Name: rs1212446647
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.

rs1212446647

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chrX:19074563-19074579 (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)₇ / del(T)₆ / del(T)₅ / del(…
del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₈ / dup(T)₉
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₅=0.000521 (138/264690, TOPMED)
delTTT=0.01461 (265/18140, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ADGRG2 : 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	18140	TTTTTTTTTTTTTTTTT=0.98291	TTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.01461, TTTTTTTTTTTTTTTT=0.00215, TTTTTTTTTTTTTTTTTTTT=0.00033, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000	0.977532	0.00653	0.015938	32
European	Sub	13910	TTTTTTTTTTTTTTTTT=0.97771	TTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.01905, TTTTTTTTTTTTTTTT=0.00280, TTTTTTTTTTTTTTTTTTTT=0.00043, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000	0.970665	0.008526	0.020809	32
African	Sub	2782	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	112	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African American	Sub	2670	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	112	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	86	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	26	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	144	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	606	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	96	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	490	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A

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

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(T)₁₇=0.999479	del(T)₅=0.000521
Allele Frequency Aggregator	Total	Global	18140	(T)₁₇=0.98291	del(T)₇=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.01461, delTT=0.00000, delT=0.00215, dupT=0.00000, dupTT=0.00000, dupTTT=0.00033
Allele Frequency Aggregator	European	Sub	13910	(T)₁₇=0.97771	del(T)₇=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.01905, delTT=0.00000, delT=0.00280, dupT=0.00000, dupTT=0.00000, dupTTT=0.00043
Allele Frequency Aggregator	African	Sub	2782	(T)₁₇=1.0000	del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	606	(T)₁₇=1.000	del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	490	(T)₁₇=1.000	del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	144	(T)₁₇=1.000	del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Asian	Sub	112	(T)₁₇=1.000	del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	South Asian	Sub	96	(T)₁₇=1.00	del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr X	NC_000023.11:g.19074573_19074579del
GRCh38.p14 chr X	NC_000023.11:g.19074574_19074579del
GRCh38.p14 chr X	NC_000023.11:g.19074575_19074579del
GRCh38.p14 chr X	NC_000023.11:g.19074576_19074579del
GRCh38.p14 chr X	NC_000023.11:g.19074577_19074579del
GRCh38.p14 chr X	NC_000023.11:g.19074578_19074579del
GRCh38.p14 chr X	NC_000023.11:g.19074579del
GRCh38.p14 chr X	NC_000023.11:g.19074579dup
GRCh38.p14 chr X	NC_000023.11:g.19074578_19074579dup
GRCh38.p14 chr X	NC_000023.11:g.19074577_19074579dup
GRCh38.p14 chr X	NC_000023.11:g.19074576_19074579dup
GRCh38.p14 chr X	NC_000023.11:g.19074575_19074579dup
GRCh38.p14 chr X	NC_000023.11:g.19074572_19074579dup
GRCh38.p14 chr X	NC_000023.11:g.19074571_19074579dup
GRCh37.p13 chr X	NC_000023.10:g.19092691_19092697del
GRCh37.p13 chr X	NC_000023.10:g.19092692_19092697del
GRCh37.p13 chr X	NC_000023.10:g.19092693_19092697del
GRCh37.p13 chr X	NC_000023.10:g.19092694_19092697del
GRCh37.p13 chr X	NC_000023.10:g.19092695_19092697del
GRCh37.p13 chr X	NC_000023.10:g.19092696_19092697del
GRCh37.p13 chr X	NC_000023.10:g.19092697del
GRCh37.p13 chr X	NC_000023.10:g.19092697dup
GRCh37.p13 chr X	NC_000023.10:g.19092696_19092697dup
GRCh37.p13 chr X	NC_000023.10:g.19092695_19092697dup
GRCh37.p13 chr X	NC_000023.10:g.19092694_19092697dup
GRCh37.p13 chr X	NC_000023.10:g.19092693_19092697dup
GRCh37.p13 chr X	NC_000023.10:g.19092690_19092697dup
GRCh37.p13 chr X	NC_000023.10:g.19092689_19092697dup
ADGRG2 RefSeqGene	NG_021304.1:g.53069_53075del
ADGRG2 RefSeqGene	NG_021304.1:g.53070_53075del
ADGRG2 RefSeqGene	NG_021304.1:g.53071_53075del
ADGRG2 RefSeqGene	NG_021304.1:g.53072_53075del
ADGRG2 RefSeqGene	NG_021304.1:g.53073_53075del
ADGRG2 RefSeqGene	NG_021304.1:g.53074_53075del
ADGRG2 RefSeqGene	NG_021304.1:g.53075del
ADGRG2 RefSeqGene	NG_021304.1:g.53075dup
ADGRG2 RefSeqGene	NG_021304.1:g.53074_53075dup
ADGRG2 RefSeqGene	NG_021304.1:g.53073_53075dup
ADGRG2 RefSeqGene	NG_021304.1:g.53072_53075dup
ADGRG2 RefSeqGene	NG_021304.1:g.53071_53075dup
ADGRG2 RefSeqGene	NG_021304.1:g.53068_53075dup
ADGRG2 RefSeqGene	NG_021304.1:g.53067_53075dup

Gene: ADGRG2, adhesion G protein-coupled receptor G2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ADGRG2 transcript variant 1	NM_001079858.3:c.-1-5734_… NM_001079858.3:c.-1-5734_-1-5728del	N/A	Intron Variant
ADGRG2 transcript variant 2	NM_001079859.3:c.-1-5734_… NM_001079859.3:c.-1-5734_-1-5728del	N/A	Intron Variant
ADGRG2 transcript variant 3	NM_001079860.3:c.-1-5734_… NM_001079860.3:c.-1-5734_-1-5728del	N/A	Intron Variant
ADGRG2 transcript variant 5	NM_001184833.2:c.-1-5734_… NM_001184833.2:c.-1-5734_-1-5728del	N/A	Intron Variant
ADGRG2 transcript variant 6	NM_001184834.2:c.-1-5734_… NM_001184834.2:c.-1-5734_-1-5728del	N/A	Intron Variant
ADGRG2 transcript variant 7	NM_001184835.2:c.-1-5734_… NM_001184835.2:c.-1-5734_-1-5728del	N/A	Intron Variant
ADGRG2 transcript variant 8	NM_001184836.2:c.-1-5734_… NM_001184836.2:c.-1-5734_-1-5728del	N/A	Intron Variant
ADGRG2 transcript variant 9	NM_001184837.2:c.-1-5734_… NM_001184837.2:c.-1-5734_-1-5728del	N/A	Intron Variant
ADGRG2 transcript variant 4	NM_005756.4:c.-1-5734_-1-… NM_005756.4:c.-1-5734_-1-5728del	N/A	Intron Variant
ADGRG2 transcript variant X2	XM_006724455.3:c.-1-5734_… XM_006724455.3:c.-1-5734_-1-5728del	N/A	Intron Variant
ADGRG2 transcript variant X6	XM_011545434.2:c.-1-5734_… XM_011545434.2:c.-1-5734_-1-5728del	N/A	Intron Variant
ADGRG2 transcript variant X3	XM_011545435.3:c.-1-5734_… XM_011545435.3:c.-1-5734_-1-5728del	N/A	Intron Variant
ADGRG2 transcript variant X1	XM_047441755.1:c.114-5734… XM_047441755.1:c.114-5734_114-5728del	N/A	Intron Variant
ADGRG2 transcript variant X4	XM_047441756.1:c.-1-5734_… XM_047441756.1:c.-1-5734_-1-5728del	N/A	Intron Variant
ADGRG2 transcript variant X5	XM_047441757.1:c.-1-5734_… XM_047441757.1:c.-1-5734_-1-5728del	N/A	Intron Variant
ADGRG2 transcript variant X7	XM_047441758.1:c.-1-5734_… XM_047441758.1:c.-1-5734_-1-5728del	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)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₈	dup(T)₉
GRCh38.p14 chr X	NC_000023.11:g.19074563_19074579=	NC_000023.11:g.19074573_19074579del	NC_000023.11:g.19074574_19074579del	NC_000023.11:g.19074575_19074579del	NC_000023.11:g.19074576_19074579del	NC_000023.11:g.19074577_19074579del	NC_000023.11:g.19074578_19074579del	NC_000023.11:g.19074579del	NC_000023.11:g.19074579dup	NC_000023.11:g.19074578_19074579dup	NC_000023.11:g.19074577_19074579dup	NC_000023.11:g.19074576_19074579dup	NC_000023.11:g.19074575_19074579dup	NC_000023.11:g.19074572_19074579dup	NC_000023.11:g.19074571_19074579dup
GRCh37.p13 chr X	NC_000023.10:g.19092681_19092697=	NC_000023.10:g.19092691_19092697del	NC_000023.10:g.19092692_19092697del	NC_000023.10:g.19092693_19092697del	NC_000023.10:g.19092694_19092697del	NC_000023.10:g.19092695_19092697del	NC_000023.10:g.19092696_19092697del	NC_000023.10:g.19092697del	NC_000023.10:g.19092697dup	NC_000023.10:g.19092696_19092697dup	NC_000023.10:g.19092695_19092697dup	NC_000023.10:g.19092694_19092697dup	NC_000023.10:g.19092693_19092697dup	NC_000023.10:g.19092690_19092697dup	NC_000023.10:g.19092689_19092697dup
ADGRG2 RefSeqGene	NG_021304.1:g.53059_53075=	NG_021304.1:g.53069_53075del	NG_021304.1:g.53070_53075del	NG_021304.1:g.53071_53075del	NG_021304.1:g.53072_53075del	NG_021304.1:g.53073_53075del	NG_021304.1:g.53074_53075del	NG_021304.1:g.53075del	NG_021304.1:g.53075dup	NG_021304.1:g.53074_53075dup	NG_021304.1:g.53073_53075dup	NG_021304.1:g.53072_53075dup	NG_021304.1:g.53071_53075dup	NG_021304.1:g.53068_53075dup	NG_021304.1:g.53067_53075dup
ADGRG2 transcript variant 1	NM_001079858.2:c.-1-5728=	NM_001079858.2:c.-1-5734_-1-5728del	NM_001079858.2:c.-1-5733_-1-5728del	NM_001079858.2:c.-1-5732_-1-5728del	NM_001079858.2:c.-1-5731_-1-5728del	NM_001079858.2:c.-1-5730_-1-5728del	NM_001079858.2:c.-1-5729_-1-5728del	NM_001079858.2:c.-1-5728del	NM_001079858.2:c.-1-5728dup	NM_001079858.2:c.-1-5729_-1-5728dup	NM_001079858.2:c.-1-5730_-1-5728dup	NM_001079858.2:c.-1-5731_-1-5728dup	NM_001079858.2:c.-1-5732_-1-5728dup	NM_001079858.2:c.-1-5735_-1-5728dup	NM_001079858.2:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 1	NM_001079858.3:c.-1-5728=	NM_001079858.3:c.-1-5734_-1-5728del	NM_001079858.3:c.-1-5733_-1-5728del	NM_001079858.3:c.-1-5732_-1-5728del	NM_001079858.3:c.-1-5731_-1-5728del	NM_001079858.3:c.-1-5730_-1-5728del	NM_001079858.3:c.-1-5729_-1-5728del	NM_001079858.3:c.-1-5728del	NM_001079858.3:c.-1-5728dup	NM_001079858.3:c.-1-5729_-1-5728dup	NM_001079858.3:c.-1-5730_-1-5728dup	NM_001079858.3:c.-1-5731_-1-5728dup	NM_001079858.3:c.-1-5732_-1-5728dup	NM_001079858.3:c.-1-5735_-1-5728dup	NM_001079858.3:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 2	NM_001079859.2:c.-1-5728=	NM_001079859.2:c.-1-5734_-1-5728del	NM_001079859.2:c.-1-5733_-1-5728del	NM_001079859.2:c.-1-5732_-1-5728del	NM_001079859.2:c.-1-5731_-1-5728del	NM_001079859.2:c.-1-5730_-1-5728del	NM_001079859.2:c.-1-5729_-1-5728del	NM_001079859.2:c.-1-5728del	NM_001079859.2:c.-1-5728dup	NM_001079859.2:c.-1-5729_-1-5728dup	NM_001079859.2:c.-1-5730_-1-5728dup	NM_001079859.2:c.-1-5731_-1-5728dup	NM_001079859.2:c.-1-5732_-1-5728dup	NM_001079859.2:c.-1-5735_-1-5728dup	NM_001079859.2:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 2	NM_001079859.3:c.-1-5728=	NM_001079859.3:c.-1-5734_-1-5728del	NM_001079859.3:c.-1-5733_-1-5728del	NM_001079859.3:c.-1-5732_-1-5728del	NM_001079859.3:c.-1-5731_-1-5728del	NM_001079859.3:c.-1-5730_-1-5728del	NM_001079859.3:c.-1-5729_-1-5728del	NM_001079859.3:c.-1-5728del	NM_001079859.3:c.-1-5728dup	NM_001079859.3:c.-1-5729_-1-5728dup	NM_001079859.3:c.-1-5730_-1-5728dup	NM_001079859.3:c.-1-5731_-1-5728dup	NM_001079859.3:c.-1-5732_-1-5728dup	NM_001079859.3:c.-1-5735_-1-5728dup	NM_001079859.3:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 3	NM_001079860.2:c.-1-5728=	NM_001079860.2:c.-1-5734_-1-5728del	NM_001079860.2:c.-1-5733_-1-5728del	NM_001079860.2:c.-1-5732_-1-5728del	NM_001079860.2:c.-1-5731_-1-5728del	NM_001079860.2:c.-1-5730_-1-5728del	NM_001079860.2:c.-1-5729_-1-5728del	NM_001079860.2:c.-1-5728del	NM_001079860.2:c.-1-5728dup	NM_001079860.2:c.-1-5729_-1-5728dup	NM_001079860.2:c.-1-5730_-1-5728dup	NM_001079860.2:c.-1-5731_-1-5728dup	NM_001079860.2:c.-1-5732_-1-5728dup	NM_001079860.2:c.-1-5735_-1-5728dup	NM_001079860.2:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 3	NM_001079860.3:c.-1-5728=	NM_001079860.3:c.-1-5734_-1-5728del	NM_001079860.3:c.-1-5733_-1-5728del	NM_001079860.3:c.-1-5732_-1-5728del	NM_001079860.3:c.-1-5731_-1-5728del	NM_001079860.3:c.-1-5730_-1-5728del	NM_001079860.3:c.-1-5729_-1-5728del	NM_001079860.3:c.-1-5728del	NM_001079860.3:c.-1-5728dup	NM_001079860.3:c.-1-5729_-1-5728dup	NM_001079860.3:c.-1-5730_-1-5728dup	NM_001079860.3:c.-1-5731_-1-5728dup	NM_001079860.3:c.-1-5732_-1-5728dup	NM_001079860.3:c.-1-5735_-1-5728dup	NM_001079860.3:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 5	NM_001184833.1:c.-1-5728=	NM_001184833.1:c.-1-5734_-1-5728del	NM_001184833.1:c.-1-5733_-1-5728del	NM_001184833.1:c.-1-5732_-1-5728del	NM_001184833.1:c.-1-5731_-1-5728del	NM_001184833.1:c.-1-5730_-1-5728del	NM_001184833.1:c.-1-5729_-1-5728del	NM_001184833.1:c.-1-5728del	NM_001184833.1:c.-1-5728dup	NM_001184833.1:c.-1-5729_-1-5728dup	NM_001184833.1:c.-1-5730_-1-5728dup	NM_001184833.1:c.-1-5731_-1-5728dup	NM_001184833.1:c.-1-5732_-1-5728dup	NM_001184833.1:c.-1-5735_-1-5728dup	NM_001184833.1:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 5	NM_001184833.2:c.-1-5728=	NM_001184833.2:c.-1-5734_-1-5728del	NM_001184833.2:c.-1-5733_-1-5728del	NM_001184833.2:c.-1-5732_-1-5728del	NM_001184833.2:c.-1-5731_-1-5728del	NM_001184833.2:c.-1-5730_-1-5728del	NM_001184833.2:c.-1-5729_-1-5728del	NM_001184833.2:c.-1-5728del	NM_001184833.2:c.-1-5728dup	NM_001184833.2:c.-1-5729_-1-5728dup	NM_001184833.2:c.-1-5730_-1-5728dup	NM_001184833.2:c.-1-5731_-1-5728dup	NM_001184833.2:c.-1-5732_-1-5728dup	NM_001184833.2:c.-1-5735_-1-5728dup	NM_001184833.2:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 6	NM_001184834.1:c.-1-5728=	NM_001184834.1:c.-1-5734_-1-5728del	NM_001184834.1:c.-1-5733_-1-5728del	NM_001184834.1:c.-1-5732_-1-5728del	NM_001184834.1:c.-1-5731_-1-5728del	NM_001184834.1:c.-1-5730_-1-5728del	NM_001184834.1:c.-1-5729_-1-5728del	NM_001184834.1:c.-1-5728del	NM_001184834.1:c.-1-5728dup	NM_001184834.1:c.-1-5729_-1-5728dup	NM_001184834.1:c.-1-5730_-1-5728dup	NM_001184834.1:c.-1-5731_-1-5728dup	NM_001184834.1:c.-1-5732_-1-5728dup	NM_001184834.1:c.-1-5735_-1-5728dup	NM_001184834.1:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 6	NM_001184834.2:c.-1-5728=	NM_001184834.2:c.-1-5734_-1-5728del	NM_001184834.2:c.-1-5733_-1-5728del	NM_001184834.2:c.-1-5732_-1-5728del	NM_001184834.2:c.-1-5731_-1-5728del	NM_001184834.2:c.-1-5730_-1-5728del	NM_001184834.2:c.-1-5729_-1-5728del	NM_001184834.2:c.-1-5728del	NM_001184834.2:c.-1-5728dup	NM_001184834.2:c.-1-5729_-1-5728dup	NM_001184834.2:c.-1-5730_-1-5728dup	NM_001184834.2:c.-1-5731_-1-5728dup	NM_001184834.2:c.-1-5732_-1-5728dup	NM_001184834.2:c.-1-5735_-1-5728dup	NM_001184834.2:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 7	NM_001184835.1:c.-1-5728=	NM_001184835.1:c.-1-5734_-1-5728del	NM_001184835.1:c.-1-5733_-1-5728del	NM_001184835.1:c.-1-5732_-1-5728del	NM_001184835.1:c.-1-5731_-1-5728del	NM_001184835.1:c.-1-5730_-1-5728del	NM_001184835.1:c.-1-5729_-1-5728del	NM_001184835.1:c.-1-5728del	NM_001184835.1:c.-1-5728dup	NM_001184835.1:c.-1-5729_-1-5728dup	NM_001184835.1:c.-1-5730_-1-5728dup	NM_001184835.1:c.-1-5731_-1-5728dup	NM_001184835.1:c.-1-5732_-1-5728dup	NM_001184835.1:c.-1-5735_-1-5728dup	NM_001184835.1:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 7	NM_001184835.2:c.-1-5728=	NM_001184835.2:c.-1-5734_-1-5728del	NM_001184835.2:c.-1-5733_-1-5728del	NM_001184835.2:c.-1-5732_-1-5728del	NM_001184835.2:c.-1-5731_-1-5728del	NM_001184835.2:c.-1-5730_-1-5728del	NM_001184835.2:c.-1-5729_-1-5728del	NM_001184835.2:c.-1-5728del	NM_001184835.2:c.-1-5728dup	NM_001184835.2:c.-1-5729_-1-5728dup	NM_001184835.2:c.-1-5730_-1-5728dup	NM_001184835.2:c.-1-5731_-1-5728dup	NM_001184835.2:c.-1-5732_-1-5728dup	NM_001184835.2:c.-1-5735_-1-5728dup	NM_001184835.2:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 8	NM_001184836.1:c.-1-5728=	NM_001184836.1:c.-1-5734_-1-5728del	NM_001184836.1:c.-1-5733_-1-5728del	NM_001184836.1:c.-1-5732_-1-5728del	NM_001184836.1:c.-1-5731_-1-5728del	NM_001184836.1:c.-1-5730_-1-5728del	NM_001184836.1:c.-1-5729_-1-5728del	NM_001184836.1:c.-1-5728del	NM_001184836.1:c.-1-5728dup	NM_001184836.1:c.-1-5729_-1-5728dup	NM_001184836.1:c.-1-5730_-1-5728dup	NM_001184836.1:c.-1-5731_-1-5728dup	NM_001184836.1:c.-1-5732_-1-5728dup	NM_001184836.1:c.-1-5735_-1-5728dup	NM_001184836.1:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 8	NM_001184836.2:c.-1-5728=	NM_001184836.2:c.-1-5734_-1-5728del	NM_001184836.2:c.-1-5733_-1-5728del	NM_001184836.2:c.-1-5732_-1-5728del	NM_001184836.2:c.-1-5731_-1-5728del	NM_001184836.2:c.-1-5730_-1-5728del	NM_001184836.2:c.-1-5729_-1-5728del	NM_001184836.2:c.-1-5728del	NM_001184836.2:c.-1-5728dup	NM_001184836.2:c.-1-5729_-1-5728dup	NM_001184836.2:c.-1-5730_-1-5728dup	NM_001184836.2:c.-1-5731_-1-5728dup	NM_001184836.2:c.-1-5732_-1-5728dup	NM_001184836.2:c.-1-5735_-1-5728dup	NM_001184836.2:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 9	NM_001184837.1:c.-1-5728=	NM_001184837.1:c.-1-5734_-1-5728del	NM_001184837.1:c.-1-5733_-1-5728del	NM_001184837.1:c.-1-5732_-1-5728del	NM_001184837.1:c.-1-5731_-1-5728del	NM_001184837.1:c.-1-5730_-1-5728del	NM_001184837.1:c.-1-5729_-1-5728del	NM_001184837.1:c.-1-5728del	NM_001184837.1:c.-1-5728dup	NM_001184837.1:c.-1-5729_-1-5728dup	NM_001184837.1:c.-1-5730_-1-5728dup	NM_001184837.1:c.-1-5731_-1-5728dup	NM_001184837.1:c.-1-5732_-1-5728dup	NM_001184837.1:c.-1-5735_-1-5728dup	NM_001184837.1:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 9	NM_001184837.2:c.-1-5728=	NM_001184837.2:c.-1-5734_-1-5728del	NM_001184837.2:c.-1-5733_-1-5728del	NM_001184837.2:c.-1-5732_-1-5728del	NM_001184837.2:c.-1-5731_-1-5728del	NM_001184837.2:c.-1-5730_-1-5728del	NM_001184837.2:c.-1-5729_-1-5728del	NM_001184837.2:c.-1-5728del	NM_001184837.2:c.-1-5728dup	NM_001184837.2:c.-1-5729_-1-5728dup	NM_001184837.2:c.-1-5730_-1-5728dup	NM_001184837.2:c.-1-5731_-1-5728dup	NM_001184837.2:c.-1-5732_-1-5728dup	NM_001184837.2:c.-1-5735_-1-5728dup	NM_001184837.2:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 4	NM_005756.3:c.-1-5728=	NM_005756.3:c.-1-5734_-1-5728del	NM_005756.3:c.-1-5733_-1-5728del	NM_005756.3:c.-1-5732_-1-5728del	NM_005756.3:c.-1-5731_-1-5728del	NM_005756.3:c.-1-5730_-1-5728del	NM_005756.3:c.-1-5729_-1-5728del	NM_005756.3:c.-1-5728del	NM_005756.3:c.-1-5728dup	NM_005756.3:c.-1-5729_-1-5728dup	NM_005756.3:c.-1-5730_-1-5728dup	NM_005756.3:c.-1-5731_-1-5728dup	NM_005756.3:c.-1-5732_-1-5728dup	NM_005756.3:c.-1-5735_-1-5728dup	NM_005756.3:c.-1-5736_-1-5728dup
ADGRG2 transcript variant 4	NM_005756.4:c.-1-5728=	NM_005756.4:c.-1-5734_-1-5728del	NM_005756.4:c.-1-5733_-1-5728del	NM_005756.4:c.-1-5732_-1-5728del	NM_005756.4:c.-1-5731_-1-5728del	NM_005756.4:c.-1-5730_-1-5728del	NM_005756.4:c.-1-5729_-1-5728del	NM_005756.4:c.-1-5728del	NM_005756.4:c.-1-5728dup	NM_005756.4:c.-1-5729_-1-5728dup	NM_005756.4:c.-1-5730_-1-5728dup	NM_005756.4:c.-1-5731_-1-5728dup	NM_005756.4:c.-1-5732_-1-5728dup	NM_005756.4:c.-1-5735_-1-5728dup	NM_005756.4:c.-1-5736_-1-5728dup
ADGRG2 transcript variant X2	XM_006724455.3:c.-1-5728=	XM_006724455.3:c.-1-5734_-1-5728del	XM_006724455.3:c.-1-5733_-1-5728del	XM_006724455.3:c.-1-5732_-1-5728del	XM_006724455.3:c.-1-5731_-1-5728del	XM_006724455.3:c.-1-5730_-1-5728del	XM_006724455.3:c.-1-5729_-1-5728del	XM_006724455.3:c.-1-5728del	XM_006724455.3:c.-1-5728dup	XM_006724455.3:c.-1-5729_-1-5728dup	XM_006724455.3:c.-1-5730_-1-5728dup	XM_006724455.3:c.-1-5731_-1-5728dup	XM_006724455.3:c.-1-5732_-1-5728dup	XM_006724455.3:c.-1-5735_-1-5728dup	XM_006724455.3:c.-1-5736_-1-5728dup
ADGRG2 transcript variant X6	XM_011545434.2:c.-1-5728=	XM_011545434.2:c.-1-5734_-1-5728del	XM_011545434.2:c.-1-5733_-1-5728del	XM_011545434.2:c.-1-5732_-1-5728del	XM_011545434.2:c.-1-5731_-1-5728del	XM_011545434.2:c.-1-5730_-1-5728del	XM_011545434.2:c.-1-5729_-1-5728del	XM_011545434.2:c.-1-5728del	XM_011545434.2:c.-1-5728dup	XM_011545434.2:c.-1-5729_-1-5728dup	XM_011545434.2:c.-1-5730_-1-5728dup	XM_011545434.2:c.-1-5731_-1-5728dup	XM_011545434.2:c.-1-5732_-1-5728dup	XM_011545434.2:c.-1-5735_-1-5728dup	XM_011545434.2:c.-1-5736_-1-5728dup
ADGRG2 transcript variant X3	XM_011545435.3:c.-1-5728=	XM_011545435.3:c.-1-5734_-1-5728del	XM_011545435.3:c.-1-5733_-1-5728del	XM_011545435.3:c.-1-5732_-1-5728del	XM_011545435.3:c.-1-5731_-1-5728del	XM_011545435.3:c.-1-5730_-1-5728del	XM_011545435.3:c.-1-5729_-1-5728del	XM_011545435.3:c.-1-5728del	XM_011545435.3:c.-1-5728dup	XM_011545435.3:c.-1-5729_-1-5728dup	XM_011545435.3:c.-1-5730_-1-5728dup	XM_011545435.3:c.-1-5731_-1-5728dup	XM_011545435.3:c.-1-5732_-1-5728dup	XM_011545435.3:c.-1-5735_-1-5728dup	XM_011545435.3:c.-1-5736_-1-5728dup
ADGRG2 transcript variant X1	XM_047441755.1:c.114-5728=	XM_047441755.1:c.114-5734_114-5728del	XM_047441755.1:c.114-5733_114-5728del	XM_047441755.1:c.114-5732_114-5728del	XM_047441755.1:c.114-5731_114-5728del	XM_047441755.1:c.114-5730_114-5728del	XM_047441755.1:c.114-5729_114-5728del	XM_047441755.1:c.114-5728del	XM_047441755.1:c.114-5728dup	XM_047441755.1:c.114-5729_114-5728dup	XM_047441755.1:c.114-5730_114-5728dup	XM_047441755.1:c.114-5731_114-5728dup	XM_047441755.1:c.114-5732_114-5728dup	XM_047441755.1:c.114-5735_114-5728dup	XM_047441755.1:c.114-5736_114-5728dup
ADGRG2 transcript variant X4	XM_047441756.1:c.-1-5728=	XM_047441756.1:c.-1-5734_-1-5728del	XM_047441756.1:c.-1-5733_-1-5728del	XM_047441756.1:c.-1-5732_-1-5728del	XM_047441756.1:c.-1-5731_-1-5728del	XM_047441756.1:c.-1-5730_-1-5728del	XM_047441756.1:c.-1-5729_-1-5728del	XM_047441756.1:c.-1-5728del	XM_047441756.1:c.-1-5728dup	XM_047441756.1:c.-1-5729_-1-5728dup	XM_047441756.1:c.-1-5730_-1-5728dup	XM_047441756.1:c.-1-5731_-1-5728dup	XM_047441756.1:c.-1-5732_-1-5728dup	XM_047441756.1:c.-1-5735_-1-5728dup	XM_047441756.1:c.-1-5736_-1-5728dup
ADGRG2 transcript variant X5	XM_047441757.1:c.-1-5728=	XM_047441757.1:c.-1-5734_-1-5728del	XM_047441757.1:c.-1-5733_-1-5728del	XM_047441757.1:c.-1-5732_-1-5728del	XM_047441757.1:c.-1-5731_-1-5728del	XM_047441757.1:c.-1-5730_-1-5728del	XM_047441757.1:c.-1-5729_-1-5728del	XM_047441757.1:c.-1-5728del	XM_047441757.1:c.-1-5728dup	XM_047441757.1:c.-1-5729_-1-5728dup	XM_047441757.1:c.-1-5730_-1-5728dup	XM_047441757.1:c.-1-5731_-1-5728dup	XM_047441757.1:c.-1-5732_-1-5728dup	XM_047441757.1:c.-1-5735_-1-5728dup	XM_047441757.1:c.-1-5736_-1-5728dup
ADGRG2 transcript variant X7	XM_047441758.1:c.-1-5728=	XM_047441758.1:c.-1-5734_-1-5728del	XM_047441758.1:c.-1-5733_-1-5728del	XM_047441758.1:c.-1-5732_-1-5728del	XM_047441758.1:c.-1-5731_-1-5728del	XM_047441758.1:c.-1-5730_-1-5728del	XM_047441758.1:c.-1-5729_-1-5728del	XM_047441758.1:c.-1-5728del	XM_047441758.1:c.-1-5728dup	XM_047441758.1:c.-1-5729_-1-5728dup	XM_047441758.1:c.-1-5730_-1-5728dup	XM_047441758.1:c.-1-5731_-1-5728dup	XM_047441758.1:c.-1-5732_-1-5728dup	XM_047441758.1:c.-1-5735_-1-5728dup	XM_047441758.1:c.-1-5736_-1-5728dup

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#.

27 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3019698552	Nov 08, 2017 (151)
2	EVA	ss3836107652	Apr 27, 2020 (154)
3	GNOMAD	ss4368639244	Apr 27, 2021 (155)
4	GNOMAD	ss4368639245	Apr 27, 2021 (155)
5	GNOMAD	ss4368639246	Apr 27, 2021 (155)
6	GNOMAD	ss4368639247	Apr 27, 2021 (155)
7	GNOMAD	ss4368639248	Apr 27, 2021 (155)
8	GNOMAD	ss4368639249	Apr 27, 2021 (155)
9	GNOMAD	ss4368639250	Apr 27, 2021 (155)
10	GNOMAD	ss4368639251	Apr 27, 2021 (155)
11	GNOMAD	ss4368639252	Apr 27, 2021 (155)
12	GNOMAD	ss4368639253	Apr 27, 2021 (155)
13	GNOMAD	ss4368639254	Apr 27, 2021 (155)
14	TOPMED	ss5116956526	Apr 27, 2021 (155)
15	TOMMO_GENOMICS	ss5233726710	Apr 27, 2021 (155)
16	TOMMO_GENOMICS	ss5233726711	Apr 27, 2021 (155)
17	TOMMO_GENOMICS	ss5233726712	Apr 27, 2021 (155)
18	1000G_HIGH_COVERAGE	ss5311950739	Oct 16, 2022 (156)
19	1000G_HIGH_COVERAGE	ss5311950740	Oct 16, 2022 (156)
20	1000G_HIGH_COVERAGE	ss5311950741	Oct 16, 2022 (156)
21	HUGCELL_USP	ss5503682586	Oct 16, 2022 (156)
22	HUGCELL_USP	ss5503682587	Oct 16, 2022 (156)
23	HUGCELL_USP	ss5503682588	Oct 16, 2022 (156)
24	HUGCELL_USP	ss5503682589	Oct 16, 2022 (156)
25	TOMMO_GENOMICS	ss5795212821	Oct 16, 2022 (156)
26	TOMMO_GENOMICS	ss5795212822	Oct 16, 2022 (156)
27	TOMMO_GENOMICS	ss5795212823	Oct 16, 2022 (156)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576300981 (NC_000023.11:19074562::T 479/62758) Row 576300982 (NC_000023.11:19074562::TT 11/62768) Row 576300983 (NC_000023.11:19074562::TTT 8/62770)...	-	Apr 27, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576300981 (NC_000023.11:19074562::T 479/62758) Row 576300982 (NC_000023.11:19074562::TT 11/62768) Row 576300983 (NC_000023.11:19074562::TTT 8/62770)...	-	Apr 27, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576300981 (NC_000023.11:19074562::T 479/62758) Row 576300982 (NC_000023.11:19074562::TT 11/62768) Row 576300983 (NC_000023.11:19074562::TTT 8/62770)...	-	Apr 27, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576300981 (NC_000023.11:19074562::T 479/62758) Row 576300982 (NC_000023.11:19074562::TT 11/62768) Row 576300983 (NC_000023.11:19074562::TTT 8/62770)...	-	Apr 27, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576300981 (NC_000023.11:19074562::T 479/62758) Row 576300982 (NC_000023.11:19074562::TT 11/62768) Row 576300983 (NC_000023.11:19074562::TTT 8/62770)...	-	Apr 27, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576300981 (NC_000023.11:19074562::T 479/62758) Row 576300982 (NC_000023.11:19074562::TT 11/62768) Row 576300983 (NC_000023.11:19074562::TTT 8/62770)...	-	Apr 27, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576300981 (NC_000023.11:19074562::T 479/62758) Row 576300982 (NC_000023.11:19074562::TT 11/62768) Row 576300983 (NC_000023.11:19074562::TTT 8/62770)...	-	Apr 27, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576300981 (NC_000023.11:19074562::T 479/62758) Row 576300982 (NC_000023.11:19074562::TT 11/62768) Row 576300983 (NC_000023.11:19074562::TTT 8/62770)...	-	Apr 27, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576300981 (NC_000023.11:19074562::T 479/62758) Row 576300982 (NC_000023.11:19074562::TT 11/62768) Row 576300983 (NC_000023.11:19074562::TTT 8/62770)...	-	Apr 27, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576300981 (NC_000023.11:19074562::T 479/62758) Row 576300982 (NC_000023.11:19074562::TT 11/62768) Row 576300983 (NC_000023.11:19074562::TTT 8/62770)...	-	Apr 27, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 576300981 (NC_000023.11:19074562::T 479/62758) Row 576300982 (NC_000023.11:19074562::TT 11/62768) Row 576300983 (NC_000023.11:19074562::TTT 8/62770)...	-	Apr 27, 2021 (155)
39	8.3KJPN Submission ignored due to conflicting rows: Row 91696017 (NC_000023.10:19092680:TTT: 1898/12560) Row 91696018 (NC_000023.10:19092680::T 21/12560) Row 91696019 (NC_000023.10:19092680::TTTTTTTTT 3/12560)	-	Apr 27, 2021 (155)
40	8.3KJPN Submission ignored due to conflicting rows: Row 91696017 (NC_000023.10:19092680:TTT: 1898/12560) Row 91696018 (NC_000023.10:19092680::T 21/12560) Row 91696019 (NC_000023.10:19092680::TTTTTTTTT 3/12560)	-	Apr 27, 2021 (155)
41	8.3KJPN Submission ignored due to conflicting rows: Row 91696017 (NC_000023.10:19092680:TTT: 1898/12560) Row 91696018 (NC_000023.10:19092680::T 21/12560) Row 91696019 (NC_000023.10:19092680::TTTTTTTTT 3/12560)	-	Apr 27, 2021 (155)
42	14KJPN Submission ignored due to conflicting rows: Row 129049925 (NC_000023.11:19074562:TTT: 2858/20436) Row 129049926 (NC_000023.11:19074562::T 28/20436) Row 129049927 (NC_000023.11:19074562:T: 14/20436)	-	Oct 16, 2022 (156)
43	14KJPN Submission ignored due to conflicting rows: Row 129049925 (NC_000023.11:19074562:TTT: 2858/20436) Row 129049926 (NC_000023.11:19074562::T 28/20436) Row 129049927 (NC_000023.11:19074562:T: 14/20436)	-	Oct 16, 2022 (156)
44	14KJPN Submission ignored due to conflicting rows: Row 129049925 (NC_000023.11:19074562:TTT: 2858/20436) Row 129049926 (NC_000023.11:19074562::T 28/20436) Row 129049927 (NC_000023.11:19074562:T: 14/20436)	-	Oct 16, 2022 (156)
45	TopMed	NC_000023.11 - 19074563	Apr 27, 2021 (155)
46	ALFA	NC_000023.11 - 19074563	Apr 27, 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
11651268029	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4368639254	NC_000023.11:19074562:TTTTTT:	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
680562883, ss4368639253, ss5116956526, ss5503682589	NC_000023.11:19074562:TTTTT:	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
11651268029	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4368639252	NC_000023.11:19074562:TTTT:	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
11651268029	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3019698552, ss5233726710	NC_000023.10:19092680:TTT:	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5503682587, ss5795212821	NC_000023.11:19074562:TTT:	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
11651268029	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4368639251, ss5311950741	NC_000023.11:19074562:TT:	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
11651268029	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4368639250, ss5311950739, ss5503682588, ss5795212823	NC_000023.11:19074562:T:	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
11651268029	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3836107652, ss5233726711	NC_000023.10:19092680::T	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4368639244, ss5311950740, ss5503682586, ss5795212822	NC_000023.11:19074562::T	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
11651268029	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4368639245	NC_000023.11:19074562::TT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
11651268029	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4368639246	NC_000023.11:19074562::TTT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
11651268029	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4368639247	NC_000023.11:19074562::TTTT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4368639248	NC_000023.11:19074562::TTTTT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4368639249	NC_000023.11:19074562::TTTTTTTT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5233726712	NC_000023.10:19092680::TTTTTTTTT	NC_000023.11:19074562:TTTTTTTTTTTT… NC_000023.11:19074562:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs1212446647

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

rs1212446647