conflicting rows: Row 5953051 (NC_000003.11:51616782::TTTTTTTT 58/4476) Row 5953052 (NC_000003.11:51616782::TTTTTTTTT 2/4364)	-	Oct 12, 2018 (152)
50	Genetic variation in the Estonian population Submission ignored due to conflicting rows: Row 5953051 (NC_000003.11:51616782::TTTTTTTT 58/4476) Row 5953052 (NC_000003.11:51616782::TTTTTTTTT 2/4364)	-	Oct 12, 2018 (152)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 107440349 (NC_000003.12:51582766::T 23/135584) Row 107440351 (NC_000003.12:51582766::TTTTTT 3/135598) Row 107440352 (NC_000003.12:51582766::TTTTTTT 16/135584)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 17072686 (NC_000003.11:51616782::TTTTTTTT 4832/16740) Row 17072687 (NC_000003.11:51616782::TTTTTTT 6/16740) Row 17072688 (NC_000003.11:51616782::TTTTTT 1/16740)...	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 17072686 (NC_000003.11:51616782::TTTTTTTT 4832/16740) Row 17072687 (NC_000003.11:51616782::TTTTTTT 6/16740) Row 17072688 (NC_000003.11:51616782::TTTTTT 1/16740)...	-	Apr 26, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 17072686 (NC_000003.11:51616782::TTTTTTTT 4832/16740) Row 17072687 (NC_000003.11:51616782::TTTTTTT 6/16740) Row 17072688 (NC_000003.11:51616782::TTTTTT 1/16740)...	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 17072686 (NC_000003.11:51616782::TTTTTTTT 4832/16740) Row 17072687 (NC_000003.11:51616782::TTTTTTT 6/16740) Row 17072688 (NC_000003.11:51616782::TTTTTT 1/16740)...	-	Apr 26, 2021 (155)
74	14KJPN Submission ignored due to conflicting rows: Row 24588280 (NC_000003.12:51582766::TTTTTTTT 7507/28222) Row 24588281 (NC_000003.12:51582766::TTTTTTT 5/28222) Row 24588283 (NC_000003.12:51582766::TTTTTTTTT 11/28222)	-	Oct 12, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 24588280 (NC_000003.12:51582766::TTTTTTTT 7507/28222) Row 24588281 (NC_000003.12:51582766::TTTTTTT 5/28222) Row 24588283 (NC_000003.12:51582766::TTTTTTTTT 11/28222)	-	Oct 12, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 24588280 (NC_000003.12:51582766::TTTTTTTT 7507/28222) Row 24588281 (NC_000003.12:51582766::TTTTTTT 5/28222) Row 24588283 (NC_000003.12:51582766::TTTTTTTTT 11/28222)	-	Oct 12, 2022 (156)
77	TopMed	NC_000003.12 - 51582767	Apr 26, 2021 (155)
78	ALFA	NC_000003.12 - 51582767	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
401615266, ss4070893032, ss4564237711	NC_000003.12:51582766:TT:	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTT	(self)
184862877	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTT	(self)
ss3784310740	NC_000003.11:51616782:T:	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTT	(self)
ss3709205269, ss4070893031	NC_000003.12:51582766:T:	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTT	(self)
184862877	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTT	(self)
ss4070893012, ss5254040880, ss5453435439	NC_000003.12:51582766::T	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTT	(self)
184862877	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTT	(self)
ss3709205270	NC_000003.12:51582767::T	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTT	(self)
184862877	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5159103381	NC_000003.11:51616782::TTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4070893014	NC_000003.12:51582766::TTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5159103380, ss5825736868	NC_000003.11:51616782::TTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4070893015, ss5690751177	NC_000003.12:51582766::TTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
184862877	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss553020310	NC_000003.10:51591822::TTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss663413282, ss2992293903, ss3660214803, ss5159103379	NC_000003.11:51616782::TTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3064046969, ss3065879794, ss4070893016, ss5254040876, ss5453435440, ss5690751176, ss5803727009	NC_000003.12:51582766::TTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
184862877	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3709205271	NC_000003.12:51582767::TTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss83179664	NT_022517.18:51556792::TTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3660214804, ss5159103382	NC_000003.11:51616782::TTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4070893017, ss5254040878, ss5690751179	NC_000003.12:51582766::TTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
184862877	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4070893018	NC_000003.12:51582766::TTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4070893019	NC_000003.12:51582766::TTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
184862877	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4070893020, ss5254040879	NC_000003.12:51582766::TTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
184862877	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070893021	NC_000003.12:51582766::TTTTTTTTTTT… NC_000003.12:51582766::TTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070893022	NC_000003.12:51582766::TTTTTTTTTTT… NC_000003.12:51582766::TTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070893023	NC_000003.12:51582766::TTTTTTTTTTT… NC_000003.12:51582766::TTTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
184862877	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070893024, ss5254040877	NC_000003.12:51582766::TTTTTTTTTTT… NC_000003.12:51582766::TTTTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
184862877	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070893025	NC_000003.12:51582766::TTTTTTTTTTT… NC_000003.12:51582766::TTTTTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070893026	NC_000003.12:51582766::TTTTTTTTTTT… NC_000003.12:51582766::TTTTTTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070893027	NC_000003.12:51582766::TTTTTTTTTTT… NC_000003.12:51582766::TTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070893028	NC_000003.12:51582766::TTTTTTTTTTT… NC_000003.12:51582766::TTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4070893029	NC_000003.12:51582766::TTTTTTTTTTT… NC_000003.12:51582766::TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:51582766:TTTTTTTTTT:T… NC_000003.12:51582766:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs61245532

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

rs61245532