Name: rs10707508
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.

rs10707508

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:436064-436084 (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)₁₂ / del(T)₁₁ / del(T)₁₀ / d…
del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₆ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / insTTTC(T)₂₂ / dup(T)₄ / ins(T)₄C(T)₂₂ / dup(T)₅ / ins(T)₅C(T)₂₂ / dup(T)₆ / dup(T)₁₁ / ins(T)₁₄C(T)₂₂ / dup(T)₂₁ / ins(T)₂₃ / ins(T)₂₃C(T)₂₂ / ins(T)₂₇
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.03173 (351/11063, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ANO9 : Intron Variant
LOC105376506 : 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	Alt HMOZ	HTRZ	HWEP
Total	Global	11063	TTTTTTTTTTTTTTTTTTTTT=0.95842	TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00163, TTTTTTTTTTTTTTTTTTTT=0.03173, TTTTTTTTTTTTTTTTTTTTTT=0.00768, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00027, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00027, TTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.939819	0.002584	0.057596	9
European	Sub	9337	TTTTTTTTTTTTTTTTTTTTT=0.9507	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0019, TTTTTTTTTTTTTTTTTTTT=0.0376, TTTTTTTTTTTTTTTTTTTTTT=0.0091, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0003, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0003, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.928415	0.003074	0.068511	6
African	Sub	1020	TTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	32	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	988	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	20	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	16	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	70	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	354	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	32	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	230	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	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	11063	(T)₂₁=0.95842	del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₆=0.00000, delTTT=0.00000, delTT=0.00163, delT=0.03173, dupT=0.00768, dupTT=0.00000, ins(T)₂₃=0.00027, ins(T)₂₇=0.00027
Allele Frequency Aggregator	European	Sub	9337	(T)₂₁=0.9507	del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₆=0.0000, delTTT=0.0000, delTT=0.0019, delT=0.0376, dupT=0.0091, dupTT=0.0000, ins(T)₂₃=0.0003, ins(T)₂₇=0.0003
Allele Frequency Aggregator	African	Sub	1020	(T)₂₁=1.0000	del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₆=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, ins(T)₂₃=0.0000, ins(T)₂₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	354	(T)₂₁=1.000	del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₆=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, ins(T)₂₃=0.000, ins(T)₂₇=0.000
Allele Frequency Aggregator	Other	Sub	230	(T)₂₁=1.000	del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₆=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, ins(T)₂₃=0.000, ins(T)₂₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	70	(T)₂₁=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₆=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, ins(T)₂₃=0.00, ins(T)₂₇=0.00
Allele Frequency Aggregator	South Asian	Sub	32	(T)₂₁=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₆=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, ins(T)₂₃=0.00, ins(T)₂₇=0.00
Allele Frequency Aggregator	Asian	Sub	20	(T)₂₁=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₆=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, ins(T)₂₃=0.00, ins(T)₂₇=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 11	NC_000011.10:g.436073_436084del
GRCh38.p14 chr 11	NC_000011.10:g.436074_436084del
GRCh38.p14 chr 11	NC_000011.10:g.436075_436084del
GRCh38.p14 chr 11	NC_000011.10:g.436076_436084del
GRCh38.p14 chr 11	NC_000011.10:g.436079_436084del
GRCh38.p14 chr 11	NC_000011.10:g.436081_436084del
GRCh38.p14 chr 11	NC_000011.10:g.436082_436084del
GRCh38.p14 chr 11	NC_000011.10:g.436083_436084del
GRCh38.p14 chr 11	NC_000011.10:g.436084del
GRCh38.p14 chr 11	NC_000011.10:g.436084dup
GRCh38.p14 chr 11	NC_000011.10:g.436083_436084dup
GRCh38.p14 chr 11	NC_000011.10:g.436082_436084dup
GRCh38.p14 chr 11	NC_000011.10:g.436064_436084T[24]CTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 11	NC_000011.10:g.436081_436084dup
GRCh38.p14 chr 11	NC_000011.10:g.436064_436084T[25]CTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 11	NC_000011.10:g.436080_436084dup
GRCh38.p14 chr 11	NC_000011.10:g.436064_436084T[26]CTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 11	NC_000011.10:g.436079_436084dup
GRCh38.p14 chr 11	NC_000011.10:g.436074_436084dup
GRCh38.p14 chr 11	NC_000011.10:g.436064_436084T[35]CTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 11	NC_000011.10:g.436064_436084dup
GRCh38.p14 chr 11	NC_000011.10:g.436084_436085insTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 11	NC_000011.10:g.436064_436084T[44]CTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 11	NC_000011.10:g.436084_436085insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 11	NC_000011.9:g.436073_436084del
GRCh37.p13 chr 11	NC_000011.9:g.436074_436084del
GRCh37.p13 chr 11	NC_000011.9:g.436075_436084del
GRCh37.p13 chr 11	NC_000011.9:g.436076_436084del
GRCh37.p13 chr 11	NC_000011.9:g.436079_436084del
GRCh37.p13 chr 11	NC_000011.9:g.436081_436084del
GRCh37.p13 chr 11	NC_000011.9:g.436082_436084del
GRCh37.p13 chr 11	NC_000011.9:g.436083_436084del
GRCh37.p13 chr 11	NC_000011.9:g.436084del
GRCh37.p13 chr 11	NC_000011.9:g.436084dup
GRCh37.p13 chr 11	NC_000011.9:g.436083_436084dup
GRCh37.p13 chr 11	NC_000011.9:g.436082_436084dup
GRCh37.p13 chr 11	NC_000011.9:g.436064_436084T[24]CTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 11	NC_000011.9:g.436081_436084dup
GRCh37.p13 chr 11	NC_000011.9:g.436064_436084T[25]CTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 11	NC_000011.9:g.436080_436084dup
GRCh37.p13 chr 11	NC_000011.9:g.436064_436084T[26]CTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 11	NC_000011.9:g.436079_436084dup
GRCh37.p13 chr 11	NC_000011.9:g.436074_436084dup
GRCh37.p13 chr 11	NC_000011.9:g.436064_436084T[35]CTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 11	NC_000011.9:g.436064_436084dup
GRCh37.p13 chr 11	NC_000011.9:g.436084_436085insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 11	NC_000011.9:g.436064_436084T[44]CTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 11	NC_000011.9:g.436084_436085insTTTTTTTTTTTTTTTTTTTTTTTTTTT
ANO9 RefSeqGene	NG_052610.1:g.10937_10948del
ANO9 RefSeqGene	NG_052610.1:g.10938_10948del
ANO9 RefSeqGene	NG_052610.1:g.10939_10948del
ANO9 RefSeqGene	NG_052610.1:g.10940_10948del
ANO9 RefSeqGene	NG_052610.1:g.10943_10948del
ANO9 RefSeqGene	NG_052610.1:g.10945_10948del
ANO9 RefSeqGene	NG_052610.1:g.10946_10948del
ANO9 RefSeqGene	NG_052610.1:g.10947_10948del
ANO9 RefSeqGene	NG_052610.1:g.10948del
ANO9 RefSeqGene	NG_052610.1:g.10948dup
ANO9 RefSeqGene	NG_052610.1:g.10947_10948dup
ANO9 RefSeqGene	NG_052610.1:g.10946_10948dup
ANO9 RefSeqGene	NG_052610.1:g.10928_10948A[22]GAAAAAAAAAAAAAAAAAAAAAAAA[1]
ANO9 RefSeqGene	NG_052610.1:g.10945_10948dup
ANO9 RefSeqGene	NG_052610.1:g.10928_10948A[22]GAAAAAAAAAAAAAAAAAAAAAAAAA[1]
ANO9 RefSeqGene	NG_052610.1:g.10944_10948dup
ANO9 RefSeqGene	NG_052610.1:g.10928_10948A[22]GAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
ANO9 RefSeqGene	NG_052610.1:g.10943_10948dup
ANO9 RefSeqGene	NG_052610.1:g.10938_10948dup
ANO9 RefSeqGene	NG_052610.1:g.10928_10948A[22]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
ANO9 RefSeqGene	NG_052610.1:g.10928_10948dup
ANO9 RefSeqGene	NG_052610.1:g.10948_10949insAAAAAAAAAAAAAAAAAAAAAAA
ANO9 RefSeqGene	NG_052610.1:g.10928_10948A[22]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
ANO9 RefSeqGene	NG_052610.1:g.10948_10949insAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: ANO9, anoctamin 9 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ANO9 transcript variant 1	NM_001012302.3:c.7-1977_7… NM_001012302.3:c.7-1977_7-1966del	N/A	Intron Variant
ANO9 transcript variant 2	NM_001347882.2:c.-506-197… NM_001347882.2:c.-506-1977_-506-1966del	N/A	Intron Variant

Gene: LOC105376506, uncharacterized LOC105376506 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105376506 transcript variant X3	XR_001748090.2:n.	N/A	Intron Variant
LOC105376506 transcript variant X1	XR_007062541.1:n.	N/A	Intron Variant
LOC105376506 transcript variant X2	XR_007062542.1:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₁=	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₆	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	insTTTC(T)₂₂	dup(T)₄	ins(T)₄C(T)₂₂	dup(T)₅	ins(T)₅C(T)₂₂	dup(T)₆	dup(T)₁₁	ins(T)₁₄C(T)₂₂	dup(T)₂₁	ins(T)₂₃	ins(T)₂₃C(T)₂₂	ins(T)₂₇
GRCh38.p14 chr 11	NC_000011.10:g.436064_436084=	NC_000011.10:g.436073_436084del	NC_000011.10:g.436074_436084del	NC_000011.10:g.436075_436084del	NC_000011.10:g.436076_436084del	NC_000011.10:g.436079_436084del	NC_000011.10:g.436081_436084del	NC_000011.10:g.436082_436084del	NC_000011.10:g.436083_436084del	NC_000011.10:g.436084del	NC_000011.10:g.436084dup	NC_000011.10:g.436083_436084dup	NC_000011.10:g.436082_436084dup	NC_000011.10:g.436064_436084T[24]CTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000011.10:g.436081_436084dup	NC_000011.10:g.436064_436084T[25]CTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000011.10:g.436080_436084dup	NC_000011.10:g.436064_436084T[26]CTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000011.10:g.436079_436084dup	NC_000011.10:g.436074_436084dup	NC_000011.10:g.436064_436084T[35]CTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000011.10:g.436064_436084dup	NC_000011.10:g.436084_436085insTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:g.436064_436084T[44]CTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000011.10:g.436084_436085insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 11	NC_000011.9:g.436064_436084=	NC_000011.9:g.436073_436084del	NC_000011.9:g.436074_436084del	NC_000011.9:g.436075_436084del	NC_000011.9:g.436076_436084del	NC_000011.9:g.436079_436084del	NC_000011.9:g.436081_436084del	NC_000011.9:g.436082_436084del	NC_000011.9:g.436083_436084del	NC_000011.9:g.436084del	NC_000011.9:g.436084dup	NC_000011.9:g.436083_436084dup	NC_000011.9:g.436082_436084dup	NC_000011.9:g.436064_436084T[24]CTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000011.9:g.436081_436084dup	NC_000011.9:g.436064_436084T[25]CTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000011.9:g.436080_436084dup	NC_000011.9:g.436064_436084T[26]CTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000011.9:g.436079_436084dup	NC_000011.9:g.436074_436084dup	NC_000011.9:g.436064_436084T[35]CTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000011.9:g.436064_436084dup	NC_000011.9:g.436084_436085insTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.9:g.436064_436084T[44]CTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000011.9:g.436084_436085insTTTTTTTTTTTTTTTTTTTTTTTTTTT
ANO9 RefSeqGene	NG_052610.1:g.10928_10948=	NG_052610.1:g.10937_10948del	NG_052610.1:g.10938_10948del	NG_052610.1:g.10939_10948del	NG_052610.1:g.10940_10948del	NG_052610.1:g.10943_10948del	NG_052610.1:g.10945_10948del	NG_052610.1:g.10946_10948del	NG_052610.1:g.10947_10948del	NG_052610.1:g.10948del	NG_052610.1:g.10948dup	NG_052610.1:g.10947_10948dup	NG_052610.1:g.10946_10948dup	NG_052610.1:g.10928_10948A[22]GAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_052610.1:g.10945_10948dup	NG_052610.1:g.10928_10948A[22]GAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_052610.1:g.10944_10948dup	NG_052610.1:g.10928_10948A[22]GAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_052610.1:g.10943_10948dup	NG_052610.1:g.10938_10948dup	NG_052610.1:g.10928_10948A[22]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_052610.1:g.10928_10948dup	NG_052610.1:g.10948_10949insAAAAAAAAAAAAAAAAAAAAAAA	NG_052610.1:g.10928_10948A[22]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_052610.1:g.10948_10949insAAAAAAAAAAAAAAAAAAAAAAAAAAA
ANO9 transcript variant 1	NM_001012302.2:c.7-1966=	NM_001012302.2:c.7-1977_7-1966del	NM_001012302.2:c.7-1976_7-1966del	NM_001012302.2:c.7-1975_7-1966del	NM_001012302.2:c.7-1974_7-1966del	NM_001012302.2:c.7-1971_7-1966del	NM_001012302.2:c.7-1969_7-1966del	NM_001012302.2:c.7-1968_7-1966del	NM_001012302.2:c.7-1967_7-1966del	NM_001012302.2:c.7-1966del	NM_001012302.2:c.7-1966dup	NM_001012302.2:c.7-1967_7-1966dup	NM_001012302.2:c.7-1968_7-1966dup	NM_001012302.2:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAA	NM_001012302.2:c.7-1969_7-1966dup	NM_001012302.2:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAA	NM_001012302.2:c.7-1970_7-1966dup	NM_001012302.2:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAAA	NM_001012302.2:c.7-1971_7-1966dup	NM_001012302.2:c.7-1976_7-1966dup	NM_001012302.2:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAA	NM_001012302.2:c.7-1986_7-1966dup	NM_001012302.2:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAA	NM_001012302.2:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAA	NM_001012302.2:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAAAAAA
ANO9 transcript variant 1	NM_001012302.3:c.7-1966=	NM_001012302.3:c.7-1977_7-1966del	NM_001012302.3:c.7-1976_7-1966del	NM_001012302.3:c.7-1975_7-1966del	NM_001012302.3:c.7-1974_7-1966del	NM_001012302.3:c.7-1971_7-1966del	NM_001012302.3:c.7-1969_7-1966del	NM_001012302.3:c.7-1968_7-1966del	NM_001012302.3:c.7-1967_7-1966del	NM_001012302.3:c.7-1966del	NM_001012302.3:c.7-1966dup	NM_001012302.3:c.7-1967_7-1966dup	NM_001012302.3:c.7-1968_7-1966dup	NM_001012302.3:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAA	NM_001012302.3:c.7-1969_7-1966dup	NM_001012302.3:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAA	NM_001012302.3:c.7-1970_7-1966dup	NM_001012302.3:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAAA	NM_001012302.3:c.7-1971_7-1966dup	NM_001012302.3:c.7-1976_7-1966dup	NM_001012302.3:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAA	NM_001012302.3:c.7-1986_7-1966dup	NM_001012302.3:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAA	NM_001012302.3:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAA	NM_001012302.3:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAAAAAA
ANO9 transcript variant 2	NM_001347882.2:c.-506-1966=	NM_001347882.2:c.-506-1977_-506-1966del	NM_001347882.2:c.-506-1976_-506-1966del	NM_001347882.2:c.-506-1975_-506-1966del	NM_001347882.2:c.-506-1974_-506-1966del	NM_001347882.2:c.-506-1971_-506-1966del	NM_001347882.2:c.-506-1969_-506-1966del	NM_001347882.2:c.-506-1968_-506-1966del	NM_001347882.2:c.-506-1967_-506-1966del	NM_001347882.2:c.-506-1966del	NM_001347882.2:c.-506-1966dup	NM_001347882.2:c.-506-1967_-506-1966dup	NM_001347882.2:c.-506-1968_-506-1966dup	NM_001347882.2:c.-506-1966_-506-1965insAAAAAAAAAAAAAAAAAAAAAAGAAA	NM_001347882.2:c.-506-1969_-506-1966dup	NM_001347882.2:c.-506-1966_-506-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAA	NM_001347882.2:c.-506-1970_-506-1966dup	NM_001347882.2:c.-506-1966_-506-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAAA	NM_001347882.2:c.-506-1971_-506-1966dup	NM_001347882.2:c.-506-1976_-506-1966dup	NM_001347882.2:c.-506-1966_-506-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAA	NM_001347882.2:c.-506-1986_-506-1966dup	NM_001347882.2:c.-506-1966_-506-1965insAAAAAAAAAAAAAAAAAAAAAAA	NM_001347882.2:c.-506-1966_-506-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAA	NM_001347882.2:c.-506-1966_-506-1965insAAAAAAAAAAAAAAAAAAAAAAAAAAA
ANO9 transcript variant X1	XM_005252885.1:c.7-1966=	XM_005252885.1:c.7-1977_7-1966del	XM_005252885.1:c.7-1976_7-1966del	XM_005252885.1:c.7-1975_7-1966del	XM_005252885.1:c.7-1974_7-1966del	XM_005252885.1:c.7-1971_7-1966del	XM_005252885.1:c.7-1969_7-1966del	XM_005252885.1:c.7-1968_7-1966del	XM_005252885.1:c.7-1967_7-1966del	XM_005252885.1:c.7-1966del	XM_005252885.1:c.7-1966dup	XM_005252885.1:c.7-1967_7-1966dup	XM_005252885.1:c.7-1968_7-1966dup	XM_005252885.1:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAA	XM_005252885.1:c.7-1969_7-1966dup	XM_005252885.1:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAA	XM_005252885.1:c.7-1970_7-1966dup	XM_005252885.1:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAAA	XM_005252885.1:c.7-1971_7-1966dup	XM_005252885.1:c.7-1976_7-1966dup	XM_005252885.1:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAA	XM_005252885.1:c.7-1986_7-1966dup	XM_005252885.1:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAA	XM_005252885.1:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAA	XM_005252885.1:c.7-1966_7-1965insAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

40 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PJP	ss294685047	May 09, 2011 (137)
2	SWEGEN	ss3007446620	Nov 08, 2017 (151)
3	ACPOP	ss3737840490	Jul 13, 2019 (153)
4	ACPOP	ss3737840491	Jul 13, 2019 (153)
5	GNOMAD	ss4228653058	Apr 26, 2021 (155)
6	GNOMAD	ss4228653059	Apr 26, 2021 (155)
7	GNOMAD	ss4228653060	Apr 26, 2021 (155)
8	GNOMAD	ss4228653061	Apr 26, 2021 (155)
9	GNOMAD	ss4228653062	Apr 26, 2021 (155)
10	GNOMAD	ss4228653063	Apr 26, 2021 (155)
11	GNOMAD	ss4228653064	Apr 26, 2021 (155)
12	GNOMAD	ss4228653065	Apr 26, 2021 (155)
13	GNOMAD	ss4228653066	Apr 26, 2021 (155)
14	GNOMAD	ss4228653067	Apr 26, 2021 (155)
15	GNOMAD	ss4228653068	Apr 26, 2021 (155)
16	GNOMAD	ss4228653069	Apr 26, 2021 (155)
17	GNOMAD	ss4228653070	Apr 26, 2021 (155)
18	GNOMAD	ss4228653071	Apr 26, 2021 (155)
19	GNOMAD	ss4228653072	Apr 26, 2021 (155)
20	GNOMAD	ss4228653073	Apr 26, 2021 (155)
21	GNOMAD	ss4228653074	Apr 26, 2021 (155)
22	GNOMAD	ss4228653075	Apr 26, 2021 (155)
23	GNOMAD	ss4228653076	Apr 26, 2021 (155)
24	GNOMAD	ss4228653077	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5200287266	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5200287267	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5200287268	Apr 26, 2021 (155)
28	1000G_HIGH_COVERAGE	ss5286097609	Oct 16, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5286097610	Oct 16, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5286097611	Oct 16, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5286097612	Oct 16, 2022 (156)
32	HUGCELL_USP	ss5481449945	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5481449946	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5481449947	Oct 16, 2022 (156)
35	SANFORD_IMAGENETICS	ss5650456810	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5746924779	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5746924780	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5746924781	Oct 16, 2022 (156)
39	YY_MCH	ss5812048742	Oct 16, 2022 (156)
40	EVA	ss5849821817	Oct 16, 2022 (156)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368969044 (NC_000011.10:436063::T 1902/91704) Row 368969045 (NC_000011.10:436063::TT 134/91714) Row 368969046 (NC_000011.10:436063::TTT 17/91706)...	-	Apr 26, 2021 (155)
61	Northern Sweden Submission ignored due to conflicting rows: Row 11125355 (NC_000011.9:436063::TTTTTTTTTTTTTTTTTTTTT 3/578) Row 11125356 (NC_000011.9:436063::TTTTTTTTTTTTTTTTTTTTTTTTTTT 2/578)	-	Jul 13, 2019 (153)
62	Northern Sweden Submission ignored due to conflicting rows: Row 11125355 (NC_000011.9:436063::TTTTTTTTTTTTTTTTTTTTT 3/578) Row 11125356 (NC_000011.9:436063::TTTTTTTTTTTTTTTTTTTTTTTTTTT 2/578)	-	Jul 13, 2019 (153)
63	8.3KJPN Submission ignored due to conflicting rows: Row 58256573 (NC_000011.9:436063:T: 7035/16282) Row 58256574 (NC_000011.9:436063:TT: 20/16282) Row 58256575 (NC_000011.9:436063::T 15/16282)	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 58256573 (NC_000011.9:436063:T: 7035/16282) Row 58256574 (NC_000011.9:436063:TT: 20/16282) Row 58256575 (NC_000011.9:436063::T 15/16282)	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 58256573 (NC_000011.9:436063:T: 7035/16282) Row 58256574 (NC_000011.9:436063:TT: 20/16282) Row 58256575 (NC_000011.9:436063::T 15/16282)	-	Apr 26, 2021 (155)
66	14KJPN Submission ignored due to conflicting rows: Row 80761883 (NC_000011.10:436063:T: 10135/22910) Row 80761884 (NC_000011.10:436063:TT: 30/22910) Row 80761885 (NC_000011.10:436063::T 17/22910)	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 80761883 (NC_000011.10:436063:T: 10135/22910) Row 80761884 (NC_000011.10:436063:TT: 30/22910) Row 80761885 (NC_000011.10:436063::T 17/22910)	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 80761883 (NC_000011.10:436063:T: 10135/22910) Row 80761884 (NC_000011.10:436063:TT: 30/22910) Row 80761885 (NC_000011.10:436063::T 17/22910)	-	Oct 16, 2022 (156)
69	ALFA	NC_000011.10 - 436064	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)
rs142523505	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4228653077	NC_000011.10:436063:TTTTTTTTTTTT:	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
3427058169	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4228653076	NC_000011.10:436063:TTTTTTTTTTT:	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
3427058169	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
3427058169	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4228653075	NC_000011.10:436063:TTTTTTTTT:	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
3427058169	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4228653074	NC_000011.10:436063:TTTTTT:	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
3427058169	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4228653073	NC_000011.10:436063:TTTT:	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4228653072, ss5286097612	NC_000011.10:436063:TTT:	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
3427058169	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5200287267	NC_000011.9:436063:TT:	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5286097610, ss5481449947, ss5746924780	NC_000011.10:436063:TT:	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
3427058169	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss294685047	NC_000011.8:426083:T:	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3007446620, ss5200287266, ss5650456810	NC_000011.9:436063:T:	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5286097609, ss5481449945, ss5746924779, ss5812048742, ss5849821817	NC_000011.10:436063:T:	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
3427058169	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5200287268	NC_000011.9:436063::T	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4228653058, ss5286097611, ss5481449946, ss5746924781	NC_000011.10:436063::T	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
3427058169	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4228653059	NC_000011.10:436063::TT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
3427058169	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4228653060	NC_000011.10:436063::TTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4228653066	NC_000011.10:436063::TTTTTTTTTTTTT… NC_000011.10:436063::TTTTTTTTTTTTTTTTTTTTTTTTCT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4228653061	NC_000011.10:436063::TTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4228653067	NC_000011.10:436063::TTTTTTTTTTTTT… NC_000011.10:436063::TTTTTTTTTTTTTTTTTTTTTTTTTCT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4228653062	NC_000011.10:436063::TTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4228653068	NC_000011.10:436063::TTTTTTTTTTTTT… NC_000011.10:436063::TTTTTTTTTTTTTTTTTTTTTTTTTTCT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4228653063	NC_000011.10:436063::TTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4228653064	NC_000011.10:436063::TTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4228653070	NC_000011.10:436063::TTTTTTTTTTTTT… NC_000011.10:436063::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3737840490	NC_000011.9:436063::TTTTTTTTTTTTTT… NC_000011.9:436063::TTTTTTTTTTTTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4228653065	NC_000011.10:436063::TTTTTTTTTTTTT… NC_000011.10:436063::TTTTTTTTTTTTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3427058169	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4228653071	NC_000011.10:436063::TTTTTTTTTTTTT… NC_000011.10:436063::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3737840491	NC_000011.9:436063::TTTTTTTTTTTTTT… NC_000011.9:436063::TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4228653069	NC_000011.10:436063::TTTTTTTTTTTTT… NC_000011.10:436063::TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3427058169	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:436063:TTTTTTTTTTTTTT… NC_000011.10:436063:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs10707508

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs10707508