SNP Links for Gene (Select 729911) - SNP

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Select item 14915677641.

rs1491567764 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 15:79281993 (GRCh38)
15:79574335 (GRCh37)
Canonical SPDI:: NC_000015.10:79281992:CT:
Gene:: ANKRD34C (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00004/1 (TOMMO)
-=0.00008/2 (GnomAD)
HGVS:: NC_000015.10:g.79281993_79281994del, NC_000015.9:g.79574335_79574336del

Select item 14915495292.

rs1491549529 [Homo sapiens]

Variant type:: DEL
Alleles:: CG>- [Show Flanks]
Chromosome:: 15:79277269 (GRCh38)
15:79569611 (GRCh37)
Canonical SPDI:: NC_000015.10:79277268:CG:
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000084/1 (ALFA)
-=0.000021/3 (GnomAD)
-=0.000035/1 (TOMMO)
HGVS:: NC_000015.10:g.79277269_79277270del, NC_000015.9:g.79569611_79569612del

Select item 14915473673.

rs1491547367 has merged into rs371497172 [Homo sapiens]

Variant type:: DELINS
Alleles:: AG>-,AGAG [Show Flanks]
Chromosome:: 15:79230968 (GRCh38)
15:79523310 (GRCh37)
Canonical SPDI:: NC_000015.10:79230955:AGAGAGAGAGAGAG:AGAGAGAGAGAG,NC_000015.10:79230955:AGAGAGAGAGAGAG:AGAGAGAGAGAGAGAG
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAGAGAGAGAGAGAG=0./0 (ALFA)
-=0.000166/44 (TOPMED)
HGVS:: NC_000015.10:g.79230956AG[6], NC_000015.10:g.79230956AG[8], NC_000015.9:g.79523298AG[6], NC_000015.9:g.79523298AG[8]

Select item 14915215824.

rs1491521582 [Homo sapiens]

Variant type:: DEL
Alleles:: CC>- [Show Flanks]
Chromosome:: 15:79278007 (GRCh38)
15:79570349 (GRCh37)
Canonical SPDI:: NC_000015.10:79278006:CC:
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00009/6 (GnomAD)
-=0.00029/4 (TOMMO)
HGVS:: NC_000015.10:g.79278007_79278008del, NC_000015.9:g.79570349_79570350del

Select item 14914984385.

rs1491498438 [Homo sapiens]

Variant type:: INS
Alleles:: ->C,G [Show Flanks]
Chromosome:: 15:79199681 (GRCh38)
15:79492024 (GRCh37)
Canonical SPDI:: NC_000015.10:79199681::C,NC_000015.10:79199681::G
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NC_000015.10:g.79199681_79199682insC, NC_000015.10:g.79199681_79199682insG, NC_000015.9:g.79492023_79492024insC, NC_000015.9:g.79492023_79492024insG

Select item 14914887166.

rs1491488716 has merged into rs371532586 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT [Show Flanks]
Chromosome:: 15:79203923 (GRCh38)
15:79496265 (GRCh37)
Canonical SPDI:: NC_000015.10:79203913:TTTTTTTTTTTT:TTTTTTTTT,NC_000015.10:79203913:TTTTTTTTTTTT:TTTTTTTTTT,NC_000015.10:79203913:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000015.10:79203913:TTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000015.10:79203913:TTTTTTTTTTTT:TTTTTTTTTTTTTT
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
T=0.001667/1 (NorthernSweden)
HGVS:: NC_000015.10:g.79203923_79203925del, NC_000015.10:g.79203924_79203925del, NC_000015.10:g.79203925del, NC_000015.10:g.79203925dup, NC_000015.10:g.79203924_79203925dup, NC_000015.9:g.79496265_79496267del, NC_000015.9:g.79496266_79496267del, NC_000015.9:g.79496267del, NC_000015.9:g.79496267dup, NC_000015.9:g.79496266_79496267dup

Select item 14914450407.

rs1491445040 [Homo sapiens]

Variant type:: INS
Alleles:: ->TT,TTT,TTTCTT [Show Flanks]
Chromosome:: 15:79278007 (GRCh38)
15:79570350 (GRCh37)
Canonical SPDI:: NC_000015.10:79278007::TT,NC_000015.10:79278007::TTT,NC_000015.10:79278007::TTTCTT
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTCTT=0./0 (ALFA)
TTT=0.00176/119 (GnomAD)
TTT=0.01269/213 (TOMMO)
TTT=0.01365/25 (Korea1K)
HGVS:: NC_000015.10:g.79278007_79278008insTT, NC_000015.10:g.79278007_79278008insTTT, NC_000015.10:g.79278007_79278008insTTTCTT, NC_000015.9:g.79570349_79570350insTT, NC_000015.9:g.79570349_79570350insTTT, NC_000015.9:g.79570349_79570350insTTTCTT

Select item 14914369438.

rs1491436943 has merged into rs1241871129 [Homo sapiens]

Variant type:: DELINS
Alleles:: CGTG>-,CGTGCGTG [Show Flanks]
Chromosome:: 15:79233445 (GRCh38)
15:79525787 (GRCh37)
Canonical SPDI:: NC_000015.10:79233441:GTGCGTG:GTG,NC_000015.10:79233441:GTGCGTG:GTGCGTGCGTG
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGCGTGCGTG=0./0 (ALFA)
-=0.00008/4 (GnomAD)
-=0.00021/3 (TOMMO)
-=0.00117/2 (Korea1K)
HGVS:: NC_000015.10:g.79233445_79233448del, NC_000015.10:g.79233445_79233448dup, NC_000015.9:g.79525787_79525790del, NC_000015.9:g.79525787_79525790dup

Select item 14914097439.

rs1491409743 has merged into rs35479682 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGG>-,GG,GGGG [Show Flanks]
Chromosome:: 15:79277275 (GRCh38)
15:79569617 (GRCh37)
Canonical SPDI:: NC_000015.10:79277269:GGGGGGGG:GGGGG,NC_000015.10:79277269:GGGGGGGG:GGGGGGG,NC_000015.10:79277269:GGGGGGGG:GGGGGGGGG
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGGGGG=0.00007/1 (ALFA)
-=0.00004/1 (TOMMO)
HGVS:: NC_000015.10:g.79277275_79277277del, NC_000015.10:g.79277277del, NC_000015.10:g.79277277dup, NC_000015.9:g.79569617_79569619del, NC_000015.9:g.79569619del, NC_000015.9:g.79569619dup

Select item 149137268010.

rs1491372680 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TCTT [Show Flanks]
Chromosome:: 15:79199665 (GRCh38)
15:79492008 (GRCh37)
Canonical SPDI:: NC_000015.10:79199665:TT:TTTCTT
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTTCTT=0./0 (ALFA)
TTTC=0.0042/256 (GnomAD)
HGVS:: NC_000015.10:g.79199667_79199668insTCTT, NC_000015.9:g.79492009_79492010insTCTT

Select item 149136529511.

rs1491365295 has merged into rs578001084 [Homo sapiens]

Variant type:: DELINS
Alleles:: TG>-,TGTG,TGTGTG,TGTGTGTG,TGTGTGTGTG,TGTGTGTGTGTG,TGTGTGTGTGTGTG,TGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTG [Show Flanks]
Chromosome:: 15:79233443 (GRCh38)
15:79525785 (GRCh37)
Canonical SPDI:: NC_000015.10:79233440:TGTG:TG,NC_000015.10:79233440:TGTG:TGTGTG,NC_000015.10:79233440:TGTG:TGTGTGTG,NC_000015.10:79233440:TGTG:TGTGTGTGTG,NC_000015.10:79233440:TGTG:TGTGTGTGTGTG,NC_000015.10:79233440:TGTG:TGTGTGTGTGTGTG,NC_000015.10:79233440:TGTG:TGTGTGTGTGTGTGTG,NC_000015.10:79233440:TGTG:TGTGTGTGTGTGTGTGTG,NC_000015.10:79233440:TGTG:TGTGTGTGTGTGTGTGTGTG
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGTGTG=0./0 (ALFA)
-=0.000023/6 (TOPMED)
HGVS:: NC_000015.10:g.79233441TG[1], NC_000015.10:g.79233441TG[3], NC_000015.10:g.79233441TG[4], NC_000015.10:g.79233441TG[5], NC_000015.10:g.79233441TG[6], NC_000015.10:g.79233441TG[7], NC_000015.10:g.79233441TG[8], NC_000015.10:g.79233441TG[9], NC_000015.10:g.79233441TG[10], NC_000015.9:g.79525783TG[1], NC_000015.9:g.79525783TG[3], NC_000015.9:g.79525783TG[4], NC_000015.9:g.79525783TG[5], NC_000015.9:g.79525783TG[6], NC_000015.9:g.79525783TG[7], NC_000015.9:g.79525783TG[8], NC_000015.9:g.79525783TG[9], NC_000015.9:g.79525783TG[10]

Select item 149134256512.

rs1491342565 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CCTT [Show Flanks]
Chromosome:: 15:79199671 (GRCh38)
15:79492014 (GRCh37)
Canonical SPDI:: NC_000015.10:79199671:CTT:CTTCCTT
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CTTCCTT=0./0 (ALFA)
CTTC=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.79199674_79199675insCCTT, NC_000015.9:g.79492016_79492017insCCTT

Select item 149133066213.

rs1491330662 has merged into rs1388226567 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT [Show Flanks]
Chromosome:: 15:79199682 (GRCh38)
15:79492024 (GRCh37)
Canonical SPDI:: NC_000015.10:79199680:TTT:T,NC_000015.10:79199680:TTT:TT,NC_000015.10:79199680:TTT:TTTT
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.00005/1 (TOMMO)
HGVS:: NC_000015.10:g.79199682_79199683del, NC_000015.10:g.79199683del, NC_000015.10:g.79199683dup, NC_000015.9:g.79492024_79492025del, NC_000015.9:g.79492025del, NC_000015.9:g.79492025dup

Select item 149132658714.

rs1491326587 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 15:79252616 (GRCh38)
15:79544958 (GRCh37)
Canonical SPDI:: NC_000015.10:79252615:AT:
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000015.10:g.79252616_79252617del, NC_000015.9:g.79544958_79544959del

Select item 149131139015.

rs1491311390 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 15:79278015 (GRCh38)
15:79570357 (GRCh37)
Canonical SPDI:: NC_000015.10:79278013:TCT:T
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00008/1 (ALFA)
-=0.00055/1 (Korea1K)
-=0.00065/45 (GnomAD)
HGVS:: NC_000015.10:g.79278015_79278016del, NC_000015.9:g.79570357_79570358del

Select item 149127749016.

rs1491277490 has merged into rs138444560 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTATTT,TTT,TTTTT [Show Flanks]
Chromosome:: 15:79199666 (GRCh38)
15:79492008 (GRCh37)
Canonical SPDI:: NC_000015.10:79199664:TTT:T,NC_000015.10:79199664:TTT:TT,NC_000015.10:79199664:TTT:TTTATTT,NC_000015.10:79199664:TTT:TTTT,NC_000015.10:79199664:TTT:TTTTTT
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.075/3 (GENOME_DK)
HGVS:: NC_000015.10:g.79199666_79199667del, NC_000015.10:g.79199667del, NC_000015.10:g.79199667_79199668insATTT, NC_000015.10:g.79199667dup, NC_000015.10:g.79199665_79199667dup, NC_000015.9:g.79492008_79492009del, NC_000015.9:g.79492009del, NC_000015.9:g.79492009_79492010insATTT, NC_000015.9:g.79492009dup, NC_000015.9:g.79492007_79492009dup

Select item 149124625817.

rs1491246258 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT [Show Flanks]
Chromosome:: 15:79199672 (GRCh38)
15:79492014 (GRCh37)
Canonical SPDI:: NC_000015.10:79199670:TCT:T,NC_000015.10:79199670:TCT:TCTCT
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TCTCT=0./0 (ALFA)
HGVS:: NC_000015.10:g.79199672_79199673del, NC_000015.10:g.79199672_79199673dup, NC_000015.9:g.79492014_79492015del, NC_000015.9:g.79492014_79492015dup

Select item 149124048818.

rs1491240488 has merged into rs759368918 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 15:79282006 (GRCh38)
15:79574348 (GRCh37)
Canonical SPDI:: NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:79281993:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ANKRD34C (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
TTTT=0./0 (GENOME_DK)
-=0.1197/28 (NorthernSweden)
HGVS:: NC_000015.10:g.79282006_79282025del, NC_000015.10:g.79282007_79282025del, NC_000015.10:g.79282008_79282025del, NC_000015.10:g.79282009_79282025del, NC_000015.10:g.79282010_79282025del, NC_000015.10:g.79282011_79282025del, NC_000015.10:g.79282012_79282025del, NC_000015.10:g.79282013_79282025del, NC_000015.10:g.79282014_79282025del, NC_000015.10:g.79282015_79282025del, NC_000015.10:g.79282016_79282025del, NC_000015.10:g.79282017_79282025del, NC_000015.10:g.79282018_79282025del, NC_000015.10:g.79282019_79282025del, NC_000015.10:g.79282020_79282025del, NC_000015.10:g.79282021_79282025del, NC_000015.10:g.79282022_79282025del, NC_000015.10:g.79282023_79282025del, NC_000015.10:g.79282024_79282025del, NC_000015.10:g.79282025del, NC_000015.10:g.79282025dup, NC_000015.10:g.79282024_79282025dup, NC_000015.10:g.79282023_79282025dup, NC_000015.10:g.79282022_79282025dup, NC_000015.10:g.79282021_79282025dup, NC_000015.10:g.79282020_79282025dup, NC_000015.10:g.79282019_79282025dup, NC_000015.10:g.79282018_79282025dup, NC_000015.10:g.79282017_79282025dup, NC_000015.10:g.79282013_79282025dup, NC_000015.10:g.79282011_79282025dup, NC_000015.10:g.79282010_79282025dup, NC_000015.10:g.79282009_79282025dup, NC_000015.10:g.79282008_79282025dup, NC_000015.10:g.79282002_79282025dup, NC_000015.10:g.79282000_79282025dup, NC_000015.10:g.79281998_79282025dup, NC_000015.9:g.79574348_79574367del, NC_000015.9:g.79574349_79574367del, NC_000015.9:g.79574350_79574367del, NC_000015.9:g.79574351_79574367del, NC_000015.9:g.79574352_79574367del, NC_000015.9:g.79574353_79574367del, NC_000015.9:g.79574354_79574367del, NC_000015.9:g.79574355_79574367del, NC_000015.9:g.79574356_79574367del, NC_000015.9:g.79574357_79574367del, NC_000015.9:g.79574358_79574367del, NC_000015.9:g.79574359_79574367del, NC_000015.9:g.79574360_79574367del, NC_000015.9:g.79574361_79574367del, NC_000015.9:g.79574362_79574367del, NC_000015.9:g.79574363_79574367del, NC_000015.9:g.79574364_79574367del, NC_000015.9:g.79574365_79574367del, NC_000015.9:g.79574366_79574367del, NC_000015.9:g.79574367del, NC_000015.9:g.79574367dup, NC_000015.9:g.79574366_79574367dup, NC_000015.9:g.79574365_79574367dup, NC_000015.9:g.79574364_79574367dup, NC_000015.9:g.79574363_79574367dup, NC_000015.9:g.79574362_79574367dup, NC_000015.9:g.79574361_79574367dup, NC_000015.9:g.79574360_79574367dup, NC_000015.9:g.79574359_79574367dup, NC_000015.9:g.79574355_79574367dup, NC_000015.9:g.79574353_79574367dup, NC_000015.9:g.79574352_79574367dup, NC_000015.9:g.79574351_79574367dup, NC_000015.9:g.79574350_79574367dup, NC_000015.9:g.79574344_79574367dup, NC_000015.9:g.79574342_79574367dup, NC_000015.9:g.79574340_79574367dup

Select item 149123836919.

rs1491238369 has merged into rs541058285 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTTT [Show Flanks]
Chromosome:: 15:79199670 (GRCh38)
15:79492012 (GRCh37)
Canonical SPDI:: NC_000015.10:79199668:TTT:T,NC_000015.10:79199668:TTT:TT,NC_000015.10:79199668:TTT:TTTT,NC_000015.10:79199668:TTT:TTTTTT
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.03167/19 (NorthernSweden)
HGVS:: NC_000015.10:g.79199670_79199671del, NC_000015.10:g.79199671del, NC_000015.10:g.79199671dup, NC_000015.10:g.79199669_79199671dup, NC_000015.9:g.79492012_79492013del, NC_000015.9:g.79492013del, NC_000015.9:g.79492013dup, NC_000015.9:g.79492011_79492013dup

Select item 149123752620.

rs1491237526 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTT>-,CTTCTT [Show Flanks]
Chromosome:: 15:79199672 (GRCh38)
15:79492014 (GRCh37)
Canonical SPDI:: NC_000015.10:79199669:TTCTT:TT,NC_000015.10:79199669:TTCTT:TTCTTCTT
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTCTTCTT=0.00008/1 (ALFA)
-=0.0002/17 (GnomAD)
TTC=0.00089/15 (TOMMO)
TTC=0.02333/14 (NorthernSweden)
HGVS:: NC_000015.10:g.79199672_79199674del, NC_000015.10:g.79199672_79199674dup, NC_000015.9:g.79492014_79492016del, NC_000015.9:g.79492014_79492016dup

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