Name: rs1478649919
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.

rs1478649919

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:35685724 (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: A>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.000007 (1/139716, GnomAD)
C=0.00009 (1/10680, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ARPP21 : 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	10680	A=0.99991	C=0.00009	0.999813	0.000187	0
European	Sub	6962	A=0.9999	C=0.0001	0.999713	0.000287	0
African	Sub	2294	A=1.0000	C=0.0000	1.0	0.0	N/A
African Others	Sub	84	A=1.00	C=0.00	1.0	0.0	N/A
African American	Sub	2210	A=1.0000	C=0.0000	1.0	0.0	N/A
Asian	Sub	108	A=1.000	C=0.000	1.0	0.0	N/A
East Asian	Sub	84	A=1.00	C=0.00	1.0	0.0	N/A
Other Asian	Sub	24	A=1.00	C=0.00	1.0	0.0	N/A
Latin American 1	Sub	146	A=1.000	C=0.000	1.0	0.0	N/A
Latin American 2	Sub	610	A=1.000	C=0.000	1.0	0.0	N/A
South Asian	Sub	94	A=1.00	C=0.00	1.0	0.0	N/A
Other	Sub	466	A=1.000	C=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
gnomAD - Genomes	Global	Study-wide	139716	A=0.999993	C=0.000007
gnomAD - Genomes	European	Sub	75662	A=0.99999	C=0.00001
gnomAD - Genomes	African	Sub	41964	A=1.00000	C=0.00000
gnomAD - Genomes	American	Sub	13568	A=1.00000	C=0.00000
gnomAD - Genomes	Ashkenazi Jewish	Sub	3308	A=1.0000	C=0.0000
gnomAD - Genomes	East Asian	Sub	3074	A=1.0000	C=0.0000
gnomAD - Genomes	Other	Sub	2140	A=1.0000	C=0.0000
Allele Frequency Aggregator	Total	Global	10680	A=0.99991	C=0.00009
Allele Frequency Aggregator	European	Sub	6962	A=0.9999	C=0.0001
Allele Frequency Aggregator	African	Sub	2294	A=1.0000	C=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	A=1.000	C=0.000
Allele Frequency Aggregator	Other	Sub	466	A=1.000	C=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	A=1.000	C=0.000
Allele Frequency Aggregator	Asian	Sub	108	A=1.000	C=0.000
Allele Frequency Aggregator	South Asian	Sub	94	A=1.00	C=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.35685724A>C
GRCh37.p13 chr 3	NC_000003.11:g.35727216A>C
ARPP21 RefSeqGene	NG_050660.1:g.51551A>C

Gene: ARPP21, cAMP regulated phosphoprotein 21 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ARPP21 transcript variant 6	NM_001267617.2:c.261+1909… NM_001267617.2:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 8	NM_001267619.2:c.261+1909… NM_001267619.2:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 21	NM_001385484.1:c.261+1909… NM_001385484.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 23	NM_001385485.1:c.261+1909… NM_001385485.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 20	NM_001385486.1:c.261+1909… NM_001385486.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 24	NM_001385487.1:c.261+1909… NM_001385487.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 14	NM_001385488.1:c.261+1909… NM_001385488.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 15	NM_001385489.1:c.261+1909… NM_001385489.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 29	NM_001385490.1:c.261+1909… NM_001385490.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 48	NM_001385491.1:c.261+1909… NM_001385491.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 10	NM_001385492.1:c.261+1909… NM_001385492.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 33	NM_001385495.1:c.261+1909… NM_001385495.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 47	NM_001385496.1:c.261+1909… NM_001385496.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 13	NM_001385497.1:c.261+1909… NM_001385497.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 49	NM_001385517.1:c.261+1909… NM_001385517.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 39	NM_001385536.1:c.261+1909… NM_001385536.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 46	NM_001385556.1:c.261+1909… NM_001385556.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 36	NM_001385558.1:c.261+1909… NM_001385558.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 28	NM_001385562.1:c.261+1909… NM_001385562.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 41	NM_001385563.1:c.261+1909… NM_001385563.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 22	NM_001385564.1:c.261+1909… NM_001385564.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 12	NM_001385565.1:c.261+1909… NM_001385565.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 45	NM_001385566.1:c.261+1909… NM_001385566.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 35	NM_001385567.1:c.261+1909… NM_001385567.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 42	NM_001385573.1:c.261+1909… NM_001385573.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 9	NM_001385574.1:c.261+1909… NM_001385574.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 11	NM_001385576.1:c.261+1909… NM_001385576.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 16	NM_001385577.1:c.261+1909… NM_001385577.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 17	NM_001385578.1:c.261+1909… NM_001385578.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 18	NM_001385580.1:c.261+1909… NM_001385580.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 19	NM_001385581.1:c.261+1909… NM_001385581.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 43	NM_001385582.1:c.261+1909… NM_001385582.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 44	NM_001385584.1:c.261+1909… NM_001385584.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 40	NM_001385585.1:c.261+1909… NM_001385585.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 25	NM_001385587.1:c.261+1909… NM_001385587.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 26	NM_001385588.2:c.261+1909… NM_001385588.2:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 37	NM_001385589.1:c.261+1909… NM_001385589.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 38	NM_001385590.1:c.261+1909… NM_001385590.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 34	NM_001385591.1:c.261+1909… NM_001385591.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 31	NM_001385592.1:c.261+1909… NM_001385592.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 32	NM_001385593.1:c.261+1909… NM_001385593.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 30	NM_001385594.1:c.261+1909… NM_001385594.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 27	NM_001385595.1:c.261+1909… NM_001385595.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 1	NM_016300.5:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant 3	NM_001025068.1:c.*1695=	N/A	3 Prime UTR Variant
ARPP21 transcript variant 4	NM_001025069.1:c.*1695=	N/A	3 Prime UTR Variant
ARPP21 transcript variant 7	NM_001267618.2:c.*1695=	N/A	3 Prime UTR Variant
ARPP21 transcript variant 2	NM_198399.2:c.*1695=	N/A	3 Prime UTR Variant
ARPP21 transcript variant 5	NM_001267616.2:c.*1695=	N/A	3 Prime UTR Variant
ARPP21 transcript variant 50	NR_169632.1:n.	N/A	Intron Variant
ARPP21 transcript variant 51	NR_169633.1:n.	N/A	Intron Variant
ARPP21 transcript variant 52	NR_169635.1:n.	N/A	Intron Variant
ARPP21 transcript variant 53	NR_169644.1:n.	N/A	Intron Variant
ARPP21 transcript variant 54	NR_169645.1:n.	N/A	Intron Variant
ARPP21 transcript variant 55	NR_169646.1:n.	N/A	Intron Variant
ARPP21 transcript variant 56	NR_169647.1:n.	N/A	Intron Variant
ARPP21 transcript variant 57	NR_170705.1:n.	N/A	Intron Variant
ARPP21 transcript variant 58	NR_170706.1:n.	N/A	Intron Variant
ARPP21 transcript variant 59	NR_170707.1:n.	N/A	Intron Variant
ARPP21 transcript variant X2	XM_011533299.4:c.261+1909… XM_011533299.4:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X3	XM_011533300.4:c.261+1909… XM_011533300.4:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X5	XM_011533301.4:c.261+1909… XM_011533301.4:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X8	XM_011533302.4:c.261+1909… XM_011533302.4:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X4	XM_011533303.4:c.261+1909… XM_011533303.4:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X1	XM_017005574.3:c.261+1909… XM_017005574.3:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X7	XM_017005575.3:c.261+1909… XM_017005575.3:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X12	XM_017005580.3:c.261+1909… XM_017005580.3:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X13	XM_017005584.3:c.261+1909… XM_017005584.3:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X15	XM_017005590.3:c.261+1909… XM_017005590.3:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X16	XM_017005591.3:c.261+1909… XM_017005591.3:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X18	XM_017005596.3:c.261+1909… XM_017005596.3:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X19	XM_017005598.3:c.261+1909… XM_017005598.3:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X6	XM_024453320.2:c.261+1909… XM_024453320.2:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X14	XM_024453322.2:c.261+1909… XM_024453322.2:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X20	XM_024453323.2:c.261+1909… XM_024453323.2:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X9	XM_047447337.1:c.261+1909… XM_047447337.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X10	XM_047447338.1:c.261+1909… XM_047447338.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X11	XM_047447339.1:c.261+1909… XM_047447339.1:c.261+1909A>C	N/A	Intron Variant
ARPP21 transcript variant X17	XM_047447340.1:c.261+1909… XM_047447340.1:c.261+1909A>C	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	A=	C
GRCh38.p14 chr 3	NC_000003.12:g.35685724=	NC_000003.12:g.35685724A>C
GRCh37.p13 chr 3	NC_000003.11:g.35727216=	NC_000003.11:g.35727216A>C
ARPP21 RefSeqGene	NG_050660.1:g.51551=	NG_050660.1:g.51551A>C
ARPP21 transcript variant 5	NM_001267616.2:c.*1695=	NM_001267616.2:c.*1695A>C
ARPP21 transcript variant 5	NM_001267616.1:c.*1695=	NM_001267616.1:c.*1695A>C
ARPP21 transcript variant 7	NM_001267618.2:c.*1695=	NM_001267618.2:c.*1695A>C
ARPP21 transcript variant 7	NM_001267618.1:c.*1695=	NM_001267618.1:c.*1695A>C
ARPP21 transcript variant 2	NM_198399.2:c.*1695=	NM_198399.2:c.*1695A>C
ARPP21 transcript variant 2	NM_198399.1:c.*1695=	NM_198399.1:c.*1695A>C
ARPP21 transcript variant 4	NM_001025069.1:c.*1695=	NM_001025069.1:c.*1695A>C
ARPP21 transcript variant 3	NM_001025068.1:c.*1695=	NM_001025068.1:c.*1695A>C
ARPP21 transcript variant 6	NM_001267617.1:c.261+1909=	NM_001267617.1:c.261+1909A>C
ARPP21 transcript variant 6	NM_001267617.2:c.261+1909=	NM_001267617.2:c.261+1909A>C
ARPP21 transcript variant 8	NM_001267619.1:c.261+1909=	NM_001267619.1:c.261+1909A>C
ARPP21 transcript variant 8	NM_001267619.2:c.261+1909=	NM_001267619.2:c.261+1909A>C
ARPP21 transcript variant 21	NM_001385484.1:c.261+1909=	NM_001385484.1:c.261+1909A>C
ARPP21 transcript variant 23	NM_001385485.1:c.261+1909=	NM_001385485.1:c.261+1909A>C
ARPP21 transcript variant 20	NM_001385486.1:c.261+1909=	NM_001385486.1:c.261+1909A>C
ARPP21 transcript variant 24	NM_001385487.1:c.261+1909=	NM_001385487.1:c.261+1909A>C
ARPP21 transcript variant 14	NM_001385488.1:c.261+1909=	NM_001385488.1:c.261+1909A>C
ARPP21 transcript variant 15	NM_001385489.1:c.261+1909=	NM_001385489.1:c.261+1909A>C
ARPP21 transcript variant 29	NM_001385490.1:c.261+1909=	NM_001385490.1:c.261+1909A>C
ARPP21 transcript variant 48	NM_001385491.1:c.261+1909=	NM_001385491.1:c.261+1909A>C
ARPP21 transcript variant 10	NM_001385492.1:c.261+1909=	NM_001385492.1:c.261+1909A>C
ARPP21 transcript variant 33	NM_001385495.1:c.261+1909=	NM_001385495.1:c.261+1909A>C
ARPP21 transcript variant 47	NM_001385496.1:c.261+1909=	NM_001385496.1:c.261+1909A>C
ARPP21 transcript variant 13	NM_001385497.1:c.261+1909=	NM_001385497.1:c.261+1909A>C
ARPP21 transcript variant 49	NM_001385517.1:c.261+1909=	NM_001385517.1:c.261+1909A>C
ARPP21 transcript variant 39	NM_001385536.1:c.261+1909=	NM_001385536.1:c.261+1909A>C
ARPP21 transcript variant 46	NM_001385556.1:c.261+1909=	NM_001385556.1:c.261+1909A>C
ARPP21 transcript variant 36	NM_001385558.1:c.261+1909=	NM_001385558.1:c.261+1909A>C
ARPP21 transcript variant 28	NM_001385562.1:c.261+1909=	NM_001385562.1:c.261+1909A>C
ARPP21 transcript variant 41	NM_001385563.1:c.261+1909=	NM_001385563.1:c.261+1909A>C
ARPP21 transcript variant 22	NM_001385564.1:c.261+1909=	NM_001385564.1:c.261+1909A>C
ARPP21 transcript variant 12	NM_001385565.1:c.261+1909=	NM_001385565.1:c.261+1909A>C
ARPP21 transcript variant 45	NM_001385566.1:c.261+1909=	NM_001385566.1:c.261+1909A>C
ARPP21 transcript variant 35	NM_001385567.1:c.261+1909=	NM_001385567.1:c.261+1909A>C
ARPP21 transcript variant 42	NM_001385573.1:c.261+1909=	NM_001385573.1:c.261+1909A>C
ARPP21 transcript variant 9	NM_001385574.1:c.261+1909=	NM_001385574.1:c.261+1909A>C
ARPP21 transcript variant 11	NM_001385576.1:c.261+1909=	NM_001385576.1:c.261+1909A>C
ARPP21 transcript variant 16	NM_001385577.1:c.261+1909=	NM_001385577.1:c.261+1909A>C
ARPP21 transcript variant 17	NM_001385578.1:c.261+1909=	NM_001385578.1:c.261+1909A>C
ARPP21 transcript variant 18	NM_001385580.1:c.261+1909=	NM_001385580.1:c.261+1909A>C
ARPP21 transcript variant 19	NM_001385581.1:c.261+1909=	NM_001385581.1:c.261+1909A>C
ARPP21 transcript variant 43	NM_001385582.1:c.261+1909=	NM_001385582.1:c.261+1909A>C
ARPP21 transcript variant 44	NM_001385584.1:c.261+1909=	NM_001385584.1:c.261+1909A>C
ARPP21 transcript variant 40	NM_001385585.1:c.261+1909=	NM_001385585.1:c.261+1909A>C
ARPP21 transcript variant 25	NM_001385587.1:c.261+1909=	NM_001385587.1:c.261+1909A>C
ARPP21 transcript variant 26	NM_001385588.2:c.261+1909=	NM_001385588.2:c.261+1909A>C
ARPP21 transcript variant 37	NM_001385589.1:c.261+1909=	NM_001385589.1:c.261+1909A>C
ARPP21 transcript variant 38	NM_001385590.1:c.261+1909=	NM_001385590.1:c.261+1909A>C
ARPP21 transcript variant 34	NM_001385591.1:c.261+1909=	NM_001385591.1:c.261+1909A>C
ARPP21 transcript variant 31	NM_001385592.1:c.261+1909=	NM_001385592.1:c.261+1909A>C
ARPP21 transcript variant 32	NM_001385593.1:c.261+1909=	NM_001385593.1:c.261+1909A>C
ARPP21 transcript variant 30	NM_001385594.1:c.261+1909=	NM_001385594.1:c.261+1909A>C
ARPP21 transcript variant 27	NM_001385595.1:c.261+1909=	NM_001385595.1:c.261+1909A>C
ARPP21 transcript variant 1	NM_016300.4:c.261+1909=	NM_016300.4:c.261+1909A>C
ARPP21 transcript variant 1	NM_016300.5:c.261+1909=	NM_016300.5:c.261+1909A>C
ARPP21 transcript variant X1	XM_005264810.1:c.261+1909=	XM_005264810.1:c.261+1909A>C
ARPP21 transcript variant X7	XM_005264811.1:c.261+1909=	XM_005264811.1:c.261+1909A>C
ARPP21 transcript variant X3	XM_005264812.1:c.261+1909=	XM_005264812.1:c.261+1909A>C
ARPP21 transcript variant X4	XM_005264813.1:c.261+1909=	XM_005264813.1:c.261+1909A>C
ARPP21 transcript variant X5	XM_005264814.1:c.261+1909=	XM_005264814.1:c.261+1909A>C
ARPP21 transcript variant X6	XM_005264815.1:c.261+1909=	XM_005264815.1:c.261+1909A>C
ARPP21 transcript variant X7	XM_005264816.1:c.261+1909=	XM_005264816.1:c.261+1909A>C
ARPP21 transcript variant X8	XM_005264817.1:c.261+1909=	XM_005264817.1:c.261+1909A>C
ARPP21 transcript variant X9	XM_005264818.1:c.261+1909=	XM_005264818.1:c.261+1909A>C
ARPP21 transcript variant X10	XM_005264819.1:c.261+1909=	XM_005264819.1:c.261+1909A>C
ARPP21 transcript variant X11	XM_005264820.1:c.261+1909=	XM_005264820.1:c.261+1909A>C
ARPP21 transcript variant X12	XM_005264821.1:c.261+1909=	XM_005264821.1:c.261+1909A>C
ARPP21 transcript variant X13	XM_005264822.1:c.261+1909=	XM_005264822.1:c.261+1909A>C
ARPP21 transcript variant X2	XM_011533299.4:c.261+1909=	XM_011533299.4:c.261+1909A>C
ARPP21 transcript variant X3	XM_011533300.4:c.261+1909=	XM_011533300.4:c.261+1909A>C
ARPP21 transcript variant X5	XM_011533301.4:c.261+1909=	XM_011533301.4:c.261+1909A>C
ARPP21 transcript variant X8	XM_011533302.4:c.261+1909=	XM_011533302.4:c.261+1909A>C
ARPP21 transcript variant X4	XM_011533303.4:c.261+1909=	XM_011533303.4:c.261+1909A>C
ARPP21 transcript variant X1	XM_017005574.3:c.261+1909=	XM_017005574.3:c.261+1909A>C
ARPP21 transcript variant X7	XM_017005575.3:c.261+1909=	XM_017005575.3:c.261+1909A>C
ARPP21 transcript variant X12	XM_017005580.3:c.261+1909=	XM_017005580.3:c.261+1909A>C
ARPP21 transcript variant X13	XM_017005584.3:c.261+1909=	XM_017005584.3:c.261+1909A>C
ARPP21 transcript variant X15	XM_017005590.3:c.261+1909=	XM_017005590.3:c.261+1909A>C
ARPP21 transcript variant X16	XM_017005591.3:c.261+1909=	XM_017005591.3:c.261+1909A>C
ARPP21 transcript variant X18	XM_017005596.3:c.261+1909=	XM_017005596.3:c.261+1909A>C
ARPP21 transcript variant X19	XM_017005598.3:c.261+1909=	XM_017005598.3:c.261+1909A>C
ARPP21 transcript variant X6	XM_024453320.2:c.261+1909=	XM_024453320.2:c.261+1909A>C
ARPP21 transcript variant X14	XM_024453322.2:c.261+1909=	XM_024453322.2:c.261+1909A>C
ARPP21 transcript variant X20	XM_024453323.2:c.261+1909=	XM_024453323.2:c.261+1909A>C
ARPP21 transcript variant X9	XM_047447337.1:c.261+1909=	XM_047447337.1:c.261+1909A>C
ARPP21 transcript variant X10	XM_047447338.1:c.261+1909=	XM_047447338.1:c.261+1909A>C
ARPP21 transcript variant X11	XM_047447339.1:c.261+1909=	XM_047447339.1:c.261+1909A>C
ARPP21 transcript variant X17	XM_047447340.1:c.261+1909=	XM_047447340.1:c.261+1909A>C

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#.

1 SubSNP, 2 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GNOMAD	ss2791588865	Nov 08, 2017 (151)
2	gnomAD - Genomes	NC_000003.12 - 35685724	Apr 27, 2021 (155)
3	ALFA	NC_000003.12 - 35685724	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
ss2791588865	NC_000003.11:35727215:A:C	NC_000003.12:35685723:A:C	(self)
104290620, 7609484045	NC_000003.12:35685723:A:C	NC_000003.12:35685723:A:C	(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 rs1478649919

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

rs1478649919