Name: rs35612117
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.

rs35612117

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:69446874-69446889 (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)₇ / del(A)₆ / del…
del(A)₁₃ / del(A)₇ / del(A)₆ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₈ / ins(A)₁₉ / ins(A)₂₂ / ins(A)₃₄
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₃=0.0000 (0/3222, ALFA)
del(A)₇=0.0000 (0/3222, ALFA)
del(A)₆=0.0000 (0/3222, ALFA) (+ 6 more)
delAA=0.0000 (0/3222, ALFA)
delA=0.0000 (0/3222, ALFA)
dupA=0.0000 (0/3222, ALFA)
dupAA=0.0000 (0/3222, ALFA)
dupAAA=0.0000 (0/3222, ALFA)
dup(A)₄=0.0000 (0/3222, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC39A9 : 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	3222	AAAAAAAAAAAAAAAA=1.0000	AAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	1740	AAAAAAAAAAAAAAAA=1.0000	AAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1024	AAAAAAAAAAAAAAAA=1.0000	AAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	46	AAAAAAAAAAAAAAAA=1.00	AAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	978	AAAAAAAAAAAAAAAA=1.000	AAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	50	AAAAAAAAAAAAAAAA=1.00	AAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	34	AAAAAAAAAAAAAAAA=1.00	AAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	16	AAAAAAAAAAAAAAAA=1.00	AAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	40	AAAAAAAAAAAAAAAA=1.00	AAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	206	AAAAAAAAAAAAAAAA=1.000	AAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	22	AAAAAAAAAAAAAAAA=1.00	AAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	140	AAAAAAAAAAAAAAAA=1.000	AAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=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	3222	(A)₁₆=1.0000	del(A)₁₃=0.0000, del(A)₇=0.0000, del(A)₆=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	European	Sub	1740	(A)₁₆=1.0000	del(A)₁₃=0.0000, del(A)₇=0.0000, del(A)₆=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	1024	(A)₁₆=1.0000	del(A)₁₃=0.0000, del(A)₇=0.0000, del(A)₆=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	206	(A)₁₆=1.000	del(A)₁₃=0.000, del(A)₇=0.000, del(A)₆=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	140	(A)₁₆=1.000	del(A)₁₃=0.000, del(A)₇=0.000, del(A)₆=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	Asian	Sub	50	(A)₁₆=1.00	del(A)₁₃=0.00, del(A)₇=0.00, del(A)₆=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	Latin American 1	Sub	40	(A)₁₆=1.00	del(A)₁₃=0.00, del(A)₇=0.00, del(A)₆=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	22	(A)₁₆=1.00	del(A)₁₃=0.00, del(A)₇=0.00, del(A)₆=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 14	NC_000014.9:g.69446877_69446889del
GRCh38.p14 chr 14	NC_000014.9:g.69446883_69446889del
GRCh38.p14 chr 14	NC_000014.9:g.69446884_69446889del
GRCh38.p14 chr 14	NC_000014.9:g.69446886_69446889del
GRCh38.p14 chr 14	NC_000014.9:g.69446887_69446889del
GRCh38.p14 chr 14	NC_000014.9:g.69446888_69446889del
GRCh38.p14 chr 14	NC_000014.9:g.69446889del
GRCh38.p14 chr 14	NC_000014.9:g.69446889dup
GRCh38.p14 chr 14	NC_000014.9:g.69446888_69446889dup
GRCh38.p14 chr 14	NC_000014.9:g.69446887_69446889dup
GRCh38.p14 chr 14	NC_000014.9:g.69446886_69446889dup
GRCh38.p14 chr 14	NC_000014.9:g.69446885_69446889dup
GRCh38.p14 chr 14	NC_000014.9:g.69446884_69446889dup
GRCh38.p14 chr 14	NC_000014.9:g.69446883_69446889dup
GRCh38.p14 chr 14	NC_000014.9:g.69446882_69446889dup
GRCh38.p14 chr 14	NC_000014.9:g.69446889_69446890insAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 14	NC_000014.9:g.69446889_69446890insAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 14	NC_000014.9:g.69446889_69446890insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 14	NC_000014.8:g.69913594_69913606del
GRCh37.p13 chr 14	NC_000014.8:g.69913600_69913606del
GRCh37.p13 chr 14	NC_000014.8:g.69913601_69913606del
GRCh37.p13 chr 14	NC_000014.8:g.69913603_69913606del
GRCh37.p13 chr 14	NC_000014.8:g.69913604_69913606del
GRCh37.p13 chr 14	NC_000014.8:g.69913605_69913606del
GRCh37.p13 chr 14	NC_000014.8:g.69913606del
GRCh37.p13 chr 14	NC_000014.8:g.69913606dup
GRCh37.p13 chr 14	NC_000014.8:g.69913605_69913606dup
GRCh37.p13 chr 14	NC_000014.8:g.69913604_69913606dup
GRCh37.p13 chr 14	NC_000014.8:g.69913603_69913606dup
GRCh37.p13 chr 14	NC_000014.8:g.69913602_69913606dup
GRCh37.p13 chr 14	NC_000014.8:g.69913601_69913606dup
GRCh37.p13 chr 14	NC_000014.8:g.69913600_69913606dup
GRCh37.p13 chr 14	NC_000014.8:g.69913599_69913606dup
GRCh37.p13 chr 14	NC_000014.8:g.69913606_69913607insAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 14	NC_000014.8:g.69913606_69913607insAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 14	NC_000014.8:g.69913606_69913607insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: SLC39A9, solute carrier family 39 member 9 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC39A9 transcript variant 2	NM_001252148.2:c.403+4611… NM_001252148.2:c.403+4611_403+4623del	N/A	Intron Variant
SLC39A9 transcript variant 3	NM_001252150.2:c.403+4611… NM_001252150.2:c.403+4611_403+4623del	N/A	Intron Variant
SLC39A9 transcript variant 4	NM_001252151.2:c.49+4611_… NM_001252151.2:c.49+4611_49+4623del	N/A	Intron Variant
SLC39A9 transcript variant 5	NM_001252152.2:c.49+4611_… NM_001252152.2:c.49+4611_49+4623del	N/A	Intron Variant
SLC39A9 transcript variant 6	NM_001330185.2:c.206-6364… NM_001330185.2:c.206-6364_206-6352del	N/A	Intron Variant
SLC39A9 transcript variant 1	NM_018375.5:c.403+4611_40… NM_018375.5:c.403+4611_403+4623del	N/A	Intron Variant
SLC39A9 transcript variant X1	XM_024449648.2:c.49+4611_… XM_024449648.2:c.49+4611_49+4623del	N/A	Intron Variant
SLC39A9 transcript variant X2	XM_047431550.1:c.49+4611_… XM_047431550.1:c.49+4611_49+4623del	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)₁₆=	del(A)₁₃	del(A)₇	del(A)₆	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₈	ins(A)₁₉	ins(A)₂₂	ins(A)₃₄
GRCh38.p14 chr 14	NC_000014.9:g.69446874_69446889=	NC_000014.9:g.69446877_69446889del	NC_000014.9:g.69446883_69446889del	NC_000014.9:g.69446884_69446889del	NC_000014.9:g.69446886_69446889del	NC_000014.9:g.69446887_69446889del	NC_000014.9:g.69446888_69446889del	NC_000014.9:g.69446889del	NC_000014.9:g.69446889dup	NC_000014.9:g.69446888_69446889dup	NC_000014.9:g.69446887_69446889dup	NC_000014.9:g.69446886_69446889dup	NC_000014.9:g.69446885_69446889dup	NC_000014.9:g.69446884_69446889dup	NC_000014.9:g.69446883_69446889dup	NC_000014.9:g.69446882_69446889dup	NC_000014.9:g.69446889_69446890insAAAAAAAAAAAAAAAAAAA	NC_000014.9:g.69446889_69446890insAAAAAAAAAAAAAAAAAAAAAA	NC_000014.9:g.69446889_69446890insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 14	NC_000014.8:g.69913591_69913606=	NC_000014.8:g.69913594_69913606del	NC_000014.8:g.69913600_69913606del	NC_000014.8:g.69913601_69913606del	NC_000014.8:g.69913603_69913606del	NC_000014.8:g.69913604_69913606del	NC_000014.8:g.69913605_69913606del	NC_000014.8:g.69913606del	NC_000014.8:g.69913606dup	NC_000014.8:g.69913605_69913606dup	NC_000014.8:g.69913604_69913606dup	NC_000014.8:g.69913603_69913606dup	NC_000014.8:g.69913602_69913606dup	NC_000014.8:g.69913601_69913606dup	NC_000014.8:g.69913600_69913606dup	NC_000014.8:g.69913599_69913606dup	NC_000014.8:g.69913606_69913607insAAAAAAAAAAAAAAAAAAA	NC_000014.8:g.69913606_69913607insAAAAAAAAAAAAAAAAAAAAAA	NC_000014.8:g.69913606_69913607insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC39A9 transcript variant 2	NM_001252148.1:c.403+4608=	NM_001252148.1:c.403+4611_403+4623del	NM_001252148.1:c.403+4617_403+4623del	NM_001252148.1:c.403+4618_403+4623del	NM_001252148.1:c.403+4620_403+4623del	NM_001252148.1:c.403+4621_403+4623del	NM_001252148.1:c.403+4622_403+4623del	NM_001252148.1:c.403+4623del	NM_001252148.1:c.403+4623dup	NM_001252148.1:c.403+4622_403+4623dup	NM_001252148.1:c.403+4621_403+4623dup	NM_001252148.1:c.403+4620_403+4623dup	NM_001252148.1:c.403+4619_403+4623dup	NM_001252148.1:c.403+4618_403+4623dup	NM_001252148.1:c.403+4617_403+4623dup	NM_001252148.1:c.403+4616_403+4623dup	NM_001252148.1:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAA	NM_001252148.1:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAAAAA	NM_001252148.1:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC39A9 transcript variant 2	NM_001252148.2:c.403+4608=	NM_001252148.2:c.403+4611_403+4623del	NM_001252148.2:c.403+4617_403+4623del	NM_001252148.2:c.403+4618_403+4623del	NM_001252148.2:c.403+4620_403+4623del	NM_001252148.2:c.403+4621_403+4623del	NM_001252148.2:c.403+4622_403+4623del	NM_001252148.2:c.403+4623del	NM_001252148.2:c.403+4623dup	NM_001252148.2:c.403+4622_403+4623dup	NM_001252148.2:c.403+4621_403+4623dup	NM_001252148.2:c.403+4620_403+4623dup	NM_001252148.2:c.403+4619_403+4623dup	NM_001252148.2:c.403+4618_403+4623dup	NM_001252148.2:c.403+4617_403+4623dup	NM_001252148.2:c.403+4616_403+4623dup	NM_001252148.2:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAA	NM_001252148.2:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAAAAA	NM_001252148.2:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC39A9 transcript variant 3	NM_001252150.1:c.403+4608=	NM_001252150.1:c.403+4611_403+4623del	NM_001252150.1:c.403+4617_403+4623del	NM_001252150.1:c.403+4618_403+4623del	NM_001252150.1:c.403+4620_403+4623del	NM_001252150.1:c.403+4621_403+4623del	NM_001252150.1:c.403+4622_403+4623del	NM_001252150.1:c.403+4623del	NM_001252150.1:c.403+4623dup	NM_001252150.1:c.403+4622_403+4623dup	NM_001252150.1:c.403+4621_403+4623dup	NM_001252150.1:c.403+4620_403+4623dup	NM_001252150.1:c.403+4619_403+4623dup	NM_001252150.1:c.403+4618_403+4623dup	NM_001252150.1:c.403+4617_403+4623dup	NM_001252150.1:c.403+4616_403+4623dup	NM_001252150.1:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAA	NM_001252150.1:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAAAAA	NM_001252150.1:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC39A9 transcript variant 3	NM_001252150.2:c.403+4608=	NM_001252150.2:c.403+4611_403+4623del	NM_001252150.2:c.403+4617_403+4623del	NM_001252150.2:c.403+4618_403+4623del	NM_001252150.2:c.403+4620_403+4623del	NM_001252150.2:c.403+4621_403+4623del	NM_001252150.2:c.403+4622_403+4623del	NM_001252150.2:c.403+4623del	NM_001252150.2:c.403+4623dup	NM_001252150.2:c.403+4622_403+4623dup	NM_001252150.2:c.403+4621_403+4623dup	NM_001252150.2:c.403+4620_403+4623dup	NM_001252150.2:c.403+4619_403+4623dup	NM_001252150.2:c.403+4618_403+4623dup	NM_001252150.2:c.403+4617_403+4623dup	NM_001252150.2:c.403+4616_403+4623dup	NM_001252150.2:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAA	NM_001252150.2:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAAAAA	NM_001252150.2:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC39A9 transcript variant 4	NM_001252151.1:c.49+4608=	NM_001252151.1:c.49+4611_49+4623del	NM_001252151.1:c.49+4617_49+4623del	NM_001252151.1:c.49+4618_49+4623del	NM_001252151.1:c.49+4620_49+4623del	NM_001252151.1:c.49+4621_49+4623del	NM_001252151.1:c.49+4622_49+4623del	NM_001252151.1:c.49+4623del	NM_001252151.1:c.49+4623dup	NM_001252151.1:c.49+4622_49+4623dup	NM_001252151.1:c.49+4621_49+4623dup	NM_001252151.1:c.49+4620_49+4623dup	NM_001252151.1:c.49+4619_49+4623dup	NM_001252151.1:c.49+4618_49+4623dup	NM_001252151.1:c.49+4617_49+4623dup	NM_001252151.1:c.49+4616_49+4623dup	NM_001252151.1:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAA	NM_001252151.1:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAAAAA	NM_001252151.1:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC39A9 transcript variant 4	NM_001252151.2:c.49+4608=	NM_001252151.2:c.49+4611_49+4623del	NM_001252151.2:c.49+4617_49+4623del	NM_001252151.2:c.49+4618_49+4623del	NM_001252151.2:c.49+4620_49+4623del	NM_001252151.2:c.49+4621_49+4623del	NM_001252151.2:c.49+4622_49+4623del	NM_001252151.2:c.49+4623del	NM_001252151.2:c.49+4623dup	NM_001252151.2:c.49+4622_49+4623dup	NM_001252151.2:c.49+4621_49+4623dup	NM_001252151.2:c.49+4620_49+4623dup	NM_001252151.2:c.49+4619_49+4623dup	NM_001252151.2:c.49+4618_49+4623dup	NM_001252151.2:c.49+4617_49+4623dup	NM_001252151.2:c.49+4616_49+4623dup	NM_001252151.2:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAA	NM_001252151.2:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAAAAA	NM_001252151.2:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC39A9 transcript variant 5	NM_001252152.1:c.49+4608=	NM_001252152.1:c.49+4611_49+4623del	NM_001252152.1:c.49+4617_49+4623del	NM_001252152.1:c.49+4618_49+4623del	NM_001252152.1:c.49+4620_49+4623del	NM_001252152.1:c.49+4621_49+4623del	NM_001252152.1:c.49+4622_49+4623del	NM_001252152.1:c.49+4623del	NM_001252152.1:c.49+4623dup	NM_001252152.1:c.49+4622_49+4623dup	NM_001252152.1:c.49+4621_49+4623dup	NM_001252152.1:c.49+4620_49+4623dup	NM_001252152.1:c.49+4619_49+4623dup	NM_001252152.1:c.49+4618_49+4623dup	NM_001252152.1:c.49+4617_49+4623dup	NM_001252152.1:c.49+4616_49+4623dup	NM_001252152.1:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAA	NM_001252152.1:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAAAAA	NM_001252152.1:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC39A9 transcript variant 5	NM_001252152.2:c.49+4608=	NM_001252152.2:c.49+4611_49+4623del	NM_001252152.2:c.49+4617_49+4623del	NM_001252152.2:c.49+4618_49+4623del	NM_001252152.2:c.49+4620_49+4623del	NM_001252152.2:c.49+4621_49+4623del	NM_001252152.2:c.49+4622_49+4623del	NM_001252152.2:c.49+4623del	NM_001252152.2:c.49+4623dup	NM_001252152.2:c.49+4622_49+4623dup	NM_001252152.2:c.49+4621_49+4623dup	NM_001252152.2:c.49+4620_49+4623dup	NM_001252152.2:c.49+4619_49+4623dup	NM_001252152.2:c.49+4618_49+4623dup	NM_001252152.2:c.49+4617_49+4623dup	NM_001252152.2:c.49+4616_49+4623dup	NM_001252152.2:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAA	NM_001252152.2:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAAAAA	NM_001252152.2:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC39A9 transcript variant 6	NM_001330185.2:c.206-6367=	NM_001330185.2:c.206-6364_206-6352del	NM_001330185.2:c.206-6358_206-6352del	NM_001330185.2:c.206-6357_206-6352del	NM_001330185.2:c.206-6355_206-6352del	NM_001330185.2:c.206-6354_206-6352del	NM_001330185.2:c.206-6353_206-6352del	NM_001330185.2:c.206-6352del	NM_001330185.2:c.206-6352dup	NM_001330185.2:c.206-6353_206-6352dup	NM_001330185.2:c.206-6354_206-6352dup	NM_001330185.2:c.206-6355_206-6352dup	NM_001330185.2:c.206-6356_206-6352dup	NM_001330185.2:c.206-6357_206-6352dup	NM_001330185.2:c.206-6358_206-6352dup	NM_001330185.2:c.206-6359_206-6352dup	NM_001330185.2:c.206-6352_206-6351insAAAAAAAAAAAAAAAAAAA	NM_001330185.2:c.206-6352_206-6351insAAAAAAAAAAAAAAAAAAAAAA	NM_001330185.2:c.206-6352_206-6351insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC39A9 transcript variant 1	NM_018375.4:c.403+4608=	NM_018375.4:c.403+4611_403+4623del	NM_018375.4:c.403+4617_403+4623del	NM_018375.4:c.403+4618_403+4623del	NM_018375.4:c.403+4620_403+4623del	NM_018375.4:c.403+4621_403+4623del	NM_018375.4:c.403+4622_403+4623del	NM_018375.4:c.403+4623del	NM_018375.4:c.403+4623dup	NM_018375.4:c.403+4622_403+4623dup	NM_018375.4:c.403+4621_403+4623dup	NM_018375.4:c.403+4620_403+4623dup	NM_018375.4:c.403+4619_403+4623dup	NM_018375.4:c.403+4618_403+4623dup	NM_018375.4:c.403+4617_403+4623dup	NM_018375.4:c.403+4616_403+4623dup	NM_018375.4:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAA	NM_018375.4:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAAAAA	NM_018375.4:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC39A9 transcript variant 1	NM_018375.5:c.403+4608=	NM_018375.5:c.403+4611_403+4623del	NM_018375.5:c.403+4617_403+4623del	NM_018375.5:c.403+4618_403+4623del	NM_018375.5:c.403+4620_403+4623del	NM_018375.5:c.403+4621_403+4623del	NM_018375.5:c.403+4622_403+4623del	NM_018375.5:c.403+4623del	NM_018375.5:c.403+4623dup	NM_018375.5:c.403+4622_403+4623dup	NM_018375.5:c.403+4621_403+4623dup	NM_018375.5:c.403+4620_403+4623dup	NM_018375.5:c.403+4619_403+4623dup	NM_018375.5:c.403+4618_403+4623dup	NM_018375.5:c.403+4617_403+4623dup	NM_018375.5:c.403+4616_403+4623dup	NM_018375.5:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAA	NM_018375.5:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAAAAA	NM_018375.5:c.403+4623_403+4624insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC39A9 transcript variant X1	XM_005267834.1:c.206-6367=	XM_005267834.1:c.206-6364_206-6352del	XM_005267834.1:c.206-6358_206-6352del	XM_005267834.1:c.206-6357_206-6352del	XM_005267834.1:c.206-6355_206-6352del	XM_005267834.1:c.206-6354_206-6352del	XM_005267834.1:c.206-6353_206-6352del	XM_005267834.1:c.206-6352del	XM_005267834.1:c.206-6352dup	XM_005267834.1:c.206-6353_206-6352dup	XM_005267834.1:c.206-6354_206-6352dup	XM_005267834.1:c.206-6355_206-6352dup	XM_005267834.1:c.206-6356_206-6352dup	XM_005267834.1:c.206-6357_206-6352dup	XM_005267834.1:c.206-6358_206-6352dup	XM_005267834.1:c.206-6359_206-6352dup	XM_005267834.1:c.206-6352_206-6351insAAAAAAAAAAAAAAAAAAA	XM_005267834.1:c.206-6352_206-6351insAAAAAAAAAAAAAAAAAAAAAA	XM_005267834.1:c.206-6352_206-6351insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC39A9 transcript variant X1	XM_024449648.2:c.49+4608=	XM_024449648.2:c.49+4611_49+4623del	XM_024449648.2:c.49+4617_49+4623del	XM_024449648.2:c.49+4618_49+4623del	XM_024449648.2:c.49+4620_49+4623del	XM_024449648.2:c.49+4621_49+4623del	XM_024449648.2:c.49+4622_49+4623del	XM_024449648.2:c.49+4623del	XM_024449648.2:c.49+4623dup	XM_024449648.2:c.49+4622_49+4623dup	XM_024449648.2:c.49+4621_49+4623dup	XM_024449648.2:c.49+4620_49+4623dup	XM_024449648.2:c.49+4619_49+4623dup	XM_024449648.2:c.49+4618_49+4623dup	XM_024449648.2:c.49+4617_49+4623dup	XM_024449648.2:c.49+4616_49+4623dup	XM_024449648.2:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAA	XM_024449648.2:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAAAAA	XM_024449648.2:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC39A9 transcript variant X2	XM_047431550.1:c.49+4608=	XM_047431550.1:c.49+4611_49+4623del	XM_047431550.1:c.49+4617_49+4623del	XM_047431550.1:c.49+4618_49+4623del	XM_047431550.1:c.49+4620_49+4623del	XM_047431550.1:c.49+4621_49+4623del	XM_047431550.1:c.49+4622_49+4623del	XM_047431550.1:c.49+4623del	XM_047431550.1:c.49+4623dup	XM_047431550.1:c.49+4622_49+4623dup	XM_047431550.1:c.49+4621_49+4623dup	XM_047431550.1:c.49+4620_49+4623dup	XM_047431550.1:c.49+4619_49+4623dup	XM_047431550.1:c.49+4618_49+4623dup	XM_047431550.1:c.49+4617_49+4623dup	XM_047431550.1:c.49+4616_49+4623dup	XM_047431550.1:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAA	XM_047431550.1:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAAAAA	XM_047431550.1:c.49+4623_49+4624insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

57 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40442520	Mar 15, 2006 (126)
2	ABI	ss40476376	Oct 12, 2018 (152)
3	HGSV	ss82245917	Sep 08, 2015 (146)
4	HGSV	ss82327597	Sep 08, 2015 (146)
5	GMI	ss289228352	May 04, 2012 (137)
6	SSMP	ss664239969	Apr 01, 2015 (144)
7	HAMMER_LAB	ss1807974336	Sep 08, 2015 (146)
8	SWEGEN	ss3012401567	Nov 08, 2017 (151)
9	URBANLAB	ss3650231284	Oct 12, 2018 (152)
10	EVA_DECODE	ss3696921621	Jul 13, 2019 (153)
11	EVA_DECODE	ss3696921622	Jul 13, 2019 (153)
12	EVA_DECODE	ss3696921623	Jul 13, 2019 (153)
13	EVA_DECODE	ss3696921624	Jul 13, 2019 (153)
14	EVA_DECODE	ss3696921625	Jul 13, 2019 (153)
15	EVA_DECODE	ss3696921626	Jul 13, 2019 (153)
16	PACBIO	ss3787699489	Jul 13, 2019 (153)
17	PACBIO	ss3792732298	Jul 13, 2019 (153)
18	PACBIO	ss3797616605	Jul 13, 2019 (153)
19	EVA	ss3833981829	Apr 27, 2020 (154)
20	KOGIC	ss3975172617	Apr 27, 2020 (154)
21	KOGIC	ss3975172618	Apr 27, 2020 (154)
22	KOGIC	ss3975172619	Apr 27, 2020 (154)
23	KOGIC	ss3975172620	Apr 27, 2020 (154)
24	GNOMAD	ss4280180492	Apr 26, 2021 (155)
25	GNOMAD	ss4280180493	Apr 26, 2021 (155)
26	GNOMAD	ss4280180494	Apr 26, 2021 (155)
27	GNOMAD	ss4280180495	Apr 26, 2021 (155)
28	GNOMAD	ss4280180496	Apr 26, 2021 (155)
29	GNOMAD	ss4280180497	Apr 26, 2021 (155)
30	GNOMAD	ss4280180498	Apr 26, 2021 (155)
31	GNOMAD	ss4280180499	Apr 26, 2021 (155)
32	GNOMAD	ss4280180500	Apr 26, 2021 (155)
33	GNOMAD	ss4280180501	Apr 26, 2021 (155)
34	GNOMAD	ss4280180502	Apr 26, 2021 (155)
35	GNOMAD	ss4280180503	Apr 26, 2021 (155)
36	GNOMAD	ss4280180504	Apr 26, 2021 (155)
37	TOPMED	ss4974930876	Apr 26, 2021 (155)
38	TOPMED	ss4974930877	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5213787737	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5213787738	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5213787739	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5213787740	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5213787741	Apr 26, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5296653860	Oct 16, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5296653861	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5296653863	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5296653864	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5296653865	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5490654871	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5490654872	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5490654873	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5490654874	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5766751152	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5766751153	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5766751154	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5766751155	Oct 16, 2022 (156)
57	EVA	ss5851086374	Oct 16, 2022 (156)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454749444 (NC_000014.9:69446873::A 22683/81910) Row 454749445 (NC_000014.9:69446873::AA 152/82194) Row 454749446 (NC_000014.9:69446873::AAA 5/82270)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454749444 (NC_000014.9:69446873::A 22683/81910) Row 454749445 (NC_000014.9:69446873::AA 152/82194) Row 454749446 (NC_000014.9:69446873::AAA 5/82270)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454749444 (NC_000014.9:69446873::A 22683/81910) Row 454749445 (NC_000014.9:69446873::AA 152/82194) Row 454749446 (NC_000014.9:69446873::AAA 5/82270)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454749444 (NC_000014.9:69446873::A 22683/81910) Row 454749445 (NC_000014.9:69446873::AA 152/82194) Row 454749446 (NC_000014.9:69446873::AAA 5/82270)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454749444 (NC_000014.9:69446873::A 22683/81910) Row 454749445 (NC_000014.9:69446873::AA 152/82194) Row 454749446 (NC_000014.9:69446873::AAA 5/82270)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454749444 (NC_000014.9:69446873::A 22683/81910) Row 454749445 (NC_000014.9:69446873::AA 152/82194) Row 454749446 (NC_000014.9:69446873::AAA 5/82270)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454749444 (NC_000014.9:69446873::A 22683/81910) Row 454749445 (NC_000014.9:69446873::AA 152/82194) Row 454749446 (NC_000014.9:69446873::AAA 5/82270)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454749444 (NC_000014.9:69446873::A 22683/81910) Row 454749445 (NC_000014.9:69446873::AA 152/82194) Row 454749446 (NC_000014.9:69446873::AAA 5/82270)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454749444 (NC_000014.9:69446873::A 22683/81910) Row 454749445 (NC_000014.9:69446873::AA 152/82194) Row 454749446 (NC_000014.9:69446873::AAA 5/82270)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454749444 (NC_000014.9:69446873::A 22683/81910) Row 454749445 (NC_000014.9:69446873::AA 152/82194) Row 454749446 (NC_000014.9:69446873::AAA 5/82270)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454749444 (NC_000014.9:69446873::A 22683/81910) Row 454749445 (NC_000014.9:69446873::AA 152/82194) Row 454749446 (NC_000014.9:69446873::AAA 5/82270)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454749444 (NC_000014.9:69446873::A 22683/81910) Row 454749445 (NC_000014.9:69446873::AA 152/82194) Row 454749446 (NC_000014.9:69446873::AAA 5/82270)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454749444 (NC_000014.9:69446873::A 22683/81910) Row 454749445 (NC_000014.9:69446873::AA 152/82194) Row 454749446 (NC_000014.9:69446873::AAA 5/82270)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454749444 (NC_000014.9:69446873::A 22683/81910) Row 454749445 (NC_000014.9:69446873::AA 152/82194) Row 454749446 (NC_000014.9:69446873::AAA 5/82270)...	-	Apr 26, 2021 (155)
72	Korean Genome Project Submission ignored due to conflicting rows: Row 31550618 (NC_000014.9:69446873:AA: 64/1802) Row 31550619 (NC_000014.9:69446875::A 273/1802) Row 31550620 (NC_000014.9:69446874:A: 378/1802)...	-	Apr 27, 2020 (154)
73	Korean Genome Project Submission ignored due to conflicting rows: Row 31550618 (NC_000014.9:69446873:AA: 64/1802) Row 31550619 (NC_000014.9:69446875::A 273/1802) Row 31550620 (NC_000014.9:69446874:A: 378/1802)...	-	Apr 27, 2020 (154)
74	Korean Genome Project Submission ignored due to conflicting rows: Row 31550618 (NC_000014.9:69446873:AA: 64/1802) Row 31550619 (NC_000014.9:69446875::A 273/1802) Row 31550620 (NC_000014.9:69446874:A: 378/1802)...	-	Apr 27, 2020 (154)
75	Korean Genome Project Submission ignored due to conflicting rows: Row 31550618 (NC_000014.9:69446873:AA: 64/1802) Row 31550619 (NC_000014.9:69446875::A 273/1802) Row 31550620 (NC_000014.9:69446874:A: 378/1802)...	-	Apr 27, 2020 (154)
76	8.3KJPN Submission ignored due to conflicting rows: Row 71757044 (NC_000014.8:69913590:A: 2868/16574) Row 71757045 (NC_000014.8:69913590::A 2195/16574) Row 71757046 (NC_000014.8:69913590:AA: 737/16574)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 71757044 (NC_000014.8:69913590:A: 2868/16574) Row 71757045 (NC_000014.8:69913590::A 2195/16574) Row 71757046 (NC_000014.8:69913590:AA: 737/16574)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 71757044 (NC_000014.8:69913590:A: 2868/16574) Row 71757045 (NC_000014.8:69913590::A 2195/16574) Row 71757046 (NC_000014.8:69913590:AA: 737/16574)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 71757044 (NC_000014.8:69913590:A: 2868/16574) Row 71757045 (NC_000014.8:69913590::A 2195/16574) Row 71757046 (NC_000014.8:69913590:AA: 737/16574)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 71757044 (NC_000014.8:69913590:A: 2868/16574) Row 71757045 (NC_000014.8:69913590::A 2195/16574) Row 71757046 (NC_000014.8:69913590:AA: 737/16574)...	-	Apr 26, 2021 (155)
81	14KJPN Submission ignored due to conflicting rows: Row 100588256 (NC_000014.9:69446873::A 3296/27652) Row 100588257 (NC_000014.9:69446873:A: 4549/27652) Row 100588258 (NC_000014.9:69446873:AA: 1262/27652)...	-	Oct 16, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 100588256 (NC_000014.9:69446873::A 3296/27652) Row 100588257 (NC_000014.9:69446873:A: 4549/27652) Row 100588258 (NC_000014.9:69446873:AA: 1262/27652)...	-	Oct 16, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 100588256 (NC_000014.9:69446873::A 3296/27652) Row 100588257 (NC_000014.9:69446873:A: 4549/27652) Row 100588258 (NC_000014.9:69446873:AA: 1262/27652)...	-	Oct 16, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 100588256 (NC_000014.9:69446873::A 3296/27652) Row 100588257 (NC_000014.9:69446873:A: 4549/27652) Row 100588258 (NC_000014.9:69446873:AA: 1262/27652)...	-	Oct 16, 2022 (156)
85	TopMed Submission ignored due to conflicting rows: Row 190476535 (NC_000014.9:69446873:AAAAAAA: 1/264690) Row 190476536 (NC_000014.9:69446873:AAAAAAAAAAAAA: 2/264690)	-	Apr 26, 2021 (155)
86	TopMed Submission ignored due to conflicting rows: Row 190476535 (NC_000014.9:69446873:AAAAAAA: 1/264690) Row 190476536 (NC_000014.9:69446873:AAAAAAAAAAAAA: 2/264690)	-	Apr 26, 2021 (155)
87	ALFA	NC_000014.9 - 69446874	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)
rs61682827	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4280180504, ss4974930877	NC_000014.9:69446873:AAAAAAAAAAAAA:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAA	(self)
6621388484	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAA	(self)
ss4974930876	NC_000014.9:69446873:AAAAAAA:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
6621388484	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
6621388484	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4280180503	NC_000014.9:69446873:AAAA:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss5213787741	NC_000014.8:69913590:AAA:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3696921626, ss4280180502	NC_000014.9:69446873:AAA:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5213787739	NC_000014.8:69913590:AA:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3975172617, ss4280180501, ss5296653863, ss5490654874, ss5766751154	NC_000014.9:69446873:AA:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
6621388484	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3696921625	NC_000014.9:69446874:AA:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss289228352	NC_000014.7:68983343:A:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss82245917, ss82327597	NC_000014.7:68983358:A:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss664239969, ss1807974336, ss3012401567, ss5213787737	NC_000014.8:69913590:A:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3650231284, ss5296653860, ss5490654872, ss5766751153, ss5851086374	NC_000014.9:69446873:A:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
6621388484	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3975172619	NC_000014.9:69446874:A:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3696921624	NC_000014.9:69446875:A:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss40442520	NT_026437.12:50913590:A:	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3787699489, ss3792732298, ss3797616605, ss3833981829, ss5213787738	NC_000014.8:69913590::A	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4280180492, ss5296653861, ss5490654871, ss5766751152	NC_000014.9:69446873::A	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
6621388484	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3975172618	NC_000014.9:69446875::A	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3696921623	NC_000014.9:69446876::A	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss40476376	NT_026437.12:50913591::A	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5213787740	NC_000014.8:69913590::AA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4280180493, ss5296653864, ss5490654873, ss5766751155	NC_000014.9:69446873::AA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
6621388484	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3975172620	NC_000014.9:69446875::AA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3696921622	NC_000014.9:69446876::AA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4280180494, ss5296653865	NC_000014.9:69446873::AAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
6621388484	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
6621388484	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4280180495	NC_000014.9:69446873::AAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4280180496	NC_000014.9:69446873::AAAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3696921621	NC_000014.9:69446876::AAAAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4280180497	NC_000014.9:69446873::AAAAAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4280180498	NC_000014.9:69446873::AAAAAAAAAAAA… NC_000014.9:69446873::AAAAAAAAAAAAAAAAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4280180499	NC_000014.9:69446873::AAAAAAAAAAAA… NC_000014.9:69446873::AAAAAAAAAAAAAAAAAAAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4280180500	NC_000014.9:69446873::AAAAAAAAAAAA… NC_000014.9:69446873::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000014.9:69446873:AAAAAAAAAAAAA… NC_000014.9:69446873:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs35612117

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

rs35612117