Name: rs1162225428
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.

rs1162225428

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:148334428-148334448 (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)₁₁ / del(A)₈ / del(A)₇ / del…
del(A)₁₁ / del(A)₈ / del(A)₇ / del(A)₅ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₁₃
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₁=0.000 (0/828, ALFA)
del(A)₈=0.000 (0/828, ALFA)
del(A)₇=0.000 (0/828, ALFA) (+ 9 more)
del(A)₅=0.000 (0/828, ALFA)
delAAA=0.000 (0/828, ALFA)
delAA=0.000 (0/828, ALFA)
delA=0.000 (0/828, ALFA)
dupA=0.000 (0/828, ALFA)
dupAA=0.000 (0/828, ALFA)
dupAAA=0.000 (0/828, ALFA)
dup(A)₄=0.000 (0/828, ALFA)
dup(A)₅=0.000 (0/828, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SASH1 : 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	828	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	440	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	316	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	18	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	298	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	14	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	12	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	6	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	36	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	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	828	(A)₂₁=1.000	del(A)₁₁=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	European	Sub	440	(A)₂₁=1.000	del(A)₁₁=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	African	Sub	316	(A)₂₁=1.000	del(A)₁₁=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Other	Sub	36	(A)₂₁=1.00	del(A)₁₁=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	14	(A)₂₁=1.00	del(A)₁₁=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 2	Sub	12	(A)₂₁=1.00	del(A)₁₁=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	6	(A)₂₁=1.0	del(A)₁₁=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₅=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0
Allele Frequency Aggregator	Asian	Sub	4	(A)₂₁=1.0	del(A)₁₁=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₅=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=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 6	NC_000006.12:g.148334438_148334448del
GRCh38.p14 chr 6	NC_000006.12:g.148334441_148334448del
GRCh38.p14 chr 6	NC_000006.12:g.148334442_148334448del
GRCh38.p14 chr 6	NC_000006.12:g.148334444_148334448del
GRCh38.p14 chr 6	NC_000006.12:g.148334446_148334448del
GRCh38.p14 chr 6	NC_000006.12:g.148334447_148334448del
GRCh38.p14 chr 6	NC_000006.12:g.148334448del
GRCh38.p14 chr 6	NC_000006.12:g.148334448dup
GRCh38.p14 chr 6	NC_000006.12:g.148334447_148334448dup
GRCh38.p14 chr 6	NC_000006.12:g.148334446_148334448dup
GRCh38.p14 chr 6	NC_000006.12:g.148334445_148334448dup
GRCh38.p14 chr 6	NC_000006.12:g.148334444_148334448dup
GRCh38.p14 chr 6	NC_000006.12:g.148334443_148334448dup
GRCh38.p14 chr 6	NC_000006.12:g.148334436_148334448dup
GRCh37.p13 chr 6	NC_000006.11:g.148655574_148655584del
GRCh37.p13 chr 6	NC_000006.11:g.148655577_148655584del
GRCh37.p13 chr 6	NC_000006.11:g.148655578_148655584del
GRCh37.p13 chr 6	NC_000006.11:g.148655580_148655584del
GRCh37.p13 chr 6	NC_000006.11:g.148655582_148655584del
GRCh37.p13 chr 6	NC_000006.11:g.148655583_148655584del
GRCh37.p13 chr 6	NC_000006.11:g.148655584del
GRCh37.p13 chr 6	NC_000006.11:g.148655584dup
GRCh37.p13 chr 6	NC_000006.11:g.148655583_148655584dup
GRCh37.p13 chr 6	NC_000006.11:g.148655582_148655584dup
GRCh37.p13 chr 6	NC_000006.11:g.148655581_148655584dup
GRCh37.p13 chr 6	NC_000006.11:g.148655580_148655584dup
GRCh37.p13 chr 6	NC_000006.11:g.148655579_148655584dup
GRCh37.p13 chr 6	NC_000006.11:g.148655572_148655584dup
SASH1 RefSeqGene	NG_051927.1:g.67163_67173del
SASH1 RefSeqGene	NG_051927.1:g.67166_67173del
SASH1 RefSeqGene	NG_051927.1:g.67167_67173del
SASH1 RefSeqGene	NG_051927.1:g.67169_67173del
SASH1 RefSeqGene	NG_051927.1:g.67171_67173del
SASH1 RefSeqGene	NG_051927.1:g.67172_67173del
SASH1 RefSeqGene	NG_051927.1:g.67173del
SASH1 RefSeqGene	NG_051927.1:g.67173dup
SASH1 RefSeqGene	NG_051927.1:g.67172_67173dup
SASH1 RefSeqGene	NG_051927.1:g.67171_67173dup
SASH1 RefSeqGene	NG_051927.1:g.67170_67173dup
SASH1 RefSeqGene	NG_051927.1:g.67169_67173dup
SASH1 RefSeqGene	NG_051927.1:g.67168_67173dup
SASH1 RefSeqGene	NG_051927.1:g.67161_67173dup

Gene: SASH1, SAM and SH3 domain containing 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SASH1 transcript variant 2	NM_001346505.2:c.22-55696… NM_001346505.2:c.22-55696_22-55686del	N/A	Intron Variant
SASH1 transcript variant 3	NM_001346506.2:c.	N/A	Genic Upstream Transcript Variant
SASH1 transcript variant 4	NM_001346507.2:c.	N/A	Genic Upstream Transcript Variant
SASH1 transcript variant 5	NM_001346508.2:c.	N/A	Genic Upstream Transcript Variant
SASH1 transcript variant 6	NM_001346509.2:c.	N/A	Genic Upstream Transcript Variant
SASH1 transcript variant 1	NM_015278.5:c.	N/A	Genic Upstream Transcript Variant
SASH1 transcript variant X2	XM_017010599.2:c.46-55696… XM_017010599.2:c.46-55696_46-55686del	N/A	Intron Variant
SASH1 transcript variant X3	XM_017010600.2:c.22-55696… XM_017010600.2:c.22-55696_22-55686del	N/A	Intron Variant
SASH1 transcript variant X9	XM_024446384.2:c.46-55696… XM_024446384.2:c.46-55696_46-55686del	N/A	Intron Variant
SASH1 transcript variant X5	XM_047418497.1:c.-22-5569… XM_047418497.1:c.-22-55696_-22-55686del	N/A	Intron Variant
SASH1 transcript variant X1	XM_017010598.3:c.	N/A	Genic Upstream Transcript Variant
SASH1 transcript variant X6	XM_017010605.2:c.	N/A	Genic Upstream Transcript Variant
SASH1 transcript variant X10	XM_024446385.2:c.	N/A	Genic Upstream Transcript Variant
SASH1 transcript variant X4	XM_047418496.1:c.	N/A	Genic Upstream Transcript Variant
SASH1 transcript variant X7	XM_047418498.1:c.	N/A	Genic Upstream Transcript Variant
SASH1 transcript variant X8	XM_047418499.1:c.	N/A	Genic Upstream Transcript Variant
SASH1 transcript variant X11	XM_047418500.1:c.	N/A	Genic Upstream Transcript 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)₂₁=	del(A)₁₁	del(A)₈	del(A)₇	del(A)₅	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₁₃
GRCh38.p14 chr 6	NC_000006.12:g.148334428_148334448=	NC_000006.12:g.148334438_148334448del	NC_000006.12:g.148334441_148334448del	NC_000006.12:g.148334442_148334448del	NC_000006.12:g.148334444_148334448del	NC_000006.12:g.148334446_148334448del	NC_000006.12:g.148334447_148334448del	NC_000006.12:g.148334448del	NC_000006.12:g.148334448dup	NC_000006.12:g.148334447_148334448dup	NC_000006.12:g.148334446_148334448dup	NC_000006.12:g.148334445_148334448dup	NC_000006.12:g.148334444_148334448dup	NC_000006.12:g.148334443_148334448dup	NC_000006.12:g.148334436_148334448dup
GRCh37.p13 chr 6	NC_000006.11:g.148655564_148655584=	NC_000006.11:g.148655574_148655584del	NC_000006.11:g.148655577_148655584del	NC_000006.11:g.148655578_148655584del	NC_000006.11:g.148655580_148655584del	NC_000006.11:g.148655582_148655584del	NC_000006.11:g.148655583_148655584del	NC_000006.11:g.148655584del	NC_000006.11:g.148655584dup	NC_000006.11:g.148655583_148655584dup	NC_000006.11:g.148655582_148655584dup	NC_000006.11:g.148655581_148655584dup	NC_000006.11:g.148655580_148655584dup	NC_000006.11:g.148655579_148655584dup	NC_000006.11:g.148655572_148655584dup
SASH1 RefSeqGene	NG_051927.1:g.67153_67173=	NG_051927.1:g.67163_67173del	NG_051927.1:g.67166_67173del	NG_051927.1:g.67167_67173del	NG_051927.1:g.67169_67173del	NG_051927.1:g.67171_67173del	NG_051927.1:g.67172_67173del	NG_051927.1:g.67173del	NG_051927.1:g.67173dup	NG_051927.1:g.67172_67173dup	NG_051927.1:g.67171_67173dup	NG_051927.1:g.67170_67173dup	NG_051927.1:g.67169_67173dup	NG_051927.1:g.67168_67173dup	NG_051927.1:g.67161_67173dup
SASH1 transcript variant 2	NM_001346505.2:c.22-55706=	NM_001346505.2:c.22-55696_22-55686del	NM_001346505.2:c.22-55693_22-55686del	NM_001346505.2:c.22-55692_22-55686del	NM_001346505.2:c.22-55690_22-55686del	NM_001346505.2:c.22-55688_22-55686del	NM_001346505.2:c.22-55687_22-55686del	NM_001346505.2:c.22-55686del	NM_001346505.2:c.22-55686dup	NM_001346505.2:c.22-55687_22-55686dup	NM_001346505.2:c.22-55688_22-55686dup	NM_001346505.2:c.22-55689_22-55686dup	NM_001346505.2:c.22-55690_22-55686dup	NM_001346505.2:c.22-55691_22-55686dup	NM_001346505.2:c.22-55698_22-55686dup
SASH1 transcript variant X2	XM_017010599.2:c.46-55706=	XM_017010599.2:c.46-55696_46-55686del	XM_017010599.2:c.46-55693_46-55686del	XM_017010599.2:c.46-55692_46-55686del	XM_017010599.2:c.46-55690_46-55686del	XM_017010599.2:c.46-55688_46-55686del	XM_017010599.2:c.46-55687_46-55686del	XM_017010599.2:c.46-55686del	XM_017010599.2:c.46-55686dup	XM_017010599.2:c.46-55687_46-55686dup	XM_017010599.2:c.46-55688_46-55686dup	XM_017010599.2:c.46-55689_46-55686dup	XM_017010599.2:c.46-55690_46-55686dup	XM_017010599.2:c.46-55691_46-55686dup	XM_017010599.2:c.46-55698_46-55686dup
SASH1 transcript variant X3	XM_017010600.2:c.22-55706=	XM_017010600.2:c.22-55696_22-55686del	XM_017010600.2:c.22-55693_22-55686del	XM_017010600.2:c.22-55692_22-55686del	XM_017010600.2:c.22-55690_22-55686del	XM_017010600.2:c.22-55688_22-55686del	XM_017010600.2:c.22-55687_22-55686del	XM_017010600.2:c.22-55686del	XM_017010600.2:c.22-55686dup	XM_017010600.2:c.22-55687_22-55686dup	XM_017010600.2:c.22-55688_22-55686dup	XM_017010600.2:c.22-55689_22-55686dup	XM_017010600.2:c.22-55690_22-55686dup	XM_017010600.2:c.22-55691_22-55686dup	XM_017010600.2:c.22-55698_22-55686dup
SASH1 transcript variant X9	XM_024446384.2:c.46-55706=	XM_024446384.2:c.46-55696_46-55686del	XM_024446384.2:c.46-55693_46-55686del	XM_024446384.2:c.46-55692_46-55686del	XM_024446384.2:c.46-55690_46-55686del	XM_024446384.2:c.46-55688_46-55686del	XM_024446384.2:c.46-55687_46-55686del	XM_024446384.2:c.46-55686del	XM_024446384.2:c.46-55686dup	XM_024446384.2:c.46-55687_46-55686dup	XM_024446384.2:c.46-55688_46-55686dup	XM_024446384.2:c.46-55689_46-55686dup	XM_024446384.2:c.46-55690_46-55686dup	XM_024446384.2:c.46-55691_46-55686dup	XM_024446384.2:c.46-55698_46-55686dup
SASH1 transcript variant X5	XM_047418497.1:c.-22-55706=	XM_047418497.1:c.-22-55696_-22-55686del	XM_047418497.1:c.-22-55693_-22-55686del	XM_047418497.1:c.-22-55692_-22-55686del	XM_047418497.1:c.-22-55690_-22-55686del	XM_047418497.1:c.-22-55688_-22-55686del	XM_047418497.1:c.-22-55687_-22-55686del	XM_047418497.1:c.-22-55686del	XM_047418497.1:c.-22-55686dup	XM_047418497.1:c.-22-55687_-22-55686dup	XM_047418497.1:c.-22-55688_-22-55686dup	XM_047418497.1:c.-22-55689_-22-55686dup	XM_047418497.1:c.-22-55690_-22-55686dup	XM_047418497.1:c.-22-55691_-22-55686dup	XM_047418497.1:c.-22-55698_-22-55686dup

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#.

39 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3000153494	Nov 08, 2017 (151)
2	URBANLAB	ss3648495327	Oct 12, 2018 (152)
3	EVA_DECODE	ss3718529976	Jul 13, 2019 (153)
4	EVA_DECODE	ss3718529977	Jul 13, 2019 (153)
5	EVA_DECODE	ss3718529978	Jul 13, 2019 (153)
6	EVA_DECODE	ss3718529979	Jul 13, 2019 (153)
7	EVA_DECODE	ss3718529980	Jul 13, 2019 (153)
8	EVA	ss3830254603	Apr 26, 2020 (154)
9	GNOMAD	ss4153696740	Apr 26, 2021 (155)
10	GNOMAD	ss4153696741	Apr 26, 2021 (155)
11	GNOMAD	ss4153696742	Apr 26, 2021 (155)
12	GNOMAD	ss4153696743	Apr 26, 2021 (155)
13	GNOMAD	ss4153696744	Apr 26, 2021 (155)
14	GNOMAD	ss4153696745	Apr 26, 2021 (155)
15	GNOMAD	ss4153696746	Apr 26, 2021 (155)
16	GNOMAD	ss4153696747	Apr 26, 2021 (155)
17	GNOMAD	ss4153696748	Apr 26, 2021 (155)
18	GNOMAD	ss4153696749	Apr 26, 2021 (155)
19	GNOMAD	ss4153696750	Apr 26, 2021 (155)
20	GNOMAD	ss4153696751	Apr 26, 2021 (155)
21	GNOMAD	ss4153696752	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5180508448	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5180508449	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5180508450	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5180508451	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5180508452	Apr 26, 2021 (155)
27	1000G_HIGH_COVERAGE	ss5270804974	Oct 13, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5270804975	Oct 13, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5270804976	Oct 13, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5270804978	Oct 13, 2022 (156)
31	HUGCELL_USP	ss5468208098	Oct 13, 2022 (156)
32	HUGCELL_USP	ss5468208099	Oct 13, 2022 (156)
33	HUGCELL_USP	ss5468208100	Oct 13, 2022 (156)
34	TOMMO_GENOMICS	ss5719555305	Oct 13, 2022 (156)
35	TOMMO_GENOMICS	ss5719555306	Oct 13, 2022 (156)
36	TOMMO_GENOMICS	ss5719555307	Oct 13, 2022 (156)
37	TOMMO_GENOMICS	ss5719555308	Oct 13, 2022 (156)
38	EVA	ss5843165778	Oct 13, 2022 (156)
39	EVA	ss5843165779	Oct 13, 2022 (156)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 244916024 (NC_000006.12:148334427::A 219/59410) Row 244916025 (NC_000006.12:148334427::AA 4722/59414) Row 244916026 (NC_000006.12:148334427::AAA 4888/59404)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 244916024 (NC_000006.12:148334427::A 219/59410) Row 244916025 (NC_000006.12:148334427::AA 4722/59414) Row 244916026 (NC_000006.12:148334427::AAA 4888/59404)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 244916024 (NC_000006.12:148334427::A 219/59410) Row 244916025 (NC_000006.12:148334427::AA 4722/59414) Row 244916026 (NC_000006.12:148334427::AAA 4888/59404)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 244916024 (NC_000006.12:148334427::A 219/59410) Row 244916025 (NC_000006.12:148334427::AA 4722/59414) Row 244916026 (NC_000006.12:148334427::AAA 4888/59404)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 244916024 (NC_000006.12:148334427::A 219/59410) Row 244916025 (NC_000006.12:148334427::AA 4722/59414) Row 244916026 (NC_000006.12:148334427::AAA 4888/59404)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 244916024 (NC_000006.12:148334427::A 219/59410) Row 244916025 (NC_000006.12:148334427::AA 4722/59414) Row 244916026 (NC_000006.12:148334427::AAA 4888/59404)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 244916024 (NC_000006.12:148334427::A 219/59410) Row 244916025 (NC_000006.12:148334427::AA 4722/59414) Row 244916026 (NC_000006.12:148334427::AAA 4888/59404)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 244916024 (NC_000006.12:148334427::A 219/59410) Row 244916025 (NC_000006.12:148334427::AA 4722/59414) Row 244916026 (NC_000006.12:148334427::AAA 4888/59404)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 244916024 (NC_000006.12:148334427::A 219/59410) Row 244916025 (NC_000006.12:148334427::AA 4722/59414) Row 244916026 (NC_000006.12:148334427::AAA 4888/59404)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 244916024 (NC_000006.12:148334427::A 219/59410) Row 244916025 (NC_000006.12:148334427::AA 4722/59414) Row 244916026 (NC_000006.12:148334427::AAA 4888/59404)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 244916024 (NC_000006.12:148334427::A 219/59410) Row 244916025 (NC_000006.12:148334427::AA 4722/59414) Row 244916026 (NC_000006.12:148334427::AAA 4888/59404)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 244916024 (NC_000006.12:148334427::A 219/59410) Row 244916025 (NC_000006.12:148334427::AA 4722/59414) Row 244916026 (NC_000006.12:148334427::AAA 4888/59404)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 244916024 (NC_000006.12:148334427::A 219/59410) Row 244916025 (NC_000006.12:148334427::AA 4722/59414) Row 244916026 (NC_000006.12:148334427::AAA 4888/59404)...	-	Apr 26, 2021 (155)
53	8.3KJPN Submission ignored due to conflicting rows: Row 38477755 (NC_000006.11:148655563:A: 6655/15712) Row 38477756 (NC_000006.11:148655563::AA 3134/15712) Row 38477757 (NC_000006.11:148655563::AAA 75/15712)...	-	Apr 26, 2021 (155)
54	8.3KJPN Submission ignored due to conflicting rows: Row 38477755 (NC_000006.11:148655563:A: 6655/15712) Row 38477756 (NC_000006.11:148655563::AA 3134/15712) Row 38477757 (NC_000006.11:148655563::AAA 75/15712)...	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 38477755 (NC_000006.11:148655563:A: 6655/15712) Row 38477756 (NC_000006.11:148655563::AA 3134/15712) Row 38477757 (NC_000006.11:148655563::AAA 75/15712)...	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 38477755 (NC_000006.11:148655563:A: 6655/15712) Row 38477756 (NC_000006.11:148655563::AA 3134/15712) Row 38477757 (NC_000006.11:148655563::AAA 75/15712)...	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 38477755 (NC_000006.11:148655563:A: 6655/15712) Row 38477756 (NC_000006.11:148655563::AA 3134/15712) Row 38477757 (NC_000006.11:148655563::AAA 75/15712)...	-	Apr 26, 2021 (155)
58	14KJPN Submission ignored due to conflicting rows: Row 53392409 (NC_000006.12:148334427:A: 11880/24040) Row 53392410 (NC_000006.12:148334427::AA 4745/24040) Row 53392411 (NC_000006.12:148334427::AAA 81/24040)...	-	Oct 13, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 53392409 (NC_000006.12:148334427:A: 11880/24040) Row 53392410 (NC_000006.12:148334427::AA 4745/24040) Row 53392411 (NC_000006.12:148334427::AAA 81/24040)...	-	Oct 13, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 53392409 (NC_000006.12:148334427:A: 11880/24040) Row 53392410 (NC_000006.12:148334427::AA 4745/24040) Row 53392411 (NC_000006.12:148334427::AAA 81/24040)...	-	Oct 13, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 53392409 (NC_000006.12:148334427:A: 11880/24040) Row 53392410 (NC_000006.12:148334427::AA 4745/24040) Row 53392411 (NC_000006.12:148334427::AAA 81/24040)...	-	Oct 13, 2022 (156)
62	ALFA	NC_000006.12 - 148334428	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
13716712974	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4153696752	NC_000006.12:148334427:AAAAAAAA:	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
13716712974	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4153696751	NC_000006.12:148334427:AAAAAAA:	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
13716712974	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3000153494	NC_000006.11:148655563:AAAAA:	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3718529980, ss4153696750, ss5270804978	NC_000006.12:148334427:AAAAA:	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
13716712974	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4153696749	NC_000006.12:148334427:AAA:	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
13716712974	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5180508451, ss5843165778	NC_000006.11:148655563:AA:	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4153696748, ss5468208100, ss5719555308	NC_000006.12:148334427:AA:	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
13716712974	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3718529979	NC_000006.12:148334430:AA:	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3830254603, ss5180508448	NC_000006.11:148655563:A:	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3648495327, ss4153696747, ss5468208098, ss5719555305	NC_000006.12:148334427:A:	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
13716712974	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3718529978	NC_000006.12:148334431:A:	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5180508452	NC_000006.11:148655563::A	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4153696740	NC_000006.12:148334427::A	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
13716712974	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5180508449, ss5843165779	NC_000006.11:148655563::AA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4153696741, ss5270804976, ss5468208099, ss5719555306	NC_000006.12:148334427::AA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
13716712974	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3718529977	NC_000006.12:148334432::AA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5180508450	NC_000006.11:148655563::AAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4153696742, ss5270804974, ss5719555307	NC_000006.12:148334427::AAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
13716712974	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3718529976	NC_000006.12:148334432::AAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4153696743, ss5270804975	NC_000006.12:148334427::AAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13716712974	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4153696744	NC_000006.12:148334427::AAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
13716712974	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4153696745	NC_000006.12:148334427::AAAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4153696746	NC_000006.12:148334427::AAAAAAAAAA… NC_000006.12:148334427::AAAAAAAAAAAAA	NC_000006.12:148334427:AAAAAAAAAAA… NC_000006.12:148334427:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs1162225428

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

Genome context:

Select flank length:

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

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1162225428