Name: rs35359938
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.

rs35359938

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:69136114-69136132 (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(T)₉ / del(T)₈ / del(T)₇ / del(…
del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.2304 (1261/5474, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DCAF5 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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	5474	(T)₁₉=0.5954	del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0002, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1704, dupTT=0.2304, dupTTT=0.0035, dup(T)₄=0.0002, dup(T)₅=0.0000
Allele Frequency Aggregator	European	Sub	5130	(T)₁₉=0.5692	del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0002, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1813, dupTT=0.2454, dupTTT=0.0037, dup(T)₄=0.0002, dup(T)₅=0.0000
Allele Frequency Aggregator	African	Sub	262	(T)₁₉=1.000	del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Other	Sub	34	(T)₁₉=0.85	del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.09, dupTT=0.06, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	20	(T)₁₉=1.00	del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	Latin American 2	Sub	16	(T)₁₉=1.00	del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(T)₁₉=1.00	del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	Asian	Sub	0	(T)₁₉=0	del(T)₉=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₅=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=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 14	NC_000014.9:g.69136124_69136132del
GRCh38.p14 chr 14	NC_000014.9:g.69136125_69136132del
GRCh38.p14 chr 14	NC_000014.9:g.69136126_69136132del
GRCh38.p14 chr 14	NC_000014.9:g.69136127_69136132del
GRCh38.p14 chr 14	NC_000014.9:g.69136128_69136132del
GRCh38.p14 chr 14	NC_000014.9:g.69136129_69136132del
GRCh38.p14 chr 14	NC_000014.9:g.69136130_69136132del
GRCh38.p14 chr 14	NC_000014.9:g.69136131_69136132del
GRCh38.p14 chr 14	NC_000014.9:g.69136132del
GRCh38.p14 chr 14	NC_000014.9:g.69136132dup
GRCh38.p14 chr 14	NC_000014.9:g.69136131_69136132dup
GRCh38.p14 chr 14	NC_000014.9:g.69136130_69136132dup
GRCh38.p14 chr 14	NC_000014.9:g.69136129_69136132dup
GRCh38.p14 chr 14	NC_000014.9:g.69136128_69136132dup
GRCh38.p14 chr 14	NC_000014.9:g.69136127_69136132dup
GRCh38.p14 chr 14	NC_000014.9:g.69136126_69136132dup
GRCh38.p14 chr 14	NC_000014.9:g.69136124_69136132dup
GRCh38.p14 chr 14	NC_000014.9:g.69136123_69136132dup
GRCh38.p14 chr 14	NC_000014.9:g.69136122_69136132dup
GRCh37.p13 chr 14	NC_000014.8:g.69602841_69602849del
GRCh37.p13 chr 14	NC_000014.8:g.69602842_69602849del
GRCh37.p13 chr 14	NC_000014.8:g.69602843_69602849del
GRCh37.p13 chr 14	NC_000014.8:g.69602844_69602849del
GRCh37.p13 chr 14	NC_000014.8:g.69602845_69602849del
GRCh37.p13 chr 14	NC_000014.8:g.69602846_69602849del
GRCh37.p13 chr 14	NC_000014.8:g.69602847_69602849del
GRCh37.p13 chr 14	NC_000014.8:g.69602848_69602849del
GRCh37.p13 chr 14	NC_000014.8:g.69602849del
GRCh37.p13 chr 14	NC_000014.8:g.69602849dup
GRCh37.p13 chr 14	NC_000014.8:g.69602848_69602849dup
GRCh37.p13 chr 14	NC_000014.8:g.69602847_69602849dup
GRCh37.p13 chr 14	NC_000014.8:g.69602846_69602849dup
GRCh37.p13 chr 14	NC_000014.8:g.69602845_69602849dup
GRCh37.p13 chr 14	NC_000014.8:g.69602844_69602849dup
GRCh37.p13 chr 14	NC_000014.8:g.69602843_69602849dup
GRCh37.p13 chr 14	NC_000014.8:g.69602841_69602849dup
GRCh37.p13 chr 14	NC_000014.8:g.69602840_69602849dup
GRCh37.p13 chr 14	NC_000014.8:g.69602839_69602849dup

Gene: DCAF5, DDB1 and CUL4 associated factor 5 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DCAF5 transcript variant 2	NM_001284206.1:c.215-1376… NM_001284206.1:c.215-13762_215-13754del	N/A	Intron Variant
DCAF5 transcript variant 3	NM_001284207.1:c.-32-1376… NM_001284207.1:c.-32-13762_-32-13754del	N/A	Intron Variant
DCAF5 transcript variant 4	NM_001284208.2:c.215-1376… NM_001284208.2:c.215-13762_215-13754del	N/A	Intron Variant
DCAF5 transcript variant 1	NM_003861.3:c.215-13762_2… NM_003861.3:c.215-13762_215-13754del	N/A	Intron Variant
DCAF5 transcript variant X1	XM_006720297.3:c.215-1376… XM_006720297.3:c.215-13762_215-13754del	N/A	Intron Variant
DCAF5 transcript variant X2	XM_006720298.3:c.215-1376… XM_006720298.3:c.215-13762_215-13754del	N/A	Intron Variant
DCAF5 transcript variant X3	XM_006720299.4:c.-32-1376… XM_006720299.4:c.-32-13762_-32-13754del	N/A	Intron Variant
DCAF5 transcript variant X7	XM_011537278.2:c.-33+1330… XM_011537278.2:c.-33+13309_-33+13317del	N/A	Intron Variant
DCAF5 transcript variant X4	XM_011537279.3:c.-32-1376… XM_011537279.3:c.-32-13762_-32-13754del	N/A	Intron Variant
DCAF5 transcript variant X5	XM_017021733.2:c.-32-1376… XM_017021733.2:c.-32-13762_-32-13754del	N/A	Intron Variant
DCAF5 transcript variant X6	XM_047431846.1:c.-33+1330… XM_047431846.1:c.-33+13309_-33+13317del	N/A	Intron Variant
DCAF5 transcript variant X8	XM_047431847.1:c.-33+1330… XM_047431847.1:c.-33+13309_-33+13317del	N/A	Intron Variant
DCAF5 transcript variant X9	XM_011537280.4:c.	N/A	Genic Upstream Transcript Variant
DCAF5 transcript variant X10	XM_017021737.2:c.	N/A	Genic Upstream Transcript 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	(T)₁₉=	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₉	dup(T)₁₀	dup(T)₁₁
GRCh38.p14 chr 14	NC_000014.9:g.69136114_69136132=	NC_000014.9:g.69136124_69136132del	NC_000014.9:g.69136125_69136132del	NC_000014.9:g.69136126_69136132del	NC_000014.9:g.69136127_69136132del	NC_000014.9:g.69136128_69136132del	NC_000014.9:g.69136129_69136132del	NC_000014.9:g.69136130_69136132del	NC_000014.9:g.69136131_69136132del	NC_000014.9:g.69136132del	NC_000014.9:g.69136132dup	NC_000014.9:g.69136131_69136132dup	NC_000014.9:g.69136130_69136132dup	NC_000014.9:g.69136129_69136132dup	NC_000014.9:g.69136128_69136132dup	NC_000014.9:g.69136127_69136132dup	NC_000014.9:g.69136126_69136132dup	NC_000014.9:g.69136124_69136132dup	NC_000014.9:g.69136123_69136132dup	NC_000014.9:g.69136122_69136132dup
GRCh37.p13 chr 14	NC_000014.8:g.69602831_69602849=	NC_000014.8:g.69602841_69602849del	NC_000014.8:g.69602842_69602849del	NC_000014.8:g.69602843_69602849del	NC_000014.8:g.69602844_69602849del	NC_000014.8:g.69602845_69602849del	NC_000014.8:g.69602846_69602849del	NC_000014.8:g.69602847_69602849del	NC_000014.8:g.69602848_69602849del	NC_000014.8:g.69602849del	NC_000014.8:g.69602849dup	NC_000014.8:g.69602848_69602849dup	NC_000014.8:g.69602847_69602849dup	NC_000014.8:g.69602846_69602849dup	NC_000014.8:g.69602845_69602849dup	NC_000014.8:g.69602844_69602849dup	NC_000014.8:g.69602843_69602849dup	NC_000014.8:g.69602841_69602849dup	NC_000014.8:g.69602840_69602849dup	NC_000014.8:g.69602839_69602849dup
DCAF5 transcript variant 2	NM_001284206.1:c.215-13754=	NM_001284206.1:c.215-13762_215-13754del	NM_001284206.1:c.215-13761_215-13754del	NM_001284206.1:c.215-13760_215-13754del	NM_001284206.1:c.215-13759_215-13754del	NM_001284206.1:c.215-13758_215-13754del	NM_001284206.1:c.215-13757_215-13754del	NM_001284206.1:c.215-13756_215-13754del	NM_001284206.1:c.215-13755_215-13754del	NM_001284206.1:c.215-13754del	NM_001284206.1:c.215-13754dup	NM_001284206.1:c.215-13755_215-13754dup	NM_001284206.1:c.215-13756_215-13754dup	NM_001284206.1:c.215-13757_215-13754dup	NM_001284206.1:c.215-13758_215-13754dup	NM_001284206.1:c.215-13759_215-13754dup	NM_001284206.1:c.215-13760_215-13754dup	NM_001284206.1:c.215-13762_215-13754dup	NM_001284206.1:c.215-13763_215-13754dup	NM_001284206.1:c.215-13764_215-13754dup
DCAF5 transcript variant 3	NM_001284207.1:c.-32-13754=	NM_001284207.1:c.-32-13762_-32-13754del	NM_001284207.1:c.-32-13761_-32-13754del	NM_001284207.1:c.-32-13760_-32-13754del	NM_001284207.1:c.-32-13759_-32-13754del	NM_001284207.1:c.-32-13758_-32-13754del	NM_001284207.1:c.-32-13757_-32-13754del	NM_001284207.1:c.-32-13756_-32-13754del	NM_001284207.1:c.-32-13755_-32-13754del	NM_001284207.1:c.-32-13754del	NM_001284207.1:c.-32-13754dup	NM_001284207.1:c.-32-13755_-32-13754dup	NM_001284207.1:c.-32-13756_-32-13754dup	NM_001284207.1:c.-32-13757_-32-13754dup	NM_001284207.1:c.-32-13758_-32-13754dup	NM_001284207.1:c.-32-13759_-32-13754dup	NM_001284207.1:c.-32-13760_-32-13754dup	NM_001284207.1:c.-32-13762_-32-13754dup	NM_001284207.1:c.-32-13763_-32-13754dup	NM_001284207.1:c.-32-13764_-32-13754dup
DCAF5 transcript variant 4	NM_001284208.2:c.215-13754=	NM_001284208.2:c.215-13762_215-13754del	NM_001284208.2:c.215-13761_215-13754del	NM_001284208.2:c.215-13760_215-13754del	NM_001284208.2:c.215-13759_215-13754del	NM_001284208.2:c.215-13758_215-13754del	NM_001284208.2:c.215-13757_215-13754del	NM_001284208.2:c.215-13756_215-13754del	NM_001284208.2:c.215-13755_215-13754del	NM_001284208.2:c.215-13754del	NM_001284208.2:c.215-13754dup	NM_001284208.2:c.215-13755_215-13754dup	NM_001284208.2:c.215-13756_215-13754dup	NM_001284208.2:c.215-13757_215-13754dup	NM_001284208.2:c.215-13758_215-13754dup	NM_001284208.2:c.215-13759_215-13754dup	NM_001284208.2:c.215-13760_215-13754dup	NM_001284208.2:c.215-13762_215-13754dup	NM_001284208.2:c.215-13763_215-13754dup	NM_001284208.2:c.215-13764_215-13754dup
DCAF5 transcript variant 1	NM_003861.2:c.215-13754=	NM_003861.2:c.215-13762_215-13754del	NM_003861.2:c.215-13761_215-13754del	NM_003861.2:c.215-13760_215-13754del	NM_003861.2:c.215-13759_215-13754del	NM_003861.2:c.215-13758_215-13754del	NM_003861.2:c.215-13757_215-13754del	NM_003861.2:c.215-13756_215-13754del	NM_003861.2:c.215-13755_215-13754del	NM_003861.2:c.215-13754del	NM_003861.2:c.215-13754dup	NM_003861.2:c.215-13755_215-13754dup	NM_003861.2:c.215-13756_215-13754dup	NM_003861.2:c.215-13757_215-13754dup	NM_003861.2:c.215-13758_215-13754dup	NM_003861.2:c.215-13759_215-13754dup	NM_003861.2:c.215-13760_215-13754dup	NM_003861.2:c.215-13762_215-13754dup	NM_003861.2:c.215-13763_215-13754dup	NM_003861.2:c.215-13764_215-13754dup
DCAF5 transcript variant 1	NM_003861.3:c.215-13754=	NM_003861.3:c.215-13762_215-13754del	NM_003861.3:c.215-13761_215-13754del	NM_003861.3:c.215-13760_215-13754del	NM_003861.3:c.215-13759_215-13754del	NM_003861.3:c.215-13758_215-13754del	NM_003861.3:c.215-13757_215-13754del	NM_003861.3:c.215-13756_215-13754del	NM_003861.3:c.215-13755_215-13754del	NM_003861.3:c.215-13754del	NM_003861.3:c.215-13754dup	NM_003861.3:c.215-13755_215-13754dup	NM_003861.3:c.215-13756_215-13754dup	NM_003861.3:c.215-13757_215-13754dup	NM_003861.3:c.215-13758_215-13754dup	NM_003861.3:c.215-13759_215-13754dup	NM_003861.3:c.215-13760_215-13754dup	NM_003861.3:c.215-13762_215-13754dup	NM_003861.3:c.215-13763_215-13754dup	NM_003861.3:c.215-13764_215-13754dup
DCAF5 transcript variant X1	XM_005268161.1:c.215-13754=	XM_005268161.1:c.215-13762_215-13754del	XM_005268161.1:c.215-13761_215-13754del	XM_005268161.1:c.215-13760_215-13754del	XM_005268161.1:c.215-13759_215-13754del	XM_005268161.1:c.215-13758_215-13754del	XM_005268161.1:c.215-13757_215-13754del	XM_005268161.1:c.215-13756_215-13754del	XM_005268161.1:c.215-13755_215-13754del	XM_005268161.1:c.215-13754del	XM_005268161.1:c.215-13754dup	XM_005268161.1:c.215-13755_215-13754dup	XM_005268161.1:c.215-13756_215-13754dup	XM_005268161.1:c.215-13757_215-13754dup	XM_005268161.1:c.215-13758_215-13754dup	XM_005268161.1:c.215-13759_215-13754dup	XM_005268161.1:c.215-13760_215-13754dup	XM_005268161.1:c.215-13762_215-13754dup	XM_005268161.1:c.215-13763_215-13754dup	XM_005268161.1:c.215-13764_215-13754dup
DCAF5 transcript variant X2	XM_005268162.1:c.-32-13754=	XM_005268162.1:c.-32-13762_-32-13754del	XM_005268162.1:c.-32-13761_-32-13754del	XM_005268162.1:c.-32-13760_-32-13754del	XM_005268162.1:c.-32-13759_-32-13754del	XM_005268162.1:c.-32-13758_-32-13754del	XM_005268162.1:c.-32-13757_-32-13754del	XM_005268162.1:c.-32-13756_-32-13754del	XM_005268162.1:c.-32-13755_-32-13754del	XM_005268162.1:c.-32-13754del	XM_005268162.1:c.-32-13754dup	XM_005268162.1:c.-32-13755_-32-13754dup	XM_005268162.1:c.-32-13756_-32-13754dup	XM_005268162.1:c.-32-13757_-32-13754dup	XM_005268162.1:c.-32-13758_-32-13754dup	XM_005268162.1:c.-32-13759_-32-13754dup	XM_005268162.1:c.-32-13760_-32-13754dup	XM_005268162.1:c.-32-13762_-32-13754dup	XM_005268162.1:c.-32-13763_-32-13754dup	XM_005268162.1:c.-32-13764_-32-13754dup
DCAF5 transcript variant X1	XM_006720297.3:c.215-13754=	XM_006720297.3:c.215-13762_215-13754del	XM_006720297.3:c.215-13761_215-13754del	XM_006720297.3:c.215-13760_215-13754del	XM_006720297.3:c.215-13759_215-13754del	XM_006720297.3:c.215-13758_215-13754del	XM_006720297.3:c.215-13757_215-13754del	XM_006720297.3:c.215-13756_215-13754del	XM_006720297.3:c.215-13755_215-13754del	XM_006720297.3:c.215-13754del	XM_006720297.3:c.215-13754dup	XM_006720297.3:c.215-13755_215-13754dup	XM_006720297.3:c.215-13756_215-13754dup	XM_006720297.3:c.215-13757_215-13754dup	XM_006720297.3:c.215-13758_215-13754dup	XM_006720297.3:c.215-13759_215-13754dup	XM_006720297.3:c.215-13760_215-13754dup	XM_006720297.3:c.215-13762_215-13754dup	XM_006720297.3:c.215-13763_215-13754dup	XM_006720297.3:c.215-13764_215-13754dup
DCAF5 transcript variant X2	XM_006720298.3:c.215-13754=	XM_006720298.3:c.215-13762_215-13754del	XM_006720298.3:c.215-13761_215-13754del	XM_006720298.3:c.215-13760_215-13754del	XM_006720298.3:c.215-13759_215-13754del	XM_006720298.3:c.215-13758_215-13754del	XM_006720298.3:c.215-13757_215-13754del	XM_006720298.3:c.215-13756_215-13754del	XM_006720298.3:c.215-13755_215-13754del	XM_006720298.3:c.215-13754del	XM_006720298.3:c.215-13754dup	XM_006720298.3:c.215-13755_215-13754dup	XM_006720298.3:c.215-13756_215-13754dup	XM_006720298.3:c.215-13757_215-13754dup	XM_006720298.3:c.215-13758_215-13754dup	XM_006720298.3:c.215-13759_215-13754dup	XM_006720298.3:c.215-13760_215-13754dup	XM_006720298.3:c.215-13762_215-13754dup	XM_006720298.3:c.215-13763_215-13754dup	XM_006720298.3:c.215-13764_215-13754dup
DCAF5 transcript variant X3	XM_006720299.4:c.-32-13754=	XM_006720299.4:c.-32-13762_-32-13754del	XM_006720299.4:c.-32-13761_-32-13754del	XM_006720299.4:c.-32-13760_-32-13754del	XM_006720299.4:c.-32-13759_-32-13754del	XM_006720299.4:c.-32-13758_-32-13754del	XM_006720299.4:c.-32-13757_-32-13754del	XM_006720299.4:c.-32-13756_-32-13754del	XM_006720299.4:c.-32-13755_-32-13754del	XM_006720299.4:c.-32-13754del	XM_006720299.4:c.-32-13754dup	XM_006720299.4:c.-32-13755_-32-13754dup	XM_006720299.4:c.-32-13756_-32-13754dup	XM_006720299.4:c.-32-13757_-32-13754dup	XM_006720299.4:c.-32-13758_-32-13754dup	XM_006720299.4:c.-32-13759_-32-13754dup	XM_006720299.4:c.-32-13760_-32-13754dup	XM_006720299.4:c.-32-13762_-32-13754dup	XM_006720299.4:c.-32-13763_-32-13754dup	XM_006720299.4:c.-32-13764_-32-13754dup
DCAF5 transcript variant X7	XM_011537278.2:c.-33+13317=	XM_011537278.2:c.-33+13309_-33+13317del	XM_011537278.2:c.-33+13310_-33+13317del	XM_011537278.2:c.-33+13311_-33+13317del	XM_011537278.2:c.-33+13312_-33+13317del	XM_011537278.2:c.-33+13313_-33+13317del	XM_011537278.2:c.-33+13314_-33+13317del	XM_011537278.2:c.-33+13315_-33+13317del	XM_011537278.2:c.-33+13316_-33+13317del	XM_011537278.2:c.-33+13317del	XM_011537278.2:c.-33+13317dup	XM_011537278.2:c.-33+13316_-33+13317dup	XM_011537278.2:c.-33+13315_-33+13317dup	XM_011537278.2:c.-33+13314_-33+13317dup	XM_011537278.2:c.-33+13313_-33+13317dup	XM_011537278.2:c.-33+13312_-33+13317dup	XM_011537278.2:c.-33+13311_-33+13317dup	XM_011537278.2:c.-33+13309_-33+13317dup	XM_011537278.2:c.-33+13308_-33+13317dup	XM_011537278.2:c.-33+13307_-33+13317dup
DCAF5 transcript variant X4	XM_011537279.3:c.-32-13754=	XM_011537279.3:c.-32-13762_-32-13754del	XM_011537279.3:c.-32-13761_-32-13754del	XM_011537279.3:c.-32-13760_-32-13754del	XM_011537279.3:c.-32-13759_-32-13754del	XM_011537279.3:c.-32-13758_-32-13754del	XM_011537279.3:c.-32-13757_-32-13754del	XM_011537279.3:c.-32-13756_-32-13754del	XM_011537279.3:c.-32-13755_-32-13754del	XM_011537279.3:c.-32-13754del	XM_011537279.3:c.-32-13754dup	XM_011537279.3:c.-32-13755_-32-13754dup	XM_011537279.3:c.-32-13756_-32-13754dup	XM_011537279.3:c.-32-13757_-32-13754dup	XM_011537279.3:c.-32-13758_-32-13754dup	XM_011537279.3:c.-32-13759_-32-13754dup	XM_011537279.3:c.-32-13760_-32-13754dup	XM_011537279.3:c.-32-13762_-32-13754dup	XM_011537279.3:c.-32-13763_-32-13754dup	XM_011537279.3:c.-32-13764_-32-13754dup
DCAF5 transcript variant X5	XM_017021733.2:c.-32-13754=	XM_017021733.2:c.-32-13762_-32-13754del	XM_017021733.2:c.-32-13761_-32-13754del	XM_017021733.2:c.-32-13760_-32-13754del	XM_017021733.2:c.-32-13759_-32-13754del	XM_017021733.2:c.-32-13758_-32-13754del	XM_017021733.2:c.-32-13757_-32-13754del	XM_017021733.2:c.-32-13756_-32-13754del	XM_017021733.2:c.-32-13755_-32-13754del	XM_017021733.2:c.-32-13754del	XM_017021733.2:c.-32-13754dup	XM_017021733.2:c.-32-13755_-32-13754dup	XM_017021733.2:c.-32-13756_-32-13754dup	XM_017021733.2:c.-32-13757_-32-13754dup	XM_017021733.2:c.-32-13758_-32-13754dup	XM_017021733.2:c.-32-13759_-32-13754dup	XM_017021733.2:c.-32-13760_-32-13754dup	XM_017021733.2:c.-32-13762_-32-13754dup	XM_017021733.2:c.-32-13763_-32-13754dup	XM_017021733.2:c.-32-13764_-32-13754dup
DCAF5 transcript variant X6	XM_047431846.1:c.-33+13317=	XM_047431846.1:c.-33+13309_-33+13317del	XM_047431846.1:c.-33+13310_-33+13317del	XM_047431846.1:c.-33+13311_-33+13317del	XM_047431846.1:c.-33+13312_-33+13317del	XM_047431846.1:c.-33+13313_-33+13317del	XM_047431846.1:c.-33+13314_-33+13317del	XM_047431846.1:c.-33+13315_-33+13317del	XM_047431846.1:c.-33+13316_-33+13317del	XM_047431846.1:c.-33+13317del	XM_047431846.1:c.-33+13317dup	XM_047431846.1:c.-33+13316_-33+13317dup	XM_047431846.1:c.-33+13315_-33+13317dup	XM_047431846.1:c.-33+13314_-33+13317dup	XM_047431846.1:c.-33+13313_-33+13317dup	XM_047431846.1:c.-33+13312_-33+13317dup	XM_047431846.1:c.-33+13311_-33+13317dup	XM_047431846.1:c.-33+13309_-33+13317dup	XM_047431846.1:c.-33+13308_-33+13317dup	XM_047431846.1:c.-33+13307_-33+13317dup
DCAF5 transcript variant X8	XM_047431847.1:c.-33+13317=	XM_047431847.1:c.-33+13309_-33+13317del	XM_047431847.1:c.-33+13310_-33+13317del	XM_047431847.1:c.-33+13311_-33+13317del	XM_047431847.1:c.-33+13312_-33+13317del	XM_047431847.1:c.-33+13313_-33+13317del	XM_047431847.1:c.-33+13314_-33+13317del	XM_047431847.1:c.-33+13315_-33+13317del	XM_047431847.1:c.-33+13316_-33+13317del	XM_047431847.1:c.-33+13317del	XM_047431847.1:c.-33+13317dup	XM_047431847.1:c.-33+13316_-33+13317dup	XM_047431847.1:c.-33+13315_-33+13317dup	XM_047431847.1:c.-33+13314_-33+13317dup	XM_047431847.1:c.-33+13313_-33+13317dup	XM_047431847.1:c.-33+13312_-33+13317dup	XM_047431847.1:c.-33+13311_-33+13317dup	XM_047431847.1:c.-33+13309_-33+13317dup	XM_047431847.1:c.-33+13308_-33+13317dup	XM_047431847.1:c.-33+13307_-33+13317dup

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#.

54 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40433076	Mar 14, 2006 (126)
2	ABI	ss40485740	Mar 15, 2006 (126)
3	HGSV	ss80036964	Dec 03, 2013 (138)
4	HUMANGENOME_JCVI	ss95644477	Dec 05, 2013 (138)
5	PJP	ss294837172	May 09, 2011 (137)
6	BILGI_BIOE	ss666630850	Apr 25, 2013 (138)
7	EVA_UK10K_ALSPAC	ss1708104713	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1708104714	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1708104854	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1708104857	Apr 01, 2015 (144)
11	SWEGEN	ss3012398425	Nov 08, 2017 (151)
12	SWEGEN	ss3012398426	Nov 08, 2017 (151)
13	SWEGEN	ss3012398427	Nov 08, 2017 (151)
14	EVA_DECODE	ss3696917749	Jul 13, 2019 (153)
15	EVA_DECODE	ss3696917750	Jul 13, 2019 (153)
16	EVA_DECODE	ss3696917751	Jul 13, 2019 (153)
17	EVA_DECODE	ss3696917752	Jul 13, 2019 (153)
18	EVA_DECODE	ss3696917753	Jul 13, 2019 (153)
19	EVA_DECODE	ss3696917754	Jul 13, 2019 (153)
20	PACBIO	ss3797616167	Jul 13, 2019 (153)
21	EVA	ss3833980735	Apr 27, 2020 (154)
22	GNOMAD	ss4280144881	Apr 26, 2021 (155)
23	GNOMAD	ss4280144883	Apr 26, 2021 (155)
24	GNOMAD	ss4280144884	Apr 26, 2021 (155)
25	GNOMAD	ss4280144885	Apr 26, 2021 (155)
26	GNOMAD	ss4280144886	Apr 26, 2021 (155)
27	GNOMAD	ss4280144887	Apr 26, 2021 (155)
28	GNOMAD	ss4280144888	Apr 26, 2021 (155)
29	GNOMAD	ss4280144889	Apr 26, 2021 (155)
30	GNOMAD	ss4280144891	Apr 26, 2021 (155)
31	GNOMAD	ss4280144892	Apr 26, 2021 (155)
32	GNOMAD	ss4280144893	Apr 26, 2021 (155)
33	GNOMAD	ss4280144894	Apr 26, 2021 (155)
34	GNOMAD	ss4280144895	Apr 26, 2021 (155)
35	GNOMAD	ss4280144896	Apr 26, 2021 (155)
36	GNOMAD	ss4280144897	Apr 26, 2021 (155)
37	GNOMAD	ss4280144898	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5213778685	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5213778686	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5213778687	Apr 26, 2021 (155)
41	1000G_HIGH_COVERAGE	ss5296646717	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5296646718	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5296646719	Oct 16, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5296646720	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5490648331	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5490648332	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5490648333	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5490648334	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5766739302	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5766739303	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5766739304	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5766739305	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5766739307	Oct 16, 2022 (156)
54	YY_MCH	ss5814856279	Oct 16, 2022 (156)
55	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 35830773 (NC_000014.8:69602830::TT 1081/3854) Row 35830774 (NC_000014.8:69602830::T 2467/3854)	-	Oct 12, 2018 (152)
56	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 35830773 (NC_000014.8:69602830::TT 1081/3854) Row 35830774 (NC_000014.8:69602830::T 2467/3854)	-	Oct 12, 2018 (152)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454690217 (NC_000014.9:69136113::T 36416/114890) Row 454690219 (NC_000014.9:69136113::TT 43070/114834) Row 454690220 (NC_000014.9:69136113::TTT 832/114922)...	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 71747992 (NC_000014.8:69602830::TT 15154/16588) Row 71747993 (NC_000014.8:69602830::TTT 149/16588) Row 71747994 (NC_000014.8:69602830::T 66/16588)	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 71747992 (NC_000014.8:69602830::TT 15154/16588) Row 71747993 (NC_000014.8:69602830::TTT 149/16588) Row 71747994 (NC_000014.8:69602830::T 66/16588)	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 71747992 (NC_000014.8:69602830::TT 15154/16588) Row 71747993 (NC_000014.8:69602830::TTT 149/16588) Row 71747994 (NC_000014.8:69602830::T 66/16588)	-	Apr 26, 2021 (155)
77	14KJPN Submission ignored due to conflicting rows: Row 100576406 (NC_000014.9:69136113::TT 26048/28256) Row 100576407 (NC_000014.9:69136113::TTT 231/28256) Row 100576408 (NC_000014.9:69136113::T 101/28256)...	-	Oct 16, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 100576406 (NC_000014.9:69136113::TT 26048/28256) Row 100576407 (NC_000014.9:69136113::TTT 231/28256) Row 100576408 (NC_000014.9:69136113::T 101/28256)...	-	Oct 16, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 100576406 (NC_000014.9:69136113::TT 26048/28256) Row 100576407 (NC_000014.9:69136113::TTT 231/28256) Row 100576408 (NC_000014.9:69136113::T 101/28256)...	-	Oct 16, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 100576406 (NC_000014.9:69136113::TT 26048/28256) Row 100576407 (NC_000014.9:69136113::TTT 231/28256) Row 100576408 (NC_000014.9:69136113::T 101/28256)...	-	Oct 16, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 100576406 (NC_000014.9:69136113::TT 26048/28256) Row 100576407 (NC_000014.9:69136113::TTT 231/28256) Row 100576408 (NC_000014.9:69136113::T 101/28256)...	-	Oct 16, 2022 (156)
82	UK 10K study - Twins Submission ignored due to conflicting rows: Row 35830773 (NC_000014.8:69602830::TT 965/3708) Row 35830774 (NC_000014.8:69602830::T 2400/3708)	-	Oct 12, 2018 (152)
83	UK 10K study - Twins Submission ignored due to conflicting rows: Row 35830773 (NC_000014.8:69602830::TT 965/3708) Row 35830774 (NC_000014.8:69602830::T 2400/3708)	-	Oct 12, 2018 (152)
84	ALFA	NC_000014.9 - 69136114	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).

Associated ID	History Updated (Build)
rs35778219	Oct 16, 2006 (127)
rs142107365	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4280144898	NC_000014.9:69136113:TTTTTTTTT:	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
4538422891	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4280144897	NC_000014.9:69136113:TTTTTTTT:	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
4538422891	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4280144896	NC_000014.9:69136113:TTTTTTT:	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
4538422891	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4280144895	NC_000014.9:69136113:TTTTTT:	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
4538422891	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4280144894, ss5296646719, ss5766739307	NC_000014.9:69136113:TTTTT:	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
4538422891	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4280144893	NC_000014.9:69136113:TTTT:	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4280144892	NC_000014.9:69136113:TTT:	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
4538422891	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4280144891	NC_000014.9:69136113:TT:	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
4538422891	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3696917749, ss5490648334, ss5766739305	NC_000014.9:69136113:T:	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
4538422891	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss1708104714, ss1708104857, ss3012398426, ss3797616167, ss5213778687	NC_000014.8:69602830::T	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4280144881, ss5296646717, ss5490648332, ss5766739304	NC_000014.9:69136113::T	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
4538422891	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3696917750	NC_000014.9:69136114::T	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss40433076, ss40485740	NT_026437.12:50602830::T	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss80036964, ss95644477	NT_026437.12:50602849::T	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss294837172	NC_000014.7:68672584::TT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss666630850, ss1708104713, ss1708104854, ss3012398425, ss3833980735, ss5213778685	NC_000014.8:69602830::TT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4280144883, ss5296646718, ss5490648331, ss5766739302, ss5814856279	NC_000014.9:69136113::TT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
4538422891	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3696917751	NC_000014.9:69136114::TT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3012398427, ss5213778686	NC_000014.8:69602830::TTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280144884, ss5296646720, ss5490648333, ss5766739303	NC_000014.9:69136113::TTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
4538422891	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3696917752	NC_000014.9:69136114::TTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280144885	NC_000014.9:69136113::TTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
4538422891	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280144886	NC_000014.9:69136113::TTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
4538422891	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280144887	NC_000014.9:69136113::TTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280144888	NC_000014.9:69136113::TTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3696917753	NC_000014.9:69136114::TTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280144889	NC_000014.9:69136113::TTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3696917754	NC_000014.9:69136114::TTTTTTTTTTT	NC_000014.9:69136113:TTTTTTTTTTTTT… NC_000014.9:69136113:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs35359938

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

rs35359938