Name: rs869150232
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.

rs869150232

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:100877420-100877441 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₁₃ / del(A)₁₂ / del(A)₁₀ / d…
del(A)₁₃ / del(A)₁₂ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₆ / dup(A)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₃=0.0000 (0/3624, ALFA)
del(A)₁₂=0.0000 (0/3624, ALFA)
del(A)₁₀=0.0000 (0/3624, ALFA) (+ 12 more)
del(A)₉=0.0000 (0/3624, ALFA)
del(A)₈=0.0000 (0/3624, ALFA)
del(A)₇=0.0000 (0/3624, ALFA)
del(A)₆=0.0000 (0/3624, ALFA)
del(A)₅=0.0000 (0/3624, ALFA)
del(A)₄=0.0000 (0/3624, ALFA)
delAAA=0.0000 (0/3624, ALFA)
delAA=0.0000 (0/3624, ALFA)
delA=0.0000 (0/3624, ALFA)
dupA=0.0000 (0/3624, ALFA)
dupAA=0.0000 (0/3624, ALFA)
dupAAA=0.0000 (0/3624, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SRRT : 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	3624	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	2352	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African	Sub	984	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	38	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	946	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	6	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	6	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	40	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	116	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	18	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	108	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=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	3624	(A)₂₂=1.0000	del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	2352	(A)₂₂=1.0000	del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	984	(A)₂₂=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	116	(A)₂₂=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	108	(A)₂₂=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	40	(A)₂₂=1.00	del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	18	(A)₂₂=1.00	del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	6	(A)₂₂=1.0	del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 7	NC_000007.14:g.100877429_100877441del
GRCh38.p14 chr 7	NC_000007.14:g.100877430_100877441del
GRCh38.p14 chr 7	NC_000007.14:g.100877432_100877441del
GRCh38.p14 chr 7	NC_000007.14:g.100877433_100877441del
GRCh38.p14 chr 7	NC_000007.14:g.100877434_100877441del
GRCh38.p14 chr 7	NC_000007.14:g.100877435_100877441del
GRCh38.p14 chr 7	NC_000007.14:g.100877436_100877441del
GRCh38.p14 chr 7	NC_000007.14:g.100877437_100877441del
GRCh38.p14 chr 7	NC_000007.14:g.100877438_100877441del
GRCh38.p14 chr 7	NC_000007.14:g.100877439_100877441del
GRCh38.p14 chr 7	NC_000007.14:g.100877440_100877441del
GRCh38.p14 chr 7	NC_000007.14:g.100877441del
GRCh38.p14 chr 7	NC_000007.14:g.100877441dup
GRCh38.p14 chr 7	NC_000007.14:g.100877440_100877441dup
GRCh38.p14 chr 7	NC_000007.14:g.100877439_100877441dup
GRCh38.p14 chr 7	NC_000007.14:g.100877438_100877441dup
GRCh38.p14 chr 7	NC_000007.14:g.100877436_100877441dup
GRCh38.p14 chr 7	NC_000007.14:g.100877432_100877441dup
GRCh37.p13 chr 7	NC_000007.13:g.100475050_100475062del
GRCh37.p13 chr 7	NC_000007.13:g.100475051_100475062del
GRCh37.p13 chr 7	NC_000007.13:g.100475053_100475062del
GRCh37.p13 chr 7	NC_000007.13:g.100475054_100475062del
GRCh37.p13 chr 7	NC_000007.13:g.100475055_100475062del
GRCh37.p13 chr 7	NC_000007.13:g.100475056_100475062del
GRCh37.p13 chr 7	NC_000007.13:g.100475057_100475062del
GRCh37.p13 chr 7	NC_000007.13:g.100475058_100475062del
GRCh37.p13 chr 7	NC_000007.13:g.100475059_100475062del
GRCh37.p13 chr 7	NC_000007.13:g.100475060_100475062del
GRCh37.p13 chr 7	NC_000007.13:g.100475061_100475062del
GRCh37.p13 chr 7	NC_000007.13:g.100475062del
GRCh37.p13 chr 7	NC_000007.13:g.100475062dup
GRCh37.p13 chr 7	NC_000007.13:g.100475061_100475062dup
GRCh37.p13 chr 7	NC_000007.13:g.100475060_100475062dup
GRCh37.p13 chr 7	NC_000007.13:g.100475059_100475062dup
GRCh37.p13 chr 7	NC_000007.13:g.100475057_100475062dup
GRCh37.p13 chr 7	NC_000007.13:g.100475053_100475062dup

Gene: SRRT, serrate, RNA effector molecule (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SRRT transcript variant 3	NM_001128852.2:c.122+1717… NM_001128852.2:c.122+1717_122+1729del	N/A	Intron Variant
SRRT transcript variant 4	NM_001128853.2:c.122+1717… NM_001128853.2:c.122+1717_122+1729del	N/A	Intron Variant
SRRT transcript variant 5	NM_001128854.2:c.122+1717… NM_001128854.2:c.122+1717_122+1729del	N/A	Intron Variant
SRRT transcript variant 1	NM_015908.6:c.122+1717_12… NM_015908.6:c.122+1717_122+1729del	N/A	Intron Variant
SRRT transcript variant X1	XM_005250405.3:c.143+1717… XM_005250405.3:c.143+1717_143+1729del	N/A	Intron Variant
SRRT transcript variant X2	XM_005250406.3:c.143+1717… XM_005250406.3:c.143+1717_143+1729del	N/A	Intron Variant
SRRT transcript variant X3	XM_005250407.3:c.143+1717… XM_005250407.3:c.143+1717_143+1729del	N/A	Intron Variant
SRRT transcript variant X4	XM_005250408.2:c.143+1717… XM_005250408.2:c.143+1717_143+1729del	N/A	Intron Variant
SRRT transcript variant X5	XM_047420459.1:c.-190+171… XM_047420459.1:c.-190+1717_-190+1729del	N/A	Intron Variant
SRRT transcript variant X6	XM_047420460.1:c.-190+171… XM_047420460.1:c.-190+1717_-190+1729del	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(A)₂₂=	del(A)₁₃	del(A)₁₂	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₆	dup(A)₁₀
GRCh38.p14 chr 7	NC_000007.14:g.100877420_100877441=	NC_000007.14:g.100877429_100877441del	NC_000007.14:g.100877430_100877441del	NC_000007.14:g.100877432_100877441del	NC_000007.14:g.100877433_100877441del	NC_000007.14:g.100877434_100877441del	NC_000007.14:g.100877435_100877441del	NC_000007.14:g.100877436_100877441del	NC_000007.14:g.100877437_100877441del	NC_000007.14:g.100877438_100877441del	NC_000007.14:g.100877439_100877441del	NC_000007.14:g.100877440_100877441del	NC_000007.14:g.100877441del	NC_000007.14:g.100877441dup	NC_000007.14:g.100877440_100877441dup	NC_000007.14:g.100877439_100877441dup	NC_000007.14:g.100877438_100877441dup	NC_000007.14:g.100877436_100877441dup	NC_000007.14:g.100877432_100877441dup
GRCh37.p13 chr 7	NC_000007.13:g.100475041_100475062=	NC_000007.13:g.100475050_100475062del	NC_000007.13:g.100475051_100475062del	NC_000007.13:g.100475053_100475062del	NC_000007.13:g.100475054_100475062del	NC_000007.13:g.100475055_100475062del	NC_000007.13:g.100475056_100475062del	NC_000007.13:g.100475057_100475062del	NC_000007.13:g.100475058_100475062del	NC_000007.13:g.100475059_100475062del	NC_000007.13:g.100475060_100475062del	NC_000007.13:g.100475061_100475062del	NC_000007.13:g.100475062del	NC_000007.13:g.100475062dup	NC_000007.13:g.100475061_100475062dup	NC_000007.13:g.100475060_100475062dup	NC_000007.13:g.100475059_100475062dup	NC_000007.13:g.100475057_100475062dup	NC_000007.13:g.100475053_100475062dup
SRRT transcript variant 3	NM_001128852.1:c.122+1708=	NM_001128852.1:c.122+1717_122+1729del	NM_001128852.1:c.122+1718_122+1729del	NM_001128852.1:c.122+1720_122+1729del	NM_001128852.1:c.122+1721_122+1729del	NM_001128852.1:c.122+1722_122+1729del	NM_001128852.1:c.122+1723_122+1729del	NM_001128852.1:c.122+1724_122+1729del	NM_001128852.1:c.122+1725_122+1729del	NM_001128852.1:c.122+1726_122+1729del	NM_001128852.1:c.122+1727_122+1729del	NM_001128852.1:c.122+1728_122+1729del	NM_001128852.1:c.122+1729del	NM_001128852.1:c.122+1729dup	NM_001128852.1:c.122+1728_122+1729dup	NM_001128852.1:c.122+1727_122+1729dup	NM_001128852.1:c.122+1726_122+1729dup	NM_001128852.1:c.122+1724_122+1729dup	NM_001128852.1:c.122+1720_122+1729dup
SRRT transcript variant 3	NM_001128852.2:c.122+1708=	NM_001128852.2:c.122+1717_122+1729del	NM_001128852.2:c.122+1718_122+1729del	NM_001128852.2:c.122+1720_122+1729del	NM_001128852.2:c.122+1721_122+1729del	NM_001128852.2:c.122+1722_122+1729del	NM_001128852.2:c.122+1723_122+1729del	NM_001128852.2:c.122+1724_122+1729del	NM_001128852.2:c.122+1725_122+1729del	NM_001128852.2:c.122+1726_122+1729del	NM_001128852.2:c.122+1727_122+1729del	NM_001128852.2:c.122+1728_122+1729del	NM_001128852.2:c.122+1729del	NM_001128852.2:c.122+1729dup	NM_001128852.2:c.122+1728_122+1729dup	NM_001128852.2:c.122+1727_122+1729dup	NM_001128852.2:c.122+1726_122+1729dup	NM_001128852.2:c.122+1724_122+1729dup	NM_001128852.2:c.122+1720_122+1729dup
SRRT transcript variant 4	NM_001128853.1:c.122+1708=	NM_001128853.1:c.122+1717_122+1729del	NM_001128853.1:c.122+1718_122+1729del	NM_001128853.1:c.122+1720_122+1729del	NM_001128853.1:c.122+1721_122+1729del	NM_001128853.1:c.122+1722_122+1729del	NM_001128853.1:c.122+1723_122+1729del	NM_001128853.1:c.122+1724_122+1729del	NM_001128853.1:c.122+1725_122+1729del	NM_001128853.1:c.122+1726_122+1729del	NM_001128853.1:c.122+1727_122+1729del	NM_001128853.1:c.122+1728_122+1729del	NM_001128853.1:c.122+1729del	NM_001128853.1:c.122+1729dup	NM_001128853.1:c.122+1728_122+1729dup	NM_001128853.1:c.122+1727_122+1729dup	NM_001128853.1:c.122+1726_122+1729dup	NM_001128853.1:c.122+1724_122+1729dup	NM_001128853.1:c.122+1720_122+1729dup
SRRT transcript variant 4	NM_001128853.2:c.122+1708=	NM_001128853.2:c.122+1717_122+1729del	NM_001128853.2:c.122+1718_122+1729del	NM_001128853.2:c.122+1720_122+1729del	NM_001128853.2:c.122+1721_122+1729del	NM_001128853.2:c.122+1722_122+1729del	NM_001128853.2:c.122+1723_122+1729del	NM_001128853.2:c.122+1724_122+1729del	NM_001128853.2:c.122+1725_122+1729del	NM_001128853.2:c.122+1726_122+1729del	NM_001128853.2:c.122+1727_122+1729del	NM_001128853.2:c.122+1728_122+1729del	NM_001128853.2:c.122+1729del	NM_001128853.2:c.122+1729dup	NM_001128853.2:c.122+1728_122+1729dup	NM_001128853.2:c.122+1727_122+1729dup	NM_001128853.2:c.122+1726_122+1729dup	NM_001128853.2:c.122+1724_122+1729dup	NM_001128853.2:c.122+1720_122+1729dup
SRRT transcript variant 5	NM_001128854.1:c.122+1708=	NM_001128854.1:c.122+1717_122+1729del	NM_001128854.1:c.122+1718_122+1729del	NM_001128854.1:c.122+1720_122+1729del	NM_001128854.1:c.122+1721_122+1729del	NM_001128854.1:c.122+1722_122+1729del	NM_001128854.1:c.122+1723_122+1729del	NM_001128854.1:c.122+1724_122+1729del	NM_001128854.1:c.122+1725_122+1729del	NM_001128854.1:c.122+1726_122+1729del	NM_001128854.1:c.122+1727_122+1729del	NM_001128854.1:c.122+1728_122+1729del	NM_001128854.1:c.122+1729del	NM_001128854.1:c.122+1729dup	NM_001128854.1:c.122+1728_122+1729dup	NM_001128854.1:c.122+1727_122+1729dup	NM_001128854.1:c.122+1726_122+1729dup	NM_001128854.1:c.122+1724_122+1729dup	NM_001128854.1:c.122+1720_122+1729dup
SRRT transcript variant 5	NM_001128854.2:c.122+1708=	NM_001128854.2:c.122+1717_122+1729del	NM_001128854.2:c.122+1718_122+1729del	NM_001128854.2:c.122+1720_122+1729del	NM_001128854.2:c.122+1721_122+1729del	NM_001128854.2:c.122+1722_122+1729del	NM_001128854.2:c.122+1723_122+1729del	NM_001128854.2:c.122+1724_122+1729del	NM_001128854.2:c.122+1725_122+1729del	NM_001128854.2:c.122+1726_122+1729del	NM_001128854.2:c.122+1727_122+1729del	NM_001128854.2:c.122+1728_122+1729del	NM_001128854.2:c.122+1729del	NM_001128854.2:c.122+1729dup	NM_001128854.2:c.122+1728_122+1729dup	NM_001128854.2:c.122+1727_122+1729dup	NM_001128854.2:c.122+1726_122+1729dup	NM_001128854.2:c.122+1724_122+1729dup	NM_001128854.2:c.122+1720_122+1729dup
SRRT transcript variant 1	NM_015908.5:c.122+1708=	NM_015908.5:c.122+1717_122+1729del	NM_015908.5:c.122+1718_122+1729del	NM_015908.5:c.122+1720_122+1729del	NM_015908.5:c.122+1721_122+1729del	NM_015908.5:c.122+1722_122+1729del	NM_015908.5:c.122+1723_122+1729del	NM_015908.5:c.122+1724_122+1729del	NM_015908.5:c.122+1725_122+1729del	NM_015908.5:c.122+1726_122+1729del	NM_015908.5:c.122+1727_122+1729del	NM_015908.5:c.122+1728_122+1729del	NM_015908.5:c.122+1729del	NM_015908.5:c.122+1729dup	NM_015908.5:c.122+1728_122+1729dup	NM_015908.5:c.122+1727_122+1729dup	NM_015908.5:c.122+1726_122+1729dup	NM_015908.5:c.122+1724_122+1729dup	NM_015908.5:c.122+1720_122+1729dup
SRRT transcript variant 1	NM_015908.6:c.122+1708=	NM_015908.6:c.122+1717_122+1729del	NM_015908.6:c.122+1718_122+1729del	NM_015908.6:c.122+1720_122+1729del	NM_015908.6:c.122+1721_122+1729del	NM_015908.6:c.122+1722_122+1729del	NM_015908.6:c.122+1723_122+1729del	NM_015908.6:c.122+1724_122+1729del	NM_015908.6:c.122+1725_122+1729del	NM_015908.6:c.122+1726_122+1729del	NM_015908.6:c.122+1727_122+1729del	NM_015908.6:c.122+1728_122+1729del	NM_015908.6:c.122+1729del	NM_015908.6:c.122+1729dup	NM_015908.6:c.122+1728_122+1729dup	NM_015908.6:c.122+1727_122+1729dup	NM_015908.6:c.122+1726_122+1729dup	NM_015908.6:c.122+1724_122+1729dup	NM_015908.6:c.122+1720_122+1729dup
SRRT transcript variant X1	XM_005250404.1:c.143+1708=	XM_005250404.1:c.143+1717_143+1729del	XM_005250404.1:c.143+1718_143+1729del	XM_005250404.1:c.143+1720_143+1729del	XM_005250404.1:c.143+1721_143+1729del	XM_005250404.1:c.143+1722_143+1729del	XM_005250404.1:c.143+1723_143+1729del	XM_005250404.1:c.143+1724_143+1729del	XM_005250404.1:c.143+1725_143+1729del	XM_005250404.1:c.143+1726_143+1729del	XM_005250404.1:c.143+1727_143+1729del	XM_005250404.1:c.143+1728_143+1729del	XM_005250404.1:c.143+1729del	XM_005250404.1:c.143+1729dup	XM_005250404.1:c.143+1728_143+1729dup	XM_005250404.1:c.143+1727_143+1729dup	XM_005250404.1:c.143+1726_143+1729dup	XM_005250404.1:c.143+1724_143+1729dup	XM_005250404.1:c.143+1720_143+1729dup
SRRT transcript variant X1	XM_005250405.1:c.143+1708=	XM_005250405.1:c.143+1717_143+1729del	XM_005250405.1:c.143+1718_143+1729del	XM_005250405.1:c.143+1720_143+1729del	XM_005250405.1:c.143+1721_143+1729del	XM_005250405.1:c.143+1722_143+1729del	XM_005250405.1:c.143+1723_143+1729del	XM_005250405.1:c.143+1724_143+1729del	XM_005250405.1:c.143+1725_143+1729del	XM_005250405.1:c.143+1726_143+1729del	XM_005250405.1:c.143+1727_143+1729del	XM_005250405.1:c.143+1728_143+1729del	XM_005250405.1:c.143+1729del	XM_005250405.1:c.143+1729dup	XM_005250405.1:c.143+1728_143+1729dup	XM_005250405.1:c.143+1727_143+1729dup	XM_005250405.1:c.143+1726_143+1729dup	XM_005250405.1:c.143+1724_143+1729dup	XM_005250405.1:c.143+1720_143+1729dup
SRRT transcript variant X1	XM_005250405.3:c.143+1708=	XM_005250405.3:c.143+1717_143+1729del	XM_005250405.3:c.143+1718_143+1729del	XM_005250405.3:c.143+1720_143+1729del	XM_005250405.3:c.143+1721_143+1729del	XM_005250405.3:c.143+1722_143+1729del	XM_005250405.3:c.143+1723_143+1729del	XM_005250405.3:c.143+1724_143+1729del	XM_005250405.3:c.143+1725_143+1729del	XM_005250405.3:c.143+1726_143+1729del	XM_005250405.3:c.143+1727_143+1729del	XM_005250405.3:c.143+1728_143+1729del	XM_005250405.3:c.143+1729del	XM_005250405.3:c.143+1729dup	XM_005250405.3:c.143+1728_143+1729dup	XM_005250405.3:c.143+1727_143+1729dup	XM_005250405.3:c.143+1726_143+1729dup	XM_005250405.3:c.143+1724_143+1729dup	XM_005250405.3:c.143+1720_143+1729dup
SRRT transcript variant X2	XM_005250406.1:c.143+1708=	XM_005250406.1:c.143+1717_143+1729del	XM_005250406.1:c.143+1718_143+1729del	XM_005250406.1:c.143+1720_143+1729del	XM_005250406.1:c.143+1721_143+1729del	XM_005250406.1:c.143+1722_143+1729del	XM_005250406.1:c.143+1723_143+1729del	XM_005250406.1:c.143+1724_143+1729del	XM_005250406.1:c.143+1725_143+1729del	XM_005250406.1:c.143+1726_143+1729del	XM_005250406.1:c.143+1727_143+1729del	XM_005250406.1:c.143+1728_143+1729del	XM_005250406.1:c.143+1729del	XM_005250406.1:c.143+1729dup	XM_005250406.1:c.143+1728_143+1729dup	XM_005250406.1:c.143+1727_143+1729dup	XM_005250406.1:c.143+1726_143+1729dup	XM_005250406.1:c.143+1724_143+1729dup	XM_005250406.1:c.143+1720_143+1729dup
SRRT transcript variant X2	XM_005250406.3:c.143+1708=	XM_005250406.3:c.143+1717_143+1729del	XM_005250406.3:c.143+1718_143+1729del	XM_005250406.3:c.143+1720_143+1729del	XM_005250406.3:c.143+1721_143+1729del	XM_005250406.3:c.143+1722_143+1729del	XM_005250406.3:c.143+1723_143+1729del	XM_005250406.3:c.143+1724_143+1729del	XM_005250406.3:c.143+1725_143+1729del	XM_005250406.3:c.143+1726_143+1729del	XM_005250406.3:c.143+1727_143+1729del	XM_005250406.3:c.143+1728_143+1729del	XM_005250406.3:c.143+1729del	XM_005250406.3:c.143+1729dup	XM_005250406.3:c.143+1728_143+1729dup	XM_005250406.3:c.143+1727_143+1729dup	XM_005250406.3:c.143+1726_143+1729dup	XM_005250406.3:c.143+1724_143+1729dup	XM_005250406.3:c.143+1720_143+1729dup
SRRT transcript variant X3	XM_005250407.1:c.143+1708=	XM_005250407.1:c.143+1717_143+1729del	XM_005250407.1:c.143+1718_143+1729del	XM_005250407.1:c.143+1720_143+1729del	XM_005250407.1:c.143+1721_143+1729del	XM_005250407.1:c.143+1722_143+1729del	XM_005250407.1:c.143+1723_143+1729del	XM_005250407.1:c.143+1724_143+1729del	XM_005250407.1:c.143+1725_143+1729del	XM_005250407.1:c.143+1726_143+1729del	XM_005250407.1:c.143+1727_143+1729del	XM_005250407.1:c.143+1728_143+1729del	XM_005250407.1:c.143+1729del	XM_005250407.1:c.143+1729dup	XM_005250407.1:c.143+1728_143+1729dup	XM_005250407.1:c.143+1727_143+1729dup	XM_005250407.1:c.143+1726_143+1729dup	XM_005250407.1:c.143+1724_143+1729dup	XM_005250407.1:c.143+1720_143+1729dup
SRRT transcript variant X3	XM_005250407.3:c.143+1708=	XM_005250407.3:c.143+1717_143+1729del	XM_005250407.3:c.143+1718_143+1729del	XM_005250407.3:c.143+1720_143+1729del	XM_005250407.3:c.143+1721_143+1729del	XM_005250407.3:c.143+1722_143+1729del	XM_005250407.3:c.143+1723_143+1729del	XM_005250407.3:c.143+1724_143+1729del	XM_005250407.3:c.143+1725_143+1729del	XM_005250407.3:c.143+1726_143+1729del	XM_005250407.3:c.143+1727_143+1729del	XM_005250407.3:c.143+1728_143+1729del	XM_005250407.3:c.143+1729del	XM_005250407.3:c.143+1729dup	XM_005250407.3:c.143+1728_143+1729dup	XM_005250407.3:c.143+1727_143+1729dup	XM_005250407.3:c.143+1726_143+1729dup	XM_005250407.3:c.143+1724_143+1729dup	XM_005250407.3:c.143+1720_143+1729dup
SRRT transcript variant X4	XM_005250408.1:c.143+1708=	XM_005250408.1:c.143+1717_143+1729del	XM_005250408.1:c.143+1718_143+1729del	XM_005250408.1:c.143+1720_143+1729del	XM_005250408.1:c.143+1721_143+1729del	XM_005250408.1:c.143+1722_143+1729del	XM_005250408.1:c.143+1723_143+1729del	XM_005250408.1:c.143+1724_143+1729del	XM_005250408.1:c.143+1725_143+1729del	XM_005250408.1:c.143+1726_143+1729del	XM_005250408.1:c.143+1727_143+1729del	XM_005250408.1:c.143+1728_143+1729del	XM_005250408.1:c.143+1729del	XM_005250408.1:c.143+1729dup	XM_005250408.1:c.143+1728_143+1729dup	XM_005250408.1:c.143+1727_143+1729dup	XM_005250408.1:c.143+1726_143+1729dup	XM_005250408.1:c.143+1724_143+1729dup	XM_005250408.1:c.143+1720_143+1729dup
SRRT transcript variant X4	XM_005250408.2:c.143+1708=	XM_005250408.2:c.143+1717_143+1729del	XM_005250408.2:c.143+1718_143+1729del	XM_005250408.2:c.143+1720_143+1729del	XM_005250408.2:c.143+1721_143+1729del	XM_005250408.2:c.143+1722_143+1729del	XM_005250408.2:c.143+1723_143+1729del	XM_005250408.2:c.143+1724_143+1729del	XM_005250408.2:c.143+1725_143+1729del	XM_005250408.2:c.143+1726_143+1729del	XM_005250408.2:c.143+1727_143+1729del	XM_005250408.2:c.143+1728_143+1729del	XM_005250408.2:c.143+1729del	XM_005250408.2:c.143+1729dup	XM_005250408.2:c.143+1728_143+1729dup	XM_005250408.2:c.143+1727_143+1729dup	XM_005250408.2:c.143+1726_143+1729dup	XM_005250408.2:c.143+1724_143+1729dup	XM_005250408.2:c.143+1720_143+1729dup
SRRT transcript variant X5	XM_047420459.1:c.-190+1708=	XM_047420459.1:c.-190+1717_-190+1729del	XM_047420459.1:c.-190+1718_-190+1729del	XM_047420459.1:c.-190+1720_-190+1729del	XM_047420459.1:c.-190+1721_-190+1729del	XM_047420459.1:c.-190+1722_-190+1729del	XM_047420459.1:c.-190+1723_-190+1729del	XM_047420459.1:c.-190+1724_-190+1729del	XM_047420459.1:c.-190+1725_-190+1729del	XM_047420459.1:c.-190+1726_-190+1729del	XM_047420459.1:c.-190+1727_-190+1729del	XM_047420459.1:c.-190+1728_-190+1729del	XM_047420459.1:c.-190+1729del	XM_047420459.1:c.-190+1729dup	XM_047420459.1:c.-190+1728_-190+1729dup	XM_047420459.1:c.-190+1727_-190+1729dup	XM_047420459.1:c.-190+1726_-190+1729dup	XM_047420459.1:c.-190+1724_-190+1729dup	XM_047420459.1:c.-190+1720_-190+1729dup
SRRT transcript variant X6	XM_047420460.1:c.-190+1708=	XM_047420460.1:c.-190+1717_-190+1729del	XM_047420460.1:c.-190+1718_-190+1729del	XM_047420460.1:c.-190+1720_-190+1729del	XM_047420460.1:c.-190+1721_-190+1729del	XM_047420460.1:c.-190+1722_-190+1729del	XM_047420460.1:c.-190+1723_-190+1729del	XM_047420460.1:c.-190+1724_-190+1729del	XM_047420460.1:c.-190+1725_-190+1729del	XM_047420460.1:c.-190+1726_-190+1729del	XM_047420460.1:c.-190+1727_-190+1729del	XM_047420460.1:c.-190+1728_-190+1729del	XM_047420460.1:c.-190+1729del	XM_047420460.1:c.-190+1729dup	XM_047420460.1:c.-190+1728_-190+1729dup	XM_047420460.1:c.-190+1727_-190+1729dup	XM_047420460.1:c.-190+1726_-190+1729dup	XM_047420460.1:c.-190+1724_-190+1729dup	XM_047420460.1:c.-190+1720_-190+1729dup

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#.

46 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4279356	Mar 15, 2016 (147)
2	MCHAISSO	ss3065150226	Jan 10, 2018 (151)
3	URBANLAB	ss3648712163	Oct 12, 2018 (152)
4	EVA_DECODE	ss3720316532	Jul 13, 2019 (153)
5	EVA_DECODE	ss3720316533	Jul 13, 2019 (153)
6	EVA_DECODE	ss3720316534	Jul 13, 2019 (153)
7	EVA_DECODE	ss3720316535	Jul 13, 2019 (153)
8	PACBIO	ss3791194689	Jul 13, 2019 (153)
9	PACBIO	ss3791194690	Jul 13, 2019 (153)
10	PACBIO	ss3791194691	Jul 13, 2019 (153)
11	PACBIO	ss3796074686	Jul 13, 2019 (153)
12	PACBIO	ss3796074687	Jul 13, 2019 (153)
13	PACBIO	ss3796074688	Jul 13, 2019 (153)
14	EVA	ss3830725510	Apr 26, 2020 (154)
15	GNOMAD	ss4169550856	Apr 26, 2021 (155)
16	GNOMAD	ss4169550857	Apr 26, 2021 (155)
17	GNOMAD	ss4169550858	Apr 26, 2021 (155)
18	GNOMAD	ss4169550859	Apr 26, 2021 (155)
19	GNOMAD	ss4169550860	Apr 26, 2021 (155)
20	GNOMAD	ss4169550861	Apr 26, 2021 (155)
21	GNOMAD	ss4169550862	Apr 26, 2021 (155)
22	GNOMAD	ss4169550863	Apr 26, 2021 (155)
23	GNOMAD	ss4169550864	Apr 26, 2021 (155)
24	GNOMAD	ss4169550865	Apr 26, 2021 (155)
25	GNOMAD	ss4169550866	Apr 26, 2021 (155)
26	GNOMAD	ss4169550867	Apr 26, 2021 (155)
27	GNOMAD	ss4169550868	Apr 26, 2021 (155)
28	GNOMAD	ss4169550869	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5184704379	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5184704380	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5184704381	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5184704382	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5184704383	Apr 26, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5274061123	Oct 13, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5274061124	Oct 13, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5274061125	Oct 13, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5274061127	Oct 13, 2022 (156)
38	HUGCELL_USP	ss5471026985	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5471026986	Oct 13, 2022 (156)
40	HUGCELL_USP	ss5471026987	Oct 13, 2022 (156)
41	HUGCELL_USP	ss5471026988	Oct 13, 2022 (156)
42	HUGCELL_USP	ss5471026989	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5725431551	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5725431552	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5725431553	Oct 13, 2022 (156)
46	TOMMO_GENOMICS	ss5725431555	Oct 13, 2022 (156)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270895927 (NC_000007.14:100877419::A 1168/65236) Row 270895928 (NC_000007.14:100877419::AA 94/65264) Row 270895929 (NC_000007.14:100877419::AAA 34/65354)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270895927 (NC_000007.14:100877419::A 1168/65236) Row 270895928 (NC_000007.14:100877419::AA 94/65264) Row 270895929 (NC_000007.14:100877419::AAA 34/65354)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270895927 (NC_000007.14:100877419::A 1168/65236) Row 270895928 (NC_000007.14:100877419::AA 94/65264) Row 270895929 (NC_000007.14:100877419::AAA 34/65354)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270895927 (NC_000007.14:100877419::A 1168/65236) Row 270895928 (NC_000007.14:100877419::AA 94/65264) Row 270895929 (NC_000007.14:100877419::AAA 34/65354)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270895927 (NC_000007.14:100877419::A 1168/65236) Row 270895928 (NC_000007.14:100877419::AA 94/65264) Row 270895929 (NC_000007.14:100877419::AAA 34/65354)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270895927 (NC_000007.14:100877419::A 1168/65236) Row 270895928 (NC_000007.14:100877419::AA 94/65264) Row 270895929 (NC_000007.14:100877419::AAA 34/65354)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270895927 (NC_000007.14:100877419::A 1168/65236) Row 270895928 (NC_000007.14:100877419::AA 94/65264) Row 270895929 (NC_000007.14:100877419::AAA 34/65354)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270895927 (NC_000007.14:100877419::A 1168/65236) Row 270895928 (NC_000007.14:100877419::AA 94/65264) Row 270895929 (NC_000007.14:100877419::AAA 34/65354)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270895927 (NC_000007.14:100877419::A 1168/65236) Row 270895928 (NC_000007.14:100877419::AA 94/65264) Row 270895929 (NC_000007.14:100877419::AAA 34/65354)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270895927 (NC_000007.14:100877419::A 1168/65236) Row 270895928 (NC_000007.14:100877419::AA 94/65264) Row 270895929 (NC_000007.14:100877419::AAA 34/65354)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270895927 (NC_000007.14:100877419::A 1168/65236) Row 270895928 (NC_000007.14:100877419::AA 94/65264) Row 270895929 (NC_000007.14:100877419::AAA 34/65354)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270895927 (NC_000007.14:100877419::A 1168/65236) Row 270895928 (NC_000007.14:100877419::AA 94/65264) Row 270895929 (NC_000007.14:100877419::AAA 34/65354)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270895927 (NC_000007.14:100877419::A 1168/65236) Row 270895928 (NC_000007.14:100877419::AA 94/65264) Row 270895929 (NC_000007.14:100877419::AAA 34/65354)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270895927 (NC_000007.14:100877419::A 1168/65236) Row 270895928 (NC_000007.14:100877419::AA 94/65264) Row 270895929 (NC_000007.14:100877419::AAA 34/65354)...	-	Apr 26, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 42673686 (NC_000007.13:100475040:AAA: 8958/16360) Row 42673687 (NC_000007.13:100475040:AAAAAAA: 70/16360) Row 42673688 (NC_000007.13:100475040:AA: 25/16360)...	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 42673686 (NC_000007.13:100475040:AAA: 8958/16360) Row 42673687 (NC_000007.13:100475040:AAAAAAA: 70/16360) Row 42673688 (NC_000007.13:100475040:AA: 25/16360)...	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 42673686 (NC_000007.13:100475040:AAA: 8958/16360) Row 42673687 (NC_000007.13:100475040:AAAAAAA: 70/16360) Row 42673688 (NC_000007.13:100475040:AA: 25/16360)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 42673686 (NC_000007.13:100475040:AAA: 8958/16360) Row 42673687 (NC_000007.13:100475040:AAAAAAA: 70/16360) Row 42673688 (NC_000007.13:100475040:AA: 25/16360)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 42673686 (NC_000007.13:100475040:AAA: 8958/16360) Row 42673687 (NC_000007.13:100475040:AAAAAAA: 70/16360) Row 42673688 (NC_000007.13:100475040:AA: 25/16360)...	-	Apr 26, 2021 (155)
66	14KJPN Submission ignored due to conflicting rows: Row 59268655 (NC_000007.14:100877419:AAA: 18890/27958) Row 59268656 (NC_000007.14:100877419:AAAAAAA: 126/27958) Row 59268657 (NC_000007.14:100877419:AA: 65/27958)...	-	Oct 13, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 59268655 (NC_000007.14:100877419:AAA: 18890/27958) Row 59268656 (NC_000007.14:100877419:AAAAAAA: 126/27958) Row 59268657 (NC_000007.14:100877419:AA: 65/27958)...	-	Oct 13, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 59268655 (NC_000007.14:100877419:AAA: 18890/27958) Row 59268656 (NC_000007.14:100877419:AAAAAAA: 126/27958) Row 59268657 (NC_000007.14:100877419:AA: 65/27958)...	-	Oct 13, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 59268655 (NC_000007.14:100877419:AAA: 18890/27958) Row 59268656 (NC_000007.14:100877419:AAAAAAA: 126/27958) Row 59268657 (NC_000007.14:100877419:AA: 65/27958)...	-	Oct 13, 2022 (156)
70	ALFA	NC_000007.14 - 100877420	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
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4169550869	NC_000007.14:100877419:AAAAAAAAAA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5184704380	NC_000007.13:100475040:AAAAAAA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4169550868, ss5725431552	NC_000007.14:100877419:AAAAAAA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4169550867	NC_000007.14:100877419:AAAAAA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5184704383	NC_000007.13:100475040:AAAAA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4169550866	NC_000007.14:100877419:AAAAA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5184704382	NC_000007.13:100475040:AAAA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3720316535, ss4169550865, ss5274061127, ss5471026985, ss5725431555	NC_000007.14:100877419:AAAA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3830725510, ss5184704379	NC_000007.13:100475040:AAA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4169550864, ss5471026986, ss5725431551	NC_000007.14:100877419:AAA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3720316534	NC_000007.14:100877420:AAA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4279356	NT_007933.15:38507883:AAA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3791194689, ss3796074686, ss5184704381	NC_000007.13:100475040:AA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3648712163, ss4169550863, ss5274061123, ss5471026987, ss5725431553	NC_000007.14:100877419:AA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3720316533	NC_000007.14:100877421:AA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3791194690, ss3796074687	NC_000007.13:100475040:A:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4169550862, ss5274061124, ss5471026988	NC_000007.14:100877419:A:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3720316532	NC_000007.14:100877422:A:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3791194691, ss3796074688	NC_000007.13:100475040::A	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3065150226, ss4169550856, ss5274061125, ss5471026989	NC_000007.14:100877419::A	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4169550857	NC_000007.14:100877419::AA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4169550858	NC_000007.14:100877419::AAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
12437153499	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4169550859	NC_000007.14:100877419::AAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4169550860	NC_000007.14:100877419::AAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4169550861	NC_000007.14:100877419::AAAAAAAAAA	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3539244635	NC_000007.14:100877419:AAAAAAAAA:	NC_000007.14:100877419:AAAAAAAAAAA… NC_000007.14:100877419:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs869150232

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

rs869150232