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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.

rs312262700

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr17:59015748 (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
insTA
Variation Type
Indel Insertion and Deletion
Frequency
None
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TRIM37 : Frameshift Variant
Publications
0 citations
Genomic View
See rs on genome
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").

None
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.59015748_59015749insTA
GRCh37.p13 chr 17 NC_000017.10:g.57093109_57093110insTA
TRIM37 RefSeqGene NG_009298.1:g.96158_96159insAT
Gene: TRIM37, tripartite motif containing 37 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
TRIM37 transcript variant 1 NM_015294.6:c.2438_2439in…

NM_015294.6:c.2438_2439insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform a NP_056109.1:p.Leu813_Ile8…

NP_056109.1:p.Leu813_Ile814insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant 10 NM_001353083.2:c.1703_170…

NM_001353083.2:c.1703_1704insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform f NP_001340012.1:p.Leu568_I…

NP_001340012.1:p.Leu568_Ile569insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant 5 NM_001320989.3:c.2438_243…

NM_001320989.3:c.2438_2439insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform c NP_001307918.1:p.Leu813_I…

NP_001307918.1:p.Leu813_Ile814insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant 12 NM_001353085.2:c.1976_197…

NM_001353085.2:c.1976_1977insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform h NP_001340014.1:p.Leu659_I…

NP_001340014.1:p.Leu659_Ile660insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant 7 NM_001353082.2:c.2336_233…

NM_001353082.2:c.2336_2337insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform e NP_001340011.1:p.Leu779_I…

NP_001340011.1:p.Leu779_Ile780insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant 6 NM_001320990.3:c.2072_207…

NM_001320990.3:c.2072_2073insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform d NP_001307919.1:p.Leu691_I…

NP_001307919.1:p.Leu691_Ile692insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant 13 NM_001353086.2:c.2387_238…

NM_001353086.2:c.2387_2388insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform i NP_001340015.1:p.Leu796_I…

NP_001340015.1:p.Leu796_Ile797insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant 4 NM_001320988.3:c.2438_243…

NM_001320988.3:c.2438_2439insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform c NP_001307917.1:p.Leu813_I…

NP_001307917.1:p.Leu813_Ile814insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant 3 NM_001320987.3:c.2336_233…

NM_001320987.3:c.2336_2337insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform b NP_001307916.1:p.Leu779_I…

NP_001307916.1:p.Leu779_Ile780insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant 2 NM_001005207.5:c.2438_243…

NM_001005207.5:c.2438_2439insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform a NP_001005207.1:p.Leu813_I…

NP_001005207.1:p.Leu813_Ile814insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant 11 NM_001353084.2:c.2438_243…

NM_001353084.2:c.2438_2439insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform g NP_001340013.1:p.Leu813_I…

NP_001340013.1:p.Leu813_Ile814insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant 9 NR_148347.2:n.2755_2756in…

NR_148347.2:n.2755_2756insAT

N/A Non Coding Transcript Variant
TRIM37 transcript variant 8 NR_148346.2:n.2857_2858in…

NR_148346.2:n.2857_2858insAT

N/A Non Coding Transcript Variant
TRIM37 transcript variant X1 XM_011524831.2:c.2438_243…

XM_011524831.2:c.2438_2439insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X1 XP_011523133.1:p.Leu813_I…

XP_011523133.1:p.Leu813_Ile814insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X2 XM_017024662.2:c.2438_243…

XM_017024662.2:c.2438_2439insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X2 XP_016880151.1:p.Leu813_I…

XP_016880151.1:p.Leu813_Ile814insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X3 XM_011524832.3:c.2438_243…

XM_011524832.3:c.2438_2439insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X3 XP_011523134.1:p.Leu813_I…

XP_011523134.1:p.Leu813_Ile814insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X4 XM_017024663.3:c.2438_243…

XM_017024663.3:c.2438_2439insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X4 XP_016880152.1:p.Leu813_I…

XP_016880152.1:p.Leu813_Ile814insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X5 XM_011524833.2:c.2387_238…

XM_011524833.2:c.2387_2388insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X5 XP_011523135.1:p.Leu796_I…

XP_011523135.1:p.Leu796_Ile797insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X6 XM_005257385.2:c.2438_243…

XM_005257385.2:c.2438_2439insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X6 XP_005257442.1:p.Leu813_I…

XP_005257442.1:p.Leu813_Ile814insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X7 XM_047436106.1:c.2387_238…

XM_047436106.1:c.2387_2388insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X7 XP_047292062.1:p.Leu796_I…

XP_047292062.1:p.Leu796_Ile797insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X8 XM_011524834.2:c.2336_233…

XM_011524834.2:c.2336_2337insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X8 XP_011523136.1:p.Leu779_I…

XP_011523136.1:p.Leu779_Ile780insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X9 XM_047436107.1:c.2336_233…

XM_047436107.1:c.2336_2337insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X9 XP_047292063.1:p.Leu779_I…

XP_047292063.1:p.Leu779_Ile780insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X10 XM_047436108.1:c.2387_238…

XM_047436108.1:c.2387_2388insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X10 XP_047292064.1:p.Leu796_I…

XP_047292064.1:p.Leu796_Ile797insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X11 XM_017024665.2:c.2336_233…

XM_017024665.2:c.2336_2337insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X11 XP_016880154.1:p.Leu779_I…

XP_016880154.1:p.Leu779_Ile780insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X12 XM_047436109.1:c.2309_231…

XM_047436109.1:c.2309_2310insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X12 XP_047292065.1:p.Leu770_I…

XP_047292065.1:p.Leu770_Ile771insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X13 XM_047436110.1:c.2336_233…

XM_047436110.1:c.2336_2337insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X13 XP_047292066.1:p.Leu779_I…

XP_047292066.1:p.Leu779_Ile780insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X14 XM_011524836.2:c.2438_243…

XM_011524836.2:c.2438_2439insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X14 XP_011523138.1:p.Leu813_I…

XP_011523138.1:p.Leu813_Ile814insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X15 XM_047436111.1:c.2438_243…

XM_047436111.1:c.2438_2439insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X15 XP_047292067.1:p.Leu813_I…

XP_047292067.1:p.Leu813_Ile814insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X16 XM_017024667.2:c.2387_238…

XM_017024667.2:c.2387_2388insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X16 XP_016880156.1:p.Leu796_I…

XP_016880156.1:p.Leu796_Ile797insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X17 XM_047436112.1:c.2285_228…

XM_047436112.1:c.2285_2286insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X17 XP_047292068.1:p.Leu762_I…

XP_047292068.1:p.Leu762_Ile763insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X18 XM_047436113.1:c.2336_233…

XM_047436113.1:c.2336_2337insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X18 XP_047292069.1:p.Leu779_I…

XP_047292069.1:p.Leu779_Ile780insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X19 XM_047436114.1:c.2336_233…

XM_047436114.1:c.2336_2337insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X19 XP_047292070.1:p.Leu779_I…

XP_047292070.1:p.Leu779_Ile780insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X20 XM_047436115.1:c.2309_231…

XM_047436115.1:c.2309_2310insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X20 XP_047292071.1:p.Leu770_I…

XP_047292071.1:p.Leu770_Ile771insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X21 XM_047436116.1:c.2309_231…

XM_047436116.1:c.2309_2310insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X21 XP_047292072.1:p.Leu770_I…

XP_047292072.1:p.Leu770_Ile771insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X22 XM_017024669.3:c.2285_228…

XM_017024669.3:c.2285_2286insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X22 XP_016880158.1:p.Leu762_I…

XP_016880158.1:p.Leu762_Ile763insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X23 XM_047436117.1:c.2387_238…

XM_047436117.1:c.2387_2388insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X23 XP_047292073.1:p.Leu796_I…

XP_047292073.1:p.Leu796_Ile797insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X24 XM_047436118.1:c.2309_231…

XM_047436118.1:c.2309_2310insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X24 XP_047292074.1:p.Leu770_I…

XP_047292074.1:p.Leu770_Ile771insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X25 XM_047436119.1:c.2258_225…

XM_047436119.1:c.2258_2259insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X25 XP_047292075.1:p.Leu753_I…

XP_047292075.1:p.Leu753_Ile754insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X26 XM_047436120.1:c.2207_220…

XM_047436120.1:c.2207_2208insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X26 XP_047292076.1:p.Leu736_I…

XP_047292076.1:p.Leu736_Ile737insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X27 XM_017024670.3:c.2336_233…

XM_017024670.3:c.2336_2337insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X27 XP_016880159.1:p.Leu779_I…

XP_016880159.1:p.Leu779_Ile780insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X28 XM_047436121.1:c.2336_233…

XM_047436121.1:c.2336_2337insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X28 XP_047292077.1:p.Leu779_I…

XP_047292077.1:p.Leu779_Ile780insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X29 XM_047436122.1:c.2207_220…

XM_047436122.1:c.2207_2208insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X29 XP_047292078.1:p.Leu736_I…

XP_047292078.1:p.Leu736_Ile737insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X30 XM_047436123.1:c.2309_231…

XM_047436123.1:c.2309_2310insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X30 XP_047292079.1:p.Leu770_I…

XP_047292079.1:p.Leu770_Ile771insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X31 XM_047436124.1:c.2285_228…

XM_047436124.1:c.2285_2286insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X31 XP_047292080.1:p.Leu762_I…

XP_047292080.1:p.Leu762_Ile763insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X32 XM_047436125.1:c.2156_215…

XM_047436125.1:c.2156_2157insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X32 XP_047292081.1:p.Leu719_I…

XP_047292081.1:p.Leu719_Ile720insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X33 XM_047436126.1:c.2207_220…

XM_047436126.1:c.2207_2208insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X33 XP_047292082.1:p.Leu736_I…

XP_047292082.1:p.Leu736_Ile737insTer

L (Leu) > L (Leu) Frameshift Variant
TRIM37 transcript variant X34 XM_017024673.3:c.1703_170…

XM_017024673.3:c.1703_1704insAT

L [TTG] > L [TTATG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X34 XP_016880162.1:p.Leu568_I…

XP_016880162.1:p.Leu568_Ile569insTer

L (Leu) > L (Leu) Frameshift 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 A= insTA
GRCh38.p14 chr 17 NC_000017.11:g.59015748= NC_000017.11:g.59015748_59015749insTA
GRCh37.p13 chr 17 NC_000017.10:g.57093109= NC_000017.10:g.57093109_57093110insTA
TRIM37 RefSeqGene NG_009298.1:g.96158= NG_009298.1:g.96158_96159insAT
TRIM37 transcript variant 1 NM_015294.6:c.2438= NM_015294.6:c.2438_2439insAT
TRIM37 transcript variant 1 NM_015294.5:c.2438= NM_015294.5:c.2438_2439insAT
TRIM37 transcript variant 1 NM_015294.4:c.2438= NM_015294.4:c.2438_2439insAT
TRIM37 transcript variant 1 NM_015294.3:c.2438= NM_015294.3:c.2438_2439insAT
TRIM37 transcript variant 2 NM_001005207.5:c.2438= NM_001005207.5:c.2438_2439insAT
TRIM37 transcript variant 2 NM_001005207.4:c.2438= NM_001005207.4:c.2438_2439insAT
TRIM37 transcript variant 2 NM_001005207.3:c.2438= NM_001005207.3:c.2438_2439insAT
TRIM37 transcript variant 2 NM_001005207.2:c.2438= NM_001005207.2:c.2438_2439insAT
TRIM37 transcript variant 6 NM_001320990.3:c.2072= NM_001320990.3:c.2072_2073insAT
TRIM37 transcript variant 6 NM_001320990.2:c.2072= NM_001320990.2:c.2072_2073insAT
TRIM37 transcript variant 6 NM_001320990.1:c.2072= NM_001320990.1:c.2072_2073insAT
TRIM37 transcript variant 3 NM_001320987.3:c.2336= NM_001320987.3:c.2336_2337insAT
TRIM37 transcript variant 3 NM_001320987.2:c.2336= NM_001320987.2:c.2336_2337insAT
TRIM37 transcript variant 3 NM_001320987.1:c.2336= NM_001320987.1:c.2336_2337insAT
TRIM37 transcript variant 4 NM_001320988.3:c.2438= NM_001320988.3:c.2438_2439insAT
TRIM37 transcript variant 4 NM_001320988.2:c.2438= NM_001320988.2:c.2438_2439insAT
TRIM37 transcript variant 4 NM_001320988.1:c.2438= NM_001320988.1:c.2438_2439insAT
TRIM37 transcript variant 5 NM_001320989.3:c.2438= NM_001320989.3:c.2438_2439insAT
TRIM37 transcript variant 5 NM_001320989.2:c.2438= NM_001320989.2:c.2438_2439insAT
TRIM37 transcript variant 5 NM_001320989.1:c.2438= NM_001320989.1:c.2438_2439insAT
TRIM37 transcript variant 8 NR_148346.2:n.2857= NR_148346.2:n.2857_2858insAT
TRIM37 transcript variant 8 NR_148346.1:n.2941= NR_148346.1:n.2941_2942insAT
TRIM37 transcript variant 11 NM_001353084.2:c.2438= NM_001353084.2:c.2438_2439insAT
TRIM37 transcript variant 11 NM_001353084.1:c.2438= NM_001353084.1:c.2438_2439insAT
TRIM37 transcript variant 10 NM_001353083.2:c.1703= NM_001353083.2:c.1703_1704insAT
TRIM37 transcript variant 10 NM_001353083.1:c.1703= NM_001353083.1:c.1703_1704insAT
TRIM37 transcript variant 13 NM_001353086.2:c.2387= NM_001353086.2:c.2387_2388insAT
TRIM37 transcript variant 13 NM_001353086.1:c.2387= NM_001353086.1:c.2387_2388insAT
TRIM37 transcript variant 9 NR_148347.2:n.2755= NR_148347.2:n.2755_2756insAT
TRIM37 transcript variant 9 NR_148347.1:n.2839= NR_148347.1:n.2839_2840insAT
TRIM37 transcript variant 7 NM_001353082.2:c.2336= NM_001353082.2:c.2336_2337insAT
TRIM37 transcript variant 7 NM_001353082.1:c.2336= NM_001353082.1:c.2336_2337insAT
TRIM37 transcript variant 12 NM_001353085.2:c.1976= NM_001353085.2:c.1976_1977insAT
TRIM37 transcript variant 12 NM_001353085.1:c.1976= NM_001353085.1:c.1976_1977insAT
TRIM37 transcript variant X3 XM_011524832.3:c.2438= XM_011524832.3:c.2438_2439insAT
TRIM37 transcript variant X3 XM_011524832.2:c.2438= XM_011524832.2:c.2438_2439insAT
TRIM37 transcript variant X2 XM_011524832.1:c.2438= XM_011524832.1:c.2438_2439insAT
TRIM37 transcript variant X4 XM_017024663.3:c.2438= XM_017024663.3:c.2438_2439insAT
TRIM37 transcript variant X4 XM_017024663.2:c.2438= XM_017024663.2:c.2438_2439insAT
TRIM37 transcript variant X4 XM_017024663.1:c.2438= XM_017024663.1:c.2438_2439insAT
TRIM37 transcript variant X22 XM_017024669.3:c.2285= XM_017024669.3:c.2285_2286insAT
TRIM37 transcript variant X12 XM_017024669.2:c.2285= XM_017024669.2:c.2285_2286insAT
TRIM37 transcript variant X15 XM_017024669.1:c.2285= XM_017024669.1:c.2285_2286insAT
TRIM37 transcript variant X27 XM_017024670.3:c.2336= XM_017024670.3:c.2336_2337insAT
TRIM37 transcript variant X13 XM_017024670.2:c.2336= XM_017024670.2:c.2336_2337insAT
TRIM37 transcript variant X16 XM_017024670.1:c.2336= XM_017024670.1:c.2336_2337insAT
TRIM37 transcript variant X34 XM_017024673.3:c.1703= XM_017024673.3:c.1703_1704insAT
TRIM37 transcript variant X17 XM_017024673.2:c.1703= XM_017024673.2:c.1703_1704insAT
TRIM37 transcript variant X20 XM_017024673.1:c.1703= XM_017024673.1:c.1703_1704insAT
TRIM37 transcript variant X2 XM_017024662.2:c.2438= XM_017024662.2:c.2438_2439insAT
TRIM37 transcript variant X2 XM_017024662.1:c.2438= XM_017024662.1:c.2438_2439insAT
TRIM37 transcript variant X1 XM_011524831.2:c.2438= XM_011524831.2:c.2438_2439insAT
TRIM37 transcript variant X1 XM_011524831.1:c.2438= XM_011524831.1:c.2438_2439insAT
TRIM37 transcript variant X11 XM_017024665.2:c.2336= XM_017024665.2:c.2336_2337insAT
TRIM37 transcript variant X9 XM_017024665.1:c.2336= XM_017024665.1:c.2336_2337insAT
TRIM37 transcript variant X14 XM_011524836.2:c.2438= XM_011524836.2:c.2438_2439insAT
TRIM37 transcript variant X10 XM_011524836.1:c.2438= XM_011524836.1:c.2438_2439insAT
TRIM37 transcript variant X6 XM_005257385.2:c.2438= XM_005257385.2:c.2438_2439insAT
TRIM37 transcript variant X6 XM_005257385.1:c.2438= XM_005257385.1:c.2438_2439insAT
TRIM37 transcript variant X16 XM_017024667.2:c.2387= XM_017024667.2:c.2387_2388insAT
TRIM37 transcript variant X11 XM_017024667.1:c.2387= XM_017024667.1:c.2387_2388insAT
TRIM37 transcript variant X5 XM_011524833.2:c.2387= XM_011524833.2:c.2387_2388insAT
TRIM37 transcript variant X5 XM_011524833.1:c.2387= XM_011524833.1:c.2387_2388insAT
TRIM37 transcript variant X8 XM_011524834.2:c.2336= XM_011524834.2:c.2336_2337insAT
TRIM37 transcript variant X7 XM_011524834.1:c.2336= XM_011524834.1:c.2336_2337insAT
TRIM37 transcript variant X9 XM_047436107.1:c.2336= XM_047436107.1:c.2336_2337insAT
TRIM37 transcript variant X13 XM_047436110.1:c.2336= XM_047436110.1:c.2336_2337insAT
TRIM37 transcript variant X15 XM_047436111.1:c.2438= XM_047436111.1:c.2438_2439insAT
TRIM37 transcript variant X7 XM_047436106.1:c.2387= XM_047436106.1:c.2387_2388insAT
TRIM37 transcript variant X12 XM_047436109.1:c.2309= XM_047436109.1:c.2309_2310insAT
TRIM37 transcript variant X25 XM_047436119.1:c.2258= XM_047436119.1:c.2258_2259insAT
TRIM37 transcript variant X26 XM_047436120.1:c.2207= XM_047436120.1:c.2207_2208insAT
TRIM37 transcript variant X31 XM_047436124.1:c.2285= XM_047436124.1:c.2285_2286insAT
TRIM37 transcript variant X32 XM_047436125.1:c.2156= XM_047436125.1:c.2156_2157insAT
TRIM37 transcript variant X33 XM_047436126.1:c.2207= XM_047436126.1:c.2207_2208insAT
TRIM37 transcript variant X10 XM_047436108.1:c.2387= XM_047436108.1:c.2387_2388insAT
TRIM37 transcript variant X18 XM_047436113.1:c.2336= XM_047436113.1:c.2336_2337insAT
TRIM37 transcript variant X20 XM_047436115.1:c.2309= XM_047436115.1:c.2309_2310insAT
TRIM37 transcript variant X19 XM_047436114.1:c.2336= XM_047436114.1:c.2336_2337insAT
TRIM37 transcript variant X21 XM_047436116.1:c.2309= XM_047436116.1:c.2309_2310insAT
TRIM37 transcript variant X23 XM_047436117.1:c.2387= XM_047436117.1:c.2387_2388insAT
TRIM37 transcript variant X28 XM_047436121.1:c.2336= XM_047436121.1:c.2336_2337insAT
TRIM37 transcript variant X29 XM_047436122.1:c.2207= XM_047436122.1:c.2207_2208insAT
TRIM37 transcript variant X30 XM_047436123.1:c.2309= XM_047436123.1:c.2309_2310insAT
TRIM37 transcript variant X17 XM_047436112.1:c.2285= XM_047436112.1:c.2285_2286insAT
TRIM37 transcript variant X24 XM_047436118.1:c.2309= XM_047436118.1:c.2309_2310insAT
E3 ubiquitin-protein ligase TRIM37 isoform a NP_056109.1:p.Leu813= NP_056109.1:p.Leu813_Ile814insTer
E3 ubiquitin-protein ligase TRIM37 isoform a NP_001005207.1:p.Leu813= NP_001005207.1:p.Leu813_Ile814insTer
E3 ubiquitin-protein ligase TRIM37 isoform d NP_001307919.1:p.Leu691= NP_001307919.1:p.Leu691_Ile692insTer
E3 ubiquitin-protein ligase TRIM37 isoform b NP_001307916.1:p.Leu779= NP_001307916.1:p.Leu779_Ile780insTer
E3 ubiquitin-protein ligase TRIM37 isoform c NP_001307917.1:p.Leu813= NP_001307917.1:p.Leu813_Ile814insTer
E3 ubiquitin-protein ligase TRIM37 isoform c NP_001307918.1:p.Leu813= NP_001307918.1:p.Leu813_Ile814insTer
E3 ubiquitin-protein ligase TRIM37 isoform g NP_001340013.1:p.Leu813= NP_001340013.1:p.Leu813_Ile814insTer
E3 ubiquitin-protein ligase TRIM37 isoform f NP_001340012.1:p.Leu568= NP_001340012.1:p.Leu568_Ile569insTer
E3 ubiquitin-protein ligase TRIM37 isoform i NP_001340015.1:p.Leu796= NP_001340015.1:p.Leu796_Ile797insTer
E3 ubiquitin-protein ligase TRIM37 isoform e NP_001340011.1:p.Leu779= NP_001340011.1:p.Leu779_Ile780insTer
E3 ubiquitin-protein ligase TRIM37 isoform h NP_001340014.1:p.Leu659= NP_001340014.1:p.Leu659_Ile660insTer
E3 ubiquitin-protein ligase TRIM37 isoform X3 XP_011523134.1:p.Leu813= XP_011523134.1:p.Leu813_Ile814insTer
E3 ubiquitin-protein ligase TRIM37 isoform X4 XP_016880152.1:p.Leu813= XP_016880152.1:p.Leu813_Ile814insTer
E3 ubiquitin-protein ligase TRIM37 isoform X22 XP_016880158.1:p.Leu762= XP_016880158.1:p.Leu762_Ile763insTer
E3 ubiquitin-protein ligase TRIM37 isoform X27 XP_016880159.1:p.Leu779= XP_016880159.1:p.Leu779_Ile780insTer
E3 ubiquitin-protein ligase TRIM37 isoform X34 XP_016880162.1:p.Leu568= XP_016880162.1:p.Leu568_Ile569insTer
E3 ubiquitin-protein ligase TRIM37 isoform X2 XP_016880151.1:p.Leu813= XP_016880151.1:p.Leu813_Ile814insTer
E3 ubiquitin-protein ligase TRIM37 isoform X1 XP_011523133.1:p.Leu813= XP_011523133.1:p.Leu813_Ile814insTer
E3 ubiquitin-protein ligase TRIM37 isoform X11 XP_016880154.1:p.Leu779= XP_016880154.1:p.Leu779_Ile780insTer
E3 ubiquitin-protein ligase TRIM37 isoform X14 XP_011523138.1:p.Leu813= XP_011523138.1:p.Leu813_Ile814insTer
E3 ubiquitin-protein ligase TRIM37 isoform X6 XP_005257442.1:p.Leu813= XP_005257442.1:p.Leu813_Ile814insTer
E3 ubiquitin-protein ligase TRIM37 isoform X16 XP_016880156.1:p.Leu796= XP_016880156.1:p.Leu796_Ile797insTer
E3 ubiquitin-protein ligase TRIM37 isoform X5 XP_011523135.1:p.Leu796= XP_011523135.1:p.Leu796_Ile797insTer
E3 ubiquitin-protein ligase TRIM37 isoform X8 XP_011523136.1:p.Leu779= XP_011523136.1:p.Leu779_Ile780insTer
E3 ubiquitin-protein ligase TRIM37 isoform X9 XP_047292063.1:p.Leu779= XP_047292063.1:p.Leu779_Ile780insTer
E3 ubiquitin-protein ligase TRIM37 isoform X13 XP_047292066.1:p.Leu779= XP_047292066.1:p.Leu779_Ile780insTer
E3 ubiquitin-protein ligase TRIM37 isoform X15 XP_047292067.1:p.Leu813= XP_047292067.1:p.Leu813_Ile814insTer
E3 ubiquitin-protein ligase TRIM37 isoform X7 XP_047292062.1:p.Leu796= XP_047292062.1:p.Leu796_Ile797insTer
E3 ubiquitin-protein ligase TRIM37 isoform X12 XP_047292065.1:p.Leu770= XP_047292065.1:p.Leu770_Ile771insTer
E3 ubiquitin-protein ligase TRIM37 isoform X25 XP_047292075.1:p.Leu753= XP_047292075.1:p.Leu753_Ile754insTer
E3 ubiquitin-protein ligase TRIM37 isoform X26 XP_047292076.1:p.Leu736= XP_047292076.1:p.Leu736_Ile737insTer
E3 ubiquitin-protein ligase TRIM37 isoform X31 XP_047292080.1:p.Leu762= XP_047292080.1:p.Leu762_Ile763insTer
E3 ubiquitin-protein ligase TRIM37 isoform X32 XP_047292081.1:p.Leu719= XP_047292081.1:p.Leu719_Ile720insTer
E3 ubiquitin-protein ligase TRIM37 isoform X33 XP_047292082.1:p.Leu736= XP_047292082.1:p.Leu736_Ile737insTer
E3 ubiquitin-protein ligase TRIM37 isoform X10 XP_047292064.1:p.Leu796= XP_047292064.1:p.Leu796_Ile797insTer
E3 ubiquitin-protein ligase TRIM37 isoform X18 XP_047292069.1:p.Leu779= XP_047292069.1:p.Leu779_Ile780insTer
E3 ubiquitin-protein ligase TRIM37 isoform X20 XP_047292071.1:p.Leu770= XP_047292071.1:p.Leu770_Ile771insTer
E3 ubiquitin-protein ligase TRIM37 isoform X19 XP_047292070.1:p.Leu779= XP_047292070.1:p.Leu779_Ile780insTer
E3 ubiquitin-protein ligase TRIM37 isoform X21 XP_047292072.1:p.Leu770= XP_047292072.1:p.Leu770_Ile771insTer
E3 ubiquitin-protein ligase TRIM37 isoform X23 XP_047292073.1:p.Leu796= XP_047292073.1:p.Leu796_Ile797insTer
E3 ubiquitin-protein ligase TRIM37 isoform X28 XP_047292077.1:p.Leu779= XP_047292077.1:p.Leu779_Ile780insTer
E3 ubiquitin-protein ligase TRIM37 isoform X29 XP_047292078.1:p.Leu736= XP_047292078.1:p.Leu736_Ile737insTer
E3 ubiquitin-protein ligase TRIM37 isoform X30 XP_047292079.1:p.Leu770= XP_047292079.1:p.Leu770_Ile771insTer
E3 ubiquitin-protein ligase TRIM37 isoform X17 XP_047292068.1:p.Leu762= XP_047292068.1:p.Leu762_Ile763insTer
E3 ubiquitin-protein ligase TRIM37 isoform X24 XP_047292074.1:p.Leu770= XP_047292074.1:p.Leu770_Ile771insTer
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#.

1 SubSNP submission
No Submitter Submission ID Date (Build)
1 HEL_FIG_AEL ss715532797 Mar 01, 2013 (137)
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History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss715532797 NC_000017.11:59015747::AT NC_000017.11:59015747:A:ATA (self)
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs312262700

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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.post761+d5e8e07