SNP Links for Gene (Select 728081) - SNP

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Select item 14915383491.

rs1491538349 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GA [Show Flanks]
Chromosome:: 4:181080179 (GRCh38)
4:182001333 (GRCh37)
Canonical SPDI:: NC_000004.12:181080179:A:AGA
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AGA=0./0 (ALFA)
HGVS:: NC_000004.12:g.181080180_181080181insGA, NC_000004.11:g.182001333_182001334insGA

Select item 14915377402.

rs1491537740 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATGTGT,GT,GTGT,GTGTGT,TTGTGT [Show Flanks]
Chromosome:: 4:181151390 (GRCh38)
4:182072544 (GRCh37)
Canonical SPDI:: NC_000004.12:181151390:T:TATGTGT,NC_000004.12:181151390:T:TGT,NC_000004.12:181151390:T:TGTGT,NC_000004.12:181151390:T:TGTGTGT,NC_000004.12:181151390:T:TTTGTGT
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGT=0./0 (ALFA)
HGVS:: NC_000004.12:g.181151391_181151392insATGTGT, NC_000004.12:g.181151391_181151392insGT, NC_000004.12:g.181151391_181151392insGTGT, NC_000004.12:g.181151392GT[3], NC_000004.12:g.181151391_181151392insTTGTGT, NC_000004.11:g.182072544_182072545insATGTGT, NC_000004.11:g.182072544_182072545insGT, NC_000004.11:g.182072544_182072545insGTGT, NC_000004.11:g.182072545GT[3], NC_000004.11:g.182072544_182072545insTTGTGT

Select item 14915328243.

rs1491532824 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>-,TATA [Show Flanks]
Chromosome:: 4:181080106 (GRCh38)
4:182001259 (GRCh37)
Canonical SPDI:: NC_000004.12:181080099:TATATATA:TATATA,NC_000004.12:181080099:TATATATA:TATATATATA
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TATATATATA=0./0 (ALFA)
HGVS:: NC_000004.12:g.181080100TA[3], NC_000004.12:g.181080100TA[5], NC_000004.11:g.182001253TA[3], NC_000004.11:g.182001253TA[5]

Select item 14915234544.

rs1491523454 has merged into rs11318416 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT,TTTTTTTTTT [Show Flanks]
Chromosome:: 4:181110133 (GRCh38)
4:182031286 (GRCh37)
Canonical SPDI:: NC_000004.12:181110119:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:181110119:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:181110119:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:181110119:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:181110119:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:181110119:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
-=0.25/10 (GENOME_DK)
HGVS:: NC_000004.12:g.181110133_181110135del, NC_000004.12:g.181110134_181110135del, NC_000004.12:g.181110135del, NC_000004.12:g.181110135dup, NC_000004.12:g.181110134_181110135dup, NC_000004.12:g.181110129_181110135dup, NC_000004.11:g.182031286_182031288del, NC_000004.11:g.182031287_182031288del, NC_000004.11:g.182031288del, NC_000004.11:g.182031288dup, NC_000004.11:g.182031287_182031288dup, NC_000004.11:g.182031282_182031288dup

Select item 14915053795.

rs1491505379 has merged into rs1050595512 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGTGT>-,GT,GTGT,GTGTGTGT [Show Flanks]
Chromosome:: 4:181151317 (GRCh38)
4:182072470 (GRCh37)
Canonical SPDI:: NC_000004.12:181151308:GTGTGTGTGTGTGT:GTGTGTGT,NC_000004.12:181151308:GTGTGTGTGTGTGT:GTGTGTGTGT,NC_000004.12:181151308:GTGTGTGTGTGTGT:GTGTGTGTGTGT,NC_000004.12:181151308:GTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGTGTGTGT=0./0 (ALFA)
GT=0.00012/2 (TOMMO)
HGVS:: NC_000004.12:g.181151309GT[4], NC_000004.12:g.181151309GT[5], NC_000004.12:g.181151309GT[6], NC_000004.12:g.181151309GT[8], NC_000004.11:g.182072462GT[4], NC_000004.11:g.182072462GT[5], NC_000004.11:g.182072462GT[6], NC_000004.11:g.182072462GT[8]

Select item 14915034816.

rs1491503481 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,ATA,ATATA,ATATATA,ATATATATA,ATATATATATA,ATATATATATATA,ATATATATATATATA,ATATATATATATATATA,ATATATATATATATATATA,ATATATATATATATATATATA,ATATATATATATATATATATATA,ATATATATATATATATATATATATATA,ATGTATATA [Show Flanks]
Chromosome:: 4:181149549 (GRCh38)
4:182070703 (GRCh37)
Canonical SPDI:: NC_000004.12:181149549::A,NC_000004.12:181149549::ATA,NC_000004.12:181149549::ATATA,NC_000004.12:181149549::ATATATA,NC_000004.12:181149549::ATATATATA,NC_000004.12:181149549::ATATATATATA,NC_000004.12:181149549::ATATATATATATA,NC_000004.12:181149549::ATATATATATATATA,NC_000004.12:181149549::ATATATATATATATATA,NC_000004.12:181149549::ATATATATATATATATATA,NC_000004.12:181149549::ATATATATATATATATATATA,NC_000004.12:181149549::ATATATATATATATATATATATA,NC_000004.12:181149549::ATATATATATATATATATATATATATA,NC_000004.12:181149549::ATGTATATA
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATA=0./0 (ALFA)
ATATATATATA=0.01258/4 (NorthernSweden)
HGVS:: NC_000004.12:g.181149549_181149550insA, NC_000004.12:g.181149549_181149550insATA, NC_000004.12:g.181149549_181149550insATATA, NC_000004.12:g.181149549_181149550insATATATA, NC_000004.12:g.181149549_181149550insATATATATA, NC_000004.12:g.181149549_181149550insATATATATATA, NC_000004.12:g.181149549_181149550insATATATATATATA, NC_000004.12:g.181149549_181149550insATATATATATATATA, NC_000004.12:g.181149549_181149550insATATATATATATATATA, NC_000004.12:g.181149549_181149550insATATATATATATATATATA, NC_000004.12:g.181149549_181149550insATATATATATATATATATATA, NC_000004.12:g.181149549_181149550insATATATATATATATATATATATA, NC_000004.12:g.181149549_181149550insATATATATATATATATATATATATATA, NC_000004.12:g.181149549_181149550insATGTATATA, NC_000004.11:g.182070702_182070703insA, NC_000004.11:g.182070702_182070703insATA, NC_000004.11:g.182070702_182070703insATATA, NC_000004.11:g.182070702_182070703insATATATA, NC_000004.11:g.182070702_182070703insATATATATA, NC_000004.11:g.182070702_182070703insATATATATATA, NC_000004.11:g.182070702_182070703insATATATATATATA, NC_000004.11:g.182070702_182070703insATATATATATATATA, NC_000004.11:g.182070702_182070703insATATATATATATATATA, NC_000004.11:g.182070702_182070703insATATATATATATATATATA, NC_000004.11:g.182070702_182070703insATATATATATATATATATATA, NC_000004.11:g.182070702_182070703insATATATATATATATATATATATA, NC_000004.11:g.182070702_182070703insATATATATATATATATATATATATATA, NC_000004.11:g.182070702_182070703insATGTATATA

Select item 14914834417.

rs1491483441 [Homo sapiens]

Variant type:: INS
Alleles:: ->C,G [Show Flanks]
Chromosome:: 4:181073678 (GRCh38)
4:181994832 (GRCh37)
Canonical SPDI:: NC_000004.12:181073678::C,NC_000004.12:181073678::G
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.001342/6 (ALFA)
G=0.000781/84 (GnomAD)
G=0.002967/19 (1000Genomes)
G=0.021311/39 (Korea1K)
HGVS:: NC_000004.12:g.181073678_181073679insC, NC_000004.12:g.181073678_181073679insG, NC_000004.11:g.181994831_181994832insC, NC_000004.11:g.181994831_181994832insG

Select item 14914830598.

rs1491483059 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTTT [Show Flanks]
Chromosome:: 4:181156614 (GRCh38)
4:182077768 (GRCh37)
Canonical SPDI:: NC_000004.12:181156614:TTT:TTTGTTT
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTTGTTT=0./0 (ALFA)
TTTG=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.181156617_181156618insGTTT, NC_000004.11:g.182077770_182077771insGTTT

Select item 14914635039.

rs1491463503 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 4:181076126 (GRCh38)
4:181997280 (GRCh37)
Canonical SPDI:: NC_000004.12:181076126:A:AA
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000004.12:g.181076127dup, NC_000004.11:g.181997280dup

Select item 149140917710.

rs1491409177 has merged into rs1242774291 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATATAAT>-,ATATAATATATAAT [Show Flanks]
Chromosome:: 4:181080110 (GRCh38)
4:182001263 (GRCh37)
Canonical SPDI:: NC_000004.12:181080100:ATATATAATATATAAT:ATATATAAT,NC_000004.12:181080100:ATATATAATATATAAT:ATATATAATATATAATATATAAT
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATAATATATAATATATAAT=0./0 (ALFA)
ATATATA=0.000038/4 (GnomAD)
ATATATA=0.001596/26 (TOMMO)
HGVS:: NC_000004.12:g.181080103ATATAAT[1], NC_000004.12:g.181080103ATATAAT[3], NC_000004.11:g.182001256ATATAAT[1], NC_000004.11:g.182001256ATATAAT[3]

Select item 149140620811.

rs1491406208 has merged into rs1209013360 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 4:181149562 (GRCh38)
4:182070715 (GRCh37)
Canonical SPDI:: NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181149548:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
-=0.01919/417 (TOMMO)
HGVS:: NC_000004.12:g.181149562_181149569del, NC_000004.12:g.181149563_181149569del, NC_000004.12:g.181149564_181149569del, NC_000004.12:g.181149565_181149569del, NC_000004.12:g.181149566_181149569del, NC_000004.12:g.181149567_181149569del, NC_000004.12:g.181149568_181149569del, NC_000004.12:g.181149569del, NC_000004.12:g.181149569dup, NC_000004.12:g.181149568_181149569dup, NC_000004.12:g.181149567_181149569dup, NC_000004.12:g.181149566_181149569dup, NC_000004.12:g.181149565_181149569dup, NC_000004.12:g.181149564_181149569dup, NC_000004.12:g.181149563_181149569dup, NC_000004.12:g.181149562_181149569dup, NC_000004.12:g.181149561_181149569dup, NC_000004.12:g.181149560_181149569dup, NC_000004.12:g.181149559_181149569dup, NC_000004.12:g.181149558_181149569dup, NC_000004.12:g.181149557_181149569dup, NC_000004.12:g.181149555_181149569dup, NC_000004.11:g.182070715_182070722del, NC_000004.11:g.182070716_182070722del, NC_000004.11:g.182070717_182070722del, NC_000004.11:g.182070718_182070722del, NC_000004.11:g.182070719_182070722del, NC_000004.11:g.182070720_182070722del, NC_000004.11:g.182070721_182070722del, NC_000004.11:g.182070722del, NC_000004.11:g.182070722dup, NC_000004.11:g.182070721_182070722dup, NC_000004.11:g.182070720_182070722dup, NC_000004.11:g.182070719_182070722dup, NC_000004.11:g.182070718_182070722dup, NC_000004.11:g.182070717_182070722dup, NC_000004.11:g.182070716_182070722dup, NC_000004.11:g.182070715_182070722dup, NC_000004.11:g.182070714_182070722dup, NC_000004.11:g.182070713_182070722dup, NC_000004.11:g.182070712_182070722dup, NC_000004.11:g.182070711_182070722dup, NC_000004.11:g.182070710_182070722dup, NC_000004.11:g.182070708_182070722dup

Select item 149140281112.

rs1491402811 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATATATATATATATATATATATATATATT,ATATATATATATATATATATATATT,ATATATATATATATATATATATATTTT,ATATATATATATATATATATATT,ATATATATATATATATATATATTTT,ATATATATATATATATATATT,ATATATATATATATATATATTT,ATATATATATATATATATATTTATATATATATATT,ATATATATATATATATATATTTT,ATATATATATATATATATATTTTT,ATATATATATATATATATATTTTTTTT,ATATATATATATATATATT,ATATATATATATATATATTT,ATATATATATATATATATTTT,ATATATATATATATATATTTTT,ATATATATATATATATATTTTTT,ATATATATATATATATATTTTTTTTTTTT,ATATATATATATATATT,ATATATATATATATATTT,ATATATATATATATATTTT,ATATATATATATATATTTTTT,ATATATATATATATATTTTTTTTT,ATATATATATATATATTTTTTTTTTTT,ATATATATATATATATTTTTTTTTTTTTTT,ATATATATATATATT,ATATATATATATATTT,ATATATATATATATTTT,ATATATATATATATTTTT,ATATATATATATATTTTTT,ATATATATATATATTTTTTT,ATATATATATATATTTTTTTT,ATATATATATATATTTTTTTTT,ATATATATATATT,ATATATATATATTT,ATATATATATATTTT,ATATATATATATTTTT,ATATATATATATTTTTT,ATATATATATATTTTTTT,ATATATATATATTTTTTTT,ATATATATATATTTTTTTTTTTT,ATATATATATATTTTTTTTTTTTT,ATATATATATT,ATATATATATTT,ATATATATATTTT,ATATATATATTTTT,ATATATATATTTTTT,ATATATATATTTTTTT,ATATATATATTTTTTTT,ATATATATATTTTTTTTT,ATATATATATTTTTTTTTT,ATATATATATTTTTTTTTTTTTTT,ATATATATT,ATATATATTT,ATATATATTTT,ATATATATTTTT,ATATATATTTTTT,ATATATATTTTTTT,ATATATATTTTTTTT,ATATATATTTTTTTTT,ATATATATTTTTTTTTT,ATATATATTTTTTTTTTTTT,ATATATT,ATATATTT,ATATATTTATTTT,ATATATTTT,ATATATTTTT,ATATATTTTTT,ATATATTTTTTT,ATATATTTTTTTT,ATATATTTTTTTTT,ATATATTTTTTTTTT,ATATATTTTTTTTTTT,ATATATTTTTTTTTTTT,ATATATTTTTTTTTTTTTTTT,ATATT,ATATTT,ATATTTT,ATATTTTT,ATATTTTTT,ATATTTTTTTT,ATATTTTTTTTT,ATATTTTTTTTTT,ATATTTTTTTTTTT,ATATTTTTTTTTTTT,ATATTTTTTTTTTTTT,ATATTTTTTTTTTTTTT,ATATTTTTTTTTTTTTTTT,ATT,ATTT,ATTTT,ATTTTT,ATTTTTT,ATTTTTTTT,ATTTTTTTTT,ATTTTTTTTTT,ATTTTTTTTTTTTT,ATTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 4:181149548 (GRCh38)
4:182070702 (GRCh37)
Canonical SPDI:: NC_000004.12:181149548:T:TATATATATATATATATATATATATATATT,NC_000004.12:181149548:T:TATATATATATATATATATATATATT,NC_000004.12:181149548:T:TATATATATATATATATATATATATTTT,NC_000004.12:181149548:T:TATATATATATATATATATATATT,NC_000004.12:181149548:T:TATATATATATATATATATATATTTT,NC_000004.12:181149548:T:TATATATATATATATATATATT,NC_000004.12:181149548:T:TATATATATATATATATATATTT,NC_000004.12:181149548:T:TATATATATATATATATATATTTATATATATATATT,NC_000004.12:181149548:T:TATATATATATATATATATATTTT,NC_000004.12:181149548:T:TATATATATATATATATATATTTTT,NC_000004.12:181149548:T:TATATATATATATATATATATTTTTTTT,NC_000004.12:181149548:T:TATATATATATATATATATT,NC_000004.12:181149548:T:TATATATATATATATATATTT,NC_000004.12:181149548:T:TATATATATATATATATATTTT,NC_000004.12:181149548:T:TATATATATATATATATATTTTT,NC_000004.12:181149548:T:TATATATATATATATATATTTTTT,NC_000004.12:181149548:T:TATATATATATATATATATTTTTTTTTTTT,NC_000004.12:181149548:T:TATATATATATATATATT,NC_000004.12:181149548:T:TATATATATATATATATTT,NC_000004.12:181149548:T:TATATATATATATATATTTT,NC_000004.12:181149548:T:TATATATATATATATATTTTTT,NC_000004.12:181149548:T:TATATATATATATATATTTTTTTTT,NC_000004.12:181149548:T:TATATATATATATATATTTTTTTTTTTT,NC_000004.12:181149548:T:TATATATATATATATATTTTTTTTTTTTTTT,NC_000004.12:181149548:T:TATATATATATATATT,NC_000004.12:181149548:T:TATATATATATATATTT,NC_000004.12:181149548:T:TATATATATATATATTTT,NC_000004.12:181149548:T:TATATATATATATATTTTT,NC_000004.12:181149548:T:TATATATATATATATTTTTT,NC_000004.12:181149548:T:TATATATATATATATTTTTTT,NC_000004.12:181149548:T:TATATATATATATATTTTTTTT,NC_000004.12:181149548:T:TATATATATATATATTTTTTTTT,NC_000004.12:181149548:T:TATATATATATATT,NC_000004.12:181149548:T:TATATATATATATTT,NC_000004.12:181149548:T:TATATATATATATTTT,NC_000004.12:181149548:T:TATATATATATATTTTT,NC_000004.12:181149548:T:TATATATATATATTTTTT,NC_000004.12:181149548:T:TATATATATATATTTTTTT,NC_000004.12:181149548:T:TATATATATATATTTTTTTT,NC_000004.12:181149548:T:TATATATATATATTTTTTTTTTTT,NC_000004.12:181149548:T:TATATATATATATTTTTTTTTTTTT,NC_000004.12:181149548:T:TATATATATATT,NC_000004.12:181149548:T:TATATATATATTT,NC_000004.12:181149548:T:TATATATATATTTT,NC_000004.12:181149548:T:TATATATATATTTTT,NC_000004.12:181149548:T:TATATATATATTTTTT,NC_000004.12:181149548:T:TATATATATATTTTTTT,NC_000004.12:181149548:T:TATATATATATTTTTTTT,NC_000004.12:181149548:T:TATATATATATTTTTTTTT,NC_000004.12:181149548:T:TATATATATATTTTTTTTTT,NC_000004.12:181149548:T:TATATATATATTTTTTTTTTTTTTT,NC_000004.12:181149548:T:TATATATATT,NC_000004.12:181149548:T:TATATATATTT,NC_000004.12:181149548:T:TATATATATTTT,NC_000004.12:181149548:T:TATATATATTTTT,NC_000004.12:181149548:T:TATATATATTTTTT,NC_000004.12:181149548:T:TATATATATTTTTTT,NC_000004.12:181149548:T:TATATATATTTTTTTT,NC_000004.12:181149548:T:TATATATATTTTTTTTT,NC_000004.12:181149548:T:TATATATATTTTTTTTTT,NC_000004.12:181149548:T:TATATATATTTTTTTTTTTTT,NC_000004.12:181149548:T:TATATATT,NC_000004.12:181149548:T:TATATATTT,NC_000004.12:181149548:T:TATATATTTATTTT,NC_000004.12:181149548:T:TATATATTTT,NC_000004.12:181149548:T:TATATATTTTT,NC_000004.12:181149548:T:TATATATTTTTT,NC_000004.12:181149548:T:TATATATTTTTTT,NC_000004.12:181149548:T:TATATATTTTTTTT,NC_000004.12:181149548:T:TATATATTTTTTTTT,NC_000004.12:181149548:T:TATATATTTTTTTTTT,NC_000004.12:181149548:T:TATATATTTTTTTTTTT,NC_000004.12:181149548:T:TATATATTTTTTTTTTTT,NC_000004.12:181149548:T:TATATATTTTTTTTTTTTTTTT,NC_000004.12:181149548:T:TATATT,NC_000004.12:181149548:T:TATATTT,NC_000004.12:181149548:T:TATATTTT,NC_000004.12:181149548:T:TATATTTTT,NC_000004.12:181149548:T:TATATTTTTT,NC_000004.12:181149548:T:TATATTTTTTTT,NC_000004.12:181149548:T:TATATTTTTTTTT,NC_000004.12:181149548:T:TATATTTTTTTTTT,NC_000004.12:181149548:T:TATATTTTTTTTTTT,NC_000004.12:181149548:T:TATATTTTTTTTTTTT,NC_000004.12:181149548:T:TATATTTTTTTTTTTTT,NC_000004.12:181149548:T:TATATTTTTTTTTTTTTT,NC_000004.12:181149548:T:TATATTTTTTTTTTTTTTTT,NC_000004.12:181149548:T:TATT,NC_000004.12:181149548:T:TATTT,NC_000004.12:181149548:T:TATTTT,NC_000004.12:181149548:T:TATTTTT,NC_000004.12:181149548:T:TATTTTTT,NC_000004.12:181149548:T:TATTTTTTTT,NC_000004.12:181149548:T:TATTTTTTTTT,NC_000004.12:181149548:T:TATTTTTTTTTT,NC_000004.12:181149548:T:TATTTTTTTTTTTTT,NC_000004.12:181149548:T:TATTTTTTTTTTTTTT
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATATATATATATT=0./0 (ALFA)
TATATATATTTTTTT=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.181149549TA[14]TT[1], NC_000004.12:g.181149549TA[12]TT[1], NC_000004.12:g.181149549TA[12]T[4], NC_000004.12:g.181149549TA[11]TT[1], NC_000004.12:g.181149549TA[11]T[4], NC_000004.12:g.181149549TA[10]TT[1], NC_000004.12:g.181149549TA[10]TTT[1], NC_000004.12:g.181149549TA[10]TTTATATATATATATT[1], NC_000004.12:g.181149549TA[10]T[4], NC_000004.12:g.181149549TA[10]T[5], NC_000004.12:g.181149549TA[10]T[8], NC_000004.12:g.181149549TA[9]TT[1], NC_000004.12:g.181149549TA[9]TTT[1], NC_000004.12:g.181149549TA[9]T[4], NC_000004.12:g.181149549TA[9]T[5], NC_000004.12:g.181149549TA[9]T[6], NC_000004.12:g.181149549TA[9]T[12], NC_000004.12:g.181149549TA[8]TT[1], NC_000004.12:g.181149549TA[8]TTT[1], NC_000004.12:g.181149549TA[8]T[4], NC_000004.12:g.181149549TA[8]T[6], NC_000004.12:g.181149549TA[8]T[9], NC_000004.12:g.181149549TA[8]T[12], NC_000004.12:g.181149549TA[8]T[15], NC_000004.12:g.181149549TA[7]TT[1], NC_000004.12:g.181149549TA[7]TTT[1], NC_000004.12:g.181149549TA[7]T[4], NC_000004.12:g.181149549TA[7]T[5], NC_000004.12:g.181149549TA[7]T[6], NC_000004.12:g.181149549TA[7]T[7], NC_000004.12:g.181149549TA[7]T[8], NC_000004.12:g.181149549TA[7]T[9], NC_000004.12:g.181149549TA[6]TT[1], NC_000004.12:g.181149549TA[6]TTT[1], NC_000004.12:g.181149549TA[6]T[4], NC_000004.12:g.181149549TA[6]T[5], NC_000004.12:g.181149549TA[6]T[6], NC_000004.12:g.181149549TA[6]T[7], NC_000004.12:g.181149549TA[6]T[8], NC_000004.12:g.181149549TA[6]T[12], NC_000004.12:g.181149549TA[6]T[13], NC_000004.12:g.181149549TA[5]TT[1], NC_000004.12:g.181149549TA[5]TTT[1], NC_000004.12:g.181149549TA[5]T[4], NC_000004.12:g.181149549TA[5]T[5], NC_000004.12:g.181149549TA[5]T[6], NC_000004.12:g.181149549TA[5]T[7], NC_000004.12:g.181149549TA[5]T[8], NC_000004.12:g.181149549TA[5]T[9], NC_000004.12:g.181149549TA[5]T[10], NC_000004.12:g.181149549TA[5]T[15], NC_000004.12:g.181149549TA[4]TT[1], NC_000004.12:g.181149549TA[4]TTT[1], NC_000004.12:g.181149549TA[4]T[4], NC_000004.12:g.181149549TA[4]T[5], NC_000004.12:g.181149549TA[4]T[6], NC_000004.12:g.181149549TA[4]T[7], NC_000004.12:g.181149549TA[4]T[8], NC_000004.12:g.181149549TA[4]T[9], NC_000004.12:g.181149549TA[4]T[10], NC_000004.12:g.181149549TA[4]T[13], NC_000004.12:g.181149549TA[3]TT[1], NC_000004.12:g.181149549TA[3]TTT[1], NC_000004.12:g.181149549TA[3]TTTATTTT[1], NC_000004.12:g.181149549TA[3]T[4], NC_000004.12:g.181149549TA[3]T[5], NC_000004.12:g.181149549TA[3]T[6], NC_000004.12:g.181149549TA[3]T[7], NC_000004.12:g.181149549TA[3]T[8], NC_000004.12:g.181149549TA[3]T[9], NC_000004.12:g.181149549TA[3]T[10], NC_000004.12:g.181149549TA[3]T[11], NC_000004.12:g.181149549TA[3]T[12], NC_000004.12:g.181149549TA[3]T[16], NC_000004.12:g.181149549TA[2]TT[1], NC_000004.12:g.181149549TA[2]TTT[1], NC_000004.12:g.181149549TA[2]T[4], NC_000004.12:g.181149549TA[2]T[5], NC_000004.12:g.181149549TA[2]T[6], NC_000004.12:g.181149549TA[2]T[8], NC_000004.12:g.181149549TA[2]T[9], NC_000004.12:g.181149549TA[2]T[10], NC_000004.12:g.181149549TA[2]T[11], NC_000004.12:g.181149549TA[2]T[12], NC_000004.12:g.181149549TA[2]T[13], NC_000004.12:g.181149549TA[2]T[14], NC_000004.12:g.181149549TA[2]T[16], NC_000004.12:g.181149549_181149550insATT, NC_000004.12:g.181149549_181149550insATTT, NC_000004.12:g.181149549_181149550insATTTT, NC_000004.12:g.181149549_181149550insATTTTT, NC_000004.12:g.181149549_181149550insATTTTTT, NC_000004.12:g.181149549_181149550insATTTTTTTT, NC_000004.12:g.181149549_181149550insATTTTTTTTT, NC_000004.12:g.181149549_181149550insATTTTTTTTTT, NC_000004.12:g.181149549_181149550insATTTTTTTTTTTTT, NC_000004.12:g.181149549_181149550insATTTTTTTTTTTTTT, NC_000004.11:g.182070702TA[14]TT[1], NC_000004.11:g.182070702TA[12]TT[1], NC_000004.11:g.182070702TA[12]T[4], NC_000004.11:g.182070702TA[11]TT[1], NC_000004.11:g.182070702TA[11]T[4], NC_000004.11:g.182070702TA[10]TT[1], NC_000004.11:g.182070702TA[10]TTT[1], NC_000004.11:g.182070702TA[10]TTTATATATATATATT[1], NC_000004.11:g.182070702TA[10]T[4], NC_000004.11:g.182070702TA[10]T[5], NC_000004.11:g.182070702TA[10]T[8], NC_000004.11:g.182070702TA[9]TT[1], NC_000004.11:g.182070702TA[9]TTT[1], NC_000004.11:g.182070702TA[9]T[4], NC_000004.11:g.182070702TA[9]T[5], NC_000004.11:g.182070702TA[9]T[6], NC_000004.11:g.182070702TA[9]T[12], NC_000004.11:g.182070702TA[8]TT[1], NC_000004.11:g.182070702TA[8]TTT[1], NC_000004.11:g.182070702TA[8]T[4], NC_000004.11:g.182070702TA[8]T[6], NC_000004.11:g.182070702TA[8]T[9], NC_000004.11:g.182070702TA[8]T[12], NC_000004.11:g.182070702TA[8]T[15], NC_000004.11:g.182070702TA[7]TT[1], NC_000004.11:g.182070702TA[7]TTT[1], NC_000004.11:g.182070702TA[7]T[4], NC_000004.11:g.182070702TA[7]T[5], NC_000004.11:g.182070702TA[7]T[6], NC_000004.11:g.182070702TA[7]T[7], NC_000004.11:g.182070702TA[7]T[8], NC_000004.11:g.182070702TA[7]T[9], NC_000004.11:g.182070702TA[6]TT[1], NC_000004.11:g.182070702TA[6]TTT[1], NC_000004.11:g.182070702TA[6]T[4], NC_000004.11:g.182070702TA[6]T[5], NC_000004.11:g.182070702TA[6]T[6], NC_000004.11:g.182070702TA[6]T[7], NC_000004.11:g.182070702TA[6]T[8], NC_000004.11:g.182070702TA[6]T[12], NC_000004.11:g.182070702TA[6]T[13], NC_000004.11:g.182070702TA[5]TT[1], NC_000004.11:g.182070702TA[5]TTT[1], NC_000004.11:g.182070702TA[5]T[4], NC_000004.11:g.182070702TA[5]T[5], NC_000004.11:g.182070702TA[5]T[6], NC_000004.11:g.182070702TA[5]T[7], NC_000004.11:g.182070702TA[5]T[8], NC_000004.11:g.182070702TA[5]T[9], NC_000004.11:g.182070702TA[5]T[10], NC_000004.11:g.182070702TA[5]T[15], NC_000004.11:g.182070702TA[4]TT[1], NC_000004.11:g.182070702TA[4]TTT[1], NC_000004.11:g.182070702TA[4]T[4], NC_000004.11:g.182070702TA[4]T[5], NC_000004.11:g.182070702TA[4]T[6], NC_000004.11:g.182070702TA[4]T[7], NC_000004.11:g.182070702TA[4]T[8], NC_000004.11:g.182070702TA[4]T[9], NC_000004.11:g.182070702TA[4]T[10], NC_000004.11:g.182070702TA[4]T[13], NC_000004.11:g.182070702TA[3]TT[1], NC_000004.11:g.182070702TA[3]TTT[1], NC_000004.11:g.182070702TA[3]TTTATTTT[1], NC_000004.11:g.182070702TA[3]T[4], NC_000004.11:g.182070702TA[3]T[5], NC_000004.11:g.182070702TA[3]T[6], NC_000004.11:g.182070702TA[3]T[7], NC_000004.11:g.182070702TA[3]T[8], NC_000004.11:g.182070702TA[3]T[9], NC_000004.11:g.182070702TA[3]T[10], NC_000004.11:g.182070702TA[3]T[11], NC_000004.11:g.182070702TA[3]T[12], NC_000004.11:g.182070702TA[3]T[16], NC_000004.11:g.182070702TA[2]TT[1], NC_000004.11:g.182070702TA[2]TTT[1], NC_000004.11:g.182070702TA[2]T[4], NC_000004.11:g.182070702TA[2]T[5], NC_000004.11:g.182070702TA[2]T[6], NC_000004.11:g.182070702TA[2]T[8], NC_000004.11:g.182070702TA[2]T[9], NC_000004.11:g.182070702TA[2]T[10], NC_000004.11:g.182070702TA[2]T[11], NC_000004.11:g.182070702TA[2]T[12], NC_000004.11:g.182070702TA[2]T[13], NC_000004.11:g.182070702TA[2]T[14], NC_000004.11:g.182070702TA[2]T[16], NC_000004.11:g.182070702_182070703insATT, NC_000004.11:g.182070702_182070703insATTT, NC_000004.11:g.182070702_182070703insATTTT, NC_000004.11:g.182070702_182070703insATTTTT, NC_000004.11:g.182070702_182070703insATTTTTT, NC_000004.11:g.182070702_182070703insATTTTTTTT, NC_000004.11:g.182070702_182070703insATTTTTTTTT, NC_000004.11:g.182070702_182070703insATTTTTTTTTT, NC_000004.11:g.182070702_182070703insATTTTTTTTTTTTT, NC_000004.11:g.182070702_182070703insATTTTTTTTTTTTTT

Select item 149136650413.

rs1491366504 has merged into rs869076911 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 4:181156626 (GRCh38)
4:182077779 (GRCh37)
Canonical SPDI:: NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181156613:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000004.12:g.181156626_181156635del, NC_000004.12:g.181156628_181156635del, NC_000004.12:g.181156629_181156635del, NC_000004.12:g.181156630_181156635del, NC_000004.12:g.181156631_181156635del, NC_000004.12:g.181156632_181156635del, NC_000004.12:g.181156633_181156635del, NC_000004.12:g.181156634_181156635del, NC_000004.12:g.181156635del, NC_000004.12:g.181156635dup, NC_000004.12:g.181156634_181156635dup, NC_000004.12:g.181156633_181156635dup, NC_000004.12:g.181156632_181156635dup, NC_000004.12:g.181156631_181156635dup, NC_000004.12:g.181156630_181156635dup, NC_000004.12:g.181156629_181156635dup, NC_000004.12:g.181156628_181156635dup, NC_000004.12:g.181156627_181156635dup, NC_000004.12:g.181156626_181156635dup, NC_000004.12:g.181156625_181156635dup, NC_000004.12:g.181156624_181156635dup, NC_000004.12:g.181156623_181156635dup, NC_000004.12:g.181156622_181156635dup, NC_000004.12:g.181156635_181156636insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.181156635_181156636insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.182077779_182077788del, NC_000004.11:g.182077781_182077788del, NC_000004.11:g.182077782_182077788del, NC_000004.11:g.182077783_182077788del, NC_000004.11:g.182077784_182077788del, NC_000004.11:g.182077785_182077788del, NC_000004.11:g.182077786_182077788del, NC_000004.11:g.182077787_182077788del, NC_000004.11:g.182077788del, NC_000004.11:g.182077788dup, NC_000004.11:g.182077787_182077788dup, NC_000004.11:g.182077786_182077788dup, NC_000004.11:g.182077785_182077788dup, NC_000004.11:g.182077784_182077788dup, NC_000004.11:g.182077783_182077788dup, NC_000004.11:g.182077782_182077788dup, NC_000004.11:g.182077781_182077788dup, NC_000004.11:g.182077780_182077788dup, NC_000004.11:g.182077779_182077788dup, NC_000004.11:g.182077778_182077788dup, NC_000004.11:g.182077777_182077788dup, NC_000004.11:g.182077776_182077788dup, NC_000004.11:g.182077775_182077788dup, NC_000004.11:g.182077788_182077789insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.182077788_182077789insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149136557114.

rs1491365571 has merged into rs33911235 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 4:181071667 (GRCh38)
4:181992820 (GRCh37)
Canonical SPDI:: NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:181071653:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000004.12:g.181071667_181071670del, NC_000004.12:g.181071668_181071670del, NC_000004.12:g.181071669_181071670del, NC_000004.12:g.181071670del, NC_000004.12:g.181071670dup, NC_000004.12:g.181071669_181071670dup, NC_000004.12:g.181071668_181071670dup, NC_000004.12:g.181071667_181071670dup, NC_000004.12:g.181071661_181071670dup, NC_000004.11:g.181992820_181992823del, NC_000004.11:g.181992821_181992823del, NC_000004.11:g.181992822_181992823del, NC_000004.11:g.181992823del, NC_000004.11:g.181992823dup, NC_000004.11:g.181992822_181992823dup, NC_000004.11:g.181992821_181992823dup, NC_000004.11:g.181992820_181992823dup, NC_000004.11:g.181992814_181992823dup

Select item 149134716715.

rs1491347167 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 4:181102153 (GRCh38)
4:182023306 (GRCh37)
Canonical SPDI:: NC_000004.12:181102152:CA:
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00185/22 (ALFA)
-=0.00256/40 (TOMMO)
HGVS:: NC_000004.12:g.181102153_181102154del, NC_000004.11:g.182023306_182023307del

Select item 149132137816.

rs1491321378 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 4:181110119 (GRCh38)
4:182031272 (GRCh37)
Canonical SPDI:: NC_000004.12:181110118:AT:
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000004.12:g.181110119_181110120del, NC_000004.11:g.182031272_182031273del

Select item 149130491717.

rs1491304917 has merged into rs1009307609 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,AA,AAA [Show Flanks]
Chromosome:: 4:181068882 (GRCh38)
4:181990035 (GRCh37)
Canonical SPDI:: NC_000004.12:181068880:AAAAA:A,NC_000004.12:181068880:AAAAA:AAA,NC_000004.12:181068880:AAAAA:AAAA
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.00006/1 (TOMMO)
-=0.00056/1 (Korea1K)
HGVS:: NC_000004.12:g.181068882_181068885del, NC_000004.12:g.181068884_181068885del, NC_000004.12:g.181068885del, NC_000004.11:g.181990035_181990038del, NC_000004.11:g.181990037_181990038del, NC_000004.11:g.181990038del

Select item 149130253218.

rs1491302532 [Homo sapiens]

Variant type:: DEL
Alleles:: AG>- [Show Flanks]
Chromosome:: 4:181151308 (GRCh38)
4:182072461 (GRCh37)
Canonical SPDI:: NC_000004.12:181151307:AG:
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000004.12:g.181151308_181151309del, NC_000004.11:g.182072461_182072462del

Select item 149130246219.

rs1491302462 has merged into rs57973366 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATATATATATATAT>-,AT,ATAT,ATATAT,ATATATAT,ATATATATAT,ATATATATATAT,ATATATATATATATAT,ATATATATATATATATAT,ATATATATATATATATATAT,ATATATATATATATATATATAT,ATATATATATATATATATATATAT,ATATATATATATATATATATATATAT,ATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATAT [Show Flanks]
Chromosome:: 4:181149536 (GRCh38)
4:182070689 (GRCh37)
Canonical SPDI:: NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:181149521:ATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATAT
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATATATATAT=0./0 (ALFA)
HGVS:: NC_000004.12:g.181149522AT[7], NC_000004.12:g.181149522AT[8], NC_000004.12:g.181149522AT[9], NC_000004.12:g.181149522AT[10], NC_000004.12:g.181149522AT[11], NC_000004.12:g.181149522AT[12], NC_000004.12:g.181149522AT[13], NC_000004.12:g.181149522AT[15], NC_000004.12:g.181149522AT[16], NC_000004.12:g.181149522AT[17], NC_000004.12:g.181149522AT[18], NC_000004.12:g.181149522AT[19], NC_000004.12:g.181149522AT[20], NC_000004.12:g.181149522AT[21], NC_000004.12:g.181149522AT[22], NC_000004.12:g.181149522AT[23], NC_000004.11:g.182070675AT[7], NC_000004.11:g.182070675AT[8], NC_000004.11:g.182070675AT[9], NC_000004.11:g.182070675AT[10], NC_000004.11:g.182070675AT[11], NC_000004.11:g.182070675AT[12], NC_000004.11:g.182070675AT[13], NC_000004.11:g.182070675AT[15], NC_000004.11:g.182070675AT[16], NC_000004.11:g.182070675AT[17], NC_000004.11:g.182070675AT[18], NC_000004.11:g.182070675AT[19], NC_000004.11:g.182070675AT[20], NC_000004.11:g.182070675AT[21], NC_000004.11:g.182070675AT[22], NC_000004.11:g.182070675AT[23]

Select item 149127084020.

rs1491270840 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT [Show Flanks]
Chromosome:: 4:181151392 (GRCh38)
4:182072545 (GRCh37)
Canonical SPDI:: NC_000004.12:181151389:CTCT:CT,NC_000004.12:181151389:CTCT:CTCTCT
Gene:: LINC00290 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTCTCT=0./0 (ALFA)
HGVS:: NC_000004.12:g.181151390CT[1], NC_000004.12:g.181151390CT[3], NC_000004.11:g.182072543CT[1], NC_000004.11:g.182072543CT[3]

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