Name: rs58143466
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.

rs58143466

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:68522815-68522838 (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)₁₄ / del(A)₁₃ / del(A)₁₂ / d…
del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / 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)₅ / ins(A)₂₇
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.3980 (2057/5168, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC25A16 : 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	5168	AAAAAAAAAAAAAAAAAAAAAAAA=0.5586	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0002, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0308, AAAAAAAAAAAAAAAAAAAAAAA=0.3980, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0112, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0012, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.367932	0.193249	0.438819	12
European	Sub	4878	AAAAAAAAAAAAAAAAAAAAAAAA=0.5334	AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0002, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0326, AAAAAAAAAAAAAAAAAAAAAAA=0.4207, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0119, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0012, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.328539	0.205393	0.466067	4
African	Sub	148	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	2	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	146	AAAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	8	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	8	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	12	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	80	AAAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	2	AAAAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	40	AAAAAAAAAAAAAAAAAAAAAAAA=0.88	AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.12, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	0.8	0.05	0.15	1

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	5168	(A)₂₄=0.5586	del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₈=0.0002, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0308, delA=0.3980, dupA=0.0112, dupAA=0.0012, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	4878	(A)₂₄=0.5334	del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₈=0.0002, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0326, delA=0.4207, dupA=0.0119, dupAA=0.0012, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	148	(A)₂₄=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=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, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	80	(A)₂₄=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=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, dup(A)₄=0.00
Allele Frequency Aggregator	Other	Sub	40	(A)₂₄=0.88	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=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=0.12, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(A)₂₄=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=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, dup(A)₄=0.00
Allele Frequency Aggregator	Asian	Sub	8	(A)₂₄=1.0	del(A)₁₄=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=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, dup(A)₄=0.0
Allele Frequency Aggregator	South Asian	Sub	2	(A)₂₄=1.0	del(A)₁₄=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=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, dup(A)₄=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 10	NC_000010.11:g.68522825_68522838del
GRCh38.p14 chr 10	NC_000010.11:g.68522826_68522838del
GRCh38.p14 chr 10	NC_000010.11:g.68522827_68522838del
GRCh38.p14 chr 10	NC_000010.11:g.68522828_68522838del
GRCh38.p14 chr 10	NC_000010.11:g.68522829_68522838del
GRCh38.p14 chr 10	NC_000010.11:g.68522830_68522838del
GRCh38.p14 chr 10	NC_000010.11:g.68522831_68522838del
GRCh38.p14 chr 10	NC_000010.11:g.68522832_68522838del
GRCh38.p14 chr 10	NC_000010.11:g.68522833_68522838del
GRCh38.p14 chr 10	NC_000010.11:g.68522834_68522838del
GRCh38.p14 chr 10	NC_000010.11:g.68522835_68522838del
GRCh38.p14 chr 10	NC_000010.11:g.68522836_68522838del
GRCh38.p14 chr 10	NC_000010.11:g.68522837_68522838del
GRCh38.p14 chr 10	NC_000010.11:g.68522838del
GRCh38.p14 chr 10	NC_000010.11:g.68522838dup
GRCh38.p14 chr 10	NC_000010.11:g.68522837_68522838dup
GRCh38.p14 chr 10	NC_000010.11:g.68522836_68522838dup
GRCh38.p14 chr 10	NC_000010.11:g.68522835_68522838dup
GRCh38.p14 chr 10	NC_000010.11:g.68522834_68522838dup
GRCh38.p14 chr 10	NC_000010.11:g.68522838_68522839insAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 10	NC_000010.10:g.70282582_70282595del
GRCh37.p13 chr 10	NC_000010.10:g.70282583_70282595del
GRCh37.p13 chr 10	NC_000010.10:g.70282584_70282595del
GRCh37.p13 chr 10	NC_000010.10:g.70282585_70282595del
GRCh37.p13 chr 10	NC_000010.10:g.70282586_70282595del
GRCh37.p13 chr 10	NC_000010.10:g.70282587_70282595del
GRCh37.p13 chr 10	NC_000010.10:g.70282588_70282595del
GRCh37.p13 chr 10	NC_000010.10:g.70282589_70282595del
GRCh37.p13 chr 10	NC_000010.10:g.70282590_70282595del
GRCh37.p13 chr 10	NC_000010.10:g.70282591_70282595del
GRCh37.p13 chr 10	NC_000010.10:g.70282592_70282595del
GRCh37.p13 chr 10	NC_000010.10:g.70282593_70282595del
GRCh37.p13 chr 10	NC_000010.10:g.70282594_70282595del
GRCh37.p13 chr 10	NC_000010.10:g.70282595del
GRCh37.p13 chr 10	NC_000010.10:g.70282595dup
GRCh37.p13 chr 10	NC_000010.10:g.70282594_70282595dup
GRCh37.p13 chr 10	NC_000010.10:g.70282593_70282595dup
GRCh37.p13 chr 10	NC_000010.10:g.70282592_70282595dup
GRCh37.p13 chr 10	NC_000010.10:g.70282591_70282595dup
GRCh37.p13 chr 10	NC_000010.10:g.70282595_70282596insAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC25A16 RefSeqGene	NG_046972.1:g.9696_9709del
SLC25A16 RefSeqGene	NG_046972.1:g.9697_9709del
SLC25A16 RefSeqGene	NG_046972.1:g.9698_9709del
SLC25A16 RefSeqGene	NG_046972.1:g.9699_9709del
SLC25A16 RefSeqGene	NG_046972.1:g.9700_9709del
SLC25A16 RefSeqGene	NG_046972.1:g.9701_9709del
SLC25A16 RefSeqGene	NG_046972.1:g.9702_9709del
SLC25A16 RefSeqGene	NG_046972.1:g.9703_9709del
SLC25A16 RefSeqGene	NG_046972.1:g.9704_9709del
SLC25A16 RefSeqGene	NG_046972.1:g.9705_9709del
SLC25A16 RefSeqGene	NG_046972.1:g.9706_9709del
SLC25A16 RefSeqGene	NG_046972.1:g.9707_9709del
SLC25A16 RefSeqGene	NG_046972.1:g.9708_9709del
SLC25A16 RefSeqGene	NG_046972.1:g.9709del
SLC25A16 RefSeqGene	NG_046972.1:g.9709dup
SLC25A16 RefSeqGene	NG_046972.1:g.9708_9709dup
SLC25A16 RefSeqGene	NG_046972.1:g.9707_9709dup
SLC25A16 RefSeqGene	NG_046972.1:g.9706_9709dup
SLC25A16 RefSeqGene	NG_046972.1:g.9705_9709dup
SLC25A16 RefSeqGene	NG_046972.1:g.9709_9710insTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: SLC25A16, solute carrier family 25 member 16 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC25A16 transcript variant 2	NM_001324312.2:c.130+4418… NM_001324312.2:c.130+4418_130+4431del	N/A	Intron Variant
SLC25A16 transcript variant 3	NM_001324313.2:c.130+4418… NM_001324313.2:c.130+4418_130+4431del	N/A	Intron Variant
SLC25A16 transcript variant 4	NM_001324314.2:c.-347+441… NM_001324314.2:c.-347+4418_-347+4431del	N/A	Intron Variant
SLC25A16 transcript variant 6	NM_001324317.2:c.-139+441… NM_001324317.2:c.-139+4418_-139+4431del	N/A	Intron Variant
SLC25A16 transcript variant 1	NM_152707.4:c.130+4418_13… NM_152707.4:c.130+4418_130+4431del	N/A	Intron Variant
SLC25A16 transcript variant 5	NM_001324315.1:c.	N/A	Genic Upstream Transcript Variant
SLC25A16 transcript variant 7	NR_136737.1:n.	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)₂₄=	del(A)₁₄	del(A)₁₃	del(A)₁₂	del(A)₁₁	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)₅	ins(A)₂₇
GRCh38.p14 chr 10	NC_000010.11:g.68522815_68522838=	NC_000010.11:g.68522825_68522838del	NC_000010.11:g.68522826_68522838del	NC_000010.11:g.68522827_68522838del	NC_000010.11:g.68522828_68522838del	NC_000010.11:g.68522829_68522838del	NC_000010.11:g.68522830_68522838del	NC_000010.11:g.68522831_68522838del	NC_000010.11:g.68522832_68522838del	NC_000010.11:g.68522833_68522838del	NC_000010.11:g.68522834_68522838del	NC_000010.11:g.68522835_68522838del	NC_000010.11:g.68522836_68522838del	NC_000010.11:g.68522837_68522838del	NC_000010.11:g.68522838del	NC_000010.11:g.68522838dup	NC_000010.11:g.68522837_68522838dup	NC_000010.11:g.68522836_68522838dup	NC_000010.11:g.68522835_68522838dup	NC_000010.11:g.68522834_68522838dup	NC_000010.11:g.68522838_68522839insAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 10	NC_000010.10:g.70282572_70282595=	NC_000010.10:g.70282582_70282595del	NC_000010.10:g.70282583_70282595del	NC_000010.10:g.70282584_70282595del	NC_000010.10:g.70282585_70282595del	NC_000010.10:g.70282586_70282595del	NC_000010.10:g.70282587_70282595del	NC_000010.10:g.70282588_70282595del	NC_000010.10:g.70282589_70282595del	NC_000010.10:g.70282590_70282595del	NC_000010.10:g.70282591_70282595del	NC_000010.10:g.70282592_70282595del	NC_000010.10:g.70282593_70282595del	NC_000010.10:g.70282594_70282595del	NC_000010.10:g.70282595del	NC_000010.10:g.70282595dup	NC_000010.10:g.70282594_70282595dup	NC_000010.10:g.70282593_70282595dup	NC_000010.10:g.70282592_70282595dup	NC_000010.10:g.70282591_70282595dup	NC_000010.10:g.70282595_70282596insAAAAAAAAAAAAAAAAAAAAAAAAAAA
SLC25A16 RefSeqGene	NG_046972.1:g.9686_9709=	NG_046972.1:g.9696_9709del	NG_046972.1:g.9697_9709del	NG_046972.1:g.9698_9709del	NG_046972.1:g.9699_9709del	NG_046972.1:g.9700_9709del	NG_046972.1:g.9701_9709del	NG_046972.1:g.9702_9709del	NG_046972.1:g.9703_9709del	NG_046972.1:g.9704_9709del	NG_046972.1:g.9705_9709del	NG_046972.1:g.9706_9709del	NG_046972.1:g.9707_9709del	NG_046972.1:g.9708_9709del	NG_046972.1:g.9709del	NG_046972.1:g.9709dup	NG_046972.1:g.9708_9709dup	NG_046972.1:g.9707_9709dup	NG_046972.1:g.9706_9709dup	NG_046972.1:g.9705_9709dup	NG_046972.1:g.9709_9710insTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant 2	NM_001324312.2:c.130+4431=	NM_001324312.2:c.130+4418_130+4431del	NM_001324312.2:c.130+4419_130+4431del	NM_001324312.2:c.130+4420_130+4431del	NM_001324312.2:c.130+4421_130+4431del	NM_001324312.2:c.130+4422_130+4431del	NM_001324312.2:c.130+4423_130+4431del	NM_001324312.2:c.130+4424_130+4431del	NM_001324312.2:c.130+4425_130+4431del	NM_001324312.2:c.130+4426_130+4431del	NM_001324312.2:c.130+4427_130+4431del	NM_001324312.2:c.130+4428_130+4431del	NM_001324312.2:c.130+4429_130+4431del	NM_001324312.2:c.130+4430_130+4431del	NM_001324312.2:c.130+4431del	NM_001324312.2:c.130+4431dup	NM_001324312.2:c.130+4430_130+4431dup	NM_001324312.2:c.130+4429_130+4431dup	NM_001324312.2:c.130+4428_130+4431dup	NM_001324312.2:c.130+4427_130+4431dup	NM_001324312.2:c.130+4431_130+4432insTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant 3	NM_001324313.2:c.130+4431=	NM_001324313.2:c.130+4418_130+4431del	NM_001324313.2:c.130+4419_130+4431del	NM_001324313.2:c.130+4420_130+4431del	NM_001324313.2:c.130+4421_130+4431del	NM_001324313.2:c.130+4422_130+4431del	NM_001324313.2:c.130+4423_130+4431del	NM_001324313.2:c.130+4424_130+4431del	NM_001324313.2:c.130+4425_130+4431del	NM_001324313.2:c.130+4426_130+4431del	NM_001324313.2:c.130+4427_130+4431del	NM_001324313.2:c.130+4428_130+4431del	NM_001324313.2:c.130+4429_130+4431del	NM_001324313.2:c.130+4430_130+4431del	NM_001324313.2:c.130+4431del	NM_001324313.2:c.130+4431dup	NM_001324313.2:c.130+4430_130+4431dup	NM_001324313.2:c.130+4429_130+4431dup	NM_001324313.2:c.130+4428_130+4431dup	NM_001324313.2:c.130+4427_130+4431dup	NM_001324313.2:c.130+4431_130+4432insTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant 4	NM_001324314.2:c.-347+4431=	NM_001324314.2:c.-347+4418_-347+4431del	NM_001324314.2:c.-347+4419_-347+4431del	NM_001324314.2:c.-347+4420_-347+4431del	NM_001324314.2:c.-347+4421_-347+4431del	NM_001324314.2:c.-347+4422_-347+4431del	NM_001324314.2:c.-347+4423_-347+4431del	NM_001324314.2:c.-347+4424_-347+4431del	NM_001324314.2:c.-347+4425_-347+4431del	NM_001324314.2:c.-347+4426_-347+4431del	NM_001324314.2:c.-347+4427_-347+4431del	NM_001324314.2:c.-347+4428_-347+4431del	NM_001324314.2:c.-347+4429_-347+4431del	NM_001324314.2:c.-347+4430_-347+4431del	NM_001324314.2:c.-347+4431del	NM_001324314.2:c.-347+4431dup	NM_001324314.2:c.-347+4430_-347+4431dup	NM_001324314.2:c.-347+4429_-347+4431dup	NM_001324314.2:c.-347+4428_-347+4431dup	NM_001324314.2:c.-347+4427_-347+4431dup	NM_001324314.2:c.-347+4431_-347+4432insTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant 6	NM_001324317.2:c.-139+4431=	NM_001324317.2:c.-139+4418_-139+4431del	NM_001324317.2:c.-139+4419_-139+4431del	NM_001324317.2:c.-139+4420_-139+4431del	NM_001324317.2:c.-139+4421_-139+4431del	NM_001324317.2:c.-139+4422_-139+4431del	NM_001324317.2:c.-139+4423_-139+4431del	NM_001324317.2:c.-139+4424_-139+4431del	NM_001324317.2:c.-139+4425_-139+4431del	NM_001324317.2:c.-139+4426_-139+4431del	NM_001324317.2:c.-139+4427_-139+4431del	NM_001324317.2:c.-139+4428_-139+4431del	NM_001324317.2:c.-139+4429_-139+4431del	NM_001324317.2:c.-139+4430_-139+4431del	NM_001324317.2:c.-139+4431del	NM_001324317.2:c.-139+4431dup	NM_001324317.2:c.-139+4430_-139+4431dup	NM_001324317.2:c.-139+4429_-139+4431dup	NM_001324317.2:c.-139+4428_-139+4431dup	NM_001324317.2:c.-139+4427_-139+4431dup	NM_001324317.2:c.-139+4431_-139+4432insTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant 1	NM_152707.3:c.130+4431=	NM_152707.3:c.130+4418_130+4431del	NM_152707.3:c.130+4419_130+4431del	NM_152707.3:c.130+4420_130+4431del	NM_152707.3:c.130+4421_130+4431del	NM_152707.3:c.130+4422_130+4431del	NM_152707.3:c.130+4423_130+4431del	NM_152707.3:c.130+4424_130+4431del	NM_152707.3:c.130+4425_130+4431del	NM_152707.3:c.130+4426_130+4431del	NM_152707.3:c.130+4427_130+4431del	NM_152707.3:c.130+4428_130+4431del	NM_152707.3:c.130+4429_130+4431del	NM_152707.3:c.130+4430_130+4431del	NM_152707.3:c.130+4431del	NM_152707.3:c.130+4431dup	NM_152707.3:c.130+4430_130+4431dup	NM_152707.3:c.130+4429_130+4431dup	NM_152707.3:c.130+4428_130+4431dup	NM_152707.3:c.130+4427_130+4431dup	NM_152707.3:c.130+4431_130+4432insTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant 1	NM_152707.4:c.130+4431=	NM_152707.4:c.130+4418_130+4431del	NM_152707.4:c.130+4419_130+4431del	NM_152707.4:c.130+4420_130+4431del	NM_152707.4:c.130+4421_130+4431del	NM_152707.4:c.130+4422_130+4431del	NM_152707.4:c.130+4423_130+4431del	NM_152707.4:c.130+4424_130+4431del	NM_152707.4:c.130+4425_130+4431del	NM_152707.4:c.130+4426_130+4431del	NM_152707.4:c.130+4427_130+4431del	NM_152707.4:c.130+4428_130+4431del	NM_152707.4:c.130+4429_130+4431del	NM_152707.4:c.130+4430_130+4431del	NM_152707.4:c.130+4431del	NM_152707.4:c.130+4431dup	NM_152707.4:c.130+4430_130+4431dup	NM_152707.4:c.130+4429_130+4431dup	NM_152707.4:c.130+4428_130+4431dup	NM_152707.4:c.130+4427_130+4431dup	NM_152707.4:c.130+4431_130+4432insTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant X1	XM_005270181.1:c.130+4431=	XM_005270181.1:c.130+4418_130+4431del	XM_005270181.1:c.130+4419_130+4431del	XM_005270181.1:c.130+4420_130+4431del	XM_005270181.1:c.130+4421_130+4431del	XM_005270181.1:c.130+4422_130+4431del	XM_005270181.1:c.130+4423_130+4431del	XM_005270181.1:c.130+4424_130+4431del	XM_005270181.1:c.130+4425_130+4431del	XM_005270181.1:c.130+4426_130+4431del	XM_005270181.1:c.130+4427_130+4431del	XM_005270181.1:c.130+4428_130+4431del	XM_005270181.1:c.130+4429_130+4431del	XM_005270181.1:c.130+4430_130+4431del	XM_005270181.1:c.130+4431del	XM_005270181.1:c.130+4431dup	XM_005270181.1:c.130+4430_130+4431dup	XM_005270181.1:c.130+4429_130+4431dup	XM_005270181.1:c.130+4428_130+4431dup	XM_005270181.1:c.130+4427_130+4431dup	XM_005270181.1:c.130+4431_130+4432insTTTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant X2	XM_005270182.1:c.-347+4431=	XM_005270182.1:c.-347+4418_-347+4431del	XM_005270182.1:c.-347+4419_-347+4431del	XM_005270182.1:c.-347+4420_-347+4431del	XM_005270182.1:c.-347+4421_-347+4431del	XM_005270182.1:c.-347+4422_-347+4431del	XM_005270182.1:c.-347+4423_-347+4431del	XM_005270182.1:c.-347+4424_-347+4431del	XM_005270182.1:c.-347+4425_-347+4431del	XM_005270182.1:c.-347+4426_-347+4431del	XM_005270182.1:c.-347+4427_-347+4431del	XM_005270182.1:c.-347+4428_-347+4431del	XM_005270182.1:c.-347+4429_-347+4431del	XM_005270182.1:c.-347+4430_-347+4431del	XM_005270182.1:c.-347+4431del	XM_005270182.1:c.-347+4431dup	XM_005270182.1:c.-347+4430_-347+4431dup	XM_005270182.1:c.-347+4429_-347+4431dup	XM_005270182.1:c.-347+4428_-347+4431dup	XM_005270182.1:c.-347+4427_-347+4431dup	XM_005270182.1:c.-347+4431_-347+4432insTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

47 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81854410	Dec 14, 2007 (129)
2	PJP	ss294662319	May 09, 2011 (137)
3	PJP	ss294662320	May 09, 2011 (134)
4	SWEGEN	ss3006663553	Nov 08, 2017 (151)
5	MCHAISSO	ss3064479234	Nov 08, 2017 (151)
6	MCHAISSO	ss3065389213	Nov 08, 2017 (151)
7	EVA_DECODE	ss3690102509	Jul 13, 2019 (153)
8	EVA_DECODE	ss3690102510	Jul 13, 2019 (153)
9	EVA_DECODE	ss3690102511	Jul 13, 2019 (153)
10	EVA_DECODE	ss3690102512	Jul 13, 2019 (153)
11	EVA_DECODE	ss3690102513	Jul 13, 2019 (153)
12	PACBIO	ss3786705628	Jul 13, 2019 (153)
13	PACBIO	ss3791881784	Jul 13, 2019 (153)
14	PACBIO	ss3796763802	Jul 13, 2019 (153)
15	EVA	ss3832184523	Apr 26, 2020 (154)
16	GNOMAD	ss4220478405	Apr 26, 2021 (155)
17	GNOMAD	ss4220478406	Apr 26, 2021 (155)
18	GNOMAD	ss4220478407	Apr 26, 2021 (155)
19	GNOMAD	ss4220478408	Apr 26, 2021 (155)
20	GNOMAD	ss4220478409	Apr 26, 2021 (155)
21	GNOMAD	ss4220478410	Apr 26, 2021 (155)
22	GNOMAD	ss4220478411	Apr 26, 2021 (155)
23	GNOMAD	ss4220478412	Apr 26, 2021 (155)
24	GNOMAD	ss4220478413	Apr 26, 2021 (155)
25	GNOMAD	ss4220478414	Apr 26, 2021 (155)
26	GNOMAD	ss4220478415	Apr 26, 2021 (155)
27	GNOMAD	ss4220478416	Apr 26, 2021 (155)
28	GNOMAD	ss4220478417	Apr 26, 2021 (155)
29	GNOMAD	ss4220478418	Apr 26, 2021 (155)
30	GNOMAD	ss4220478419	Apr 26, 2021 (155)
31	GNOMAD	ss4220478420	Apr 26, 2021 (155)
32	GNOMAD	ss4220478421	Apr 26, 2021 (155)
33	GNOMAD	ss4220478422	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5198136024	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5198136025	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5198136026	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5198136027	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5198136028	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5284443914	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5479981982	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5479981983	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5479981984	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5744110394	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5744110395	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5744110396	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5744110397	Oct 16, 2022 (156)
47	YY_MCH	ss5811631394	Oct 16, 2022 (156)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355457423 (NC_000010.11:68522814::A 302/60394) Row 355457424 (NC_000010.11:68522814::AA 144/60564) Row 355457425 (NC_000010.11:68522814::AAAA 3/60576)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 56105331 (NC_000010.10:70282571:A: 10394/16546) Row 56105332 (NC_000010.10:70282571:AAAAAAAAAA: 26/16546) Row 56105333 (NC_000010.10:70282571::A 75/16546)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 56105331 (NC_000010.10:70282571:A: 10394/16546) Row 56105332 (NC_000010.10:70282571:AAAAAAAAAA: 26/16546) Row 56105333 (NC_000010.10:70282571::A 75/16546)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 56105331 (NC_000010.10:70282571:A: 10394/16546) Row 56105332 (NC_000010.10:70282571:AAAAAAAAAA: 26/16546) Row 56105333 (NC_000010.10:70282571::A 75/16546)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 56105331 (NC_000010.10:70282571:A: 10394/16546) Row 56105332 (NC_000010.10:70282571:AAAAAAAAAA: 26/16546) Row 56105333 (NC_000010.10:70282571::A 75/16546)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 56105331 (NC_000010.10:70282571:A: 10394/16546) Row 56105332 (NC_000010.10:70282571:AAAAAAAAAA: 26/16546) Row 56105333 (NC_000010.10:70282571::A 75/16546)...	-	Apr 26, 2021 (155)
71	14KJPN Submission ignored due to conflicting rows: Row 77947498 (NC_000010.11:68522814:A: 16407/26436) Row 77947499 (NC_000010.11:68522814:AA: 313/26436) Row 77947500 (NC_000010.11:68522814::A 144/26436)...	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 77947498 (NC_000010.11:68522814:A: 16407/26436) Row 77947499 (NC_000010.11:68522814:AA: 313/26436) Row 77947500 (NC_000010.11:68522814::A 144/26436)...	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 77947498 (NC_000010.11:68522814:A: 16407/26436) Row 77947499 (NC_000010.11:68522814:AA: 313/26436) Row 77947500 (NC_000010.11:68522814::A 144/26436)...	-	Oct 16, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 77947498 (NC_000010.11:68522814:A: 16407/26436) Row 77947499 (NC_000010.11:68522814:AA: 313/26436) Row 77947500 (NC_000010.11:68522814::A 144/26436)...	-	Oct 16, 2022 (156)
75	ALFA	NC_000010.11 - 68522815	Apr 26, 2021 (155)

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

Associated ID	History Updated (Build)
rs142464042	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4220478422	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4220478421	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3006663553	NC_000010.10:70282571:AAAAAAAAAAAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4220478420	NC_000010.11:68522814:AAAAAAAAAAAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4220478419	NC_000010.11:68522814:AAAAAAAAAAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5198136025	NC_000010.10:70282571:AAAAAAAAAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5744110397	NC_000010.11:68522814:AAAAAAAAAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA
ss4220478418	NC_000010.11:68522814:AAAAAAAAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3690102513, ss4220478417	NC_000010.11:68522814:AAAAAAAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5198136028	NC_000010.10:70282571:AAAAAAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4220478416	NC_000010.11:68522814:AAAAAAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4220478415	NC_000010.11:68522814:AAAAAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4220478414	NC_000010.11:68522814:AAAAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4220478413	NC_000010.11:68522814:AAAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4220478412	NC_000010.11:68522814:AAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3690102512	NC_000010.11:68522819:AAA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3786705628, ss5198136027	NC_000010.10:70282571:AA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220478411, ss5284443914, ss5479981984, ss5744110395	NC_000010.11:68522814:AA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3690102511	NC_000010.11:68522820:AA:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss81854410	NC_000010.8:69952600:A:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss294662319	NC_000010.9:69952577:A:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss294662320	NC_000010.9:69952600:A:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3791881784, ss3796763802, ss3832184523, ss5198136024	NC_000010.10:70282571:A:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3064479234, ss3065389213, ss4220478410, ss5479981982, ss5744110394, ss5811631394	NC_000010.11:68522814:A:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3690102510	NC_000010.11:68522821:A:	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5198136026	NC_000010.10:70282571::A	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220478405, ss5479981983, ss5744110396	NC_000010.11:68522814::A	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3690102509	NC_000010.11:68522822::A	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220478406	NC_000010.11:68522814::AA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220478407	NC_000010.11:68522814::AAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10866077203	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220478408	NC_000010.11:68522814::AAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220478409	NC_000010.11:68522814::AAAAAAAAAAA… NC_000010.11:68522814::AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3122755874	NC_000010.11:68522814::AAA	NC_000010.11:68522814:AAAAAAAAAAAA… NC_000010.11:68522814:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA

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

No publications for rs58143466

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

rs58143466