SNP Links for Gene (Select 148581) - SNP

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Select item 14915879121.

rs1491587912 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GGA,GGAAGAAGAAGAGGA,GGAAGAGGA,GGAAGAGGAAGAGGA,GGAAGAGGAAGAGGAAGAGGA,GGAAGAGGAAGAGGAAGAGGAAGAGGA [Show Flanks]
Chromosome:: 1:64239095 (GRCh38)
1:64704779 (GRCh37)
Canonical SPDI:: NC_000001.11:64239095:GA:GAGGA,NC_000001.11:64239095:GA:GAGGAAGAAGAAGAGGA,NC_000001.11:64239095:GA:GAGGAAGAGGA,NC_000001.11:64239095:GA:GAGGAAGAGGAAGAGGA,NC_000001.11:64239095:GA:GAGGAAGAGGAAGAGGAAGAGGA,NC_000001.11:64239095:GA:GAGGAAGAGGAAGAGGAAGAGGAAGAGGA
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAGGA=0./0 (ALFA)
HGVS:: NC_000001.11:g.64239097_64239098insGGA, NC_000001.11:g.64239097_64239098insGGAAGAAGAAGAGGA, NC_000001.11:g.64239097_64239098insGGAAGAGGA, NC_000001.11:g.64239096_64239097GAGGAA[2]GAGGA[1], NC_000001.11:g.64239096_64239097GAGGAA[3]GAGGA[1], NC_000001.11:g.64239096_64239097GAGGAA[4]GAGGA[1], NC_000001.10:g.64704780_64704781insGGA, NC_000001.10:g.64704780_64704781insGGAAGAAGAAGAGGA, NC_000001.10:g.64704780_64704781insGGAAGAGGA, NC_000001.10:g.64704779_64704780GAGGAA[2]GAGGA[1], NC_000001.10:g.64704779_64704780GAGGAA[3]GAGGA[1], NC_000001.10:g.64704779_64704780GAGGAA[4]GAGGA[1]

Select item 14915851642.

rs1491585164 has merged into rs1222465109 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>-,GAGA [Show Flanks]
Chromosome:: 1:64239147 (GRCh38)
1:64704830 (GRCh37)
Canonical SPDI:: NC_000001.11:64239145:AGA:A,NC_000001.11:64239145:AGA:AGAGA
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAGA=0./0 (ALFA)
-=0.00004/1 (GnomAD)
-=0.00008/1 (TOMMO)
HGVS:: NC_000001.11:g.64239147_64239148del, NC_000001.11:g.64239147_64239148dup, NC_000001.10:g.64704830_64704831del, NC_000001.10:g.64704830_64704831dup

Select item 14915817423.

rs1491581742 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GAAGAAGAAG [Show Flanks]
Chromosome:: 1:64239174 (GRCh38)
1:64704858 (GRCh37)
Canonical SPDI:: NC_000001.11:64239174:GAAGAAGAAG:GAAGAAGAAGGAAGAAGAAG
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GAAGAAGAAGGAAGAAGAAG=0./0 (ALFA)
GAAGAAGAAG=0.0001/9 (GnomAD)
HGVS:: NC_000001.11:g.64239175_64239184dup, NC_000001.10:g.64704858_64704867dup

Select item 14915507294.

rs1491550729 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 1:64239131 (GRCh38)
1:64704815 (GRCh37)
Canonical SPDI:: NC_000001.11:64239131:G:GG
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
G=0.00115/24 (GnomAD)
HGVS:: NC_000001.11:g.64239132dup, NC_000001.10:g.64704815dup

Select item 14915450015.

rs1491545001 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G,GAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG [Show Flanks]
Chromosome:: 1:64239122 (GRCh38)
1:64704806 (GRCh37)
Canonical SPDI:: NC_000001.11:64239122:G:GG,NC_000001.11:64239122:G:GGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239122:G:GGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239122:G:GGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239122:G:GGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239122:G:GGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
G=0.03358/54 (Korea1K)
HGVS:: NC_000001.11:g.64239123dup, NC_000001.11:g.64239123_64239124insGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239123_64239124insGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239123_64239124insGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239123_64239124insGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239123_64239124insGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704806dup, NC_000001.10:g.64704806_64704807insGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704806_64704807insGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704806_64704807insGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704806_64704807insGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704806_64704807insGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG

Select item 14915431056.

rs1491543105 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AGA,CGAGGAAGAAGAAGAAGAAGAAGA [Show Flanks]
Chromosome:: 1:64239086 (GRCh38)
1:64704770 (GRCh37)
Canonical SPDI:: NC_000001.11:64239086:GAAGA:GAAGAAGA,NC_000001.11:64239086:GAAGA:GAAGACGAGGAAGAAGAAGAAGAAGAAGA
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAAGAAGA=0./0 (ALFA)
GAA=0.00014/2 (TOMMO)
GAAGACGAGGAAGAAGAAGAAGAA=0.00032/13 (GnomAD)
HGVS:: NC_000001.11:g.64239089_64239091dup, NC_000001.11:g.64239091_64239092insCGAGGAAGAAGAAGAAGAAGAAGA, NC_000001.10:g.64704772_64704774dup, NC_000001.10:g.64704774_64704775insCGAGGAAGAAGAAGAAGAAGAAGA

Select item 14915224467.

rs1491522446 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G,GAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,GGG [Show Flanks]
Chromosome:: 1:64239110 (GRCh38)
1:64704794 (GRCh37)
Canonical SPDI:: NC_000001.11:64239110:G:GG,NC_000001.11:64239110:G:GGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239110:G:GGGG
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGG=0./0 (ALFA)
GGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAG=0.00004/1 (TOMMO)
G=0.00405/73 (GnomAD)
HGVS:: NC_000001.11:g.64239111dup, NC_000001.11:g.64239111_64239112insGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239111_64239112insGGG, NC_000001.10:g.64704794dup, NC_000001.10:g.64704794_64704795insGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704794_64704795insGGG

Select item 14915045468.

rs1491504546 [Homo sapiens]

Variant type:: DEL
Alleles:: GG>- [Show Flanks]
Chromosome:: 1:64239086 (GRCh38)
1:64704769 (GRCh37)
Canonical SPDI:: NC_000001.11:64239085:GG:
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00004/1 (TOMMO)
HGVS:: NC_000001.11:g.64239086_64239087del, NC_000001.10:g.64704769_64704770del

Select item 14914936949.

rs1491493694 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 1:64239105 (GRCh38)
1:64704788 (GRCh37)
Canonical SPDI:: NC_000001.11:64239103:AGA:A
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.00017/2 (ALFA)
-=0.00078/6 (GnomAD)
HGVS:: NC_000001.11:g.64239105_64239106del, NC_000001.10:g.64704788_64704789del

Select item 149148652710.

rs1491486527 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 1:64239126 (GRCh38)
1:64704809 (GRCh37)
Canonical SPDI:: NC_000001.11:64239124:AGA:A
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.00025/3 (ALFA)
-=0.00095/20 (GnomAD)
HGVS:: NC_000001.11:g.64239126_64239127del, NC_000001.10:g.64704809_64704810del

Select item 149146858711.

rs1491468587 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 1:64228687 (GRCh38)
1:64694371 (GRCh37)
Canonical SPDI:: NC_000001.11:64228687::C
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0.00008/1 (ALFA)
C=0.00007/2 (TOMMO)
HGVS:: NC_000001.11:g.64228687_64228688insC, NC_000001.10:g.64694370_64694371insC

Select item 149144470412.

rs1491444704 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 1:64239120 (GRCh38)
1:64704803 (GRCh37)
Canonical SPDI:: NC_000001.11:64239118:AGA:A
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.00059/7 (ALFA)
-=0.00024/4 (GnomAD)
HGVS:: NC_000001.11:g.64239120_64239121del, NC_000001.10:g.64704803_64704804del

Select item 149144395513.

rs1491443955 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G,GGG [Show Flanks]
Chromosome:: 1:64239104 (GRCh38)
1:64704788 (GRCh37)
Canonical SPDI:: NC_000001.11:64239104:G:GG,NC_000001.11:64239104:G:GGGG
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
G=0.0005/8 (GnomAD)
G=0.00179/22 (TOMMO)
HGVS:: NC_000001.11:g.64239105dup, NC_000001.11:g.64239105_64239106insGGG, NC_000001.10:g.64704788dup, NC_000001.10:g.64704788_64704789insGGG

Select item 149141427514.

rs1491414275 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,AA,AAGAA,AAGAAGAA,AAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAA,AAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAA,AAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAA,AGAAGAAGGAA [Show Flanks]
Chromosome:: 1:64239080 (GRCh38)
1:64704764 (GRCh37)
Canonical SPDI:: NC_000001.11:64239080::A,NC_000001.11:64239080::AA,NC_000001.11:64239080::AAGAA,NC_000001.11:64239080::AAGAAGAA,NC_000001.11:64239080::AAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAA,NC_000001.11:64239080::AAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAA,NC_000001.11:64239080::AAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAA,NC_000001.11:64239080::AGAAGAAGGAA
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
HGVS:: NC_000001.11:g.64239080_64239081insA, NC_000001.11:g.64239080_64239081insAA, NC_000001.11:g.64239080_64239081insAAGAA, NC_000001.11:g.64239080_64239081insAAGAAGAA, NC_000001.11:g.64239080_64239081insAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAA, NC_000001.11:g.64239080_64239081insAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAA, NC_000001.11:g.64239080_64239081insAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAA, NC_000001.11:g.64239080_64239081insAGAAGAAGGAA, NC_000001.10:g.64704763_64704764insA, NC_000001.10:g.64704763_64704764insAA, NC_000001.10:g.64704763_64704764insAAGAA, NC_000001.10:g.64704763_64704764insAAGAAGAA, NC_000001.10:g.64704763_64704764insAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAA, NC_000001.10:g.64704763_64704764insAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAA, NC_000001.10:g.64704763_64704764insAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAA, NC_000001.10:g.64704763_64704764insAGAAGAAGGAA

Select item 149140536615.

rs1491405366 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 1:64239145 (GRCh38)
1:64704828 (GRCh37)
Canonical SPDI:: NC_000001.11:64239144:AA:
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00004/1 (GnomAD)
HGVS:: NC_000001.11:g.64239145_64239146del, NC_000001.10:g.64704828_64704829del

Select item 149138090716.

rs1491380907 [Homo sapiens]

Variant type:: DELINS
Alleles:: AG>- [Show Flanks]
Chromosome:: 1:64239085 (GRCh38)
1:64704768 (GRCh37)
Canonical SPDI:: NC_000001.11:64239082:AGAG:AG
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AGAG=0./0 (ALFA)
HGVS:: NC_000001.11:g.64239083AG[1], NC_000001.10:g.64704766AG[1]

Select item 149137588217.

rs1491375882 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G,GAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG [Show Flanks]
Chromosome:: 1:64239134 (GRCh38)
1:64704818 (GRCh37)
Canonical SPDI:: NC_000001.11:64239134:G:GG,NC_000001.11:64239134:G:GGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239134:G:GGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239134:G:GGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239134:G:GGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239134:G:GGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
GGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAG=0.00059/8 (TOMMO)
HGVS:: NC_000001.11:g.64239135dup, NC_000001.11:g.64239135_64239136insGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239135_64239136insGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239135_64239136insGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239135_64239136insGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239135GGAAGA[5]GG[1], NC_000001.10:g.64704818dup, NC_000001.10:g.64704818_64704819insGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704818_64704819insGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704818_64704819insGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704818_64704819insGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704818GGAAGA[5]GG[1]

Select item 149133861218.

rs1491338612 has merged into rs59774097 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTT>-,T,TTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:64228696 (GRCh38)
1:64694379 (GRCh37)
Canonical SPDI:: NC_000001.11:64228686:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000001.11:64228686:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:64228686:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:64228686:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:64228686:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:64228686:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:64228686:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:64228686:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:64228686:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:64228686:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:64228686:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:64228686:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:64228686:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:64228686:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000001.11:g.64228696_64228707del, NC_000001.11:g.64228697_64228707del, NC_000001.11:g.64228699_64228707del, NC_000001.11:g.64228703_64228707del, NC_000001.11:g.64228704_64228707del, NC_000001.11:g.64228705_64228707del, NC_000001.11:g.64228706_64228707del, NC_000001.11:g.64228707del, NC_000001.11:g.64228707dup, NC_000001.11:g.64228706_64228707dup, NC_000001.11:g.64228705_64228707dup, NC_000001.11:g.64228704_64228707dup, NC_000001.11:g.64228703_64228707dup, NC_000001.11:g.64228702_64228707dup, NC_000001.10:g.64694379_64694390del, NC_000001.10:g.64694380_64694390del, NC_000001.10:g.64694382_64694390del, NC_000001.10:g.64694386_64694390del, NC_000001.10:g.64694387_64694390del, NC_000001.10:g.64694388_64694390del, NC_000001.10:g.64694389_64694390del, NC_000001.10:g.64694390del, NC_000001.10:g.64694390dup, NC_000001.10:g.64694389_64694390dup, NC_000001.10:g.64694388_64694390dup, NC_000001.10:g.64694387_64694390dup, NC_000001.10:g.64694386_64694390dup, NC_000001.10:g.64694385_64694390dup

Select item 149133852919.

rs1491338529 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G,GAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGACG,GAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,GAAGAGG [Show Flanks]
Chromosome:: 1:64239119 (GRCh38)
1:64704803 (GRCh37)
Canonical SPDI:: NC_000001.11:64239119:G:GG,NC_000001.11:64239119:G:GGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239119:G:GGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239119:G:GGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGACG,NC_000001.11:64239119:G:GGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239119:G:GGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239119:G:GGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239119:G:GGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239119:G:GGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239119:G:GGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG,NC_000001.11:64239119:G:GGAAGAGG
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
HGVS:: NC_000001.11:g.64239120dup, NC_000001.11:g.64239120_64239121insGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239120_64239121insGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239120_64239121insGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGACG, NC_000001.11:g.64239120_64239121insGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239120_64239121insGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239120_64239121insGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239120_64239121insGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239120_64239121insGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239120_64239121insGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.11:g.64239120_64239121insGAAGAGG, NC_000001.10:g.64704803dup, NC_000001.10:g.64704803_64704804insGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704803_64704804insGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704803_64704804insGAAGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGACG, NC_000001.10:g.64704803_64704804insGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704803_64704804insGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704803_64704804insGAAGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704803_64704804insGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704803_64704804insGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704803_64704804insGAAGAAGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGG, NC_000001.10:g.64704803_64704804insGAAGAGG

Select item 149133741220.

rs1491337412 has merged into rs1376551804 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGA>-,GGAGGA [Show Flanks]
Chromosome:: 1:64239086 (GRCh38)
1:64704769 (GRCh37)
Canonical SPDI:: NC_000001.11:64239083:GAGGA:GA,NC_000001.11:64239083:GAGGA:GAGGAGGA
Gene:: UBE2U (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAGGAGGA=0./0 (ALFA)
-=0.00819/129 (TOMMO)
-=0.01173/742 (GnomAD)
HGVS:: NC_000001.11:g.64239086_64239088del, NC_000001.11:g.64239086_64239088dup, NC_000001.10:g.64704769_64704771del, NC_000001.10:g.64704769_64704771dup

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