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Select item 14915738891.

rs1491573889 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GG [Show Flanks]
Chromosome:: X:110442248 (GRCh38)
X:109685477 (GRCh37)
Canonical SPDI:: NC_000023.11:110442248:G:GGG
Gene:: RTL9 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000023.11:g.110442249_110442250insGG, NC_000023.10:g.109685477_109685478insGG, NG_016469.2:g.2985_2986insCC, NG_016402.2:g.28193_28194insGG

Select item 14915720992.

rs1491572099 has merged into rs57937918 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTT>-,T,TT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: X:110387868 (GRCh38)
X:109631096 (GRCh37)
Canonical SPDI:: NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110387857:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
-=0.475/19 (GENOME_DK)
HGVS:: NC_000023.11:g.110387868_110387879del, NC_000023.11:g.110387869_110387879del, NC_000023.11:g.110387870_110387879del, NC_000023.11:g.110387873_110387879del, NC_000023.11:g.110387874_110387879del, NC_000023.11:g.110387875_110387879del, NC_000023.11:g.110387876_110387879del, NC_000023.11:g.110387877_110387879del, NC_000023.11:g.110387878_110387879del, NC_000023.11:g.110387879del, NC_000023.11:g.110387879dup, NC_000023.11:g.110387878_110387879dup, NC_000023.11:g.110387877_110387879dup, NC_000023.11:g.110387876_110387879dup, NC_000023.11:g.110387875_110387879dup, NC_000023.11:g.110387874_110387879dup, NC_000023.11:g.110387873_110387879dup, NC_000023.11:g.110387872_110387879dup, NC_000023.10:g.109631096_109631107del, NC_000023.10:g.109631097_109631107del, NC_000023.10:g.109631098_109631107del, NC_000023.10:g.109631101_109631107del, NC_000023.10:g.109631102_109631107del, NC_000023.10:g.109631103_109631107del, NC_000023.10:g.109631104_109631107del, NC_000023.10:g.109631105_109631107del, NC_000023.10:g.109631106_109631107del, NC_000023.10:g.109631107del, NC_000023.10:g.109631107dup, NC_000023.10:g.109631106_109631107dup, NC_000023.10:g.109631105_109631107dup, NC_000023.10:g.109631104_109631107dup, NC_000023.10:g.109631103_109631107dup, NC_000023.10:g.109631102_109631107dup, NC_000023.10:g.109631101_109631107dup, NC_000023.10:g.109631100_109631107dup, NG_016469.2:g.57365_57376del, NG_016469.2:g.57366_57376del, NG_016469.2:g.57367_57376del, NG_016469.2:g.57370_57376del, NG_016469.2:g.57371_57376del, NG_016469.2:g.57372_57376del, NG_016469.2:g.57373_57376del, NG_016469.2:g.57374_57376del, NG_016469.2:g.57375_57376del, NG_016469.2:g.57376del, NG_016469.2:g.57376dup, NG_016469.2:g.57375_57376dup, NG_016469.2:g.57374_57376dup, NG_016469.2:g.57373_57376dup, NG_016469.2:g.57372_57376dup, NG_016469.2:g.57371_57376dup, NG_016469.2:g.57370_57376dup, NG_016469.2:g.57369_57376dup

Select item 14915619423.

rs1491561942 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: X:110429458 (GRCh38)
X:109672686 (GRCh37)
Canonical SPDI:: NC_000023.11:110429455:GTGT:GT
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: GTGT=0./0 (ALFA)
HGVS:: NC_000023.11:g.110429456GT[1], NC_000023.10:g.109672684GT[1], NG_016469.2:g.15775AC[1], NG_016402.2:g.15400GT[1]

Select item 14914593094.

rs1491459309 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,G [Show Flanks]
Chromosome:: X:110405100 (GRCh38)
X:109648329 (GRCh37)
Canonical SPDI:: NC_000023.11:110405100::A,NC_000023.11:110405100::G
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.110405100_110405101insA, NC_000023.11:g.110405100_110405101insG, NC_000023.10:g.109648328_109648329insA, NC_000023.10:g.109648328_109648329insG, NG_016469.2:g.40133_40134insT, NG_016469.2:g.40133_40134insC

Select item 14914046245.

rs1491404624 has merged into rs908737506 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGTGTGTGTGTGTGTGT>-,GT,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
Chromosome:: X:110442271 (GRCh38)
X:109685499 (GRCh37)
Canonical SPDI:: NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000023.11:110442247:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Gene:: RTL9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGTGTGTGTGTGTGTGTGT=0./0 (ALFA)
-=0.000057/15 (TOPMED)
HGVS:: NC_000023.11:g.110442249GT[11], NC_000023.11:g.110442249GT[12], NC_000023.11:g.110442249GT[13], NC_000023.11:g.110442249GT[14], NC_000023.11:g.110442249GT[15], NC_000023.11:g.110442249GT[16], NC_000023.11:g.110442249GT[17], NC_000023.11:g.110442249GT[18], NC_000023.11:g.110442249GT[19], NC_000023.11:g.110442249GT[21], NC_000023.11:g.110442249GT[22], NC_000023.11:g.110442249GT[23], NC_000023.11:g.110442249GT[24], NC_000023.11:g.110442249GT[25], NC_000023.11:g.110442249GT[26], NC_000023.10:g.109685477GT[11], NC_000023.10:g.109685477GT[12], NC_000023.10:g.109685477GT[13], NC_000023.10:g.109685477GT[14], NC_000023.10:g.109685477GT[15], NC_000023.10:g.109685477GT[16], NC_000023.10:g.109685477GT[17], NC_000023.10:g.109685477GT[18], NC_000023.10:g.109685477GT[19], NC_000023.10:g.109685477GT[21], NC_000023.10:g.109685477GT[22], NC_000023.10:g.109685477GT[23], NC_000023.10:g.109685477GT[24], NC_000023.10:g.109685477GT[25], NC_000023.10:g.109685477GT[26], NG_016469.2:g.2947CA[11], NG_016469.2:g.2947CA[12], NG_016469.2:g.2947CA[13], NG_016469.2:g.2947CA[14], NG_016469.2:g.2947CA[15], NG_016469.2:g.2947CA[16], NG_016469.2:g.2947CA[17], NG_016469.2:g.2947CA[18], NG_016469.2:g.2947CA[19], NG_016469.2:g.2947CA[21], NG_016469.2:g.2947CA[22], NG_016469.2:g.2947CA[23], NG_016469.2:g.2947CA[24], NG_016469.2:g.2947CA[25], NG_016469.2:g.2947CA[26], NG_016402.2:g.28193GT[11], NG_016402.2:g.28193GT[12], NG_016402.2:g.28193GT[13], NG_016402.2:g.28193GT[14], NG_016402.2:g.28193GT[15], NG_016402.2:g.28193GT[16], NG_016402.2:g.28193GT[17], NG_016402.2:g.28193GT[18], NG_016402.2:g.28193GT[19], NG_016402.2:g.28193GT[21], NG_016402.2:g.28193GT[22], NG_016402.2:g.28193GT[23], NG_016402.2:g.28193GT[24], NG_016402.2:g.28193GT[25], NG_016402.2:g.28193GT[26]

Select item 14913448516.

rs1491344851 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: X:110429456 (GRCh38)
X:109672685 (GRCh37)
Canonical SPDI:: NC_000023.11:110429456:T:TT
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
HGVS:: NC_000023.11:g.110429457dup, NC_000023.10:g.109672685dup, NG_016469.2:g.15777dup, NG_016402.2:g.15401dup

Select item 14912992727.

rs1491299272 has merged into rs1181988453 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: X:110447125 (GRCh38)
X:109690353 (GRCh37)
Canonical SPDI:: NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110447111:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: RTL9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
-=0.000019/5 (TOPMED)
HGVS:: NC_000023.11:g.110447125_110447135del, NC_000023.11:g.110447126_110447135del, NC_000023.11:g.110447127_110447135del, NC_000023.11:g.110447128_110447135del, NC_000023.11:g.110447129_110447135del, NC_000023.11:g.110447130_110447135del, NC_000023.11:g.110447131_110447135del, NC_000023.11:g.110447132_110447135del, NC_000023.11:g.110447133_110447135del, NC_000023.11:g.110447134_110447135del, NC_000023.11:g.110447135del, NC_000023.11:g.110447135dup, NC_000023.11:g.110447134_110447135dup, NC_000023.11:g.110447133_110447135dup, NC_000023.11:g.110447132_110447135dup, NC_000023.11:g.110447131_110447135dup, NC_000023.11:g.110447130_110447135dup, NC_000023.11:g.110447129_110447135dup, NC_000023.11:g.110447128_110447135dup, NC_000023.11:g.110447127_110447135dup, NC_000023.11:g.110447126_110447135dup, NC_000023.11:g.110447125_110447135dup, NC_000023.11:g.110447124_110447135dup, NC_000023.11:g.110447121_110447135dup, NC_000023.11:g.110447120_110447135dup, NC_000023.11:g.110447119_110447135dup, NC_000023.11:g.110447118_110447135dup, NC_000023.11:g.110447116_110447135dup, NC_000023.11:g.110447113_110447135dup, NC_000023.11:g.110447135_110447136insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.110447135_110447136insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.109690353_109690363del, NC_000023.10:g.109690354_109690363del, NC_000023.10:g.109690355_109690363del, NC_000023.10:g.109690356_109690363del, NC_000023.10:g.109690357_109690363del, NC_000023.10:g.109690358_109690363del, NC_000023.10:g.109690359_109690363del, NC_000023.10:g.109690360_109690363del, NC_000023.10:g.109690361_109690363del, NC_000023.10:g.109690362_109690363del, NC_000023.10:g.109690363del, NC_000023.10:g.109690363dup, NC_000023.10:g.109690362_109690363dup, NC_000023.10:g.109690361_109690363dup, NC_000023.10:g.109690360_109690363dup, NC_000023.10:g.109690359_109690363dup, NC_000023.10:g.109690358_109690363dup, NC_000023.10:g.109690357_109690363dup, NC_000023.10:g.109690356_109690363dup, NC_000023.10:g.109690355_109690363dup, NC_000023.10:g.109690354_109690363dup, NC_000023.10:g.109690353_109690363dup, NC_000023.10:g.109690352_109690363dup, NC_000023.10:g.109690349_109690363dup, NC_000023.10:g.109690348_109690363dup, NC_000023.10:g.109690347_109690363dup, NC_000023.10:g.109690346_109690363dup, NC_000023.10:g.109690344_109690363dup, NC_000023.10:g.109690341_109690363dup, NC_000023.10:g.109690363_109690364insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.109690363_109690364insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016402.2:g.33069_33079del, NG_016402.2:g.33070_33079del, NG_016402.2:g.33071_33079del, NG_016402.2:g.33072_33079del, NG_016402.2:g.33073_33079del, NG_016402.2:g.33074_33079del, NG_016402.2:g.33075_33079del, NG_016402.2:g.33076_33079del, NG_016402.2:g.33077_33079del, NG_016402.2:g.33078_33079del, NG_016402.2:g.33079del, NG_016402.2:g.33079dup, NG_016402.2:g.33078_33079dup, NG_016402.2:g.33077_33079dup, NG_016402.2:g.33076_33079dup, NG_016402.2:g.33075_33079dup, NG_016402.2:g.33074_33079dup, NG_016402.2:g.33073_33079dup, NG_016402.2:g.33072_33079dup, NG_016402.2:g.33071_33079dup, NG_016402.2:g.33070_33079dup, NG_016402.2:g.33069_33079dup, NG_016402.2:g.33068_33079dup, NG_016402.2:g.33065_33079dup, NG_016402.2:g.33064_33079dup, NG_016402.2:g.33063_33079dup, NG_016402.2:g.33062_33079dup, NG_016402.2:g.33060_33079dup, NG_016402.2:g.33057_33079dup, NG_016402.2:g.33079_33080insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016402.2:g.33079_33080insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14912627868.

rs1491262786 has merged into rs781098261 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTCTCTCTCTCTCTCT>-,CTCT,CTCTCTCT,CTCTCTCTCT,CTCTCTCTCTCT,CTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT [Show Flanks]
Chromosome:: X:110442233 (GRCh38)
X:109685461 (GRCh37)
Canonical SPDI:: NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000023.11:110442221:TCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTCTCTCTCTCTCT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.110442223CT[5], NC_000023.11:g.110442223CT[7], NC_000023.11:g.110442223CT[9], NC_000023.11:g.110442223CT[10], NC_000023.11:g.110442223CT[11], NC_000023.11:g.110442223CT[12], NC_000023.11:g.110442223CT[14], NC_000023.11:g.110442223CT[15], NC_000023.11:g.110442223CT[16], NC_000023.11:g.110442223CT[17], NC_000023.11:g.110442223CT[18], NC_000023.11:g.110442223CT[19], NC_000023.11:g.110442223CT[20], NC_000023.11:g.110442223CT[21], NC_000023.11:g.110442223CT[22], NC_000023.11:g.110442223CT[23], NC_000023.10:g.109685451CT[5], NC_000023.10:g.109685451CT[7], NC_000023.10:g.109685451CT[9], NC_000023.10:g.109685451CT[10], NC_000023.10:g.109685451CT[11], NC_000023.10:g.109685451CT[12], NC_000023.10:g.109685451CT[14], NC_000023.10:g.109685451CT[15], NC_000023.10:g.109685451CT[16], NC_000023.10:g.109685451CT[17], NC_000023.10:g.109685451CT[18], NC_000023.10:g.109685451CT[19], NC_000023.10:g.109685451CT[20], NC_000023.10:g.109685451CT[21], NC_000023.10:g.109685451CT[22], NC_000023.10:g.109685451CT[23], NG_016469.2:g.2987GA[5], NG_016469.2:g.2987GA[7], NG_016469.2:g.2987GA[9], NG_016469.2:g.2987GA[10], NG_016469.2:g.2987GA[11], NG_016469.2:g.2987GA[12], NG_016469.2:g.2987GA[14], NG_016469.2:g.2987GA[15], NG_016469.2:g.2987GA[16], NG_016469.2:g.2987GA[17], NG_016469.2:g.2987GA[18], NG_016469.2:g.2987GA[19], NG_016469.2:g.2987GA[20], NG_016469.2:g.2987GA[21], NG_016469.2:g.2987GA[22], NG_016469.2:g.2987GA[23], NG_016402.2:g.28167CT[5], NG_016402.2:g.28167CT[7], NG_016402.2:g.28167CT[9], NG_016402.2:g.28167CT[10], NG_016402.2:g.28167CT[11], NG_016402.2:g.28167CT[12], NG_016402.2:g.28167CT[14], NG_016402.2:g.28167CT[15], NG_016402.2:g.28167CT[16], NG_016402.2:g.28167CT[17], NG_016402.2:g.28167CT[18], NG_016402.2:g.28167CT[19], NG_016402.2:g.28167CT[20], NG_016402.2:g.28167CT[21], NG_016402.2:g.28167CT[22], NG_016402.2:g.28167CT[23]

Select item 14912478339.

rs1491247833 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GT [Show Flanks]
Chromosome:: X:110447112 (GRCh38)
X:109690341 (GRCh37)
Canonical SPDI:: NC_000023.11:110447112:T:TGT
Gene:: RTL9 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000023.11:g.110447113_110447114insGT, NC_000023.10:g.109690341_109690342insGT, NG_016402.2:g.33057_33058insGT

Select item 149120505010.

rs1491205050 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CCTCTC [Show Flanks]
Chromosome:: X:110442222 (GRCh38)
X:109685451 (GRCh37)
Canonical SPDI:: NC_000023.11:110442222:CTCTC:CTCTCCCTCTC
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: CTCTCCCTCTC=0./0 (ALFA)
HGVS:: NC_000023.11:g.110442223_110442227CT[2]CCCTCTC[1], NC_000023.10:g.109685451_109685455CT[2]CCCTCTC[1], NG_016469.2:g.3007_3011GA[2]GGGAGAG[1], NG_016402.2:g.28167_28171CT[2]CCCTCTC[1]

Select item 149119133911.

rs1491191339 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTTTTTTTTTTTT [Show Flanks]
Chromosome:: X:110429459 (GRCh38)
X:109672688 (GRCh37)
Canonical SPDI:: NC_000023.11:110429459:TTTTTTTTTTTT:TTTTTTTTTTTTGTTTTTTTTTTTT
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
HGVS:: NC_000023.11:g.110429460_110429471T[12]GTTTTTTTTTTTT[1], NC_000023.10:g.109672688_109672699T[12]GTTTTTTTTTTTT[1], NG_016469.2:g.15763_15774A[12]CAAAAAAAAAAAA[1], NG_016402.2:g.15404_15415T[12]GTTTTTTTTTTTT[1]

Select item 149108001712.

rs1491080017 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: X:110429472 (GRCh38)
X:109672701 (GRCh37)
Canonical SPDI:: NC_000023.11:110429472::G
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000023.11:g.110429472_110429473insG, NC_000023.10:g.109672700_109672701insG, NG_016469.2:g.15761_15762insC, NG_016402.2:g.15416_15417insG

Select item 149105730313.

rs1491057303 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: X:110442220 (GRCh38)
X:109685449 (GRCh37)
Canonical SPDI:: NC_000023.11:110442220::C
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.110442220_110442221insC, NC_000023.10:g.109685448_109685449insC, NG_016469.2:g.3013_3014insG, NG_016402.2:g.28164_28165insC

Select item 149103685214.

rs1491036852 has merged into rs377409601 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT [Show Flanks]
Chromosome:: X:110392291 (GRCh38)
X:109635519 (GRCh37)
Canonical SPDI:: NC_000023.11:110392272:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000023.11:110392272:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000023.11:110392272:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000023.11:110392272:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110392272:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110392272:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110392272:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110392272:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110392272:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:110392272:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000023.11:g.110392291_110392294del, NC_000023.11:g.110392292_110392294del, NC_000023.11:g.110392293_110392294del, NC_000023.11:g.110392294del, NC_000023.11:g.110392294dup, NC_000023.11:g.110392293_110392294dup, NC_000023.11:g.110392292_110392294dup, NC_000023.11:g.110392291_110392294dup, NC_000023.11:g.110392290_110392294dup, NC_000023.11:g.110392289_110392294dup, NC_000023.10:g.109635519_109635522del, NC_000023.10:g.109635520_109635522del, NC_000023.10:g.109635521_109635522del, NC_000023.10:g.109635522del, NC_000023.10:g.109635522dup, NC_000023.10:g.109635521_109635522dup, NC_000023.10:g.109635520_109635522dup, NC_000023.10:g.109635519_109635522dup, NC_000023.10:g.109635518_109635522dup, NC_000023.10:g.109635517_109635522dup, NG_016469.2:g.52958_52961del, NG_016469.2:g.52959_52961del, NG_016469.2:g.52960_52961del, NG_016469.2:g.52961del, NG_016469.2:g.52961dup, NG_016469.2:g.52960_52961dup, NG_016469.2:g.52959_52961dup, NG_016469.2:g.52958_52961dup, NG_016469.2:g.52957_52961dup, NG_016469.2:g.52956_52961dup

Select item 149091635915.

rs1490916359 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: X:110446548 (GRCh38)
X:109689776 (GRCh37)
Canonical SPDI:: NC_000023.11:110446547:T:A
Gene:: RTL9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.110446548T>A, NC_000023.10:g.109689776T>A, NG_016402.2:g.32492T>A

Select item 149087319916.

rs1490873199 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:110387504 (GRCh38)
X:109630732 (GRCh37)
Canonical SPDI:: NC_000023.11:110387503:G:A
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000142/2 (ALFA)
A=0.000004/1 (TOPMED)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.110387504G>A, NC_000023.10:g.109630732G>A, NG_016469.2:g.57730C>T

Select item 149085808517.

rs1490858085 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: X:110391452 (GRCh38)
X:109634680 (GRCh37)
Canonical SPDI:: NC_000023.11:110391451:C:A
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.110391452C>A, NC_000023.10:g.109634680C>A, NG_016469.2:g.53782G>T

Select item 149083924618.

rs1490839246 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:110427611 (GRCh38)
X:109670839 (GRCh37)
Canonical SPDI:: NC_000023.11:110427610:T:G
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.110427611T>G, NC_000023.10:g.109670839T>G, NG_016469.2:g.17623A>C, NG_016402.2:g.13555T>G

Select item 149080570919.

rs1490805709 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:110405519 (GRCh38)
X:109648747 (GRCh37)
Canonical SPDI:: NC_000023.11:110405518:A:G
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.110405519A>G, NC_000023.10:g.109648747A>G, NG_016469.2:g.39715T>C

Select item 149073161920.

rs1490731619 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:110380474 (GRCh38)
X:109623702 (GRCh37)
Canonical SPDI:: NC_000023.11:110380473:A:G
Gene:: AMMECR1 (Varview), RTL9 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.110380474A>G, NC_000023.10:g.109623702A>G, NG_016469.2:g.64760T>C

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