Name: rs1491043686
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.

rs1491043686

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:88057756-88057757 (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: insT
Variation Type: Insertion
Frequency: insT=0.00000 (0/10680, ALFA)
insT=0.0006 (1/1584, GnomAD)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BANP : 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	10680	=1.00000	T=0.00000	1.0	N/A
European	Sub	6962	=1.0000	T=0.0000	1.0	N/A
African	Sub	2294	=1.0000	T=0.0000	1.0	N/A
African Others	Sub	84	=1.00	T=0.00	1.0	N/A
African American	Sub	2210	=1.0000	T=0.0000	1.0	N/A
Asian	Sub	108	=1.000	T=0.000	1.0	N/A
East Asian	Sub	84	=1.00	T=0.00	1.0	N/A
Other Asian	Sub	24	=1.00	T=0.00	1.0	N/A
Latin American 1	Sub	146	=1.000	T=0.000	1.0	N/A
Latin American 2	Sub	610	=1.000	T=0.000	1.0	N/A
South Asian	Sub	94	=1.00	T=0.00	1.0	N/A
Other	Sub	466	=1.000	T=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	10680	- No frequency provided	insT=0.00000
Allele Frequency Aggregator	European	Sub	6962	- No frequency provided	insT=0.0000
Allele Frequency Aggregator	African	Sub	2294	- No frequency provided	insT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	- No frequency provided	insT=0.000
Allele Frequency Aggregator	Other	Sub	466	- No frequency provided	insT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	- No frequency provided	insT=0.000
Allele Frequency Aggregator	Asian	Sub	108	- No frequency provided	insT=0.000
Allele Frequency Aggregator	South Asian	Sub	94	- No frequency provided	insT=0.00
gnomAD - Genomes	Global	Study-wide	1584	- No frequency provided	insT=0.0006
gnomAD - Genomes	African	Sub	1518	- No frequency provided	insT=0.0007
gnomAD - Genomes	American	Sub	34	- No frequency provided	insT=0.00
gnomAD - Genomes	European	Sub	20	- No frequency provided	insT=0.00
gnomAD - Genomes	Other	Sub	8	- No frequency provided	insT=0.0
gnomAD - Genomes	Ashkenazi Jewish	Sub	4	- No frequency provided	insT=0.0
gnomAD - Genomes	East Asian	Sub	0	- No frequency provided	insT=0

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 16	NC_000016.10:g.88057756_88057757insT
GRCh37.p13 chr 16	NC_000016.9:g.88091362_88091363insT
BANP RefSeqGene	NG_029918.1:g.111325_111326insT

Gene: BANP, BTG3 associated nuclear protein (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BANP transcript variant 3	NM_001173539.2:c.1303-143… NM_001173539.2:c.1303-14313_1303-14312insT	N/A	Intron Variant
BANP transcript variant 4	NM_001173540.2:c.1213-751… NM_001173540.2:c.1213-7511_1213-7510insT	N/A	Intron Variant
BANP transcript variant 5	NM_001173541.2:c.1186-143… NM_001173541.2:c.1186-14313_1186-14312insT	N/A	Intron Variant
BANP transcript variant 6	NM_001173542.1:c.1312-143… NM_001173542.1:c.1312-14313_1312-14312insT	N/A	Intron Variant
BANP transcript variant 7	NM_001173543.1:c.1279-751… NM_001173543.1:c.1279-7511_1279-7510insT	N/A	Intron Variant
BANP transcript variant 8	NM_001384916.1:c.1195-143… NM_001384916.1:c.1195-14313_1195-14312insT	N/A	Intron Variant
BANP transcript variant 9	NM_001384918.1:c.1303-143… NM_001384918.1:c.1303-14313_1303-14312insT	N/A	Intron Variant
BANP transcript variant 10	NM_001384919.1:c.1303-143… NM_001384919.1:c.1303-14313_1303-14312insT	N/A	Intron Variant
BANP transcript variant 11	NM_001384920.1:c.1303-143… NM_001384920.1:c.1303-14313_1303-14312insT	N/A	Intron Variant
BANP transcript variant 12	NM_001384921.1:c.1186-143… NM_001384921.1:c.1186-14313_1186-14312insT	N/A	Intron Variant
BANP transcript variant 13	NM_001384922.1:c.1186-143… NM_001384922.1:c.1186-14313_1186-14312insT	N/A	Intron Variant
BANP transcript variant 14	NM_001384923.1:c.1186-143… NM_001384923.1:c.1186-14313_1186-14312insT	N/A	Intron Variant
BANP transcript variant 15	NM_001384925.1:c.1312-143… NM_001384925.1:c.1312-14313_1312-14312insT	N/A	Intron Variant
BANP transcript variant 16	NM_001384926.1:c.1312-143… NM_001384926.1:c.1312-14313_1312-14312insT	N/A	Intron Variant
BANP transcript variant 17	NM_001384927.1:c.1312-143… NM_001384927.1:c.1312-14313_1312-14312insT	N/A	Intron Variant
BANP transcript variant 18	NM_001384928.1:c.1330-143… NM_001384928.1:c.1330-14313_1330-14312insT	N/A	Intron Variant
BANP transcript variant 19	NM_001384929.1:c.1330-143… NM_001384929.1:c.1330-14313_1330-14312insT	N/A	Intron Variant
BANP transcript variant 20	NM_001384931.1:c.1321-143… NM_001384931.1:c.1321-14313_1321-14312insT	N/A	Intron Variant
BANP transcript variant 21	NM_001384935.1:c.1321-143… NM_001384935.1:c.1321-14313_1321-14312insT	N/A	Intron Variant
BANP transcript variant 22	NM_001384936.1:c.1213-143… NM_001384936.1:c.1213-14313_1213-14312insT	N/A	Intron Variant
BANP transcript variant 23	NM_001384937.1:c.1213-143… NM_001384937.1:c.1213-14313_1213-14312insT	N/A	Intron Variant
BANP transcript variant 24	NM_001384938.1:c.1204-143… NM_001384938.1:c.1204-14313_1204-14312insT	N/A	Intron Variant
BANP transcript variant 25	NM_001384939.1:c.1003-143… NM_001384939.1:c.1003-14313_1003-14312insT	N/A	Intron Variant
BANP transcript variant 26	NM_001384940.1:c.1003-143… NM_001384940.1:c.1003-14313_1003-14312insT	N/A	Intron Variant
BANP transcript variant 27	NM_001384941.1:c.994-1431… NM_001384941.1:c.994-14313_994-14312insT	N/A	Intron Variant
BANP transcript variant 28	NM_001384942.1:c.994-1431… NM_001384942.1:c.994-14313_994-14312insT	N/A	Intron Variant
BANP transcript variant 29	NM_001384943.1:c.886-1431… NM_001384943.1:c.886-14313_886-14312insT	N/A	Intron Variant
BANP transcript variant 30	NM_001384944.1:c.877-1431… NM_001384944.1:c.877-14313_877-14312insT	N/A	Intron Variant
BANP transcript variant 31	NM_001386991.1:c.1312-751… NM_001386991.1:c.1312-7511_1312-7510insT	N/A	Intron Variant
BANP transcript variant 32	NM_001386992.1:c.1303-751… NM_001386992.1:c.1303-7511_1303-7510insT	N/A	Intron Variant
BANP transcript variant 1	NM_017869.4:c.1195-14313_… NM_017869.4:c.1195-14313_1195-14312insT	N/A	Intron Variant
BANP transcript variant 2	NM_079837.3:c.1195-7511_1… NM_079837.3:c.1195-7511_1195-7510insT	N/A	Intron Variant
BANP transcript variant X1	XM_011523170.2:c.1330-751… XM_011523170.2:c.1330-7511_1330-7510insT	N/A	Intron Variant
BANP transcript variant X2	XM_011523174.3:c.1330-751… XM_011523174.3:c.1330-7511_1330-7510insT	N/A	Intron Variant
BANP transcript variant X6	XM_011523175.4:c.1330-751… XM_011523175.4:c.1330-7511_1330-7510insT	N/A	Intron Variant
BANP transcript variant X5	XM_011523176.3:c.1330-751… XM_011523176.3:c.1330-7511_1330-7510insT	N/A	Intron Variant
BANP transcript variant X7	XM_011523178.2:c.1321-751… XM_011523178.2:c.1321-7511_1321-7510insT	N/A	Intron Variant
BANP transcript variant X8	XM_011523180.3:c.1312-751… XM_011523180.3:c.1312-7511_1312-7510insT	N/A	Intron Variant
BANP transcript variant X12	XM_017023379.3:c.1303-751… XM_017023379.3:c.1303-7511_1303-7510insT	N/A	Intron Variant
BANP transcript variant X19	XM_017023380.2:c.1186-751… XM_017023380.2:c.1186-7511_1186-7510insT	N/A	Intron Variant
BANP transcript variant X22	XM_024450327.2:c.1003-751… XM_024450327.2:c.1003-7511_1003-7510insT	N/A	Intron Variant
BANP transcript variant X3	XM_047434280.1:c.1330-751… XM_047434280.1:c.1330-7511_1330-7510insT	N/A	Intron Variant
BANP transcript variant X4	XM_047434281.1:c.1330-751… XM_047434281.1:c.1330-7511_1330-7510insT	N/A	Intron Variant
BANP transcript variant X9	XM_047434283.1:c.1312-751… XM_047434283.1:c.1312-7511_1312-7510insT	N/A	Intron Variant
BANP transcript variant X10	XM_047434284.1:c.1312-751… XM_047434284.1:c.1312-7511_1312-7510insT	N/A	Intron Variant
BANP transcript variant X11	XM_047434285.1:c.1303-751… XM_047434285.1:c.1303-7511_1303-7510insT	N/A	Intron Variant
BANP transcript variant X13	XM_047434286.1:c.1303-751… XM_047434286.1:c.1303-7511_1303-7510insT	N/A	Intron Variant
BANP transcript variant X14	XM_047434287.1:c.1303-751… XM_047434287.1:c.1303-7511_1303-7510insT	N/A	Intron Variant
BANP transcript variant X15	XM_047434288.1:c.1303-143… XM_047434288.1:c.1303-14313_1303-14312insT	N/A	Intron Variant
BANP transcript variant X16	XM_047434290.1:c.1303-143… XM_047434290.1:c.1303-14313_1303-14312insT	N/A	Intron Variant
BANP transcript variant X17	XM_047434291.1:c.1303-143… XM_047434291.1:c.1303-14313_1303-14312insT	N/A	Intron Variant
BANP transcript variant X18	XM_047434292.1:c.1204-751… XM_047434292.1:c.1204-7511_1204-7510insT	N/A	Intron Variant
BANP transcript variant X20	XM_047434293.1:c.1186-751… XM_047434293.1:c.1186-7511_1186-7510insT	N/A	Intron Variant
BANP transcript variant X21	XM_047434294.1:c.1186-751… XM_047434294.1:c.1186-7511_1186-7510insT	N/A	Intron Variant
BANP transcript variant X23	XM_047434295.1:c.994-7511… XM_047434295.1:c.994-7511_994-7510insT	N/A	Intron Variant
BANP transcript variant X24	XM_047434296.1:c.967-7511… XM_047434296.1:c.967-7511_967-7510insT	N/A	Intron Variant
BANP transcript variant X25	XM_047434297.1:c.994-1431… XM_047434297.1:c.994-14313_994-14312insT	N/A	Intron Variant
BANP transcript variant X26	XM_047434298.1:c.886-7511… XM_047434298.1:c.886-7511_886-7510insT	N/A	Intron Variant
BANP transcript variant X27	XM_047434299.1:c.877-7511… XM_047434299.1:c.877-7511_877-7510insT	N/A	Intron Variant
BANP transcript variant X28	XM_047434300.1:c.877-1431… XM_047434300.1:c.877-14313_877-14312insT	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	=	insT
GRCh38.p14 chr 16	NC_000016.10:g.88057756_88057757=	NC_000016.10:g.88057756_88057757insT
GRCh37.p13 chr 16	NC_000016.9:g.88091362_88091363=	NC_000016.9:g.88091362_88091363insT
BANP RefSeqGene	NG_029918.1:g.111325_111326=	NG_029918.1:g.111325_111326insT
BANP transcript variant 3	NM_001173539.1:c.1303-14312=	NM_001173539.1:c.1303-14313_1303-14312insT
BANP transcript variant 3	NM_001173539.2:c.1303-14312=	NM_001173539.2:c.1303-14313_1303-14312insT
BANP transcript variant 4	NM_001173540.1:c.1213-7510=	NM_001173540.1:c.1213-7511_1213-7510insT
BANP transcript variant 4	NM_001173540.2:c.1213-7510=	NM_001173540.2:c.1213-7511_1213-7510insT
BANP transcript variant 5	NM_001173541.1:c.1186-14312=	NM_001173541.1:c.1186-14313_1186-14312insT
BANP transcript variant 5	NM_001173541.2:c.1186-14312=	NM_001173541.2:c.1186-14313_1186-14312insT
BANP transcript variant 6	NM_001173542.1:c.1312-14312=	NM_001173542.1:c.1312-14313_1312-14312insT
BANP transcript variant 7	NM_001173543.1:c.1279-7510=	NM_001173543.1:c.1279-7511_1279-7510insT
BANP transcript variant 8	NM_001384916.1:c.1195-14312=	NM_001384916.1:c.1195-14313_1195-14312insT
BANP transcript variant 9	NM_001384918.1:c.1303-14312=	NM_001384918.1:c.1303-14313_1303-14312insT
BANP transcript variant 10	NM_001384919.1:c.1303-14312=	NM_001384919.1:c.1303-14313_1303-14312insT
BANP transcript variant 11	NM_001384920.1:c.1303-14312=	NM_001384920.1:c.1303-14313_1303-14312insT
BANP transcript variant 12	NM_001384921.1:c.1186-14312=	NM_001384921.1:c.1186-14313_1186-14312insT
BANP transcript variant 13	NM_001384922.1:c.1186-14312=	NM_001384922.1:c.1186-14313_1186-14312insT
BANP transcript variant 14	NM_001384923.1:c.1186-14312=	NM_001384923.1:c.1186-14313_1186-14312insT
BANP transcript variant 15	NM_001384925.1:c.1312-14312=	NM_001384925.1:c.1312-14313_1312-14312insT
BANP transcript variant 16	NM_001384926.1:c.1312-14312=	NM_001384926.1:c.1312-14313_1312-14312insT
BANP transcript variant 17	NM_001384927.1:c.1312-14312=	NM_001384927.1:c.1312-14313_1312-14312insT
BANP transcript variant 18	NM_001384928.1:c.1330-14312=	NM_001384928.1:c.1330-14313_1330-14312insT
BANP transcript variant 19	NM_001384929.1:c.1330-14312=	NM_001384929.1:c.1330-14313_1330-14312insT
BANP transcript variant 20	NM_001384931.1:c.1321-14312=	NM_001384931.1:c.1321-14313_1321-14312insT
BANP transcript variant 21	NM_001384935.1:c.1321-14312=	NM_001384935.1:c.1321-14313_1321-14312insT
BANP transcript variant 22	NM_001384936.1:c.1213-14312=	NM_001384936.1:c.1213-14313_1213-14312insT
BANP transcript variant 23	NM_001384937.1:c.1213-14312=	NM_001384937.1:c.1213-14313_1213-14312insT
BANP transcript variant 24	NM_001384938.1:c.1204-14312=	NM_001384938.1:c.1204-14313_1204-14312insT
BANP transcript variant 25	NM_001384939.1:c.1003-14312=	NM_001384939.1:c.1003-14313_1003-14312insT
BANP transcript variant 26	NM_001384940.1:c.1003-14312=	NM_001384940.1:c.1003-14313_1003-14312insT
BANP transcript variant 27	NM_001384941.1:c.994-14312=	NM_001384941.1:c.994-14313_994-14312insT
BANP transcript variant 28	NM_001384942.1:c.994-14312=	NM_001384942.1:c.994-14313_994-14312insT
BANP transcript variant 29	NM_001384943.1:c.886-14312=	NM_001384943.1:c.886-14313_886-14312insT
BANP transcript variant 30	NM_001384944.1:c.877-14312=	NM_001384944.1:c.877-14313_877-14312insT
BANP transcript variant 31	NM_001386991.1:c.1312-7510=	NM_001386991.1:c.1312-7511_1312-7510insT
BANP transcript variant 32	NM_001386992.1:c.1303-7510=	NM_001386992.1:c.1303-7511_1303-7510insT
BANP transcript variant 1	NM_017869.3:c.1195-14312=	NM_017869.3:c.1195-14313_1195-14312insT
BANP transcript variant 1	NM_017869.4:c.1195-14312=	NM_017869.4:c.1195-14313_1195-14312insT
BANP transcript variant 2	NM_079837.2:c.1195-7510=	NM_079837.2:c.1195-7511_1195-7510insT
BANP transcript variant 2	NM_079837.3:c.1195-7510=	NM_079837.3:c.1195-7511_1195-7510insT
BANP transcript variant X1	XM_005256007.1:c.1279-7510=	XM_005256007.1:c.1279-7511_1279-7510insT
BANP transcript variant X2	XM_005256008.1:c.1330-14312=	XM_005256008.1:c.1330-14313_1330-14312insT
BANP transcript variant X3	XM_005256009.1:c.1312-14312=	XM_005256009.1:c.1312-14313_1312-14312insT
BANP transcript variant X4	XM_005256010.1:c.1003-14312=	XM_005256010.1:c.1003-14313_1003-14312insT
BANP transcript variant X5	XM_005256011.1:c.1003-14312=	XM_005256011.1:c.1003-14313_1003-14312insT
BANP transcript variant X6	XM_005256012.1:c.886-14312=	XM_005256012.1:c.886-14313_886-14312insT
BANP transcript variant X1	XM_011523170.2:c.1330-7510=	XM_011523170.2:c.1330-7511_1330-7510insT
BANP transcript variant X2	XM_011523174.3:c.1330-7510=	XM_011523174.3:c.1330-7511_1330-7510insT
BANP transcript variant X6	XM_011523175.4:c.1330-7510=	XM_011523175.4:c.1330-7511_1330-7510insT
BANP transcript variant X5	XM_011523176.3:c.1330-7510=	XM_011523176.3:c.1330-7511_1330-7510insT
BANP transcript variant X7	XM_011523178.2:c.1321-7510=	XM_011523178.2:c.1321-7511_1321-7510insT
BANP transcript variant X8	XM_011523180.3:c.1312-7510=	XM_011523180.3:c.1312-7511_1312-7510insT
BANP transcript variant X12	XM_017023379.3:c.1303-7510=	XM_017023379.3:c.1303-7511_1303-7510insT
BANP transcript variant X19	XM_017023380.2:c.1186-7510=	XM_017023380.2:c.1186-7511_1186-7510insT
BANP transcript variant X22	XM_024450327.2:c.1003-7510=	XM_024450327.2:c.1003-7511_1003-7510insT
BANP transcript variant X3	XM_047434280.1:c.1330-7510=	XM_047434280.1:c.1330-7511_1330-7510insT
BANP transcript variant X4	XM_047434281.1:c.1330-7510=	XM_047434281.1:c.1330-7511_1330-7510insT
BANP transcript variant X9	XM_047434283.1:c.1312-7510=	XM_047434283.1:c.1312-7511_1312-7510insT
BANP transcript variant X10	XM_047434284.1:c.1312-7510=	XM_047434284.1:c.1312-7511_1312-7510insT
BANP transcript variant X11	XM_047434285.1:c.1303-7510=	XM_047434285.1:c.1303-7511_1303-7510insT
BANP transcript variant X13	XM_047434286.1:c.1303-7510=	XM_047434286.1:c.1303-7511_1303-7510insT
BANP transcript variant X14	XM_047434287.1:c.1303-7510=	XM_047434287.1:c.1303-7511_1303-7510insT
BANP transcript variant X15	XM_047434288.1:c.1303-14312=	XM_047434288.1:c.1303-14313_1303-14312insT
BANP transcript variant X16	XM_047434290.1:c.1303-14312=	XM_047434290.1:c.1303-14313_1303-14312insT
BANP transcript variant X17	XM_047434291.1:c.1303-14312=	XM_047434291.1:c.1303-14313_1303-14312insT
BANP transcript variant X18	XM_047434292.1:c.1204-7510=	XM_047434292.1:c.1204-7511_1204-7510insT
BANP transcript variant X20	XM_047434293.1:c.1186-7510=	XM_047434293.1:c.1186-7511_1186-7510insT
BANP transcript variant X21	XM_047434294.1:c.1186-7510=	XM_047434294.1:c.1186-7511_1186-7510insT
BANP transcript variant X23	XM_047434295.1:c.994-7510=	XM_047434295.1:c.994-7511_994-7510insT
BANP transcript variant X24	XM_047434296.1:c.967-7510=	XM_047434296.1:c.967-7511_967-7510insT
BANP transcript variant X25	XM_047434297.1:c.994-14312=	XM_047434297.1:c.994-14313_994-14312insT
BANP transcript variant X26	XM_047434298.1:c.886-7510=	XM_047434298.1:c.886-7511_886-7510insT
BANP transcript variant X27	XM_047434299.1:c.877-7510=	XM_047434299.1:c.877-7511_877-7510insT
BANP transcript variant X28	XM_047434300.1:c.877-14312=	XM_047434300.1:c.877-14313_877-14312insT

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	ss2946473311	Nov 17, 2017 (151)
2	gnomAD - Genomes	NC_000016.10 - 88057757	Apr 27, 2021 (155)
3	ALFA	NC_000016.10 - 88057757	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
ss2946473311	NC_000016.9:88091362::T	NC_000016.10:88057756::T	(self)
498425099, 5542166130	NC_000016.10:88057756::T	NC_000016.10:88057756::T	(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 rs1491043686

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

rs1491043686