Name: rs1229164919
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.

rs1229164919

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chrX:72943773-72943804 (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(GAG)₇ / del(GAG)₄ / del(GAG)₃ …
del(GAG)₇ / del(GAG)₄ / del(GAG)₃ / del(GAG)₂ / delGAG / dupGAG / dup(GAG)₂ / dup(GAG)₃
Variation Type: Indel Insertion and Deletion
Frequency: del(GAG)₇=0.00000 (0/11158, ALFA)
del(GAG)₄=0.00000 (0/11158, ALFA)
del(GAG)₃=0.00000 (0/11158, ALFA) (+ 5 more)
del(GAG)₂=0.00000 (0/11158, ALFA)
delGAG=0.00000 (0/11158, ALFA)
dupGAG=0.00000 (0/11158, ALFA)
dup(GAG)₂=0.00000 (0/11158, ALFA)
dup(GAG)₃=0.00000 (0/11158, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DMRTC1 : Non Coding Transcript Variant
FAM226A : 2KB Upstream 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	HWEP
Total	Global	11158	AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=1.00000	AGGAGGAGGAG=0.00000, AGGAGGAGGAGGAGGAGGAG=0.00000, AGGAGGAGGAGGAGGAGGAGGAG=0.00000, AGGAGGAGGAGGAGGAGGAGGAGGAG=0.00000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00000	1.0	N/A
European	Sub	7242	AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=1.0000	AGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000	1.0	N/A
African	Sub	2588	AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=1.0000	AGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000	1.0	N/A
African Others	Sub	100	AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=1.00	AGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00	1.0	N/A
African American	Sub	2488	AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=1.0000	AGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.0000	1.0	N/A
Asian	Sub	102	AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=1.000	AGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000	1.0	N/A
East Asian	Sub	80	AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=1.00	AGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00	1.0	N/A
Other Asian	Sub	22	AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=1.00	AGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00	1.0	N/A
Latin American 1	Sub	138	AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=1.000	AGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000	1.0	N/A
Latin American 2	Sub	558	AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=1.000	AGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000	1.0	N/A
South Asian	Sub	86	AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=1.00	AGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.00	1.0	N/A
Other	Sub	444	AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=1.000	AGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000, AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG=0.000	1.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	11158	(AGG)₁₀AG=1.00000	del(GAG)₇=0.00000, del(GAG)₄=0.00000, del(GAG)₃=0.00000, del(GAG)₂=0.00000, delGAG=0.00000, dupGAG=0.00000, dup(GAG)₂=0.00000, dup(GAG)₃=0.00000
Allele Frequency Aggregator	European	Sub	7242	(AGG)₁₀AG=1.0000	del(GAG)₇=0.0000, del(GAG)₄=0.0000, del(GAG)₃=0.0000, del(GAG)₂=0.0000, delGAG=0.0000, dupGAG=0.0000, dup(GAG)₂=0.0000, dup(GAG)₃=0.0000
Allele Frequency Aggregator	African	Sub	2588	(AGG)₁₀AG=1.0000	del(GAG)₇=0.0000, del(GAG)₄=0.0000, del(GAG)₃=0.0000, del(GAG)₂=0.0000, delGAG=0.0000, dupGAG=0.0000, dup(GAG)₂=0.0000, dup(GAG)₃=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	558	(AGG)₁₀AG=1.000	del(GAG)₇=0.000, del(GAG)₄=0.000, del(GAG)₃=0.000, del(GAG)₂=0.000, delGAG=0.000, dupGAG=0.000, dup(GAG)₂=0.000, dup(GAG)₃=0.000
Allele Frequency Aggregator	Other	Sub	444	(AGG)₁₀AG=1.000	del(GAG)₇=0.000, del(GAG)₄=0.000, del(GAG)₃=0.000, del(GAG)₂=0.000, delGAG=0.000, dupGAG=0.000, dup(GAG)₂=0.000, dup(GAG)₃=0.000
Allele Frequency Aggregator	Latin American 1	Sub	138	(AGG)₁₀AG=1.000	del(GAG)₇=0.000, del(GAG)₄=0.000, del(GAG)₃=0.000, del(GAG)₂=0.000, delGAG=0.000, dupGAG=0.000, dup(GAG)₂=0.000, dup(GAG)₃=0.000
Allele Frequency Aggregator	Asian	Sub	102	(AGG)₁₀AG=1.000	del(GAG)₇=0.000, del(GAG)₄=0.000, del(GAG)₃=0.000, del(GAG)₂=0.000, delGAG=0.000, dupGAG=0.000, dup(GAG)₂=0.000, dup(GAG)₃=0.000
Allele Frequency Aggregator	South Asian	Sub	86	(AGG)₁₀AG=1.00	del(GAG)₇=0.00, del(GAG)₄=0.00, del(GAG)₃=0.00, del(GAG)₂=0.00, delGAG=0.00, dupGAG=0.00, dup(GAG)₂=0.00, dup(GAG)₃=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.72943775GAG[3]
GRCh38.p14 chr X	NC_000023.11:g.72943775GAG[6]
GRCh38.p14 chr X	NC_000023.11:g.72943775GAG[7]
GRCh38.p14 chr X	NC_000023.11:g.72943775GAG[8]
GRCh38.p14 chr X	NC_000023.11:g.72943775GAG[9]
GRCh38.p14 chr X	NC_000023.11:g.72943775GAG[11]
GRCh38.p14 chr X	NC_000023.11:g.72943775GAG[12]
GRCh38.p14 chr X	NC_000023.11:g.72943775GAG[13]
GRCh37.p13 chr X fix patch HG1438_PATCH	NW_004070882.1:g.632792GAG[3]
GRCh37.p13 chr X fix patch HG1438_PATCH	NW_004070882.1:g.632792GAG[6]
GRCh37.p13 chr X fix patch HG1438_PATCH	NW_004070882.1:g.632792GAG[7]
GRCh37.p13 chr X fix patch HG1438_PATCH	NW_004070882.1:g.632792GAG[8]
GRCh37.p13 chr X fix patch HG1438_PATCH	NW_004070882.1:g.632792GAG[9]
GRCh37.p13 chr X fix patch HG1438_PATCH	NW_004070882.1:g.632792GAG[11]
GRCh37.p13 chr X fix patch HG1438_PATCH	NW_004070882.1:g.632792GAG[12]
GRCh37.p13 chr X fix patch HG1438_PATCH	NW_004070882.1:g.632792GAG[13]
GRCh37.p13 chr X	NC_000023.10:g.72163614GAG[5]
GRCh37.p13 chr X	NC_000023.10:g.72163614GAG[8]
GRCh37.p13 chr X	NC_000023.10:g.72163614GAG[9]
GRCh37.p13 chr X	NC_000023.10:g.72163614GAG[10]
GRCh37.p13 chr X	NC_000023.10:g.72163614GAG[11]
GRCh37.p13 chr X	NC_000023.10:g.72163614GAG[13]
GRCh37.p13 chr X	NC_000023.10:g.72163614GAG[14]
GRCh37.p13 chr X	NC_000023.10:g.72163614GAG[15]

Gene: DMRTC1, DMRT like family C1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DMRTC1 transcript variant 2	NM_001386923.1:c.-339_-30… NM_001386923.1:c.-339_-308=	N/A	5 Prime UTR Variant
DMRTC1 transcript variant 3	NM_001386924.1:c.-247_-21… NM_001386924.1:c.-247_-216=	N/A	5 Prime UTR Variant
DMRTC1 transcript variant 1	NM_033053.3:c.-324_-293=	N/A	5 Prime UTR Variant
DMRTC1 transcript variant 4	NR_170342.1:n.36CCT[3]	N/A	Non Coding Transcript Variant
DMRTC1 transcript variant 4	NR_170342.1:n.36CCT[6]	N/A	Non Coding Transcript Variant
DMRTC1 transcript variant 4	NR_170342.1:n.36CCT[7]	N/A	Non Coding Transcript Variant
DMRTC1 transcript variant 4	NR_170342.1:n.36CCT[8]	N/A	Non Coding Transcript Variant
DMRTC1 transcript variant 4	NR_170342.1:n.36CCT[9]	N/A	Non Coding Transcript Variant
DMRTC1 transcript variant 4	NR_170342.1:n.36CCT[11]	N/A	Non Coding Transcript Variant
DMRTC1 transcript variant 4	NR_170342.1:n.36CCT[12]	N/A	Non Coding Transcript Variant
DMRTC1 transcript variant 4	NR_170342.1:n.36CCT[13]	N/A	Non Coding Transcript Variant

Gene: FAM226A, family with sequence similarity 226 member A (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
FAM226A transcript	NR_026595.2:n.	N/A	Upstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(AGG)₁₀AG=	del(GAG)₇	del(GAG)₄	del(GAG)₃	del(GAG)₂	delGAG	dupGAG	dup(GAG)₂	dup(GAG)₃
GRCh38.p14 chr X	NC_000023.11:g.72943773_72943804=	NC_000023.11:g.72943775GAG[3]	NC_000023.11:g.72943775GAG[6]	NC_000023.11:g.72943775GAG[7]	NC_000023.11:g.72943775GAG[8]	NC_000023.11:g.72943775GAG[9]	NC_000023.11:g.72943775GAG[11]	NC_000023.11:g.72943775GAG[12]	NC_000023.11:g.72943775GAG[13]
GRCh37.p13 chr X fix patch HG1438_PATCH	NW_004070882.1:g.632790_632821=	NW_004070882.1:g.632792GAG[3]	NW_004070882.1:g.632792GAG[6]	NW_004070882.1:g.632792GAG[7]	NW_004070882.1:g.632792GAG[8]	NW_004070882.1:g.632792GAG[9]	NW_004070882.1:g.632792GAG[11]	NW_004070882.1:g.632792GAG[12]	NW_004070882.1:g.632792GAG[13]
GRCh37.p13 chr X	NC_000023.10:g.72163612_72163649=	NC_000023.10:g.72163614GAG[5]	NC_000023.10:g.72163614GAG[8]	NC_000023.10:g.72163614GAG[9]	NC_000023.10:g.72163614GAG[10]	NC_000023.10:g.72163614GAG[11]	NC_000023.10:g.72163614GAG[13]	NC_000023.10:g.72163614GAG[14]	NC_000023.10:g.72163614GAG[15]
DMRTC1 transcript variant 1	NM_033053.3:c.-324_-293=	NM_033053.3:c.-322CCT[3]	NM_033053.3:c.-322CCT[6]	NM_033053.3:c.-322CCT[7]	NM_033053.3:c.-322CCT[8]	NM_033053.3:c.-322CCT[9]	NM_033053.3:c.-322CCT[11]	NM_033053.3:c.-322CCT[12]	NM_033053.3:c.-322CCT[13]
DMRTC1 transcript variant 4	NR_170342.1:n.34_65=	NR_170342.1:n.36CCT[3]	NR_170342.1:n.36CCT[6]	NR_170342.1:n.36CCT[7]	NR_170342.1:n.36CCT[8]	NR_170342.1:n.36CCT[9]	NR_170342.1:n.36CCT[11]	NR_170342.1:n.36CCT[12]	NR_170342.1:n.36CCT[13]
DMRTC1 transcript variant 2	NM_001386923.1:c.-339_-308=	NM_001386923.1:c.-337CCT[3]	NM_001386923.1:c.-337CCT[6]	NM_001386923.1:c.-337CCT[7]	NM_001386923.1:c.-337CCT[8]	NM_001386923.1:c.-337CCT[9]	NM_001386923.1:c.-337CCT[11]	NM_001386923.1:c.-337CCT[12]	NM_001386923.1:c.-337CCT[13]
DMRTC1 transcript variant 3	NM_001386924.1:c.-247_-216=	NM_001386924.1:c.-245CCT[3]	NM_001386924.1:c.-245CCT[6]	NM_001386924.1:c.-245CCT[7]	NM_001386924.1:c.-245CCT[8]	NM_001386924.1:c.-245CCT[9]	NM_001386924.1:c.-245CCT[11]	NM_001386924.1:c.-245CCT[12]	NM_001386924.1:c.-245CCT[13]

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#.

6 SubSNP, 6 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUGCELL_USP	ss5504463774	Oct 17, 2022 (156)
2	TOMMO_GENOMICS	ss5796860202	Oct 17, 2022 (156)
3	TOMMO_GENOMICS	ss5796860203	Oct 17, 2022 (156)
4	TOMMO_GENOMICS	ss5796860204	Oct 17, 2022 (156)
5	TOMMO_GENOMICS	ss5796860205	Oct 17, 2022 (156)
6	TOMMO_GENOMICS	ss5796860206	Oct 17, 2022 (156)
7	14KJPN Submission ignored due to conflicting rows: Row 130697306 (NC_000023.11:72943772:AGG: 11/6128) Row 130697307 (NC_000023.11:72943772::AGGAGG 32/6128) Row 130697308 (NC_000023.11:72943772::AGG 153/6128)...	-	Oct 17, 2022 (156)
8	14KJPN Submission ignored due to conflicting rows: Row 130697306 (NC_000023.11:72943772:AGG: 11/6128) Row 130697307 (NC_000023.11:72943772::AGGAGG 32/6128) Row 130697308 (NC_000023.11:72943772::AGG 153/6128)...	-	Oct 17, 2022 (156)
9	14KJPN Submission ignored due to conflicting rows: Row 130697306 (NC_000023.11:72943772:AGG: 11/6128) Row 130697307 (NC_000023.11:72943772::AGGAGG 32/6128) Row 130697308 (NC_000023.11:72943772::AGG 153/6128)...	-	Oct 17, 2022 (156)
10	14KJPN Submission ignored due to conflicting rows: Row 130697306 (NC_000023.11:72943772:AGG: 11/6128) Row 130697307 (NC_000023.11:72943772::AGGAGG 32/6128) Row 130697308 (NC_000023.11:72943772::AGG 153/6128)...	-	Oct 17, 2022 (156)
11	14KJPN Submission ignored due to conflicting rows: Row 130697306 (NC_000023.11:72943772:AGG: 11/6128) Row 130697307 (NC_000023.11:72943772::AGGAGG 32/6128) Row 130697308 (NC_000023.11:72943772::AGG 153/6128)...	-	Oct 17, 2022 (156)
12	ALFA	NC_000023.11 - 72943773	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
1880595764	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAG	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAG	(self)
1880595764	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAG	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAG	(self)
1880595764	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAG	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAG	(self)
ss5796860205	NC_000023.11:72943772:AGGAGG:	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAG	(self)
1880595764	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAG	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAG	(self)
ss5796860202	NC_000023.11:72943772:AGG:	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAGGAG	(self)
1880595764	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAGGAG	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAGGAG	(self)
ss5796860204	NC_000023.11:72943772::AGG	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG	(self)
1880595764	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG	(self)
ss5504463774, ss5796860203	NC_000023.11:72943772::AGGAGG	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG	(self)
1880595764	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG	(self)
ss5796860206	NC_000023.11:72943772::AGGAGGAGG	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG
1880595764	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG	NC_000023.11:72943772:AGGAGGAGGAGG… NC_000023.11:72943772:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG:AGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAG	(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 rs1229164919

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1229164919