Name: rs368567940
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.

rs368567940

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chrX:150373467-150373490 (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(CA)₅ / del(CA)₄ / del(CA)₃ / d…
del(CA)₅ / del(CA)₄ / del(CA)₃ / delCACA / delCA / dupCA / dupCACA / dup(CA)₃ / dup(CA)₄
Variation Type: Indel Insertion and Deletion
Frequency: delCA=0.323099 (85521/264690, TOPMED)
dupCACA=0.0019 (12/6230, ALFA)
(CA)₁₂=0.4951 (1869/3775, 1000G) (+ 1 more)
dupCA=0.2 (2/8, KOREAN)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MAMLD1 : 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	HWEP
Total	Global	6230	CACACACACACACACACACACACA=0.9960	CACACACACACACA=0.0000, CACACACACACACACA=0.0000, CACACACACACACACACA=0.0000, CACACACACACACACACACA=0.0000, CACACACACACACACACACACA=0.0008, CACACACACACACACACACACACACA=0.0013, CACACACACACACACACACACACACACA=0.0019, CACACACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACACACA=0.0000	0.998069	0.001931	32
European	Sub	4208	CACACACACACACACACACACACA=0.9941	CACACACACACACA=0.0000, CACACACACACACACA=0.0000, CACACACACACACACACA=0.0000, CACACACACACACACACACA=0.0000, CACACACACACACACACACACA=0.0012, CACACACACACACACACACACACACA=0.0019, CACACACACACACACACACACACACACA=0.0029, CACACACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACACACA=0.0000	0.997139	0.002861	32
African	Sub	1164	CACACACACACACACACACACACA=1.0000	CACACACACACACA=0.0000, CACACACACACACACA=0.0000, CACACACACACACACACA=0.0000, CACACACACACACACACACA=0.0000, CACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACACACA=0.0000	1.0	0.0	N/A
African Others	Sub	52	CACACACACACACACACACACACA=1.00	CACACACACACACA=0.00, CACACACACACACACA=0.00, CACACACACACACACACA=0.00, CACACACACACACACACACA=0.00, CACACACACACACACACACACA=0.00, CACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACA=0.00	1.0	0.0	N/A
African American	Sub	1112	CACACACACACACACACACACACA=1.0000	CACACACACACACA=0.0000, CACACACACACACACA=0.0000, CACACACACACACACACA=0.0000, CACACACACACACACACACA=0.0000, CACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACACA=0.0000, CACACACACACACACACACACACACACACACA=0.0000	1.0	0.0	N/A
Asian	Sub	92	CACACACACACACACACACACACA=1.00	CACACACACACACA=0.00, CACACACACACACACA=0.00, CACACACACACACACACA=0.00, CACACACACACACACACACA=0.00, CACACACACACACACACACACA=0.00, CACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACA=0.00	1.0	0.0	N/A
East Asian	Sub	74	CACACACACACACACACACACACA=1.00	CACACACACACACA=0.00, CACACACACACACACA=0.00, CACACACACACACACACA=0.00, CACACACACACACACACACA=0.00, CACACACACACACACACACACA=0.00, CACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACA=0.00	1.0	0.0	N/A
Other Asian	Sub	18	CACACACACACACACACACACACA=1.00	CACACACACACACA=0.00, CACACACACACACACA=0.00, CACACACACACACACACA=0.00, CACACACACACACACACACA=0.00, CACACACACACACACACACACA=0.00, CACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACA=0.00	1.0	0.0	N/A
Latin American 1	Sub	70	CACACACACACACACACACACACA=1.00	CACACACACACACA=0.00, CACACACACACACACA=0.00, CACACACACACACACACA=0.00, CACACACACACACACACACA=0.00, CACACACACACACACACACACA=0.00, CACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACA=0.00	1.0	0.0	N/A
Latin American 2	Sub	400	CACACACACACACACACACACACA=1.000	CACACACACACACA=0.000, CACACACACACACACA=0.000, CACACACACACACACACA=0.000, CACACACACACACACACACA=0.000, CACACACACACACACACACACA=0.000, CACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACA=0.000	1.0	0.0	N/A
South Asian	Sub	58	CACACACACACACACACACACACA=1.00	CACACACACACACA=0.00, CACACACACACACACA=0.00, CACACACACACACACACA=0.00, CACACACACACACACACACA=0.00, CACACACACACACACACACACA=0.00, CACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACA=0.00, CACACACACACACACACACACACACACACACA=0.00	1.0	0.0	N/A
Other	Sub	238	CACACACACACACACACACACACA=1.000	CACACACACACACA=0.000, CACACACACACACACA=0.000, CACACACACACACACACA=0.000, CACACACACACACACACACA=0.000, CACACACACACACACACACACA=0.000, CACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACA=0.000, CACACACACACACACACACACACACACACACA=0.000	1.0	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
TopMed	Global	Study-wide	264690	(CA)₁₂=0.676901	delCA=0.323099
Allele Frequency Aggregator	Total	Global	6230	(CA)₁₂=0.9960	del(CA)₅=0.0000, del(CA)₄=0.0000, del(CA)₃=0.0000, delCACA=0.0000, delCA=0.0008, dupCA=0.0013, dupCACA=0.0019, dup(CA)₃=0.0000, dup(CA)₄=0.0000
Allele Frequency Aggregator	European	Sub	4208	(CA)₁₂=0.9941	del(CA)₅=0.0000, del(CA)₄=0.0000, del(CA)₃=0.0000, delCACA=0.0000, delCA=0.0012, dupCA=0.0019, dupCACA=0.0029, dup(CA)₃=0.0000, dup(CA)₄=0.0000
Allele Frequency Aggregator	African	Sub	1164	(CA)₁₂=1.0000	del(CA)₅=0.0000, del(CA)₄=0.0000, del(CA)₃=0.0000, delCACA=0.0000, delCA=0.0000, dupCA=0.0000, dupCACA=0.0000, dup(CA)₃=0.0000, dup(CA)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	400	(CA)₁₂=1.000	del(CA)₅=0.000, del(CA)₄=0.000, del(CA)₃=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000
Allele Frequency Aggregator	Other	Sub	238	(CA)₁₂=1.000	del(CA)₅=0.000, del(CA)₄=0.000, del(CA)₃=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000
Allele Frequency Aggregator	Asian	Sub	92	(CA)₁₂=1.00	del(CA)₅=0.00, del(CA)₄=0.00, del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	70	(CA)₁₂=1.00	del(CA)₅=0.00, del(CA)₄=0.00, del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	58	(CA)₁₂=1.00	del(CA)₅=0.00, del(CA)₄=0.00, del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00
1000Genomes	Global	Study-wide	3775	- No frequency provided	dupCA=0.5049
1000Genomes	African	Sub	1003	- No frequency provided	dupCA=0.2512
1000Genomes	Europe	Sub	766	- No frequency provided	dupCA=0.433
1000Genomes	East Asian	Sub	764	- No frequency provided	dupCA=0.665
1000Genomes	South Asian	Sub	718	- No frequency provided	dupCA=0.649
1000Genomes	American	Sub	524	- No frequency provided	dupCA=0.664
KOREAN population from KRGDB	KOREAN	Study-wide	8	- No frequency provided	dupCA=0.2

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 X	NC_000023.11:g.150373467CA[7]
GRCh38.p14 chr X	NC_000023.11:g.150373467CA[8]
GRCh38.p14 chr X	NC_000023.11:g.150373467CA[9]
GRCh38.p14 chr X	NC_000023.11:g.150373467CA[10]
GRCh38.p14 chr X	NC_000023.11:g.150373467CA[11]
GRCh38.p14 chr X	NC_000023.11:g.150373467CA[13]
GRCh38.p14 chr X	NC_000023.11:g.150373467CA[14]
GRCh38.p14 chr X	NC_000023.11:g.150373467CA[15]
GRCh38.p14 chr X	NC_000023.11:g.150373467CA[16]
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5897865CA[7]
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5897865CA[8]
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5897865CA[9]
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5897865CA[10]
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5897865CA[11]
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5897865CA[13]
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5897865CA[14]
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5897865CA[15]
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5897865CA[16]
MAMLD1 RefSeqGene	NG_017093.2:g.15170CA[7]
MAMLD1 RefSeqGene	NG_017093.2:g.15170CA[8]
MAMLD1 RefSeqGene	NG_017093.2:g.15170CA[9]
MAMLD1 RefSeqGene	NG_017093.2:g.15170CA[10]
MAMLD1 RefSeqGene	NG_017093.2:g.15170CA[11]
MAMLD1 RefSeqGene	NG_017093.2:g.15170CA[13]
MAMLD1 RefSeqGene	NG_017093.2:g.15170CA[14]
MAMLD1 RefSeqGene	NG_017093.2:g.15170CA[15]
MAMLD1 RefSeqGene	NG_017093.2:g.15170CA[16]
GRCh37.p13 chr X	NC_000023.10:g.149541736delinsACA
GRCh37.p13 chr X	NC_000023.10:g.149541736_149541743del
GRCh37.p13 chr X	NC_000023.10:g.149541736_149541741del
GRCh37.p13 chr X	NC_000023.10:g.149541736_149541739del
GRCh37.p13 chr X	NC_000023.10:g.149541722TC[7]
GRCh37.p13 chr X	NC_000023.10:g.149541736T>A
GRCh37.p13 chr X	NC_000023.10:g.149541736delinsACACA
GRCh37.p13 chr X	NC_000023.10:g.149541736delinsACACACA
GRCh37.p13 chr X	NC_000023.10:g.149541736delinsACACACACA
GRCh37.p13 chr X	NC_000023.10:g.149541736delinsACACACACACA

Gene: MAMLD1, mastermind like domain containing 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MAMLD1 transcript variant 1	NM_001177465.3:c.-64+9937… NM_001177465.3:c.-64+9937CA[7]	N/A	Intron Variant
MAMLD1 transcript variant 3	NM_001177466.3:c.-64+1058… NM_001177466.3:c.-64+10581CA[7]	N/A	Intron Variant
MAMLD1 transcript variant 4	NM_001400512.1:c.-64+9937… NM_001400512.1:c.-64+9937CA[7]	N/A	Intron Variant
MAMLD1 transcript variant 5	NM_001400513.1:c.-64+1058… NM_001400513.1:c.-64+10581CA[7]	N/A	Intron Variant
MAMLD1 transcript variant 6	NM_001400514.1:c.-64+1058… NM_001400514.1:c.-64+10581CA[7]	N/A	Intron Variant
MAMLD1 transcript variant 7	NM_001400515.1:c.-64+1058… NM_001400515.1:c.-64+10581CA[7]	N/A	Intron Variant
MAMLD1 transcript variant 2	NM_005491.5:c.-64+9937CA[… NM_005491.5:c.-64+9937CA[7]	N/A	Intron Variant
MAMLD1 transcript variant X1	XM_011531092.4:c.-64+1058… XM_011531092.4:c.-64+10581CA[7]	N/A	Intron Variant
MAMLD1 transcript variant X2	XM_024452317.2:c.-64+1058… XM_024452317.2:c.-64+10581CA[7]	N/A	Intron Variant
MAMLD1 transcript variant X3	XM_047441709.1:c.-193-271… XM_047441709.1:c.-193-271CA[7]	N/A	Intron Variant
MAMLD1 transcript variant X4	XM_047441710.1:c.-64+8938… XM_047441710.1:c.-64+8938CA[7]	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	(CA)₁₂=	del(CA)₅	del(CA)₄	del(CA)₃	delCACA	delCA	dupCA	dupCACA	dup(CA)₃	dup(CA)₄
GRCh38.p14 chr X	NC_000023.11:g.150373467_150373490=	NC_000023.11:g.150373467CA[7]	NC_000023.11:g.150373467CA[8]	NC_000023.11:g.150373467CA[9]	NC_000023.11:g.150373467CA[10]	NC_000023.11:g.150373467CA[11]	NC_000023.11:g.150373467CA[13]	NC_000023.11:g.150373467CA[14]	NC_000023.11:g.150373467CA[15]	NC_000023.11:g.150373467CA[16]
GRCh37.p13 chr X fix patch HG1459_PATCH	NW_004070890.2:g.5897865_5897888=	NW_004070890.2:g.5897865CA[7]	NW_004070890.2:g.5897865CA[8]	NW_004070890.2:g.5897865CA[9]	NW_004070890.2:g.5897865CA[10]	NW_004070890.2:g.5897865CA[11]	NW_004070890.2:g.5897865CA[13]	NW_004070890.2:g.5897865CA[14]	NW_004070890.2:g.5897865CA[15]	NW_004070890.2:g.5897865CA[16]
MAMLD1 RefSeqGene	NG_017093.2:g.15170_15193=	NG_017093.2:g.15170CA[7]	NG_017093.2:g.15170CA[8]	NG_017093.2:g.15170CA[9]	NG_017093.2:g.15170CA[10]	NG_017093.2:g.15170CA[11]	NG_017093.2:g.15170CA[13]	NG_017093.2:g.15170CA[14]	NG_017093.2:g.15170CA[15]	NG_017093.2:g.15170CA[16]
GRCh37.p13 chr X	NC_000023.10:g.149541736delinsACA	NC_000023.10:g.149541736_149541743del	NC_000023.10:g.149541736_149541741del	NC_000023.10:g.149541736_149541739del	NC_000023.10:g.149541722TC[7]	NC_000023.10:g.149541736T>A	NC_000023.10:g.149541736delinsACACA	NC_000023.10:g.149541736delinsACACACA	NC_000023.10:g.149541736delinsACACACACA	NC_000023.10:g.149541736delinsACACACACACA
MAMLD1 transcript variant 1	NM_001177465.1:c.-64+9939delinsACA	NM_001177465.1:c.-64+9939_-64+9946del	NM_001177465.1:c.-64+9939_-64+9944del	NM_001177465.1:c.-64+9939_-64+9942del	NM_001177465.1:c.-64+9924CT[7]	NM_001177465.1:c.-64+9939T>A	NM_001177465.1:c.-64+9939delinsACACA	NM_001177465.1:c.-64+9939delinsACACACA	NM_001177465.1:c.-64+9939delinsACACACACA	NM_001177465.1:c.-64+9939delinsACACACACACA
MAMLD1 transcript variant 1	NM_001177465.3:c.-64+9937=	NM_001177465.3:c.-64+9937CA[7]	NM_001177465.3:c.-64+9937CA[8]	NM_001177465.3:c.-64+9937CA[9]	NM_001177465.3:c.-64+9937CA[10]	NM_001177465.3:c.-64+9937CA[11]	NM_001177465.3:c.-64+9937CA[13]	NM_001177465.3:c.-64+9937CA[14]	NM_001177465.3:c.-64+9937CA[15]	NM_001177465.3:c.-64+9937CA[16]
MAMLD1 transcript variant 3	NM_001177466.3:c.-64+10581=	NM_001177466.3:c.-64+10581CA[7]	NM_001177466.3:c.-64+10581CA[8]	NM_001177466.3:c.-64+10581CA[9]	NM_001177466.3:c.-64+10581CA[10]	NM_001177466.3:c.-64+10581CA[11]	NM_001177466.3:c.-64+10581CA[13]	NM_001177466.3:c.-64+10581CA[14]	NM_001177466.3:c.-64+10581CA[15]	NM_001177466.3:c.-64+10581CA[16]
MAMLD1 transcript variant 4	NM_001400512.1:c.-64+9937=	NM_001400512.1:c.-64+9937CA[7]	NM_001400512.1:c.-64+9937CA[8]	NM_001400512.1:c.-64+9937CA[9]	NM_001400512.1:c.-64+9937CA[10]	NM_001400512.1:c.-64+9937CA[11]	NM_001400512.1:c.-64+9937CA[13]	NM_001400512.1:c.-64+9937CA[14]	NM_001400512.1:c.-64+9937CA[15]	NM_001400512.1:c.-64+9937CA[16]
MAMLD1 transcript variant 5	NM_001400513.1:c.-64+10581=	NM_001400513.1:c.-64+10581CA[7]	NM_001400513.1:c.-64+10581CA[8]	NM_001400513.1:c.-64+10581CA[9]	NM_001400513.1:c.-64+10581CA[10]	NM_001400513.1:c.-64+10581CA[11]	NM_001400513.1:c.-64+10581CA[13]	NM_001400513.1:c.-64+10581CA[14]	NM_001400513.1:c.-64+10581CA[15]	NM_001400513.1:c.-64+10581CA[16]
MAMLD1 transcript variant 6	NM_001400514.1:c.-64+10581=	NM_001400514.1:c.-64+10581CA[7]	NM_001400514.1:c.-64+10581CA[8]	NM_001400514.1:c.-64+10581CA[9]	NM_001400514.1:c.-64+10581CA[10]	NM_001400514.1:c.-64+10581CA[11]	NM_001400514.1:c.-64+10581CA[13]	NM_001400514.1:c.-64+10581CA[14]	NM_001400514.1:c.-64+10581CA[15]	NM_001400514.1:c.-64+10581CA[16]
MAMLD1 transcript variant 7	NM_001400515.1:c.-64+10581=	NM_001400515.1:c.-64+10581CA[7]	NM_001400515.1:c.-64+10581CA[8]	NM_001400515.1:c.-64+10581CA[9]	NM_001400515.1:c.-64+10581CA[10]	NM_001400515.1:c.-64+10581CA[11]	NM_001400515.1:c.-64+10581CA[13]	NM_001400515.1:c.-64+10581CA[14]	NM_001400515.1:c.-64+10581CA[15]	NM_001400515.1:c.-64+10581CA[16]
MAMLD1 transcript variant 2	NM_005491.5:c.-64+9937=	NM_005491.5:c.-64+9937CA[7]	NM_005491.5:c.-64+9937CA[8]	NM_005491.5:c.-64+9937CA[9]	NM_005491.5:c.-64+9937CA[10]	NM_005491.5:c.-64+9937CA[11]	NM_005491.5:c.-64+9937CA[13]	NM_005491.5:c.-64+9937CA[14]	NM_005491.5:c.-64+9937CA[15]	NM_005491.5:c.-64+9937CA[16]
MAMLD1 transcript variant X1	XM_005274634.1:c.-64+9939delinsACA	XM_005274634.1:c.-64+9939_-64+9946del	XM_005274634.1:c.-64+9939_-64+9944del	XM_005274634.1:c.-64+9939_-64+9942del	XM_005274634.1:c.-64+9924CT[7]	XM_005274634.1:c.-64+9939T>A	XM_005274634.1:c.-64+9939delinsACACA	XM_005274634.1:c.-64+9939delinsACACACA	XM_005274634.1:c.-64+9939delinsACACACACA	XM_005274634.1:c.-64+9939delinsACACACACACA
MAMLD1 transcript variant X2	XM_005274635.1:c.-64+10583delinsACA	XM_005274635.1:c.-64+10583_-64+10590del	XM_005274635.1:c.-64+10583_-64+10588del	XM_005274635.1:c.-64+10583_-64+10586del	XM_005274635.1:c.-64+10568CT[7]	XM_005274635.1:c.-64+10583T>A	XM_005274635.1:c.-64+10583delinsACACA	XM_005274635.1:c.-64+10583delinsACACACA	XM_005274635.1:c.-64+10583delinsACACACACA	XM_005274635.1:c.-64+10583delinsACACACACACA
MAMLD1 transcript variant X3	XM_005274636.1:c.-64+9939delinsACA	XM_005274636.1:c.-64+9939_-64+9946del	XM_005274636.1:c.-64+9939_-64+9944del	XM_005274636.1:c.-64+9939_-64+9942del	XM_005274636.1:c.-64+9924CT[7]	XM_005274636.1:c.-64+9939T>A	XM_005274636.1:c.-64+9939delinsACACA	XM_005274636.1:c.-64+9939delinsACACACA	XM_005274636.1:c.-64+9939delinsACACACACA	XM_005274636.1:c.-64+9939delinsACACACACACA
MAMLD1 transcript variant X4	XM_005274637.1:c.-19+9939delinsACA	XM_005274637.1:c.-19+9939_-19+9946del	XM_005274637.1:c.-19+9939_-19+9944del	XM_005274637.1:c.-19+9939_-19+9942del	XM_005274637.1:c.-19+9924CT[7]	XM_005274637.1:c.-19+9939T>A	XM_005274637.1:c.-19+9939delinsACACA	XM_005274637.1:c.-19+9939delinsACACACA	XM_005274637.1:c.-19+9939delinsACACACACA	XM_005274637.1:c.-19+9939delinsACACACACACA
MAMLD1 transcript variant X5	XM_005274638.1:c.-19+10583delinsACA	XM_005274638.1:c.-19+10583_-19+10590del	XM_005274638.1:c.-19+10583_-19+10588del	XM_005274638.1:c.-19+10583_-19+10586del	XM_005274638.1:c.-19+10568CT[7]	XM_005274638.1:c.-19+10583T>A	XM_005274638.1:c.-19+10583delinsACACA	XM_005274638.1:c.-19+10583delinsACACACA	XM_005274638.1:c.-19+10583delinsACACACACA	XM_005274638.1:c.-19+10583delinsACACACACACA
MAMLD1 transcript variant X8	XM_005274641.1:c.-64+9939delinsACA	XM_005274641.1:c.-64+9939_-64+9946del	XM_005274641.1:c.-64+9939_-64+9944del	XM_005274641.1:c.-64+9939_-64+9942del	XM_005274641.1:c.-64+9924CT[7]	XM_005274641.1:c.-64+9939T>A	XM_005274641.1:c.-64+9939delinsACACA	XM_005274641.1:c.-64+9939delinsACACACA	XM_005274641.1:c.-64+9939delinsACACACACA	XM_005274641.1:c.-64+9939delinsACACACACACA
MAMLD1 transcript variant X2	XM_005278161.1:c.-64+9937=	XM_005278161.1:c.-64+9937CA[7]	XM_005278161.1:c.-64+9937CA[8]	XM_005278161.1:c.-64+9937CA[9]	XM_005278161.1:c.-64+9937CA[10]	XM_005278161.1:c.-64+9937CA[11]	XM_005278161.1:c.-64+9937CA[13]	XM_005278161.1:c.-64+9937CA[14]	XM_005278161.1:c.-64+9937CA[15]	XM_005278161.1:c.-64+9937CA[16]
MAMLD1 transcript variant X5	XM_005278164.1:c.-19+10581=	XM_005278164.1:c.-19+10581CA[7]	XM_005278164.1:c.-19+10581CA[8]	XM_005278164.1:c.-19+10581CA[9]	XM_005278164.1:c.-19+10581CA[10]	XM_005278164.1:c.-19+10581CA[11]	XM_005278164.1:c.-19+10581CA[13]	XM_005278164.1:c.-19+10581CA[14]	XM_005278164.1:c.-19+10581CA[15]	XM_005278164.1:c.-19+10581CA[16]
MAMLD1 transcript variant X6	XM_005278165.1:c.-64+9937=	XM_005278165.1:c.-64+9937CA[7]	XM_005278165.1:c.-64+9937CA[8]	XM_005278165.1:c.-64+9937CA[9]	XM_005278165.1:c.-64+9937CA[10]	XM_005278165.1:c.-64+9937CA[11]	XM_005278165.1:c.-64+9937CA[13]	XM_005278165.1:c.-64+9937CA[14]	XM_005278165.1:c.-64+9937CA[15]	XM_005278165.1:c.-64+9937CA[16]
MAMLD1 transcript variant X1	XM_011531092.4:c.-64+10581=	XM_011531092.4:c.-64+10581CA[7]	XM_011531092.4:c.-64+10581CA[8]	XM_011531092.4:c.-64+10581CA[9]	XM_011531092.4:c.-64+10581CA[10]	XM_011531092.4:c.-64+10581CA[11]	XM_011531092.4:c.-64+10581CA[13]	XM_011531092.4:c.-64+10581CA[14]	XM_011531092.4:c.-64+10581CA[15]	XM_011531092.4:c.-64+10581CA[16]
MAMLD1 transcript variant X2	XM_024452317.2:c.-64+10581=	XM_024452317.2:c.-64+10581CA[7]	XM_024452317.2:c.-64+10581CA[8]	XM_024452317.2:c.-64+10581CA[9]	XM_024452317.2:c.-64+10581CA[10]	XM_024452317.2:c.-64+10581CA[11]	XM_024452317.2:c.-64+10581CA[13]	XM_024452317.2:c.-64+10581CA[14]	XM_024452317.2:c.-64+10581CA[15]	XM_024452317.2:c.-64+10581CA[16]
MAMLD1 transcript variant X3	XM_047441709.1:c.-193-271=	XM_047441709.1:c.-193-271CA[7]	XM_047441709.1:c.-193-271CA[8]	XM_047441709.1:c.-193-271CA[9]	XM_047441709.1:c.-193-271CA[10]	XM_047441709.1:c.-193-271CA[11]	XM_047441709.1:c.-193-271CA[13]	XM_047441709.1:c.-193-271CA[14]	XM_047441709.1:c.-193-271CA[15]	XM_047441709.1:c.-193-271CA[16]
MAMLD1 transcript variant X4	XM_047441710.1:c.-64+8938=	XM_047441710.1:c.-64+8938CA[7]	XM_047441710.1:c.-64+8938CA[8]	XM_047441710.1:c.-64+8938CA[9]	XM_047441710.1:c.-64+8938CA[10]	XM_047441710.1:c.-64+8938CA[11]	XM_047441710.1:c.-64+8938CA[13]	XM_047441710.1:c.-64+8938CA[14]	XM_047441710.1:c.-64+8938CA[15]	XM_047441710.1:c.-64+8938CA[16]

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#.

58 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77903493	Oct 13, 2018 (152)
2	HGSV	ss80302759	Oct 13, 2018 (152)
3	HGSV	ss83774118	Oct 13, 2018 (152)
4	GMI	ss478864206	Oct 13, 2018 (152)
5	TISHKOFF	ss555103278	Apr 25, 2013 (138)
6	TISHKOFF	ss562785755	Apr 25, 2013 (138)
7	SSMP	ss664553072	Apr 09, 2015 (144)
8	DDI	ss1536953126	Apr 09, 2015 (144)
9	DDI	ss1536953127	Apr 09, 2015 (144)
10	1000GENOMES	ss1556608488	Apr 09, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1709896538	Apr 09, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1709896544	Apr 09, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1709896546	Apr 09, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1709896554	Apr 09, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1709896564	Apr 09, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1709896567	Apr 09, 2015 (144)
17	SYSTEMSBIOZJU	ss2629796457	Oct 13, 2018 (152)
18	SWEGEN	ss3020791206	Oct 13, 2018 (152)
19	SWEGEN	ss3020791207	Oct 13, 2018 (152)
20	SWEGEN	ss3020791208	Oct 13, 2018 (152)
21	SWEGEN	ss3020791211	Oct 13, 2018 (152)
22	SWEGEN	ss3020791212	Oct 13, 2018 (152)
23	SWEGEN	ss3020791213	Oct 13, 2018 (152)
24	MCHAISSO	ss3065281111	Nov 08, 2017 (151)
25	URBANLAB	ss3651351793	Oct 13, 2018 (152)
26	KHV_HUMAN_GENOMES	ss3823503190	Jul 14, 2019 (153)
27	EVA	ss3836358686	Apr 27, 2020 (154)
28	EVA	ss3836358687	Apr 27, 2020 (154)
29	EVA	ss3847317287	Apr 27, 2020 (154)
30	KRGDB	ss3943217575	Apr 27, 2020 (154)
31	GNOMAD	ss4380740679	Apr 26, 2021 (155)
32	GNOMAD	ss4380740680	Apr 26, 2021 (155)
33	GNOMAD	ss4380740683	Apr 26, 2021 (155)
34	GNOMAD	ss4380740684	Apr 26, 2021 (155)
35	GNOMAD	ss4380740685	Apr 26, 2021 (155)
36	GNOMAD	ss4380740686	Apr 26, 2021 (155)
37	TOPMED	ss5140903165	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5236720078	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5236720082	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5236720083	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5236720084	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5236720087	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5236720088	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5236720089	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5236720090	Apr 26, 2021 (155)
46	1000G_HIGH_COVERAGE	ss5314291800	Oct 13, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5314291801	Oct 13, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5314291802	Oct 13, 2022 (156)
49	HUGCELL_USP	ss5505652864	Oct 13, 2022 (156)
50	HUGCELL_USP	ss5505652865	Oct 13, 2022 (156)
51	HUGCELL_USP	ss5505652867	Oct 13, 2022 (156)
52	HUGCELL_USP	ss5505652869	Oct 13, 2022 (156)
53	TOMMO_GENOMICS	ss5799226626	Oct 13, 2022 (156)
54	TOMMO_GENOMICS	ss5799226627	Oct 13, 2022 (156)
55	TOMMO_GENOMICS	ss5799226628	Oct 13, 2022 (156)
56	TOMMO_GENOMICS	ss5799226630	Oct 13, 2022 (156)
57	EVA	ss5857235408	Oct 13, 2022 (156)
58	EVA	ss5981176366	Oct 13, 2022 (156)
59	1000Genomes	NC_000023.10 - 149541735	Oct 13, 2018 (152)
60	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 46567137 (NC_000023.10:149541720:CT: 53/2889) Row 46567141 (NC_000023.10:149541734::CA 1025/2889) Row 46567142 (NC_000023.10:149541734::CACA 480/2889)	-	Oct 13, 2018 (152)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 46567137 (NC_000023.10:149541720:CT: 53/2889) Row 46567141 (NC_000023.10:149541734::CA 1025/2889) Row 46567142 (NC_000023.10:149541734::CACA 480/2889)	-	Oct 13, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 46567137 (NC_000023.10:149541720:CT: 53/2889) Row 46567141 (NC_000023.10:149541734::CA 1025/2889) Row 46567142 (NC_000023.10:149541734::CACA 480/2889)	-	Oct 13, 2018 (152)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594022340 (NC_000023.11:150373466::CA 9200/95783) Row 594022341 (NC_000023.11:150373466::CACA 50/95907) Row 594022344 (NC_000023.11:150373466:CA: 30136/95429)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594022340 (NC_000023.11:150373466::CA 9200/95783) Row 594022341 (NC_000023.11:150373466::CACA 50/95907) Row 594022344 (NC_000023.11:150373466:CA: 30136/95429)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594022340 (NC_000023.11:150373466::CA 9200/95783) Row 594022341 (NC_000023.11:150373466::CACA 50/95907) Row 594022344 (NC_000023.11:150373466:CA: 30136/95429)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594022340 (NC_000023.11:150373466::CA 9200/95783) Row 594022341 (NC_000023.11:150373466::CACA 50/95907) Row 594022344 (NC_000023.11:150373466:CA: 30136/95429)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594022340 (NC_000023.11:150373466::CA 9200/95783) Row 594022341 (NC_000023.11:150373466::CACA 50/95907) Row 594022344 (NC_000023.11:150373466:CA: 30136/95429)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 594022340 (NC_000023.11:150373466::CA 9200/95783) Row 594022341 (NC_000023.11:150373466::CACA 50/95907) Row 594022344 (NC_000023.11:150373466:CA: 30136/95429)...	-	Apr 26, 2021 (155)
69	KOREAN population from KRGDB	NC_000023.10 - 149541735	Apr 27, 2020 (154)
70	8.3KJPN Submission ignored due to conflicting rows: Row 94689385 (NC_000023.10:149541720:CT: 220/12331) Row 94689389 (NC_000023.10:149541734::CA 9037/12754) Row 94689390 (NC_000023.10:149541734::CACA 15/12754)...	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 94689385 (NC_000023.10:149541720:CT: 220/12331) Row 94689389 (NC_000023.10:149541734::CA 9037/12754) Row 94689390 (NC_000023.10:149541734::CACA 15/12754)...	-	Apr 26, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 94689385 (NC_000023.10:149541720:CT: 220/12331) Row 94689389 (NC_000023.10:149541734::CA 9037/12754) Row 94689390 (NC_000023.10:149541734::CACA 15/12754)...	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 94689385 (NC_000023.10:149541720:CT: 220/12331) Row 94689389 (NC_000023.10:149541734::CA 9037/12754) Row 94689390 (NC_000023.10:149541734::CACA 15/12754)...	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 94689385 (NC_000023.10:149541720:CT: 220/12331) Row 94689389 (NC_000023.10:149541734::CA 9037/12754) Row 94689390 (NC_000023.10:149541734::CACA 15/12754)...	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 94689385 (NC_000023.10:149541720:CT: 220/12331) Row 94689389 (NC_000023.10:149541734::CA 9037/12754) Row 94689390 (NC_000023.10:149541734::CACA 15/12754)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 94689385 (NC_000023.10:149541720:CT: 220/12331) Row 94689389 (NC_000023.10:149541734::CA 9037/12754) Row 94689390 (NC_000023.10:149541734::CACA 15/12754)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 94689385 (NC_000023.10:149541720:CT: 220/12331) Row 94689389 (NC_000023.10:149541734::CA 9037/12754) Row 94689390 (NC_000023.10:149541734::CACA 15/12754)...	-	Apr 26, 2021 (155)
78	14KJPN Submission ignored due to conflicting rows: Row 133063730 (NC_000023.11:150373466:CACA: 377/22219) Row 133063731 (NC_000023.11:150373466:CA: 2605/22219) Row 133063732 (NC_000023.11:150373466:CACACA: 4/22219)...	-	Oct 13, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 133063730 (NC_000023.11:150373466:CACA: 377/22219) Row 133063731 (NC_000023.11:150373466:CA: 2605/22219) Row 133063732 (NC_000023.11:150373466:CACACA: 4/22219)...	-	Oct 13, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 133063730 (NC_000023.11:150373466:CACA: 377/22219) Row 133063731 (NC_000023.11:150373466:CA: 2605/22219) Row 133063732 (NC_000023.11:150373466:CACACA: 4/22219)...	-	Oct 13, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 133063730 (NC_000023.11:150373466:CACA: 377/22219) Row 133063731 (NC_000023.11:150373466:CA: 2605/22219) Row 133063732 (NC_000023.11:150373466:CACACA: 4/22219)...	-	Oct 13, 2022 (156)
82	TopMed	NC_000023.11 - 150373467	Apr 26, 2021 (155)
83	UK 10K study - Twins Submission ignored due to conflicting rows: Row 46567137 (NC_000023.10:149541720:CT: 96/3708) Row 46567141 (NC_000023.10:149541734::CA 1269/3708) Row 46567142 (NC_000023.10:149541734::CACA 604/3708)	-	Oct 13, 2018 (152)
84	UK 10K study - Twins Submission ignored due to conflicting rows: Row 46567137 (NC_000023.10:149541720:CT: 96/3708) Row 46567141 (NC_000023.10:149541734::CA 1269/3708) Row 46567142 (NC_000023.10:149541734::CACA 604/3708)	-	Oct 13, 2018 (152)
85	UK 10K study - Twins Submission ignored due to conflicting rows: Row 46567137 (NC_000023.10:149541720:CT: 96/3708) Row 46567141 (NC_000023.10:149541734::CA 1269/3708) Row 46567142 (NC_000023.10:149541734::CACA 604/3708)	-	Oct 13, 2018 (152)
86	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 10230779 (NC_000023.10:149541734::CA 30/47) Row 10230780 (NC_000023.10:149541736::CACA 39/48)	-	Jul 14, 2019 (153)
87	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 10230779 (NC_000023.10:149541734::CA 30/47) Row 10230780 (NC_000023.10:149541736::CACA 39/48)	-	Jul 14, 2019 (153)
88	ALFA	NC_000023.11 - 150373467	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
ss4380740686	NC_000023.11:150373466:CACACACACA:	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACA	(self)
1708752196	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACA	(self)
1708752196	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACA	(self)
ss4380740685, ss5799226628	NC_000023.11:150373466:CACACA:	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACA	(self)
1708752196	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACA	(self)
ss5236720084	NC_000023.10:149541734:CTCA:	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACA	(self)
ss4380740684, ss5314291800, ss5505652867, ss5799226626	NC_000023.11:150373466:CACA:	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACA	(self)
1708752196	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACA	(self)
ss1709896538, ss1709896554, ss5236720078	NC_000023.10:149541720:CT:	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACA	(self)
ss3836358687, ss5236720089	NC_000023.10:149541736:CA:	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACA	(self)
ss555103278	NC_000023.10:149541754:CA:	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACA	(self)
704509522, ss3651351793, ss3847317287, ss4380740683, ss5140903165, ss5314291801, ss5505652864, ss5799226627, ss5857235408	NC_000023.11:150373466:CA:	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACA	(self)
1708752196	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACA	(self)
ss478864206	NC_000023.9:149292393::AC	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACA	(self)
84562599, 50394969, ss1536953126, ss1556608488, ss1709896544, ss1709896564, ss3020791207, ss3836358686, ss3943217575, ss5236720082	NC_000023.10:149541734::CA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACA	(self)
ss562785755	NC_000023.10:149541735:T:ACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACA	(self)
ss1536953127, ss3020791213, ss5236720088	NC_000023.10:149541736::CA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACA	(self)
ss3065281111, ss3823503190, ss4380740679, ss5314291802, ss5505652865, ss5799226630	NC_000023.11:150373466::CA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACA	(self)
1708752196	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACA	(self)
ss83774118	NT_167198.1:459694::CA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACA	(self)
ss1709896546, ss1709896567, ss3020791206, ss5236720083	NC_000023.10:149541734::CACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACACA	(self)
ss664553072, ss2629796457, ss3020791212, ss5236720087	NC_000023.10:149541736::CACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACACA	(self)
ss4380740680, ss5505652869	NC_000023.11:150373466::CACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACACA	(self)
1708752196	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACACA	(self)
ss77903493	NT_167198.1:459694::CACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACACA	(self)
ss3020791208	NC_000023.10:149541734::CACACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACACACA	(self)
ss3020791211, ss5236720090, ss5981176366	NC_000023.10:149541736::CACACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACACACA	(self)
1708752196	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACACACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACACACA	(self)
ss80302759	NT_167198.1:459694::CACACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACACACA	(self)
1708752196	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACACACACA	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACACACACACACACACACA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3624733736	NC_000023.11:150373466:CACACACA:	NC_000023.11:150373466:CACACACACAC… NC_000023.11:150373466:CACACACACACACACACACACACA:CACACACACACACACA

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

No publications for rs368567940

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

rs368567940