SNP Links for Gene (Select 54971) - SNP

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Select item 14915766251.

rs1491576625 has merged into rs5818659 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTTTT [Show Flanks]
Chromosome:: 16:88056474 (GRCh38)
16:88090080 (GRCh37)
Canonical SPDI:: NC_000016.10:88056461:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000016.10:88056461:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000016.10:88056461:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000016.10:88056461:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000016.10:88056461:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000016.10:88056461:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000016.10:88056461:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000016.10:88056461:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
-=0.251797/1261 (1000Genomes)
-=0.292384/77391 (TOPMED)
HGVS:: NC_000016.10:g.88056474_88056476del, NC_000016.10:g.88056475_88056476del, NC_000016.10:g.88056476del, NC_000016.10:g.88056476dup, NC_000016.10:g.88056475_88056476dup, NC_000016.10:g.88056474_88056476dup, NC_000016.10:g.88056473_88056476dup, NC_000016.10:g.88056469_88056476dup, NC_000016.9:g.88090080_88090082del, NC_000016.9:g.88090081_88090082del, NC_000016.9:g.88090082del, NC_000016.9:g.88090082dup, NC_000016.9:g.88090081_88090082dup, NC_000016.9:g.88090080_88090082dup, NC_000016.9:g.88090079_88090082dup, NC_000016.9:g.88090075_88090082dup, NG_029918.1:g.110043_110045del, NG_029918.1:g.110044_110045del, NG_029918.1:g.110045del, NG_029918.1:g.110045dup, NG_029918.1:g.110044_110045dup, NG_029918.1:g.110043_110045dup, NG_029918.1:g.110042_110045dup, NG_029918.1:g.110038_110045dup

Select item 14915665242.

rs1491566524 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 16:88001257 (GRCh38)
16:88034864 (GRCh37)
Canonical SPDI:: NC_000016.10:88001257:A:AA
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AA=0./0 (ALFA)
HGVS:: NC_000016.10:g.88001258dup, NC_000016.9:g.88034864dup, NG_029918.1:g.54827dup

Select item 14915353683.

rs1491535368 [Homo sapiens]

Variant type:: DELINS
Alleles:: CC>- [Show Flanks]
Chromosome:: 16:88000320 (GRCh38)
16:88033926 (GRCh37)
Canonical SPDI:: NC_000016.10:88000318:CCC:C
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: -=0.0453/33 (Korea1K)
-=0.0493/316 (1000Genomes)
-=0.2786/1750 (TOMMO)
HGVS:: NC_000016.10:g.88000320_88000321del, NC_000016.9:g.88033926_88033927del, NG_029918.1:g.53889_53890del

Select item 14915122454.

rs1491512245 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 16:88041587 (GRCh38)
16:88075193 (GRCh37)
Canonical SPDI:: NC_000016.10:88041585:TGT:T
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.88041587_88041588del, NC_000016.9:g.88075193_88075194del, NG_029918.1:g.95156_95157del

Select item 14914899495.

rs1491489949 has merged into rs11349895 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAA>-,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 16:88006956 (GRCh38)
16:88040562 (GRCh37)
Canonical SPDI:: NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88006947:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAA=0./0 (ALFA)
HGVS:: NC_000016.10:g.88006956_88006970del, NC_000016.10:g.88006959_88006970del, NC_000016.10:g.88006960_88006970del, NC_000016.10:g.88006962_88006970del, NC_000016.10:g.88006963_88006970del, NC_000016.10:g.88006964_88006970del, NC_000016.10:g.88006965_88006970del, NC_000016.10:g.88006966_88006970del, NC_000016.10:g.88006967_88006970del, NC_000016.10:g.88006968_88006970del, NC_000016.10:g.88006969_88006970del, NC_000016.10:g.88006970del, NC_000016.10:g.88006970dup, NC_000016.10:g.88006969_88006970dup, NC_000016.10:g.88006968_88006970dup, NC_000016.10:g.88006967_88006970dup, NC_000016.10:g.88006966_88006970dup, NC_000016.10:g.88006960_88006970dup, NC_000016.10:g.88006951_88006970dup, NC_000016.10:g.88006970_88006971insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000016.9:g.88040562_88040576del, NC_000016.9:g.88040565_88040576del, NC_000016.9:g.88040566_88040576del, NC_000016.9:g.88040568_88040576del, NC_000016.9:g.88040569_88040576del, NC_000016.9:g.88040570_88040576del, NC_000016.9:g.88040571_88040576del, NC_000016.9:g.88040572_88040576del, NC_000016.9:g.88040573_88040576del, NC_000016.9:g.88040574_88040576del, NC_000016.9:g.88040575_88040576del, NC_000016.9:g.88040576del, NC_000016.9:g.88040576dup, NC_000016.9:g.88040575_88040576dup, NC_000016.9:g.88040574_88040576dup, NC_000016.9:g.88040573_88040576dup, NC_000016.9:g.88040572_88040576dup, NC_000016.9:g.88040566_88040576dup, NC_000016.9:g.88040557_88040576dup, NC_000016.9:g.88040576_88040577insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029918.1:g.60525_60539del, NG_029918.1:g.60528_60539del, NG_029918.1:g.60529_60539del, NG_029918.1:g.60531_60539del, NG_029918.1:g.60532_60539del, NG_029918.1:g.60533_60539del, NG_029918.1:g.60534_60539del, NG_029918.1:g.60535_60539del, NG_029918.1:g.60536_60539del, NG_029918.1:g.60537_60539del, NG_029918.1:g.60538_60539del, NG_029918.1:g.60539del, NG_029918.1:g.60539dup, NG_029918.1:g.60538_60539dup, NG_029918.1:g.60537_60539dup, NG_029918.1:g.60536_60539dup, NG_029918.1:g.60535_60539dup, NG_029918.1:g.60529_60539dup, NG_029918.1:g.60520_60539dup, NG_029918.1:g.60539_60540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14914494146.

rs1491449414 has merged into rs59989652 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 16:88029319 (GRCh38)
16:88062925 (GRCh37)
Canonical SPDI:: NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88029306:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
-=0.01/5 (NorthernSweden)
HGVS:: NC_000016.10:g.88029319_88029328del, NC_000016.10:g.88029320_88029328del, NC_000016.10:g.88029321_88029328del, NC_000016.10:g.88029322_88029328del, NC_000016.10:g.88029323_88029328del, NC_000016.10:g.88029324_88029328del, NC_000016.10:g.88029325_88029328del, NC_000016.10:g.88029326_88029328del, NC_000016.10:g.88029327_88029328del, NC_000016.10:g.88029328del, NC_000016.10:g.88029328dup, NC_000016.10:g.88029327_88029328dup, NC_000016.10:g.88029326_88029328dup, NC_000016.10:g.88029325_88029328dup, NC_000016.10:g.88029319_88029328dup, NC_000016.9:g.88062925_88062934del, NC_000016.9:g.88062926_88062934del, NC_000016.9:g.88062927_88062934del, NC_000016.9:g.88062928_88062934del, NC_000016.9:g.88062929_88062934del, NC_000016.9:g.88062930_88062934del, NC_000016.9:g.88062931_88062934del, NC_000016.9:g.88062932_88062934del, NC_000016.9:g.88062933_88062934del, NC_000016.9:g.88062934del, NC_000016.9:g.88062934dup, NC_000016.9:g.88062933_88062934dup, NC_000016.9:g.88062932_88062934dup, NC_000016.9:g.88062931_88062934dup, NC_000016.9:g.88062925_88062934dup, NG_029918.1:g.82888_82897del, NG_029918.1:g.82889_82897del, NG_029918.1:g.82890_82897del, NG_029918.1:g.82891_82897del, NG_029918.1:g.82892_82897del, NG_029918.1:g.82893_82897del, NG_029918.1:g.82894_82897del, NG_029918.1:g.82895_82897del, NG_029918.1:g.82896_82897del, NG_029918.1:g.82897del, NG_029918.1:g.82897dup, NG_029918.1:g.82896_82897dup, NG_029918.1:g.82895_82897dup, NG_029918.1:g.82894_82897dup, NG_029918.1:g.82888_82897dup

Select item 14914304977.

rs1491430497 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 16:88006947 (GRCh38)
16:88040553 (GRCh37)
Canonical SPDI:: NC_000016.10:88006946:CA:
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.01939/230 (ALFA)
-=0.00457/128 (TOMMO)
HGVS:: NC_000016.10:g.88006947_88006948del, NC_000016.9:g.88040553_88040554del, NG_029918.1:g.60516_60517del

Select item 14913519018.

rs1491351901 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 16:88041586 (GRCh38)
16:88075193 (GRCh37)
Canonical SPDI:: NC_000016.10:88041586:G:GG
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GG=0.001119/5 (ALFA)
G=0.000029/4 (GnomAD)
HGVS:: NC_000016.10:g.88041587dup, NC_000016.9:g.88075193dup, NG_029918.1:g.95156dup

Select item 14912137599.

rs1491213759 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 16:88056462 (GRCh38)
16:88090069 (GRCh37)
Canonical SPDI:: NC_000016.10:88056462::C
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
C=0.000209/5 (GnomAD)
C=0.000248/4 (TOMMO)
HGVS:: NC_000016.10:g.88056462_88056463insC, NC_000016.9:g.88090068_88090069insC, NG_029918.1:g.110031_110032insC

Select item 149119731410.

rs1491197314 has merged into rs59786663 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTCTTTAAGTAATTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTCCCTAAAATTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTCCTTAAATTATGATATTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTCTTTAAATTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTAAAATTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTAAATTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 16:87976484 (GRCh38)
16:88010090 (GRCh37)
Canonical SPDI:: NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTCTTTAAGTAATTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTCCCTAAAATTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTCCTTAAATTATGATATTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTAAATTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTAAAATTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAAATTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:87976474:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: BANP (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
-=0.4227/2117 (1000Genomes)
HGVS:: NC_000016.10:g.87976484_87976489del, NC_000016.10:g.87976485_87976489del, NC_000016.10:g.87976486_87976489del, NC_000016.10:g.87976487_87976489del, NC_000016.10:g.87976488_87976489del, NC_000016.10:g.87976489del, NC_000016.10:g.87976489dup, NC_000016.10:g.87976488_87976489dup, NC_000016.10:g.87976487_87976489dup, NC_000016.10:g.87976486_87976489dup, NC_000016.10:g.87976485_87976489dup, NC_000016.10:g.87976484_87976489dup, NC_000016.10:g.87976483_87976489dup, NC_000016.10:g.87976482_87976489dup, NC_000016.10:g.87976481_87976489dup, NC_000016.10:g.87976480_87976489dup, NC_000016.10:g.87976479_87976489dup, NC_000016.10:g.87976475_87976489T[26]CTTTAAGTAATTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000016.10:g.87976478_87976489dup, NC_000016.10:g.87976475_87976489T[27]CCCTAAAATTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000016.10:g.87976475_87976489T[27]CCTTAAATTATGATATTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000016.10:g.87976477_87976489dup, NC_000016.10:g.87976475_87976489T[28]CTTTAAATTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000016.10:g.87976476_87976489dup, NC_000016.10:g.87976475_87976489T[29]A[4]T[24], NC_000016.10:g.87976475_87976489dup, NC_000016.10:g.87976489_87976490insTTTTTTTTTTTTTTTTTTTT, NC_000016.10:g.87976475_87976489T[35]AAATTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000016.10:g.87976475_87976489T[38]ATTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000016.10:g.87976489_87976490insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.10:g.87976489_87976490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.10:g.87976489_87976490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.10:g.87976489_87976490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.10:g.87976489_87976490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.10:g.87976489_87976490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.10:g.87976489_87976490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.10:g.87976489_87976490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.10:g.87976489_87976490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.10:g.87976489_87976490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.9:g.88010090_88010095del, NC_000016.9:g.88010091_88010095del, NC_000016.9:g.88010092_88010095del, NC_000016.9:g.88010093_88010095del, NC_000016.9:g.88010094_88010095del, NC_000016.9:g.88010095del, NC_000016.9:g.88010095dup, NC_000016.9:g.88010094_88010095dup, NC_000016.9:g.88010093_88010095dup, NC_000016.9:g.88010092_88010095dup, NC_000016.9:g.88010091_88010095dup, NC_000016.9:g.88010090_88010095dup, NC_000016.9:g.88010089_88010095dup, NC_000016.9:g.88010088_88010095dup, NC_000016.9:g.88010087_88010095dup, NC_000016.9:g.88010086_88010095dup, NC_000016.9:g.88010085_88010095dup, NC_000016.9:g.88010081_88010095T[26]CTTTAAGTAATTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000016.9:g.88010084_88010095dup, NC_000016.9:g.88010081_88010095T[27]CCCTAAAATTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000016.9:g.88010081_88010095T[27]CCTTAAATTATGATATTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000016.9:g.88010083_88010095dup, NC_000016.9:g.88010081_88010095T[28]CTTTAAATTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000016.9:g.88010082_88010095dup, NC_000016.9:g.88010081_88010095T[29]A[4]T[24], NC_000016.9:g.88010081_88010095dup, NC_000016.9:g.88010095_88010096insTTTTTTTTTTTTTTTTTTTT, NC_000016.9:g.88010081_88010095T[35]AAATTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000016.9:g.88010081_88010095T[38]ATTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000016.9:g.88010095_88010096insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.9:g.88010095_88010096insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.9:g.88010095_88010096insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.9:g.88010095_88010096insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.9:g.88010095_88010096insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.9:g.88010095_88010096insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.9:g.88010095_88010096insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.9:g.88010095_88010096insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.9:g.88010095_88010096insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.9:g.88010095_88010096insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029918.1:g.30053_30058del, NG_029918.1:g.30054_30058del, NG_029918.1:g.30055_30058del, NG_029918.1:g.30056_30058del, NG_029918.1:g.30057_30058del, NG_029918.1:g.30058del, NG_029918.1:g.30058dup, NG_029918.1:g.30057_30058dup, NG_029918.1:g.30056_30058dup, NG_029918.1:g.30055_30058dup, NG_029918.1:g.30054_30058dup, NG_029918.1:g.30053_30058dup, NG_029918.1:g.30052_30058dup, NG_029918.1:g.30051_30058dup, NG_029918.1:g.30050_30058dup, NG_029918.1:g.30049_30058dup, NG_029918.1:g.30048_30058dup, NG_029918.1:g.30044_30058T[26]CTTTAAGTAATTTTTTTTTTTTTTTTTTTTTTTT[1], NG_029918.1:g.30047_30058dup, NG_029918.1:g.30044_30058T[27]CCCTAAAATTTTTTTTTTTTTTTTTTTTTTTT[1], NG_029918.1:g.30044_30058T[27]CCTTAAATTATGATATTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_029918.1:g.30046_30058dup, NG_029918.1:g.30044_30058T[28]CTTTAAATTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_029918.1:g.30045_30058dup, NG_029918.1:g.30044_30058T[29]A[4]T[24], NG_029918.1:g.30044_30058dup, NG_029918.1:g.30058_30059insTTTTTTTTTTTTTTTTTTTT, NG_029918.1:g.30044_30058T[35]AAATTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_029918.1:g.30044_30058T[38]ATTTTTTTTTTTTTTTTTTTTTTTT[1], NG_029918.1:g.30058_30059insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029918.1:g.30058_30059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029918.1:g.30058_30059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029918.1:g.30058_30059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029918.1:g.30058_30059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029918.1:g.30058_30059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029918.1:g.30058_30059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029918.1:g.30058_30059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029918.1:g.30058_30059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029918.1:g.30058_30059insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149115665211.

rs1491156652 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 16:88001257 (GRCh38)
16:88034863 (GRCh37)
Canonical SPDI:: NC_000016.10:88001256:TA:
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: -=0.158333/95 (NorthernSweden)
-=0.162334/20544 (GnomAD)
-=0.236727/1516 (1000Genomes)
-=0.313761/5237 (TOMMO)
HGVS:: NC_000016.10:g.88001257_88001258del, NC_000016.9:g.88034863_88034864del, NG_029918.1:g.54826_54827del

Select item 149114752612.

rs1491147526 [Homo sapiens]

Variant type:: INS
Alleles:: ->AT [Show Flanks]
Chromosome:: 16:88000319 (GRCh38)
16:88033926 (GRCh37)
Canonical SPDI:: NC_000016.10:88000319::AT
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: AT=0.0041/26 (TOMMO)
HGVS:: NC_000016.10:g.88000319_88000320insAT, NC_000016.9:g.88033925_88033926insAT, NG_029918.1:g.53888_53889insAT

Select item 149111995713.

rs1491119957 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 16:88029306 (GRCh38)
16:88062912 (GRCh37)
Canonical SPDI:: NC_000016.10:88029305:CA:
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00101/12 (ALFA)
-=0.00061/17 (TOMMO)
HGVS:: NC_000016.10:g.88029306_88029307del, NC_000016.9:g.88062912_88062913del, NG_029918.1:g.82875_82876del

Select item 149109311114.

rs1491093111 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTTTTTTTTT [Show Flanks]
Chromosome:: 16:87976475 (GRCh38)
16:88010082 (GRCh37)
Canonical SPDI:: NC_000016.10:87976475:TTTTTTTTT:TTTTTTTTTGTTTTTTTTT
Gene:: BANP (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TTTTTTTTTGTTTTTTTTT=0./0 (ALFA)
TTTTTTTTTG=0.00017/2 (GnomAD)
HGVS:: NC_000016.10:g.87976476_87976484T[9]GTTTTTTTTT[1], NC_000016.9:g.88010082_88010090T[9]GTTTTTTTTT[1], NG_029918.1:g.30045_30053T[9]GTTTTTTTTT[1]

Select item 149108250615.

rs1491082506 has merged into rs60313647 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA [Show Flanks]
Chromosome:: 16:88029621 (GRCh38)
16:88063227 (GRCh37)
Canonical SPDI:: NC_000016.10:88029610:AAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000016.10:88029610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:88029610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:88029610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:88029610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000016.10:88029610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:88029610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000016.10:88029610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000016.10:88029610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000016.10:88029610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000016.10:88029610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
-=0.3091/1548 (1000Genomes)
HGVS:: NC_000016.10:g.88029621_88029627del, NC_000016.10:g.88029623_88029627del, NC_000016.10:g.88029624_88029627del, NC_000016.10:g.88029625_88029627del, NC_000016.10:g.88029626_88029627del, NC_000016.10:g.88029627del, NC_000016.10:g.88029627dup, NC_000016.10:g.88029626_88029627dup, NC_000016.10:g.88029625_88029627dup, NC_000016.10:g.88029624_88029627dup, NC_000016.10:g.88029623_88029627dup, NC_000016.9:g.88063227_88063233del, NC_000016.9:g.88063229_88063233del, NC_000016.9:g.88063230_88063233del, NC_000016.9:g.88063231_88063233del, NC_000016.9:g.88063232_88063233del, NC_000016.9:g.88063233del, NC_000016.9:g.88063233dup, NC_000016.9:g.88063232_88063233dup, NC_000016.9:g.88063231_88063233dup, NC_000016.9:g.88063230_88063233dup, NC_000016.9:g.88063229_88063233dup, NG_029918.1:g.83190_83196del, NG_029918.1:g.83192_83196del, NG_029918.1:g.83193_83196del, NG_029918.1:g.83194_83196del, NG_029918.1:g.83195_83196del, NG_029918.1:g.83196del, NG_029918.1:g.83196dup, NG_029918.1:g.83195_83196dup, NG_029918.1:g.83194_83196dup, NG_029918.1:g.83193_83196dup, NG_029918.1:g.83192_83196dup

Select item 149104368616.

rs1491043686 [Homo sapiens]

Variant type:: INS
Alleles:: ->T [Show Flanks]
Chromosome:: 16:88057756 (GRCh38)
16:88091363 (GRCh37)
Canonical SPDI:: NC_000016.10:88057756::T
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.00063/1 (GnomAD)
HGVS:: NC_000016.10:g.88057756_88057757insT, NC_000016.9:g.88091362_88091363insT, NG_029918.1:g.111325_111326insT

Select item 149100757717.

rs1491007577 has merged into rs10624509 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA [Show Flanks]
Chromosome:: 16:87971027 (GRCh38)
16:88004633 (GRCh37)
Canonical SPDI:: NC_000016.10:87971016:AAAAAAAAAAAAAA:AAAAAAAAAA,NC_000016.10:87971016:AAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000016.10:87971016:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:87971016:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:87971016:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000016.10:87971016:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:87971016:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000016.10:87971016:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000016.10:87971016:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000016.10:87971016:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA
Gene:: BANP (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000016.10:g.87971027_87971030del, NC_000016.10:g.87971028_87971030del, NC_000016.10:g.87971029_87971030del, NC_000016.10:g.87971030del, NC_000016.10:g.87971030dup, NC_000016.10:g.87971029_87971030dup, NC_000016.10:g.87971028_87971030dup, NC_000016.10:g.87971027_87971030dup, NC_000016.10:g.87971026_87971030dup, NC_000016.10:g.87971025_87971030dup, NC_000016.9:g.88004633_88004636del, NC_000016.9:g.88004634_88004636del, NC_000016.9:g.88004635_88004636del, NC_000016.9:g.88004636del, NC_000016.9:g.88004636dup, NC_000016.9:g.88004635_88004636dup, NC_000016.9:g.88004634_88004636dup, NC_000016.9:g.88004633_88004636dup, NC_000016.9:g.88004632_88004636dup, NC_000016.9:g.88004631_88004636dup, NG_029918.1:g.24596_24599del, NG_029918.1:g.24597_24599del, NG_029918.1:g.24598_24599del, NG_029918.1:g.24599del, NG_029918.1:g.24599dup, NG_029918.1:g.24598_24599dup, NG_029918.1:g.24597_24599dup, NG_029918.1:g.24596_24599dup, NG_029918.1:g.24595_24599dup, NG_029918.1:g.24594_24599dup

Select item 149100563118.

rs1491005631 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: 16:87968499 (GRCh38)
16:88002105 (GRCh37)
Canonical SPDI:: NC_000016.10:87968497:ATA:A
Gene:: BANP (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.005058/60 (ALFA)
-=0.004696/655 (GnomAD)
HGVS:: NC_000016.10:g.87968499_87968500del, NC_000016.9:g.88002105_88002106del, NG_029918.1:g.22068_22069del

Select item 149097089819.

rs1490970898 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 16:88035866 (GRCh38)
16:88069472 (GRCh37)
Canonical SPDI:: NC_000016.10:88035865:G:A,NC_000016.10:88035865:G:T
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.88035866G>A, NC_000016.10:g.88035866G>T, NC_000016.9:g.88069472G>A, NC_000016.9:g.88069472G>T, NG_029918.1:g.89435G>A, NG_029918.1:g.89435G>T

Select item 149096651720.

rs1490966517 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:88072978 (GRCh38)
16:88106584 (GRCh37)
Canonical SPDI:: NC_000016.10:88072977:C:T
Gene:: BANP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000016.10:g.88072978C>T, NC_000016.9:g.88106584C>T, NG_029918.1:g.126547C>T

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