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dbSNP Short Genetic Variations

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.

rs60117388

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr17:75905942-75905951 (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(C)5 / delCC / delC / dupC / du…

del(C)5 / delCC / delC / dupC / dupCC / dupCCC / dup(C)4 / dup(C)5 / dup(C)6 / dup(C)7 / dup(C)8 / dup(C)9 / dup(C)10

Variation Type
Indel Insertion and Deletion
Frequency
delC=0.0758 (715/9427, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
MRPL38 : 2KB Upstream 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 9427 CCCCCCCCCC=0.8897 CCCCC=0.0000, CCCCCCCC=0.0012, CCCCCCCCC=0.0758, CCCCCCCCCCC=0.0326, CCCCCCCCCCCC=0.0007, CCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCC=0.0000 0.864991 0.015596 0.119413 32
European Sub 7875 CCCCCCCCCC=0.8683 CCCCC=0.0000, CCCCCCCC=0.0014, CCCCCCCCC=0.0904, CCCCCCCCCCC=0.0390, CCCCCCCCCCCC=0.0009, CCCCCCCCCCCCC=0.0000, CCCCCCCCCCCCCC=0.0000 0.83608 0.019034 0.144886 31
African Sub 874 CCCCCCCCCC=1.000 CCCCC=0.000, CCCCCCCC=0.000, CCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000 1.0 0.0 0.0 N/A
African Others Sub 34 CCCCCCCCCC=1.00 CCCCC=0.00, CCCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00 1.0 0.0 0.0 N/A
African American Sub 840 CCCCCCCCCC=1.000 CCCCC=0.000, CCCCCCCC=0.000, CCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000 1.0 0.0 0.0 N/A
Asian Sub 50 CCCCCCCCCC=1.00 CCCCC=0.00, CCCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00 1.0 0.0 0.0 N/A
East Asian Sub 42 CCCCCCCCCC=1.00 CCCCC=0.00, CCCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 8 CCCCCCCCCC=1.0 CCCCC=0.0, CCCCCCCC=0.0, CCCCCCCCC=0.0, CCCCCCCCCCC=0.0, CCCCCCCCCCCC=0.0, CCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCC=0.0 1.0 0.0 0.0 N/A
Latin American 1 Sub 74 CCCCCCCCCC=1.00 CCCCC=0.00, CCCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00 1.0 0.0 0.0 N/A
Latin American 2 Sub 294 CCCCCCCCCC=1.000 CCCCC=0.000, CCCCCCCC=0.000, CCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000 1.0 0.0 0.0 N/A
South Asian Sub 44 CCCCCCCCCC=1.00 CCCCC=0.00, CCCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00 1.0 0.0 0.0 N/A
Other Sub 216 CCCCCCCCCC=0.986 CCCCC=0.000, CCCCCCCC=0.000, CCCCCCCCC=0.014, CCCCCCCCCCC=0.000, CCCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000 0.972222 0.0 0.027778 0


Help

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").

Download
Study Population Group Sample Size Ref Allele Alt Allele
Allele Frequency Aggregator Total Global 9427 (C)10=0.8897 del(C)5=0.0000, delCC=0.0012, delC=0.0758, dupC=0.0326, dupCC=0.0007, dupCCC=0.0000, dup(C)4=0.0000
Allele Frequency Aggregator European Sub 7875 (C)10=0.8683 del(C)5=0.0000, delCC=0.0014, delC=0.0904, dupC=0.0390, dupCC=0.0009, dupCCC=0.0000, dup(C)4=0.0000
Allele Frequency Aggregator African Sub 874 (C)10=1.000 del(C)5=0.000, delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000, dupCCC=0.000, dup(C)4=0.000
Allele Frequency Aggregator Latin American 2 Sub 294 (C)10=1.000 del(C)5=0.000, delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000, dupCCC=0.000, dup(C)4=0.000
Allele Frequency Aggregator Other Sub 216 (C)10=0.986 del(C)5=0.000, delCC=0.000, delC=0.014, dupC=0.000, dupCC=0.000, dupCCC=0.000, dup(C)4=0.000
Allele Frequency Aggregator Latin American 1 Sub 74 (C)10=1.00 del(C)5=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00, dup(C)4=0.00
Allele Frequency Aggregator Asian Sub 50 (C)10=1.00 del(C)5=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00, dup(C)4=0.00
Allele Frequency Aggregator South Asian Sub 44 (C)10=1.00 del(C)5=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00, dup(C)4=0.00
Help

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 17 NC_000017.11:g.75905947_75905951del
GRCh38.p14 chr 17 NC_000017.11:g.75905950_75905951del
GRCh38.p14 chr 17 NC_000017.11:g.75905951del
GRCh38.p14 chr 17 NC_000017.11:g.75905951dup
GRCh38.p14 chr 17 NC_000017.11:g.75905950_75905951dup
GRCh38.p14 chr 17 NC_000017.11:g.75905949_75905951dup
GRCh38.p14 chr 17 NC_000017.11:g.75905948_75905951dup
GRCh38.p14 chr 17 NC_000017.11:g.75905947_75905951dup
GRCh38.p14 chr 17 NC_000017.11:g.75905946_75905951dup
GRCh38.p14 chr 17 NC_000017.11:g.75905945_75905951dup
GRCh38.p14 chr 17 NC_000017.11:g.75905944_75905951dup
GRCh38.p14 chr 17 NC_000017.11:g.75905943_75905951dup
GRCh38.p14 chr 17 NC_000017.11:g.75905942_75905951dup
GRCh37.p13 chr 17 NC_000017.10:g.73902028_73902032del
GRCh37.p13 chr 17 NC_000017.10:g.73902031_73902032del
GRCh37.p13 chr 17 NC_000017.10:g.73902032del
GRCh37.p13 chr 17 NC_000017.10:g.73902032dup
GRCh37.p13 chr 17 NC_000017.10:g.73902031_73902032dup
GRCh37.p13 chr 17 NC_000017.10:g.73902030_73902032dup
GRCh37.p13 chr 17 NC_000017.10:g.73902029_73902032dup
GRCh37.p13 chr 17 NC_000017.10:g.73902028_73902032dup
GRCh37.p13 chr 17 NC_000017.10:g.73902027_73902032dup
GRCh37.p13 chr 17 NC_000017.10:g.73902026_73902032dup
GRCh37.p13 chr 17 NC_000017.10:g.73902025_73902032dup
GRCh37.p13 chr 17 NC_000017.10:g.73902024_73902032dup
GRCh37.p13 chr 17 NC_000017.10:g.73902023_73902032dup
Gene: MRPL38, mitochondrial ribosomal protein L38 (minus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
MRPL38 transcript NM_032478.4:c. N/A Upstream Transcript Variant
Help

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
Help

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 (C)10= del(C)5 delCC delC dupC dupCC dupCCC dup(C)4 dup(C)5 dup(C)6 dup(C)7 dup(C)8 dup(C)9 dup(C)10
GRCh38.p14 chr 17 NC_000017.11:g.75905942_75905951= NC_000017.11:g.75905947_75905951del NC_000017.11:g.75905950_75905951del NC_000017.11:g.75905951del NC_000017.11:g.75905951dup NC_000017.11:g.75905950_75905951dup NC_000017.11:g.75905949_75905951dup NC_000017.11:g.75905948_75905951dup NC_000017.11:g.75905947_75905951dup NC_000017.11:g.75905946_75905951dup NC_000017.11:g.75905945_75905951dup NC_000017.11:g.75905944_75905951dup NC_000017.11:g.75905943_75905951dup NC_000017.11:g.75905942_75905951dup
GRCh37.p13 chr 17 NC_000017.10:g.73902023_73902032= NC_000017.10:g.73902028_73902032del NC_000017.10:g.73902031_73902032del NC_000017.10:g.73902032del NC_000017.10:g.73902032dup NC_000017.10:g.73902031_73902032dup NC_000017.10:g.73902030_73902032dup NC_000017.10:g.73902029_73902032dup NC_000017.10:g.73902028_73902032dup NC_000017.10:g.73902027_73902032dup NC_000017.10:g.73902026_73902032dup NC_000017.10:g.73902025_73902032dup NC_000017.10:g.73902024_73902032dup NC_000017.10:g.73902023_73902032dup
Help

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, 25 Frequency submissions
No Submitter Submission ID Date (Build)
1 HGSV ss81114539 Sep 08, 2015 (146)
2 HGSV ss81116393 Sep 08, 2015 (146)
3 HGSV ss81188519 Sep 08, 2015 (146)
4 HGSV ss81646388 Sep 08, 2015 (146)
5 GMI ss289338902 May 04, 2012 (137)
6 1000GENOMES ss327808459 May 09, 2011 (137)
7 1000GENOMES ss327935784 May 09, 2011 (137)
8 LUNTER ss552543514 Apr 25, 2013 (138)
9 LUNTER ss552901166 Apr 25, 2013 (138)
10 LUNTER ss553627004 Apr 25, 2013 (138)
11 SSMP ss664377064 Apr 01, 2015 (144)
12 HAMMER_LAB ss1808883927 Sep 08, 2015 (146)
13 HAMMER_LAB ss1808883928 Sep 08, 2015 (146)
14 SYSTEMSBIOZJU ss2629081932 Nov 08, 2017 (151)
15 MCHAISSO ss3063877869 Jan 10, 2018 (151)
16 EVA_DECODE ss3700926561 Jul 13, 2019 (153)
17 EVA_DECODE ss3700926562 Jul 13, 2019 (153)
18 EVA_DECODE ss3700926563 Jul 13, 2019 (153)
19 EVA_DECODE ss3700926564 Jul 13, 2019 (153)
20 ACPOP ss3742221408 Jul 13, 2019 (153)
21 ACPOP ss3742221409 Jul 13, 2019 (153)
22 EVA ss3834980950 Apr 27, 2020 (154)
23 KOGIC ss3979303563 Apr 27, 2020 (154)
24 KOGIC ss3979303564 Apr 27, 2020 (154)
25 GNOMAD ss4315762575 Apr 27, 2021 (155)
26 GNOMAD ss4315762576 Apr 27, 2021 (155)
27 GNOMAD ss4315762577 Apr 27, 2021 (155)
28 GNOMAD ss4315762578 Apr 27, 2021 (155)
29 GNOMAD ss4315762579 Apr 27, 2021 (155)
30 GNOMAD ss4315762580 Apr 27, 2021 (155)
31 GNOMAD ss4315762581 Apr 27, 2021 (155)
32 GNOMAD ss4315762582 Apr 27, 2021 (155)
33 GNOMAD ss4315762583 Apr 27, 2021 (155)
34 GNOMAD ss4315762584 Apr 27, 2021 (155)
35 GNOMAD ss4315762585 Apr 27, 2021 (155)
36 GNOMAD ss4315762586 Apr 27, 2021 (155)
37 TOMMO_GENOMICS ss5223506287 Apr 27, 2021 (155)
38 TOMMO_GENOMICS ss5223506288 Apr 27, 2021 (155)
39 TOMMO_GENOMICS ss5223506289 Apr 27, 2021 (155)
40 TOMMO_GENOMICS ss5223506290 Apr 27, 2021 (155)
41 1000G_HIGH_COVERAGE ss5303955544 Oct 16, 2022 (156)
42 1000G_HIGH_COVERAGE ss5303955545 Oct 16, 2022 (156)
43 1000G_HIGH_COVERAGE ss5303955546 Oct 16, 2022 (156)
44 1000G_HIGH_COVERAGE ss5303955547 Oct 16, 2022 (156)
45 1000G_HIGH_COVERAGE ss5303955548 Oct 16, 2022 (156)
46 1000G_HIGH_COVERAGE ss5303955549 Oct 16, 2022 (156)
47 HUGCELL_USP ss5496918341 Oct 16, 2022 (156)
48 HUGCELL_USP ss5496918343 Oct 16, 2022 (156)
49 HUGCELL_USP ss5496918344 Oct 16, 2022 (156)
50 HUGCELL_USP ss5496918345 Oct 16, 2022 (156)
51 TOMMO_GENOMICS ss5780059989 Oct 16, 2022 (156)
52 TOMMO_GENOMICS ss5780059990 Oct 16, 2022 (156)
53 TOMMO_GENOMICS ss5780059992 Oct 16, 2022 (156)
54 TOMMO_GENOMICS ss5780059993 Oct 16, 2022 (156)
55 EVA ss5834296277 Oct 16, 2022 (156)
56 EVA ss5834296278 Oct 16, 2022 (156)
57 EVA ss5851898621 Oct 16, 2022 (156)
58 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 514048604 (NC_000017.11:75905941::C 8904/94450)
Row 514048605 (NC_000017.11:75905941::CC 1879/94848)
Row 514048606 (NC_000017.11:75905941::CCC 310/95170)...

- Apr 27, 2021 (155)
59 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 514048604 (NC_000017.11:75905941::C 8904/94450)
Row 514048605 (NC_000017.11:75905941::CC 1879/94848)
Row 514048606 (NC_000017.11:75905941::CCC 310/95170)...

- Apr 27, 2021 (155)
60 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 514048604 (NC_000017.11:75905941::C 8904/94450)
Row 514048605 (NC_000017.11:75905941::CC 1879/94848)
Row 514048606 (NC_000017.11:75905941::CCC 310/95170)...

- Apr 27, 2021 (155)
61 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 514048604 (NC_000017.11:75905941::C 8904/94450)
Row 514048605 (NC_000017.11:75905941::CC 1879/94848)
Row 514048606 (NC_000017.11:75905941::CCC 310/95170)...

- Apr 27, 2021 (155)
62 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 514048604 (NC_000017.11:75905941::C 8904/94450)
Row 514048605 (NC_000017.11:75905941::CC 1879/94848)
Row 514048606 (NC_000017.11:75905941::CCC 310/95170)...

- Apr 27, 2021 (155)
63 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 514048604 (NC_000017.11:75905941::C 8904/94450)
Row 514048605 (NC_000017.11:75905941::CC 1879/94848)
Row 514048606 (NC_000017.11:75905941::CCC 310/95170)...

- Apr 27, 2021 (155)
64 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 514048604 (NC_000017.11:75905941::C 8904/94450)
Row 514048605 (NC_000017.11:75905941::CC 1879/94848)
Row 514048606 (NC_000017.11:75905941::CCC 310/95170)...

- Apr 27, 2021 (155)
65 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 514048604 (NC_000017.11:75905941::C 8904/94450)
Row 514048605 (NC_000017.11:75905941::CC 1879/94848)
Row 514048606 (NC_000017.11:75905941::CCC 310/95170)...

- Apr 27, 2021 (155)
66 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 514048604 (NC_000017.11:75905941::C 8904/94450)
Row 514048605 (NC_000017.11:75905941::CC 1879/94848)
Row 514048606 (NC_000017.11:75905941::CCC 310/95170)...

- Apr 27, 2021 (155)
67 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 514048604 (NC_000017.11:75905941::C 8904/94450)
Row 514048605 (NC_000017.11:75905941::CC 1879/94848)
Row 514048606 (NC_000017.11:75905941::CCC 310/95170)...

- Apr 27, 2021 (155)
68 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 514048604 (NC_000017.11:75905941::C 8904/94450)
Row 514048605 (NC_000017.11:75905941::CC 1879/94848)
Row 514048606 (NC_000017.11:75905941::CCC 310/95170)...

- Apr 27, 2021 (155)
69 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 514048604 (NC_000017.11:75905941::C 8904/94450)
Row 514048605 (NC_000017.11:75905941::CC 1879/94848)
Row 514048606 (NC_000017.11:75905941::CCC 310/95170)...

- Apr 27, 2021 (155)
70 Korean Genome Project

Submission ignored due to conflicting rows:
Row 35681564 (NC_000017.11:75905942::C 174/1754)
Row 35681565 (NC_000017.11:75905941:C: 474/1754)

- Apr 27, 2020 (154)
71 Korean Genome Project

Submission ignored due to conflicting rows:
Row 35681564 (NC_000017.11:75905942::C 174/1754)
Row 35681565 (NC_000017.11:75905941:C: 474/1754)

- Apr 27, 2020 (154)
72 Northern Sweden

Submission ignored due to conflicting rows:
Row 15506273 (NC_000017.10:73902022:C: 99/592)
Row 15506274 (NC_000017.10:73902022::C 38/592)

- Jul 13, 2019 (153)
73 Northern Sweden

Submission ignored due to conflicting rows:
Row 15506273 (NC_000017.10:73902022:C: 99/592)
Row 15506274 (NC_000017.10:73902022::C 38/592)

- Jul 13, 2019 (153)
74 8.3KJPN

Submission ignored due to conflicting rows:
Row 81475594 (NC_000017.10:73902022:C: 4036/16356)
Row 81475595 (NC_000017.10:73902022::C 1380/16356)
Row 81475596 (NC_000017.10:73902022:CC: 19/16356)...

- Apr 27, 2021 (155)
75 8.3KJPN

Submission ignored due to conflicting rows:
Row 81475594 (NC_000017.10:73902022:C: 4036/16356)
Row 81475595 (NC_000017.10:73902022::C 1380/16356)
Row 81475596 (NC_000017.10:73902022:CC: 19/16356)...

- Apr 27, 2021 (155)
76 8.3KJPN

Submission ignored due to conflicting rows:
Row 81475594 (NC_000017.10:73902022:C: 4036/16356)
Row 81475595 (NC_000017.10:73902022::C 1380/16356)
Row 81475596 (NC_000017.10:73902022:CC: 19/16356)...

- Apr 27, 2021 (155)
77 8.3KJPN

Submission ignored due to conflicting rows:
Row 81475594 (NC_000017.10:73902022:C: 4036/16356)
Row 81475595 (NC_000017.10:73902022::C 1380/16356)
Row 81475596 (NC_000017.10:73902022:CC: 19/16356)...

- Apr 27, 2021 (155)
78 14KJPN

Submission ignored due to conflicting rows:
Row 113897093 (NC_000017.11:75905941:C: 6899/27820)
Row 113897094 (NC_000017.11:75905941::C 2459/27820)
Row 113897096 (NC_000017.11:75905941::CC 37/27820)...

- Oct 16, 2022 (156)
79 14KJPN

Submission ignored due to conflicting rows:
Row 113897093 (NC_000017.11:75905941:C: 6899/27820)
Row 113897094 (NC_000017.11:75905941::C 2459/27820)
Row 113897096 (NC_000017.11:75905941::CC 37/27820)...

- Oct 16, 2022 (156)
80 14KJPN

Submission ignored due to conflicting rows:
Row 113897093 (NC_000017.11:75905941:C: 6899/27820)
Row 113897094 (NC_000017.11:75905941::C 2459/27820)
Row 113897096 (NC_000017.11:75905941::CC 37/27820)...

- Oct 16, 2022 (156)
81 14KJPN

Submission ignored due to conflicting rows:
Row 113897093 (NC_000017.11:75905941:C: 6899/27820)
Row 113897094 (NC_000017.11:75905941::C 2459/27820)
Row 113897096 (NC_000017.11:75905941::CC 37/27820)...

- Oct 16, 2022 (156)
82 ALFA NC_000017.11 - 75905942 Apr 27, 2021 (155)
Help

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)
rs139128350 May 11, 2012 (137)
rs377331681 May 13, 2013 (138)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss4315762586 NC_000017.11:75905941:CCCCC: NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCC

(self)
4419206466 NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCC

NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCC

(self)
ss5223506289 NC_000017.10:73902022:CC: NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCC

(self)
ss3063877869, ss4315762585, ss5303955549, ss5496918345, ss5780059993 NC_000017.11:75905941:CC: NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCC

(self)
4419206466 NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCC

NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCC

(self)
ss3700926564 NC_000017.11:75905949:CC: NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCC

(self)
ss289338902, ss327808459, ss327935784, ss552543514, ss552901166, ss553627004 NC_000017.9:71413617:C: NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCC

(self)
ss81114539, ss81116393, ss81188519, ss81646388 NC_000017.9:71413626:C: NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCC

(self)
ss664377064, ss1808883928, ss3742221408, ss5223506287, ss5834296277 NC_000017.10:73902022:C: NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCC

(self)
ss3979303564, ss5303955544, ss5496918341, ss5780059989, ss5851898621 NC_000017.11:75905941:C: NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCC

(self)
4419206466 NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCC

NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCC

(self)
ss3700926563 NC_000017.11:75905950:C: NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCC

(self)
ss1808883927, ss2629081932, ss3742221409, ss3834980950, ss5223506288 NC_000017.10:73902022::C NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCC

(self)
ss4315762575, ss5303955545, ss5496918343, ss5780059990 NC_000017.11:75905941::C NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCC

(self)
4419206466 NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCC

NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCC

(self)
ss3979303563 NC_000017.11:75905942::C NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCC

(self)
ss3700926562 NC_000017.11:75905951::C NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCC

(self)
ss5223506290 NC_000017.10:73902022::CC NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCC

(self)
ss4315762576, ss5303955546, ss5496918344, ss5780059992 NC_000017.11:75905941::CC NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCC

(self)
4419206466 NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCC

NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCC

(self)
ss3700926561 NC_000017.11:75905951::CC NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCC

(self)
ss5834296278 NC_000017.10:73902022::CCC NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCCC

ss4315762577, ss5303955547 NC_000017.11:75905941::CCC NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCCC

(self)
4419206466 NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCCC

NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCCC

(self)
ss4315762578, ss5303955548 NC_000017.11:75905941::CCCC NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCCCC

(self)
4419206466 NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCCCC

NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCCCC

(self)
ss4315762579 NC_000017.11:75905941::CCCCC NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCCCCC

(self)
ss4315762580 NC_000017.11:75905941::CCCCCC NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCCCCCC

(self)
ss4315762581 NC_000017.11:75905941::CCCCCCC NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCCCCCCC

(self)
ss4315762582 NC_000017.11:75905941::CCCCCCCC NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCCCCCCCC

(self)
ss4315762583 NC_000017.11:75905941::CCCCCCCCC NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCCCCCCCCC

(self)
ss4315762584 NC_000017.11:75905941::CCCCCCCCCC NC_000017.11:75905941:CCCCCCCCCC:C…

NC_000017.11:75905941:CCCCCCCCCC:CCCCCCCCCCCCCCCCCCCC

(self)
Help

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

No publications for rs60117388

Help

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.

Software version is: 2.0.1.post820+afb47a3d