Name: rs60845242
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.

rs60845242

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:68495782-68495801 (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)₉ / del(A)₈ / del(A)₇ / del(…
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 / dup(A)₆ / dup(A)₇ / dup(A)₉ / dup(A)₁₁ / dup(A)₁₂ / dup(A)₁₃ / ins(A)₂₅
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₉=0.000 (0/476, ALFA)
del(A)₈=0.000 (0/476, ALFA)
del(A)₇=0.000 (0/476, ALFA) (+ 10 more)
del(A)₆=0.000 (0/476, ALFA)
del(A)₅=0.000 (0/476, ALFA)
del(A)₄=0.000 (0/476, ALFA)
delAA=0.000 (0/476, ALFA)
delA=0.000 (0/476, ALFA)
dupA=0.000 (0/476, ALFA)
dupAA=0.000 (0/476, ALFA)
dupAAA=0.000 (0/476, ALFA)
dup(A)₄=0.000 (0/476, ALFA)
dup(A)₅=0.000 (0/476, 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	476	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	264	AAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	96	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	2	AAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African American	Sub	94	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	2	AAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	AAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	6	AAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	74	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	6	AAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	28	AAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=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	476	(A)₂₀=1.000	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, 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	264	(A)₂₀=1.000	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, 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	96	(A)₂₀=1.00	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, 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	74	(A)₂₀=1.00	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, 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	Other	Sub	28	(A)₂₀=1.00	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, 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	6	(A)₂₀=1.0	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, 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	South Asian	Sub	6	(A)₂₀=1.0	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, 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	2	(A)₂₀=1.0	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, 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 10	NC_000010.11:g.68495793_68495801del
GRCh38.p14 chr 10	NC_000010.11:g.68495794_68495801del
GRCh38.p14 chr 10	NC_000010.11:g.68495795_68495801del
GRCh38.p14 chr 10	NC_000010.11:g.68495796_68495801del
GRCh38.p14 chr 10	NC_000010.11:g.68495797_68495801del
GRCh38.p14 chr 10	NC_000010.11:g.68495798_68495801del
GRCh38.p14 chr 10	NC_000010.11:g.68495799_68495801del
GRCh38.p14 chr 10	NC_000010.11:g.68495800_68495801del
GRCh38.p14 chr 10	NC_000010.11:g.68495801del
GRCh38.p14 chr 10	NC_000010.11:g.68495801dup
GRCh38.p14 chr 10	NC_000010.11:g.68495800_68495801dup
GRCh38.p14 chr 10	NC_000010.11:g.68495799_68495801dup
GRCh38.p14 chr 10	NC_000010.11:g.68495798_68495801dup
GRCh38.p14 chr 10	NC_000010.11:g.68495797_68495801dup
GRCh38.p14 chr 10	NC_000010.11:g.68495796_68495801dup
GRCh38.p14 chr 10	NC_000010.11:g.68495795_68495801dup
GRCh38.p14 chr 10	NC_000010.11:g.68495793_68495801dup
GRCh38.p14 chr 10	NC_000010.11:g.68495791_68495801dup
GRCh38.p14 chr 10	NC_000010.11:g.68495790_68495801dup
GRCh38.p14 chr 10	NC_000010.11:g.68495789_68495801dup
GRCh38.p14 chr 10	NC_000010.11:g.68495801_68495802insAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 10	NC_000010.10:g.70255550_70255558del
GRCh37.p13 chr 10	NC_000010.10:g.70255551_70255558del
GRCh37.p13 chr 10	NC_000010.10:g.70255552_70255558del
GRCh37.p13 chr 10	NC_000010.10:g.70255553_70255558del
GRCh37.p13 chr 10	NC_000010.10:g.70255554_70255558del
GRCh37.p13 chr 10	NC_000010.10:g.70255555_70255558del
GRCh37.p13 chr 10	NC_000010.10:g.70255556_70255558del
GRCh37.p13 chr 10	NC_000010.10:g.70255557_70255558del
GRCh37.p13 chr 10	NC_000010.10:g.70255558del
GRCh37.p13 chr 10	NC_000010.10:g.70255558dup
GRCh37.p13 chr 10	NC_000010.10:g.70255557_70255558dup
GRCh37.p13 chr 10	NC_000010.10:g.70255556_70255558dup
GRCh37.p13 chr 10	NC_000010.10:g.70255555_70255558dup
GRCh37.p13 chr 10	NC_000010.10:g.70255554_70255558dup
GRCh37.p13 chr 10	NC_000010.10:g.70255553_70255558dup
GRCh37.p13 chr 10	NC_000010.10:g.70255552_70255558dup
GRCh37.p13 chr 10	NC_000010.10:g.70255550_70255558dup
GRCh37.p13 chr 10	NC_000010.10:g.70255548_70255558dup
GRCh37.p13 chr 10	NC_000010.10:g.70255547_70255558dup
GRCh37.p13 chr 10	NC_000010.10:g.70255546_70255558dup
GRCh37.p13 chr 10	NC_000010.10:g.70255558_70255559insAAAAAAAAAAAAAAAAAAAAAAAAA
SLC25A16 RefSeqGene	NG_046972.1:g.36734_36742del
SLC25A16 RefSeqGene	NG_046972.1:g.36735_36742del
SLC25A16 RefSeqGene	NG_046972.1:g.36736_36742del
SLC25A16 RefSeqGene	NG_046972.1:g.36737_36742del
SLC25A16 RefSeqGene	NG_046972.1:g.36738_36742del
SLC25A16 RefSeqGene	NG_046972.1:g.36739_36742del
SLC25A16 RefSeqGene	NG_046972.1:g.36740_36742del
SLC25A16 RefSeqGene	NG_046972.1:g.36741_36742del
SLC25A16 RefSeqGene	NG_046972.1:g.36742del
SLC25A16 RefSeqGene	NG_046972.1:g.36742dup
SLC25A16 RefSeqGene	NG_046972.1:g.36741_36742dup
SLC25A16 RefSeqGene	NG_046972.1:g.36740_36742dup
SLC25A16 RefSeqGene	NG_046972.1:g.36739_36742dup
SLC25A16 RefSeqGene	NG_046972.1:g.36738_36742dup
SLC25A16 RefSeqGene	NG_046972.1:g.36737_36742dup
SLC25A16 RefSeqGene	NG_046972.1:g.36736_36742dup
SLC25A16 RefSeqGene	NG_046972.1:g.36734_36742dup
SLC25A16 RefSeqGene	NG_046972.1:g.36732_36742dup
SLC25A16 RefSeqGene	NG_046972.1:g.36731_36742dup
SLC25A16 RefSeqGene	NG_046972.1:g.36730_36742dup
SLC25A16 RefSeqGene	NG_046972.1:g.36742_36743insTTTTTTTTTTTTTTTTTTTTTTTTT

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.422-2220… NM_001324312.2:c.422-2220_422-2212del	N/A	Intron Variant
SLC25A16 transcript variant 3	NM_001324313.2:c.422-2220… NM_001324313.2:c.422-2220_422-2212del	N/A	Intron Variant
SLC25A16 transcript variant 4	NM_001324314.2:c.128-2220… NM_001324314.2:c.128-2220_128-2212del	N/A	Intron Variant
SLC25A16 transcript variant 5	NM_001324315.1:c.128-2220… NM_001324315.1:c.128-2220_128-2212del	N/A	Intron Variant
SLC25A16 transcript variant 6	NM_001324317.2:c.20-2220_… NM_001324317.2:c.20-2220_20-2212del	N/A	Intron Variant
SLC25A16 transcript variant 1	NM_152707.4:c.422-2220_42… NM_152707.4:c.422-2220_422-2212del	N/A	Intron Variant
SLC25A16 transcript variant 7	NR_136737.1:n.	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(A)₂₀=	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	dup(A)₆	dup(A)₇	dup(A)₉	dup(A)₁₁	dup(A)₁₂	dup(A)₁₃	ins(A)₂₅
GRCh38.p14 chr 10	NC_000010.11:g.68495782_68495801=	NC_000010.11:g.68495793_68495801del	NC_000010.11:g.68495794_68495801del	NC_000010.11:g.68495795_68495801del	NC_000010.11:g.68495796_68495801del	NC_000010.11:g.68495797_68495801del	NC_000010.11:g.68495798_68495801del	NC_000010.11:g.68495799_68495801del	NC_000010.11:g.68495800_68495801del	NC_000010.11:g.68495801del	NC_000010.11:g.68495801dup	NC_000010.11:g.68495800_68495801dup	NC_000010.11:g.68495799_68495801dup	NC_000010.11:g.68495798_68495801dup	NC_000010.11:g.68495797_68495801dup	NC_000010.11:g.68495796_68495801dup	NC_000010.11:g.68495795_68495801dup	NC_000010.11:g.68495793_68495801dup	NC_000010.11:g.68495791_68495801dup	NC_000010.11:g.68495790_68495801dup	NC_000010.11:g.68495789_68495801dup	NC_000010.11:g.68495801_68495802insAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 10	NC_000010.10:g.70255539_70255558=	NC_000010.10:g.70255550_70255558del	NC_000010.10:g.70255551_70255558del	NC_000010.10:g.70255552_70255558del	NC_000010.10:g.70255553_70255558del	NC_000010.10:g.70255554_70255558del	NC_000010.10:g.70255555_70255558del	NC_000010.10:g.70255556_70255558del	NC_000010.10:g.70255557_70255558del	NC_000010.10:g.70255558del	NC_000010.10:g.70255558dup	NC_000010.10:g.70255557_70255558dup	NC_000010.10:g.70255556_70255558dup	NC_000010.10:g.70255555_70255558dup	NC_000010.10:g.70255554_70255558dup	NC_000010.10:g.70255553_70255558dup	NC_000010.10:g.70255552_70255558dup	NC_000010.10:g.70255550_70255558dup	NC_000010.10:g.70255548_70255558dup	NC_000010.10:g.70255547_70255558dup	NC_000010.10:g.70255546_70255558dup	NC_000010.10:g.70255558_70255559insAAAAAAAAAAAAAAAAAAAAAAAAA
SLC25A16 RefSeqGene	NG_046972.1:g.36723_36742=	NG_046972.1:g.36734_36742del	NG_046972.1:g.36735_36742del	NG_046972.1:g.36736_36742del	NG_046972.1:g.36737_36742del	NG_046972.1:g.36738_36742del	NG_046972.1:g.36739_36742del	NG_046972.1:g.36740_36742del	NG_046972.1:g.36741_36742del	NG_046972.1:g.36742del	NG_046972.1:g.36742dup	NG_046972.1:g.36741_36742dup	NG_046972.1:g.36740_36742dup	NG_046972.1:g.36739_36742dup	NG_046972.1:g.36738_36742dup	NG_046972.1:g.36737_36742dup	NG_046972.1:g.36736_36742dup	NG_046972.1:g.36734_36742dup	NG_046972.1:g.36732_36742dup	NG_046972.1:g.36731_36742dup	NG_046972.1:g.36730_36742dup	NG_046972.1:g.36742_36743insTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant 2	NM_001324312.2:c.422-2212=	NM_001324312.2:c.422-2220_422-2212del	NM_001324312.2:c.422-2219_422-2212del	NM_001324312.2:c.422-2218_422-2212del	NM_001324312.2:c.422-2217_422-2212del	NM_001324312.2:c.422-2216_422-2212del	NM_001324312.2:c.422-2215_422-2212del	NM_001324312.2:c.422-2214_422-2212del	NM_001324312.2:c.422-2213_422-2212del	NM_001324312.2:c.422-2212del	NM_001324312.2:c.422-2212dup	NM_001324312.2:c.422-2213_422-2212dup	NM_001324312.2:c.422-2214_422-2212dup	NM_001324312.2:c.422-2215_422-2212dup	NM_001324312.2:c.422-2216_422-2212dup	NM_001324312.2:c.422-2217_422-2212dup	NM_001324312.2:c.422-2218_422-2212dup	NM_001324312.2:c.422-2220_422-2212dup	NM_001324312.2:c.422-2222_422-2212dup	NM_001324312.2:c.422-2223_422-2212dup	NM_001324312.2:c.422-2224_422-2212dup	NM_001324312.2:c.422-2212_422-2211insTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant 3	NM_001324313.2:c.422-2212=	NM_001324313.2:c.422-2220_422-2212del	NM_001324313.2:c.422-2219_422-2212del	NM_001324313.2:c.422-2218_422-2212del	NM_001324313.2:c.422-2217_422-2212del	NM_001324313.2:c.422-2216_422-2212del	NM_001324313.2:c.422-2215_422-2212del	NM_001324313.2:c.422-2214_422-2212del	NM_001324313.2:c.422-2213_422-2212del	NM_001324313.2:c.422-2212del	NM_001324313.2:c.422-2212dup	NM_001324313.2:c.422-2213_422-2212dup	NM_001324313.2:c.422-2214_422-2212dup	NM_001324313.2:c.422-2215_422-2212dup	NM_001324313.2:c.422-2216_422-2212dup	NM_001324313.2:c.422-2217_422-2212dup	NM_001324313.2:c.422-2218_422-2212dup	NM_001324313.2:c.422-2220_422-2212dup	NM_001324313.2:c.422-2222_422-2212dup	NM_001324313.2:c.422-2223_422-2212dup	NM_001324313.2:c.422-2224_422-2212dup	NM_001324313.2:c.422-2212_422-2211insTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant 4	NM_001324314.2:c.128-2212=	NM_001324314.2:c.128-2220_128-2212del	NM_001324314.2:c.128-2219_128-2212del	NM_001324314.2:c.128-2218_128-2212del	NM_001324314.2:c.128-2217_128-2212del	NM_001324314.2:c.128-2216_128-2212del	NM_001324314.2:c.128-2215_128-2212del	NM_001324314.2:c.128-2214_128-2212del	NM_001324314.2:c.128-2213_128-2212del	NM_001324314.2:c.128-2212del	NM_001324314.2:c.128-2212dup	NM_001324314.2:c.128-2213_128-2212dup	NM_001324314.2:c.128-2214_128-2212dup	NM_001324314.2:c.128-2215_128-2212dup	NM_001324314.2:c.128-2216_128-2212dup	NM_001324314.2:c.128-2217_128-2212dup	NM_001324314.2:c.128-2218_128-2212dup	NM_001324314.2:c.128-2220_128-2212dup	NM_001324314.2:c.128-2222_128-2212dup	NM_001324314.2:c.128-2223_128-2212dup	NM_001324314.2:c.128-2224_128-2212dup	NM_001324314.2:c.128-2212_128-2211insTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant 5	NM_001324315.1:c.128-2212=	NM_001324315.1:c.128-2220_128-2212del	NM_001324315.1:c.128-2219_128-2212del	NM_001324315.1:c.128-2218_128-2212del	NM_001324315.1:c.128-2217_128-2212del	NM_001324315.1:c.128-2216_128-2212del	NM_001324315.1:c.128-2215_128-2212del	NM_001324315.1:c.128-2214_128-2212del	NM_001324315.1:c.128-2213_128-2212del	NM_001324315.1:c.128-2212del	NM_001324315.1:c.128-2212dup	NM_001324315.1:c.128-2213_128-2212dup	NM_001324315.1:c.128-2214_128-2212dup	NM_001324315.1:c.128-2215_128-2212dup	NM_001324315.1:c.128-2216_128-2212dup	NM_001324315.1:c.128-2217_128-2212dup	NM_001324315.1:c.128-2218_128-2212dup	NM_001324315.1:c.128-2220_128-2212dup	NM_001324315.1:c.128-2222_128-2212dup	NM_001324315.1:c.128-2223_128-2212dup	NM_001324315.1:c.128-2224_128-2212dup	NM_001324315.1:c.128-2212_128-2211insTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant 6	NM_001324317.2:c.20-2212=	NM_001324317.2:c.20-2220_20-2212del	NM_001324317.2:c.20-2219_20-2212del	NM_001324317.2:c.20-2218_20-2212del	NM_001324317.2:c.20-2217_20-2212del	NM_001324317.2:c.20-2216_20-2212del	NM_001324317.2:c.20-2215_20-2212del	NM_001324317.2:c.20-2214_20-2212del	NM_001324317.2:c.20-2213_20-2212del	NM_001324317.2:c.20-2212del	NM_001324317.2:c.20-2212dup	NM_001324317.2:c.20-2213_20-2212dup	NM_001324317.2:c.20-2214_20-2212dup	NM_001324317.2:c.20-2215_20-2212dup	NM_001324317.2:c.20-2216_20-2212dup	NM_001324317.2:c.20-2217_20-2212dup	NM_001324317.2:c.20-2218_20-2212dup	NM_001324317.2:c.20-2220_20-2212dup	NM_001324317.2:c.20-2222_20-2212dup	NM_001324317.2:c.20-2223_20-2212dup	NM_001324317.2:c.20-2224_20-2212dup	NM_001324317.2:c.20-2212_20-2211insTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant 1	NM_152707.3:c.422-2212=	NM_152707.3:c.422-2220_422-2212del	NM_152707.3:c.422-2219_422-2212del	NM_152707.3:c.422-2218_422-2212del	NM_152707.3:c.422-2217_422-2212del	NM_152707.3:c.422-2216_422-2212del	NM_152707.3:c.422-2215_422-2212del	NM_152707.3:c.422-2214_422-2212del	NM_152707.3:c.422-2213_422-2212del	NM_152707.3:c.422-2212del	NM_152707.3:c.422-2212dup	NM_152707.3:c.422-2213_422-2212dup	NM_152707.3:c.422-2214_422-2212dup	NM_152707.3:c.422-2215_422-2212dup	NM_152707.3:c.422-2216_422-2212dup	NM_152707.3:c.422-2217_422-2212dup	NM_152707.3:c.422-2218_422-2212dup	NM_152707.3:c.422-2220_422-2212dup	NM_152707.3:c.422-2222_422-2212dup	NM_152707.3:c.422-2223_422-2212dup	NM_152707.3:c.422-2224_422-2212dup	NM_152707.3:c.422-2212_422-2211insTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant 1	NM_152707.4:c.422-2212=	NM_152707.4:c.422-2220_422-2212del	NM_152707.4:c.422-2219_422-2212del	NM_152707.4:c.422-2218_422-2212del	NM_152707.4:c.422-2217_422-2212del	NM_152707.4:c.422-2216_422-2212del	NM_152707.4:c.422-2215_422-2212del	NM_152707.4:c.422-2214_422-2212del	NM_152707.4:c.422-2213_422-2212del	NM_152707.4:c.422-2212del	NM_152707.4:c.422-2212dup	NM_152707.4:c.422-2213_422-2212dup	NM_152707.4:c.422-2214_422-2212dup	NM_152707.4:c.422-2215_422-2212dup	NM_152707.4:c.422-2216_422-2212dup	NM_152707.4:c.422-2217_422-2212dup	NM_152707.4:c.422-2218_422-2212dup	NM_152707.4:c.422-2220_422-2212dup	NM_152707.4:c.422-2222_422-2212dup	NM_152707.4:c.422-2223_422-2212dup	NM_152707.4:c.422-2224_422-2212dup	NM_152707.4:c.422-2212_422-2211insTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant X1	XM_005270181.1:c.422-2212=	XM_005270181.1:c.422-2220_422-2212del	XM_005270181.1:c.422-2219_422-2212del	XM_005270181.1:c.422-2218_422-2212del	XM_005270181.1:c.422-2217_422-2212del	XM_005270181.1:c.422-2216_422-2212del	XM_005270181.1:c.422-2215_422-2212del	XM_005270181.1:c.422-2214_422-2212del	XM_005270181.1:c.422-2213_422-2212del	XM_005270181.1:c.422-2212del	XM_005270181.1:c.422-2212dup	XM_005270181.1:c.422-2213_422-2212dup	XM_005270181.1:c.422-2214_422-2212dup	XM_005270181.1:c.422-2215_422-2212dup	XM_005270181.1:c.422-2216_422-2212dup	XM_005270181.1:c.422-2217_422-2212dup	XM_005270181.1:c.422-2218_422-2212dup	XM_005270181.1:c.422-2220_422-2212dup	XM_005270181.1:c.422-2222_422-2212dup	XM_005270181.1:c.422-2223_422-2212dup	XM_005270181.1:c.422-2224_422-2212dup	XM_005270181.1:c.422-2212_422-2211insTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant X2	XM_005270182.1:c.128-2212=	XM_005270182.1:c.128-2220_128-2212del	XM_005270182.1:c.128-2219_128-2212del	XM_005270182.1:c.128-2218_128-2212del	XM_005270182.1:c.128-2217_128-2212del	XM_005270182.1:c.128-2216_128-2212del	XM_005270182.1:c.128-2215_128-2212del	XM_005270182.1:c.128-2214_128-2212del	XM_005270182.1:c.128-2213_128-2212del	XM_005270182.1:c.128-2212del	XM_005270182.1:c.128-2212dup	XM_005270182.1:c.128-2213_128-2212dup	XM_005270182.1:c.128-2214_128-2212dup	XM_005270182.1:c.128-2215_128-2212dup	XM_005270182.1:c.128-2216_128-2212dup	XM_005270182.1:c.128-2217_128-2212dup	XM_005270182.1:c.128-2218_128-2212dup	XM_005270182.1:c.128-2220_128-2212dup	XM_005270182.1:c.128-2222_128-2212dup	XM_005270182.1:c.128-2223_128-2212dup	XM_005270182.1:c.128-2224_128-2212dup	XM_005270182.1:c.128-2212_128-2211insTTTTTTTTTTTTTTTTTTTTTTTTT
SLC25A16 transcript variant X3	XM_005270183.1:c.-3+652=	XM_005270183.1:c.-3+644_-3+652del	XM_005270183.1:c.-3+645_-3+652del	XM_005270183.1:c.-3+646_-3+652del	XM_005270183.1:c.-3+647_-3+652del	XM_005270183.1:c.-3+648_-3+652del	XM_005270183.1:c.-3+649_-3+652del	XM_005270183.1:c.-3+650_-3+652del	XM_005270183.1:c.-3+651_-3+652del	XM_005270183.1:c.-3+652del	XM_005270183.1:c.-3+652dup	XM_005270183.1:c.-3+651_-3+652dup	XM_005270183.1:c.-3+650_-3+652dup	XM_005270183.1:c.-3+649_-3+652dup	XM_005270183.1:c.-3+648_-3+652dup	XM_005270183.1:c.-3+647_-3+652dup	XM_005270183.1:c.-3+646_-3+652dup	XM_005270183.1:c.-3+644_-3+652dup	XM_005270183.1:c.-3+642_-3+652dup	XM_005270183.1:c.-3+641_-3+652dup	XM_005270183.1:c.-3+640_-3+652dup	XM_005270183.1:c.-3+652_-3+653insTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

57 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80449428	Dec 15, 2007 (129)
2	HGSV	ss82525768	Dec 15, 2007 (129)
3	HUMANGENOME_JCVI	ss95544672	Feb 04, 2009 (130)
4	PJP	ss294662303	May 09, 2011 (137)
5	PJP	ss294662304	May 09, 2011 (137)
6	SWEGEN	ss3006663186	Nov 08, 2017 (151)
7	URBANLAB	ss3649399676	Oct 12, 2018 (152)
8	EVA_DECODE	ss3690102041	Jul 13, 2019 (153)
9	EVA_DECODE	ss3690102042	Jul 13, 2019 (153)
10	EVA_DECODE	ss3690102043	Jul 13, 2019 (153)
11	EVA_DECODE	ss3690102044	Jul 13, 2019 (153)
12	EVA_DECODE	ss3690102045	Jul 13, 2019 (153)
13	PACBIO	ss3786705588	Jul 13, 2019 (153)
14	PACBIO	ss3796763774	Jul 13, 2019 (153)
15	PACBIO	ss3796763775	Jul 13, 2019 (153)
16	EVA	ss3832184362	Apr 26, 2020 (154)
17	GNOMAD	ss4220474922	Apr 26, 2021 (155)
18	GNOMAD	ss4220474923	Apr 26, 2021 (155)
19	GNOMAD	ss4220474924	Apr 26, 2021 (155)
20	GNOMAD	ss4220474925	Apr 26, 2021 (155)
21	GNOMAD	ss4220474926	Apr 26, 2021 (155)
22	GNOMAD	ss4220474927	Apr 26, 2021 (155)
23	GNOMAD	ss4220474928	Apr 26, 2021 (155)
24	GNOMAD	ss4220474929	Apr 26, 2021 (155)
25	GNOMAD	ss4220474930	Apr 26, 2021 (155)
26	GNOMAD	ss4220474931	Apr 26, 2021 (155)
27	GNOMAD	ss4220474932	Apr 26, 2021 (155)
28	GNOMAD	ss4220474933	Apr 26, 2021 (155)
29	GNOMAD	ss4220474934	Apr 26, 2021 (155)
30	GNOMAD	ss4220474935	Apr 26, 2021 (155)
31	GNOMAD	ss4220474936	Apr 26, 2021 (155)
32	GNOMAD	ss4220474937	Apr 26, 2021 (155)
33	GNOMAD	ss4220474938	Apr 26, 2021 (155)
34	GNOMAD	ss4220474939	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5198134953	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5198134954	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5198134955	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5198134956	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5198134957	Apr 26, 2021 (155)
40	1000G_HIGH_COVERAGE	ss5284443119	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5284443120	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5284443122	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5284443123	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5479981264	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5479981265	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5479981266	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5479981267	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5479981268	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5744108881	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5744108882	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5744108883	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5744108884	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5744108885	Oct 16, 2022 (156)
54	EVA	ss5824554025	Oct 16, 2022 (156)
55	EVA	ss5824554026	Oct 16, 2022 (156)
56	EVA	ss5824554027	Oct 16, 2022 (156)
57	EVA	ss5849616506	Oct 16, 2022 (156)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 355451392 (NC_000010.11:68495781::A 2418/83676) Row 355451393 (NC_000010.11:68495781::AA 637/83682) Row 355451394 (NC_000010.11:68495781::AAA 55873/83442)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 56104260 (NC_000010.10:70255538::AAA 10785/15626) Row 56104261 (NC_000010.10:70255538::AAAA 122/15626) Row 56104262 (NC_000010.10:70255538:A: 139/15626)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 56104260 (NC_000010.10:70255538::AAA 10785/15626) Row 56104261 (NC_000010.10:70255538::AAAA 122/15626) Row 56104262 (NC_000010.10:70255538:A: 139/15626)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 56104260 (NC_000010.10:70255538::AAA 10785/15626) Row 56104261 (NC_000010.10:70255538::AAAA 122/15626) Row 56104262 (NC_000010.10:70255538:A: 139/15626)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 56104260 (NC_000010.10:70255538::AAA 10785/15626) Row 56104261 (NC_000010.10:70255538::AAAA 122/15626) Row 56104262 (NC_000010.10:70255538:A: 139/15626)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 56104260 (NC_000010.10:70255538::AAA 10785/15626) Row 56104261 (NC_000010.10:70255538::AAAA 122/15626) Row 56104262 (NC_000010.10:70255538:A: 139/15626)...	-	Apr 26, 2021 (155)
81	14KJPN Submission ignored due to conflicting rows: Row 77945985 (NC_000010.11:68495781::AAA 20209/27404) Row 77945986 (NC_000010.11:68495781:A: 284/27404) Row 77945987 (NC_000010.11:68495781::AA 127/27404)...	-	Oct 16, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 77945985 (NC_000010.11:68495781::AAA 20209/27404) Row 77945986 (NC_000010.11:68495781:A: 284/27404) Row 77945987 (NC_000010.11:68495781::AA 127/27404)...	-	Oct 16, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 77945985 (NC_000010.11:68495781::AAA 20209/27404) Row 77945986 (NC_000010.11:68495781:A: 284/27404) Row 77945987 (NC_000010.11:68495781::AA 127/27404)...	-	Oct 16, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 77945985 (NC_000010.11:68495781::AAA 20209/27404) Row 77945986 (NC_000010.11:68495781:A: 284/27404) Row 77945987 (NC_000010.11:68495781::AA 127/27404)...	-	Oct 16, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 77945985 (NC_000010.11:68495781::AAA 20209/27404) Row 77945986 (NC_000010.11:68495781:A: 284/27404) Row 77945987 (NC_000010.11:68495781::AA 127/27404)...	-	Oct 16, 2022 (156)
86	ALFA	NC_000010.11 - 68495782	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)
rs72401375	May 11, 2012 (137)
rs72413165	May 11, 2012 (137)
rs145818048	May 11, 2012 (137)
rs148971366	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4220474939	NC_000010.11:68495781:AAAAAAAAA:	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
10670344658	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
10670344658	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4220474938	NC_000010.11:68495781:AAAAAAA:	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
10670344658	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
10670344658	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
10670344658	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4220474937	NC_000010.11:68495781:AAAA:	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
10670344658	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4220474936	NC_000010.11:68495781:AAA:	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4220474935	NC_000010.11:68495781:AA:	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
10670344658	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3006663186, ss5198134955	NC_000010.10:70255538:A:	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3690102045, ss4220474934, ss5284443120, ss5479981267, ss5744108882	NC_000010.11:68495781:A:	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
10670344658	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4220474922, ss5284443123, ss5479981268	NC_000010.11:68495781::A	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
10670344658	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3690102044	NC_000010.11:68495782::A	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3786705588, ss3796763774, ss5198134956, ss5824554026	NC_000010.10:70255538::AA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220474923, ss5479981264, ss5744108883	NC_000010.11:68495781::AA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
10670344658	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3690102043	NC_000010.11:68495782::AA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss294662303	NC_000010.9:69925545::AAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss294662304	NC_000010.9:69925562::AAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3796763775, ss5198134953, ss5824554025	NC_000010.10:70255538::AAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3649399676, ss4220474924, ss5284443119, ss5479981265, ss5744108881	NC_000010.11:68495781::AAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
10670344658	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3690102042	NC_000010.11:68495782::AAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss80449428, ss95544672	NT_030059.13:21060022::AAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3832184362, ss5198134954, ss5824554027	NC_000010.10:70255538::AAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220474925, ss5284443122, ss5479981266, ss5744108885, ss5849616506	NC_000010.11:68495781::AAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
10670344658	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3690102041	NC_000010.11:68495782::AAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss82525768	NT_030059.13:21060022::AAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5198134957	NC_000010.10:70255538::AAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220474926, ss5744108884	NC_000010.11:68495781::AAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
10670344658	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220474927	NC_000010.11:68495781::AAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220474928	NC_000010.11:68495781::AAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220474929	NC_000010.11:68495781::AAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220474930	NC_000010.11:68495781::AAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220474931	NC_000010.11:68495781::AAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220474932	NC_000010.11:68495781::AAAAAAAAAAA… NC_000010.11:68495781::AAAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4220474933	NC_000010.11:68495781::AAAAAAAAAAA… NC_000010.11:68495781::AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3122750390	NC_000010.11:68495781:AAAAAA:	NC_000010.11:68495781:AAAAAAAAAAAA… NC_000010.11:68495781:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA

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

No publications for rs60845242

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

rs60845242