Name: rs1491362964
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.

rs1491362964

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:73037572-73037573 (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: insA / insAA / insATA / insATATA /…
insA / insAA / insATA / insATATA / ins(AT)₃A / ins(AT)₄A / ins(AT)₅A / ins(AT)₆A / ins(AT)₇A / ins(AT)₈A / ins(AT)₉A / insATATTTA
Variation Type: Insertion
Frequency: insA=0.00000 (0/11632, ALFA)
insAA=0.00000 (0/11632, ALFA)
insATA=0.00000 (0/11632, ALFA) (+ 6 more)
insATATA=0.00000 (0/11632, ALFA)
ins(AT)₃A=0.00000 (0/11632, ALFA)
ins(AT)₄A=0.00000 (0/11632, ALFA)
ins(AT)₅A=0.00000 (0/11632, ALFA)
insATATTTA=0.00000 (0/11632, ALFA)
insA=0.007 (6/834, Korea1K)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: P4HA1 : 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	HWEP
Total	Global	11632	=1.00000	A=0.00000, AA=0.00000, ATA=0.00000, ATATA=0.00000, ATATATA=0.00000, ATATATATA=0.00000, ATATATATATA=0.00000, ATATTTA=0.00000	1.0	N/A
European	Sub	7464	=1.0000	A=0.0000, AA=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATA=0.0000, ATATTTA=0.0000	1.0	N/A
African	Sub	2776	=1.0000	A=0.0000, AA=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATA=0.0000, ATATTTA=0.0000	1.0	N/A
African Others	Sub	108	=1.000	A=0.000, AA=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=0.000, ATATTTA=0.000	1.0	N/A
African American	Sub	2668	=1.0000	A=0.0000, AA=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATA=0.0000, ATATTTA=0.0000	1.0	N/A
Asian	Sub	104	=1.000	A=0.000, AA=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=0.000, ATATTTA=0.000	1.0	N/A
East Asian	Sub	80	=1.00	A=0.00, AA=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATA=0.00, ATATTTA=0.00	1.0	N/A
Other Asian	Sub	24	=1.00	A=0.00, AA=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATA=0.00, ATATTTA=0.00	1.0	N/A
Latin American 1	Sub	142	=1.000	A=0.000, AA=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=0.000, ATATTTA=0.000	1.0	N/A
Latin American 2	Sub	590	=1.000	A=0.000, AA=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=0.000, ATATTTA=0.000	1.0	N/A
South Asian	Sub	94	=1.00	A=0.00, AA=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATA=0.00, ATATTTA=0.00	1.0	N/A
Other	Sub	462	=1.000	A=0.000, AA=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=0.000, ATATTTA=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	11632	- No frequency provided	insA=0.00000, insAA=0.00000, insATA=0.00000, insATATA=0.00000, ins(AT)₃A=0.00000, ins(AT)₄A=0.00000, ins(AT)₅A=0.00000, insATATTTA=0.00000
Allele Frequency Aggregator	European	Sub	7464	- No frequency provided	insA=0.0000, insAA=0.0000, insATA=0.0000, insATATA=0.0000, ins(AT)₃A=0.0000, ins(AT)₄A=0.0000, ins(AT)₅A=0.0000, insATATTTA=0.0000
Allele Frequency Aggregator	African	Sub	2776	- No frequency provided	insA=0.0000, insAA=0.0000, insATA=0.0000, insATATA=0.0000, ins(AT)₃A=0.0000, ins(AT)₄A=0.0000, ins(AT)₅A=0.0000, insATATTTA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	590	- No frequency provided	insA=0.000, insAA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₅A=0.000, insATATTTA=0.000
Allele Frequency Aggregator	Other	Sub	462	- No frequency provided	insA=0.000, insAA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₅A=0.000, insATATTTA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	142	- No frequency provided	insA=0.000, insAA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₅A=0.000, insATATTTA=0.000
Allele Frequency Aggregator	Asian	Sub	104	- No frequency provided	insA=0.000, insAA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₅A=0.000, insATATTTA=0.000
Allele Frequency Aggregator	South Asian	Sub	94	- No frequency provided	insA=0.00, insAA=0.00, insATA=0.00, insATATA=0.00, ins(AT)₃A=0.00, ins(AT)₄A=0.00, ins(AT)₅A=0.00, insATATTTA=0.00
Korean Genome Project	KOREAN	Study-wide	834	- No frequency provided	insA=0.007

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 10	NC_000010.11:g.73037572_73037573insA
GRCh38.p14 chr 10	NC_000010.11:g.73037572_73037573insAA
GRCh38.p14 chr 10	NC_000010.11:g.73037572_73037573insATA
GRCh38.p14 chr 10	NC_000010.11:g.73037572_73037573insATATA
GRCh38.p14 chr 10	NC_000010.11:g.73037572_73037573insATATATA
GRCh38.p14 chr 10	NC_000010.11:g.73037572_73037573insATATATATA
GRCh38.p14 chr 10	NC_000010.11:g.73037572_73037573insATATATATATA
GRCh38.p14 chr 10	NC_000010.11:g.73037572_73037573insATATATATATATA
GRCh38.p14 chr 10	NC_000010.11:g.73037572_73037573insATATATATATATATA
GRCh38.p14 chr 10	NC_000010.11:g.73037572_73037573insATATATATATATATATA
GRCh38.p14 chr 10	NC_000010.11:g.73037572_73037573insATATATATATATATATATA
GRCh38.p14 chr 10	NC_000010.11:g.73037572_73037573insATATTTA
GRCh37.p13 chr 10	NC_000010.10:g.74797330_74797331insA
GRCh37.p13 chr 10	NC_000010.10:g.74797330_74797331insAA
GRCh37.p13 chr 10	NC_000010.10:g.74797330_74797331insATA
GRCh37.p13 chr 10	NC_000010.10:g.74797330_74797331insATATA
GRCh37.p13 chr 10	NC_000010.10:g.74797330_74797331insATATATA
GRCh37.p13 chr 10	NC_000010.10:g.74797330_74797331insATATATATA
GRCh37.p13 chr 10	NC_000010.10:g.74797330_74797331insATATATATATA
GRCh37.p13 chr 10	NC_000010.10:g.74797330_74797331insATATATATATATA
GRCh37.p13 chr 10	NC_000010.10:g.74797330_74797331insATATATATATATATA
GRCh37.p13 chr 10	NC_000010.10:g.74797330_74797331insATATATATATATATATA
GRCh37.p13 chr 10	NC_000010.10:g.74797330_74797331insATATATATATATATATATA
GRCh37.p13 chr 10	NC_000010.10:g.74797330_74797331insATATTTA

Gene: P4HA1, prolyl 4-hydroxylase subunit alpha 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
P4HA1 transcript variant 1	NM_000917.4:c.1148+6314_1… NM_000917.4:c.1148+6314_1148+6315insT	N/A	Intron Variant
P4HA1 transcript variant 2	NM_001017962.3:c.1149-720… NM_001017962.3:c.1149-7203_1149-7202insT	N/A	Intron Variant
P4HA1 transcript variant 3	NM_001142595.2:c.1149-720… NM_001142595.2:c.1149-7203_1149-7202insT	N/A	Intron Variant
P4HA1 transcript variant 4	NM_001142596.2:c.1148+631… NM_001142596.2:c.1148+6314_1148+6315insT	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	=	insA	insAA	insATA	insATATA	ins(AT)₃A	ins(AT)₄A	ins(AT)₅A	ins(AT)₆A	ins(AT)₇A	ins(AT)₈A	ins(AT)₉A	insATATTTA
GRCh38.p14 chr 10	NC_000010.11:g.73037572_73037573=	NC_000010.11:g.73037572_73037573insA	NC_000010.11:g.73037572_73037573insAA	NC_000010.11:g.73037572_73037573insATA	NC_000010.11:g.73037572_73037573insATATA	NC_000010.11:g.73037572_73037573insATATATA	NC_000010.11:g.73037572_73037573insATATATATA	NC_000010.11:g.73037572_73037573insATATATATATA	NC_000010.11:g.73037572_73037573insATATATATATATA	NC_000010.11:g.73037572_73037573insATATATATATATATA	NC_000010.11:g.73037572_73037573insATATATATATATATATA	NC_000010.11:g.73037572_73037573insATATATATATATATATATA	NC_000010.11:g.73037572_73037573insATATTTA
GRCh37.p13 chr 10	NC_000010.10:g.74797330_74797331=	NC_000010.10:g.74797330_74797331insA	NC_000010.10:g.74797330_74797331insAA	NC_000010.10:g.74797330_74797331insATA	NC_000010.10:g.74797330_74797331insATATA	NC_000010.10:g.74797330_74797331insATATATA	NC_000010.10:g.74797330_74797331insATATATATA	NC_000010.10:g.74797330_74797331insATATATATATA	NC_000010.10:g.74797330_74797331insATATATATATATA	NC_000010.10:g.74797330_74797331insATATATATATATATA	NC_000010.10:g.74797330_74797331insATATATATATATATATA	NC_000010.10:g.74797330_74797331insATATATATATATATATATA	NC_000010.10:g.74797330_74797331insATATTTA
P4HA1 transcript variant 1	NM_000917.3:c.1148+6314=	NM_000917.3:c.1148+6314_1148+6315insT	NM_000917.3:c.1148+6314_1148+6315insTT	NM_000917.3:c.1148+6314_1148+6315insTAT	NM_000917.3:c.1148+6314_1148+6315insTATAT	NM_000917.3:c.1148+6314_1148+6315insTATATAT	NM_000917.3:c.1148+6314_1148+6315insTATATATAT	NM_000917.3:c.1148+6314_1148+6315insTATATATATAT	NM_000917.3:c.1148+6314_1148+6315insTATATATATATAT	NM_000917.3:c.1148+6314_1148+6315insTATATATATATATAT	NM_000917.3:c.1148+6314_1148+6315insTATATATATATATATAT	NM_000917.3:c.1148+6314_1148+6315insTATATATATATATATATAT	NM_000917.3:c.1148+6314_1148+6315insTAAATAT
P4HA1 transcript variant 1	NM_000917.4:c.1148+6314=	NM_000917.4:c.1148+6314_1148+6315insT	NM_000917.4:c.1148+6314_1148+6315insTT	NM_000917.4:c.1148+6314_1148+6315insTAT	NM_000917.4:c.1148+6314_1148+6315insTATAT	NM_000917.4:c.1148+6314_1148+6315insTATATAT	NM_000917.4:c.1148+6314_1148+6315insTATATATAT	NM_000917.4:c.1148+6314_1148+6315insTATATATATAT	NM_000917.4:c.1148+6314_1148+6315insTATATATATATAT	NM_000917.4:c.1148+6314_1148+6315insTATATATATATATAT	NM_000917.4:c.1148+6314_1148+6315insTATATATATATATATAT	NM_000917.4:c.1148+6314_1148+6315insTATATATATATATATATAT	NM_000917.4:c.1148+6314_1148+6315insTAAATAT
P4HA1 transcript variant 2	NM_001017962.2:c.1149-7203=	NM_001017962.2:c.1149-7203_1149-7202insT	NM_001017962.2:c.1149-7203_1149-7202insTT	NM_001017962.2:c.1149-7203_1149-7202insTAT	NM_001017962.2:c.1149-7203_1149-7202insTATAT	NM_001017962.2:c.1149-7203_1149-7202insTATATAT	NM_001017962.2:c.1149-7203_1149-7202insTATATATAT	NM_001017962.2:c.1149-7203_1149-7202insTATATATATAT	NM_001017962.2:c.1149-7203_1149-7202insTATATATATATAT	NM_001017962.2:c.1149-7203_1149-7202insTATATATATATATAT	NM_001017962.2:c.1149-7203_1149-7202insTATATATATATATATAT	NM_001017962.2:c.1149-7203_1149-7202insTATATATATATATATATAT	NM_001017962.2:c.1149-7203_1149-7202insTAAATAT
P4HA1 transcript variant 2	NM_001017962.3:c.1149-7203=	NM_001017962.3:c.1149-7203_1149-7202insT	NM_001017962.3:c.1149-7203_1149-7202insTT	NM_001017962.3:c.1149-7203_1149-7202insTAT	NM_001017962.3:c.1149-7203_1149-7202insTATAT	NM_001017962.3:c.1149-7203_1149-7202insTATATAT	NM_001017962.3:c.1149-7203_1149-7202insTATATATAT	NM_001017962.3:c.1149-7203_1149-7202insTATATATATAT	NM_001017962.3:c.1149-7203_1149-7202insTATATATATATAT	NM_001017962.3:c.1149-7203_1149-7202insTATATATATATATAT	NM_001017962.3:c.1149-7203_1149-7202insTATATATATATATATAT	NM_001017962.3:c.1149-7203_1149-7202insTATATATATATATATATAT	NM_001017962.3:c.1149-7203_1149-7202insTAAATAT
P4HA1 transcript variant 3	NM_001142595.1:c.1149-7203=	NM_001142595.1:c.1149-7203_1149-7202insT	NM_001142595.1:c.1149-7203_1149-7202insTT	NM_001142595.1:c.1149-7203_1149-7202insTAT	NM_001142595.1:c.1149-7203_1149-7202insTATAT	NM_001142595.1:c.1149-7203_1149-7202insTATATAT	NM_001142595.1:c.1149-7203_1149-7202insTATATATAT	NM_001142595.1:c.1149-7203_1149-7202insTATATATATAT	NM_001142595.1:c.1149-7203_1149-7202insTATATATATATAT	NM_001142595.1:c.1149-7203_1149-7202insTATATATATATATAT	NM_001142595.1:c.1149-7203_1149-7202insTATATATATATATATAT	NM_001142595.1:c.1149-7203_1149-7202insTATATATATATATATATAT	NM_001142595.1:c.1149-7203_1149-7202insTAAATAT
P4HA1 transcript variant 3	NM_001142595.2:c.1149-7203=	NM_001142595.2:c.1149-7203_1149-7202insT	NM_001142595.2:c.1149-7203_1149-7202insTT	NM_001142595.2:c.1149-7203_1149-7202insTAT	NM_001142595.2:c.1149-7203_1149-7202insTATAT	NM_001142595.2:c.1149-7203_1149-7202insTATATAT	NM_001142595.2:c.1149-7203_1149-7202insTATATATAT	NM_001142595.2:c.1149-7203_1149-7202insTATATATATAT	NM_001142595.2:c.1149-7203_1149-7202insTATATATATATAT	NM_001142595.2:c.1149-7203_1149-7202insTATATATATATATAT	NM_001142595.2:c.1149-7203_1149-7202insTATATATATATATATAT	NM_001142595.2:c.1149-7203_1149-7202insTATATATATATATATATAT	NM_001142595.2:c.1149-7203_1149-7202insTAAATAT
P4HA1 transcript variant 4	NM_001142596.1:c.1148+6314=	NM_001142596.1:c.1148+6314_1148+6315insT	NM_001142596.1:c.1148+6314_1148+6315insTT	NM_001142596.1:c.1148+6314_1148+6315insTAT	NM_001142596.1:c.1148+6314_1148+6315insTATAT	NM_001142596.1:c.1148+6314_1148+6315insTATATAT	NM_001142596.1:c.1148+6314_1148+6315insTATATATAT	NM_001142596.1:c.1148+6314_1148+6315insTATATATATAT	NM_001142596.1:c.1148+6314_1148+6315insTATATATATATAT	NM_001142596.1:c.1148+6314_1148+6315insTATATATATATATAT	NM_001142596.1:c.1148+6314_1148+6315insTATATATATATATATAT	NM_001142596.1:c.1148+6314_1148+6315insTATATATATATATATATAT	NM_001142596.1:c.1148+6314_1148+6315insTAAATAT
P4HA1 transcript variant 4	NM_001142596.2:c.1148+6314=	NM_001142596.2:c.1148+6314_1148+6315insT	NM_001142596.2:c.1148+6314_1148+6315insTT	NM_001142596.2:c.1148+6314_1148+6315insTAT	NM_001142596.2:c.1148+6314_1148+6315insTATAT	NM_001142596.2:c.1148+6314_1148+6315insTATATAT	NM_001142596.2:c.1148+6314_1148+6315insTATATATAT	NM_001142596.2:c.1148+6314_1148+6315insTATATATATAT	NM_001142596.2:c.1148+6314_1148+6315insTATATATATATAT	NM_001142596.2:c.1148+6314_1148+6315insTATATATATATATAT	NM_001142596.2:c.1148+6314_1148+6315insTATATATATATATATAT	NM_001142596.2:c.1148+6314_1148+6315insTATATATATATATATATAT	NM_001142596.2:c.1148+6314_1148+6315insTAAATAT
P4HA1 transcript variant X1	XM_005269870.1:c.1148+6314=	XM_005269870.1:c.1148+6314_1148+6315insT	XM_005269870.1:c.1148+6314_1148+6315insTT	XM_005269870.1:c.1148+6314_1148+6315insTAT	XM_005269870.1:c.1148+6314_1148+6315insTATAT	XM_005269870.1:c.1148+6314_1148+6315insTATATAT	XM_005269870.1:c.1148+6314_1148+6315insTATATATAT	XM_005269870.1:c.1148+6314_1148+6315insTATATATATAT	XM_005269870.1:c.1148+6314_1148+6315insTATATATATATAT	XM_005269870.1:c.1148+6314_1148+6315insTATATATATATATAT	XM_005269870.1:c.1148+6314_1148+6315insTATATATATATATATAT	XM_005269870.1:c.1148+6314_1148+6315insTATATATATATATATATAT	XM_005269870.1:c.1148+6314_1148+6315insTAAATAT

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#.

18 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	KOGIC	ss3968165335	Apr 26, 2020 (154)
2	GNOMAD	ss4221030748	Apr 26, 2021 (155)
3	GNOMAD	ss4221030749	Apr 26, 2021 (155)
4	GNOMAD	ss4221030750	Apr 26, 2021 (155)
5	GNOMAD	ss4221030751	Apr 26, 2021 (155)
6	GNOMAD	ss4221030752	Apr 26, 2021 (155)
7	GNOMAD	ss4221030753	Apr 26, 2021 (155)
8	TOMMO_GENOMICS	ss5198287232	Apr 26, 2021 (155)
9	TOMMO_GENOMICS	ss5198287233	Apr 26, 2021 (155)
10	TOMMO_GENOMICS	ss5198287234	Apr 26, 2021 (155)
11	TOMMO_GENOMICS	ss5198287235	Apr 26, 2021 (155)
12	TOMMO_GENOMICS	ss5198287236	Apr 26, 2021 (155)
13	TOMMO_GENOMICS	ss5744308592	Oct 16, 2022 (156)
14	TOMMO_GENOMICS	ss5744308593	Oct 16, 2022 (156)
15	TOMMO_GENOMICS	ss5744308594	Oct 16, 2022 (156)
16	TOMMO_GENOMICS	ss5744308595	Oct 16, 2022 (156)
17	TOMMO_GENOMICS	ss5744308596	Oct 16, 2022 (156)
18	YY_MCH	ss5811660861	Oct 16, 2022 (156)
19	gnomAD - Genomes Submission ignored due to conflicting rows: Row 356385680 (NC_000010.11:73037572::A 175/14518) Row 356385681 (NC_000010.11:73037572::ATATATATATA 3/14708) Row 356385682 (NC_000010.11:73037572::ATATATATATATA 3/14716)...	-	Apr 26, 2021 (155)
20	gnomAD - Genomes Submission ignored due to conflicting rows: Row 356385680 (NC_000010.11:73037572::A 175/14518) Row 356385681 (NC_000010.11:73037572::ATATATATATA 3/14708) Row 356385682 (NC_000010.11:73037572::ATATATATATATA 3/14716)...	-	Apr 26, 2021 (155)
21	gnomAD - Genomes Submission ignored due to conflicting rows: Row 356385680 (NC_000010.11:73037572::A 175/14518) Row 356385681 (NC_000010.11:73037572::ATATATATATA 3/14708) Row 356385682 (NC_000010.11:73037572::ATATATATATATA 3/14716)...	-	Apr 26, 2021 (155)
22	gnomAD - Genomes Submission ignored due to conflicting rows: Row 356385680 (NC_000010.11:73037572::A 175/14518) Row 356385681 (NC_000010.11:73037572::ATATATATATA 3/14708) Row 356385682 (NC_000010.11:73037572::ATATATATATATA 3/14716)...	-	Apr 26, 2021 (155)
23	gnomAD - Genomes Submission ignored due to conflicting rows: Row 356385680 (NC_000010.11:73037572::A 175/14518) Row 356385681 (NC_000010.11:73037572::ATATATATATA 3/14708) Row 356385682 (NC_000010.11:73037572::ATATATATATATA 3/14716)...	-	Apr 26, 2021 (155)
24	gnomAD - Genomes Submission ignored due to conflicting rows: Row 356385680 (NC_000010.11:73037572::A 175/14518) Row 356385681 (NC_000010.11:73037572::ATATATATATA 3/14708) Row 356385682 (NC_000010.11:73037572::ATATATATATATA 3/14716)...	-	Apr 26, 2021 (155)
25	Korean Genome Project	NC_000010.11 - 73037573	Apr 26, 2020 (154)
26	8.3KJPN Submission ignored due to conflicting rows: Row 56256539 (NC_000010.10:74797330::ATATA 33/11506) Row 56256540 (NC_000010.10:74797330::A 282/11506) Row 56256541 (NC_000010.10:74797330::ATA 53/11506)...	-	Apr 26, 2021 (155)
27	8.3KJPN Submission ignored due to conflicting rows: Row 56256539 (NC_000010.10:74797330::ATATA 33/11506) Row 56256540 (NC_000010.10:74797330::A 282/11506) Row 56256541 (NC_000010.10:74797330::ATA 53/11506)...	-	Apr 26, 2021 (155)
28	8.3KJPN Submission ignored due to conflicting rows: Row 56256539 (NC_000010.10:74797330::ATATA 33/11506) Row 56256540 (NC_000010.10:74797330::A 282/11506) Row 56256541 (NC_000010.10:74797330::ATA 53/11506)...	-	Apr 26, 2021 (155)
29	8.3KJPN Submission ignored due to conflicting rows: Row 56256539 (NC_000010.10:74797330::ATATA 33/11506) Row 56256540 (NC_000010.10:74797330::A 282/11506) Row 56256541 (NC_000010.10:74797330::ATA 53/11506)...	-	Apr 26, 2021 (155)
30	8.3KJPN Submission ignored due to conflicting rows: Row 56256539 (NC_000010.10:74797330::ATATA 33/11506) Row 56256540 (NC_000010.10:74797330::A 282/11506) Row 56256541 (NC_000010.10:74797330::ATA 53/11506)...	-	Apr 26, 2021 (155)
31	14KJPN Submission ignored due to conflicting rows: Row 78145696 (NC_000010.11:73037572::A 836/25478) Row 78145697 (NC_000010.11:73037572::ATATA 130/25478) Row 78145698 (NC_000010.11:73037572::ATA 162/25478)...	-	Oct 16, 2022 (156)
32	14KJPN Submission ignored due to conflicting rows: Row 78145696 (NC_000010.11:73037572::A 836/25478) Row 78145697 (NC_000010.11:73037572::ATATA 130/25478) Row 78145698 (NC_000010.11:73037572::ATA 162/25478)...	-	Oct 16, 2022 (156)
33	14KJPN Submission ignored due to conflicting rows: Row 78145696 (NC_000010.11:73037572::A 836/25478) Row 78145697 (NC_000010.11:73037572::ATATA 130/25478) Row 78145698 (NC_000010.11:73037572::ATA 162/25478)...	-	Oct 16, 2022 (156)
34	14KJPN Submission ignored due to conflicting rows: Row 78145696 (NC_000010.11:73037572::A 836/25478) Row 78145697 (NC_000010.11:73037572::ATATA 130/25478) Row 78145698 (NC_000010.11:73037572::ATA 162/25478)...	-	Oct 16, 2022 (156)
35	14KJPN Submission ignored due to conflicting rows: Row 78145696 (NC_000010.11:73037572::A 836/25478) Row 78145697 (NC_000010.11:73037572::ATATA 130/25478) Row 78145698 (NC_000010.11:73037572::ATA 162/25478)...	-	Oct 16, 2022 (156)
36	ALFA	NC_000010.11 - 73037573	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
ss5198287233	NC_000010.10:74797330::A	NC_000010.11:73037572::A	(self)
24543336, 3027651194, ss3968165335, ss4221030748, ss5744308592, ss5811660861	NC_000010.11:73037572::A	NC_000010.11:73037572::A	(self)
3027651194	NC_000010.11:73037572::AA	NC_000010.11:73037572::AA	(self)
ss5198287234	NC_000010.10:74797330::ATA	NC_000010.11:73037572::ATA	(self)
3027651194, ss5744308594	NC_000010.11:73037572::ATA	NC_000010.11:73037572::ATA	(self)
ss5198287232	NC_000010.10:74797330::ATATA	NC_000010.11:73037572::ATATA	(self)
3027651194, ss5744308593	NC_000010.11:73037572::ATATA	NC_000010.11:73037572::ATATA	(self)
ss5198287235	NC_000010.10:74797330::ATATATA	NC_000010.11:73037572::ATATATA	(self)
3027651194, ss5744308595	NC_000010.11:73037572::ATATATA	NC_000010.11:73037572::ATATATA	(self)
3027651194, ss5744308596	NC_000010.11:73037572::ATATATATA	NC_000010.11:73037572::ATATATATA	(self)
3027651194, ss4221030749	NC_000010.11:73037572::ATATATATATA	NC_000010.11:73037572::ATATATATATA	(self)
ss5198287236	NC_000010.10:74797330::ATATATATATA… NC_000010.10:74797330::ATATATATATATA	NC_000010.11:73037572::ATATATATATA… NC_000010.11:73037572::ATATATATATATA	(self)
ss4221030750	NC_000010.11:73037572::ATATATATATA… NC_000010.11:73037572::ATATATATATATA	NC_000010.11:73037572::ATATATATATA… NC_000010.11:73037572::ATATATATATATA	(self)
ss4221030751	NC_000010.11:73037572::ATATATATATA… NC_000010.11:73037572::ATATATATATATATA	NC_000010.11:73037572::ATATATATATA… NC_000010.11:73037572::ATATATATATATATA	(self)
ss4221030752	NC_000010.11:73037572::ATATATATATA… NC_000010.11:73037572::ATATATATATATATATA	NC_000010.11:73037572::ATATATATATA… NC_000010.11:73037572::ATATATATATATATATA	(self)
ss4221030753	NC_000010.11:73037572::ATATATATATA… NC_000010.11:73037572::ATATATATATATATATATA	NC_000010.11:73037572::ATATATATATA… NC_000010.11:73037572::ATATATATATATATATATA	(self)
3027651194	NC_000010.11:73037572::ATATTTA	NC_000010.11:73037572::ATATTTA	(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 rs1491362964

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

rs1491362964