Name: rs1491195459
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.

rs1491195459

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:32044931-32044932 (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: ins(A)₁₇G / ins(A)₁₃G / ins(A)₆C /…
ins(A)₁₇G / ins(A)₁₃G / ins(A)₆C / insAAAG / insAAG / insAG / insG
Variation Type: Insertion
Frequency: ins(A)₆C=0.00000 (0/11782, ALFA)
insAAG=0.00000 (0/11782, ALFA)
insAG=0.00000 (0/11782, ALFA) (+ 1 more)
insG=0.00000 (0/11782, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NRG1 : Intron Variant
NRG1-IT1 : 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	11782	=1.00000	AAAAAAC=0.00000, AAG=0.00000, AG=0.00000, G=0.00000	1.0	N/A
European	Sub	7616	=1.0000	AAAAAAC=0.0000, AAG=0.0000, AG=0.0000, G=0.0000	1.0	N/A
African	Sub	2740	=1.0000	AAAAAAC=0.0000, AAG=0.0000, AG=0.0000, G=0.0000	1.0	N/A
African Others	Sub	102	=1.000	AAAAAAC=0.000, AAG=0.000, AG=0.000, G=0.000	1.0	N/A
African American	Sub	2638	=1.0000	AAAAAAC=0.0000, AAG=0.0000, AG=0.0000, G=0.0000	1.0	N/A
Asian	Sub	108	=1.000	AAAAAAC=0.000, AAG=0.000, AG=0.000, G=0.000	1.0	N/A
East Asian	Sub	84	=1.00	AAAAAAC=0.00, AAG=0.00, AG=0.00, G=0.00	1.0	N/A
Other Asian	Sub	24	=1.00	AAAAAAC=0.00, AAG=0.00, AG=0.00, G=0.00	1.0	N/A
Latin American 1	Sub	146	=1.000	AAAAAAC=0.000, AAG=0.000, AG=0.000, G=0.000	1.0	N/A
Latin American 2	Sub	610	=1.000	AAAAAAC=0.000, AAG=0.000, AG=0.000, G=0.000	1.0	N/A
South Asian	Sub	94	=1.00	AAAAAAC=0.00, AAG=0.00, AG=0.00, G=0.00	1.0	N/A
Other	Sub	468	=1.000	AAAAAAC=0.000, AAG=0.000, AG=0.000, G=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	11782	- No frequency provided	ins(A)₆C=0.00000, insAAG=0.00000, insAG=0.00000, insG=0.00000
Allele Frequency Aggregator	European	Sub	7616	- No frequency provided	ins(A)₆C=0.0000, insAAG=0.0000, insAG=0.0000, insG=0.0000
Allele Frequency Aggregator	African	Sub	2740	- No frequency provided	ins(A)₆C=0.0000, insAAG=0.0000, insAG=0.0000, insG=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	- No frequency provided	ins(A)₆C=0.000, insAAG=0.000, insAG=0.000, insG=0.000
Allele Frequency Aggregator	Other	Sub	468	- No frequency provided	ins(A)₆C=0.000, insAAG=0.000, insAG=0.000, insG=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	- No frequency provided	ins(A)₆C=0.000, insAAG=0.000, insAG=0.000, insG=0.000
Allele Frequency Aggregator	Asian	Sub	108	- No frequency provided	ins(A)₆C=0.000, insAAG=0.000, insAG=0.000, insG=0.000
Allele Frequency Aggregator	South Asian	Sub	94	- No frequency provided	ins(A)₆C=0.00, insAAG=0.00, insAG=0.00, insG=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 8	NC_000008.11:g.32044931_32044932insAAAAAAAAAAAAAAAAAG
GRCh38.p14 chr 8	NC_000008.11:g.32044931_32044932insAAAAAAAAAAAAAG
GRCh38.p14 chr 8	NC_000008.11:g.32044931_32044932insAAAAAAC
GRCh38.p14 chr 8	NC_000008.11:g.32044931_32044932insAAAG
GRCh38.p14 chr 8	NC_000008.11:g.32044931_32044932insAAG
GRCh38.p14 chr 8	NC_000008.11:g.32044931_32044932insAG
GRCh38.p14 chr 8	NC_000008.11:g.32044931_32044932insG
GRCh37.p13 chr 8	NC_000008.10:g.31902447_31902448insAAAAAAAAAAAAAAAAAG
GRCh37.p13 chr 8	NC_000008.10:g.31902447_31902448insAAAAAAAAAAAAAG
GRCh37.p13 chr 8	NC_000008.10:g.31902447_31902448insAAAAAAC
GRCh37.p13 chr 8	NC_000008.10:g.31902447_31902448insAAAG
GRCh37.p13 chr 8	NC_000008.10:g.31902447_31902448insAAG
GRCh37.p13 chr 8	NC_000008.10:g.31902447_31902448insAG
GRCh37.p13 chr 8	NC_000008.10:g.31902447_31902448insG
NRG1 RefSeqGene	NG_012005.2:g.410710_410711insAAAAAAAAAAAAAAAAAG
NRG1 RefSeqGene	NG_012005.2:g.410710_410711insAAAAAAAAAAAAAG
NRG1 RefSeqGene	NG_012005.2:g.410710_410711insAAAAAAC
NRG1 RefSeqGene	NG_012005.2:g.410710_410711insAAAG
NRG1 RefSeqGene	NG_012005.2:g.410710_410711insAAG
NRG1 RefSeqGene	NG_012005.2:g.410710_410711insAG
NRG1 RefSeqGene	NG_012005.2:g.410710_410711insG

Gene: NRG1, neuregulin 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NRG1 transcript variant HRG-beta1c	NM_001159995.3:c.37+40550… NM_001159995.3:c.37+405500_37+405501insAAAAAAAAAAAAAAAAAG	N/A	Intron Variant
NRG1 transcript variant HRG-beta1b	NM_001159999.3:c.37+40550… NM_001159999.3:c.37+405500_37+405501insAAAAAAAAAAAAAAAAAG	N/A	Intron Variant
NRG1 transcript variant HRG-beta1d	NM_001160001.3:c.37+40550… NM_001160001.3:c.37+405500_37+405501insAAAAAAAAAAAAAAAAAG	N/A	Intron Variant
NRG1 transcript variant fetal-a-IV-1	NM_001322201.2:c.-556+405… NM_001322201.2:c.-556+405500_-556+405501insAAAAAAAAAAAAAAAAAG	N/A	Intron Variant
NRG1 transcript variant fetal-c-IV-2	NM_001322202.2:c.-505+405… NM_001322202.2:c.-505+405500_-505+405501insAAAAAAAAAAAAAAAAAG	N/A	Intron Variant
NRG1 transcript variant GGF2	NM_013962.3:c.745+404202_… NM_013962.3:c.745+404202_745+404203insAAAAAAAAAAAAAAAAAG	N/A	Intron Variant
NRG1 transcript variant ndf43c	NM_001159996.3:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant HRG-gamma2	NM_001160002.2:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant ndf43b	NM_001160004.3:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant HRG-beta3b	NM_001160005.2:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant HRG-gamma3	NM_001160007.2:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant HRG-beta2b	NM_001160008.2:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant VI-1	NM_001322197.2:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant NRG-III-beta1a	NM_001322205.2:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant III-2	NM_001322206.2:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant III-3	NM_001322207.2:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant HRG-gamma	NM_004495.4:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant HRG-beta1	NM_013956.5:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant HRG-beta2	NM_013957.5:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant HRG-beta3	NM_013958.4:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant SMDF	NM_013959.4:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant ndf43	NM_013960.5:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant HRG-alpha	NM_013964.5:c.	N/A	Genic Upstream Transcript Variant
NRG1 transcript variant X1	XM_011544512.3:c.745+4042… XM_011544512.3:c.745+404202_745+404203insAAAAAAAAAAAAAAAAAG	N/A	Intron Variant
NRG1 transcript variant X2	XM_017013367.2:c.745+4042… XM_017013367.2:c.745+404202_745+404203insAAAAAAAAAAAAAAAAAG	N/A	Intron Variant
NRG1 transcript variant X4	XM_017013371.3:c.745+4042… XM_017013371.3:c.745+404202_745+404203insAAAAAAAAAAAAAAAAAG	N/A	Intron Variant
NRG1 transcript variant X5	XM_017013372.3:c.745+4042… XM_017013372.3:c.745+404202_745+404203insAAAAAAAAAAAAAAAAAG	N/A	Intron Variant
NRG1 transcript variant X3	XM_017013368.3:c.	N/A	Genic Upstream Transcript Variant

Gene: NRG1-IT1, NRG1 intronic transcript 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NRG1-IT1 transcript variant 1	NR_104156.1:n.	N/A	Intron Variant
NRG1-IT1 transcript variant 2	NR_104157.1:n.	N/A	Intron Variant
NRG1-IT1 transcript variant 3	NR_104158.1:n.	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	=	ins(A)₁₇G	ins(A)₁₃G	ins(A)₆C	insAAAG	insAAG	insAG	insG
GRCh38.p14 chr 8	NC_000008.11:g.32044931_32044932=	NC_000008.11:g.32044931_32044932insAAAAAAAAAAAAAAAAAG	NC_000008.11:g.32044931_32044932insAAAAAAAAAAAAAG	NC_000008.11:g.32044931_32044932insAAAAAAC	NC_000008.11:g.32044931_32044932insAAAG	NC_000008.11:g.32044931_32044932insAAG	NC_000008.11:g.32044931_32044932insAG	NC_000008.11:g.32044931_32044932insG
GRCh37.p13 chr 8	NC_000008.10:g.31902447_31902448=	NC_000008.10:g.31902447_31902448insAAAAAAAAAAAAAAAAAG	NC_000008.10:g.31902447_31902448insAAAAAAAAAAAAAG	NC_000008.10:g.31902447_31902448insAAAAAAC	NC_000008.10:g.31902447_31902448insAAAG	NC_000008.10:g.31902447_31902448insAAG	NC_000008.10:g.31902447_31902448insAG	NC_000008.10:g.31902447_31902448insG
NRG1 RefSeqGene	NG_012005.2:g.410710_410711=	NG_012005.2:g.410710_410711insAAAAAAAAAAAAAAAAAG	NG_012005.2:g.410710_410711insAAAAAAAAAAAAAG	NG_012005.2:g.410710_410711insAAAAAAC	NG_012005.2:g.410710_410711insAAAG	NG_012005.2:g.410710_410711insAAG	NG_012005.2:g.410710_410711insAG	NG_012005.2:g.410710_410711insG
NRG1 transcript variant HRG-beta1c	NM_001159995.1:c.37+405501=	NM_001159995.1:c.37+405500_37+405501insAAAAAAAAAAAAAAAAAG	NM_001159995.1:c.37+405500_37+405501insAAAAAAAAAAAAAG	NM_001159995.1:c.37+405500_37+405501insAAAAAAC	NM_001159995.1:c.37+405500_37+405501insAAAG	NM_001159995.1:c.37+405500_37+405501insAAG	NM_001159995.1:c.37+405500_37+405501insAG	NM_001159995.1:c.37+405500_37+405501insG
NRG1 transcript variant HRG-beta1c	NM_001159995.3:c.37+405501=	NM_001159995.3:c.37+405500_37+405501insAAAAAAAAAAAAAAAAAG	NM_001159995.3:c.37+405500_37+405501insAAAAAAAAAAAAAG	NM_001159995.3:c.37+405500_37+405501insAAAAAAC	NM_001159995.3:c.37+405500_37+405501insAAAG	NM_001159995.3:c.37+405500_37+405501insAAG	NM_001159995.3:c.37+405500_37+405501insAG	NM_001159995.3:c.37+405500_37+405501insG
NRG1 transcript variant HRG-beta1b	NM_001159999.1:c.37+405501=	NM_001159999.1:c.37+405500_37+405501insAAAAAAAAAAAAAAAAAG	NM_001159999.1:c.37+405500_37+405501insAAAAAAAAAAAAAG	NM_001159999.1:c.37+405500_37+405501insAAAAAAC	NM_001159999.1:c.37+405500_37+405501insAAAG	NM_001159999.1:c.37+405500_37+405501insAAG	NM_001159999.1:c.37+405500_37+405501insAG	NM_001159999.1:c.37+405500_37+405501insG
NRG1 transcript variant HRG-beta1b	NM_001159999.3:c.37+405501=	NM_001159999.3:c.37+405500_37+405501insAAAAAAAAAAAAAAAAAG	NM_001159999.3:c.37+405500_37+405501insAAAAAAAAAAAAAG	NM_001159999.3:c.37+405500_37+405501insAAAAAAC	NM_001159999.3:c.37+405500_37+405501insAAAG	NM_001159999.3:c.37+405500_37+405501insAAG	NM_001159999.3:c.37+405500_37+405501insAG	NM_001159999.3:c.37+405500_37+405501insG
NRG1 transcript variant HRG-beta1d	NM_001160001.1:c.37+405501=	NM_001160001.1:c.37+405500_37+405501insAAAAAAAAAAAAAAAAAG	NM_001160001.1:c.37+405500_37+405501insAAAAAAAAAAAAAG	NM_001160001.1:c.37+405500_37+405501insAAAAAAC	NM_001160001.1:c.37+405500_37+405501insAAAG	NM_001160001.1:c.37+405500_37+405501insAAG	NM_001160001.1:c.37+405500_37+405501insAG	NM_001160001.1:c.37+405500_37+405501insG
NRG1 transcript variant HRG-beta1d	NM_001160001.3:c.37+405501=	NM_001160001.3:c.37+405500_37+405501insAAAAAAAAAAAAAAAAAG	NM_001160001.3:c.37+405500_37+405501insAAAAAAAAAAAAAG	NM_001160001.3:c.37+405500_37+405501insAAAAAAC	NM_001160001.3:c.37+405500_37+405501insAAAG	NM_001160001.3:c.37+405500_37+405501insAAG	NM_001160001.3:c.37+405500_37+405501insAG	NM_001160001.3:c.37+405500_37+405501insG
NRG1 transcript variant fetal-a-IV-1	NM_001322201.2:c.-556+405501=	NM_001322201.2:c.-556+405500_-556+405501insAAAAAAAAAAAAAAAAAG	NM_001322201.2:c.-556+405500_-556+405501insAAAAAAAAAAAAAG	NM_001322201.2:c.-556+405500_-556+405501insAAAAAAC	NM_001322201.2:c.-556+405500_-556+405501insAAAG	NM_001322201.2:c.-556+405500_-556+405501insAAG	NM_001322201.2:c.-556+405500_-556+405501insAG	NM_001322201.2:c.-556+405500_-556+405501insG
NRG1 transcript variant fetal-c-IV-2	NM_001322202.2:c.-505+405501=	NM_001322202.2:c.-505+405500_-505+405501insAAAAAAAAAAAAAAAAAG	NM_001322202.2:c.-505+405500_-505+405501insAAAAAAAAAAAAAG	NM_001322202.2:c.-505+405500_-505+405501insAAAAAAC	NM_001322202.2:c.-505+405500_-505+405501insAAAG	NM_001322202.2:c.-505+405500_-505+405501insAAG	NM_001322202.2:c.-505+405500_-505+405501insAG	NM_001322202.2:c.-505+405500_-505+405501insG
NRG1 transcript variant GGF2	NM_013962.2:c.745+404203=	NM_013962.2:c.745+404202_745+404203insAAAAAAAAAAAAAAAAAG	NM_013962.2:c.745+404202_745+404203insAAAAAAAAAAAAAG	NM_013962.2:c.745+404202_745+404203insAAAAAAC	NM_013962.2:c.745+404202_745+404203insAAAG	NM_013962.2:c.745+404202_745+404203insAAG	NM_013962.2:c.745+404202_745+404203insAG	NM_013962.2:c.745+404202_745+404203insG
NRG1 transcript variant GGF2	NM_013962.3:c.745+404203=	NM_013962.3:c.745+404202_745+404203insAAAAAAAAAAAAAAAAAG	NM_013962.3:c.745+404202_745+404203insAAAAAAAAAAAAAG	NM_013962.3:c.745+404202_745+404203insAAAAAAC	NM_013962.3:c.745+404202_745+404203insAAAG	NM_013962.3:c.745+404202_745+404203insAAG	NM_013962.3:c.745+404202_745+404203insAG	NM_013962.3:c.745+404202_745+404203insG
NRG1 transcript variant X4	XM_005273488.1:c.121+404203=	XM_005273488.1:c.121+404202_121+404203insAAAAAAAAAAAAAAAAAG	XM_005273488.1:c.121+404202_121+404203insAAAAAAAAAAAAAG	XM_005273488.1:c.121+404202_121+404203insAAAAAAC	XM_005273488.1:c.121+404202_121+404203insAAAG	XM_005273488.1:c.121+404202_121+404203insAAG	XM_005273488.1:c.121+404202_121+404203insAG	XM_005273488.1:c.121+404202_121+404203insG
NRG1 transcript variant X1	XM_011544512.3:c.745+404203=	XM_011544512.3:c.745+404202_745+404203insAAAAAAAAAAAAAAAAAG	XM_011544512.3:c.745+404202_745+404203insAAAAAAAAAAAAAG	XM_011544512.3:c.745+404202_745+404203insAAAAAAC	XM_011544512.3:c.745+404202_745+404203insAAAG	XM_011544512.3:c.745+404202_745+404203insAAG	XM_011544512.3:c.745+404202_745+404203insAG	XM_011544512.3:c.745+404202_745+404203insG
NRG1 transcript variant X2	XM_017013367.2:c.745+404203=	XM_017013367.2:c.745+404202_745+404203insAAAAAAAAAAAAAAAAAG	XM_017013367.2:c.745+404202_745+404203insAAAAAAAAAAAAAG	XM_017013367.2:c.745+404202_745+404203insAAAAAAC	XM_017013367.2:c.745+404202_745+404203insAAAG	XM_017013367.2:c.745+404202_745+404203insAAG	XM_017013367.2:c.745+404202_745+404203insAG	XM_017013367.2:c.745+404202_745+404203insG
NRG1 transcript variant X4	XM_017013371.3:c.745+404203=	XM_017013371.3:c.745+404202_745+404203insAAAAAAAAAAAAAAAAAG	XM_017013371.3:c.745+404202_745+404203insAAAAAAAAAAAAAG	XM_017013371.3:c.745+404202_745+404203insAAAAAAC	XM_017013371.3:c.745+404202_745+404203insAAAG	XM_017013371.3:c.745+404202_745+404203insAAG	XM_017013371.3:c.745+404202_745+404203insAG	XM_017013371.3:c.745+404202_745+404203insG
NRG1 transcript variant X5	XM_017013372.3:c.745+404203=	XM_017013372.3:c.745+404202_745+404203insAAAAAAAAAAAAAAAAAG	XM_017013372.3:c.745+404202_745+404203insAAAAAAAAAAAAAG	XM_017013372.3:c.745+404202_745+404203insAAAAAAC	XM_017013372.3:c.745+404202_745+404203insAAAG	XM_017013372.3:c.745+404202_745+404203insAAG	XM_017013372.3:c.745+404202_745+404203insAG	XM_017013372.3:c.745+404202_745+404203insG

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#.

11 SubSNP, 8 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GNOMAD	ss4181890328	Apr 26, 2021 (155)
2	GNOMAD	ss4181890329	Apr 26, 2021 (155)
3	GNOMAD	ss4181890330	Apr 26, 2021 (155)
4	GNOMAD	ss4181890331	Apr 26, 2021 (155)
5	GNOMAD	ss4181890332	Apr 26, 2021 (155)
6	GNOMAD	ss4181890333	Apr 26, 2021 (155)
7	GNOMAD	ss4181890334	Apr 26, 2021 (155)
8	1000G_HIGH_COVERAGE	ss5276652360	Oct 16, 2022 (156)
9	1000G_HIGH_COVERAGE	ss5276652361	Oct 16, 2022 (156)
10	HUGCELL_USP	ss5473272829	Oct 16, 2022 (156)
11	SANFORD_IMAGENETICS	ss5645107713	Oct 16, 2022 (156)
12	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291824178 (NC_000008.11:32044931::AAAAAAAAAAAAAAAAAG 2/120958) Row 291824179 (NC_000008.11:32044931::AAAAAAAAAAAAAG 3/120958) Row 291824180 (NC_000008.11:32044931::AAAAAAC 1/120958)...	-	Apr 26, 2021 (155)
13	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291824178 (NC_000008.11:32044931::AAAAAAAAAAAAAAAAAG 2/120958) Row 291824179 (NC_000008.11:32044931::AAAAAAAAAAAAAG 3/120958) Row 291824180 (NC_000008.11:32044931::AAAAAAC 1/120958)...	-	Apr 26, 2021 (155)
14	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291824178 (NC_000008.11:32044931::AAAAAAAAAAAAAAAAAG 2/120958) Row 291824179 (NC_000008.11:32044931::AAAAAAAAAAAAAG 3/120958) Row 291824180 (NC_000008.11:32044931::AAAAAAC 1/120958)...	-	Apr 26, 2021 (155)
15	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291824178 (NC_000008.11:32044931::AAAAAAAAAAAAAAAAAG 2/120958) Row 291824179 (NC_000008.11:32044931::AAAAAAAAAAAAAG 3/120958) Row 291824180 (NC_000008.11:32044931::AAAAAAC 1/120958)...	-	Apr 26, 2021 (155)
16	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291824178 (NC_000008.11:32044931::AAAAAAAAAAAAAAAAAG 2/120958) Row 291824179 (NC_000008.11:32044931::AAAAAAAAAAAAAG 3/120958) Row 291824180 (NC_000008.11:32044931::AAAAAAC 1/120958)...	-	Apr 26, 2021 (155)
17	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291824178 (NC_000008.11:32044931::AAAAAAAAAAAAAAAAAG 2/120958) Row 291824179 (NC_000008.11:32044931::AAAAAAAAAAAAAG 3/120958) Row 291824180 (NC_000008.11:32044931::AAAAAAC 1/120958)...	-	Apr 26, 2021 (155)
18	gnomAD - Genomes Submission ignored due to conflicting rows: Row 291824178 (NC_000008.11:32044931::AAAAAAAAAAAAAAAAAG 2/120958) Row 291824179 (NC_000008.11:32044931::AAAAAAAAAAAAAG 3/120958) Row 291824180 (NC_000008.11:32044931::AAAAAAC 1/120958)...	-	Apr 26, 2021 (155)
19	ALFA	NC_000008.11 - 32044932	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
ss4181890328	NC_000008.11:32044931::AAAAAAAAAAA… NC_000008.11:32044931::AAAAAAAAAAAAAAAAAG	NC_000008.11:32044931::AAAAAAAAAAA… NC_000008.11:32044931::AAAAAAAAAAAAAAAAAG	(self)
ss4181890329	NC_000008.11:32044931::AAAAAAAAAAA… NC_000008.11:32044931::AAAAAAAAAAAAAG	NC_000008.11:32044931::AAAAAAAAAAA… NC_000008.11:32044931::AAAAAAAAAAAAAG	(self)
6783355973, ss4181890330	NC_000008.11:32044931::AAAAAAC	NC_000008.11:32044931::AAAAAAC	(self)
ss4181890331	NC_000008.11:32044931::AAAG	NC_000008.11:32044931::AAAG	(self)
6783355973, ss4181890332, ss5276652361	NC_000008.11:32044931::AAG	NC_000008.11:32044931::AAG	(self)
ss5645107713	NC_000008.10:31902447::AG	NC_000008.11:32044931::AG
6783355973, ss4181890333, ss5276652360, ss5473272829	NC_000008.11:32044931::AG	NC_000008.11:32044931::AG	(self)
6783355973, ss4181890334	NC_000008.11:32044931::G	NC_000008.11:32044931::G	(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 rs1491195459

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

rs1491195459