Name: rs777175392
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.

rs777175392

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:68844295-68844315 (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)₁₃ / del(T)₁₂ / del(T)₁₁ / d…
del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₁ / dup(T)₁₅ / ins(T)₂₈ / ins(T)₃₃
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₃=0.000004 (1/264690, TOPMED)
dupT=0.4254 (2139/5028, ALFA)
(T)₂₁=0.1 (1/8, KOREAN)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: STOX1 : 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	5028	TTTTTTTTTTTTTTTTTTTTT=0.4934	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0044, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.4254, TTTTTTTTTTTTTTTTTTTTTTTT=0.0181, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0527, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0014, TTTTTTTTTTTTTTTTTTTTTTT=0.0046	0.501593	0.385071	0.113336	32
European	Sub	4696	TTTTTTTTTTTTTTTTTTTTT=0.4589	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0047, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.4542, TTTTTTTTTTTTTTTTTTTTTTTT=0.0194, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0564, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0015, TTTTTTTTTTTTTTTTTTTTTTT=0.0049	0.462334	0.415066	0.1226	32
African	Sub	262	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	12	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	250	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	18	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	10	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	2	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	16	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	6	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	28	TTTTTTTTTTTTTTTTTTTTT=0.79	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.21, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	0.785714	0.214286	0.0	8

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
TopMed	Global	Study-wide	264690	(T)₂₁=0.999996	del(T)₁₃=0.000004
Allele Frequency Aggregator	Total	Global	5028	(T)₂₁=0.4934	del(T)₁₃=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0044, delTT=0.0000, delT=0.0000, dupT=0.4254, dupTT=0.0046, dupTTT=0.0181, dup(T)₄=0.0527, dup(T)₁₁=0.0014
Allele Frequency Aggregator	European	Sub	4696	(T)₂₁=0.4589	del(T)₁₃=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0047, delTT=0.0000, delT=0.0000, dupT=0.4542, dupTT=0.0049, dupTTT=0.0194, dup(T)₄=0.0564, dup(T)₁₁=0.0015
Allele Frequency Aggregator	African	Sub	262	(T)₂₁=1.000	del(T)₁₃=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₁₁=0.000
Allele Frequency Aggregator	Other	Sub	28	(T)₂₁=0.79	del(T)₁₃=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.21, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₁₁=0.00
Allele Frequency Aggregator	Asian	Sub	18	(T)₂₁=1.00	del(T)₁₃=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₁₁=0.00
Allele Frequency Aggregator	Latin American 2	Sub	16	(T)₂₁=1.00	del(T)₁₃=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₁₁=0.00
Allele Frequency Aggregator	South Asian	Sub	6	(T)₂₁=1.0	del(T)₁₃=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₁₁=0.0
Allele Frequency Aggregator	Latin American 1	Sub	2	(T)₂₁=1.0	del(T)₁₃=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₁₁=0.0
KOREAN population from KRGDB	KOREAN	Study-wide	8	- No frequency provided	dupT=0.9

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 10	NC_000010.11:g.68844303_68844315del
GRCh38.p14 chr 10	NC_000010.11:g.68844304_68844315del
GRCh38.p14 chr 10	NC_000010.11:g.68844305_68844315del
GRCh38.p14 chr 10	NC_000010.11:g.68844306_68844315del
GRCh38.p14 chr 10	NC_000010.11:g.68844307_68844315del
GRCh38.p14 chr 10	NC_000010.11:g.68844308_68844315del
GRCh38.p14 chr 10	NC_000010.11:g.68844309_68844315del
GRCh38.p14 chr 10	NC_000010.11:g.68844310_68844315del
GRCh38.p14 chr 10	NC_000010.11:g.68844312_68844315del
GRCh38.p14 chr 10	NC_000010.11:g.68844313_68844315del
GRCh38.p14 chr 10	NC_000010.11:g.68844314_68844315del
GRCh38.p14 chr 10	NC_000010.11:g.68844315del
GRCh38.p14 chr 10	NC_000010.11:g.68844315dup
GRCh38.p14 chr 10	NC_000010.11:g.68844314_68844315dup
GRCh38.p14 chr 10	NC_000010.11:g.68844313_68844315dup
GRCh38.p14 chr 10	NC_000010.11:g.68844312_68844315dup
GRCh38.p14 chr 10	NC_000010.11:g.68844311_68844315dup
GRCh38.p14 chr 10	NC_000010.11:g.68844310_68844315dup
GRCh38.p14 chr 10	NC_000010.11:g.68844309_68844315dup
GRCh38.p14 chr 10	NC_000010.11:g.68844308_68844315dup
GRCh38.p14 chr 10	NC_000010.11:g.68844307_68844315dup
GRCh38.p14 chr 10	NC_000010.11:g.68844305_68844315dup
GRCh38.p14 chr 10	NC_000010.11:g.68844301_68844315dup
GRCh38.p14 chr 10	NC_000010.11:g.68844315_68844316insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.68844315_68844316insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.70604059_70604071del
GRCh37.p13 chr 10	NC_000010.10:g.70604060_70604071del
GRCh37.p13 chr 10	NC_000010.10:g.70604061_70604071del
GRCh37.p13 chr 10	NC_000010.10:g.70604062_70604071del
GRCh37.p13 chr 10	NC_000010.10:g.70604063_70604071del
GRCh37.p13 chr 10	NC_000010.10:g.70604064_70604071del
GRCh37.p13 chr 10	NC_000010.10:g.70604065_70604071del
GRCh37.p13 chr 10	NC_000010.10:g.70604066_70604071del
GRCh37.p13 chr 10	NC_000010.10:g.70604068_70604071del
GRCh37.p13 chr 10	NC_000010.10:g.70604069_70604071del
GRCh37.p13 chr 10	NC_000010.10:g.70604070_70604071del
GRCh37.p13 chr 10	NC_000010.10:g.70604071del
GRCh37.p13 chr 10	NC_000010.10:g.70604071dup
GRCh37.p13 chr 10	NC_000010.10:g.70604070_70604071dup
GRCh37.p13 chr 10	NC_000010.10:g.70604069_70604071dup
GRCh37.p13 chr 10	NC_000010.10:g.70604068_70604071dup
GRCh37.p13 chr 10	NC_000010.10:g.70604067_70604071dup
GRCh37.p13 chr 10	NC_000010.10:g.70604066_70604071dup
GRCh37.p13 chr 10	NC_000010.10:g.70604065_70604071dup
GRCh37.p13 chr 10	NC_000010.10:g.70604064_70604071dup
GRCh37.p13 chr 10	NC_000010.10:g.70604063_70604071dup
GRCh37.p13 chr 10	NC_000010.10:g.70604061_70604071dup
GRCh37.p13 chr 10	NC_000010.10:g.70604057_70604071dup
GRCh37.p13 chr 10	NC_000010.10:g.70604071_70604072insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.70604071_70604072insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
STOX1 RefSeqGene	NG_012975.2:g.21767_21779del
STOX1 RefSeqGene	NG_012975.2:g.21768_21779del
STOX1 RefSeqGene	NG_012975.2:g.21769_21779del
STOX1 RefSeqGene	NG_012975.2:g.21770_21779del
STOX1 RefSeqGene	NG_012975.2:g.21771_21779del
STOX1 RefSeqGene	NG_012975.2:g.21772_21779del
STOX1 RefSeqGene	NG_012975.2:g.21773_21779del
STOX1 RefSeqGene	NG_012975.2:g.21774_21779del
STOX1 RefSeqGene	NG_012975.2:g.21776_21779del
STOX1 RefSeqGene	NG_012975.2:g.21777_21779del
STOX1 RefSeqGene	NG_012975.2:g.21778_21779del
STOX1 RefSeqGene	NG_012975.2:g.21779del
STOX1 RefSeqGene	NG_012975.2:g.21779dup
STOX1 RefSeqGene	NG_012975.2:g.21778_21779dup
STOX1 RefSeqGene	NG_012975.2:g.21777_21779dup
STOX1 RefSeqGene	NG_012975.2:g.21776_21779dup
STOX1 RefSeqGene	NG_012975.2:g.21775_21779dup
STOX1 RefSeqGene	NG_012975.2:g.21774_21779dup
STOX1 RefSeqGene	NG_012975.2:g.21773_21779dup
STOX1 RefSeqGene	NG_012975.2:g.21772_21779dup
STOX1 RefSeqGene	NG_012975.2:g.21771_21779dup
STOX1 RefSeqGene	NG_012975.2:g.21769_21779dup
STOX1 RefSeqGene	NG_012975.2:g.21765_21779dup
STOX1 RefSeqGene	NG_012975.2:g.21779_21780insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
STOX1 RefSeqGene	NG_012975.2:g.21779_21780insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: STOX1, storkhead box 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
STOX1 transcript variant 3	NM_001130159.3:c.310+1637… NM_001130159.3:c.310+16370_310+16382del	N/A	Intron Variant
STOX1 transcript variant 4	NM_001130160.3:c.310+1637… NM_001130160.3:c.310+16370_310+16382del	N/A	Intron Variant
STOX1 transcript variant 2	NM_001130161.4:c.310+1637… NM_001130161.4:c.310+16370_310+16382del	N/A	Intron Variant
STOX1 transcript variant 1	NM_152709.5:c.310+16370_3… NM_152709.5:c.310+16370_310+16382del	N/A	Intron Variant
STOX1 transcript variant X1	XM_011539454.3:c.-21+1603… XM_011539454.3:c.-21+16034_-21+16046del	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)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₁	dup(T)₁₅	ins(T)₂₈	ins(T)₃₃
GRCh38.p14 chr 10	NC_000010.11:g.68844295_68844315=	NC_000010.11:g.68844303_68844315del	NC_000010.11:g.68844304_68844315del	NC_000010.11:g.68844305_68844315del	NC_000010.11:g.68844306_68844315del	NC_000010.11:g.68844307_68844315del	NC_000010.11:g.68844308_68844315del	NC_000010.11:g.68844309_68844315del	NC_000010.11:g.68844310_68844315del	NC_000010.11:g.68844312_68844315del	NC_000010.11:g.68844313_68844315del	NC_000010.11:g.68844314_68844315del	NC_000010.11:g.68844315del	NC_000010.11:g.68844315dup	NC_000010.11:g.68844314_68844315dup	NC_000010.11:g.68844313_68844315dup	NC_000010.11:g.68844312_68844315dup	NC_000010.11:g.68844311_68844315dup	NC_000010.11:g.68844310_68844315dup	NC_000010.11:g.68844309_68844315dup	NC_000010.11:g.68844308_68844315dup	NC_000010.11:g.68844307_68844315dup	NC_000010.11:g.68844305_68844315dup	NC_000010.11:g.68844301_68844315dup	NC_000010.11:g.68844315_68844316insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.68844315_68844316insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.70604051_70604071=	NC_000010.10:g.70604059_70604071del	NC_000010.10:g.70604060_70604071del	NC_000010.10:g.70604061_70604071del	NC_000010.10:g.70604062_70604071del	NC_000010.10:g.70604063_70604071del	NC_000010.10:g.70604064_70604071del	NC_000010.10:g.70604065_70604071del	NC_000010.10:g.70604066_70604071del	NC_000010.10:g.70604068_70604071del	NC_000010.10:g.70604069_70604071del	NC_000010.10:g.70604070_70604071del	NC_000010.10:g.70604071del	NC_000010.10:g.70604071dup	NC_000010.10:g.70604070_70604071dup	NC_000010.10:g.70604069_70604071dup	NC_000010.10:g.70604068_70604071dup	NC_000010.10:g.70604067_70604071dup	NC_000010.10:g.70604066_70604071dup	NC_000010.10:g.70604065_70604071dup	NC_000010.10:g.70604064_70604071dup	NC_000010.10:g.70604063_70604071dup	NC_000010.10:g.70604061_70604071dup	NC_000010.10:g.70604057_70604071dup	NC_000010.10:g.70604071_70604072insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.70604071_70604072insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
STOX1 RefSeqGene	NG_012975.2:g.21759_21779=	NG_012975.2:g.21767_21779del	NG_012975.2:g.21768_21779del	NG_012975.2:g.21769_21779del	NG_012975.2:g.21770_21779del	NG_012975.2:g.21771_21779del	NG_012975.2:g.21772_21779del	NG_012975.2:g.21773_21779del	NG_012975.2:g.21774_21779del	NG_012975.2:g.21776_21779del	NG_012975.2:g.21777_21779del	NG_012975.2:g.21778_21779del	NG_012975.2:g.21779del	NG_012975.2:g.21779dup	NG_012975.2:g.21778_21779dup	NG_012975.2:g.21777_21779dup	NG_012975.2:g.21776_21779dup	NG_012975.2:g.21775_21779dup	NG_012975.2:g.21774_21779dup	NG_012975.2:g.21773_21779dup	NG_012975.2:g.21772_21779dup	NG_012975.2:g.21771_21779dup	NG_012975.2:g.21769_21779dup	NG_012975.2:g.21765_21779dup	NG_012975.2:g.21779_21780insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NG_012975.2:g.21779_21780insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
STOX1 transcript variant 3	NM_001130159.2:c.310+16361=	NM_001130159.2:c.310+16369_310+16381del	NM_001130159.2:c.310+16370_310+16381del	NM_001130159.2:c.310+16371_310+16381del	NM_001130159.2:c.310+16372_310+16381del	NM_001130159.2:c.310+16373_310+16381del	NM_001130159.2:c.310+16374_310+16381del	NM_001130159.2:c.310+16375_310+16381del	NM_001130159.2:c.310+16376_310+16381del	NM_001130159.2:c.310+16378_310+16381del	NM_001130159.2:c.310+16379_310+16381del	NM_001130159.2:c.310+16380_310+16381del	NM_001130159.2:c.310+16381del	NM_001130159.2:c.310+16381dup	NM_001130159.2:c.310+16380_310+16381dup	NM_001130159.2:c.310+16379_310+16381dup	NM_001130159.2:c.310+16378_310+16381dup	NM_001130159.2:c.310+16377_310+16381dup	NM_001130159.2:c.310+16376_310+16381dup	NM_001130159.2:c.310+16375_310+16381dup	NM_001130159.2:c.310+16374_310+16381dup	NM_001130159.2:c.310+16373_310+16381dup	NM_001130159.2:c.310+16371_310+16381dup	NM_001130159.2:c.310+16367_310+16381dup	NM_001130159.2:c.310+16381_310+16382insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001130159.2:c.310+16381_310+16382insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
STOX1 transcript variant 3	NM_001130159.3:c.310+16362=	NM_001130159.3:c.310+16370_310+16382del	NM_001130159.3:c.310+16371_310+16382del	NM_001130159.3:c.310+16372_310+16382del	NM_001130159.3:c.310+16373_310+16382del	NM_001130159.3:c.310+16374_310+16382del	NM_001130159.3:c.310+16375_310+16382del	NM_001130159.3:c.310+16376_310+16382del	NM_001130159.3:c.310+16377_310+16382del	NM_001130159.3:c.310+16379_310+16382del	NM_001130159.3:c.310+16380_310+16382del	NM_001130159.3:c.310+16381_310+16382del	NM_001130159.3:c.310+16382del	NM_001130159.3:c.310+16382dup	NM_001130159.3:c.310+16381_310+16382dup	NM_001130159.3:c.310+16380_310+16382dup	NM_001130159.3:c.310+16379_310+16382dup	NM_001130159.3:c.310+16378_310+16382dup	NM_001130159.3:c.310+16377_310+16382dup	NM_001130159.3:c.310+16376_310+16382dup	NM_001130159.3:c.310+16375_310+16382dup	NM_001130159.3:c.310+16374_310+16382dup	NM_001130159.3:c.310+16372_310+16382dup	NM_001130159.3:c.310+16368_310+16382dup	NM_001130159.3:c.310+16382_310+16383insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001130159.3:c.310+16382_310+16383insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
STOX1 transcript variant 4	NM_001130160.2:c.310+16361=	NM_001130160.2:c.310+16369_310+16381del	NM_001130160.2:c.310+16370_310+16381del	NM_001130160.2:c.310+16371_310+16381del	NM_001130160.2:c.310+16372_310+16381del	NM_001130160.2:c.310+16373_310+16381del	NM_001130160.2:c.310+16374_310+16381del	NM_001130160.2:c.310+16375_310+16381del	NM_001130160.2:c.310+16376_310+16381del	NM_001130160.2:c.310+16378_310+16381del	NM_001130160.2:c.310+16379_310+16381del	NM_001130160.2:c.310+16380_310+16381del	NM_001130160.2:c.310+16381del	NM_001130160.2:c.310+16381dup	NM_001130160.2:c.310+16380_310+16381dup	NM_001130160.2:c.310+16379_310+16381dup	NM_001130160.2:c.310+16378_310+16381dup	NM_001130160.2:c.310+16377_310+16381dup	NM_001130160.2:c.310+16376_310+16381dup	NM_001130160.2:c.310+16375_310+16381dup	NM_001130160.2:c.310+16374_310+16381dup	NM_001130160.2:c.310+16373_310+16381dup	NM_001130160.2:c.310+16371_310+16381dup	NM_001130160.2:c.310+16367_310+16381dup	NM_001130160.2:c.310+16381_310+16382insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001130160.2:c.310+16381_310+16382insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
STOX1 transcript variant 4	NM_001130160.3:c.310+16362=	NM_001130160.3:c.310+16370_310+16382del	NM_001130160.3:c.310+16371_310+16382del	NM_001130160.3:c.310+16372_310+16382del	NM_001130160.3:c.310+16373_310+16382del	NM_001130160.3:c.310+16374_310+16382del	NM_001130160.3:c.310+16375_310+16382del	NM_001130160.3:c.310+16376_310+16382del	NM_001130160.3:c.310+16377_310+16382del	NM_001130160.3:c.310+16379_310+16382del	NM_001130160.3:c.310+16380_310+16382del	NM_001130160.3:c.310+16381_310+16382del	NM_001130160.3:c.310+16382del	NM_001130160.3:c.310+16382dup	NM_001130160.3:c.310+16381_310+16382dup	NM_001130160.3:c.310+16380_310+16382dup	NM_001130160.3:c.310+16379_310+16382dup	NM_001130160.3:c.310+16378_310+16382dup	NM_001130160.3:c.310+16377_310+16382dup	NM_001130160.3:c.310+16376_310+16382dup	NM_001130160.3:c.310+16375_310+16382dup	NM_001130160.3:c.310+16374_310+16382dup	NM_001130160.3:c.310+16372_310+16382dup	NM_001130160.3:c.310+16368_310+16382dup	NM_001130160.3:c.310+16382_310+16383insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001130160.3:c.310+16382_310+16383insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
STOX1 transcript variant 2	NM_001130161.2:c.310+16361=	NM_001130161.2:c.310+16369_310+16381del	NM_001130161.2:c.310+16370_310+16381del	NM_001130161.2:c.310+16371_310+16381del	NM_001130161.2:c.310+16372_310+16381del	NM_001130161.2:c.310+16373_310+16381del	NM_001130161.2:c.310+16374_310+16381del	NM_001130161.2:c.310+16375_310+16381del	NM_001130161.2:c.310+16376_310+16381del	NM_001130161.2:c.310+16378_310+16381del	NM_001130161.2:c.310+16379_310+16381del	NM_001130161.2:c.310+16380_310+16381del	NM_001130161.2:c.310+16381del	NM_001130161.2:c.310+16381dup	NM_001130161.2:c.310+16380_310+16381dup	NM_001130161.2:c.310+16379_310+16381dup	NM_001130161.2:c.310+16378_310+16381dup	NM_001130161.2:c.310+16377_310+16381dup	NM_001130161.2:c.310+16376_310+16381dup	NM_001130161.2:c.310+16375_310+16381dup	NM_001130161.2:c.310+16374_310+16381dup	NM_001130161.2:c.310+16373_310+16381dup	NM_001130161.2:c.310+16371_310+16381dup	NM_001130161.2:c.310+16367_310+16381dup	NM_001130161.2:c.310+16381_310+16382insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001130161.2:c.310+16381_310+16382insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
STOX1 transcript variant 2	NM_001130161.4:c.310+16362=	NM_001130161.4:c.310+16370_310+16382del	NM_001130161.4:c.310+16371_310+16382del	NM_001130161.4:c.310+16372_310+16382del	NM_001130161.4:c.310+16373_310+16382del	NM_001130161.4:c.310+16374_310+16382del	NM_001130161.4:c.310+16375_310+16382del	NM_001130161.4:c.310+16376_310+16382del	NM_001130161.4:c.310+16377_310+16382del	NM_001130161.4:c.310+16379_310+16382del	NM_001130161.4:c.310+16380_310+16382del	NM_001130161.4:c.310+16381_310+16382del	NM_001130161.4:c.310+16382del	NM_001130161.4:c.310+16382dup	NM_001130161.4:c.310+16381_310+16382dup	NM_001130161.4:c.310+16380_310+16382dup	NM_001130161.4:c.310+16379_310+16382dup	NM_001130161.4:c.310+16378_310+16382dup	NM_001130161.4:c.310+16377_310+16382dup	NM_001130161.4:c.310+16376_310+16382dup	NM_001130161.4:c.310+16375_310+16382dup	NM_001130161.4:c.310+16374_310+16382dup	NM_001130161.4:c.310+16372_310+16382dup	NM_001130161.4:c.310+16368_310+16382dup	NM_001130161.4:c.310+16382_310+16383insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001130161.4:c.310+16382_310+16383insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
STOX1 transcript variant 5	NM_001130162.2:c.-21+16025=	NM_001130162.2:c.-21+16033_-21+16045del	NM_001130162.2:c.-21+16034_-21+16045del	NM_001130162.2:c.-21+16035_-21+16045del	NM_001130162.2:c.-21+16036_-21+16045del	NM_001130162.2:c.-21+16037_-21+16045del	NM_001130162.2:c.-21+16038_-21+16045del	NM_001130162.2:c.-21+16039_-21+16045del	NM_001130162.2:c.-21+16040_-21+16045del	NM_001130162.2:c.-21+16042_-21+16045del	NM_001130162.2:c.-21+16043_-21+16045del	NM_001130162.2:c.-21+16044_-21+16045del	NM_001130162.2:c.-21+16045del	NM_001130162.2:c.-21+16045dup	NM_001130162.2:c.-21+16044_-21+16045dup	NM_001130162.2:c.-21+16043_-21+16045dup	NM_001130162.2:c.-21+16042_-21+16045dup	NM_001130162.2:c.-21+16041_-21+16045dup	NM_001130162.2:c.-21+16040_-21+16045dup	NM_001130162.2:c.-21+16039_-21+16045dup	NM_001130162.2:c.-21+16038_-21+16045dup	NM_001130162.2:c.-21+16037_-21+16045dup	NM_001130162.2:c.-21+16035_-21+16045dup	NM_001130162.2:c.-21+16031_-21+16045dup	NM_001130162.2:c.-21+16045_-21+16046insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001130162.2:c.-21+16045_-21+16046insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
STOX1 transcript variant 1	NM_152709.4:c.310+16361=	NM_152709.4:c.310+16369_310+16381del	NM_152709.4:c.310+16370_310+16381del	NM_152709.4:c.310+16371_310+16381del	NM_152709.4:c.310+16372_310+16381del	NM_152709.4:c.310+16373_310+16381del	NM_152709.4:c.310+16374_310+16381del	NM_152709.4:c.310+16375_310+16381del	NM_152709.4:c.310+16376_310+16381del	NM_152709.4:c.310+16378_310+16381del	NM_152709.4:c.310+16379_310+16381del	NM_152709.4:c.310+16380_310+16381del	NM_152709.4:c.310+16381del	NM_152709.4:c.310+16381dup	NM_152709.4:c.310+16380_310+16381dup	NM_152709.4:c.310+16379_310+16381dup	NM_152709.4:c.310+16378_310+16381dup	NM_152709.4:c.310+16377_310+16381dup	NM_152709.4:c.310+16376_310+16381dup	NM_152709.4:c.310+16375_310+16381dup	NM_152709.4:c.310+16374_310+16381dup	NM_152709.4:c.310+16373_310+16381dup	NM_152709.4:c.310+16371_310+16381dup	NM_152709.4:c.310+16367_310+16381dup	NM_152709.4:c.310+16381_310+16382insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_152709.4:c.310+16381_310+16382insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
STOX1 transcript variant 1	NM_152709.5:c.310+16362=	NM_152709.5:c.310+16370_310+16382del	NM_152709.5:c.310+16371_310+16382del	NM_152709.5:c.310+16372_310+16382del	NM_152709.5:c.310+16373_310+16382del	NM_152709.5:c.310+16374_310+16382del	NM_152709.5:c.310+16375_310+16382del	NM_152709.5:c.310+16376_310+16382del	NM_152709.5:c.310+16377_310+16382del	NM_152709.5:c.310+16379_310+16382del	NM_152709.5:c.310+16380_310+16382del	NM_152709.5:c.310+16381_310+16382del	NM_152709.5:c.310+16382del	NM_152709.5:c.310+16382dup	NM_152709.5:c.310+16381_310+16382dup	NM_152709.5:c.310+16380_310+16382dup	NM_152709.5:c.310+16379_310+16382dup	NM_152709.5:c.310+16378_310+16382dup	NM_152709.5:c.310+16377_310+16382dup	NM_152709.5:c.310+16376_310+16382dup	NM_152709.5:c.310+16375_310+16382dup	NM_152709.5:c.310+16374_310+16382dup	NM_152709.5:c.310+16372_310+16382dup	NM_152709.5:c.310+16368_310+16382dup	NM_152709.5:c.310+16382_310+16383insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_152709.5:c.310+16382_310+16383insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
STOX1 transcript variant X1	XM_005269605.1:c.-21+15299=	XM_005269605.1:c.-21+15307_-21+15319del	XM_005269605.1:c.-21+15308_-21+15319del	XM_005269605.1:c.-21+15309_-21+15319del	XM_005269605.1:c.-21+15310_-21+15319del	XM_005269605.1:c.-21+15311_-21+15319del	XM_005269605.1:c.-21+15312_-21+15319del	XM_005269605.1:c.-21+15313_-21+15319del	XM_005269605.1:c.-21+15314_-21+15319del	XM_005269605.1:c.-21+15316_-21+15319del	XM_005269605.1:c.-21+15317_-21+15319del	XM_005269605.1:c.-21+15318_-21+15319del	XM_005269605.1:c.-21+15319del	XM_005269605.1:c.-21+15319dup	XM_005269605.1:c.-21+15318_-21+15319dup	XM_005269605.1:c.-21+15317_-21+15319dup	XM_005269605.1:c.-21+15316_-21+15319dup	XM_005269605.1:c.-21+15315_-21+15319dup	XM_005269605.1:c.-21+15314_-21+15319dup	XM_005269605.1:c.-21+15313_-21+15319dup	XM_005269605.1:c.-21+15312_-21+15319dup	XM_005269605.1:c.-21+15311_-21+15319dup	XM_005269605.1:c.-21+15309_-21+15319dup	XM_005269605.1:c.-21+15305_-21+15319dup	XM_005269605.1:c.-21+15319_-21+15320insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005269605.1:c.-21+15319_-21+15320insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
STOX1 transcript variant X1	XM_011539454.3:c.-21+16026=	XM_011539454.3:c.-21+16034_-21+16046del	XM_011539454.3:c.-21+16035_-21+16046del	XM_011539454.3:c.-21+16036_-21+16046del	XM_011539454.3:c.-21+16037_-21+16046del	XM_011539454.3:c.-21+16038_-21+16046del	XM_011539454.3:c.-21+16039_-21+16046del	XM_011539454.3:c.-21+16040_-21+16046del	XM_011539454.3:c.-21+16041_-21+16046del	XM_011539454.3:c.-21+16043_-21+16046del	XM_011539454.3:c.-21+16044_-21+16046del	XM_011539454.3:c.-21+16045_-21+16046del	XM_011539454.3:c.-21+16046del	XM_011539454.3:c.-21+16046dup	XM_011539454.3:c.-21+16045_-21+16046dup	XM_011539454.3:c.-21+16044_-21+16046dup	XM_011539454.3:c.-21+16043_-21+16046dup	XM_011539454.3:c.-21+16042_-21+16046dup	XM_011539454.3:c.-21+16041_-21+16046dup	XM_011539454.3:c.-21+16040_-21+16046dup	XM_011539454.3:c.-21+16039_-21+16046dup	XM_011539454.3:c.-21+16038_-21+16046dup	XM_011539454.3:c.-21+16036_-21+16046dup	XM_011539454.3:c.-21+16032_-21+16046dup	XM_011539454.3:c.-21+16046_-21+16047insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_011539454.3:c.-21+16046_-21+16047insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

55 SubSNP, 37 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95544828	Oct 12, 2018 (152)
2	PJP	ss294662510	Oct 12, 2018 (152)
3	EVA_UK10K_ALSPAC	ss1706787352	Apr 01, 2015 (144)
4	EVA_UK10K_ALSPAC	ss1706787354	Apr 01, 2015 (144)
5	EVA_UK10K_TWINSUK	ss1706787668	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1706787669	Apr 01, 2015 (144)
7	SWEGEN	ss3006667785	Nov 08, 2017 (151)
8	EVA_DECODE	ss3690107743	Jul 13, 2019 (153)
9	EVA_DECODE	ss3690107744	Jul 13, 2019 (153)
10	EVA_DECODE	ss3690107745	Jul 13, 2019 (153)
11	EVA_DECODE	ss3690107746	Jul 13, 2019 (153)
12	EVA	ss3832186025	Apr 26, 2020 (154)
13	KRGDB	ss3922532462	Apr 26, 2020 (154)
14	GNOMAD	ss4220521814	Apr 26, 2021 (155)
15	GNOMAD	ss4220521815	Apr 26, 2021 (155)
16	GNOMAD	ss4220521816	Apr 26, 2021 (155)
17	GNOMAD	ss4220521817	Apr 26, 2021 (155)
18	GNOMAD	ss4220521818	Apr 26, 2021 (155)
19	GNOMAD	ss4220521819	Apr 26, 2021 (155)
20	GNOMAD	ss4220521820	Apr 26, 2021 (155)
21	GNOMAD	ss4220521821	Apr 26, 2021 (155)
22	GNOMAD	ss4220521822	Apr 26, 2021 (155)
23	GNOMAD	ss4220521823	Apr 26, 2021 (155)
24	GNOMAD	ss4220521824	Apr 26, 2021 (155)
25	GNOMAD	ss4220521825	Apr 26, 2021 (155)
26	GNOMAD	ss4220521827	Apr 26, 2021 (155)
27	GNOMAD	ss4220521828	Apr 26, 2021 (155)
28	GNOMAD	ss4220521829	Apr 26, 2021 (155)
29	GNOMAD	ss4220521830	Apr 26, 2021 (155)
30	GNOMAD	ss4220521831	Apr 26, 2021 (155)
31	GNOMAD	ss4220521832	Apr 26, 2021 (155)
32	GNOMAD	ss4220521833	Apr 26, 2021 (155)
33	GNOMAD	ss4220521834	Apr 26, 2021 (155)
34	TOPMED	ss4856386932	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5198147881	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5198147882	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5198147883	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5198147884	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5198147885	Apr 26, 2021 (155)
40	1000G_HIGH_COVERAGE	ss5284452970	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5284452971	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5284452972	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5284452973	Oct 16, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5284452974	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5479989960	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5479989961	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5479989962	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5479989963	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5744126360	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5744126361	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5744126362	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5744126364	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5744126365	Oct 16, 2022 (156)
54	EVA	ss5824557750	Oct 16, 2022 (156)
55	EVA	ss5824557751	Oct 16, 2022 (156)
56	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 27920385 (NC_000010.10:70604050::TT 2033/3854) Row 27920386 (NC_000010.10:70604050::TTT 1527/3854)	-	Oct 12, 2018 (152)
57	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 27920385 (NC_000010.10:70604050::TT 2033/3854) Row 27920386 (NC_000010.10:70604050::TTT 1527/3854)	-	Oct 12, 2018 (152)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355528501 (NC_000010.11:68844294::T 70136/96972) Row 355528502 (NC_000010.11:68844294::TT 812/96592) Row 355528503 (NC_000010.11:68844294::TTT 388/96562)...	-	Apr 26, 2021 (155)
78	KOREAN population from KRGDB	NC_000010.10 - 70604051	Apr 26, 2020 (154)
79	8.3KJPN Submission ignored due to conflicting rows: Row 56117188 (NC_000010.10:70604050::T 7775/16112) Row 56117189 (NC_000010.10:70604050:T: 156/16112) Row 56117190 (NC_000010.10:70604050::TT 53/16112)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 56117188 (NC_000010.10:70604050::T 7775/16112) Row 56117189 (NC_000010.10:70604050:T: 156/16112) Row 56117190 (NC_000010.10:70604050::TT 53/16112)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 56117188 (NC_000010.10:70604050::T 7775/16112) Row 56117189 (NC_000010.10:70604050:T: 156/16112) Row 56117190 (NC_000010.10:70604050::TT 53/16112)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 56117188 (NC_000010.10:70604050::T 7775/16112) Row 56117189 (NC_000010.10:70604050:T: 156/16112) Row 56117190 (NC_000010.10:70604050::TT 53/16112)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 56117188 (NC_000010.10:70604050::T 7775/16112) Row 56117189 (NC_000010.10:70604050:T: 156/16112) Row 56117190 (NC_000010.10:70604050::TT 53/16112)...	-	Apr 26, 2021 (155)
84	14KJPN Submission ignored due to conflicting rows: Row 77963464 (NC_000010.11:68844294::T 15369/28176) Row 77963465 (NC_000010.11:68844294:T: 316/28176) Row 77963466 (NC_000010.11:68844294::TT 61/28176)...	-	Oct 16, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 77963464 (NC_000010.11:68844294::T 15369/28176) Row 77963465 (NC_000010.11:68844294:T: 316/28176) Row 77963466 (NC_000010.11:68844294::TT 61/28176)...	-	Oct 16, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 77963464 (NC_000010.11:68844294::T 15369/28176) Row 77963465 (NC_000010.11:68844294:T: 316/28176) Row 77963466 (NC_000010.11:68844294::TT 61/28176)...	-	Oct 16, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 77963464 (NC_000010.11:68844294::T 15369/28176) Row 77963465 (NC_000010.11:68844294:T: 316/28176) Row 77963466 (NC_000010.11:68844294::TT 61/28176)...	-	Oct 16, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 77963464 (NC_000010.11:68844294::T 15369/28176) Row 77963465 (NC_000010.11:68844294:T: 316/28176) Row 77963466 (NC_000010.11:68844294::TT 61/28176)...	-	Oct 16, 2022 (156)
89	TopMed	NC_000010.11 - 68844295	Apr 26, 2021 (155)
90	UK 10K study - Twins Submission ignored due to conflicting rows: Row 27920385 (NC_000010.10:70604050::TT 2009/3708) Row 27920386 (NC_000010.10:70604050::TTT 1421/3708)	-	Oct 12, 2018 (152)
91	UK 10K study - Twins Submission ignored due to conflicting rows: Row 27920385 (NC_000010.10:70604050::TT 2009/3708) Row 27920386 (NC_000010.10:70604050::TTT 1421/3708)	-	Oct 12, 2018 (152)
92	ALFA	NC_000010.11 - 68844295	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
71932587, ss4856386932	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTT:	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss4220521834	NC_000010.11:68844294:TTTTTTTTTTTT:	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4220521833, ss5284452974	NC_000010.11:68844294:TTTTTTTTT:	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4220521832	NC_000010.11:68844294:TTTTTTTT:	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4220521831	NC_000010.11:68844294:TTTTTTT:	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4220521830	NC_000010.11:68844294:TTTTTT:	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3006667785	NC_000010.10:70604050:TTT:	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3690107743, ss4220521829, ss5479989963	NC_000010.11:68844294:TTT:	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4220521828, ss5284452972	NC_000010.11:68844294:TT:	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5198147882	NC_000010.10:70604050:T:	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4220521827, ss5284452971, ss5479989960, ss5744126361	NC_000010.11:68844294:T:	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3690107744	NC_000010.11:68844296:T:	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss294662510	NC_000010.9:70274057::T	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
29709856, ss3832186025, ss3922532462, ss5198147881	NC_000010.10:70604050::T	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4220521814, ss5284452970, ss5479989961, ss5744126360	NC_000010.11:68844294::T	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3690107745	NC_000010.11:68844297::T	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss95544828	NT_030059.13:21408535::T	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss1706787352, ss1706787668, ss5198147883, ss5824557750	NC_000010.10:70604050::TT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4220521815, ss5284452973, ss5479989962, ss5744126362	NC_000010.11:68844294::TT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3690107746	NC_000010.11:68844297::TT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1706787354, ss1706787669, ss5198147885, ss5824557751	NC_000010.10:70604050::TTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4220521816, ss5744126365	NC_000010.11:68844294::TTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5198147884	NC_000010.10:70604050::TTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4220521817, ss5744126364	NC_000010.11:68844294::TTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4220521818	NC_000010.11:68844294::TTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4220521819	NC_000010.11:68844294::TTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4220521820	NC_000010.11:68844294::TTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4220521821	NC_000010.11:68844294::TTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4220521822	NC_000010.11:68844294::TTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4782737513	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4220521823	NC_000010.11:68844294::TTTTTTTTTTT… NC_000010.11:68844294::TTTTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4220521824	NC_000010.11:68844294::TTTTTTTTTTT… NC_000010.11:68844294::TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4220521825	NC_000010.11:68844294::TTTTTTTTTTT… NC_000010.11:68844294::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:68844294:TTTTTTTTTTTT… NC_000010.11:68844294:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs777175392

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

rs777175392