SNP Links for Gene (Select 5468) - SNP

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Select item 14915732371.

rs1491573237 has merged into rs11321700 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA [Show Flanks]
Chromosome:: 3:12341194 (GRCh38)
3:12382693 (GRCh37)
Canonical SPDI:: NC_000003.12:12341182:AAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000003.12:12341182:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000003.12:12341182:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000003.12:12341182:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA
Gene:: PPARG (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0.0002/1 (ALFA)
A=0.2997/175 (NorthernSweden)
A=0.3227/1616 (1000Genomes)
HGVS:: NC_000003.12:g.12341194_12341196del, NC_000003.12:g.12341195_12341196del, NC_000003.12:g.12341196del, NC_000003.12:g.12341196dup, NC_000003.11:g.12382693_12382695del, NC_000003.11:g.12382694_12382695del, NC_000003.11:g.12382695del, NC_000003.11:g.12382695dup, NG_011749.1:g.58345_58347del, NG_011749.1:g.58346_58347del, NG_011749.1:g.58347del, NG_011749.1:g.58347dup

Select item 14915243552.

rs1491524355 [Homo sapiens]

Variant type:: DEL
Alleles:: GG>- [Show Flanks]
Chromosome:: 3:12448303 (GRCh38)
3:12489802 (GRCh37)
Canonical SPDI:: NC_000003.12:12448302:GG:
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.12448303_12448304del, NC_000003.11:g.12489802_12489803del

Select item 14915226903.

rs1491522690 [Homo sapiens]

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

Select item 14915192534.

rs1491519253 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 3:12310791 (GRCh38)
3:12352290 (GRCh37)
Canonical SPDI:: NC_000003.12:12310790:TA:
Gene:: PPARG (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00011/3 (TOMMO)
HGVS:: NC_000003.12:g.12310791_12310792del, NC_000003.11:g.12352290_12352291del, NG_011749.1:g.27942_27943del

Select item 14914841605.

rs1491484160 has merged into rs71063823 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 3:12354764 (GRCh38)
3:12396263 (GRCh37)
Canonical SPDI:: NC_000003.12:12354753:AAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000003.12:12354753:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000003.12:12354753:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000003.12:12354753:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:12354753:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000003.12:12354753:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:12354753:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000003.12:12354753:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000003.12:12354753:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000003.12:12354753:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000003.12:12354753:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:12354753:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:12354753:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: PPARG (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
AA=0.4275/2141 (1000Genomes)
HGVS:: NC_000003.12:g.12354764_12354771del, NC_000003.12:g.12354766_12354771del, NC_000003.12:g.12354767_12354771del, NC_000003.12:g.12354768_12354771del, NC_000003.12:g.12354769_12354771del, NC_000003.12:g.12354770_12354771del, NC_000003.12:g.12354771del, NC_000003.12:g.12354771dup, NC_000003.12:g.12354770_12354771dup, NC_000003.12:g.12354769_12354771dup, NC_000003.12:g.12354768_12354771dup, NC_000003.12:g.12354767_12354771dup, NC_000003.12:g.12354765_12354771dup, NC_000003.11:g.12396263_12396270del, NC_000003.11:g.12396265_12396270del, NC_000003.11:g.12396266_12396270del, NC_000003.11:g.12396267_12396270del, NC_000003.11:g.12396268_12396270del, NC_000003.11:g.12396269_12396270del, NC_000003.11:g.12396270del, NC_000003.11:g.12396270dup, NC_000003.11:g.12396269_12396270dup, NC_000003.11:g.12396268_12396270dup, NC_000003.11:g.12396267_12396270dup, NC_000003.11:g.12396266_12396270dup, NC_000003.11:g.12396264_12396270dup, NG_011749.1:g.71915_71922del, NG_011749.1:g.71917_71922del, NG_011749.1:g.71918_71922del, NG_011749.1:g.71919_71922del, NG_011749.1:g.71920_71922del, NG_011749.1:g.71921_71922del, NG_011749.1:g.71922del, NG_011749.1:g.71922dup, NG_011749.1:g.71921_71922dup, NG_011749.1:g.71920_71922dup, NG_011749.1:g.71919_71922dup, NG_011749.1:g.71918_71922dup, NG_011749.1:g.71916_71922dup

Select item 14914464306.

rs1491446430 has merged into rs5741526 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT [Show Flanks]
Chromosome:: 3:12295524 (GRCh38)
3:12337023 (GRCh37)
Canonical SPDI:: NC_000003.12:12295514:TTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000003.12:12295514:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:12295514:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:12295514:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:12295514:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:12295514:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:12295514:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT
Gene:: PPARG (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
-=0.2516/1260 (1000Genomes)
-=0.2898/1117 (ALSPAC)
HGVS:: NC_000003.12:g.12295524_12295530del, NC_000003.12:g.12295527_12295530del, NC_000003.12:g.12295528_12295530del, NC_000003.12:g.12295529_12295530del, NC_000003.12:g.12295530del, NC_000003.12:g.12295530dup, NC_000003.12:g.12295529_12295530dup, NC_000003.11:g.12337023_12337029del, NC_000003.11:g.12337026_12337029del, NC_000003.11:g.12337027_12337029del, NC_000003.11:g.12337028_12337029del, NC_000003.11:g.12337029del, NC_000003.11:g.12337029dup, NC_000003.11:g.12337028_12337029dup, NG_011749.1:g.12675_12681del, NG_011749.1:g.12678_12681del, NG_011749.1:g.12679_12681del, NG_011749.1:g.12680_12681del, NG_011749.1:g.12681del, NG_011749.1:g.12681dup, NG_011749.1:g.12680_12681dup

Select item 14914461437.

rs1491446143 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 3:12285905 (GRCh38)
3:12327405 (GRCh37)
Canonical SPDI:: NC_000003.12:12285905:T:TT
Gene:: PPARG (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
T=0./0 (TWINSUK)
T=0.000053/14 (TOPMED)
T=0.000061/8 (GnomAD)
T=0.000259/1 (ALSPAC)
HGVS:: NC_000003.12:g.12285906dup, NC_000003.11:g.12327405dup, NG_011749.1:g.3057dup

Select item 14914362498.

rs1491436249 [Homo sapiens]

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

Select item 14914038329.

rs1491403832 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 3:12469878 (GRCh38)
3:12511378 (GRCh37)
Canonical SPDI:: NC_000003.12:12469878:G:GG
HGVS:: NC_000003.12:g.12469879dup, NC_000003.11:g.12511378dup

Select item 149139014910.

rs1491390149 has merged into rs71628749 [Homo sapiens]

Variant type:: DELINS
Alleles:: GG>-,G [Show Flanks]
Chromosome:: 3:12308372 (GRCh38)
3:12349871 (GRCh37)
Canonical SPDI:: NC_000003.12:12308370:GGG:G,NC_000003.12:12308370:GGG:GG
Gene:: PPARG (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
-=0.02516/1928 (GnomAD)
-=0.08049/1302 (TOMMO)
HGVS:: NC_000003.12:g.12308372_12308373del, NC_000003.12:g.12308373del, NC_000003.11:g.12349871_12349872del, NC_000003.11:g.12349872del, NG_011749.1:g.25523_25524del, NG_011749.1:g.25524del

Select item 149138769711.

rs1491387697 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 3:12354753 (GRCh38)
3:12396252 (GRCh37)
Canonical SPDI:: NC_000003.12:12354752:CA:
Gene:: PPARG (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00717/85 (ALFA)
-=0.00152/43 (TOMMO)
HGVS:: NC_000003.12:g.12354753_12354754del, NC_000003.11:g.12396252_12396253del, NG_011749.1:g.71904_71905del

Select item 149135555112.

rs1491355551 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 3:12413816 (GRCh38)
3:12455315 (GRCh37)
Canonical SPDI:: NC_000003.12:12413815:CA:
Gene:: PPARG (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.00152/18 (ALFA)
HGVS:: NC_000003.12:g.12413816_12413817del, NC_000003.11:g.12455315_12455316del, NG_011749.1:g.130967_130968del

Select item 149135480813.

rs1491354808 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 3:12446864 (GRCh38)
3:12488364 (GRCh37)
Canonical SPDI:: NC_000003.12:12446864::A
Validated:: by frequency,by cluster
MAF:: A=0.014444/1999 (GnomAD)
A=0.017021/109 (1000Genomes)
HGVS:: NC_000003.12:g.12446864_12446865insA, NC_000003.11:g.12488363_12488364insA

Select item 149134312614.

rs1491343126 [Homo sapiens]

Variant type:: INS
Alleles:: ->TC,TTC,TTTC [Show Flanks]
Chromosome:: 3:12417887 (GRCh38)
3:12459387 (GRCh37)
Canonical SPDI:: NC_000003.12:12417887::TC,NC_000003.12:12417887::TTC,NC_000003.12:12417887::TTTC
Gene:: PPARG (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTC=0./0 (ALFA)
TTC=0.005037/601 (GnomAD)
HGVS:: NC_000003.12:g.12417887_12417888insTC, NC_000003.12:g.12417887_12417888insTTC, NC_000003.12:g.12417887_12417888insTTTC, NC_000003.11:g.12459386_12459387insTC, NC_000003.11:g.12459386_12459387insTTC, NC_000003.11:g.12459386_12459387insTTTC, NG_011749.1:g.135038_135039insTC, NG_011749.1:g.135038_135039insTTC, NG_011749.1:g.135038_135039insTTTC

Select item 149133981315.

rs1491339813 has merged into rs72200690 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTCT>-,CT,CTCTCT,CTCTCTCT [Show Flanks]
Chromosome:: 3:12445652 (GRCh38)
3:12487151 (GRCh37)
Canonical SPDI:: NC_000003.12:12445642:TCTCTCTCTCTCT:TCTCTCTCT,NC_000003.12:12445642:TCTCTCTCTCTCT:TCTCTCTCTCT,NC_000003.12:12445642:TCTCTCTCTCTCT:TCTCTCTCTCTCTCT,NC_000003.12:12445642:TCTCTCTCTCTCT:TCTCTCTCTCTCTCTCT
Validated:: by frequency,by alfa,by cluster
MAF:: TCTCTCTCTCT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
TC=0.011667/7 (NorthernSweden)
TC=0.055131/924 (TOMMO)
HGVS:: NC_000003.12:g.12445644CT[4], NC_000003.12:g.12445644CT[5], NC_000003.12:g.12445644CT[7], NC_000003.12:g.12445644CT[8], NC_000003.11:g.12487143CT[4], NC_000003.11:g.12487143CT[5], NC_000003.11:g.12487143CT[7], NC_000003.11:g.12487143CT[8], NG_082926.1:g.1192CT[4], NG_082926.1:g.1192CT[5], NG_082926.1:g.1192CT[7], NG_082926.1:g.1192CT[8]

Select item 149133839716.

rs1491338397 [Homo sapiens]

Variant type:: DELINS
Alleles:: GG>- [Show Flanks]
Chromosome:: 3:12446865 (GRCh38)
3:12488364 (GRCh37)
Canonical SPDI:: NC_000003.12:12446863:GGG:G
Validated:: by frequency,by alfa
MAF:: G=0.000084/1 (ALFA)
-=0.00008/10 (GnomAD)
HGVS:: NC_000003.12:g.12446865_12446866del, NC_000003.11:g.12488364_12488365del

Select item 149131881217.

rs1491318812 [Homo sapiens]

Variant type:: INS
Alleles:: ->GG [Show Flanks]
Chromosome:: 3:12412447 (GRCh38)
3:12453947 (GRCh37)
Canonical SPDI:: NC_000003.12:12412447::GG
Gene:: PPARG (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: GG=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.12412447_12412448insGG, NC_000003.11:g.12453946_12453947insGG, NG_011749.1:g.129598_129599insGG

Select item 149126953518.

rs1491269535 has merged into rs770971383 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA,AAAAA,AAAAAAA,AAAAAAAAA [Show Flanks]
Chromosome:: 3:12469876 (GRCh38)
3:12511375 (GRCh37)
Canonical SPDI:: NC_000003.12:12469865:AAAAAAAAAAAAA:AAAAAAAAAA,NC_000003.12:12469865:AAAAAAAAAAAAA:AAAAAAAAAAA,NC_000003.12:12469865:AAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000003.12:12469865:AAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:12469865:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000003.12:12469865:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000003.12:12469865:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
-=0.01375/8 (NorthernSweden)
HGVS:: NC_000003.12:g.12469876_12469878del, NC_000003.12:g.12469877_12469878del, NC_000003.12:g.12469878del, NC_000003.12:g.12469878dup, NC_000003.12:g.12469877_12469878dup, NC_000003.12:g.12469875_12469878dup, NC_000003.12:g.12469873_12469878dup, NC_000003.11:g.12511375_12511377del, NC_000003.11:g.12511376_12511377del, NC_000003.11:g.12511377del, NC_000003.11:g.12511377dup, NC_000003.11:g.12511376_12511377dup, NC_000003.11:g.12511374_12511377dup, NC_000003.11:g.12511372_12511377dup

Select item 149126727019.

rs1491267270 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 3:12469865 (GRCh38)
3:12511364 (GRCh37)
Canonical SPDI:: NC_000003.12:12469864:CA:
Validated:: by frequency,by alfa
MAF:: -=0.00034/4 (ALFA)
HGVS:: NC_000003.12:g.12469865_12469866del, NC_000003.11:g.12511364_12511365del

Select item 149126634220.

rs1491266342 has merged into rs869086237 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCCCTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 3:12417910 (GRCh38)
3:12459409 (GRCh37)
Canonical SPDI:: NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCCCTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:12417902:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: PPARG (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTT=0./0 (ALFA)
HGVS:: NC_000003.12:g.12417910_12417925del, NC_000003.12:g.12417911_12417925del, NC_000003.12:g.12417912_12417925del, NC_000003.12:g.12417913_12417925del, NC_000003.12:g.12417914_12417925del, NC_000003.12:g.12417915_12417925del, NC_000003.12:g.12417916_12417925del, NC_000003.12:g.12417917_12417925del, NC_000003.12:g.12417918_12417925del, NC_000003.12:g.12417919_12417925del, NC_000003.12:g.12417920_12417925del, NC_000003.12:g.12417921_12417925del, NC_000003.12:g.12417922_12417925del, NC_000003.12:g.12417923_12417925del, NC_000003.12:g.12417924_12417925del, NC_000003.12:g.12417925del, NC_000003.12:g.12417903_12417925T[23]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.12417925dup, NC_000003.12:g.12417924_12417925dup, NC_000003.12:g.12417923_12417925dup, NC_000003.12:g.12417922_12417925dup, NC_000003.12:g.12417921_12417925dup, NC_000003.12:g.12417920_12417925dup, NC_000003.12:g.12417919_12417925dup, NC_000003.12:g.12417903_12417925T[30]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.12417918_12417925dup, NC_000003.12:g.12417903_12417925T[31]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.12417917_12417925dup, NC_000003.12:g.12417903_12417925T[32]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.12417916_12417925dup, NC_000003.12:g.12417903_12417925T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.12417915_12417925dup, NC_000003.12:g.12417903_12417925T[34]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.12417903_12417925T[34]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.12417914_12417925dup, NC_000003.12:g.12417912_12417925dup, NC_000003.12:g.12417911_12417925dup, NC_000003.12:g.12417903_12417925T[38]CTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.12417910_12417925dup, NC_000003.12:g.12417903_12417925T[39]CCCTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.12417909_12417925dup, NC_000003.12:g.12417903_12417925T[40]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.12417908_12417925dup, NC_000003.12:g.12417903_12417925T[41]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.12417907_12417925dup, NC_000003.12:g.12417906_12417925dup, NC_000003.12:g.12417903_12417925T[43]CTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.12417905_12417925dup, NC_000003.12:g.12417904_12417925dup, NC_000003.12:g.12417903_12417925dup, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417903_12417925T[49]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417903_12417925T[52]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.12417925_12417926insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459409_12459424del, NC_000003.11:g.12459410_12459424del, NC_000003.11:g.12459411_12459424del, NC_000003.11:g.12459412_12459424del, NC_000003.11:g.12459413_12459424del, NC_000003.11:g.12459414_12459424del, NC_000003.11:g.12459415_12459424del, NC_000003.11:g.12459416_12459424del, NC_000003.11:g.12459417_12459424del, NC_000003.11:g.12459418_12459424del, NC_000003.11:g.12459419_12459424del, NC_000003.11:g.12459420_12459424del, NC_000003.11:g.12459421_12459424del, NC_000003.11:g.12459422_12459424del, NC_000003.11:g.12459423_12459424del, NC_000003.11:g.12459424del, NC_000003.11:g.12459402_12459424T[23]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.12459424dup, NC_000003.11:g.12459423_12459424dup, NC_000003.11:g.12459422_12459424dup, NC_000003.11:g.12459421_12459424dup, NC_000003.11:g.12459420_12459424dup, NC_000003.11:g.12459419_12459424dup, NC_000003.11:g.12459418_12459424dup, NC_000003.11:g.12459402_12459424T[30]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.12459417_12459424dup, NC_000003.11:g.12459402_12459424T[31]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.12459416_12459424dup, NC_000003.11:g.12459402_12459424T[32]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.12459415_12459424dup, NC_000003.11:g.12459402_12459424T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.12459414_12459424dup, NC_000003.11:g.12459402_12459424T[34]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.12459402_12459424T[34]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.12459413_12459424dup, NC_000003.11:g.12459411_12459424dup, NC_000003.11:g.12459410_12459424dup, NC_000003.11:g.12459402_12459424T[38]CTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.12459409_12459424dup, NC_000003.11:g.12459402_12459424T[39]CCCTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.12459408_12459424dup, NC_000003.11:g.12459402_12459424T[40]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.12459407_12459424dup, NC_000003.11:g.12459402_12459424T[41]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.12459406_12459424dup, NC_000003.11:g.12459405_12459424dup, NC_000003.11:g.12459402_12459424T[43]CTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.12459404_12459424dup, NC_000003.11:g.12459403_12459424dup, NC_000003.11:g.12459402_12459424dup, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459402_12459424T[49]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459402_12459424T[52]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.12459424_12459425insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135061_135076del, NG_011749.1:g.135062_135076del, NG_011749.1:g.135063_135076del, NG_011749.1:g.135064_135076del, NG_011749.1:g.135065_135076del, NG_011749.1:g.135066_135076del, NG_011749.1:g.135067_135076del, NG_011749.1:g.135068_135076del, NG_011749.1:g.135069_135076del, NG_011749.1:g.135070_135076del, NG_011749.1:g.135071_135076del, NG_011749.1:g.135072_135076del, NG_011749.1:g.135073_135076del, NG_011749.1:g.135074_135076del, NG_011749.1:g.135075_135076del, NG_011749.1:g.135076del, NG_011749.1:g.135054_135076T[23]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_011749.1:g.135076dup, NG_011749.1:g.135075_135076dup, NG_011749.1:g.135074_135076dup, NG_011749.1:g.135073_135076dup, NG_011749.1:g.135072_135076dup, NG_011749.1:g.135071_135076dup, NG_011749.1:g.135070_135076dup, NG_011749.1:g.135054_135076T[30]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_011749.1:g.135069_135076dup, NG_011749.1:g.135054_135076T[31]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_011749.1:g.135068_135076dup, NG_011749.1:g.135054_135076T[32]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_011749.1:g.135067_135076dup, NG_011749.1:g.135054_135076T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_011749.1:g.135066_135076dup, NG_011749.1:g.135054_135076T[34]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_011749.1:g.135054_135076T[34]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_011749.1:g.135065_135076dup, NG_011749.1:g.135063_135076dup, NG_011749.1:g.135062_135076dup, NG_011749.1:g.135054_135076T[38]CTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_011749.1:g.135061_135076dup, NG_011749.1:g.135054_135076T[39]CCCTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_011749.1:g.135060_135076dup, NG_011749.1:g.135054_135076T[40]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_011749.1:g.135059_135076dup, NG_011749.1:g.135054_135076T[41]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_011749.1:g.135058_135076dup, NG_011749.1:g.135057_135076dup, NG_011749.1:g.135054_135076T[43]CTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_011749.1:g.135056_135076dup, NG_011749.1:g.135055_135076dup, NG_011749.1:g.135054_135076dup, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135054_135076T[49]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135054_135076T[52]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011749.1:g.135076_135077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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