SNP Links for Nucleotide (Select 806904734) - SNP

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Select item 14915515101.

rs1491551510 [Homo sapiens]

Variant type:: DEL
Alleles:: TC>- [Show Flanks]
Chromosome:: X:43721876 (GRCh38)
X:43581123 (GRCh37)
Canonical SPDI:: NC_000023.11:43721875:TC:
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.43721876_43721877del, NC_000023.10:g.43581123_43581124del, NG_008957.2:g.70716_70717del

Select item 14914524662.

rs1491452466 has merged into rs764561924 [Homo sapiens]

Variant type:: DELINS
Alleles:: GC>-,GCGC [Show Flanks]
Chromosome:: X:43692039 (GRCh38)
X:43551287 (GRCh37)
Canonical SPDI:: NC_000023.11:43692037:CGC:C,NC_000023.11:43692037:CGC:CGCGC
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.0249/230 (ALFA)
-=0.125/5 (GENOME_DK)
HGVS:: NC_000023.11:g.43692039_43692040del, NC_000023.11:g.43692039_43692040dup, NC_000023.10:g.43551287_43551288del, NC_000023.10:g.43551287_43551288dup, NG_008957.2:g.40879_40880del, NG_008957.2:g.40879_40880dup

Select item 14913768473.

rs1491376847 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTTT,CTTTTCTTT [Show Flanks]
Chromosome:: X:43684875 (GRCh38)
X:43544124 (GRCh37)
Canonical SPDI:: NC_000023.11:43684875:TTT:TTTCTTT,NC_000023.11:43684875:TTT:TTTCTTTTCTTT
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTTCTTTTCTTT=0./0 (ALFA)
HGVS:: NC_000023.11:g.43684878_43684879insCTTT, NC_000023.11:g.43684876_43684878TTTCT[2]TT[1], NC_000023.10:g.43544126_43544127insCTTT, NC_000023.10:g.43544124_43544126TTTCT[2]TT[1], NG_008957.2:g.33718_33719insCTTT, NG_008957.2:g.33716_33718TTTCT[2]TT[1]

Select item 14913698964.

rs1491369896 has merged into rs201207592 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTT>-,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: X:43684886 (GRCh38)
X:43544134 (GRCh37)
Canonical SPDI:: NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43684874:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
T=0.3862/1458 (1000Genomes)
HGVS:: NC_000023.11:g.43684886_43684894del, NC_000023.11:g.43684888_43684894del, NC_000023.11:g.43684889_43684894del, NC_000023.11:g.43684891_43684894del, NC_000023.11:g.43684892_43684894del, NC_000023.11:g.43684893_43684894del, NC_000023.11:g.43684894del, NC_000023.11:g.43684894dup, NC_000023.11:g.43684893_43684894dup, NC_000023.11:g.43684892_43684894dup, NC_000023.11:g.43684891_43684894dup, NC_000023.11:g.43684890_43684894dup, NC_000023.11:g.43684889_43684894dup, NC_000023.11:g.43684888_43684894dup, NC_000023.11:g.43684887_43684894dup, NC_000023.11:g.43684886_43684894dup, NC_000023.11:g.43684885_43684894dup, NC_000023.11:g.43684884_43684894dup, NC_000023.11:g.43684883_43684894dup, NC_000023.11:g.43684882_43684894dup, NC_000023.11:g.43684881_43684894dup, NC_000023.11:g.43684880_43684894dup, NC_000023.11:g.43684879_43684894dup, NC_000023.11:g.43684876_43684894dup, NC_000023.11:g.43684875_43684894dup, NC_000023.11:g.43684894_43684895insTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.43684894_43684895insTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.43684894_43684895insTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.43684894_43684895insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.11:g.43684894_43684895insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.43544134_43544142del, NC_000023.10:g.43544136_43544142del, NC_000023.10:g.43544137_43544142del, NC_000023.10:g.43544139_43544142del, NC_000023.10:g.43544140_43544142del, NC_000023.10:g.43544141_43544142del, NC_000023.10:g.43544142del, NC_000023.10:g.43544142dup, NC_000023.10:g.43544141_43544142dup, NC_000023.10:g.43544140_43544142dup, NC_000023.10:g.43544139_43544142dup, NC_000023.10:g.43544138_43544142dup, NC_000023.10:g.43544137_43544142dup, NC_000023.10:g.43544136_43544142dup, NC_000023.10:g.43544135_43544142dup, NC_000023.10:g.43544134_43544142dup, NC_000023.10:g.43544133_43544142dup, NC_000023.10:g.43544132_43544142dup, NC_000023.10:g.43544131_43544142dup, NC_000023.10:g.43544130_43544142dup, NC_000023.10:g.43544129_43544142dup, NC_000023.10:g.43544128_43544142dup, NC_000023.10:g.43544127_43544142dup, NC_000023.10:g.43544124_43544142dup, NC_000023.10:g.43544123_43544142dup, NC_000023.10:g.43544142_43544143insTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.43544142_43544143insTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.43544142_43544143insTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.43544142_43544143insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000023.10:g.43544142_43544143insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008957.2:g.33726_33734del, NG_008957.2:g.33728_33734del, NG_008957.2:g.33729_33734del, NG_008957.2:g.33731_33734del, NG_008957.2:g.33732_33734del, NG_008957.2:g.33733_33734del, NG_008957.2:g.33734del, NG_008957.2:g.33734dup, NG_008957.2:g.33733_33734dup, NG_008957.2:g.33732_33734dup, NG_008957.2:g.33731_33734dup, NG_008957.2:g.33730_33734dup, NG_008957.2:g.33729_33734dup, NG_008957.2:g.33728_33734dup, NG_008957.2:g.33727_33734dup, NG_008957.2:g.33726_33734dup, NG_008957.2:g.33725_33734dup, NG_008957.2:g.33724_33734dup, NG_008957.2:g.33723_33734dup, NG_008957.2:g.33722_33734dup, NG_008957.2:g.33721_33734dup, NG_008957.2:g.33720_33734dup, NG_008957.2:g.33719_33734dup, NG_008957.2:g.33716_33734dup, NG_008957.2:g.33715_33734dup, NG_008957.2:g.33734_33735insTTTTTTTTTTTTTTTTTTTTT, NG_008957.2:g.33734_33735insTTTTTTTTTTTTTTTTTTTTTT, NG_008957.2:g.33734_33735insTTTTTTTTTTTTTTTTTTTTTTT, NG_008957.2:g.33734_33735insTTTTTTTTTTTTTTTTTTTTTTTT, NG_008957.2:g.33734_33735insTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14913676265.

rs1491367626 [Homo sapiens]

Variant type:: INS
Alleles:: ->AT [Show Flanks]
Chromosome:: X:43693804 (GRCh38)
X:43553052 (GRCh37)
Canonical SPDI:: NC_000023.11:43693804::AT
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AT=0./0 (ALFA)
AT=0.000049/5 (GnomAD)
AT=0.000208/1 (1000Genomes)
HGVS:: NC_000023.11:g.43693804_43693805insAT, NC_000023.10:g.43553051_43553052insAT, NG_008957.2:g.42644_42645insAT

Select item 14912403456.

rs1491240345 has merged into rs768785097 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT [Show Flanks]
Chromosome:: X:43681892 (GRCh38)
X:43541140 (GRCh37)
Canonical SPDI:: NC_000023.11:43681880:TTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000023.11:43681880:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000023.11:43681880:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000023.11:43681880:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000023.11:43681880:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000023.11:43681880:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000023.11:43681880:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000023.11:43681880:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000023.11:43681880:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
-=0.24079/909 (1000Genomes)
HGVS:: NC_000023.11:g.43681892_43681895del, NC_000023.11:g.43681893_43681895del, NC_000023.11:g.43681894_43681895del, NC_000023.11:g.43681895del, NC_000023.11:g.43681895dup, NC_000023.11:g.43681894_43681895dup, NC_000023.11:g.43681893_43681895dup, NC_000023.11:g.43681892_43681895dup, NC_000023.11:g.43681891_43681895dup, NC_000023.10:g.43541140_43541143del, NC_000023.10:g.43541141_43541143del, NC_000023.10:g.43541142_43541143del, NC_000023.10:g.43541143del, NC_000023.10:g.43541143dup, NC_000023.10:g.43541142_43541143dup, NC_000023.10:g.43541141_43541143dup, NC_000023.10:g.43541140_43541143dup, NC_000023.10:g.43541139_43541143dup, NG_008957.2:g.30732_30735del, NG_008957.2:g.30733_30735del, NG_008957.2:g.30734_30735del, NG_008957.2:g.30735del, NG_008957.2:g.30735dup, NG_008957.2:g.30734_30735dup, NG_008957.2:g.30733_30735dup, NG_008957.2:g.30732_30735dup, NG_008957.2:g.30731_30735dup

Select item 14912332357.

rs1491233235 [Homo sapiens]

Variant type:: DELINS
Alleles:: GC>- [Show Flanks]
Chromosome:: X:43692043 (GRCh38)
X:43551291 (GRCh37)
Canonical SPDI:: NC_000023.11:43692041:CGC:C
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: -=0.00023/3 (TOMMO)
HGVS:: NC_000023.11:g.43692043_43692044del, NC_000023.10:g.43551291_43551292del, NG_008957.2:g.40883_40884del

Select item 14911674858.

rs1491167485 [Homo sapiens]

Variant type:: DELINS
Alleles:: GC>- [Show Flanks]
Chromosome:: X:43693805 (GRCh38)
X:43553052 (GRCh37)
Canonical SPDI:: NC_000023.11:43693803:CGC:C
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.00002/2 (GnomAD)
HGVS:: NC_000023.11:g.43693805_43693806del, NC_000023.10:g.43553052_43553053del, NG_008957.2:g.42645_42646del

Select item 14911361799.

rs1491136179 has merged into rs758339663 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT,TTTTTT,TTTTTTTTT,TTTTTTTTTTTTT [Show Flanks]
Chromosome:: X:43708675 (GRCh38)
X:43567922 (GRCh37)
Canonical SPDI:: NC_000023.11:43708662:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000023.11:43708662:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000023.11:43708662:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000023.11:43708662:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000023.11:43708662:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000023.11:43708662:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000023.11:43708662:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000023.11:43708662:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
T=0.175/7 (GENOME_DK)
HGVS:: NC_000023.11:g.43708675_43708677del, NC_000023.11:g.43708676_43708677del, NC_000023.11:g.43708677del, NC_000023.11:g.43708677dup, NC_000023.11:g.43708676_43708677dup, NC_000023.11:g.43708675_43708677dup, NC_000023.11:g.43708672_43708677dup, NC_000023.11:g.43708668_43708677dup, NC_000023.10:g.43567922_43567924del, NC_000023.10:g.43567923_43567924del, NC_000023.10:g.43567924del, NC_000023.10:g.43567924dup, NC_000023.10:g.43567923_43567924dup, NC_000023.10:g.43567922_43567924dup, NC_000023.10:g.43567919_43567924dup, NC_000023.10:g.43567915_43567924dup, NG_008957.2:g.57515_57517del, NG_008957.2:g.57516_57517del, NG_008957.2:g.57517del, NG_008957.2:g.57517dup, NG_008957.2:g.57516_57517dup, NG_008957.2:g.57515_57517dup, NG_008957.2:g.57512_57517dup, NG_008957.2:g.57508_57517dup

Select item 149111199010.

rs1491111990 [Homo sapiens]

Variant type:: INS
Alleles:: ->ACAT,AT [Show Flanks]
Chromosome:: X:43692042 (GRCh38)
X:43551291 (GRCh37)
Canonical SPDI:: NC_000023.11:43692042::ACAT,NC_000023.11:43692042::AT
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AT=0./0 (ALFA)
HGVS:: NC_000023.11:g.43692042_43692043insACAT, NC_000023.11:g.43692042_43692043insAT, NC_000023.10:g.43551290_43551291insACAT, NC_000023.10:g.43551290_43551291insAT, NG_008957.2:g.40882_40883insACAT, NG_008957.2:g.40882_40883insAT

Select item 149107539111.

rs1491075391 has merged into rs397717487 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATAT>-,AT,ATATAT,ATATATAT,ATATATATAT,ATATATATATAT,ATATATATATATAT,ATATATATGAACTGTGTTTATATATATATATATATATAT [Show Flanks]
Chromosome:: X:43657287 (GRCh38)
X:43516535 (GRCh37)
Canonical SPDI:: NC_000023.11:43657273:TATATATATATATATAT:TATATATATATAT,NC_000023.11:43657273:TATATATATATATATAT:TATATATATATATAT,NC_000023.11:43657273:TATATATATATATATAT:TATATATATATATATATAT,NC_000023.11:43657273:TATATATATATATATAT:TATATATATATATATATATAT,NC_000023.11:43657273:TATATATATATATATAT:TATATATATATATATATATATAT,NC_000023.11:43657273:TATATATATATATATAT:TATATATATATATATATATATATAT,NC_000023.11:43657273:TATATATATATATATAT:TATATATATATATATATATATATATAT,NC_000023.11:43657273:TATATATATATATATAT:TATATATATATATATATATATGAACTGTGTTTATATATATATATATATATAT
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATATATATATATATATAT=0./0 (ALFA)
-=0.325/13 (GENOME_DK)
TATA=0.4167/20 (Vietnamese)
-=0.4946/1867 (1000Genomes)
HGVS:: NC_000023.11:g.43657275AT[6], NC_000023.11:g.43657275AT[7], NC_000023.11:g.43657275AT[9], NC_000023.11:g.43657275AT[10], NC_000023.11:g.43657275AT[11], NC_000023.11:g.43657275AT[12], NC_000023.11:g.43657275AT[13], NC_000023.11:g.43657274_43657290TA[10]TGAACTGTGTTTATATATATATATATATATAT[1], NC_000023.10:g.43516523AT[6], NC_000023.10:g.43516523AT[7], NC_000023.10:g.43516523AT[9], NC_000023.10:g.43516523AT[10], NC_000023.10:g.43516523AT[11], NC_000023.10:g.43516523AT[12], NC_000023.10:g.43516523AT[13], NC_000023.10:g.43516522_43516538TA[10]TGAACTGTGTTTATATATATATATATATATAT[1], NG_008957.2:g.6115AT[6], NG_008957.2:g.6115AT[7], NG_008957.2:g.6115AT[9], NG_008957.2:g.6115AT[10], NG_008957.2:g.6115AT[11], NG_008957.2:g.6115AT[12], NG_008957.2:g.6115AT[13], NG_008957.2:g.6114_6130TA[10]TGAACTGTGTTTATATATATATATATATATAT[1]

Select item 149103975512.

rs1491039755 has merged into rs370833081 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT [Show Flanks]
Chromosome:: X:43653787 (GRCh38)
X:43513035 (GRCh37)
Canonical SPDI:: NC_000023.11:43653775:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000023.11:43653775:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000023.11:43653775:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000023.11:43653775:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000023.11:43653775:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000023.11:43653775:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000023.11:43653775:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT
Gene:: MAOA (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.13245/500 (1000Genomes)
HGVS:: NC_000023.11:g.43653787_43653792del, NC_000023.11:g.43653790_43653792del, NC_000023.11:g.43653791_43653792del, NC_000023.11:g.43653792del, NC_000023.11:g.43653792dup, NC_000023.11:g.43653791_43653792dup, NC_000023.11:g.43653790_43653792dup, NC_000023.10:g.43513035_43513040del, NC_000023.10:g.43513038_43513040del, NC_000023.10:g.43513039_43513040del, NC_000023.10:g.43513040del, NC_000023.10:g.43513040dup, NC_000023.10:g.43513039_43513040dup, NC_000023.10:g.43513038_43513040dup, NG_008957.2:g.2627_2632del, NG_008957.2:g.2630_2632del, NG_008957.2:g.2631_2632del, NG_008957.2:g.2632del, NG_008957.2:g.2632dup, NG_008957.2:g.2631_2632dup, NG_008957.2:g.2630_2632dup

Select item 149100172813.

rs1491001728 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:43666874 (GRCh38)
X:43526122 (GRCh37)
Canonical SPDI:: NC_000023.11:43666873:G:T
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.43666874G>T, NC_000023.10:g.43526122G>T, NG_008957.2:g.15714G>T

Select item 149097662414.

rs1490976624 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: X:43667904 (GRCh38)
X:43527152 (GRCh37)
Canonical SPDI:: NC_000023.11:43667903:T:A
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.43667904T>A, NC_000023.10:g.43527152T>A, NG_008957.2:g.16744T>A

Select item 149097223515.

rs1490972235 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAT>- [Show Flanks]
Chromosome:: X:43719582 (GRCh38)
X:43578829 (GRCh37)
Canonical SPDI:: NC_000023.11:43719579:ATGAT:AT
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.43719582_43719584del, NC_000023.10:g.43578829_43578831del, NG_008957.2:g.68422_68424del

Select item 149094629616.

rs1490946296 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGG>- [Show Flanks]
Chromosome:: X:43716063 (GRCh38)
X:43575310 (GRCh37)
Canonical SPDI:: NC_000023.11:43716060:GGGGG:GG
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0.000142/2 (ALFA)
-=0.000023/6 (TOPMED)
-=0.000208/1 (1000Genomes)
-=0.014413/185 (TOMMO)
HGVS:: NC_000023.11:g.43716063_43716065del, NC_000023.10:g.43575310_43575312del, NG_008957.2:g.64903_64905del

Select item 149089709617.

rs1490897096 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: X:43687947 (GRCh38)
X:43547195 (GRCh37)
Canonical SPDI:: NC_000023.11:43687946:A:G,NC_000023.11:43687946:A:T
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.43687947A>G, NC_000023.11:g.43687947A>T, NC_000023.10:g.43547195A>G, NC_000023.10:g.43547195A>T, NG_008957.2:g.36787A>G, NG_008957.2:g.36787A>T

Select item 149087705818.

rs1490877058 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: X:43706151 (GRCh38)
X:43565398 (GRCh37)
Canonical SPDI:: NC_000023.11:43706150:A:
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.43706151del, NC_000023.10:g.43565398del, NG_008957.2:g.54991del

Select item 149082596819.

rs1490825968 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: X:43679024 (GRCh38)
X:43538272 (GRCh37)
Canonical SPDI:: NC_000023.11:43679023:A:C
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.43679024A>C, NC_000023.10:g.43538272A>C, NG_008957.2:g.27864A>C

Select item 149080440720.

rs1490804407 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:43699637 (GRCh38)
X:43558884 (GRCh37)
Canonical SPDI:: NC_000023.11:43699636:T:C
Gene:: MAOA (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.43699637T>C, NC_000023.10:g.43558884T>C, NG_008957.2:g.48477T>C

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