SNP Links for Nucleotide (Select 594191171) - SNP

Links from Nucleotide

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Select item 14914811651.

rs1491481165 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:3016430 (GRCh38)
6:3016664 (GRCh37)
Canonical SPDI:: NC_000006.12:3016429:CA:
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00472/56 (ALFA)
-=0.00177/50 (TOMMO)
HGVS:: NC_000006.12:g.3016430_3016431del, NC_000006.11:g.3016664_3016665del, NG_034013.1:g.21615_21616del

Select item 14914053752.

rs1491405375 [Homo sapiens]

Variant type:: DELINS
Alleles:: AG>- [Show Flanks]
Chromosome:: 6:3004896 (GRCh38)
6:3005130 (GRCh37)
Canonical SPDI:: NC_000006.12:3004893:AGAG:AG
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.3004894AG[1], NC_000006.11:g.3005128AG[1], NG_034013.1:g.10079AG[1]

Select item 14913930543.

rs1491393054 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GAGTCTCGCTCTGTCT [Show Flanks]
Chromosome:: 6:3004894 (GRCh38)
6:3005129 (GRCh37)
Canonical SPDI:: NC_000006.12:3004894:GAGTCTCGCTCTGTCT:GAGTCTCGCTCTGTCTGAGTCTCGCTCTGTCT
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GAGTCTCGCTCTGTCTGAGTCTCGCTCTGTCT=0./0 (ALFA)
GAGTCTCGCTCTGTCT=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.3004895_3004910dup, NC_000006.11:g.3005129_3005144dup, NG_034013.1:g.10080_10095dup

Select item 14913375104.

rs1491337510 has merged into rs36118697 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAA>-,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:3016442 (GRCh38)
6:3016676 (GRCh37)
Canonical SPDI:: NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:3016430:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000006.12:g.3016442_3016450del, NC_000006.12:g.3016445_3016450del, NC_000006.12:g.3016446_3016450del, NC_000006.12:g.3016447_3016450del, NC_000006.12:g.3016448_3016450del, NC_000006.12:g.3016449_3016450del, NC_000006.12:g.3016450del, NC_000006.12:g.3016450dup, NC_000006.12:g.3016449_3016450dup, NC_000006.12:g.3016448_3016450dup, NC_000006.12:g.3016447_3016450dup, NC_000006.12:g.3016446_3016450dup, NC_000006.12:g.3016445_3016450dup, NC_000006.12:g.3016444_3016450dup, NC_000006.12:g.3016443_3016450dup, NC_000006.12:g.3016442_3016450dup, NC_000006.12:g.3016441_3016450dup, NC_000006.12:g.3016440_3016450dup, NC_000006.12:g.3016439_3016450dup, NC_000006.12:g.3016438_3016450dup, NC_000006.12:g.3016437_3016450dup, NC_000006.12:g.3016436_3016450dup, NC_000006.12:g.3016435_3016450dup, NC_000006.12:g.3016434_3016450dup, NC_000006.12:g.3016433_3016450dup, NC_000006.12:g.3016432_3016450dup, NC_000006.12:g.3016431_3016450dup, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.3016450_3016451insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016676_3016684del, NC_000006.11:g.3016679_3016684del, NC_000006.11:g.3016680_3016684del, NC_000006.11:g.3016681_3016684del, NC_000006.11:g.3016682_3016684del, NC_000006.11:g.3016683_3016684del, NC_000006.11:g.3016684del, NC_000006.11:g.3016684dup, NC_000006.11:g.3016683_3016684dup, NC_000006.11:g.3016682_3016684dup, NC_000006.11:g.3016681_3016684dup, NC_000006.11:g.3016680_3016684dup, NC_000006.11:g.3016679_3016684dup, NC_000006.11:g.3016678_3016684dup, NC_000006.11:g.3016677_3016684dup, NC_000006.11:g.3016676_3016684dup, NC_000006.11:g.3016675_3016684dup, NC_000006.11:g.3016674_3016684dup, NC_000006.11:g.3016673_3016684dup, NC_000006.11:g.3016672_3016684dup, NC_000006.11:g.3016671_3016684dup, NC_000006.11:g.3016670_3016684dup, NC_000006.11:g.3016669_3016684dup, NC_000006.11:g.3016668_3016684dup, NC_000006.11:g.3016667_3016684dup, NC_000006.11:g.3016666_3016684dup, NC_000006.11:g.3016665_3016684dup, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.3016684_3016685insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21627_21635del, NG_034013.1:g.21630_21635del, NG_034013.1:g.21631_21635del, NG_034013.1:g.21632_21635del, NG_034013.1:g.21633_21635del, NG_034013.1:g.21634_21635del, NG_034013.1:g.21635del, NG_034013.1:g.21635dup, NG_034013.1:g.21634_21635dup, NG_034013.1:g.21633_21635dup, NG_034013.1:g.21632_21635dup, NG_034013.1:g.21631_21635dup, NG_034013.1:g.21630_21635dup, NG_034013.1:g.21629_21635dup, NG_034013.1:g.21628_21635dup, NG_034013.1:g.21627_21635dup, NG_034013.1:g.21626_21635dup, NG_034013.1:g.21625_21635dup, NG_034013.1:g.21624_21635dup, NG_034013.1:g.21623_21635dup, NG_034013.1:g.21622_21635dup, NG_034013.1:g.21621_21635dup, NG_034013.1:g.21620_21635dup, NG_034013.1:g.21619_21635dup, NG_034013.1:g.21618_21635dup, NG_034013.1:g.21617_21635dup, NG_034013.1:g.21616_21635dup, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034013.1:g.21635_21636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14913158345.

rs1491315834 [Homo sapiens]

Variant type:: DELINS
Alleles:: TG>- [Show Flanks]
Chromosome:: 6:3004939 (GRCh38)
6:3005173 (GRCh37)
Canonical SPDI:: NC_000006.12:3004937:GTG:G
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000224/1 (ALFA)
-=0.000057/8 (GnomAD)
-=0.000223/1 (Estonian)
HGVS:: NC_000006.12:g.3004939_3004940del, NC_000006.11:g.3005173_3005174del, NG_034013.1:g.10124_10125del

Select item 14912686776.

rs1491268677 [Homo sapiens]

Variant type:: INS
Alleles:: ->CA [Show Flanks]
Chromosome:: 6:3004938 (GRCh38)
6:3005173 (GRCh37)
Canonical SPDI:: NC_000006.12:3004938::CA
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CA=0./0 (ALFA)
HGVS:: NC_000006.12:g.3004938_3004939insCA, NC_000006.11:g.3005172_3005173insCA, NG_034013.1:g.10123_10124insCA

Select item 14911669957.

rs1491166995 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>- [Show Flanks]
Chromosome:: 6:3010232 (GRCh38)
6:3010466 (GRCh37)
Canonical SPDI:: NC_000006.12:3010230:TAT:T
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: -=0.000006/1 (GnomAD_exomes)
-=0.000015/1 (ExAC)
HGVS:: NC_000006.12:g.3010232_3010233del, NC_000006.11:g.3010466_3010467del, NG_034013.1:g.15417_15418del

Select item 14910782788.

rs1491078278 has merged into rs113900840 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA [Show Flanks]
Chromosome:: 6:3000537 (GRCh38)
6:3000771 (GRCh37)
Canonical SPDI:: NC_000006.12:3000527:AAAAAAAAAAA:AAAAAAAAA,NC_000006.12:3000527:AAAAAAAAAAA:AAAAAAAAAA,NC_000006.12:3000527:AAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:3000527:AAAAAAAAAAA:AAAAAAAAAAAAA
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
-=0.268/1198 (Estonian)
-=0.2724/1010 (TWINSUK)
-=0.2763/1065 (ALSPAC)
-=0.2809/168 (NorthernSweden)
-=0.3/12 (GENOME_DK)
-=0.3288/1564 (1000Genomes)
HGVS:: NC_000006.12:g.3000537_3000538del, NC_000006.12:g.3000538del, NC_000006.12:g.3000538dup, NC_000006.12:g.3000537_3000538dup, NC_000006.11:g.3000771_3000772del, NC_000006.11:g.3000772del, NC_000006.11:g.3000772dup, NC_000006.11:g.3000771_3000772dup, NG_034013.1:g.5722_5723del, NG_034013.1:g.5723del, NG_034013.1:g.5723dup, NG_034013.1:g.5722_5723dup

Select item 14908312399.

rs1490831239 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:3000528 (GRCh38)
6:3000762 (GRCh37)
Canonical SPDI:: NC_000006.12:3000527:A:G
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.00034/4 (ALFA)
G=0.00022/13 (GnomAD)
A=0.47222/17 (SGDP_PRJ)
HGVS:: NC_000006.12:g.3000528A>G, NC_000006.11:g.3000762A>G, NG_034013.1:g.5713A>G

Select item 149064438210.

rs1490644382 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 6:2999734 (GRCh38)
6:2999968 (GRCh37)
Canonical SPDI:: NC_000006.12:2999733:C:A,NC_000006.12:2999733:C:T
Gene:: NQO2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000006.12:g.2999734C>A, NC_000006.12:g.2999734C>T, NC_000006.11:g.2999968C>A, NC_000006.11:g.2999968C>T, NG_034013.1:g.4919C>A, NG_034013.1:g.4919C>T

Select item 149044788711.

rs1490447887 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:3013428 (GRCh38)
6:3013662 (GRCh37)
Canonical SPDI:: NC_000006.12:3013427:C:T
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000224/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000006.12:g.3013428C>T, NC_000006.11:g.3013662C>T, NG_034013.1:g.18613C>T

Select item 149039214812.

rs1490392148 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:3003726 (GRCh38)
6:3003960 (GRCh37)
Canonical SPDI:: NC_000006.12:3003725:T:C
Gene:: NQO2 (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.3003726T>C, NC_000006.11:g.3003960T>C, NG_034013.1:g.8911T>C, NM_001290221.2:c.-306T>C, NM_001290221.1:c.-306T>C

Select item 149038266013.

rs1490382660 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 6:3002836 (GRCh38)
6:3003070 (GRCh37)
Canonical SPDI:: NC_000006.12:3002835:T:
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.3002836del, NC_000006.11:g.3003070del, NG_034013.1:g.8021del

Select item 149021670814.

rs1490216708 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:3014573 (GRCh38)
6:3014807 (GRCh37)
Canonical SPDI:: NC_000006.12:3014572:A:G
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000021/3 (GnomAD)
G=0.000023/6 (TOPMED)
HGVS:: NC_000006.12:g.3014573A>G, NC_000006.11:g.3014807A>G, NG_034013.1:g.19758A>G

Select item 149010781715.

rs1490107817 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:3017946 (GRCh38)
6:3018180 (GRCh37)
Canonical SPDI:: NC_000006.12:3017945:T:C
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.3017946T>C, NC_000006.11:g.3018180T>C, NG_034013.1:g.23131T>C

Select item 149005762016.

rs1490057620 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:2997553 (GRCh38)
6:2997787 (GRCh37)
Canonical SPDI:: NC_000006.12:2997552:G:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.2997553G>C, NC_000006.11:g.2997787G>C, NG_034013.1:g.2738G>C

Select item 148989371117.

rs1489893711 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:2996581 (GRCh38)
6:2996815 (GRCh37)
Canonical SPDI:: NC_000006.12:2996580:G:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.2996581G>T, NC_000006.11:g.2996815G>T, NG_034013.1:g.1766G>T

Select item 148984483818.

rs1489844838 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:3009400 (GRCh38)
6:3009634 (GRCh37)
Canonical SPDI:: NC_000006.12:3009399:C:T
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000006.12:g.3009400C>T, NC_000006.11:g.3009634C>T, NG_034013.1:g.14585C>T

Select item 148982700419.

rs1489827004 has merged into rs1387277887 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTTC>-,CTTCCTTC [Show Flanks]
Chromosome:: 6:2998830 (GRCh38)
6:2999064 (GRCh37)
Canonical SPDI:: NC_000006.12:2998820:CCTTCCTTCCTTC:CCTTCCTTC,NC_000006.12:2998820:CCTTCCTTCCTTC:CCTTCCTTCCTTCCTTC
Gene:: NQO2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CCTTCCTTCCTTCCTTC=0./0 (ALFA)
CCTT=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.2998822CTTC[2], NC_000006.12:g.2998822CTTC[4], NC_000006.11:g.2999056CTTC[2], NC_000006.11:g.2999056CTTC[4], NG_034013.1:g.4007CTTC[2], NG_034013.1:g.4007CTTC[4]

Select item 148971217120.

rs1489712171 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:3016593 (GRCh38)
6:3016827 (GRCh37)
Canonical SPDI:: NC_000006.12:3016592:C:T
Gene:: NQO2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000006.12:g.3016593C>T, NC_000006.11:g.3016827C>T, NG_034013.1:g.21778C>T

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