SNP Links for Nucleotide (Select 164414399) - SNP

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Links from Nucleotide

Items: 1 to 20 of 550

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Select item 14908165511.

rs1490816551 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 15:84569952 (GRCh38)
15:85113183 (GRCh37)
Canonical SPDI:: NC_000015.10:84569951:A:G,NC_000015.10:84569951:A:T
Gene:: UBE2Q2P1 (Varview), LINC00933 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.84569952A>G, NC_000015.10:g.84569952A>T, NC_000015.9:g.85113183A>G, NC_000015.9:g.85113183A>T, NW_025791797.1:g.1061798A>G, NW_025791797.1:g.1061798A>T, NR_003661.2:n.844T>C, NR_003661.2:n.844T>A, NM_207382.1:c.-253T>C, NM_207382.1:c.-253T>A

Select item 14904777652.

rs1490477765 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:84570322 (GRCh38)
15:85113553 (GRCh37)
Canonical SPDI:: NC_000015.10:84570321:T:C
Gene:: UBE2Q2P1 (Varview), LINC00933 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000015.10:g.84570322T>C, NC_000015.9:g.85113553T>C, NW_025791797.1:g.1062168T>C, NR_003661.2:n.474A>G, NM_207382.1:c.-623A>G

Select item 14901415223.

rs1490141522 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:84554975 (GRCh38)
15:85098206 (GRCh37)
Canonical SPDI:: NC_000015.10:84554974:G:A
Gene:: UBE2Q2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.84554975G>A, NC_000015.9:g.85098206G>A, NW_025791797.1:g.1046821G>A, NR_003661.2:n.1387C>T, NM_207382.1:c.291C>T

Select item 14874475954.

rs1487447595 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 15:84554982 (GRCh38)
15:85098213 (GRCh37)
Canonical SPDI:: NC_000015.10:84554981:G:A,NC_000015.10:84554981:G:C
Gene:: UBE2Q2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000015.10:g.84554982G>A, NC_000015.10:g.84554982G>C, NC_000015.9:g.85098213G>A, NC_000015.9:g.85098213G>C, NW_025791797.1:g.1046828G>A, NW_025791797.1:g.1046828G>C, NR_003661.2:n.1380C>T, NR_003661.2:n.1380C>G, NM_207382.1:c.284C>T, NM_207382.1:c.284C>G

Select item 14865158675.

rs1486515867 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:84570513 (GRCh38)
15:85113744 (GRCh37)
Canonical SPDI:: NC_000015.10:84570512:T:C
Gene:: UBE2Q2P1 (Varview), LINC00933 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.84570513T>C, NC_000015.9:g.85113744T>C, NW_025791797.1:g.1062359T>C, NR_003661.2:n.283A>G, NM_207382.1:c.-814A>G

Select item 14849856146.

rs1484985614 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 15:84527197 (GRCh38)
15:85070428 (GRCh37)
Canonical SPDI:: NC_000015.10:84527196:A:T
Gene:: UBE2Q2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: T=0.00106/30 (TOMMO)
T=0.01065/31 (KOREAN)
HGVS:: NC_000015.10:g.84527197A>T, NC_000015.9:g.85070428A>T, NW_025791797.1:g.1019043A>T, NR_003661.2:n.2149T>A, NM_207382.1:c.*513T>A

Select item 14847148637.

rs1484714863 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 15:84570541 (GRCh38)
15:85113772 (GRCh37)
Canonical SPDI:: NC_000015.10:84570540:C:G
Gene:: UBE2Q2P1 (Varview), LINC00933 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.84570541C>G, NC_000015.9:g.85113772C>G, NW_025791797.1:g.1062387C>G, NR_003661.2:n.255G>C, NM_207382.1:c.-842G>C

Select item 14805214668.

rs1480521466 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:84569669 (GRCh38)
15:85112900 (GRCh37)
Canonical SPDI:: NC_000015.10:84569668:A:G
Gene:: UBE2Q2P1 (Varview), LINC00933 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.84569669A>G, NC_000015.9:g.85112900A>G, NW_025791797.1:g.1061515A>G, NR_003661.2:n.1127T>C, NM_207382.1:c.31T>C

Select item 14797027169.

rs1479702716 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 15:84570304 (GRCh38)
15:85113535 (GRCh37)
Canonical SPDI:: NC_000015.10:84570303:G:A,NC_000015.10:84570303:G:T
Gene:: UBE2Q2P1 (Varview), LINC00933 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
T=0.000558/1 (Korea1K)
HGVS:: NC_000015.10:g.84570304G>A, NC_000015.10:g.84570304G>T, NC_000015.9:g.85113535G>A, NC_000015.9:g.85113535G>T, NW_025791797.1:g.1062150G>A, NW_025791797.1:g.1062150G>T, NR_003661.2:n.492C>T, NR_003661.2:n.492C>A, NM_207382.1:c.-605C>T, NM_207382.1:c.-605C>A

Select item 147943013810.

rs1479430138 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 15:84542187 (GRCh38)
15:85085418 (GRCh37)
Canonical SPDI:: NC_000015.10:84542186:A:C
Gene:: UBE2Q2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000396/6 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000036/5 (GnomAD)
HGVS:: NC_000015.10:g.84542187A>C, NC_000015.9:g.85085418A>C, NW_025791797.1:g.1034033A>C, NR_003661.2:n.1551T>G, NM_207382.1:c.455T>G

Select item 147586183111.

rs1475861831 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:84569747 (GRCh38)
15:85112978 (GRCh37)
Canonical SPDI:: NC_000015.10:84569746:T:C
Gene:: UBE2Q2P1 (Varview), LINC00933 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000015.10:g.84569747T>C, NC_000015.9:g.85112978T>C, NW_025791797.1:g.1061593T>C, NR_003661.2:n.1049A>G, NM_207382.1:c.-48A>G

Select item 147468687612.

rs1474686876 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:84527229 (GRCh38)
15:85070460 (GRCh37)
Canonical SPDI:: NC_000015.10:84527228:G:A
Gene:: UBE2Q2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000015/2 (GnomAD)
HGVS:: NC_000015.10:g.84527229G>A, NC_000015.9:g.85070460G>A, NW_025791797.1:g.1019075G>A, NR_003661.2:n.2117C>T, NM_207382.1:c.*481C>T

Select item 147221833513.

rs1472218335 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:84527560 (GRCh38)
15:85070791 (GRCh37)
Canonical SPDI:: NC_000015.10:84527559:T:C
Gene:: UBE2Q2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.84527560T>C, NC_000015.9:g.85070791T>C, NW_025791797.1:g.1019406T>C, NR_003661.2:n.1786A>G, NM_207382.1:c.*150A>G

Select item 147192625114.

rs1471926251 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 15:84570081 (GRCh38)
15:85113313 (GRCh37)
Canonical SPDI:: NC_000015.10:84570081:C:CC
Gene:: UBE2Q2P1 (Varview), LINC00933 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0.000071/1 (ALFA)
C=0.000021/3 (GnomAD)
C=0.00003/8 (TOPMED)
HGVS:: NC_000015.10:g.84570082dup, NC_000015.9:g.85113313dup, NW_025791797.1:g.1061928dup, NR_003661.2:n.714dup, NM_207382.1:c.-383dup

Select item 147047922815.

rs1470479228 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:84570362 (GRCh38)
15:85113593 (GRCh37)
Canonical SPDI:: NC_000015.10:84570361:C:T
Gene:: UBE2Q2P1 (Varview), LINC00933 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.00006/1 (TOMMO)
HGVS:: NC_000015.10:g.84570362C>T, NC_000015.9:g.85113593C>T, NW_025791797.1:g.1062208C>T, NR_003661.2:n.434G>A, NM_207382.1:c.-663G>A

Select item 147001584916.

rs1470015849 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 15:84569792 (GRCh38)
15:85113023 (GRCh37)
Canonical SPDI:: NC_000015.10:84569791:T:A
Gene:: UBE2Q2P1 (Varview), LINC00933 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.84569792T>A, NC_000015.9:g.85113023T>A, NW_025791797.1:g.1061638T>A, NR_003661.2:n.1004A>T, NM_207382.1:c.-93A>T

Select item 146890807917.

rs1468908079 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 15:84570355 (GRCh38)
15:85113586 (GRCh37)
Canonical SPDI:: NC_000015.10:84570354:G:A,NC_000015.10:84570354:G:C,NC_000015.10:84570354:G:T
Gene:: UBE2Q2P1 (Varview), LINC00933 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000015.10:g.84570355G>A, NC_000015.10:g.84570355G>C, NC_000015.10:g.84570355G>T, NC_000015.9:g.85113586G>A, NC_000015.9:g.85113586G>C, NC_000015.9:g.85113586G>T, NW_025791797.1:g.1062201G>A, NW_025791797.1:g.1062201G>C, NW_025791797.1:g.1062201G>T, NR_003661.2:n.441C>T, NR_003661.2:n.441C>G, NR_003661.2:n.441C>A, NM_207382.1:c.-656C>T, NM_207382.1:c.-656C>G, NM_207382.1:c.-656C>A

Select item 146743690418.

rs1467436904 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 15:84542221 (GRCh38)
15:85085452 (GRCh37)
Canonical SPDI:: NC_000015.10:84542220:C:A
Gene:: UBE2Q2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000132/2 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.84542221C>A, NC_000015.9:g.85085452C>A, NW_025791797.1:g.1034067C>A, NR_003661.2:n.1517G>T, NM_207382.1:c.421G>T

Select item 146701585619.

rs1467015856 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTTTT>- [Show Flanks]
Chromosome:: 15:84538571 (GRCh38)
15:85081802 (GRCh37)
Canonical SPDI:: NC_000015.10:84538566:TTTTCTTTT:TTTT
Gene:: UBE2Q2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TTTT=0./0 (ALFA)
HGVS:: NC_000015.10:g.84538571_84538575del, NC_000015.9:g.85081802_85081806del, NW_025791797.1:g.1030417_1030421del, NR_003661.2:n.1639_1643del, NM_207382.1:c.*3_*7del

Select item 146643169820.

rs1466431698 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:84527594 (GRCh38)
15:85070825 (GRCh37)
Canonical SPDI:: NC_000015.10:84527593:T:C
Gene:: UBE2Q2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000015.10:g.84527594T>C, NC_000015.9:g.85070825T>C, NW_025791797.1:g.1019440T>C, NR_003661.2:n.1752A>G, NM_207382.1:c.*116A>G

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