Name: rs36073563
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.

rs36073563

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:144888596-144888620 (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)₁₃ / del(A)₈ / del(A)₇ / del…
del(A)₁₃ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₆ / dup(A)₂₅
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₃=0.00000 (0/11254, ALFA)
del(A)₈=0.00000 (0/11254, ALFA)
del(A)₇=0.00000 (0/11254, ALFA) (+ 9 more)
del(A)₆=0.00000 (0/11254, ALFA)
del(A)₄=0.00000 (0/11254, ALFA)
delAAA=0.00000 (0/11254, ALFA)
delAA=0.00000 (0/11254, ALFA)
delA=0.00000 (0/11254, ALFA)
dupA=0.00000 (0/11254, ALFA)
dupAA=0.00000 (0/11254, ALFA)
dupAAA=0.00000 (0/11254, ALFA)
dup(A)₄=0.00000 (0/11254, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF250 : 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	11254	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00000	AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00000	1.0	N/A
European	Sub	8972	AAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1324	AAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	50	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	1274	AAAAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	60	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	42	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	18	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	96	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	362	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	84	AAAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	356	AAAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=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	11254	(A)₂₅=1.00000	del(A)₁₃=0.00000, del(A)₈=0.00000, del(A)₇=0.00000, del(A)₆=0.00000, del(A)₄=0.00000, delAAA=0.00000, delAA=0.00000, delA=0.00000, dupA=0.00000, dupAA=0.00000, dupAAA=0.00000, dup(A)₄=0.00000
Allele Frequency Aggregator	European	Sub	8972	(A)₂₅=1.0000	del(A)₁₃=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=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
Allele Frequency Aggregator	African	Sub	1324	(A)₂₅=1.0000	del(A)₁₃=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=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
Allele Frequency Aggregator	Latin American 2	Sub	362	(A)₂₅=1.000	del(A)₁₃=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=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
Allele Frequency Aggregator	Other	Sub	356	(A)₂₅=1.000	del(A)₁₃=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=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
Allele Frequency Aggregator	Latin American 1	Sub	96	(A)₂₅=1.00	del(A)₁₃=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=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
Allele Frequency Aggregator	South Asian	Sub	84	(A)₂₅=1.00	del(A)₁₃=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=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
Allele Frequency Aggregator	Asian	Sub	60	(A)₂₅=1.00	del(A)₁₃=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=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

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.144888608_144888620del
GRCh38.p14 chr 8	NC_000008.11:g.144888613_144888620del
GRCh38.p14 chr 8	NC_000008.11:g.144888614_144888620del
GRCh38.p14 chr 8	NC_000008.11:g.144888615_144888620del
GRCh38.p14 chr 8	NC_000008.11:g.144888617_144888620del
GRCh38.p14 chr 8	NC_000008.11:g.144888618_144888620del
GRCh38.p14 chr 8	NC_000008.11:g.144888619_144888620del
GRCh38.p14 chr 8	NC_000008.11:g.144888620del
GRCh38.p14 chr 8	NC_000008.11:g.144888620dup
GRCh38.p14 chr 8	NC_000008.11:g.144888619_144888620dup
GRCh38.p14 chr 8	NC_000008.11:g.144888618_144888620dup
GRCh38.p14 chr 8	NC_000008.11:g.144888617_144888620dup
GRCh38.p14 chr 8	NC_000008.11:g.144888615_144888620dup
GRCh38.p14 chr 8	NC_000008.11:g.144888596_144888620dup
GRCh37.p13 chr 8	NC_000008.10:g.146113993_146114005del
GRCh37.p13 chr 8	NC_000008.10:g.146113998_146114005del
GRCh37.p13 chr 8	NC_000008.10:g.146113999_146114005del
GRCh37.p13 chr 8	NC_000008.10:g.146114000_146114005del
GRCh37.p13 chr 8	NC_000008.10:g.146114002_146114005del
GRCh37.p13 chr 8	NC_000008.10:g.146114003_146114005del
GRCh37.p13 chr 8	NC_000008.10:g.146114004_146114005del
GRCh37.p13 chr 8	NC_000008.10:g.146114005del
GRCh37.p13 chr 8	NC_000008.10:g.146114005dup
GRCh37.p13 chr 8	NC_000008.10:g.146114004_146114005dup
GRCh37.p13 chr 8	NC_000008.10:g.146114003_146114005dup
GRCh37.p13 chr 8	NC_000008.10:g.146114002_146114005dup
GRCh37.p13 chr 8	NC_000008.10:g.146114000_146114005dup
GRCh37.p13 chr 8	NC_000008.10:g.146113981_146114005dup

Gene: ZNF250, zinc finger protein 250 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF250 transcript variant 2	NM_001109689.4:c.283+973_… NM_001109689.4:c.283+973_283+985del	N/A	Intron Variant
ZNF250 transcript variant 3	NM_001363098.2:c.298+973_… NM_001363098.2:c.298+973_298+985del	N/A	Intron Variant
ZNF250 transcript variant 4	NM_001363099.2:c.298+973_… NM_001363099.2:c.298+973_298+985del	N/A	Intron Variant
ZNF250 transcript variant 5	NM_001363100.2:c.283+973_… NM_001363100.2:c.283+973_283+985del	N/A	Intron Variant
ZNF250 transcript variant 6	NM_001363101.2:c.283+973_… NM_001363101.2:c.283+973_283+985del	N/A	Intron Variant
ZNF250 transcript variant 7	NM_001363102.2:c.283+973_… NM_001363102.2:c.283+973_283+985del	N/A	Intron Variant
ZNF250 transcript variant 8	NM_001363103.2:c.283+973_… NM_001363103.2:c.283+973_283+985del	N/A	Intron Variant
ZNF250 transcript variant 9	NM_001363104.2:c.298+973_… NM_001363104.2:c.298+973_298+985del	N/A	Intron Variant
ZNF250 transcript variant 10	NM_001363105.2:c.283+973_… NM_001363105.2:c.283+973_283+985del	N/A	Intron Variant
ZNF250 transcript variant 11	NM_001363106.2:c.283+973_… NM_001363106.2:c.283+973_283+985del	N/A	Intron Variant
ZNF250 transcript variant 12	NM_001363107.2:c.283+973_… NM_001363107.2:c.283+973_283+985del	N/A	Intron Variant
ZNF250 transcript variant 1	NM_021061.5:c.298+973_298… NM_021061.5:c.298+973_298+985del	N/A	Intron Variant
ZNF250 transcript variant X1	XM_047422064.1:c.298+973_… XM_047422064.1:c.298+973_298+985del	N/A	Intron Variant
ZNF250 transcript variant X2	XM_047422065.1:c.283+973_… XM_047422065.1:c.283+973_283+985del	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)₂₅=	del(A)₁₃	del(A)₈	del(A)₇	del(A)₆	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₆	dup(A)₂₅
GRCh38.p14 chr 8	NC_000008.11:g.144888596_144888620=	NC_000008.11:g.144888608_144888620del	NC_000008.11:g.144888613_144888620del	NC_000008.11:g.144888614_144888620del	NC_000008.11:g.144888615_144888620del	NC_000008.11:g.144888617_144888620del	NC_000008.11:g.144888618_144888620del	NC_000008.11:g.144888619_144888620del	NC_000008.11:g.144888620del	NC_000008.11:g.144888620dup	NC_000008.11:g.144888619_144888620dup	NC_000008.11:g.144888618_144888620dup	NC_000008.11:g.144888617_144888620dup	NC_000008.11:g.144888615_144888620dup	NC_000008.11:g.144888596_144888620dup
GRCh37.p13 chr 8	NC_000008.10:g.146113981_146114005=	NC_000008.10:g.146113993_146114005del	NC_000008.10:g.146113998_146114005del	NC_000008.10:g.146113999_146114005del	NC_000008.10:g.146114000_146114005del	NC_000008.10:g.146114002_146114005del	NC_000008.10:g.146114003_146114005del	NC_000008.10:g.146114004_146114005del	NC_000008.10:g.146114005del	NC_000008.10:g.146114005dup	NC_000008.10:g.146114004_146114005dup	NC_000008.10:g.146114003_146114005dup	NC_000008.10:g.146114002_146114005dup	NC_000008.10:g.146114000_146114005dup	NC_000008.10:g.146113981_146114005dup
ZNF250 transcript variant 2	NM_001109689.3:c.283+985=	NM_001109689.3:c.283+973_283+985del	NM_001109689.3:c.283+978_283+985del	NM_001109689.3:c.283+979_283+985del	NM_001109689.3:c.283+980_283+985del	NM_001109689.3:c.283+982_283+985del	NM_001109689.3:c.283+983_283+985del	NM_001109689.3:c.283+984_283+985del	NM_001109689.3:c.283+985del	NM_001109689.3:c.283+985dup	NM_001109689.3:c.283+984_283+985dup	NM_001109689.3:c.283+983_283+985dup	NM_001109689.3:c.283+982_283+985dup	NM_001109689.3:c.283+980_283+985dup	NM_001109689.3:c.283+961_283+985dup
ZNF250 transcript variant 2	NM_001109689.4:c.283+985=	NM_001109689.4:c.283+973_283+985del	NM_001109689.4:c.283+978_283+985del	NM_001109689.4:c.283+979_283+985del	NM_001109689.4:c.283+980_283+985del	NM_001109689.4:c.283+982_283+985del	NM_001109689.4:c.283+983_283+985del	NM_001109689.4:c.283+984_283+985del	NM_001109689.4:c.283+985del	NM_001109689.4:c.283+985dup	NM_001109689.4:c.283+984_283+985dup	NM_001109689.4:c.283+983_283+985dup	NM_001109689.4:c.283+982_283+985dup	NM_001109689.4:c.283+980_283+985dup	NM_001109689.4:c.283+961_283+985dup
ZNF250 transcript variant 3	NM_001363098.2:c.298+985=	NM_001363098.2:c.298+973_298+985del	NM_001363098.2:c.298+978_298+985del	NM_001363098.2:c.298+979_298+985del	NM_001363098.2:c.298+980_298+985del	NM_001363098.2:c.298+982_298+985del	NM_001363098.2:c.298+983_298+985del	NM_001363098.2:c.298+984_298+985del	NM_001363098.2:c.298+985del	NM_001363098.2:c.298+985dup	NM_001363098.2:c.298+984_298+985dup	NM_001363098.2:c.298+983_298+985dup	NM_001363098.2:c.298+982_298+985dup	NM_001363098.2:c.298+980_298+985dup	NM_001363098.2:c.298+961_298+985dup
ZNF250 transcript variant 4	NM_001363099.2:c.298+985=	NM_001363099.2:c.298+973_298+985del	NM_001363099.2:c.298+978_298+985del	NM_001363099.2:c.298+979_298+985del	NM_001363099.2:c.298+980_298+985del	NM_001363099.2:c.298+982_298+985del	NM_001363099.2:c.298+983_298+985del	NM_001363099.2:c.298+984_298+985del	NM_001363099.2:c.298+985del	NM_001363099.2:c.298+985dup	NM_001363099.2:c.298+984_298+985dup	NM_001363099.2:c.298+983_298+985dup	NM_001363099.2:c.298+982_298+985dup	NM_001363099.2:c.298+980_298+985dup	NM_001363099.2:c.298+961_298+985dup
ZNF250 transcript variant 5	NM_001363100.2:c.283+985=	NM_001363100.2:c.283+973_283+985del	NM_001363100.2:c.283+978_283+985del	NM_001363100.2:c.283+979_283+985del	NM_001363100.2:c.283+980_283+985del	NM_001363100.2:c.283+982_283+985del	NM_001363100.2:c.283+983_283+985del	NM_001363100.2:c.283+984_283+985del	NM_001363100.2:c.283+985del	NM_001363100.2:c.283+985dup	NM_001363100.2:c.283+984_283+985dup	NM_001363100.2:c.283+983_283+985dup	NM_001363100.2:c.283+982_283+985dup	NM_001363100.2:c.283+980_283+985dup	NM_001363100.2:c.283+961_283+985dup
ZNF250 transcript variant 6	NM_001363101.2:c.283+985=	NM_001363101.2:c.283+973_283+985del	NM_001363101.2:c.283+978_283+985del	NM_001363101.2:c.283+979_283+985del	NM_001363101.2:c.283+980_283+985del	NM_001363101.2:c.283+982_283+985del	NM_001363101.2:c.283+983_283+985del	NM_001363101.2:c.283+984_283+985del	NM_001363101.2:c.283+985del	NM_001363101.2:c.283+985dup	NM_001363101.2:c.283+984_283+985dup	NM_001363101.2:c.283+983_283+985dup	NM_001363101.2:c.283+982_283+985dup	NM_001363101.2:c.283+980_283+985dup	NM_001363101.2:c.283+961_283+985dup
ZNF250 transcript variant 7	NM_001363102.2:c.283+985=	NM_001363102.2:c.283+973_283+985del	NM_001363102.2:c.283+978_283+985del	NM_001363102.2:c.283+979_283+985del	NM_001363102.2:c.283+980_283+985del	NM_001363102.2:c.283+982_283+985del	NM_001363102.2:c.283+983_283+985del	NM_001363102.2:c.283+984_283+985del	NM_001363102.2:c.283+985del	NM_001363102.2:c.283+985dup	NM_001363102.2:c.283+984_283+985dup	NM_001363102.2:c.283+983_283+985dup	NM_001363102.2:c.283+982_283+985dup	NM_001363102.2:c.283+980_283+985dup	NM_001363102.2:c.283+961_283+985dup
ZNF250 transcript variant 8	NM_001363103.2:c.283+985=	NM_001363103.2:c.283+973_283+985del	NM_001363103.2:c.283+978_283+985del	NM_001363103.2:c.283+979_283+985del	NM_001363103.2:c.283+980_283+985del	NM_001363103.2:c.283+982_283+985del	NM_001363103.2:c.283+983_283+985del	NM_001363103.2:c.283+984_283+985del	NM_001363103.2:c.283+985del	NM_001363103.2:c.283+985dup	NM_001363103.2:c.283+984_283+985dup	NM_001363103.2:c.283+983_283+985dup	NM_001363103.2:c.283+982_283+985dup	NM_001363103.2:c.283+980_283+985dup	NM_001363103.2:c.283+961_283+985dup
ZNF250 transcript variant 9	NM_001363104.2:c.298+985=	NM_001363104.2:c.298+973_298+985del	NM_001363104.2:c.298+978_298+985del	NM_001363104.2:c.298+979_298+985del	NM_001363104.2:c.298+980_298+985del	NM_001363104.2:c.298+982_298+985del	NM_001363104.2:c.298+983_298+985del	NM_001363104.2:c.298+984_298+985del	NM_001363104.2:c.298+985del	NM_001363104.2:c.298+985dup	NM_001363104.2:c.298+984_298+985dup	NM_001363104.2:c.298+983_298+985dup	NM_001363104.2:c.298+982_298+985dup	NM_001363104.2:c.298+980_298+985dup	NM_001363104.2:c.298+961_298+985dup
ZNF250 transcript variant 10	NM_001363105.2:c.283+985=	NM_001363105.2:c.283+973_283+985del	NM_001363105.2:c.283+978_283+985del	NM_001363105.2:c.283+979_283+985del	NM_001363105.2:c.283+980_283+985del	NM_001363105.2:c.283+982_283+985del	NM_001363105.2:c.283+983_283+985del	NM_001363105.2:c.283+984_283+985del	NM_001363105.2:c.283+985del	NM_001363105.2:c.283+985dup	NM_001363105.2:c.283+984_283+985dup	NM_001363105.2:c.283+983_283+985dup	NM_001363105.2:c.283+982_283+985dup	NM_001363105.2:c.283+980_283+985dup	NM_001363105.2:c.283+961_283+985dup
ZNF250 transcript variant 11	NM_001363106.2:c.283+985=	NM_001363106.2:c.283+973_283+985del	NM_001363106.2:c.283+978_283+985del	NM_001363106.2:c.283+979_283+985del	NM_001363106.2:c.283+980_283+985del	NM_001363106.2:c.283+982_283+985del	NM_001363106.2:c.283+983_283+985del	NM_001363106.2:c.283+984_283+985del	NM_001363106.2:c.283+985del	NM_001363106.2:c.283+985dup	NM_001363106.2:c.283+984_283+985dup	NM_001363106.2:c.283+983_283+985dup	NM_001363106.2:c.283+982_283+985dup	NM_001363106.2:c.283+980_283+985dup	NM_001363106.2:c.283+961_283+985dup
ZNF250 transcript variant 12	NM_001363107.2:c.283+985=	NM_001363107.2:c.283+973_283+985del	NM_001363107.2:c.283+978_283+985del	NM_001363107.2:c.283+979_283+985del	NM_001363107.2:c.283+980_283+985del	NM_001363107.2:c.283+982_283+985del	NM_001363107.2:c.283+983_283+985del	NM_001363107.2:c.283+984_283+985del	NM_001363107.2:c.283+985del	NM_001363107.2:c.283+985dup	NM_001363107.2:c.283+984_283+985dup	NM_001363107.2:c.283+983_283+985dup	NM_001363107.2:c.283+982_283+985dup	NM_001363107.2:c.283+980_283+985dup	NM_001363107.2:c.283+961_283+985dup
ZNF250 transcript variant 1	NM_021061.4:c.298+985=	NM_021061.4:c.298+973_298+985del	NM_021061.4:c.298+978_298+985del	NM_021061.4:c.298+979_298+985del	NM_021061.4:c.298+980_298+985del	NM_021061.4:c.298+982_298+985del	NM_021061.4:c.298+983_298+985del	NM_021061.4:c.298+984_298+985del	NM_021061.4:c.298+985del	NM_021061.4:c.298+985dup	NM_021061.4:c.298+984_298+985dup	NM_021061.4:c.298+983_298+985dup	NM_021061.4:c.298+982_298+985dup	NM_021061.4:c.298+980_298+985dup	NM_021061.4:c.298+961_298+985dup
ZNF250 transcript variant 1	NM_021061.5:c.298+985=	NM_021061.5:c.298+973_298+985del	NM_021061.5:c.298+978_298+985del	NM_021061.5:c.298+979_298+985del	NM_021061.5:c.298+980_298+985del	NM_021061.5:c.298+982_298+985del	NM_021061.5:c.298+983_298+985del	NM_021061.5:c.298+984_298+985del	NM_021061.5:c.298+985del	NM_021061.5:c.298+985dup	NM_021061.5:c.298+984_298+985dup	NM_021061.5:c.298+983_298+985dup	NM_021061.5:c.298+982_298+985dup	NM_021061.5:c.298+980_298+985dup	NM_021061.5:c.298+961_298+985dup
ZNF250 transcript variant X5	XM_005272327.1:c.283+985=	XM_005272327.1:c.283+973_283+985del	XM_005272327.1:c.283+978_283+985del	XM_005272327.1:c.283+979_283+985del	XM_005272327.1:c.283+980_283+985del	XM_005272327.1:c.283+982_283+985del	XM_005272327.1:c.283+983_283+985del	XM_005272327.1:c.283+984_283+985del	XM_005272327.1:c.283+985del	XM_005272327.1:c.283+985dup	XM_005272327.1:c.283+984_283+985dup	XM_005272327.1:c.283+983_283+985dup	XM_005272327.1:c.283+982_283+985dup	XM_005272327.1:c.283+980_283+985dup	XM_005272327.1:c.283+961_283+985dup
ZNF250 transcript variant X2	XM_005272328.1:c.283+985=	XM_005272328.1:c.283+973_283+985del	XM_005272328.1:c.283+978_283+985del	XM_005272328.1:c.283+979_283+985del	XM_005272328.1:c.283+980_283+985del	XM_005272328.1:c.283+982_283+985del	XM_005272328.1:c.283+983_283+985del	XM_005272328.1:c.283+984_283+985del	XM_005272328.1:c.283+985del	XM_005272328.1:c.283+985dup	XM_005272328.1:c.283+984_283+985dup	XM_005272328.1:c.283+983_283+985dup	XM_005272328.1:c.283+982_283+985dup	XM_005272328.1:c.283+980_283+985dup	XM_005272328.1:c.283+961_283+985dup
ZNF250 transcript variant X3	XM_005272329.1:c.283+985=	XM_005272329.1:c.283+973_283+985del	XM_005272329.1:c.283+978_283+985del	XM_005272329.1:c.283+979_283+985del	XM_005272329.1:c.283+980_283+985del	XM_005272329.1:c.283+982_283+985del	XM_005272329.1:c.283+983_283+985del	XM_005272329.1:c.283+984_283+985del	XM_005272329.1:c.283+985del	XM_005272329.1:c.283+985dup	XM_005272329.1:c.283+984_283+985dup	XM_005272329.1:c.283+983_283+985dup	XM_005272329.1:c.283+982_283+985dup	XM_005272329.1:c.283+980_283+985dup	XM_005272329.1:c.283+961_283+985dup
ZNF250 transcript variant X4	XM_005272330.1:c.298+985=	XM_005272330.1:c.298+973_298+985del	XM_005272330.1:c.298+978_298+985del	XM_005272330.1:c.298+979_298+985del	XM_005272330.1:c.298+980_298+985del	XM_005272330.1:c.298+982_298+985del	XM_005272330.1:c.298+983_298+985del	XM_005272330.1:c.298+984_298+985del	XM_005272330.1:c.298+985del	XM_005272330.1:c.298+985dup	XM_005272330.1:c.298+984_298+985dup	XM_005272330.1:c.298+983_298+985dup	XM_005272330.1:c.298+982_298+985dup	XM_005272330.1:c.298+980_298+985dup	XM_005272330.1:c.298+961_298+985dup
ZNF250 transcript variant X5	XM_005272331.1:c.283+985=	XM_005272331.1:c.283+973_283+985del	XM_005272331.1:c.283+978_283+985del	XM_005272331.1:c.283+979_283+985del	XM_005272331.1:c.283+980_283+985del	XM_005272331.1:c.283+982_283+985del	XM_005272331.1:c.283+983_283+985del	XM_005272331.1:c.283+984_283+985del	XM_005272331.1:c.283+985del	XM_005272331.1:c.283+985dup	XM_005272331.1:c.283+984_283+985dup	XM_005272331.1:c.283+983_283+985dup	XM_005272331.1:c.283+982_283+985dup	XM_005272331.1:c.283+980_283+985dup	XM_005272331.1:c.283+961_283+985dup
ZNF250 transcript variant X1	XM_047422064.1:c.298+985=	XM_047422064.1:c.298+973_298+985del	XM_047422064.1:c.298+978_298+985del	XM_047422064.1:c.298+979_298+985del	XM_047422064.1:c.298+980_298+985del	XM_047422064.1:c.298+982_298+985del	XM_047422064.1:c.298+983_298+985del	XM_047422064.1:c.298+984_298+985del	XM_047422064.1:c.298+985del	XM_047422064.1:c.298+985dup	XM_047422064.1:c.298+984_298+985dup	XM_047422064.1:c.298+983_298+985dup	XM_047422064.1:c.298+982_298+985dup	XM_047422064.1:c.298+980_298+985dup	XM_047422064.1:c.298+961_298+985dup
ZNF250 transcript variant X2	XM_047422065.1:c.283+985=	XM_047422065.1:c.283+973_283+985del	XM_047422065.1:c.283+978_283+985del	XM_047422065.1:c.283+979_283+985del	XM_047422065.1:c.283+980_283+985del	XM_047422065.1:c.283+982_283+985del	XM_047422065.1:c.283+983_283+985del	XM_047422065.1:c.283+984_283+985del	XM_047422065.1:c.283+985del	XM_047422065.1:c.283+985dup	XM_047422065.1:c.283+984_283+985dup	XM_047422065.1:c.283+983_283+985dup	XM_047422065.1:c.283+982_283+985dup	XM_047422065.1:c.283+980_283+985dup	XM_047422065.1:c.283+961_283+985dup

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#.

30 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss43202608	Mar 15, 2006 (126)
2	GNOMAD	ss4195789615	Apr 26, 2021 (155)
3	GNOMAD	ss4195789616	Apr 26, 2021 (155)
4	GNOMAD	ss4195789617	Apr 26, 2021 (155)
5	GNOMAD	ss4195789618	Apr 26, 2021 (155)
6	GNOMAD	ss4195789619	Apr 26, 2021 (155)
7	GNOMAD	ss4195789620	Apr 26, 2021 (155)
8	GNOMAD	ss4195789621	Apr 26, 2021 (155)
9	GNOMAD	ss4195789622	Apr 26, 2021 (155)
10	GNOMAD	ss4195789623	Apr 26, 2021 (155)
11	GNOMAD	ss4195789624	Apr 26, 2021 (155)
12	GNOMAD	ss4195789625	Apr 26, 2021 (155)
13	GNOMAD	ss4195789626	Apr 26, 2021 (155)
14	GNOMAD	ss4195789627	Apr 26, 2021 (155)
15	TOMMO_GENOMICS	ss5191608770	Apr 26, 2021 (155)
16	TOMMO_GENOMICS	ss5191608771	Apr 26, 2021 (155)
17	TOMMO_GENOMICS	ss5191608772	Apr 26, 2021 (155)
18	TOMMO_GENOMICS	ss5191608773	Apr 26, 2021 (155)
19	TOMMO_GENOMICS	ss5191608774	Apr 26, 2021 (155)
20	HUGCELL_USP	ss5475750966	Oct 16, 2022 (156)
21	HUGCELL_USP	ss5475750967	Oct 16, 2022 (156)
22	HUGCELL_USP	ss5475750968	Oct 16, 2022 (156)
23	HUGCELL_USP	ss5475750969	Oct 16, 2022 (156)
24	HUGCELL_USP	ss5475750970	Oct 16, 2022 (156)
25	TOMMO_GENOMICS	ss5734525974	Oct 16, 2022 (156)
26	TOMMO_GENOMICS	ss5734525975	Oct 16, 2022 (156)
27	TOMMO_GENOMICS	ss5734525976	Oct 16, 2022 (156)
28	TOMMO_GENOMICS	ss5734525977	Oct 16, 2022 (156)
29	EVA	ss5831414196	Oct 16, 2022 (156)
30	EVA	ss5831414197	Oct 16, 2022 (156)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 315024524 (NC_000008.11:144888595::A 3182/47780) Row 315024525 (NC_000008.11:144888595::AA 149/49350) Row 315024526 (NC_000008.11:144888595::AAA 10/50000)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 315024524 (NC_000008.11:144888595::A 3182/47780) Row 315024525 (NC_000008.11:144888595::AA 149/49350) Row 315024526 (NC_000008.11:144888595::AAA 10/50000)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 315024524 (NC_000008.11:144888595::A 3182/47780) Row 315024525 (NC_000008.11:144888595::AA 149/49350) Row 315024526 (NC_000008.11:144888595::AAA 10/50000)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 315024524 (NC_000008.11:144888595::A 3182/47780) Row 315024525 (NC_000008.11:144888595::AA 149/49350) Row 315024526 (NC_000008.11:144888595::AAA 10/50000)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 315024524 (NC_000008.11:144888595::A 3182/47780) Row 315024525 (NC_000008.11:144888595::AA 149/49350) Row 315024526 (NC_000008.11:144888595::AAA 10/50000)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 315024524 (NC_000008.11:144888595::A 3182/47780) Row 315024525 (NC_000008.11:144888595::AA 149/49350) Row 315024526 (NC_000008.11:144888595::AAA 10/50000)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 315024524 (NC_000008.11:144888595::A 3182/47780) Row 315024525 (NC_000008.11:144888595::AA 149/49350) Row 315024526 (NC_000008.11:144888595::AAA 10/50000)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 315024524 (NC_000008.11:144888595::A 3182/47780) Row 315024525 (NC_000008.11:144888595::AA 149/49350) Row 315024526 (NC_000008.11:144888595::AAA 10/50000)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 315024524 (NC_000008.11:144888595::A 3182/47780) Row 315024525 (NC_000008.11:144888595::AA 149/49350) Row 315024526 (NC_000008.11:144888595::AAA 10/50000)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 315024524 (NC_000008.11:144888595::A 3182/47780) Row 315024525 (NC_000008.11:144888595::AA 149/49350) Row 315024526 (NC_000008.11:144888595::AAA 10/50000)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 315024524 (NC_000008.11:144888595::A 3182/47780) Row 315024525 (NC_000008.11:144888595::AA 149/49350) Row 315024526 (NC_000008.11:144888595::AAA 10/50000)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 315024524 (NC_000008.11:144888595::A 3182/47780) Row 315024525 (NC_000008.11:144888595::AA 149/49350) Row 315024526 (NC_000008.11:144888595::AAA 10/50000)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 315024524 (NC_000008.11:144888595::A 3182/47780) Row 315024525 (NC_000008.11:144888595::AA 149/49350) Row 315024526 (NC_000008.11:144888595::AAA 10/50000)...	-	Apr 26, 2021 (155)
44	8.3KJPN Submission ignored due to conflicting rows: Row 49578077 (NC_000008.10:146113980:AA: 4563/16588) Row 49578078 (NC_000008.10:146113980::A 1433/16588) Row 49578079 (NC_000008.10:146113980:A: 570/16588)...	-	Apr 26, 2021 (155)
45	8.3KJPN Submission ignored due to conflicting rows: Row 49578077 (NC_000008.10:146113980:AA: 4563/16588) Row 49578078 (NC_000008.10:146113980::A 1433/16588) Row 49578079 (NC_000008.10:146113980:A: 570/16588)...	-	Apr 26, 2021 (155)
46	8.3KJPN Submission ignored due to conflicting rows: Row 49578077 (NC_000008.10:146113980:AA: 4563/16588) Row 49578078 (NC_000008.10:146113980::A 1433/16588) Row 49578079 (NC_000008.10:146113980:A: 570/16588)...	-	Apr 26, 2021 (155)
47	8.3KJPN Submission ignored due to conflicting rows: Row 49578077 (NC_000008.10:146113980:AA: 4563/16588) Row 49578078 (NC_000008.10:146113980::A 1433/16588) Row 49578079 (NC_000008.10:146113980:A: 570/16588)...	-	Apr 26, 2021 (155)
48	8.3KJPN Submission ignored due to conflicting rows: Row 49578077 (NC_000008.10:146113980:AA: 4563/16588) Row 49578078 (NC_000008.10:146113980::A 1433/16588) Row 49578079 (NC_000008.10:146113980:A: 570/16588)...	-	Apr 26, 2021 (155)
49	14KJPN Submission ignored due to conflicting rows: Row 68363078 (NC_000008.11:144888595:AA: 8136/28162) Row 68363079 (NC_000008.11:144888595::A 2686/28162) Row 68363080 (NC_000008.11:144888595:A: 988/28162)...	-	Oct 16, 2022 (156)
50	14KJPN Submission ignored due to conflicting rows: Row 68363078 (NC_000008.11:144888595:AA: 8136/28162) Row 68363079 (NC_000008.11:144888595::A 2686/28162) Row 68363080 (NC_000008.11:144888595:A: 988/28162)...	-	Oct 16, 2022 (156)
51	14KJPN Submission ignored due to conflicting rows: Row 68363078 (NC_000008.11:144888595:AA: 8136/28162) Row 68363079 (NC_000008.11:144888595::A 2686/28162) Row 68363080 (NC_000008.11:144888595:A: 988/28162)...	-	Oct 16, 2022 (156)
52	14KJPN Submission ignored due to conflicting rows: Row 68363078 (NC_000008.11:144888595:AA: 8136/28162) Row 68363079 (NC_000008.11:144888595::A 2686/28162) Row 68363080 (NC_000008.11:144888595:A: 988/28162)...	-	Oct 16, 2022 (156)
53	ALFA	NC_000008.11 - 144888596	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
8458511478	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4195789627	NC_000008.11:144888595:AAAAAAAA:	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
8458511478	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4195789626	NC_000008.11:144888595:AAAAAAA:	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
8458511478	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4195789625	NC_000008.11:144888595:AAAAAA:	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
8458511478	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4195789624	NC_000008.11:144888595:AAAA:	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
8458511478	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5191608773	NC_000008.10:146113980:AAA:	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4195789623, ss5475750970, ss5734525977	NC_000008.11:144888595:AAA:	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
8458511478	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5191608770	NC_000008.10:146113980:AA:	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4195789622, ss5475750967, ss5734525974	NC_000008.11:144888595:AA:	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
8458511478	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5191608772	NC_000008.10:146113980:A:	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4195789621, ss5475750969, ss5734525976	NC_000008.11:144888595:A:	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
8458511478	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss43202608	NT_037704.5:681416:A:	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5191608771	NC_000008.10:146113980::A	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4195789615, ss5475750966, ss5734525975	NC_000008.11:144888595::A	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
8458511478	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5191608774, ss5831414196	NC_000008.10:146113980::AA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4195789616, ss5475750968	NC_000008.11:144888595::AA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
8458511478	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5831414197	NC_000008.10:146113980::AAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA
ss4195789617	NC_000008.11:144888595::AAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
8458511478	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4195789618	NC_000008.11:144888595::AAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
8458511478	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4195789619	NC_000008.11:144888595::AAAAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4195789620	NC_000008.11:144888595::AAAAAAAAAA… NC_000008.11:144888595::AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2478484658	NC_000008.10:146113980:AAAAAAAA:	NC_000008.11:144888595:AAAAAAAAAAA… NC_000008.11:144888595:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs36073563

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

rs36073563