SNP Links for Gene (Select 57862) - SNP

Links from Gene

Items: 1 to 20 of 10932

<< First< Prev

Page of 547

Next >Last >>

Select item 14915536541.

rs1491553654 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTT [Show Flanks]
Chromosome:: 14:73912170 (GRCh38)
14:74378874 (GRCh37)
Canonical SPDI:: NC_000014.9:73912170:TT:TTCTT
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000014.9:g.73912172_73912173insCTT, NC_000014.8:g.74378875_74378876insCTT

Select item 14915509452.

rs1491550945 has merged into rs113156661 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:73927100 (GRCh38)
14:74393803 (GRCh37)
Canonical SPDI:: NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTT,NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:73927089:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ZNF410 (Varview), FAM161B (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
-=0.3826/544 (1000Genomes)
HGVS:: NC_000014.9:g.73927100_73927103del, NC_000014.9:g.73927101_73927103del, NC_000014.9:g.73927102_73927103del, NC_000014.9:g.73927103del, NC_000014.9:g.73927103dup, NC_000014.9:g.73927102_73927103dup, NC_000014.9:g.73927101_73927103dup, NC_000014.9:g.73927093_73927103dup, NC_000014.8:g.74393803_74393806del, NC_000014.8:g.74393804_74393806del, NC_000014.8:g.74393805_74393806del, NC_000014.8:g.74393806del, NC_000014.8:g.74393806dup, NC_000014.8:g.74393805_74393806dup, NC_000014.8:g.74393804_74393806dup, NC_000014.8:g.74393796_74393806dup

Select item 14915116783.

rs1491511678 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 14:73889811 (GRCh38)
14:74356515 (GRCh37)
Canonical SPDI:: NC_000014.9:73889811:C:CC
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000014.9:g.73889812dup, NC_000014.8:g.74356515dup

Select item 14914514524.

rs1491451452 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 14:73889431 (GRCh38)
14:74356134 (GRCh37)
Canonical SPDI:: NC_000014.9:73889430:CA:
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000014.9:g.73889431_73889432del, NC_000014.8:g.74356134_74356135del

Select item 14914204645.

rs1491420464 has merged into rs34227581 [Homo sapiens]

Variant type:: DELINS
Alleles:: GG>-,G,GGG,GGGG,GGGGG,GGGGGG [Show Flanks]
Chromosome:: 14:73909615 (GRCh38)
14:74376318 (GRCh37)
Canonical SPDI:: NC_000014.9:73909607:GGGGGGGGG:GGGGGGG,NC_000014.9:73909607:GGGGGGGGG:GGGGGGGG,NC_000014.9:73909607:GGGGGGGGG:GGGGGGGGGG,NC_000014.9:73909607:GGGGGGGGG:GGGGGGGGGGG,NC_000014.9:73909607:GGGGGGGGG:GGGGGGGGGGGG,NC_000014.9:73909607:GGGGGGGGG:GGGGGGGGGGGGG
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGGGGGGGGG=0./0 (ALFA)
-=0.126/631 (1000Genomes)
HGVS:: NC_000014.9:g.73909615_73909616del, NC_000014.9:g.73909616del, NC_000014.9:g.73909616dup, NC_000014.9:g.73909615_73909616dup, NC_000014.9:g.73909614_73909616dup, NC_000014.9:g.73909613_73909616dup, NC_000014.8:g.74376318_74376319del, NC_000014.8:g.74376319del, NC_000014.8:g.74376319dup, NC_000014.8:g.74376318_74376319dup, NC_000014.8:g.74376317_74376319dup, NC_000014.8:g.74376316_74376319dup

Select item 14914023336.

rs1491402333 has merged into rs34162465 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTT>-,T,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:73912178 (GRCh38)
14:74378881 (GRCh37)
Canonical SPDI:: NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73912169:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTT=0./0 (ALFA)
T=0.3005/1505 (1000Genomes)
HGVS:: NC_000014.9:g.73912178_73912189del, NC_000014.9:g.73912179_73912189del, NC_000014.9:g.73912182_73912189del, NC_000014.9:g.73912183_73912189del, NC_000014.9:g.73912184_73912189del, NC_000014.9:g.73912185_73912189del, NC_000014.9:g.73912186_73912189del, NC_000014.9:g.73912187_73912189del, NC_000014.9:g.73912188_73912189del, NC_000014.9:g.73912189del, NC_000014.9:g.73912189dup, NC_000014.9:g.73912188_73912189dup, NC_000014.9:g.73912187_73912189dup, NC_000014.9:g.73912186_73912189dup, NC_000014.9:g.73912185_73912189dup, NC_000014.9:g.73912184_73912189dup, NC_000014.8:g.74378881_74378892del, NC_000014.8:g.74378882_74378892del, NC_000014.8:g.74378885_74378892del, NC_000014.8:g.74378886_74378892del, NC_000014.8:g.74378887_74378892del, NC_000014.8:g.74378888_74378892del, NC_000014.8:g.74378889_74378892del, NC_000014.8:g.74378890_74378892del, NC_000014.8:g.74378891_74378892del, NC_000014.8:g.74378892del, NC_000014.8:g.74378892dup, NC_000014.8:g.74378891_74378892dup, NC_000014.8:g.74378890_74378892dup, NC_000014.8:g.74378889_74378892dup, NC_000014.8:g.74378888_74378892dup, NC_000014.8:g.74378887_74378892dup

Select item 14913423107.

rs1491342310 has merged into rs71115932 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:73918695 (GRCh38)
14:74385398 (GRCh37)
Canonical SPDI:: NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73918686:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000014.9:g.73918695_73918714del, NC_000014.9:g.73918697_73918714del, NC_000014.9:g.73918698_73918714del, NC_000014.9:g.73918699_73918714del, NC_000014.9:g.73918700_73918714del, NC_000014.9:g.73918701_73918714del, NC_000014.9:g.73918702_73918714del, NC_000014.9:g.73918703_73918714del, NC_000014.9:g.73918704_73918714del, NC_000014.9:g.73918705_73918714del, NC_000014.9:g.73918706_73918714del, NC_000014.9:g.73918707_73918714del, NC_000014.9:g.73918708_73918714del, NC_000014.9:g.73918709_73918714del, NC_000014.9:g.73918710_73918714del, NC_000014.9:g.73918711_73918714del, NC_000014.9:g.73918712_73918714del, NC_000014.9:g.73918713_73918714del, NC_000014.9:g.73918714del, NC_000014.9:g.73918714dup, NC_000014.9:g.73918713_73918714dup, NC_000014.9:g.73918712_73918714dup, NC_000014.9:g.73918711_73918714dup, NC_000014.9:g.73918710_73918714dup, NC_000014.9:g.73918707_73918714dup, NC_000014.8:g.74385398_74385417del, NC_000014.8:g.74385400_74385417del, NC_000014.8:g.74385401_74385417del, NC_000014.8:g.74385402_74385417del, NC_000014.8:g.74385403_74385417del, NC_000014.8:g.74385404_74385417del, NC_000014.8:g.74385405_74385417del, NC_000014.8:g.74385406_74385417del, NC_000014.8:g.74385407_74385417del, NC_000014.8:g.74385408_74385417del, NC_000014.8:g.74385409_74385417del, NC_000014.8:g.74385410_74385417del, NC_000014.8:g.74385411_74385417del, NC_000014.8:g.74385412_74385417del, NC_000014.8:g.74385413_74385417del, NC_000014.8:g.74385414_74385417del, NC_000014.8:g.74385415_74385417del, NC_000014.8:g.74385416_74385417del, NC_000014.8:g.74385417del, NC_000014.8:g.74385417dup, NC_000014.8:g.74385416_74385417dup, NC_000014.8:g.74385415_74385417dup, NC_000014.8:g.74385414_74385417dup, NC_000014.8:g.74385413_74385417dup, NC_000014.8:g.74385410_74385417dup

Select item 14913281608.

rs1491328160 has merged into rs34227581 [Homo sapiens]

Variant type:: DELINS
Alleles:: GG>-,G,GGG,GGGG,GGGGG,GGGGGG [Show Flanks]
Chromosome:: 14:73909615 (GRCh38)
14:74376318 (GRCh37)
Canonical SPDI:: NC_000014.9:73909607:GGGGGGGGG:GGGGGGG,NC_000014.9:73909607:GGGGGGGGG:GGGGGGGG,NC_000014.9:73909607:GGGGGGGGG:GGGGGGGGGG,NC_000014.9:73909607:GGGGGGGGG:GGGGGGGGGGG,NC_000014.9:73909607:GGGGGGGGG:GGGGGGGGGGGG,NC_000014.9:73909607:GGGGGGGGG:GGGGGGGGGGGGG
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGGGGGGGGG=0./0 (ALFA)
-=0.126/631 (1000Genomes)
HGVS:: NC_000014.9:g.73909615_73909616del, NC_000014.9:g.73909616del, NC_000014.9:g.73909616dup, NC_000014.9:g.73909615_73909616dup, NC_000014.9:g.73909614_73909616dup, NC_000014.9:g.73909613_73909616dup, NC_000014.8:g.74376318_74376319del, NC_000014.8:g.74376319del, NC_000014.8:g.74376319dup, NC_000014.8:g.74376318_74376319dup, NC_000014.8:g.74376317_74376319dup, NC_000014.8:g.74376316_74376319dup

Select item 14912860149.

rs1491286014 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 14:73916545 (GRCh38)
14:74383249 (GRCh37)
Canonical SPDI:: NC_000014.9:73916545:A:AA
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000029/4 (GnomAD)
A=0.000312/2 (1000Genomes)
HGVS:: NC_000014.9:g.73916546dup, NC_000014.8:g.74383249dup

Select item 149125882710.

rs1491258827 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 14:73918686 (GRCh38)
14:74385389 (GRCh37)
Canonical SPDI:: NC_000014.9:73918685:CT:
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000027/3 (GnomAD)
HGVS:: NC_000014.9:g.73918686_73918687del, NC_000014.8:g.74385389_74385390del

Select item 149123121211.

rs1491231212 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TATATATATATATATATATATATATATATGTATA,TATATATATATATATATATATATATATGTATA,TATATATATATATATATATATATATGTATA,TATATATATATATATATATATATGTATA,TATATATATATATATATATATGTATA,TATATATATATATATATATGTATA,TATATATATATATATATATGTGTATA,TATATATATATATATATGTATA,TATATATATATATATGTATA,TATATATATATATGTATA,TATATATATATGTATA,TATATATATGTATA,TATATATGTATA,TATATGTATA,TATGTATA,TATGTATATATATATGTATA,TGTATA [Show Flanks]
Chromosome:: 14:73905991 (GRCh38)
14:74372695 (GRCh37)
Canonical SPDI:: NC_000014.9:73905991:TATA:TATATATATATATATATATATATATATATATATGTATA,NC_000014.9:73905991:TATA:TATATATATATATATATATATATATATATATGTATA,NC_000014.9:73905991:TATA:TATATATATATATATATATATATATATATGTATA,NC_000014.9:73905991:TATA:TATATATATATATATATATATATATATGTATA,NC_000014.9:73905991:TATA:TATATATATATATATATATATATATGTATA,NC_000014.9:73905991:TATA:TATATATATATATATATATATATGTATA,NC_000014.9:73905991:TATA:TATATATATATATATATATATATGTGTATA,NC_000014.9:73905991:TATA:TATATATATATATATATATATGTATA,NC_000014.9:73905991:TATA:TATATATATATATATATATGTATA,NC_000014.9:73905991:TATA:TATATATATATATATATGTATA,NC_000014.9:73905991:TATA:TATATATATATATATGTATA,NC_000014.9:73905991:TATA:TATATATATATATGTATA,NC_000014.9:73905991:TATA:TATATATATATGTATA,NC_000014.9:73905991:TATA:TATATATATGTATA,NC_000014.9:73905991:TATA:TATATATGTATA,NC_000014.9:73905991:TATA:TATATATGTATATATATATGTATA,NC_000014.9:73905991:TATA:TATATGTATA
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATGTATA=0./0 (ALFA)
TATATATATATATATATATG=0.00167/1 (NorthernSweden)
HGVS:: NC_000014.9:g.73905992_73905995TA[16]TGTATA[1], NC_000014.9:g.73905992_73905995TA[15]TGTATA[1], NC_000014.9:g.73905992_73905995TA[14]TGTATA[1], NC_000014.9:g.73905992_73905995TA[13]TGTATA[1], NC_000014.9:g.73905992_73905995TA[12]TGTATA[1], NC_000014.9:g.73905992_73905995TA[11]TGTATA[1], NC_000014.9:g.73905992_73905995TA[11]TG[2]TA[2], NC_000014.9:g.73905992_73905995TA[10]TGTATA[1], NC_000014.9:g.73905992_73905995TA[9]TGTATA[1], NC_000014.9:g.73905992_73905995TA[8]TGTATA[1], NC_000014.9:g.73905992_73905995TA[7]TGTATA[1], NC_000014.9:g.73905992_73905995TA[6]TGTATA[1], NC_000014.9:g.73905992_73905995TA[5]TGTATA[1], NC_000014.9:g.73905992_73905995TA[4]TGTATA[1], NC_000014.9:g.73905992_73905995TA[3]TGTATA[1], NC_000014.9:g.73905995_73905996insTATGTATATATATATGTATA, NC_000014.9:g.73905992_73905995TA[2]TGTATA[1], NC_000014.8:g.74372695_74372698TA[16]TGTATA[1], NC_000014.8:g.74372695_74372698TA[15]TGTATA[1], NC_000014.8:g.74372695_74372698TA[14]TGTATA[1], NC_000014.8:g.74372695_74372698TA[13]TGTATA[1], NC_000014.8:g.74372695_74372698TA[12]TGTATA[1], NC_000014.8:g.74372695_74372698TA[11]TGTATA[1], NC_000014.8:g.74372695_74372698TA[11]TG[2]TA[2], NC_000014.8:g.74372695_74372698TA[10]TGTATA[1], NC_000014.8:g.74372695_74372698TA[9]TGTATA[1], NC_000014.8:g.74372695_74372698TA[8]TGTATA[1], NC_000014.8:g.74372695_74372698TA[7]TGTATA[1], NC_000014.8:g.74372695_74372698TA[6]TGTATA[1], NC_000014.8:g.74372695_74372698TA[5]TGTATA[1], NC_000014.8:g.74372695_74372698TA[4]TGTATA[1], NC_000014.8:g.74372695_74372698TA[3]TGTATA[1], NC_000014.8:g.74372698_74372699insTATGTATATATATATGTATA, NC_000014.8:g.74372695_74372698TA[2]TGTATA[1]

Select item 149111292412.

rs1491112924 has merged into rs755623044 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 14:73910763 (GRCh38)
14:74377466 (GRCh37)
Canonical SPDI:: NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000014.9:g.73910763_73910773del, NC_000014.9:g.73910766_73910773del, NC_000014.9:g.73910767_73910773del, NC_000014.9:g.73910768_73910773del, NC_000014.9:g.73910769_73910773del, NC_000014.9:g.73910770_73910773del, NC_000014.9:g.73910771_73910773del, NC_000014.9:g.73910772_73910773del, NC_000014.9:g.73910773del, NC_000014.9:g.73910773dup, NC_000014.9:g.73910772_73910773dup, NC_000014.9:g.73910771_73910773dup, NC_000014.9:g.73910770_73910773dup, NC_000014.9:g.73910768_73910773dup, NC_000014.8:g.74377466_74377476del, NC_000014.8:g.74377469_74377476del, NC_000014.8:g.74377470_74377476del, NC_000014.8:g.74377471_74377476del, NC_000014.8:g.74377472_74377476del, NC_000014.8:g.74377473_74377476del, NC_000014.8:g.74377474_74377476del, NC_000014.8:g.74377475_74377476del, NC_000014.8:g.74377476del, NC_000014.8:g.74377476dup, NC_000014.8:g.74377475_74377476dup, NC_000014.8:g.74377474_74377476dup, NC_000014.8:g.74377473_74377476dup, NC_000014.8:g.74377471_74377476dup

Select item 149110902413.

rs1491109024 has merged into rs11461357 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:73927844 (GRCh38)
14:74394547 (GRCh37)
Canonical SPDI:: NC_000014.9:73927832:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000014.9:73927832:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:73927832:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:73927832:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:73927832:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:73927832:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:73927832:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000014.9:73927832:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73927832:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ZNF410 (Varview), FAM161B (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
T=0.4397/2202 (1000Genomes)
HGVS:: NC_000014.9:g.73927844_73927848del, NC_000014.9:g.73927847_73927848del, NC_000014.9:g.73927848del, NC_000014.9:g.73927848dup, NC_000014.9:g.73927847_73927848dup, NC_000014.9:g.73927846_73927848dup, NC_000014.9:g.73927845_73927848dup, NC_000014.9:g.73927844_73927848dup, NC_000014.9:g.73927841_73927848dup, NC_000014.8:g.74394547_74394551del, NC_000014.8:g.74394550_74394551del, NC_000014.8:g.74394551del, NC_000014.8:g.74394551dup, NC_000014.8:g.74394550_74394551dup, NC_000014.8:g.74394549_74394551dup, NC_000014.8:g.74394548_74394551dup, NC_000014.8:g.74394547_74394551dup, NC_000014.8:g.74394544_74394551dup

Select item 149107407714.

rs1491074077 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 14:73925148 (GRCh38)
14:74391851 (GRCh37)
Canonical SPDI:: NC_000014.9:73925146:TGT:T
Gene:: ZNF410 (Varview), FAM161B (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: -=0.000021/3 (GnomAD)
HGVS:: NC_000014.9:g.73925148_73925149del, NC_000014.8:g.74391851_74391852del

Select item 149095841915.

rs1490958419 has merged into rs755623044 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 14:73910763 (GRCh38)
14:74377466 (GRCh37)
Canonical SPDI:: NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73910753:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000014.9:g.73910763_73910773del, NC_000014.9:g.73910766_73910773del, NC_000014.9:g.73910767_73910773del, NC_000014.9:g.73910768_73910773del, NC_000014.9:g.73910769_73910773del, NC_000014.9:g.73910770_73910773del, NC_000014.9:g.73910771_73910773del, NC_000014.9:g.73910772_73910773del, NC_000014.9:g.73910773del, NC_000014.9:g.73910773dup, NC_000014.9:g.73910772_73910773dup, NC_000014.9:g.73910771_73910773dup, NC_000014.9:g.73910770_73910773dup, NC_000014.9:g.73910768_73910773dup, NC_000014.8:g.74377466_74377476del, NC_000014.8:g.74377469_74377476del, NC_000014.8:g.74377470_74377476del, NC_000014.8:g.74377471_74377476del, NC_000014.8:g.74377472_74377476del, NC_000014.8:g.74377473_74377476del, NC_000014.8:g.74377474_74377476del, NC_000014.8:g.74377475_74377476del, NC_000014.8:g.74377476del, NC_000014.8:g.74377476dup, NC_000014.8:g.74377475_74377476dup, NC_000014.8:g.74377474_74377476dup, NC_000014.8:g.74377473_74377476dup, NC_000014.8:g.74377471_74377476dup

Select item 149092169116.

rs1490921691 [Homo sapiens]

Variant type:: INS
Alleles:: ->CT [Show Flanks]
Chromosome:: 14:73893976 (GRCh38)
14:74360680 (GRCh37)
Canonical SPDI:: NC_000014.9:73893976::CT
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000014.9:g.73893976_73893977insCT, NC_000014.8:g.74360679_74360680insCT

Select item 149089687317.

rs1490896873 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:73887811 (GRCh38)
14:74354514 (GRCh37)
Canonical SPDI:: NC_000014.9:73887810:G:A
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.73887811G>A, NC_000014.8:g.74354514G>A

Select item 149087438318.

rs1490874383 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 14:73898644 (GRCh38)
14:74365347 (GRCh37)
Canonical SPDI:: NC_000014.9:73898643:T:A
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000043/6 (GnomAD)
A=0.000057/15 (TOPMED)
HGVS:: NC_000014.9:g.73898644T>A, NC_000014.8:g.74365347T>A

Select item 149085860519.

rs1490858605 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:73900725 (GRCh38)
14:74367428 (GRCh37)
Canonical SPDI:: NC_000014.9:73900724:A:G
Gene:: ZNF410 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0.00007/1 (ALFA)
HGVS:: NC_000014.9:g.73900725A>G, NC_000014.8:g.74367428A>G

Select item 149085537220.

rs1490855372 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 14:73904079 (GRCh38)
14:74370782 (GRCh37)
Canonical SPDI:: NC_000014.9:73904078:G:T
Gene:: ZNF410 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.73904079G>T, NC_000014.8:g.74370782G>T, NM_021188.3:c.700G>T, NM_021188.2:c.700G>T, NM_001242924.2:c.751G>T, NM_001242924.1:c.751G>T, NM_001242928.2:c.141G>T, NM_001242928.1:c.141G>T, NR_040251.2:n.874G>T, NR_040251.1:n.1118G>T, NM_001242926.2:c.700G>T, NM_001242926.1:c.700G>T, NM_001242927.2:c.481G>T, NM_001242927.1:c.481G>T, NP_067011.1:p.Ala234Ser, NP_001229853.1:p.Ala251Ser, NP_001229857.1:p.Gln47His, NP_001229855.1:p.Ala234Ser, NP_001229856.1:p.Ala161Ser

<< First< Prev

Page of 547

Next >Last >>

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 10932

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity