Name: rs1187184475
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.

rs1187184475

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:29450743-29450762 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₈ / del(A)₇ / del(A)₆ / del(…
del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₇
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₈=0.0000 (0/9484, ALFA)
del(A)₇=0.0000 (0/9484, ALFA)
del(A)₆=0.0000 (0/9484, ALFA) (+ 11 more)
del(A)₅=0.0000 (0/9484, ALFA)
del(A)₄=0.0000 (0/9484, ALFA)
delAAA=0.0000 (0/9484, ALFA)
delAA=0.0000 (0/9484, ALFA)
delA=0.0000 (0/9484, ALFA)
dupA=0.0000 (0/9484, ALFA)
dupAA=0.0000 (0/9484, ALFA)
dupAAA=0.0000 (0/9484, ALFA)
dup(A)₄=0.0000 (0/9484, ALFA)
dup(A)₅=0.0000 (0/9484, ALFA)
dup(A)₇=0.0000 (0/9484, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BOLA2-SMG1P6 : 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	9484	AAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	6674	AAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1664	AAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	60	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	1604	AAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	82	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	62	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	20	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	110	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Latin American 2	Sub	520	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	62	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	372	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=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	9484	(A)₂₀=1.0000	del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₇=0.0000
Allele Frequency Aggregator	European	Sub	6674	(A)₂₀=1.0000	del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₇=0.0000
Allele Frequency Aggregator	African	Sub	1664	(A)₂₀=1.0000	del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	520	(A)₂₀=1.000	del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₇=0.000
Allele Frequency Aggregator	Other	Sub	372	(A)₂₀=1.000	del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	110	(A)₂₀=1.000	del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₇=0.000
Allele Frequency Aggregator	Asian	Sub	82	(A)₂₀=1.00	del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	62	(A)₂₀=1.00	del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₇=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 16	NC_000016.10:g.29450755_29450762del
GRCh38.p14 chr 16	NC_000016.10:g.29450756_29450762del
GRCh38.p14 chr 16	NC_000016.10:g.29450757_29450762del
GRCh38.p14 chr 16	NC_000016.10:g.29450758_29450762del
GRCh38.p14 chr 16	NC_000016.10:g.29450759_29450762del
GRCh38.p14 chr 16	NC_000016.10:g.29450760_29450762del
GRCh38.p14 chr 16	NC_000016.10:g.29450761_29450762del
GRCh38.p14 chr 16	NC_000016.10:g.29450762del
GRCh38.p14 chr 16	NC_000016.10:g.29450762dup
GRCh38.p14 chr 16	NC_000016.10:g.29450761_29450762dup
GRCh38.p14 chr 16	NC_000016.10:g.29450760_29450762dup
GRCh38.p14 chr 16	NC_000016.10:g.29450759_29450762dup
GRCh38.p14 chr 16	NC_000016.10:g.29450758_29450762dup
GRCh38.p14 chr 16	NC_000016.10:g.29450756_29450762dup
GRCh37.p13 chr 16	NC_000016.9:g.29462076_29462083del
GRCh37.p13 chr 16	NC_000016.9:g.29462077_29462083del
GRCh37.p13 chr 16	NC_000016.9:g.29462078_29462083del
GRCh37.p13 chr 16	NC_000016.9:g.29462079_29462083del
GRCh37.p13 chr 16	NC_000016.9:g.29462080_29462083del
GRCh37.p13 chr 16	NC_000016.9:g.29462081_29462083del
GRCh37.p13 chr 16	NC_000016.9:g.29462082_29462083del
GRCh37.p13 chr 16	NC_000016.9:g.29462083del
GRCh37.p13 chr 16	NC_000016.9:g.29462083dup
GRCh37.p13 chr 16	NC_000016.9:g.29462082_29462083dup
GRCh37.p13 chr 16	NC_000016.9:g.29462081_29462083dup
GRCh37.p13 chr 16	NC_000016.9:g.29462080_29462083dup
GRCh37.p13 chr 16	NC_000016.9:g.29462079_29462083dup
GRCh37.p13 chr 16	NC_000016.9:g.29462077_29462083dup

Gene: BOLA2-SMG1P6, BOLA2-SMG1P6 readthrough (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BOLA2-SMG1P6 transcript variant 1	NM_001320622.1:c.321+3266… NM_001320622.1:c.321+3266_321+3273del	N/A	Intron Variant
BOLA2-SMG1P6 transcript variant 2	NM_001320623.1:c.359+3266… NM_001320623.1:c.359+3266_359+3273del	N/A	Intron Variant
BOLA2-SMG1P6 transcript variant 3	NM_001320624.1:c.261+3441… NM_001320624.1:c.261+3441_261+3448del	N/A	Intron Variant
BOLA2-SMG1P6 transcript variant 4	NM_001320625.1:c.5+3441_5… NM_001320625.1:c.5+3441_5+3448del	N/A	Intron Variant
BOLA2-SMG1P6 transcript variant 5	NM_001320627.1:c.-16+3266… NM_001320627.1:c.-16+3266_-16+3273del	N/A	Intron Variant
BOLA2-SMG1P6 transcript variant 6	NM_001320628.1:c.-16+3266… NM_001320628.1:c.-16+3266_-16+3273del	N/A	Intron Variant
BOLA2-SMG1P6 transcript variant 7	NR_135316.1: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	(A)₂₀=	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₇
GRCh38.p14 chr 16	NC_000016.10:g.29450743_29450762=	NC_000016.10:g.29450755_29450762del	NC_000016.10:g.29450756_29450762del	NC_000016.10:g.29450757_29450762del	NC_000016.10:g.29450758_29450762del	NC_000016.10:g.29450759_29450762del	NC_000016.10:g.29450760_29450762del	NC_000016.10:g.29450761_29450762del	NC_000016.10:g.29450762del	NC_000016.10:g.29450762dup	NC_000016.10:g.29450761_29450762dup	NC_000016.10:g.29450760_29450762dup	NC_000016.10:g.29450759_29450762dup	NC_000016.10:g.29450758_29450762dup	NC_000016.10:g.29450756_29450762dup
GRCh37.p13 chr 16	NC_000016.9:g.29462064_29462083=	NC_000016.9:g.29462076_29462083del	NC_000016.9:g.29462077_29462083del	NC_000016.9:g.29462078_29462083del	NC_000016.9:g.29462079_29462083del	NC_000016.9:g.29462080_29462083del	NC_000016.9:g.29462081_29462083del	NC_000016.9:g.29462082_29462083del	NC_000016.9:g.29462083del	NC_000016.9:g.29462083dup	NC_000016.9:g.29462082_29462083dup	NC_000016.9:g.29462081_29462083dup	NC_000016.9:g.29462080_29462083dup	NC_000016.9:g.29462079_29462083dup	NC_000016.9:g.29462077_29462083dup
BOLA2-SMG1P6 transcript variant 1	NM_001320622.1:c.321+3273=	NM_001320622.1:c.321+3266_321+3273del	NM_001320622.1:c.321+3267_321+3273del	NM_001320622.1:c.321+3268_321+3273del	NM_001320622.1:c.321+3269_321+3273del	NM_001320622.1:c.321+3270_321+3273del	NM_001320622.1:c.321+3271_321+3273del	NM_001320622.1:c.321+3272_321+3273del	NM_001320622.1:c.321+3273del	NM_001320622.1:c.321+3273dup	NM_001320622.1:c.321+3272_321+3273dup	NM_001320622.1:c.321+3271_321+3273dup	NM_001320622.1:c.321+3270_321+3273dup	NM_001320622.1:c.321+3269_321+3273dup	NM_001320622.1:c.321+3267_321+3273dup
BOLA2-SMG1P6 transcript variant 2	NM_001320623.1:c.359+3273=	NM_001320623.1:c.359+3266_359+3273del	NM_001320623.1:c.359+3267_359+3273del	NM_001320623.1:c.359+3268_359+3273del	NM_001320623.1:c.359+3269_359+3273del	NM_001320623.1:c.359+3270_359+3273del	NM_001320623.1:c.359+3271_359+3273del	NM_001320623.1:c.359+3272_359+3273del	NM_001320623.1:c.359+3273del	NM_001320623.1:c.359+3273dup	NM_001320623.1:c.359+3272_359+3273dup	NM_001320623.1:c.359+3271_359+3273dup	NM_001320623.1:c.359+3270_359+3273dup	NM_001320623.1:c.359+3269_359+3273dup	NM_001320623.1:c.359+3267_359+3273dup
BOLA2-SMG1P6 transcript variant 3	NM_001320624.1:c.261+3448=	NM_001320624.1:c.261+3441_261+3448del	NM_001320624.1:c.261+3442_261+3448del	NM_001320624.1:c.261+3443_261+3448del	NM_001320624.1:c.261+3444_261+3448del	NM_001320624.1:c.261+3445_261+3448del	NM_001320624.1:c.261+3446_261+3448del	NM_001320624.1:c.261+3447_261+3448del	NM_001320624.1:c.261+3448del	NM_001320624.1:c.261+3448dup	NM_001320624.1:c.261+3447_261+3448dup	NM_001320624.1:c.261+3446_261+3448dup	NM_001320624.1:c.261+3445_261+3448dup	NM_001320624.1:c.261+3444_261+3448dup	NM_001320624.1:c.261+3442_261+3448dup
BOLA2-SMG1P6 transcript variant 4	NM_001320625.1:c.5+3448=	NM_001320625.1:c.5+3441_5+3448del	NM_001320625.1:c.5+3442_5+3448del	NM_001320625.1:c.5+3443_5+3448del	NM_001320625.1:c.5+3444_5+3448del	NM_001320625.1:c.5+3445_5+3448del	NM_001320625.1:c.5+3446_5+3448del	NM_001320625.1:c.5+3447_5+3448del	NM_001320625.1:c.5+3448del	NM_001320625.1:c.5+3448dup	NM_001320625.1:c.5+3447_5+3448dup	NM_001320625.1:c.5+3446_5+3448dup	NM_001320625.1:c.5+3445_5+3448dup	NM_001320625.1:c.5+3444_5+3448dup	NM_001320625.1:c.5+3442_5+3448dup
BOLA2-SMG1P6 transcript variant 5	NM_001320627.1:c.-16+3273=	NM_001320627.1:c.-16+3266_-16+3273del	NM_001320627.1:c.-16+3267_-16+3273del	NM_001320627.1:c.-16+3268_-16+3273del	NM_001320627.1:c.-16+3269_-16+3273del	NM_001320627.1:c.-16+3270_-16+3273del	NM_001320627.1:c.-16+3271_-16+3273del	NM_001320627.1:c.-16+3272_-16+3273del	NM_001320627.1:c.-16+3273del	NM_001320627.1:c.-16+3273dup	NM_001320627.1:c.-16+3272_-16+3273dup	NM_001320627.1:c.-16+3271_-16+3273dup	NM_001320627.1:c.-16+3270_-16+3273dup	NM_001320627.1:c.-16+3269_-16+3273dup	NM_001320627.1:c.-16+3267_-16+3273dup
BOLA2-SMG1P6 transcript variant 6	NM_001320628.1:c.-16+3273=	NM_001320628.1:c.-16+3266_-16+3273del	NM_001320628.1:c.-16+3267_-16+3273del	NM_001320628.1:c.-16+3268_-16+3273del	NM_001320628.1:c.-16+3269_-16+3273del	NM_001320628.1:c.-16+3270_-16+3273del	NM_001320628.1:c.-16+3271_-16+3273del	NM_001320628.1:c.-16+3272_-16+3273del	NM_001320628.1:c.-16+3273del	NM_001320628.1:c.-16+3273dup	NM_001320628.1:c.-16+3272_-16+3273dup	NM_001320628.1:c.-16+3271_-16+3273dup	NM_001320628.1:c.-16+3270_-16+3273dup	NM_001320628.1:c.-16+3269_-16+3273dup	NM_001320628.1:c.-16+3267_-16+3273dup
BOLA2 transcript variant X1	XM_005255415.1:c.359+3273=	XM_005255415.1:c.359+3266_359+3273del	XM_005255415.1:c.359+3267_359+3273del	XM_005255415.1:c.359+3268_359+3273del	XM_005255415.1:c.359+3269_359+3273del	XM_005255415.1:c.359+3270_359+3273del	XM_005255415.1:c.359+3271_359+3273del	XM_005255415.1:c.359+3272_359+3273del	XM_005255415.1:c.359+3273del	XM_005255415.1:c.359+3273dup	XM_005255415.1:c.359+3272_359+3273dup	XM_005255415.1:c.359+3271_359+3273dup	XM_005255415.1:c.359+3270_359+3273dup	XM_005255415.1:c.359+3269_359+3273dup	XM_005255415.1:c.359+3267_359+3273dup
BOLA2 transcript variant X2	XM_005255416.1:c.-16+3273=	XM_005255416.1:c.-16+3266_-16+3273del	XM_005255416.1:c.-16+3267_-16+3273del	XM_005255416.1:c.-16+3268_-16+3273del	XM_005255416.1:c.-16+3269_-16+3273del	XM_005255416.1:c.-16+3270_-16+3273del	XM_005255416.1:c.-16+3271_-16+3273del	XM_005255416.1:c.-16+3272_-16+3273del	XM_005255416.1:c.-16+3273del	XM_005255416.1:c.-16+3273dup	XM_005255416.1:c.-16+3272_-16+3273dup	XM_005255416.1:c.-16+3271_-16+3273dup	XM_005255416.1:c.-16+3270_-16+3273dup	XM_005255416.1:c.-16+3269_-16+3273dup	XM_005255416.1:c.-16+3267_-16+3273dup

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#.

36 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3699120519	Jul 13, 2019 (153)
2	EVA_DECODE	ss3699120520	Jul 13, 2019 (153)
3	EVA_DECODE	ss3699120521	Jul 13, 2019 (153)
4	EVA_DECODE	ss3699120522	Jul 13, 2019 (153)
5	EVA_DECODE	ss3699120523	Jul 13, 2019 (153)
6	EVA_DECODE	ss3699120524	Jul 13, 2019 (153)
7	PACBIO	ss3788019903	Jul 13, 2019 (153)
8	KOGIC	ss3977386977	Apr 27, 2020 (154)
9	KOGIC	ss3977386978	Apr 27, 2020 (154)
10	KOGIC	ss3977386979	Apr 27, 2020 (154)
11	GNOMAD	ss4299340425	Apr 26, 2021 (155)
12	GNOMAD	ss4299340426	Apr 26, 2021 (155)
13	GNOMAD	ss4299340427	Apr 26, 2021 (155)
14	GNOMAD	ss4299340428	Apr 26, 2021 (155)
15	GNOMAD	ss4299340429	Apr 26, 2021 (155)
16	GNOMAD	ss4299340430	Apr 26, 2021 (155)
17	GNOMAD	ss4299340431	Apr 26, 2021 (155)
18	GNOMAD	ss4299340432	Apr 26, 2021 (155)
19	GNOMAD	ss4299340433	Apr 26, 2021 (155)
20	GNOMAD	ss4299340434	Apr 26, 2021 (155)
21	GNOMAD	ss4299340435	Apr 26, 2021 (155)
22	GNOMAD	ss4299340436	Apr 26, 2021 (155)
23	GNOMAD	ss4299340437	Apr 26, 2021 (155)
24	GNOMAD	ss4299340438	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5219140959	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5219140960	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5219140961	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5219140962	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5219140963	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5219140964	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5773830262	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5773830263	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5773830264	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5773830265	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5773830266	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5773830267	Oct 16, 2022 (156)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002306 (NC_000016.10:29450742::A 71/19286) Row 487002307 (NC_000016.10:29450742::AA 125/19288) Row 487002308 (NC_000016.10:29450742::AAA 4/19282)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002306 (NC_000016.10:29450742::A 71/19286) Row 487002307 (NC_000016.10:29450742::AA 125/19288) Row 487002308 (NC_000016.10:29450742::AAA 4/19282)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002306 (NC_000016.10:29450742::A 71/19286) Row 487002307 (NC_000016.10:29450742::AA 125/19288) Row 487002308 (NC_000016.10:29450742::AAA 4/19282)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002306 (NC_000016.10:29450742::A 71/19286) Row 487002307 (NC_000016.10:29450742::AA 125/19288) Row 487002308 (NC_000016.10:29450742::AAA 4/19282)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002306 (NC_000016.10:29450742::A 71/19286) Row 487002307 (NC_000016.10:29450742::AA 125/19288) Row 487002308 (NC_000016.10:29450742::AAA 4/19282)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002306 (NC_000016.10:29450742::A 71/19286) Row 487002307 (NC_000016.10:29450742::AA 125/19288) Row 487002308 (NC_000016.10:29450742::AAA 4/19282)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002306 (NC_000016.10:29450742::A 71/19286) Row 487002307 (NC_000016.10:29450742::AA 125/19288) Row 487002308 (NC_000016.10:29450742::AAA 4/19282)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002306 (NC_000016.10:29450742::A 71/19286) Row 487002307 (NC_000016.10:29450742::AA 125/19288) Row 487002308 (NC_000016.10:29450742::AAA 4/19282)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002306 (NC_000016.10:29450742::A 71/19286) Row 487002307 (NC_000016.10:29450742::AA 125/19288) Row 487002308 (NC_000016.10:29450742::AAA 4/19282)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002306 (NC_000016.10:29450742::A 71/19286) Row 487002307 (NC_000016.10:29450742::AA 125/19288) Row 487002308 (NC_000016.10:29450742::AAA 4/19282)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002306 (NC_000016.10:29450742::A 71/19286) Row 487002307 (NC_000016.10:29450742::AA 125/19288) Row 487002308 (NC_000016.10:29450742::AAA 4/19282)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002306 (NC_000016.10:29450742::A 71/19286) Row 487002307 (NC_000016.10:29450742::AA 125/19288) Row 487002308 (NC_000016.10:29450742::AAA 4/19282)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002306 (NC_000016.10:29450742::A 71/19286) Row 487002307 (NC_000016.10:29450742::AA 125/19288) Row 487002308 (NC_000016.10:29450742::AAA 4/19282)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002306 (NC_000016.10:29450742::A 71/19286) Row 487002307 (NC_000016.10:29450742::AA 125/19288) Row 487002308 (NC_000016.10:29450742::AAA 4/19282)...	-	Apr 26, 2021 (155)
51	Korean Genome Project Submission ignored due to conflicting rows: Row 33764978 (NC_000016.10:29450745:AAAA: 65/534) Row 33764979 (NC_000016.10:29450744:AAAAA: 14/534) Row 33764980 (NC_000016.10:29450747:AA: 10/534)	-	Apr 27, 2020 (154)
52	Korean Genome Project Submission ignored due to conflicting rows: Row 33764978 (NC_000016.10:29450745:AAAA: 65/534) Row 33764979 (NC_000016.10:29450744:AAAAA: 14/534) Row 33764980 (NC_000016.10:29450747:AA: 10/534)	-	Apr 27, 2020 (154)
53	Korean Genome Project Submission ignored due to conflicting rows: Row 33764978 (NC_000016.10:29450745:AAAA: 65/534) Row 33764979 (NC_000016.10:29450744:AAAAA: 14/534) Row 33764980 (NC_000016.10:29450747:AA: 10/534)	-	Apr 27, 2020 (154)
54	8.3KJPN Submission ignored due to conflicting rows: Row 77110266 (NC_000016.9:29462063:AAAA: 1160/13086) Row 77110267 (NC_000016.9:29462063:AAAAAAA: 85/13086) Row 77110268 (NC_000016.9:29462063:AAAAA: 589/13086)...	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 77110266 (NC_000016.9:29462063:AAAA: 1160/13086) Row 77110267 (NC_000016.9:29462063:AAAAAAA: 85/13086) Row 77110268 (NC_000016.9:29462063:AAAAA: 589/13086)...	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 77110266 (NC_000016.9:29462063:AAAA: 1160/13086) Row 77110267 (NC_000016.9:29462063:AAAAAAA: 85/13086) Row 77110268 (NC_000016.9:29462063:AAAAA: 589/13086)...	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 77110266 (NC_000016.9:29462063:AAAA: 1160/13086) Row 77110267 (NC_000016.9:29462063:AAAAAAA: 85/13086) Row 77110268 (NC_000016.9:29462063:AAAAA: 589/13086)...	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 77110266 (NC_000016.9:29462063:AAAA: 1160/13086) Row 77110267 (NC_000016.9:29462063:AAAAAAA: 85/13086) Row 77110268 (NC_000016.9:29462063:AAAAA: 589/13086)...	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 77110266 (NC_000016.9:29462063:AAAA: 1160/13086) Row 77110267 (NC_000016.9:29462063:AAAAAAA: 85/13086) Row 77110268 (NC_000016.9:29462063:AAAAA: 589/13086)...	-	Apr 26, 2021 (155)
60	14KJPN Submission ignored due to conflicting rows: Row 107667366 (NC_000016.10:29450742:A: 523/23136) Row 107667367 (NC_000016.10:29450742:AAAA: 1887/23136) Row 107667368 (NC_000016.10:29450742:AA: 187/23136)...	-	Oct 16, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 107667366 (NC_000016.10:29450742:A: 523/23136) Row 107667367 (NC_000016.10:29450742:AAAA: 1887/23136) Row 107667368 (NC_000016.10:29450742:AA: 187/23136)...	-	Oct 16, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 107667366 (NC_000016.10:29450742:A: 523/23136) Row 107667367 (NC_000016.10:29450742:AAAA: 1887/23136) Row 107667368 (NC_000016.10:29450742:AA: 187/23136)...	-	Oct 16, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 107667366 (NC_000016.10:29450742:A: 523/23136) Row 107667367 (NC_000016.10:29450742:AAAA: 1887/23136) Row 107667368 (NC_000016.10:29450742:AA: 187/23136)...	-	Oct 16, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 107667366 (NC_000016.10:29450742:A: 523/23136) Row 107667367 (NC_000016.10:29450742:AAAA: 1887/23136) Row 107667368 (NC_000016.10:29450742:AA: 187/23136)...	-	Oct 16, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 107667366 (NC_000016.10:29450742:A: 523/23136) Row 107667367 (NC_000016.10:29450742:AAAA: 1887/23136) Row 107667368 (NC_000016.10:29450742:AA: 187/23136)...	-	Oct 16, 2022 (156)
66	ALFA	NC_000016.10 - 29450743	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
ss3699120524, ss4299340438	NC_000016.10:29450742:AAAAAAAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
15426873014	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss5219140960	NC_000016.9:29462063:AAAAAAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4299340437, ss5773830266	NC_000016.10:29450742:AAAAAAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
15426873014	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5219140964	NC_000016.9:29462063:AAAAAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4299340436	NC_000016.10:29450742:AAAAAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
15426873014	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3699120523	NC_000016.10:29450744:AAAAAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3788019903, ss5219140961	NC_000016.9:29462063:AAAAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4299340435, ss5773830265	NC_000016.10:29450742:AAAAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
15426873014	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3977386978	NC_000016.10:29450744:AAAAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5219140959	NC_000016.9:29462063:AAAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4299340434, ss5773830263	NC_000016.10:29450742:AAAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
15426873014	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3977386977	NC_000016.10:29450745:AAAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3699120522	NC_000016.10:29450746:AAAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4299340433	NC_000016.10:29450742:AAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
15426873014	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3699120521	NC_000016.10:29450747:AAA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5219140962	NC_000016.9:29462063:AA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4299340432, ss5773830264	NC_000016.10:29450742:AA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
15426873014	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3977386979	NC_000016.10:29450747:AA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3699120520	NC_000016.10:29450748:AA:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5219140963	NC_000016.9:29462063:A:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4299340431, ss5773830262	NC_000016.10:29450742:A:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
15426873014	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3699120519	NC_000016.10:29450749:A:	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4299340425, ss5773830267	NC_000016.10:29450742::A	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
15426873014	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4299340426	NC_000016.10:29450742::AA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
15426873014	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4299340427	NC_000016.10:29450742::AAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
15426873014	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4299340428	NC_000016.10:29450742::AAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
15426873014	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4299340429	NC_000016.10:29450742::AAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
15426873014	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4299340430	NC_000016.10:29450742::AAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
15426873014	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000016.10:29450742:AAAAAAAAAAAA… NC_000016.10:29450742:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs1187184475

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1187184475