SNP Links for Gene (Select 10673) - SNP

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Select item 14914696461.

rs1491469646 [Homo sapiens]

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

Select item 14913178122.

rs1491317812 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 13:108282862 (GRCh38)
13:108935211 (GRCh37)
Canonical SPDI:: NC_000013.11:108282862:T:TT
Gene:: TNFSF13B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
T=0.000035/1 (TOMMO)
HGVS:: NC_000013.11:g.108282863dup, NC_000013.10:g.108935211dup, NG_029524.1:g.18235dup

Select item 14912189823.

rs1491218982 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: 13:108282863 (GRCh38)
13:108935211 (GRCh37)
Canonical SPDI:: NC_000013.11:108282861:ATA:A
Gene:: TNFSF13B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.108282863_108282864del, NC_000013.10:g.108935211_108935212del, NG_029524.1:g.18235_18236del

Select item 14911839614.

rs1491183961 has merged into rs58093140 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 13:108307031 (GRCh38)
13:108959379 (GRCh37)
Canonical SPDI:: NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:108307016:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: TNFSF13B (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
-=0.2806/1405 (1000Genomes)
-=0.3158/12 (GENOME_DK)
HGVS:: NC_000013.11:g.108307031_108307047del, NC_000013.11:g.108307032_108307047del, NC_000013.11:g.108307033_108307047del, NC_000013.11:g.108307034_108307047del, NC_000013.11:g.108307035_108307047del, NC_000013.11:g.108307036_108307047del, NC_000013.11:g.108307037_108307047del, NC_000013.11:g.108307038_108307047del, NC_000013.11:g.108307039_108307047del, NC_000013.11:g.108307040_108307047del, NC_000013.11:g.108307041_108307047del, NC_000013.11:g.108307042_108307047del, NC_000013.11:g.108307043_108307047del, NC_000013.11:g.108307044_108307047del, NC_000013.11:g.108307045_108307047del, NC_000013.11:g.108307046_108307047del, NC_000013.11:g.108307047del, NC_000013.11:g.108307047dup, NC_000013.11:g.108307046_108307047dup, NC_000013.11:g.108307045_108307047dup, NC_000013.11:g.108307044_108307047dup, NC_000013.11:g.108307043_108307047dup, NC_000013.11:g.108307042_108307047dup, NC_000013.11:g.108307041_108307047dup, NC_000013.11:g.108307040_108307047dup, NC_000013.11:g.108307039_108307047dup, NC_000013.11:g.108307038_108307047dup, NC_000013.11:g.108307037_108307047dup, NC_000013.11:g.108307036_108307047dup, NC_000013.11:g.108307035_108307047dup, NC_000013.11:g.108307034_108307047dup, NC_000013.11:g.108307033_108307047dup, NC_000013.11:g.108307032_108307047dup, NC_000013.11:g.108307028_108307047dup, NC_000013.11:g.108307022_108307047dup, NC_000013.11:g.108307021_108307047dup, NC_000013.11:g.108307019_108307047dup, NC_000013.11:g.108307047_108307048insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.11:g.108307047_108307048insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.10:g.108959379_108959395del, NC_000013.10:g.108959380_108959395del, NC_000013.10:g.108959381_108959395del, NC_000013.10:g.108959382_108959395del, NC_000013.10:g.108959383_108959395del, NC_000013.10:g.108959384_108959395del, NC_000013.10:g.108959385_108959395del, NC_000013.10:g.108959386_108959395del, NC_000013.10:g.108959387_108959395del, NC_000013.10:g.108959388_108959395del, NC_000013.10:g.108959389_108959395del, NC_000013.10:g.108959390_108959395del, NC_000013.10:g.108959391_108959395del, NC_000013.10:g.108959392_108959395del, NC_000013.10:g.108959393_108959395del, NC_000013.10:g.108959394_108959395del, NC_000013.10:g.108959395del, NC_000013.10:g.108959395dup, NC_000013.10:g.108959394_108959395dup, NC_000013.10:g.108959393_108959395dup, NC_000013.10:g.108959392_108959395dup, NC_000013.10:g.108959391_108959395dup, NC_000013.10:g.108959390_108959395dup, NC_000013.10:g.108959389_108959395dup, NC_000013.10:g.108959388_108959395dup, NC_000013.10:g.108959387_108959395dup, NC_000013.10:g.108959386_108959395dup, NC_000013.10:g.108959385_108959395dup, NC_000013.10:g.108959384_108959395dup, NC_000013.10:g.108959383_108959395dup, NC_000013.10:g.108959382_108959395dup, NC_000013.10:g.108959381_108959395dup, NC_000013.10:g.108959380_108959395dup, NC_000013.10:g.108959376_108959395dup, NC_000013.10:g.108959370_108959395dup, NC_000013.10:g.108959369_108959395dup, NC_000013.10:g.108959367_108959395dup, NC_000013.10:g.108959395_108959396insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.10:g.108959395_108959396insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029524.1:g.42403_42419del, NG_029524.1:g.42404_42419del, NG_029524.1:g.42405_42419del, NG_029524.1:g.42406_42419del, NG_029524.1:g.42407_42419del, NG_029524.1:g.42408_42419del, NG_029524.1:g.42409_42419del, NG_029524.1:g.42410_42419del, NG_029524.1:g.42411_42419del, NG_029524.1:g.42412_42419del, NG_029524.1:g.42413_42419del, NG_029524.1:g.42414_42419del, NG_029524.1:g.42415_42419del, NG_029524.1:g.42416_42419del, NG_029524.1:g.42417_42419del, NG_029524.1:g.42418_42419del, NG_029524.1:g.42419del, NG_029524.1:g.42419dup, NG_029524.1:g.42418_42419dup, NG_029524.1:g.42417_42419dup, NG_029524.1:g.42416_42419dup, NG_029524.1:g.42415_42419dup, NG_029524.1:g.42414_42419dup, NG_029524.1:g.42413_42419dup, NG_029524.1:g.42412_42419dup, NG_029524.1:g.42411_42419dup, NG_029524.1:g.42410_42419dup, NG_029524.1:g.42409_42419dup, NG_029524.1:g.42408_42419dup, NG_029524.1:g.42407_42419dup, NG_029524.1:g.42406_42419dup, NG_029524.1:g.42405_42419dup, NG_029524.1:g.42404_42419dup, NG_029524.1:g.42400_42419dup, NG_029524.1:g.42394_42419dup, NG_029524.1:g.42393_42419dup, NG_029524.1:g.42391_42419dup, NG_029524.1:g.42419_42420insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029524.1:g.42419_42420insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_006573.5:c.*93_*109del, NM_006573.5:c.*94_*109del, NM_006573.5:c.*95_*109del, NM_006573.5:c.*96_*109del, NM_006573.5:c.*97_*109del, NM_006573.5:c.*98_*109del, NM_006573.5:c.*99_*109del, NM_006573.5:c.*100_*109del, NM_006573.5:c.*101_*109del, NM_006573.5:c.*102_*109del, NM_006573.5:c.*103_*109del, NM_006573.5:c.*104_*109del, NM_006573.5:c.*105_*109del, NM_006573.5:c.*106_*109del, NM_006573.5:c.*107_*109del, NM_006573.5:c.*108_*109del, NM_006573.5:c.*109del, NM_006573.5:c.*109dup, NM_006573.5:c.*108_*109dup, NM_006573.5:c.*107_*109dup, NM_006573.5:c.*106_*109dup, NM_006573.5:c.*105_*109dup, NM_006573.5:c.*104_*109dup, NM_006573.5:c.*103_*109dup, NM_006573.5:c.*102_*109dup, NM_006573.5:c.*101_*109dup, NM_006573.5:c.*100_*109dup, NM_006573.5:c.*99_*109dup, NM_006573.5:c.*98_*109dup, NM_006573.5:c.*97_*109dup, NM_006573.5:c.*96_*109dup, NM_006573.5:c.*95_*109dup, NM_006573.5:c.*94_*109dup, NM_006573.5:c.*90_*109dup, NM_006573.5:c.*84_*109dup, NM_006573.5:c.*83_*109dup, NM_006573.5:c.*81_*109dup, NM_006573.5:c.*109_*110insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_006573.5:c.*109_*110insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_006573.4:c.*93_*109del, NM_006573.4:c.*94_*109del, NM_006573.4:c.*95_*109del, NM_006573.4:c.*96_*109del, NM_006573.4:c.*97_*109del, NM_006573.4:c.*98_*109del, NM_006573.4:c.*99_*109del, NM_006573.4:c.*100_*109del, NM_006573.4:c.*101_*109del, NM_006573.4:c.*102_*109del, NM_006573.4:c.*103_*109del, NM_006573.4:c.*104_*109del, NM_006573.4:c.*105_*109del, NM_006573.4:c.*106_*109del, NM_006573.4:c.*107_*109del, NM_006573.4:c.*108_*109del, NM_006573.4:c.*109del, NM_006573.4:c.*109dup, NM_006573.4:c.*108_*109dup, NM_006573.4:c.*107_*109dup, NM_006573.4:c.*106_*109dup, NM_006573.4:c.*105_*109dup, NM_006573.4:c.*104_*109dup, NM_006573.4:c.*103_*109dup, NM_006573.4:c.*102_*109dup, NM_006573.4:c.*101_*109dup, NM_006573.4:c.*100_*109dup, NM_006573.4:c.*99_*109dup, NM_006573.4:c.*98_*109dup, NM_006573.4:c.*97_*109dup, NM_006573.4:c.*96_*109dup, NM_006573.4:c.*95_*109dup, NM_006573.4:c.*94_*109dup, NM_006573.4:c.*90_*109dup, NM_006573.4:c.*84_*109dup, NM_006573.4:c.*83_*109dup, NM_006573.4:c.*81_*109dup, NM_006573.4:c.*109_*110insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_006573.4:c.*109_*110insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001145645.2:c.*93_*109del, NM_001145645.2:c.*94_*109del, NM_001145645.2:c.*95_*109del, NM_001145645.2:c.*96_*109del, NM_001145645.2:c.*97_*109del, NM_001145645.2:c.*98_*109del, NM_001145645.2:c.*99_*109del, NM_001145645.2:c.*100_*109del, NM_001145645.2:c.*101_*109del, NM_001145645.2:c.*102_*109del, NM_001145645.2:c.*103_*109del, NM_001145645.2:c.*104_*109del, NM_001145645.2:c.*105_*109del, NM_001145645.2:c.*106_*109del, NM_001145645.2:c.*107_*109del, NM_001145645.2:c.*108_*109del, NM_001145645.2:c.*109del, NM_001145645.2:c.*109dup, NM_001145645.2:c.*108_*109dup, NM_001145645.2:c.*107_*109dup, NM_001145645.2:c.*106_*109dup, NM_001145645.2:c.*105_*109dup, NM_001145645.2:c.*104_*109dup, NM_001145645.2:c.*103_*109dup, NM_001145645.2:c.*102_*109dup, NM_001145645.2:c.*101_*109dup, NM_001145645.2:c.*100_*109dup, NM_001145645.2:c.*99_*109dup, NM_001145645.2:c.*98_*109dup, NM_001145645.2:c.*97_*109dup, NM_001145645.2:c.*96_*109dup, NM_001145645.2:c.*95_*109dup, NM_001145645.2:c.*94_*109dup, NM_001145645.2:c.*90_*109dup, NM_001145645.2:c.*84_*109dup, NM_001145645.2:c.*83_*109dup, NM_001145645.2:c.*81_*109dup, NM_001145645.2:c.*109_*110insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_001145645.2:c.*109_*110insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14911660585.

rs1491166058 has merged into rs1216744898 [Homo sapiens]

Variant type:: DELINS
Alleles:: CATA>-,CATACATA [Show Flanks]
Chromosome:: 13:108274382 (GRCh38)
13:108926730 (GRCh37)
Canonical SPDI:: NC_000013.11:108274378:ATACATA:ATA,NC_000013.11:108274378:ATACATA:ATACATACATA
Gene:: TNFSF13B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATACATACATA=0./0 (ALFA)
HGVS:: NC_000013.11:g.108274382_108274385del, NC_000013.11:g.108274382_108274385dup, NC_000013.10:g.108926730_108926733del, NC_000013.10:g.108926730_108926733dup, NG_029524.1:g.9754_9757del, NG_029524.1:g.9754_9757dup

Select item 14909844206.

rs1490984420 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:108266770 (GRCh38)
13:108919118 (GRCh37)
Canonical SPDI:: NC_000013.11:108266769:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000013.11:g.108266770C>T, NC_000013.10:g.108919118C>T, NG_029524.1:g.2142C>T

Select item 14907319917.

rs1490731991 [Homo sapiens]

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

Select item 14906856878.

rs1490685687 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:108278601 (GRCh38)
13:108930949 (GRCh37)
Canonical SPDI:: NC_000013.11:108278600:C:T
Gene:: TNFSF13B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00008/1 (ALFA)
T=0.00022/3 (TOMMO)
T=0.00059/1 (Korea1K)
T=0.09253/270 (KOREAN)
HGVS:: NC_000013.11:g.108278601C>T, NC_000013.10:g.108930949C>T, NG_029524.1:g.13973C>T

Select item 14905699909.

rs1490569990 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:108273574 (GRCh38)
13:108925922 (GRCh37)
Canonical SPDI:: NC_000013.11:108273573:A:G
Gene:: TNFSF13B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.108273574A>G, NC_000013.10:g.108925922A>G, NG_029524.1:g.8946A>G

Select item 149047983010.

rs1490479830 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:108295237 (GRCh38)
13:108947585 (GRCh37)
Canonical SPDI:: NC_000013.11:108295236:C:T
Gene:: TNFSF13B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000253/3 (ALFA)
T=0.000105/14 (GnomAD)
HGVS:: NC_000013.11:g.108295237C>T, NC_000013.10:g.108947585C>T, NG_029524.1:g.30609C>T

Select item 149035607411.

rs1490356074 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:108306276 (GRCh38)
13:108958624 (GRCh37)
Canonical SPDI:: NC_000013.11:108306275:G:A
Gene:: TNFSF13B (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.108306276G>A, NC_000013.10:g.108958624G>A, NG_029524.1:g.41648G>A

Select item 149033157312.

rs1490331573 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:108291693 (GRCh38)
13:108944041 (GRCh37)
Canonical SPDI:: NC_000013.11:108291692:A:G
Gene:: TNFSF13B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000142/2 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.108291693A>G, NC_000013.10:g.108944041A>G, NG_029524.1:g.27065A>G

Select item 149017481313.

rs1490174813 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 13:108266249 (GRCh38)
13:108918597 (GRCh37)
Canonical SPDI:: NC_000013.11:108266248:A:
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.108266249del, NC_000013.10:g.108918597del, NG_029524.1:g.1621del

Select item 149007217414.

rs1490072174 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 13:108297698 (GRCh38)
13:108950046 (GRCh37)
Canonical SPDI:: NC_000013.11:108297697:A:C
Gene:: TNFSF13B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000015/2 (GnomAD)
HGVS:: NC_000013.11:g.108297698A>C, NC_000013.10:g.108950046A>C, NG_029524.1:g.33070A>C

Select item 149004661815.

rs1490046618 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 13:108296431 (GRCh38)
13:108948779 (GRCh37)
Canonical SPDI:: NC_000013.11:108296430:G:A,NC_000013.11:108296430:G:C
Gene:: TNFSF13B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000015/2 (GnomAD)
HGVS:: NC_000013.11:g.108296431G>A, NC_000013.11:g.108296431G>C, NC_000013.10:g.108948779G>A, NC_000013.10:g.108948779G>C, NG_029524.1:g.31803G>A, NG_029524.1:g.31803G>C

Select item 148997297116.

rs1489972971 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:108280001 (GRCh38)
13:108932349 (GRCh37)
Canonical SPDI:: NC_000013.11:108280000:T:C
Gene:: TNFSF13B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.108280001T>C, NC_000013.10:g.108932349T>C, NG_029524.1:g.15373T>C

Select item 148989187817.

rs1489891878 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:108278676 (GRCh38)
13:108931024 (GRCh37)
Canonical SPDI:: NC_000013.11:108278675:T:C
Gene:: TNFSF13B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00038/5 (TOMMO)
HGVS:: NC_000013.11:g.108278676T>C, NC_000013.10:g.108931024T>C, NG_029524.1:g.14048T>C

Select item 148986028618.

rs1489860286 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:108280892 (GRCh38)
13:108933240 (GRCh37)
Canonical SPDI:: NC_000013.11:108280891:A:G
Gene:: TNFSF13B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.108280892A>G, NC_000013.10:g.108933240A>G, NG_029524.1:g.16264A>G

Select item 148973396119.

rs1489733961 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:108287640 (GRCh38)
13:108939988 (GRCh37)
Canonical SPDI:: NC_000013.11:108287639:T:C
Gene:: TNFSF13B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000013.11:g.108287640T>C, NC_000013.10:g.108939988T>C, NG_029524.1:g.23012T>C

Select item 148964646920.

rs1489646469 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:108271948 (GRCh38)
13:108924296 (GRCh37)
Canonical SPDI:: NC_000013.11:108271947:G:A
Gene:: TNFSF13B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.108271948G>A, NC_000013.10:g.108924296G>A, NG_029524.1:g.7320G>A

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