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Select item 14915869021.

rs1491586902 has merged into rs869287430 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 5:7418657 (GRCh38)
5:7418770 (GRCh37)
Canonical SPDI:: NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7418647:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ADCY2 (Varview), LOC105374646 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000005.10:g.7418657_7418673del, NC_000005.10:g.7418658_7418673del, NC_000005.10:g.7418659_7418673del, NC_000005.10:g.7418660_7418673del, NC_000005.10:g.7418661_7418673del, NC_000005.10:g.7418662_7418673del, NC_000005.10:g.7418663_7418673del, NC_000005.10:g.7418664_7418673del, NC_000005.10:g.7418665_7418673del, NC_000005.10:g.7418666_7418673del, NC_000005.10:g.7418667_7418673del, NC_000005.10:g.7418668_7418673del, NC_000005.10:g.7418669_7418673del, NC_000005.10:g.7418670_7418673del, NC_000005.10:g.7418671_7418673del, NC_000005.10:g.7418672_7418673del, NC_000005.10:g.7418673del, NC_000005.10:g.7418673dup, NC_000005.10:g.7418672_7418673dup, NC_000005.10:g.7418671_7418673dup, NC_000005.10:g.7418670_7418673dup, NC_000005.10:g.7418669_7418673dup, NC_000005.10:g.7418668_7418673dup, NC_000005.10:g.7418667_7418673dup, NC_000005.10:g.7418666_7418673dup, NC_000005.10:g.7418665_7418673dup, NC_000005.10:g.7418664_7418673dup, NC_000005.10:g.7418663_7418673dup, NC_000005.10:g.7418662_7418673dup, NC_000005.10:g.7418661_7418673dup, NC_000005.10:g.7418659_7418673dup, NC_000005.10:g.7418658_7418673dup, NC_000005.10:g.7418656_7418673dup, NC_000005.10:g.7418655_7418673dup, NC_000005.10:g.7418654_7418673dup, NC_000005.10:g.7418653_7418673dup, NC_000005.10:g.7418652_7418673dup, NC_000005.10:g.7418651_7418673dup, NC_000005.10:g.7418650_7418673dup, NC_000005.10:g.7418649_7418673dup, NC_000005.10:g.7418648_7418673dup, NC_000005.10:g.7418673_7418674insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.10:g.7418673_7418674insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.10:g.7418673_7418674insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.7418770_7418786del, NC_000005.9:g.7418771_7418786del, NC_000005.9:g.7418772_7418786del, NC_000005.9:g.7418773_7418786del, NC_000005.9:g.7418774_7418786del, NC_000005.9:g.7418775_7418786del, NC_000005.9:g.7418776_7418786del, NC_000005.9:g.7418777_7418786del, NC_000005.9:g.7418778_7418786del, NC_000005.9:g.7418779_7418786del, NC_000005.9:g.7418780_7418786del, NC_000005.9:g.7418781_7418786del, NC_000005.9:g.7418782_7418786del, NC_000005.9:g.7418783_7418786del, NC_000005.9:g.7418784_7418786del, NC_000005.9:g.7418785_7418786del, NC_000005.9:g.7418786del, NC_000005.9:g.7418786dup, NC_000005.9:g.7418785_7418786dup, NC_000005.9:g.7418784_7418786dup, NC_000005.9:g.7418783_7418786dup, NC_000005.9:g.7418782_7418786dup, NC_000005.9:g.7418781_7418786dup, NC_000005.9:g.7418780_7418786dup, NC_000005.9:g.7418779_7418786dup, NC_000005.9:g.7418778_7418786dup, NC_000005.9:g.7418777_7418786dup, NC_000005.9:g.7418776_7418786dup, NC_000005.9:g.7418775_7418786dup, NC_000005.9:g.7418774_7418786dup, NC_000005.9:g.7418772_7418786dup, NC_000005.9:g.7418771_7418786dup, NC_000005.9:g.7418769_7418786dup, NC_000005.9:g.7418768_7418786dup, NC_000005.9:g.7418767_7418786dup, NC_000005.9:g.7418766_7418786dup, NC_000005.9:g.7418765_7418786dup, NC_000005.9:g.7418764_7418786dup, NC_000005.9:g.7418763_7418786dup, NC_000005.9:g.7418762_7418786dup, NC_000005.9:g.7418761_7418786dup, NC_000005.9:g.7418786_7418787insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.7418786_7418787insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000005.9:g.7418786_7418787insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_046913.1:g.27428_27444del, NG_046913.1:g.27429_27444del, NG_046913.1:g.27430_27444del, NG_046913.1:g.27431_27444del, NG_046913.1:g.27432_27444del, NG_046913.1:g.27433_27444del, NG_046913.1:g.27434_27444del, NG_046913.1:g.27435_27444del, NG_046913.1:g.27436_27444del, NG_046913.1:g.27437_27444del, NG_046913.1:g.27438_27444del, NG_046913.1:g.27439_27444del, NG_046913.1:g.27440_27444del, NG_046913.1:g.27441_27444del, NG_046913.1:g.27442_27444del, NG_046913.1:g.27443_27444del, NG_046913.1:g.27444del, NG_046913.1:g.27444dup, NG_046913.1:g.27443_27444dup, NG_046913.1:g.27442_27444dup, NG_046913.1:g.27441_27444dup, NG_046913.1:g.27440_27444dup, NG_046913.1:g.27439_27444dup, NG_046913.1:g.27438_27444dup, NG_046913.1:g.27437_27444dup, NG_046913.1:g.27436_27444dup, NG_046913.1:g.27435_27444dup, NG_046913.1:g.27434_27444dup, NG_046913.1:g.27433_27444dup, NG_046913.1:g.27432_27444dup, NG_046913.1:g.27430_27444dup, NG_046913.1:g.27429_27444dup, NG_046913.1:g.27427_27444dup, NG_046913.1:g.27426_27444dup, NG_046913.1:g.27425_27444dup, NG_046913.1:g.27424_27444dup, NG_046913.1:g.27423_27444dup, NG_046913.1:g.27422_27444dup, NG_046913.1:g.27421_27444dup, NG_046913.1:g.27420_27444dup, NG_046913.1:g.27419_27444dup, NG_046913.1:g.27444_27445insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_046913.1:g.27444_27445insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_046913.1:g.27444_27445insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14915817902.

rs1491581790 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AC [Show Flanks]
Chromosome:: 5:7501647 (GRCh38)
5:7501761 (GRCh37)
Canonical SPDI:: NC_000005.10:7501647:C:CAC
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CAC=0./0 (ALFA)
CA=0.000004/1 (TOPMED)
CA=0.000021/1 (GnomAD)
HGVS:: NC_000005.10:g.7501648_7501649insAC, NC_000005.9:g.7501761_7501762insAC, NG_046913.1:g.110419_110420insAC

Select item 14915655163.

rs1491565516 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CCATCA [Show Flanks]
Chromosome:: 5:7741605 (GRCh38)
5:7741719 (GRCh37)
Canonical SPDI:: NC_000005.10:7741605:CATCACCATCACCATCA:CATCACCATCACCATCACCATCA
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CATCACCATCACCATCACCATCA=0./0 (ALFA)
CATCAC=0.00011/4 (GnomAD)
HGVS:: NC_000005.10:g.7741611CCATCA[3], NC_000005.9:g.7741724CCATCA[3], NG_046913.1:g.350382CCATCA[3]

Select item 14915645134.

rs1491564513 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 5:7811512 (GRCh38)
5:7811625 (GRCh37)
Canonical SPDI:: NC_000005.10:7811510:AGA:A
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.014669/174 (ALFA)
-=0.016192/2248 (GnomAD)
-=0.023363/117 (1000Genomes)
HGVS:: NC_000005.10:g.7811512_7811513del, NC_000005.9:g.7811625_7811626del, NG_046913.1:g.420283_420284del

Select item 14915633035.

rs1491563303 [Homo sapiens]

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

Select item 14915628586.

rs1491562858 has merged into rs910360437 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTT>-,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 5:7498248 (GRCh38)
5:7498361 (GRCh37)
Canonical SPDI:: NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7498239:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTT=0./0 (ALFA)
TTTTTTTTTTTTTTTTTTTT=0.00171/1 (NorthernSweden)
HGVS:: NC_000005.10:g.7498248_7498266del, NC_000005.10:g.7498250_7498266del, NC_000005.10:g.7498252_7498266del, NC_000005.10:g.7498253_7498266del, NC_000005.10:g.7498254_7498266del, NC_000005.10:g.7498255_7498266del, NC_000005.10:g.7498256_7498266del, NC_000005.10:g.7498257_7498266del, NC_000005.10:g.7498258_7498266del, NC_000005.10:g.7498259_7498266del, NC_000005.10:g.7498260_7498266del, NC_000005.10:g.7498261_7498266del, NC_000005.10:g.7498262_7498266del, NC_000005.10:g.7498263_7498266del, NC_000005.10:g.7498264_7498266del, NC_000005.10:g.7498265_7498266del, NC_000005.10:g.7498266del, NC_000005.10:g.7498266dup, NC_000005.10:g.7498265_7498266dup, NC_000005.10:g.7498264_7498266dup, NC_000005.10:g.7498263_7498266dup, NC_000005.10:g.7498262_7498266dup, NC_000005.10:g.7498261_7498266dup, NC_000005.10:g.7498260_7498266dup, NC_000005.10:g.7498249_7498266dup, NC_000005.10:g.7498247_7498266dup, NC_000005.10:g.7498241_7498266dup, NC_000005.9:g.7498361_7498379del, NC_000005.9:g.7498363_7498379del, NC_000005.9:g.7498365_7498379del, NC_000005.9:g.7498366_7498379del, NC_000005.9:g.7498367_7498379del, NC_000005.9:g.7498368_7498379del, NC_000005.9:g.7498369_7498379del, NC_000005.9:g.7498370_7498379del, NC_000005.9:g.7498371_7498379del, NC_000005.9:g.7498372_7498379del, NC_000005.9:g.7498373_7498379del, NC_000005.9:g.7498374_7498379del, NC_000005.9:g.7498375_7498379del, NC_000005.9:g.7498376_7498379del, NC_000005.9:g.7498377_7498379del, NC_000005.9:g.7498378_7498379del, NC_000005.9:g.7498379del, NC_000005.9:g.7498379dup, NC_000005.9:g.7498378_7498379dup, NC_000005.9:g.7498377_7498379dup, NC_000005.9:g.7498376_7498379dup, NC_000005.9:g.7498375_7498379dup, NC_000005.9:g.7498374_7498379dup, NC_000005.9:g.7498373_7498379dup, NC_000005.9:g.7498362_7498379dup, NC_000005.9:g.7498360_7498379dup, NC_000005.9:g.7498354_7498379dup, NG_046913.1:g.107019_107037del, NG_046913.1:g.107021_107037del, NG_046913.1:g.107023_107037del, NG_046913.1:g.107024_107037del, NG_046913.1:g.107025_107037del, NG_046913.1:g.107026_107037del, NG_046913.1:g.107027_107037del, NG_046913.1:g.107028_107037del, NG_046913.1:g.107029_107037del, NG_046913.1:g.107030_107037del, NG_046913.1:g.107031_107037del, NG_046913.1:g.107032_107037del, NG_046913.1:g.107033_107037del, NG_046913.1:g.107034_107037del, NG_046913.1:g.107035_107037del, NG_046913.1:g.107036_107037del, NG_046913.1:g.107037del, NG_046913.1:g.107037dup, NG_046913.1:g.107036_107037dup, NG_046913.1:g.107035_107037dup, NG_046913.1:g.107034_107037dup, NG_046913.1:g.107033_107037dup, NG_046913.1:g.107032_107037dup, NG_046913.1:g.107031_107037dup, NG_046913.1:g.107020_107037dup, NG_046913.1:g.107018_107037dup, NG_046913.1:g.107012_107037dup

Select item 14915621067.

rs1491562106 [Homo sapiens]

Variant type:: INS
Alleles:: ->GGAT [Show Flanks]
Chromosome:: 5:7499648 (GRCh38)
5:7499762 (GRCh37)
Canonical SPDI:: NC_000005.10:7499648::GGAT
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GGAT=0./0 (ALFA)
GGAT=0.000027/3 (GnomAD)
HGVS:: NC_000005.10:g.7499648_7499649insGGAT, NC_000005.9:g.7499761_7499762insGGAT, NG_046913.1:g.108419_108420insGGAT

Select item 14915592468.

rs1491559246 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 5:7499683 (GRCh38)
5:7499796 (GRCh37)
Canonical SPDI:: NC_000005.10:7499681:TGT:T
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000169/2 (ALFA)
-=0.000271/31 (GnomAD)
-=0.000283/5 (TOMMO)
HGVS:: NC_000005.10:g.7499683_7499684del, NC_000005.9:g.7499796_7499797del, NG_046913.1:g.108454_108455del

Select item 14915587489.

rs1491558748 [Homo sapiens]

Variant type:: DELINS
Alleles:: GG>- [Show Flanks]
Chromosome:: 5:7660235 (GRCh38)
5:7660348 (GRCh37)
Canonical SPDI:: NC_000005.10:7660233:GGG:G
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: -=0.001458/184 (GnomAD)
-=0.002811/18 (1000Genomes)
-=0.003213/54 (TOMMO)
HGVS:: NC_000005.10:g.7660235_7660236del, NC_000005.9:g.7660348_7660349del, NG_046913.1:g.269006_269007del

Select item 149155711610.

rs1491557116 [Homo sapiens]

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

Select item 149155260511.

rs1491552605 has merged into rs10662818 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTTTCTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 5:7684786 (GRCh38)
5:7684899 (GRCh37)
Canonical SPDI:: NC_000005.10:7684775:TTTTTTTTTTTTTT:TTTTTTTTTT,NC_000005.10:7684775:TTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000005.10:7684775:TTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000005.10:7684775:TTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000005.10:7684775:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:7684775:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:7684775:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000005.10:7684775:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000005.10:7684775:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000005.10:7684775:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000005.10:7684775:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTT
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
TT=0.3866/1936 (1000Genomes)
HGVS:: NC_000005.10:g.7684786_7684789del, NC_000005.10:g.7684787_7684789del, NC_000005.10:g.7684788_7684789del, NC_000005.10:g.7684789del, NC_000005.10:g.7684789dup, NC_000005.10:g.7684788_7684789dup, NC_000005.10:g.7684787_7684789dup, NC_000005.10:g.7684786_7684789dup, NC_000005.10:g.7684785_7684789dup, NC_000005.10:g.7684784_7684789dup, NC_000005.10:g.7684776_7684789T[23]CTTTTTTTTTTTTTTTTT[1], NC_000005.9:g.7684899_7684902del, NC_000005.9:g.7684900_7684902del, NC_000005.9:g.7684901_7684902del, NC_000005.9:g.7684902del, NC_000005.9:g.7684902dup, NC_000005.9:g.7684901_7684902dup, NC_000005.9:g.7684900_7684902dup, NC_000005.9:g.7684899_7684902dup, NC_000005.9:g.7684898_7684902dup, NC_000005.9:g.7684897_7684902dup, NC_000005.9:g.7684889_7684902T[23]CTTTTTTTTTTTTTTTTT[1], NG_046913.1:g.293557_293560del, NG_046913.1:g.293558_293560del, NG_046913.1:g.293559_293560del, NG_046913.1:g.293560del, NG_046913.1:g.293560dup, NG_046913.1:g.293559_293560dup, NG_046913.1:g.293558_293560dup, NG_046913.1:g.293557_293560dup, NG_046913.1:g.293556_293560dup, NG_046913.1:g.293555_293560dup, NG_046913.1:g.293547_293560T[23]CTTTTTTTTTTTTTTTTT[1]

Select item 149155255412.

rs1491552554 has merged into rs34190695 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT [Show Flanks]
Chromosome:: 5:7731267 (GRCh38)
5:7731380 (GRCh37)
Canonical SPDI:: NC_000005.10:7731253:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000005.10:7731253:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000005.10:7731253:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:7731253:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:7731253:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000005.10:7731253:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000005.10:7731253:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000005.10:7731253:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:7731253:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.32608/1633 (1000Genomes)
-=0.35/14 (GENOME_DK)
HGVS:: NC_000005.10:g.7731267_7731270del, NC_000005.10:g.7731268_7731270del, NC_000005.10:g.7731269_7731270del, NC_000005.10:g.7731270del, NC_000005.10:g.7731270dup, NC_000005.10:g.7731269_7731270dup, NC_000005.10:g.7731268_7731270dup, NC_000005.10:g.7731266_7731270dup, NC_000005.10:g.7731265_7731270dup, NC_000005.9:g.7731380_7731383del, NC_000005.9:g.7731381_7731383del, NC_000005.9:g.7731382_7731383del, NC_000005.9:g.7731383del, NC_000005.9:g.7731383dup, NC_000005.9:g.7731382_7731383dup, NC_000005.9:g.7731381_7731383dup, NC_000005.9:g.7731379_7731383dup, NC_000005.9:g.7731378_7731383dup, NG_046913.1:g.340038_340041del, NG_046913.1:g.340039_340041del, NG_046913.1:g.340040_340041del, NG_046913.1:g.340041del, NG_046913.1:g.340041dup, NG_046913.1:g.340040_340041dup, NG_046913.1:g.340039_340041dup, NG_046913.1:g.340037_340041dup, NG_046913.1:g.340036_340041dup

Select item 149154946713.

rs1491549467 has merged into rs57731885 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 5:7817838 (GRCh38)
5:7817951 (GRCh37)
Canonical SPDI:: NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:7817823:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ADCY2 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
-=0.0391/20 (NorthernSweden)
HGVS:: NC_000005.10:g.7817838_7817853del, NC_000005.10:g.7817839_7817853del, NC_000005.10:g.7817840_7817853del, NC_000005.10:g.7817841_7817853del, NC_000005.10:g.7817842_7817853del, NC_000005.10:g.7817843_7817853del, NC_000005.10:g.7817844_7817853del, NC_000005.10:g.7817845_7817853del, NC_000005.10:g.7817846_7817853del, NC_000005.10:g.7817847_7817853del, NC_000005.10:g.7817848_7817853del, NC_000005.10:g.7817849_7817853del, NC_000005.10:g.7817850_7817853del, NC_000005.10:g.7817851_7817853del, NC_000005.10:g.7817852_7817853del, NC_000005.10:g.7817853del, NC_000005.10:g.7817853dup, NC_000005.10:g.7817852_7817853dup, NC_000005.10:g.7817851_7817853dup, NC_000005.10:g.7817850_7817853dup, NC_000005.10:g.7817849_7817853dup, NC_000005.10:g.7817848_7817853dup, NC_000005.10:g.7817847_7817853dup, NC_000005.10:g.7817846_7817853dup, NC_000005.10:g.7817845_7817853dup, NC_000005.10:g.7817844_7817853dup, NC_000005.10:g.7817841_7817853dup, NC_000005.9:g.7817951_7817966del, NC_000005.9:g.7817952_7817966del, NC_000005.9:g.7817953_7817966del, NC_000005.9:g.7817954_7817966del, NC_000005.9:g.7817955_7817966del, NC_000005.9:g.7817956_7817966del, NC_000005.9:g.7817957_7817966del, NC_000005.9:g.7817958_7817966del, NC_000005.9:g.7817959_7817966del, NC_000005.9:g.7817960_7817966del, NC_000005.9:g.7817961_7817966del, NC_000005.9:g.7817962_7817966del, NC_000005.9:g.7817963_7817966del, NC_000005.9:g.7817964_7817966del, NC_000005.9:g.7817965_7817966del, NC_000005.9:g.7817966del, NC_000005.9:g.7817966dup, NC_000005.9:g.7817965_7817966dup, NC_000005.9:g.7817964_7817966dup, NC_000005.9:g.7817963_7817966dup, NC_000005.9:g.7817962_7817966dup, NC_000005.9:g.7817961_7817966dup, NC_000005.9:g.7817960_7817966dup, NC_000005.9:g.7817959_7817966dup, NC_000005.9:g.7817958_7817966dup, NC_000005.9:g.7817957_7817966dup, NC_000005.9:g.7817954_7817966dup, NG_046913.1:g.426609_426624del, NG_046913.1:g.426610_426624del, NG_046913.1:g.426611_426624del, NG_046913.1:g.426612_426624del, NG_046913.1:g.426613_426624del, NG_046913.1:g.426614_426624del, NG_046913.1:g.426615_426624del, NG_046913.1:g.426616_426624del, NG_046913.1:g.426617_426624del, NG_046913.1:g.426618_426624del, NG_046913.1:g.426619_426624del, NG_046913.1:g.426620_426624del, NG_046913.1:g.426621_426624del, NG_046913.1:g.426622_426624del, NG_046913.1:g.426623_426624del, NG_046913.1:g.426624del, NG_046913.1:g.426624dup, NG_046913.1:g.426623_426624dup, NG_046913.1:g.426622_426624dup, NG_046913.1:g.426621_426624dup, NG_046913.1:g.426620_426624dup, NG_046913.1:g.426619_426624dup, NG_046913.1:g.426618_426624dup, NG_046913.1:g.426617_426624dup, NG_046913.1:g.426616_426624dup, NG_046913.1:g.426615_426624dup, NG_046913.1:g.426612_426624dup

Select item 149154175314.

rs1491541753 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTTT [Show Flanks]
Chromosome:: 5:7573594 (GRCh38)
5:7573708 (GRCh37)
Canonical SPDI:: NC_000005.10:7573594:TTT:TTTCTTT
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000005.10:g.7573597_7573598insCTTT, NC_000005.9:g.7573710_7573711insCTTT, NG_046913.1:g.182368_182369insCTTT

Select item 149153639715.

rs1491536397 has merged into rs34653388 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAGA>-,GA [Show Flanks]
Chromosome:: 5:7589524 (GRCh38)
5:7589637 (GRCh37)
Canonical SPDI:: NC_000005.10:7589522:AGAGA:A,NC_000005.10:7589522:AGAGA:AGA
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGA=0./0 (ALFA)
-=0.028062/3022 (GnomAD)
-=0.02901/17 (NorthernSweden)
-=0.204722/789 (ALSPAC)
HGVS:: NC_000005.10:g.7589524_7589527del, NC_000005.10:g.7589524GA[1], NC_000005.9:g.7589637_7589640del, NC_000005.9:g.7589637GA[1], NG_046913.1:g.198295_198298del, NG_046913.1:g.198295GA[1]

Select item 149152064116.

rs1491520641 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 5:7724425 (GRCh38)
5:7724538 (GRCh37)
Canonical SPDI:: NC_000005.10:7724424:TA:
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000014/2 (GnomAD)
HGVS:: NC_000005.10:g.7724425_7724426del, NC_000005.9:g.7724538_7724539del, NG_046913.1:g.333196_333197del

Select item 149150488917.

rs1491504889 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 5:7817823 (GRCh38)
5:7817936 (GRCh37)
Canonical SPDI:: NC_000005.10:7817822:CA:
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000005.10:g.7817823_7817824del, NC_000005.9:g.7817936_7817937del, NG_046913.1:g.426594_426595del

Select item 149150359718.

rs1491503597 has merged into rs960087059 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA [Show Flanks]
Chromosome:: 5:7811510 (GRCh38)
5:7811623 (GRCh37)
Canonical SPDI:: NC_000005.10:7811500:AAAAAAAAAAA:AAAAAAAAA,NC_000005.10:7811500:AAAAAAAAAAA:AAAAAAAAAA,NC_000005.10:7811500:AAAAAAAAAAA:AAAAAAAAAAAA,NC_000005.10:7811500:AAAAAAAAAAA:AAAAAAAAAAAAA
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
A=0.00018/3 (TOMMO)
HGVS:: NC_000005.10:g.7811510_7811511del, NC_000005.10:g.7811511del, NC_000005.10:g.7811511dup, NC_000005.10:g.7811510_7811511dup, NC_000005.9:g.7811623_7811624del, NC_000005.9:g.7811624del, NC_000005.9:g.7811624dup, NC_000005.9:g.7811623_7811624dup, NG_046913.1:g.420281_420282del, NG_046913.1:g.420282del, NG_046913.1:g.420282dup, NG_046913.1:g.420281_420282dup

Select item 149149794519.

rs1491497945 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTTTTTT [Show Flanks]
Chromosome:: 5:7418648 (GRCh38)
5:7418762 (GRCh37)
Canonical SPDI:: NC_000005.10:7418648:TTTTTT:TTTTTTGTTTTTT
Gene:: ADCY2 (Varview), LOC105374646 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTTTTTGTTTTTT=0./0 (ALFA)
TTTTTTG=0.00036/23 (GnomAD)
HGVS:: NC_000005.10:g.7418649_7418654T[6]GTTTTTT[1], NC_000005.9:g.7418762_7418767T[6]GTTTTTT[1], NG_046913.1:g.27420_27425T[6]GTTTTTT[1]

Select item 149149675020.

rs1491496750 has merged into rs3033075 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA,AAAAA [Show Flanks]
Chromosome:: 5:7539366 (GRCh38)
5:7539479 (GRCh37)
Canonical SPDI:: NC_000005.10:7539355:AAAAAAAAAAAAA:AAAAAAAAAA,NC_000005.10:7539355:AAAAAAAAAAAAA:AAAAAAAAAAA,NC_000005.10:7539355:AAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000005.10:7539355:AAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000005.10:7539355:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA
Gene:: ADCY2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
-=0.02654/105 (1000Genomes)
A=0.175/7 (GENOME_DK)
A=0.17722/683 (ALSPAC)
A=0.18608/690 (TWINSUK)
A=0.23833/143 (NorthernSweden)
HGVS:: NC_000005.10:g.7539366_7539368del, NC_000005.10:g.7539367_7539368del, NC_000005.10:g.7539368del, NC_000005.10:g.7539368dup, NC_000005.10:g.7539367_7539368dup, NC_000005.9:g.7539479_7539481del, NC_000005.9:g.7539480_7539481del, NC_000005.9:g.7539481del, NC_000005.9:g.7539481dup, NC_000005.9:g.7539480_7539481dup, NG_046913.1:g.148137_148139del, NG_046913.1:g.148138_148139del, NG_046913.1:g.148139del, NG_046913.1:g.148139dup, NG_046913.1:g.148138_148139dup

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