SNP Links for Gene (Select 85465) - SNP

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Select item 14915138951.

rs1491513895 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->TTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Chromosome:: no mapping
Canonical SPDI:

Select item 14915095072.

rs1491509507 has merged into rs59396679 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 2:26364087 (GRCh38)
2:26586955 (GRCh37)
Canonical SPDI:: NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26364078:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
-=0.000015/4 (TOPMED)
HGVS:: NC_000002.12:g.26364087_26364099del, NC_000002.12:g.26364088_26364099del, NC_000002.12:g.26364089_26364099del, NC_000002.12:g.26364090_26364099del, NC_000002.12:g.26364092_26364099del, NC_000002.12:g.26364093_26364099del, NC_000002.12:g.26364094_26364099del, NC_000002.12:g.26364095_26364099del, NC_000002.12:g.26364096_26364099del, NC_000002.12:g.26364097_26364099del, NC_000002.12:g.26364098_26364099del, NC_000002.12:g.26364099del, NC_000002.12:g.26364099dup, NC_000002.12:g.26364098_26364099dup, NC_000002.12:g.26364097_26364099dup, NC_000002.12:g.26364096_26364099dup, NC_000002.12:g.26364095_26364099dup, NC_000002.12:g.26364094_26364099dup, NC_000002.11:g.26586955_26586967del, NC_000002.11:g.26586956_26586967del, NC_000002.11:g.26586957_26586967del, NC_000002.11:g.26586958_26586967del, NC_000002.11:g.26586960_26586967del, NC_000002.11:g.26586961_26586967del, NC_000002.11:g.26586962_26586967del, NC_000002.11:g.26586963_26586967del, NC_000002.11:g.26586964_26586967del, NC_000002.11:g.26586965_26586967del, NC_000002.11:g.26586966_26586967del, NC_000002.11:g.26586967del, NC_000002.11:g.26586967dup, NC_000002.11:g.26586966_26586967dup, NC_000002.11:g.26586965_26586967dup, NC_000002.11:g.26586964_26586967dup, NC_000002.11:g.26586963_26586967dup, NC_000002.11:g.26586962_26586967dup

Select item 14914164943.

rs1491416494 has merged into rs60220320 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAA>-,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 2:26387704 (GRCh38)
2:26610572 (GRCh37)
Canonical SPDI:: NC_000002.12:26387695:AAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000002.12:26387695:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000002.12:26387695:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000002.12:26387695:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000002.12:26387695:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000002.12:26387695:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000002.12:26387695:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000002.12:26387695:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000002.12:26387695:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:26387695:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000002.12:26387695:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000002.12:g.26387704_26387713del, NC_000002.12:g.26387708_26387713del, NC_000002.12:g.26387709_26387713del, NC_000002.12:g.26387710_26387713del, NC_000002.12:g.26387711_26387713del, NC_000002.12:g.26387712_26387713del, NC_000002.12:g.26387713del, NC_000002.12:g.26387713dup, NC_000002.12:g.26387709_26387713dup, NC_000002.12:g.26387703_26387713dup, NC_000002.12:g.26387697_26387713dup, NC_000002.11:g.26610572_26610581del, NC_000002.11:g.26610576_26610581del, NC_000002.11:g.26610577_26610581del, NC_000002.11:g.26610578_26610581del, NC_000002.11:g.26610579_26610581del, NC_000002.11:g.26610580_26610581del, NC_000002.11:g.26610581del, NC_000002.11:g.26610581dup, NC_000002.11:g.26610577_26610581dup, NC_000002.11:g.26610571_26610581dup, NC_000002.11:g.26610565_26610581dup

Select item 14913929544.

rs1491392954 has merged into rs869073468 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 2:26349006 (GRCh38)
2:26571874 (GRCh37)
Canonical SPDI:: NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000002.12:g.26349006_26349031del, NC_000002.12:g.26349007_26349031del, NC_000002.12:g.26349008_26349031del, NC_000002.12:g.26349009_26349031del, NC_000002.12:g.26349010_26349031del, NC_000002.12:g.26349011_26349031del, NC_000002.12:g.26349012_26349031del, NC_000002.12:g.26349013_26349031del, NC_000002.12:g.26349014_26349031del, NC_000002.12:g.26349015_26349031del, NC_000002.12:g.26349016_26349031del, NC_000002.12:g.26349017_26349031del, NC_000002.12:g.26349018_26349031del, NC_000002.12:g.26349019_26349031del, NC_000002.12:g.26349020_26349031del, NC_000002.12:g.26349021_26349031del, NC_000002.12:g.26349022_26349031del, NC_000002.12:g.26349023_26349031del, NC_000002.12:g.26349024_26349031del, NC_000002.12:g.26349025_26349031del, NC_000002.12:g.26349026_26349031del, NC_000002.12:g.26349027_26349031del, NC_000002.12:g.26349028_26349031del, NC_000002.12:g.26349029_26349031del, NC_000002.12:g.26349030_26349031del, NC_000002.12:g.26349031del, NC_000002.12:g.26349031dup, NC_000002.12:g.26349030_26349031dup, NC_000002.12:g.26349029_26349031dup, NC_000002.12:g.26349028_26349031dup, NC_000002.12:g.26349027_26349031dup, NC_000002.12:g.26349026_26349031dup, NC_000002.12:g.26349025_26349031dup, NC_000002.12:g.26349024_26349031dup, NC_000002.12:g.26349023_26349031dup, NC_000002.12:g.26349022_26349031dup, NC_000002.12:g.26349021_26349031dup, NC_000002.12:g.26349020_26349031dup, NC_000002.12:g.26349019_26349031dup, NC_000002.12:g.26349018_26349031dup, NC_000002.12:g.26349017_26349031dup, NC_000002.12:g.26349016_26349031dup, NC_000002.12:g.26349015_26349031dup, NC_000002.12:g.26349014_26349031dup, NC_000002.12:g.26349012_26349031dup, NC_000002.12:g.26349011_26349031dup, NC_000002.12:g.26349009_26349031dup, NC_000002.12:g.26349005_26349031dup, NC_000002.12:g.26349004_26349031dup, NC_000002.12:g.26349031_26349032insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.26571874_26571899del, NC_000002.11:g.26571875_26571899del, NC_000002.11:g.26571876_26571899del, NC_000002.11:g.26571877_26571899del, NC_000002.11:g.26571878_26571899del, NC_000002.11:g.26571879_26571899del, NC_000002.11:g.26571880_26571899del, NC_000002.11:g.26571881_26571899del, NC_000002.11:g.26571882_26571899del, NC_000002.11:g.26571883_26571899del, NC_000002.11:g.26571884_26571899del, NC_000002.11:g.26571885_26571899del, NC_000002.11:g.26571886_26571899del, NC_000002.11:g.26571887_26571899del, NC_000002.11:g.26571888_26571899del, NC_000002.11:g.26571889_26571899del, NC_000002.11:g.26571890_26571899del, NC_000002.11:g.26571891_26571899del, NC_000002.11:g.26571892_26571899del, NC_000002.11:g.26571893_26571899del, NC_000002.11:g.26571894_26571899del, NC_000002.11:g.26571895_26571899del, NC_000002.11:g.26571896_26571899del, NC_000002.11:g.26571897_26571899del, NC_000002.11:g.26571898_26571899del, NC_000002.11:g.26571899del, NC_000002.11:g.26571899dup, NC_000002.11:g.26571898_26571899dup, NC_000002.11:g.26571897_26571899dup, NC_000002.11:g.26571896_26571899dup, NC_000002.11:g.26571895_26571899dup, NC_000002.11:g.26571894_26571899dup, NC_000002.11:g.26571893_26571899dup, NC_000002.11:g.26571892_26571899dup, NC_000002.11:g.26571891_26571899dup, NC_000002.11:g.26571890_26571899dup, NC_000002.11:g.26571889_26571899dup, NC_000002.11:g.26571888_26571899dup, NC_000002.11:g.26571887_26571899dup, NC_000002.11:g.26571886_26571899dup, NC_000002.11:g.26571885_26571899dup, NC_000002.11:g.26571884_26571899dup, NC_000002.11:g.26571883_26571899dup, NC_000002.11:g.26571882_26571899dup, NC_000002.11:g.26571880_26571899dup, NC_000002.11:g.26571879_26571899dup, NC_000002.11:g.26571877_26571899dup, NC_000002.11:g.26571873_26571899dup, NC_000002.11:g.26571872_26571899dup, NC_000002.11:g.26571899_26571900insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14911399645.

rs1491139964 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 2:26364078 (GRCh38)
2:26586946 (GRCh37)
Canonical SPDI:: NC_000002.12:26364077:CT:
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.000084/1 (ALFA)
-=0.000008/1 (GnomAD)
HGVS:: NC_000002.12:g.26364078_26364079del, NC_000002.11:g.26586946_26586947del

Select item 14910624606.

rs1491062460 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TTAT,TTTTAT,TTTTTTTTAT,TTTTTTTTTTTTTTTTAT [Show Flanks]
Chromosome:: 2:26381228 (GRCh38)
2:26604097 (GRCh37)
Canonical SPDI:: NC_000002.12:26381228:T:TTTAT,NC_000002.12:26381228:T:TTTTTAT,NC_000002.12:26381228:T:TTTTTTTTTAT,NC_000002.12:26381228:T:TTTTTTTTTTTTTTTTTAT
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTTAT=0./0 (ALFA)
HGVS:: NC_000002.12:g.26381229_26381230insTTAT, NC_000002.12:g.26381229T[5]AT[1], NC_000002.12:g.26381229T[9]AT[1], NC_000002.12:g.26381229T[17]AT[1], NC_000002.11:g.26604097_26604098insTTAT, NC_000002.11:g.26604097T[5]AT[1], NC_000002.11:g.26604097T[9]AT[1], NC_000002.11:g.26604097T[17]AT[1]

Select item 14910356317.

rs1491035631 has merged into rs35795789 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA [Show Flanks]
Chromosome:: 2:26352857 (GRCh38)
2:26575725 (GRCh37)
Canonical SPDI:: NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
A=0.3099/1552 (1000Genomes)
HGVS:: NC_000002.12:g.26352857_26352859del, NC_000002.12:g.26352858_26352859del, NC_000002.12:g.26352859del, NC_000002.12:g.26352859dup, NC_000002.12:g.26352858_26352859dup, NC_000002.12:g.26352857_26352859dup, NC_000002.12:g.26352856_26352859dup, NC_000002.12:g.26352855_26352859dup, NC_000002.12:g.26352853_26352859dup, NC_000002.11:g.26575725_26575727del, NC_000002.11:g.26575726_26575727del, NC_000002.11:g.26575727del, NC_000002.11:g.26575727dup, NC_000002.11:g.26575726_26575727dup, NC_000002.11:g.26575725_26575727dup, NC_000002.11:g.26575724_26575727dup, NC_000002.11:g.26575723_26575727dup, NC_000002.11:g.26575721_26575727dup

Select item 14910254988.

rs1491025498 has merged into rs147570982 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACAC>-,AC,ACACAC,ACACACAC,ACACACACAC [Show Flanks]
Chromosome:: 2:26356968 (GRCh38)
2:26579836 (GRCh37)
Canonical SPDI:: NC_000002.12:26356956:CACACACACACACAC:CACACACACAC,NC_000002.12:26356956:CACACACACACACAC:CACACACACACAC,NC_000002.12:26356956:CACACACACACACAC:CACACACACACACACAC,NC_000002.12:26356956:CACACACACACACAC:CACACACACACACACACAC,NC_000002.12:26356956:CACACACACACACAC:CACACACACACACACACACAC
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACACACACACACACACAC=0./0 (ALFA)
CA=0.03095/155 (1000Genomes)
CA=0.03944/661 (TOMMO)
CA=0.04803/88 (Korea1K)
CA=0.09346/20 (Vietnamese)
HGVS:: NC_000002.12:g.26356958AC[5], NC_000002.12:g.26356958AC[6], NC_000002.12:g.26356958AC[8], NC_000002.12:g.26356958AC[9], NC_000002.12:g.26356958AC[10], NC_000002.11:g.26579826AC[5], NC_000002.11:g.26579826AC[6], NC_000002.11:g.26579826AC[8], NC_000002.11:g.26579826AC[9], NC_000002.11:g.26579826AC[10]

Select item 14910049959.

rs1491004995 has merged into rs57146815 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAA>-,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA [Show Flanks]
Chromosome:: 2:26376101 (GRCh38)
2:26598969 (GRCh37)
Canonical SPDI:: NC_000002.12:26376091:AAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000002.12:26376091:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000002.12:26376091:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000002.12:26376091:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000002.12:26376091:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000002.12:26376091:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000002.12:26376091:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000002.12:26376091:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000002.12:26376091:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000002.12:26376091:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
-=0.325/13 (GENOME_DK)
HGVS:: NC_000002.12:g.26376101_26376109del, NC_000002.12:g.26376105_26376109del, NC_000002.12:g.26376106_26376109del, NC_000002.12:g.26376107_26376109del, NC_000002.12:g.26376108_26376109del, NC_000002.12:g.26376109del, NC_000002.12:g.26376109dup, NC_000002.12:g.26376108_26376109dup, NC_000002.12:g.26376107_26376109dup, NC_000002.12:g.26376106_26376109dup, NC_000002.11:g.26598969_26598977del, NC_000002.11:g.26598973_26598977del, NC_000002.11:g.26598974_26598977del, NC_000002.11:g.26598975_26598977del, NC_000002.11:g.26598976_26598977del, NC_000002.11:g.26598977del, NC_000002.11:g.26598977dup, NC_000002.11:g.26598976_26598977dup, NC_000002.11:g.26598975_26598977dup, NC_000002.11:g.26598974_26598977dup

Select item 149100381010.

rs1491003810 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:26388896 (GRCh38)
2:26611764 (GRCh37)
Canonical SPDI:: NC_000002.12:26388895:G:T
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000224/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000002.12:g.26388896G>T, NC_000002.11:g.26611764G>T

Select item 149094732311.

rs1490947323 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 2:26392250 (GRCh38)
2:26615118 (GRCh37)
Canonical SPDI:: NC_000002.12:26392249:A:T
Gene:: SELENOI (Varview)
Functional Consequence:: 3_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.26392250A>T, NC_000002.11:g.26615118A>T, NM_033505.4:c.*3147A>T, NM_033505.3:c.*3147A>T, NM_033505.2:c.*3147A>T, NR_137633.2:n.4339A>T, NR_137633.1:n.4396A>T

Select item 149094446112.

rs1490944461 [Homo sapiens]

Variant type:: DELINS
Alleles:: CCT>- [Show Flanks]
Chromosome:: 2:26354496 (GRCh38)
2:26577364 (GRCh37)
Canonical SPDI:: NC_000002.12:26354493:CTCCT:CT
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CT=0./0 (ALFA)
-=0.000023/6 (TOPMED)
-=0.00005/7 (GnomAD)
HGVS:: NC_000002.12:g.26354496_26354498del, NC_000002.11:g.26577364_26577366del

Select item 149079846313.

rs1490798463 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:26386474 (GRCh38)
2:26609342 (GRCh37)
Canonical SPDI:: NC_000002.12:26386473:A:G
Gene:: SELENOI (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000002.12:g.26386474A>G, NC_000002.11:g.26609342A>G, NM_033505.4:c.1033A>G, NM_033505.3:c.1033A>G, NM_033505.2:c.1033A>G, NR_137633.2:n.1031A>G, NR_137633.1:n.1088A>G, NP_277040.1:p.Ile345Val

Select item 149078353714.

rs1490783537 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TA [Show Flanks]
Chromosome:: 2:26365681 (GRCh38)
2:26588550 (GRCh37)
Canonical SPDI:: NC_000002.12:26365681:TATA:TATATA
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATA=0./0 (ALFA)
TA=0.000008/2 (TOPMED)
TA=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.26365682TA[3], NC_000002.11:g.26588550TA[3]

Select item 149069090415.

rs1490690904 has merged into rs869073468 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 2:26349006 (GRCh38)
2:26571874 (GRCh37)
Canonical SPDI:: NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:26348996:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000002.12:g.26349006_26349031del, NC_000002.12:g.26349007_26349031del, NC_000002.12:g.26349008_26349031del, NC_000002.12:g.26349009_26349031del, NC_000002.12:g.26349010_26349031del, NC_000002.12:g.26349011_26349031del, NC_000002.12:g.26349012_26349031del, NC_000002.12:g.26349013_26349031del, NC_000002.12:g.26349014_26349031del, NC_000002.12:g.26349015_26349031del, NC_000002.12:g.26349016_26349031del, NC_000002.12:g.26349017_26349031del, NC_000002.12:g.26349018_26349031del, NC_000002.12:g.26349019_26349031del, NC_000002.12:g.26349020_26349031del, NC_000002.12:g.26349021_26349031del, NC_000002.12:g.26349022_26349031del, NC_000002.12:g.26349023_26349031del, NC_000002.12:g.26349024_26349031del, NC_000002.12:g.26349025_26349031del, NC_000002.12:g.26349026_26349031del, NC_000002.12:g.26349027_26349031del, NC_000002.12:g.26349028_26349031del, NC_000002.12:g.26349029_26349031del, NC_000002.12:g.26349030_26349031del, NC_000002.12:g.26349031del, NC_000002.12:g.26349031dup, NC_000002.12:g.26349030_26349031dup, NC_000002.12:g.26349029_26349031dup, NC_000002.12:g.26349028_26349031dup, NC_000002.12:g.26349027_26349031dup, NC_000002.12:g.26349026_26349031dup, NC_000002.12:g.26349025_26349031dup, NC_000002.12:g.26349024_26349031dup, NC_000002.12:g.26349023_26349031dup, NC_000002.12:g.26349022_26349031dup, NC_000002.12:g.26349021_26349031dup, NC_000002.12:g.26349020_26349031dup, NC_000002.12:g.26349019_26349031dup, NC_000002.12:g.26349018_26349031dup, NC_000002.12:g.26349017_26349031dup, NC_000002.12:g.26349016_26349031dup, NC_000002.12:g.26349015_26349031dup, NC_000002.12:g.26349014_26349031dup, NC_000002.12:g.26349012_26349031dup, NC_000002.12:g.26349011_26349031dup, NC_000002.12:g.26349009_26349031dup, NC_000002.12:g.26349005_26349031dup, NC_000002.12:g.26349004_26349031dup, NC_000002.12:g.26349031_26349032insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000002.11:g.26571874_26571899del, NC_000002.11:g.26571875_26571899del, NC_000002.11:g.26571876_26571899del, NC_000002.11:g.26571877_26571899del, NC_000002.11:g.26571878_26571899del, NC_000002.11:g.26571879_26571899del, NC_000002.11:g.26571880_26571899del, NC_000002.11:g.26571881_26571899del, NC_000002.11:g.26571882_26571899del, NC_000002.11:g.26571883_26571899del, NC_000002.11:g.26571884_26571899del, NC_000002.11:g.26571885_26571899del, NC_000002.11:g.26571886_26571899del, NC_000002.11:g.26571887_26571899del, NC_000002.11:g.26571888_26571899del, NC_000002.11:g.26571889_26571899del, NC_000002.11:g.26571890_26571899del, NC_000002.11:g.26571891_26571899del, NC_000002.11:g.26571892_26571899del, NC_000002.11:g.26571893_26571899del, NC_000002.11:g.26571894_26571899del, NC_000002.11:g.26571895_26571899del, NC_000002.11:g.26571896_26571899del, NC_000002.11:g.26571897_26571899del, NC_000002.11:g.26571898_26571899del, NC_000002.11:g.26571899del, NC_000002.11:g.26571899dup, NC_000002.11:g.26571898_26571899dup, NC_000002.11:g.26571897_26571899dup, NC_000002.11:g.26571896_26571899dup, NC_000002.11:g.26571895_26571899dup, NC_000002.11:g.26571894_26571899dup, NC_000002.11:g.26571893_26571899dup, NC_000002.11:g.26571892_26571899dup, NC_000002.11:g.26571891_26571899dup, NC_000002.11:g.26571890_26571899dup, NC_000002.11:g.26571889_26571899dup, NC_000002.11:g.26571888_26571899dup, NC_000002.11:g.26571887_26571899dup, NC_000002.11:g.26571886_26571899dup, NC_000002.11:g.26571885_26571899dup, NC_000002.11:g.26571884_26571899dup, NC_000002.11:g.26571883_26571899dup, NC_000002.11:g.26571882_26571899dup, NC_000002.11:g.26571880_26571899dup, NC_000002.11:g.26571879_26571899dup, NC_000002.11:g.26571877_26571899dup, NC_000002.11:g.26571873_26571899dup, NC_000002.11:g.26571872_26571899dup, NC_000002.11:g.26571899_26571900insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149064436616.

rs1490644366 has merged into rs5830006 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAAAAAA [Show Flanks]
Chromosome:: 2:26350114 (GRCh38)
2:26572982 (GRCh37)
Canonical SPDI:: NC_000002.12:26350106:AAAAAAAAAAA:AAAAAAA,NC_000002.12:26350106:AAAAAAAAAAA:AAAAAAAA,NC_000002.12:26350106:AAAAAAAAAAA:AAAAAAAAA,NC_000002.12:26350106:AAAAAAAAAAA:AAAAAAAAAA,NC_000002.12:26350106:AAAAAAAAAAA:AAAAAAAAAAAA,NC_000002.12:26350106:AAAAAAAAAAA:AAAAAAAAAAAAAAAAA
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAA=0./0 (ALFA)
A=0.01653/277 (TOMMO)
-=0.02167/13 (NorthernSweden)
-=0.075/3 (GENOME_DK)
-=0.13099/656 (1000Genomes)
HGVS:: NC_000002.12:g.26350114_26350117del, NC_000002.12:g.26350115_26350117del, NC_000002.12:g.26350116_26350117del, NC_000002.12:g.26350117del, NC_000002.12:g.26350117dup, NC_000002.12:g.26350112_26350117dup, NC_000002.11:g.26572982_26572985del, NC_000002.11:g.26572983_26572985del, NC_000002.11:g.26572984_26572985del, NC_000002.11:g.26572985del, NC_000002.11:g.26572985dup, NC_000002.11:g.26572980_26572985dup

Select item 149057770417.

rs1490577704 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:26390030 (GRCh38)
2:26612898 (GRCh37)
Canonical SPDI:: NC_000002.12:26390029:T:C
Gene:: SELENOI (Varview)
Functional Consequence:: 3_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000019/5 (TOPMED)
HGVS:: NC_000002.12:g.26390030T>C, NC_000002.11:g.26612898T>C, NM_033505.4:c.*927T>C, NM_033505.3:c.*927T>C, NM_033505.2:c.*927T>C, NR_137633.2:n.2119T>C, NR_137633.1:n.2176T>C

Select item 149045720218.

rs1490457202 [Homo sapiens]

Variant type:: DELINS
Alleles:: TCGCT>- [Show Flanks]
Chromosome:: 2:26372698 (GRCh38)
2:26595566 (GRCh37)
Canonical SPDI:: NC_000002.12:26372696:TTCGCT:T
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000002.12:g.26372698_26372702del, NC_000002.11:g.26595566_26595570del

Select item 149044032819.

rs1490440328 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:26388706 (GRCh38)
2:26611574 (GRCh37)
Canonical SPDI:: NC_000002.12:26388705:T:C
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0./0 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000002.12:g.26388706T>C, NC_000002.11:g.26611574T>C

Select item 149040848320.

rs1490408483 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 2:26357059 (GRCh38)
2:26579927 (GRCh37)
Canonical SPDI:: NC_000002.12:26357058:T:A
Gene:: SELENOI (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.26357059T>A, NC_000002.11:g.26579927T>A

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