SNP Links for Gene (Select 148741) - SNP

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Select item 14915284571.

rs1491528457 [Homo sapiens]

Variant type:: DEL
Alleles:: GC>- [Show Flanks]
Chromosome:: 1:145870891 (GRCh38)
1:145564189 (GRCh37)
Canonical SPDI:: NC_000001.11:145870890:GC:
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.145870891_145870892del, NW_003871055.3:g.2686304_2686305del, NC_000001.10:g.145564189_145564190del

Select item 14913844342.

rs1491384434 [Homo sapiens]

Variant type:: DEL
Alleles:: GC>- [Show Flanks]
Chromosome:: 1:145879948 (GRCh38)
1:145555127 (GRCh37)
Canonical SPDI:: NC_000001.11:145879947:GC:
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.145879948_145879949del, NW_003871055.3:g.2695361_2695362del, NC_000001.10:g.145555127_145555128del

Select item 14913368883.

rs1491336888 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 1:145879948 (GRCh38)
1:145555124 (GRCh37)
Canonical SPDI:: NC_000001.11:145879948:CCCC:CCCCC
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CCCCC=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.145879952dup, NW_003871055.3:g.2695365dup, NC_000001.10:g.145555127dup

Select item 14912611024.

rs1491261102 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CCA [Show Flanks]
Chromosome:: 1:145870891 (GRCh38)
1:145564184 (GRCh37)
Canonical SPDI:: NC_000001.11:145870891:CCACCA:CCACCACCA
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CCACCACCA=0./0 (ALFA)
CCA=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.145870892CCA[3], NW_003871055.3:g.2686305CCA[3], NC_000001.10:g.145564184TGG[3]

Select item 14911642795.

rs1491164279 has merged into rs59433424 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:145871163 (GRCh38)
1:145563909 (GRCh37)
Canonical SPDI:: NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:145871153:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
AAAAAAAAAAAAAAAA=0./0 (GENOME_DK)
HGVS:: NC_000001.11:g.145871163_145871181del, NC_000001.11:g.145871165_145871181del, NC_000001.11:g.145871166_145871181del, NC_000001.11:g.145871167_145871181del, NC_000001.11:g.145871168_145871181del, NC_000001.11:g.145871169_145871181del, NC_000001.11:g.145871170_145871181del, NC_000001.11:g.145871171_145871181del, NC_000001.11:g.145871172_145871181del, NC_000001.11:g.145871173_145871181del, NC_000001.11:g.145871174_145871181del, NC_000001.11:g.145871175_145871181del, NC_000001.11:g.145871176_145871181del, NC_000001.11:g.145871177_145871181del, NC_000001.11:g.145871178_145871181del, NC_000001.11:g.145871179_145871181del, NC_000001.11:g.145871180_145871181del, NC_000001.11:g.145871181del, NC_000001.11:g.145871181dup, NC_000001.11:g.145871180_145871181dup, NC_000001.11:g.145871179_145871181dup, NC_000001.11:g.145871178_145871181dup, NC_000001.11:g.145871154_145871181T[32]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.11:g.145871177_145871181dup, NC_000001.11:g.145871154_145871181T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.11:g.145871154_145871181T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.11:g.145871154_145871181T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.11:g.145871176_145871181dup, NC_000001.11:g.145871175_145871181dup, NC_000001.11:g.145871174_145871181dup, NC_000001.11:g.145871154_145871181T[36]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.11:g.145871173_145871181dup, NC_000001.11:g.145871172_145871181dup, NC_000001.11:g.145871171_145871181dup, NC_000001.11:g.145871170_145871181dup, NC_000001.11:g.145871169_145871181dup, NC_000001.11:g.145871168_145871181dup, NC_000001.11:g.145871167_145871181dup, NC_000001.11:g.145871166_145871181dup, NC_000001.11:g.145871165_145871181dup, NC_000001.11:g.145871163_145871181dup, NC_000001.11:g.145871160_145871181dup, NC_000001.11:g.145871159_145871181dup, NC_000001.11:g.145871157_145871181dup, NC_000001.11:g.145871156_145871181dup, NC_000001.11:g.145871155_145871181dup, NC_000001.11:g.145871154_145871181dup, NC_000001.11:g.145871181_145871182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.145871181_145871182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.145871181_145871182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.145871181_145871182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.145871181_145871182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.145871181_145871182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.145871181_145871182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.145871181_145871182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.145871181_145871182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.145871181_145871182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.145871181_145871182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.2686576_2686594del, NW_003871055.3:g.2686578_2686594del, NW_003871055.3:g.2686579_2686594del, NW_003871055.3:g.2686580_2686594del, NW_003871055.3:g.2686581_2686594del, NW_003871055.3:g.2686582_2686594del, NW_003871055.3:g.2686583_2686594del, NW_003871055.3:g.2686584_2686594del, NW_003871055.3:g.2686585_2686594del, NW_003871055.3:g.2686586_2686594del, NW_003871055.3:g.2686587_2686594del, NW_003871055.3:g.2686588_2686594del, NW_003871055.3:g.2686589_2686594del, NW_003871055.3:g.2686590_2686594del, NW_003871055.3:g.2686591_2686594del, NW_003871055.3:g.2686592_2686594del, NW_003871055.3:g.2686593_2686594del, NW_003871055.3:g.2686594del, NW_003871055.3:g.2686594dup, NW_003871055.3:g.2686593_2686594dup, NW_003871055.3:g.2686592_2686594dup, NW_003871055.3:g.2686591_2686594dup, NW_003871055.3:g.2686567_2686594T[32]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NW_003871055.3:g.2686590_2686594dup, NW_003871055.3:g.2686567_2686594T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NW_003871055.3:g.2686567_2686594T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NW_003871055.3:g.2686567_2686594T[33]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NW_003871055.3:g.2686589_2686594dup, NW_003871055.3:g.2686588_2686594dup, NW_003871055.3:g.2686587_2686594dup, NW_003871055.3:g.2686567_2686594T[36]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NW_003871055.3:g.2686586_2686594dup, NW_003871055.3:g.2686585_2686594dup, NW_003871055.3:g.2686584_2686594dup, NW_003871055.3:g.2686583_2686594dup, NW_003871055.3:g.2686582_2686594dup, NW_003871055.3:g.2686581_2686594dup, NW_003871055.3:g.2686580_2686594dup, NW_003871055.3:g.2686579_2686594dup, NW_003871055.3:g.2686578_2686594dup, NW_003871055.3:g.2686576_2686594dup, NW_003871055.3:g.2686573_2686594dup, NW_003871055.3:g.2686572_2686594dup, NW_003871055.3:g.2686570_2686594dup, NW_003871055.3:g.2686569_2686594dup, NW_003871055.3:g.2686568_2686594dup, NW_003871055.3:g.2686567_2686594dup, NW_003871055.3:g.2686594_2686595insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.2686594_2686595insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.2686594_2686595insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.2686594_2686595insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.2686594_2686595insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.2686594_2686595insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.2686594_2686595insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.2686594_2686595insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.2686594_2686595insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.2686594_2686595insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003871055.3:g.2686594_2686595insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.145563909_145563927del, NC_000001.10:g.145563911_145563927del, NC_000001.10:g.145563912_145563927del, NC_000001.10:g.145563913_145563927del, NC_000001.10:g.145563914_145563927del, NC_000001.10:g.145563915_145563927del, NC_000001.10:g.145563916_145563927del, NC_000001.10:g.145563917_145563927del, NC_000001.10:g.145563918_145563927del, NC_000001.10:g.145563919_145563927del, NC_000001.10:g.145563920_145563927del, NC_000001.10:g.145563921_145563927del, NC_000001.10:g.145563922_145563927del, NC_000001.10:g.145563923_145563927del, NC_000001.10:g.145563924_145563927del, NC_000001.10:g.145563925_145563927del, NC_000001.10:g.145563926_145563927del, NC_000001.10:g.145563927del, NC_000001.10:g.145563927dup, NC_000001.10:g.145563926_145563927dup, NC_000001.10:g.145563925_145563927dup, NC_000001.10:g.145563924_145563927dup, NC_000001.10:g.145563900_145563927A[36]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000001.10:g.145563923_145563927dup, NC_000001.10:g.145563900_145563927A[35]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000001.10:g.145563900_145563927A[36]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000001.10:g.145563900_145563927A[39]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000001.10:g.145563922_145563927dup, NC_000001.10:g.145563921_145563927dup, NC_000001.10:g.145563920_145563927dup, NC_000001.10:g.145563900_145563927A[36]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000001.10:g.145563919_145563927dup, NC_000001.10:g.145563918_145563927dup, NC_000001.10:g.145563917_145563927dup, NC_000001.10:g.145563916_145563927dup, NC_000001.10:g.145563915_145563927dup, NC_000001.10:g.145563914_145563927dup, NC_000001.10:g.145563913_145563927dup, NC_000001.10:g.145563912_145563927dup, NC_000001.10:g.145563911_145563927dup, NC_000001.10:g.145563909_145563927dup, NC_000001.10:g.145563906_145563927dup, NC_000001.10:g.145563905_145563927dup, NC_000001.10:g.145563903_145563927dup, NC_000001.10:g.145563902_145563927dup, NC_000001.10:g.145563901_145563927dup, NC_000001.10:g.145563900_145563927dup, NC_000001.10:g.145563927_145563928insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.145563927_145563928insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.145563927_145563928insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.145563927_145563928insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.145563927_145563928insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.145563927_145563928insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.145563927_145563928insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.145563927_145563928insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.145563927_145563928insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.145563927_145563928insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.145563927_145563928insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14907729846.

rs1490772984 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:145877117 (GRCh38)
1:145557964 (GRCh37)
Canonical SPDI:: NC_000001.11:145877116:A:T
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.145877117A>T, NW_003871055.3:g.2692530A>T, NC_000001.10:g.145557964T>A

Select item 14904062887.

rs1490406288 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:145884430 (GRCh38)
1:145550646 (GRCh37)
Canonical SPDI:: NC_000001.11:145884429:C:T
Gene:: ANKRD35 (Varview), LOC107985593 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.145884430C>T, NW_003871055.3:g.2699843C>T, NC_000001.10:g.145550646G>A

Select item 14903544718.

rs1490354471 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:145883321 (GRCh38)
1:145551755 (GRCh37)
Canonical SPDI:: NC_000001.11:145883320:G:A,NC_000001.11:145883320:G:T
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.145883321G>A, NC_000001.11:g.145883321G>T, NW_003871055.3:g.2698734G>A, NW_003871055.3:g.2698734G>T, NC_000001.10:g.145551755C>T, NC_000001.10:g.145551755C>A

Select item 14902833349.

rs1490283334 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:145877512 (GRCh38)
1:145557568 (GRCh37)
Canonical SPDI:: NC_000001.11:145877511:T:C
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.145877512T>C, NW_003871055.3:g.2692925T>C, NC_000001.10:g.145557568A>G

Select item 149016181610.

rs1490161816 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:145870232 (GRCh38)
1:145564851 (GRCh37)
Canonical SPDI:: NC_000001.11:145870231:C:G,NC_000001.11:145870231:C:T
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.145870232C>G, NC_000001.11:g.145870232C>T, NW_003871055.3:g.2685645C>G, NW_003871055.3:g.2685645C>T, NC_000001.10:g.145564851G>C, NC_000001.10:g.145564851G>A

Select item 149007331411.

rs1490073314 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 1:145869189 (GRCh38)
1:145565897 (GRCh37)
Canonical SPDI:: NC_000001.11:145869187:TGT:T
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.00003/4 (GnomAD)
HGVS:: NC_000001.11:g.145869189_145869190del, NW_003871055.3:g.2684602_2684603del, NC_000001.10:g.145565897_145565898del

Select item 149007063612.

rs1490070636 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:145885427 (GRCh38)
1:145549648 (GRCh37)
Canonical SPDI:: NC_000001.11:145885426:G:A
Gene:: ANKRD35 (Varview), LOC107985593 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000001.11:g.145885427G>A, NW_003871055.3:g.2700840G>A, NC_000001.10:g.145549648C>T

Select item 148999969313.

rs1489999693 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:145869754 (GRCh38)
1:145565332 (GRCh37)
Canonical SPDI:: NC_000001.11:145869753:C:A
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.145869754C>A, NW_003871055.3:g.2685167C>A, NC_000001.10:g.145565332G>T

Select item 148990906814.

rs1489909068 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:145868779 (GRCh38)
1:145566307 (GRCh37)
Canonical SPDI:: NC_000001.11:145868778:C:T
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.145868779C>T, NW_003871055.3:g.2684192C>T, NC_000001.10:g.145566307G>A

Select item 148990625515.

rs1489906255 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:145884907 (GRCh38)
1:145550168 (GRCh37)
Canonical SPDI:: NC_000001.11:145884906:C:G,NC_000001.11:145884906:C:T
Gene:: ANKRD35 (Varview), LOC107985593 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.145884907C>G, NC_000001.11:g.145884907C>T, NW_003871055.3:g.2700320C>G, NW_003871055.3:g.2700320C>T, NC_000001.10:g.145550168G>C, NC_000001.10:g.145550168G>A

Select item 148973974816.

rs1489739748 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 1:145876490 (GRCh38)
1:145558591 (GRCh37)
Canonical SPDI:: NC_000001.11:145876489:G:A,NC_000001.11:145876489:G:C,NC_000001.11:145876489:G:T
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.145876490G>A, NC_000001.11:g.145876490G>C, NC_000001.11:g.145876490G>T, NW_003871055.3:g.2691903G>A, NW_003871055.3:g.2691903G>C, NW_003871055.3:g.2691903G>T, NC_000001.10:g.145558591C>T, NC_000001.10:g.145558591C>G, NC_000001.10:g.145558591C>A

Select item 148922660417.

rs1489226604 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:145881837 (GRCh38)
1:145553239 (GRCh37)
Canonical SPDI:: NC_000001.11:145881836:C:A
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000014/2 (GnomAD)
A=0.00003/8 (TOPMED)
HGVS:: NC_000001.11:g.145881837C>A, NW_003871055.3:g.2697250C>A, NC_000001.10:g.145553239G>T

Select item 148914802618.

rs1489148026 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:145878975 (GRCh38)
1:145556105 (GRCh37)
Canonical SPDI:: NC_000001.11:145878974:T:C
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000026/7 (TOPMED)
HGVS:: NC_000001.11:g.145878975T>C, NW_003871055.3:g.2694388T>C, NC_000001.10:g.145556105A>G

Select item 148903631919.

rs1489036319 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:145867054 (GRCh38)
1:145568032 (GRCh37)
Canonical SPDI:: NC_000001.11:145867053:T:C
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.145867054T>C, NW_003871055.3:g.2682467T>C, NC_000001.10:g.145568032A>G

Select item 148895110420.

rs1488951104 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:145882518 (GRCh38)
1:145552558 (GRCh37)
Canonical SPDI:: NC_000001.11:145882517:C:G
Gene:: ANKRD35 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.145882518C>G, NW_003871055.3:g.2697931C>G, NC_000001.10:g.145552558G>C

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