Name: rs36047355
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.

rs36047355

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:22365401-22365422 (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)₁₂ / del(A)₁₀ / del(A)₉ / de…
del(A)₁₂ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₈
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₂=0.0000 (0/5178, ALFA)
del(A)₁₀=0.0000 (0/5178, ALFA)
del(A)₉=0.0000 (0/5178, ALFA) (+ 13 more)
del(A)₈=0.0000 (0/5178, ALFA)
del(A)₇=0.0000 (0/5178, ALFA)
del(A)₅=0.0000 (0/5178, ALFA)
del(A)₄=0.0000 (0/5178, ALFA)
delAAA=0.0000 (0/5178, ALFA)
delAA=0.0000 (0/5178, ALFA)
delA=0.0000 (0/5178, ALFA)
dupA=0.0000 (0/5178, ALFA)
dupAA=0.0000 (0/5178, ALFA)
dup(A)₄=0.0000 (0/5178, ALFA)
dup(A)₅=0.0000 (0/5178, ALFA)
dup(A)₆=0.0000 (0/5178, ALFA)
delA=0.33 (13/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC39A14 : 2KB Upstream 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	5178	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	2920	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1764	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	76	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	1688	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	28	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	26	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	2	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	52	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	178	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	30	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	206	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=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	5178	(A)₂₂=1.0000	del(A)₁₂=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	European	Sub	2920	(A)₂₂=1.0000	del(A)₁₂=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	African	Sub	1764	(A)₂₂=1.0000	del(A)₁₂=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	Other	Sub	206	(A)₂₂=1.000	del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	178	(A)₂₂=1.000	del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	52	(A)₂₂=1.00	del(A)₁₂=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	30	(A)₂₂=1.00	del(A)₁₂=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	Asian	Sub	28	(A)₂₂=1.00	del(A)₁₂=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00
The Danish reference pan genome	Danish	Study-wide	40	(A)₂₂=0.68	delA=0.33

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.22365411_22365422del
GRCh38.p14 chr 8	NC_000008.11:g.22365413_22365422del
GRCh38.p14 chr 8	NC_000008.11:g.22365414_22365422del
GRCh38.p14 chr 8	NC_000008.11:g.22365415_22365422del
GRCh38.p14 chr 8	NC_000008.11:g.22365416_22365422del
GRCh38.p14 chr 8	NC_000008.11:g.22365418_22365422del
GRCh38.p14 chr 8	NC_000008.11:g.22365419_22365422del
GRCh38.p14 chr 8	NC_000008.11:g.22365420_22365422del
GRCh38.p14 chr 8	NC_000008.11:g.22365421_22365422del
GRCh38.p14 chr 8	NC_000008.11:g.22365422del
GRCh38.p14 chr 8	NC_000008.11:g.22365422dup
GRCh38.p14 chr 8	NC_000008.11:g.22365421_22365422dup
GRCh38.p14 chr 8	NC_000008.11:g.22365420_22365422dup
GRCh38.p14 chr 8	NC_000008.11:g.22365419_22365422dup
GRCh38.p14 chr 8	NC_000008.11:g.22365418_22365422dup
GRCh38.p14 chr 8	NC_000008.11:g.22365417_22365422dup
GRCh38.p14 chr 8	NC_000008.11:g.22365415_22365422dup
GRCh37.p13 chr 8	NC_000008.10:g.22222924_22222935del
GRCh37.p13 chr 8	NC_000008.10:g.22222926_22222935del
GRCh37.p13 chr 8	NC_000008.10:g.22222927_22222935del
GRCh37.p13 chr 8	NC_000008.10:g.22222928_22222935del
GRCh37.p13 chr 8	NC_000008.10:g.22222929_22222935del
GRCh37.p13 chr 8	NC_000008.10:g.22222931_22222935del
GRCh37.p13 chr 8	NC_000008.10:g.22222932_22222935del
GRCh37.p13 chr 8	NC_000008.10:g.22222933_22222935del
GRCh37.p13 chr 8	NC_000008.10:g.22222934_22222935del
GRCh37.p13 chr 8	NC_000008.10:g.22222935del
GRCh37.p13 chr 8	NC_000008.10:g.22222935dup
GRCh37.p13 chr 8	NC_000008.10:g.22222934_22222935dup
GRCh37.p13 chr 8	NC_000008.10:g.22222933_22222935dup
GRCh37.p13 chr 8	NC_000008.10:g.22222932_22222935dup
GRCh37.p13 chr 8	NC_000008.10:g.22222931_22222935dup
GRCh37.p13 chr 8	NC_000008.10:g.22222930_22222935dup
GRCh37.p13 chr 8	NC_000008.10:g.22222928_22222935dup
SLC39A14 RefSeqGene	NG_054890.1:g.3163_3174del
SLC39A14 RefSeqGene	NG_054890.1:g.3165_3174del
SLC39A14 RefSeqGene	NG_054890.1:g.3166_3174del
SLC39A14 RefSeqGene	NG_054890.1:g.3167_3174del
SLC39A14 RefSeqGene	NG_054890.1:g.3168_3174del
SLC39A14 RefSeqGene	NG_054890.1:g.3170_3174del
SLC39A14 RefSeqGene	NG_054890.1:g.3171_3174del
SLC39A14 RefSeqGene	NG_054890.1:g.3172_3174del
SLC39A14 RefSeqGene	NG_054890.1:g.3173_3174del
SLC39A14 RefSeqGene	NG_054890.1:g.3174del
SLC39A14 RefSeqGene	NG_054890.1:g.3174dup
SLC39A14 RefSeqGene	NG_054890.1:g.3173_3174dup
SLC39A14 RefSeqGene	NG_054890.1:g.3172_3174dup
SLC39A14 RefSeqGene	NG_054890.1:g.3171_3174dup
SLC39A14 RefSeqGene	NG_054890.1:g.3170_3174dup
SLC39A14 RefSeqGene	NG_054890.1:g.3169_3174dup
SLC39A14 RefSeqGene	NG_054890.1:g.3167_3174dup

Gene: SLC39A14, solute carrier family 39 member 14 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
SLC39A14 transcript variant 1	NM_001128431.4:c.	N/A	Upstream Transcript Variant
SLC39A14 transcript variant 4	NM_001135154.3:c.	N/A	Upstream Transcript Variant
SLC39A14 transcript variant 5	NM_001351655.2:c.	N/A	Upstream Transcript Variant
SLC39A14 transcript variant 8	NM_001351656.2:c.	N/A	Upstream Transcript Variant
SLC39A14 transcript variant 6	NM_001351657.2:c.	N/A	Upstream Transcript Variant
SLC39A14 transcript variant 7	NM_001351658.2:c.	N/A	Upstream Transcript Variant
SLC39A14 transcript variant 2	NM_015359.6:c.	N/A	Upstream Transcript Variant
SLC39A14 transcript variant 3	NM_001135153.3:c.	N/A	N/A
SLC39A14 transcript variant 9	NM_001351659.2:c.	N/A	N/A
SLC39A14 transcript variant 10	NM_001351660.2:c.	N/A	N/A
SLC39A14 transcript variant X2	XM_006716324.4:c.	N/A	Upstream Transcript Variant
SLC39A14 transcript variant X1	XM_047421653.1:c.	N/A	Upstream Transcript Variant
SLC39A14 transcript variant X3	XM_047421654.1:c.	N/A	Upstream Transcript Variant
SLC39A14 transcript variant X4	XM_047421655.1:c.	N/A	N/A

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)₂₂=	del(A)₁₂	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₈
GRCh38.p14 chr 8	NC_000008.11:g.22365401_22365422=	NC_000008.11:g.22365411_22365422del	NC_000008.11:g.22365413_22365422del	NC_000008.11:g.22365414_22365422del	NC_000008.11:g.22365415_22365422del	NC_000008.11:g.22365416_22365422del	NC_000008.11:g.22365418_22365422del	NC_000008.11:g.22365419_22365422del	NC_000008.11:g.22365420_22365422del	NC_000008.11:g.22365421_22365422del	NC_000008.11:g.22365422del	NC_000008.11:g.22365422dup	NC_000008.11:g.22365421_22365422dup	NC_000008.11:g.22365420_22365422dup	NC_000008.11:g.22365419_22365422dup	NC_000008.11:g.22365418_22365422dup	NC_000008.11:g.22365417_22365422dup	NC_000008.11:g.22365415_22365422dup
GRCh37.p13 chr 8	NC_000008.10:g.22222914_22222935=	NC_000008.10:g.22222924_22222935del	NC_000008.10:g.22222926_22222935del	NC_000008.10:g.22222927_22222935del	NC_000008.10:g.22222928_22222935del	NC_000008.10:g.22222929_22222935del	NC_000008.10:g.22222931_22222935del	NC_000008.10:g.22222932_22222935del	NC_000008.10:g.22222933_22222935del	NC_000008.10:g.22222934_22222935del	NC_000008.10:g.22222935del	NC_000008.10:g.22222935dup	NC_000008.10:g.22222934_22222935dup	NC_000008.10:g.22222933_22222935dup	NC_000008.10:g.22222932_22222935dup	NC_000008.10:g.22222931_22222935dup	NC_000008.10:g.22222930_22222935dup	NC_000008.10:g.22222928_22222935dup
SLC39A14 RefSeqGene	NG_054890.1:g.3153_3174=	NG_054890.1:g.3163_3174del	NG_054890.1:g.3165_3174del	NG_054890.1:g.3166_3174del	NG_054890.1:g.3167_3174del	NG_054890.1:g.3168_3174del	NG_054890.1:g.3170_3174del	NG_054890.1:g.3171_3174del	NG_054890.1:g.3172_3174del	NG_054890.1:g.3173_3174del	NG_054890.1:g.3174del	NG_054890.1:g.3174dup	NG_054890.1:g.3173_3174dup	NG_054890.1:g.3172_3174dup	NG_054890.1:g.3171_3174dup	NG_054890.1:g.3170_3174dup	NG_054890.1:g.3169_3174dup	NG_054890.1:g.3167_3174dup

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#.

37 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss43226689	Dec 04, 2013 (138)
2	HUMANGENOME_JCVI	ss98024003	Feb 06, 2009 (137)
3	EVA_GENOME_DK	ss1577170584	Apr 01, 2015 (144)
4	EVA	ss3831065037	Apr 26, 2020 (154)
5	GNOMAD	ss4180678398	Apr 26, 2021 (155)
6	GNOMAD	ss4180678399	Apr 26, 2021 (155)
7	GNOMAD	ss4180678400	Apr 26, 2021 (155)
8	GNOMAD	ss4180678401	Apr 26, 2021 (155)
9	GNOMAD	ss4180678402	Apr 26, 2021 (155)
10	GNOMAD	ss4180678403	Apr 26, 2021 (155)
11	GNOMAD	ss4180678404	Apr 26, 2021 (155)
12	GNOMAD	ss4180678405	Apr 26, 2021 (155)
13	GNOMAD	ss4180678406	Apr 26, 2021 (155)
14	GNOMAD	ss4180678407	Apr 26, 2021 (155)
15	GNOMAD	ss4180678408	Apr 26, 2021 (155)
16	GNOMAD	ss4180678409	Apr 26, 2021 (155)
17	GNOMAD	ss4180678410	Apr 26, 2021 (155)
18	GNOMAD	ss4180678411	Apr 26, 2021 (155)
19	TOPMED	ss4778795065	Apr 26, 2021 (155)
20	TOPMED	ss4778795066	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5187743081	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5187743082	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5187743083	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5187743084	Apr 26, 2021 (155)
25	1000G_HIGH_COVERAGE	ss5276401712	Oct 16, 2022 (156)
26	1000G_HIGH_COVERAGE	ss5276401713	Oct 16, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5276401714	Oct 16, 2022 (156)
28	HUGCELL_USP	ss5473046081	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5473046082	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5473046083	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5473046084	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5729386994	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5729386995	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5729386996	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5729386997	Oct 16, 2022 (156)
36	EVA	ss5830251832	Oct 16, 2022 (156)
37	EVA	ss5888106922	Oct 16, 2022 (156)
38	The Danish reference pan genome	NC_000008.10 - 22222914	Apr 26, 2020 (154)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289782548 (NC_000008.11:22365400::A 1724/62784) Row 289782549 (NC_000008.11:22365400::AA 68/62906) Row 289782550 (NC_000008.11:22365400::AAA 5/63020)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289782548 (NC_000008.11:22365400::A 1724/62784) Row 289782549 (NC_000008.11:22365400::AA 68/62906) Row 289782550 (NC_000008.11:22365400::AAA 5/63020)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289782548 (NC_000008.11:22365400::A 1724/62784) Row 289782549 (NC_000008.11:22365400::AA 68/62906) Row 289782550 (NC_000008.11:22365400::AAA 5/63020)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289782548 (NC_000008.11:22365400::A 1724/62784) Row 289782549 (NC_000008.11:22365400::AA 68/62906) Row 289782550 (NC_000008.11:22365400::AAA 5/63020)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289782548 (NC_000008.11:22365400::A 1724/62784) Row 289782549 (NC_000008.11:22365400::AA 68/62906) Row 289782550 (NC_000008.11:22365400::AAA 5/63020)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289782548 (NC_000008.11:22365400::A 1724/62784) Row 289782549 (NC_000008.11:22365400::AA 68/62906) Row 289782550 (NC_000008.11:22365400::AAA 5/63020)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289782548 (NC_000008.11:22365400::A 1724/62784) Row 289782549 (NC_000008.11:22365400::AA 68/62906) Row 289782550 (NC_000008.11:22365400::AAA 5/63020)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289782548 (NC_000008.11:22365400::A 1724/62784) Row 289782549 (NC_000008.11:22365400::AA 68/62906) Row 289782550 (NC_000008.11:22365400::AAA 5/63020)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289782548 (NC_000008.11:22365400::A 1724/62784) Row 289782549 (NC_000008.11:22365400::AA 68/62906) Row 289782550 (NC_000008.11:22365400::AAA 5/63020)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289782548 (NC_000008.11:22365400::A 1724/62784) Row 289782549 (NC_000008.11:22365400::AA 68/62906) Row 289782550 (NC_000008.11:22365400::AAA 5/63020)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289782548 (NC_000008.11:22365400::A 1724/62784) Row 289782549 (NC_000008.11:22365400::AA 68/62906) Row 289782550 (NC_000008.11:22365400::AAA 5/63020)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289782548 (NC_000008.11:22365400::A 1724/62784) Row 289782549 (NC_000008.11:22365400::AA 68/62906) Row 289782550 (NC_000008.11:22365400::AAA 5/63020)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289782548 (NC_000008.11:22365400::A 1724/62784) Row 289782549 (NC_000008.11:22365400::AA 68/62906) Row 289782550 (NC_000008.11:22365400::AAA 5/63020)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 289782548 (NC_000008.11:22365400::A 1724/62784) Row 289782549 (NC_000008.11:22365400::AA 68/62906) Row 289782550 (NC_000008.11:22365400::AAA 5/63020)...	-	Apr 26, 2021 (155)
53	8.3KJPN Submission ignored due to conflicting rows: Row 45712388 (NC_000008.10:22222913:A: 4671/16610) Row 45712389 (NC_000008.10:22222913:AA: 6/16610) Row 45712390 (NC_000008.10:22222913::A 44/16610)...	-	Apr 26, 2021 (155)
54	8.3KJPN Submission ignored due to conflicting rows: Row 45712388 (NC_000008.10:22222913:A: 4671/16610) Row 45712389 (NC_000008.10:22222913:AA: 6/16610) Row 45712390 (NC_000008.10:22222913::A 44/16610)...	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 45712388 (NC_000008.10:22222913:A: 4671/16610) Row 45712389 (NC_000008.10:22222913:AA: 6/16610) Row 45712390 (NC_000008.10:22222913::A 44/16610)...	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 45712388 (NC_000008.10:22222913:A: 4671/16610) Row 45712389 (NC_000008.10:22222913:AA: 6/16610) Row 45712390 (NC_000008.10:22222913::A 44/16610)...	-	Apr 26, 2021 (155)
57	14KJPN Submission ignored due to conflicting rows: Row 63224098 (NC_000008.11:22365400:A: 8661/27538) Row 63224099 (NC_000008.11:22365400:AA: 7/27538) Row 63224100 (NC_000008.11:22365400::A 58/27538)...	-	Oct 16, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 63224098 (NC_000008.11:22365400:A: 8661/27538) Row 63224099 (NC_000008.11:22365400:AA: 7/27538) Row 63224100 (NC_000008.11:22365400::A 58/27538)...	-	Oct 16, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 63224098 (NC_000008.11:22365400:A: 8661/27538) Row 63224099 (NC_000008.11:22365400:AA: 7/27538) Row 63224100 (NC_000008.11:22365400::A 58/27538)...	-	Oct 16, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 63224098 (NC_000008.11:22365400:A: 8661/27538) Row 63224099 (NC_000008.11:22365400:AA: 7/27538) Row 63224100 (NC_000008.11:22365400::A 58/27538)...	-	Oct 16, 2022 (156)
61	TopMed Submission ignored due to conflicting rows: Row 616172625 (NC_000008.11:22365400:AAAAAAAAAA: 43/264690) Row 616172626 (NC_000008.11:22365400:AAAAAAAAAAAA: 1/264690)	-	Apr 26, 2021 (155)
62	TopMed Submission ignored due to conflicting rows: Row 616172625 (NC_000008.11:22365400:AAAAAAAAAA: 43/264690) Row 616172626 (NC_000008.11:22365400:AAAAAAAAAAAA: 1/264690)	-	Apr 26, 2021 (155)
63	ALFA	NC_000008.11 - 22365401	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)
rs67890605	May 11, 2012 (137)
rs67890606	Feb 27, 2009 (130)
rs67890607	Feb 27, 2009 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4180678411, ss4778795066	NC_000008.11:22365400:AAAAAAAAAAAA:	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss5830251832	NC_000008.10:22222913:AAAAAAAAAA:	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA
ss4180678410, ss4778795065	NC_000008.11:22365400:AAAAAAAAAA:	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5729386997	NC_000008.11:22365400:AAAAAAAA:	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4180678409	NC_000008.11:22365400:AAAAAAA:	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4180678408	NC_000008.11:22365400:AAAAA:	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4180678407	NC_000008.11:22365400:AAAA:	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4180678406, ss5888106922	NC_000008.11:22365400:AAA:	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5187743082	NC_000008.10:22222913:AA:	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4180678405, ss5276401714, ss5473046084, ss5729386995	NC_000008.11:22365400:AA:	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
1207852, ss1577170584, ss5187743081	NC_000008.10:22222913:A:	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4180678404, ss5276401712, ss5473046081, ss5729386994	NC_000008.11:22365400:A:	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss98024003	NT_167187.1:10081059:A:	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss43226689	NT_167187.1:10081080:A:	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3831065037, ss5187743083	NC_000008.10:22222913::A	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180678398, ss5276401713, ss5473046082, ss5729386996	NC_000008.11:22365400::A	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180678399, ss5473046083	NC_000008.11:22365400::AA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180678400	NC_000008.11:22365400::AAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180678401	NC_000008.11:22365400::AAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180678402	NC_000008.11:22365400::AAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4180678403	NC_000008.11:22365400::AAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
4086256811	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5187743084	NC_000008.10:22222913::AAAAAAAA	NC_000008.11:22365400:AAAAAAAAAAAA… NC_000008.11:22365400:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs36047355

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

rs36047355