SNP Links for Gene (Select 4676) - SNP

Links from Gene

Items: 1 to 20 of 13389

<< First< Prev

Page of 670

Next >Last >>

Select item 14915867741.

rs1491586774 has merged into rs545028521 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA,AAAAA,AAAAAA [Show Flanks]
Chromosome:: 11:2983603 (GRCh38)
11:3004833 (GRCh37)
Canonical SPDI:: NC_000011.10:2983592:AAAAAAAAAAAA:AAAAAAAAAA,NC_000011.10:2983592:AAAAAAAAAAAA:AAAAAAAAAAA,NC_000011.10:2983592:AAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:2983592:AAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000011.10:2983592:AAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000011.10:2983592:AAAAAAAAAAAA:AAAAAAAAAAAAAAAA
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
A=0.3321/1663 (1000Genomes)
A=0.3664/1412 (ALSPAC)
A=0.3735/1385 (TWINSUK)
A=0.375/15 (GENOME_DK)
HGVS:: NC_000011.10:g.2983603_2983604del, NC_000011.10:g.2983604del, NC_000011.10:g.2983604dup, NC_000011.10:g.2983603_2983604dup, NC_000011.10:g.2983602_2983604dup, NC_000011.10:g.2983601_2983604dup, NC_000011.9:g.3004833_3004834del, NC_000011.9:g.3004834del, NC_000011.9:g.3004834dup, NC_000011.9:g.3004833_3004834dup, NC_000011.9:g.3004832_3004834dup, NC_000011.9:g.3004831_3004834dup, NT_187585.1:g.214681_214682del, NT_187585.1:g.214682del, NT_187585.1:g.214682dup, NT_187585.1:g.214681_214682dup, NT_187585.1:g.214680_214682dup, NT_187585.1:g.214679_214682dup

Select item 14915677282.

rs1491567728 [Homo sapiens]

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

Select item 14914891073.

rs1491489107 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 11:2970858 (GRCh38)
11:2992088 (GRCh37)
Canonical SPDI:: NC_000011.10:2970857:CA:
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000169/2 (ALFA)
-=0.000528/54 (GnomAD)
-=0.001239/21 (TOMMO)
HGVS:: NC_000011.10:g.2970858_2970859del, NC_000011.9:g.2992088_2992089del, NT_187585.1:g.201925A>C, NT_187585.1:g.201934_201935del

Select item 14914576144.

rs1491457614 has merged into rs61176259 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTT>-,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 11:2969002 (GRCh38)
11:2990232 (GRCh37)
Canonical SPDI:: NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:2968988:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.375/15 (GENOME_DK)
HGVS:: NC_000011.10:g.2969002_2969009del, NC_000011.10:g.2969004_2969009del, NC_000011.10:g.2969005_2969009del, NC_000011.10:g.2969007_2969009del, NC_000011.10:g.2969008_2969009del, NC_000011.10:g.2969009del, NC_000011.10:g.2969009dup, NC_000011.10:g.2969008_2969009dup, NC_000011.10:g.2969007_2969009dup, NC_000011.10:g.2969006_2969009dup, NC_000011.10:g.2969005_2969009dup, NC_000011.10:g.2969004_2969009dup, NC_000011.10:g.2969003_2969009dup, NC_000011.10:g.2969002_2969009dup, NC_000011.10:g.2969000_2969009dup, NC_000011.10:g.2968999_2969009dup, NC_000011.10:g.2968995_2969009dup, NC_000011.10:g.2968994_2969009dup, NC_000011.10:g.2968992_2969009dup, NC_000011.9:g.2990232_2990239del, NC_000011.9:g.2990234_2990239del, NC_000011.9:g.2990235_2990239del, NC_000011.9:g.2990237_2990239del, NC_000011.9:g.2990238_2990239del, NC_000011.9:g.2990239del, NC_000011.9:g.2990239dup, NC_000011.9:g.2990238_2990239dup, NC_000011.9:g.2990237_2990239dup, NC_000011.9:g.2990236_2990239dup, NC_000011.9:g.2990235_2990239dup, NC_000011.9:g.2990234_2990239dup, NC_000011.9:g.2990233_2990239dup, NC_000011.9:g.2990232_2990239dup, NC_000011.9:g.2990230_2990239dup, NC_000011.9:g.2990229_2990239dup, NC_000011.9:g.2990225_2990239dup, NC_000011.9:g.2990224_2990239dup, NC_000011.9:g.2990222_2990239dup

Select item 14914083205.

rs1491408320 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 11:2987756 (GRCh38)
11:3008986 (GRCh37)
Canonical SPDI:: NC_000011.10:2987755:CA:
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000011.10:g.2987756_2987757del, NC_000011.9:g.3008986_3008987del, NT_187585.1:g.218847dup, NT_187585.1:g.218827del

Select item 14913505036.

rs1491350503 has merged into rs200984231 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,TTT,TTTT,TTTTTT,TTTTTTT [Show Flanks]
Chromosome:: 11:2945842 (GRCh38)
11:2967072 (GRCh37)
Canonical SPDI:: NC_000011.10:2945837:TTTTTTTTT:TTTT,NC_000011.10:2945837:TTTTTTTTT:TTTTTTT,NC_000011.10:2945837:TTTTTTTTT:TTTTTTTT,NC_000011.10:2945837:TTTTTTTTT:TTTTTTTTTT,NC_000011.10:2945837:TTTTTTTTT:TTTTTTTTTTT
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTT=0./0 (ALFA)
T=0.00022/1 (Estonian)
T=0.00025/4 (TOMMO)
T=0.00562/36 (1000Genomes)
HGVS:: NC_000011.10:g.2945842_2945846del, NC_000011.10:g.2945845_2945846del, NC_000011.10:g.2945846del, NC_000011.10:g.2945846dup, NC_000011.10:g.2945845_2945846dup, NC_000011.9:g.2967072_2967076del, NC_000011.9:g.2967075_2967076del, NC_000011.9:g.2967076del, NC_000011.9:g.2967076dup, NC_000011.9:g.2967075_2967076dup, NT_187585.1:g.176890_176894del, NT_187585.1:g.176893_176894del, NT_187585.1:g.176894del, NT_187585.1:g.176894dup, NT_187585.1:g.176893_176894dup

Select item 14913142587.

rs1491314258 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 11:2984166 (GRCh38)
11:3005396 (GRCh37)
Canonical SPDI:: NC_000011.10:2984165:CA:
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00017/2 (ALFA)
HGVS:: NC_000011.10:g.2984166_2984167del, NC_000011.9:g.3005396_3005397del, NT_187585.1:g.215263dup, NT_187585.1:g.215243del

Select item 14912961078.

rs1491296107 has merged into rs35188952 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAA>-,AA,AAA,AAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 11:2984175 (GRCh38)
11:3005405 (GRCh37)
Canonical SPDI:: NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2984166:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000011.10:g.2984175_2984189del, NC_000011.10:g.2984177_2984189del, NC_000011.10:g.2984178_2984189del, NC_000011.10:g.2984180_2984189del, NC_000011.10:g.2984185_2984189del, NC_000011.10:g.2984186_2984189del, NC_000011.10:g.2984187_2984189del, NC_000011.10:g.2984188_2984189del, NC_000011.10:g.2984189del, NC_000011.10:g.2984189dup, NC_000011.10:g.2984188_2984189dup, NC_000011.10:g.2984187_2984189dup, NC_000011.10:g.2984186_2984189dup, NC_000011.10:g.2984185_2984189dup, NC_000011.10:g.2984178_2984189dup, NC_000011.9:g.3005405_3005419del, NC_000011.9:g.3005407_3005419del, NC_000011.9:g.3005408_3005419del, NC_000011.9:g.3005410_3005419del, NC_000011.9:g.3005415_3005419del, NC_000011.9:g.3005416_3005419del, NC_000011.9:g.3005417_3005419del, NC_000011.9:g.3005418_3005419del, NC_000011.9:g.3005419del, NC_000011.9:g.3005419dup, NC_000011.9:g.3005418_3005419dup, NC_000011.9:g.3005417_3005419dup, NC_000011.9:g.3005416_3005419dup, NC_000011.9:g.3005415_3005419dup, NC_000011.9:g.3005408_3005419dup, NT_187585.1:g.215261_215263dup, NT_187585.1:g.215252_215263del, NT_187585.1:g.215254_215263del, NT_187585.1:g.215255_215263del, NT_187585.1:g.215257_215263del, NT_187585.1:g.215262_215263del, NT_187585.1:g.215263del, NT_187585.1:g.215263dup, NT_187585.1:g.215262_215263dup, NT_187585.1:g.215260_215263dup, NT_187585.1:g.215259_215263dup, NT_187585.1:g.215258_215263dup, NT_187585.1:g.215257_215263dup, NT_187585.1:g.215256_215263dup, NT_187585.1:g.215249_215263dup

Select item 14912333469.

rs1491233346 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 11:2963098 (GRCh38)
11:2984328 (GRCh37)
Canonical SPDI:: NC_000011.10:2963097:CA:
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00126/15 (ALFA)
HGVS:: NC_000011.10:g.2963098_2963099del, NC_000011.9:g.2984328_2984329del, NT_187585.1:g.194166dup, NT_187585.1:g.194150del

Select item 149114458910.

rs1491144589 has merged into rs55650724 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGGAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 11:2963104 (GRCh38)
11:2984334 (GRCh37)
Canonical SPDI:: NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2963098:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGGAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAA=0./0 (ALFA)
A=0.2778/1391 (1000Genomes)
HGVS:: NC_000011.10:g.2963104_2963115del, NC_000011.10:g.2963105_2963115del, NC_000011.10:g.2963107_2963115del, NC_000011.10:g.2963108_2963115del, NC_000011.10:g.2963109_2963115del, NC_000011.10:g.2963111_2963115del, NC_000011.10:g.2963112_2963115del, NC_000011.10:g.2963113_2963115del, NC_000011.10:g.2963114_2963115del, NC_000011.10:g.2963115del, NC_000011.10:g.2963115dup, NC_000011.10:g.2963114_2963115dup, NC_000011.10:g.2963113_2963115dup, NC_000011.10:g.2963111_2963115dup, NC_000011.10:g.2963110_2963115dup, NC_000011.10:g.2963109_2963115dup, NC_000011.10:g.2963108_2963115dup, NC_000011.10:g.2963107_2963115dup, NC_000011.10:g.2963106_2963115dup, NC_000011.10:g.2963105_2963115dup, NC_000011.10:g.2963104_2963115dup, NC_000011.10:g.2963103_2963115dup, NC_000011.10:g.2963101_2963115dup, NC_000011.10:g.2963100_2963115dup, NC_000011.10:g.2963099_2963115dup, NC_000011.10:g.2963115_2963116insAAAAAAAAAAAAAAAAAA, NC_000011.10:g.2963115_2963116insAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.2963115_2963116insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.2963115_2963116insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.2963115_2963116insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.2963099_2963115A[35]GGAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000011.9:g.2984334_2984345del, NC_000011.9:g.2984335_2984345del, NC_000011.9:g.2984337_2984345del, NC_000011.9:g.2984338_2984345del, NC_000011.9:g.2984339_2984345del, NC_000011.9:g.2984341_2984345del, NC_000011.9:g.2984342_2984345del, NC_000011.9:g.2984343_2984345del, NC_000011.9:g.2984344_2984345del, NC_000011.9:g.2984345del, NC_000011.9:g.2984345dup, NC_000011.9:g.2984344_2984345dup, NC_000011.9:g.2984343_2984345dup, NC_000011.9:g.2984341_2984345dup, NC_000011.9:g.2984340_2984345dup, NC_000011.9:g.2984339_2984345dup, NC_000011.9:g.2984338_2984345dup, NC_000011.9:g.2984337_2984345dup, NC_000011.9:g.2984336_2984345dup, NC_000011.9:g.2984335_2984345dup, NC_000011.9:g.2984334_2984345dup, NC_000011.9:g.2984333_2984345dup, NC_000011.9:g.2984331_2984345dup, NC_000011.9:g.2984330_2984345dup, NC_000011.9:g.2984329_2984345dup, NC_000011.9:g.2984345_2984346insAAAAAAAAAAAAAAAAAA, NC_000011.9:g.2984345_2984346insAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.2984345_2984346insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.2984345_2984346insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.2984345_2984346insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.2984329_2984345A[35]GGAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NT_187585.1:g.194166dup, NT_187585.1:g.194156_194166del, NT_187585.1:g.194157_194166del, NT_187585.1:g.194159_194166del, NT_187585.1:g.194160_194166del, NT_187585.1:g.194161_194166del, NT_187585.1:g.194163_194166del, NT_187585.1:g.194164_194166del, NT_187585.1:g.194165_194166del, NT_187585.1:g.194166del, NT_187585.1:g.194165_194166dup, NT_187585.1:g.194164_194166dup, NT_187585.1:g.194163_194166dup, NT_187585.1:g.194161_194166dup, NT_187585.1:g.194160_194166dup, NT_187585.1:g.194159_194166dup, NT_187585.1:g.194158_194166dup, NT_187585.1:g.194157_194166dup, NT_187585.1:g.194156_194166dup, NT_187585.1:g.194155_194166dup, NT_187585.1:g.194154_194166dup, NT_187585.1:g.194153_194166dup, NT_187585.1:g.194151_194166dup, NT_187585.1:g.194166_194167insAAAAAAAAAAAAAAAAA, NT_187585.1:g.194166_194167insAAAAAAAAAAAAAAAAAA, NT_187585.1:g.194166_194167insAAAAAAAAAAAAAAAAAAA, NT_187585.1:g.194166_194167insAAAAAAAAAAAAAAAAAAAA, NT_187585.1:g.194166_194167insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187585.1:g.194166_194167insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187585.1:g.194166_194167insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_187585.1:g.194151_194166A[35]GGAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]

Select item 149103327411.

rs1491033274 has merged into rs376072968 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAA>-,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA [Show Flanks]
Chromosome:: 11:2975163 (GRCh38)
11:2996393 (GRCh37)
Canonical SPDI:: NC_000011.10:2975152:AAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000011.10:2975152:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000011.10:2975152:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000011.10:2975152:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:2975152:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000011.10:2975152:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000011.10:2975152:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000011.10:2975152:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
AA=0.3948/1977 (1000Genomes)
HGVS:: NC_000011.10:g.2975163_2975169del, NC_000011.10:g.2975168_2975169del, NC_000011.10:g.2975169del, NC_000011.10:g.2975169dup, NC_000011.10:g.2975168_2975169dup, NC_000011.10:g.2975167_2975169dup, NC_000011.10:g.2975166_2975169dup, NC_000011.10:g.2975165_2975169dup, NC_000011.9:g.2996393_2996399del, NC_000011.9:g.2996398_2996399del, NC_000011.9:g.2996399del, NC_000011.9:g.2996399dup, NC_000011.9:g.2996398_2996399dup, NC_000011.9:g.2996397_2996399dup, NC_000011.9:g.2996396_2996399dup, NC_000011.9:g.2996395_2996399dup, NT_187585.1:g.206232_206238del, NT_187585.1:g.206237_206238del, NT_187585.1:g.206238del, NT_187585.1:g.206238dup, NT_187585.1:g.206237_206238dup, NT_187585.1:g.206236_206238dup, NT_187585.1:g.206235_206238dup, NT_187585.1:g.206234_206238dup

Select item 149100529812.

rs1491005298 has merged into rs34999812 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA,AAAAA,AAAAAA [Show Flanks]
Chromosome:: 11:2961515 (GRCh38)
11:2982745 (GRCh37)
Canonical SPDI:: NC_000011.10:2961501:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:2961501:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000011.10:2961501:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000011.10:2961501:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000011.10:2961501:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:2961501:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAAAA=0.0005/4 (ALFA)
-=0.2194/1099 (1000Genomes)
HGVS:: NC_000011.10:g.2961515_2961517del, NC_000011.10:g.2961516_2961517del, NC_000011.10:g.2961517del, NC_000011.10:g.2961517dup, NC_000011.10:g.2961516_2961517dup, NC_000011.10:g.2961515_2961517dup, NC_000011.9:g.2982745_2982747del, NC_000011.9:g.2982746_2982747del, NC_000011.9:g.2982747del, NC_000011.9:g.2982747dup, NC_000011.9:g.2982746_2982747dup, NC_000011.9:g.2982745_2982747dup, NT_187585.1:g.192567_192569del, NT_187585.1:g.192568_192569del, NT_187585.1:g.192569del, NT_187585.1:g.192569dup, NT_187585.1:g.192568_192569dup, NT_187585.1:g.192567_192569dup

Select item 149096385313.

rs1490963853 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:2958612 (GRCh38)
11:2979842 (GRCh37)
Canonical SPDI:: NC_000011.10:2958611:G:A,NC_000011.10:2958611:G:T
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.2958612G>A, NC_000011.10:g.2958612G>T, NC_000011.9:g.2979842G>A, NC_000011.9:g.2979842G>T, NT_187585.1:g.189662G>A, NT_187585.1:g.189662G>T

Select item 149096357314.

rs1490963573 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:2944807 (GRCh38)
11:2966037 (GRCh37)
Canonical SPDI:: NC_000011.10:2944806:T:G
Gene:: NAP1L4 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.2944807T>G, NC_000011.9:g.2966037T>G, NT_187585.1:g.175855T>G, NM_005969.4:c.*872A>C, NM_005969.3:c.*872A>C, NM_001369386.1:c.*801A>C, NM_001369378.1:c.*872A>C, NM_001369388.1:c.*801A>C, NM_001369375.1:c.*872A>C, NM_001369384.1:c.*801A>C, NM_001369376.1:c.*872A>C, NM_001369383.1:c.*801A>C, NM_001369379.1:c.*872A>C, NM_001369377.1:c.*872A>C, NM_001369381.1:c.*801A>C, NM_001369382.1:c.*801A>C, NM_001369380.1:c.*801A>C, NM_001369385.1:c.*801A>C

Select item 149075906315.

rs1490759063 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:2979094 (GRCh38)
11:3000324 (GRCh37)
Canonical SPDI:: NC_000011.10:2979093:C:A
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.2979094C>A, NC_000011.9:g.3000324C>A, NT_187585.1:g.210164C>A

Select item 149068017716.

rs1490680177 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:2987567 (GRCh38)
11:3008797 (GRCh37)
Canonical SPDI:: NC_000011.10:2987566:C:A
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.2987567C>A, NC_000011.9:g.3008797C>A, NT_187585.1:g.218638C>A

Select item 149066076717.

rs1490660767 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:2975862 (GRCh38)
11:2997092 (GRCh37)
Canonical SPDI:: NC_000011.10:2975861:G:A
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.2975862G>A, NC_000011.9:g.2997092G>A, NT_187585.1:g.206931G>A

Select item 149055514518.

rs1490555145 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:2983452 (GRCh38)
11:3004682 (GRCh37)
Canonical SPDI:: NC_000011.10:2983451:A:C
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.2983452A>C, NC_000011.9:g.3004682A>C, NT_187585.1:g.214530A>C

Select item 149049581419.

rs1490495814 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 11:2957634 (GRCh38)
11:2978864 (GRCh37)
Canonical SPDI:: NC_000011.10:2957633:TT:T
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.2957635del, NC_000011.9:g.2978865del, NT_187585.1:g.188685del

Select item 149041256020.

rs1490412560 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:2990677 (GRCh38)
11:3011907 (GRCh37)
Canonical SPDI:: NC_000011.10:2990676:C:T
Gene:: NAP1L4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.2990677C>T, NC_000011.9:g.3011907C>T, NT_187585.1:g.221747C>T, NM_018568.1:c.-359C>T

<< First< Prev

Page of 670

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 13389

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity