SNP Links for Gene (Select 4140) - SNP

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Select item 14915893351.

rs1491589335 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 14:103389528 (GRCh38)
14:103855865 (GRCh37)
Canonical SPDI:: NC_000014.9:103389527:CA:
Gene:: MARK3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00017/2 (ALFA)
HGVS:: NC_000014.9:g.103389528_103389529del, NC_000014.8:g.103855865_103855866del, NG_030339.2:g.9165_9166del

Select item 14915742352.

rs1491574235 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:103423220 (GRCh38)
14:103889558 (GRCh37)
Canonical SPDI:: NC_000014.9:103423220:T:TTTTTT,NC_000014.9:103423220:T:TTTTTTTT,NC_000014.9:103423220:T:TTTTTTTTT,NC_000014.9:103423220:T:TTTTTTTTTT,NC_000014.9:103423220:T:TTTTTTTTTTT,NC_000014.9:103423220:T:TTTTTTTTTTTTTT,NC_000014.9:103423220:T:TTTTTTTTTTTTTTTT
Gene:: MARK3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: TTTTT=0.00095/22 (GnomAD)
HGVS:: NC_000014.9:g.103423221_103423222insTTTTT, NC_000014.9:g.103423221_103423222insTTTTTTT, NC_000014.9:g.103423221_103423222insTTTTTTTT, NC_000014.9:g.103423221_103423222insTTTTTTTTT, NC_000014.9:g.103423221_103423222insTTTTTTTTTT, NC_000014.9:g.103423221_103423222insTTTTTTTTTTTTT, NC_000014.9:g.103423221_103423222insTTTTTTTTTTTTTTT, NC_000014.8:g.103889558_103889559insTTTTT, NC_000014.8:g.103889558_103889559insTTTTTTT, NC_000014.8:g.103889558_103889559insTTTTTTTT, NC_000014.8:g.103889558_103889559insTTTTTTTTT, NC_000014.8:g.103889558_103889559insTTTTTTTTTT, NC_000014.8:g.103889558_103889559insTTTTTTTTTTTTT, NC_000014.8:g.103889558_103889559insTTTTTTTTTTTTTTT, NG_030339.2:g.42858_42859insTTTTT, NG_030339.2:g.42858_42859insTTTTTTT, NG_030339.2:g.42858_42859insTTTTTTTT, NG_030339.2:g.42858_42859insTTTTTTTTT, NG_030339.2:g.42858_42859insTTTTTTTTTT, NG_030339.2:g.42858_42859insTTTTTTTTTTTTT, NG_030339.2:g.42858_42859insTTTTTTTTTTTTTTT

Select item 14915731053.

rs1491573105 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 14:103409435 (GRCh38)
14:103875772 (GRCh37)
Canonical SPDI:: NC_000014.9:103409434:TA:
Gene:: MARK3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000014.9:g.103409435_103409436del, NC_000014.8:g.103875772_103875773del, NG_030339.2:g.29072_29073del

Select item 14915689064.

rs1491568906 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 14:103450876 (GRCh38)
14:103917214 (GRCh37)
Canonical SPDI:: NC_000014.9:103450876:T:TT
Gene:: MARK3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
HGVS:: NC_000014.9:g.103450877dup, NC_000014.8:g.103917214dup, NG_030339.2:g.70514dup

Select item 14915414215.

rs1491541421 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 14:103418242 (GRCh38)
14:103884580 (GRCh37)
Canonical SPDI:: NC_000014.9:103418242:A:AA
Gene:: MARK3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: AA=0./0 (ALFA)
A=0.00006/5 (GnomAD)
HGVS:: NC_000014.9:g.103418243dup, NC_000014.8:g.103884580dup, NG_030339.2:g.37880dup

Select item 14915346586.

rs1491534658 has merged into rs10525116 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 14:103467684 (GRCh38)
14:103934021 (GRCh37)
Canonical SPDI:: NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467674:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MARK3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.103467684_103467697del, NC_000014.9:g.103467685_103467697del, NC_000014.9:g.103467686_103467697del, NC_000014.9:g.103467688_103467697del, NC_000014.9:g.103467689_103467697del, NC_000014.9:g.103467690_103467697del, NC_000014.9:g.103467691_103467697del, NC_000014.9:g.103467692_103467697del, NC_000014.9:g.103467693_103467697del, NC_000014.9:g.103467694_103467697del, NC_000014.9:g.103467695_103467697del, NC_000014.9:g.103467696_103467697del, NC_000014.9:g.103467697del, NC_000014.9:g.103467697dup, NC_000014.9:g.103467696_103467697dup, NC_000014.9:g.103467695_103467697dup, NC_000014.9:g.103467694_103467697dup, NC_000014.9:g.103467693_103467697dup, NC_000014.9:g.103467692_103467697dup, NC_000014.9:g.103467691_103467697dup, NC_000014.9:g.103467690_103467697dup, NC_000014.9:g.103467689_103467697dup, NC_000014.9:g.103467688_103467697dup, NC_000014.9:g.103467687_103467697dup, NC_000014.9:g.103467686_103467697dup, NC_000014.9:g.103467685_103467697dup, NC_000014.9:g.103467684_103467697dup, NC_000014.9:g.103467683_103467697dup, NC_000014.9:g.103467682_103467697dup, NC_000014.9:g.103467681_103467697dup, NC_000014.9:g.103467680_103467697dup, NC_000014.9:g.103467679_103467697dup, NC_000014.9:g.103467678_103467697dup, NC_000014.9:g.103467677_103467697dup, NC_000014.9:g.103467676_103467697dup, NC_000014.9:g.103467675_103467697dup, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.103467697_103467698insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934021_103934034del, NC_000014.8:g.103934022_103934034del, NC_000014.8:g.103934023_103934034del, NC_000014.8:g.103934025_103934034del, NC_000014.8:g.103934026_103934034del, NC_000014.8:g.103934027_103934034del, NC_000014.8:g.103934028_103934034del, NC_000014.8:g.103934029_103934034del, NC_000014.8:g.103934030_103934034del, NC_000014.8:g.103934031_103934034del, NC_000014.8:g.103934032_103934034del, NC_000014.8:g.103934033_103934034del, NC_000014.8:g.103934034del, NC_000014.8:g.103934034dup, NC_000014.8:g.103934033_103934034dup, NC_000014.8:g.103934032_103934034dup, NC_000014.8:g.103934031_103934034dup, NC_000014.8:g.103934030_103934034dup, NC_000014.8:g.103934029_103934034dup, NC_000014.8:g.103934028_103934034dup, NC_000014.8:g.103934027_103934034dup, NC_000014.8:g.103934026_103934034dup, NC_000014.8:g.103934025_103934034dup, NC_000014.8:g.103934024_103934034dup, NC_000014.8:g.103934023_103934034dup, NC_000014.8:g.103934022_103934034dup, NC_000014.8:g.103934021_103934034dup, NC_000014.8:g.103934020_103934034dup, NC_000014.8:g.103934019_103934034dup, NC_000014.8:g.103934018_103934034dup, NC_000014.8:g.103934017_103934034dup, NC_000014.8:g.103934016_103934034dup, NC_000014.8:g.103934015_103934034dup, NC_000014.8:g.103934014_103934034dup, NC_000014.8:g.103934013_103934034dup, NC_000014.8:g.103934012_103934034dup, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.103934034_103934035insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87321_87334del, NG_030339.2:g.87322_87334del, NG_030339.2:g.87323_87334del, NG_030339.2:g.87325_87334del, NG_030339.2:g.87326_87334del, NG_030339.2:g.87327_87334del, NG_030339.2:g.87328_87334del, NG_030339.2:g.87329_87334del, NG_030339.2:g.87330_87334del, NG_030339.2:g.87331_87334del, NG_030339.2:g.87332_87334del, NG_030339.2:g.87333_87334del, NG_030339.2:g.87334del, NG_030339.2:g.87334dup, NG_030339.2:g.87333_87334dup, NG_030339.2:g.87332_87334dup, NG_030339.2:g.87331_87334dup, NG_030339.2:g.87330_87334dup, NG_030339.2:g.87329_87334dup, NG_030339.2:g.87328_87334dup, NG_030339.2:g.87327_87334dup, NG_030339.2:g.87326_87334dup, NG_030339.2:g.87325_87334dup, NG_030339.2:g.87324_87334dup, NG_030339.2:g.87323_87334dup, NG_030339.2:g.87322_87334dup, NG_030339.2:g.87321_87334dup, NG_030339.2:g.87320_87334dup, NG_030339.2:g.87319_87334dup, NG_030339.2:g.87318_87334dup, NG_030339.2:g.87317_87334dup, NG_030339.2:g.87316_87334dup, NG_030339.2:g.87315_87334dup, NG_030339.2:g.87314_87334dup, NG_030339.2:g.87313_87334dup, NG_030339.2:g.87312_87334dup, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030339.2:g.87334_87335insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14915245117.

rs1491524511 [Homo sapiens]

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

Select item 14915171108.

rs1491517110 [Homo sapiens]

Variant type:: DEL
Alleles:: TC>- [Show Flanks]
Chromosome:: 14:103431976 (GRCh38)
14:103898313 (GRCh37)
Canonical SPDI:: NC_000014.9:103431975:TC:
Gene:: MARK3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00346/41 (ALFA)
HGVS:: NC_000014.9:g.103431976_103431977del, NC_000014.8:g.103898313_103898314del, NG_030339.2:g.51613_51614del

Select item 14914696749.

rs1491469674 has merged into rs11320440 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA [Show Flanks]
Chromosome:: 14:103467014 (GRCh38)
14:103933351 (GRCh37)
Canonical SPDI:: NC_000014.9:103467004:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000014.9:103467004:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000014.9:103467004:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000014.9:103467004:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000014.9:103467004:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000014.9:103467004:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:103467004:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:103467004:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000014.9:103467004:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000014.9:103467004:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000014.9:103467004:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103467004:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA
Gene:: MARK3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000014.9:g.103467014_103467024del, NC_000014.9:g.103467015_103467024del, NC_000014.9:g.103467017_103467024del, NC_000014.9:g.103467018_103467024del, NC_000014.9:g.103467019_103467024del, NC_000014.9:g.103467020_103467024del, NC_000014.9:g.103467021_103467024del, NC_000014.9:g.103467022_103467024del, NC_000014.9:g.103467023_103467024del, NC_000014.9:g.103467024del, NC_000014.9:g.103467024dup, NC_000014.9:g.103467023_103467024dup, NC_000014.8:g.103933351_103933361del, NC_000014.8:g.103933352_103933361del, NC_000014.8:g.103933354_103933361del, NC_000014.8:g.103933355_103933361del, NC_000014.8:g.103933356_103933361del, NC_000014.8:g.103933357_103933361del, NC_000014.8:g.103933358_103933361del, NC_000014.8:g.103933359_103933361del, NC_000014.8:g.103933360_103933361del, NC_000014.8:g.103933361del, NC_000014.8:g.103933361dup, NC_000014.8:g.103933360_103933361dup, NG_030339.2:g.86651_86661del, NG_030339.2:g.86652_86661del, NG_030339.2:g.86654_86661del, NG_030339.2:g.86655_86661del, NG_030339.2:g.86656_86661del, NG_030339.2:g.86657_86661del, NG_030339.2:g.86658_86661del, NG_030339.2:g.86659_86661del, NG_030339.2:g.86660_86661del, NG_030339.2:g.86661del, NG_030339.2:g.86661dup, NG_030339.2:g.86660_86661dup

Select item 149146653210.

rs1491466532 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 14:103444105 (GRCh38)
14:103910442 (GRCh37)
Canonical SPDI:: NC_000014.9:103444104:TA:
Gene:: MARK3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000014.9:g.103444105_103444106del, NC_000014.8:g.103910442_103910443del, NG_030339.2:g.63742_63743del

Select item 149145919311.

rs1491459193 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 14:103481785 (GRCh38)
14:103948123 (GRCh37)
Canonical SPDI:: NC_000014.9:103481785:A:AA
Gene:: MARK3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AA=0./0 (ALFA)
A=0.00037/4 (GnomAD)
HGVS:: NC_000014.9:g.103481786dup, NC_000014.8:g.103948123dup, NG_030339.2:g.101423dup

Select item 149144650212.

rs1491446502 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 14:103418242 (GRCh38)
14:103884579 (GRCh37)
Canonical SPDI:: NC_000014.9:103418241:TA:
Gene:: MARK3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00367/60 (ALFA)
HGVS:: NC_000014.9:g.103418242_103418243del, NC_000014.8:g.103884579_103884580del, NG_030339.2:g.37879_37880del

Select item 149143035313.

rs1491430353 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 14:103467674 (GRCh38)
14:103934011 (GRCh37)
Canonical SPDI:: NC_000014.9:103467673:CA:
Gene:: MARK3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000014.9:g.103467674_103467675del, NC_000014.8:g.103934011_103934012del, NG_030339.2:g.87311_87312del

Select item 149141453814.

rs1491414538 has merged into rs71126028 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 14:103472657 (GRCh38)
14:103938994 (GRCh37)
Canonical SPDI:: NC_000014.9:103472647:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000014.9:103472647:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000014.9:103472647:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:103472647:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:103472647:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000014.9:103472647:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000014.9:103472647:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000014.9:103472647:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103472647:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103472647:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103472647:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103472647:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103472647:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MARK3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
A=0.0853/427 (1000Genomes)
HGVS:: NC_000014.9:g.103472657_103472667del, NC_000014.9:g.103472662_103472667del, NC_000014.9:g.103472663_103472667del, NC_000014.9:g.103472664_103472667del, NC_000014.9:g.103472665_103472667del, NC_000014.9:g.103472666_103472667del, NC_000014.9:g.103472667del, NC_000014.9:g.103472667dup, NC_000014.9:g.103472666_103472667dup, NC_000014.9:g.103472665_103472667dup, NC_000014.9:g.103472664_103472667dup, NC_000014.9:g.103472663_103472667dup, NC_000014.9:g.103472662_103472667dup, NC_000014.8:g.103938994_103939004del, NC_000014.8:g.103938999_103939004del, NC_000014.8:g.103939000_103939004del, NC_000014.8:g.103939001_103939004del, NC_000014.8:g.103939002_103939004del, NC_000014.8:g.103939003_103939004del, NC_000014.8:g.103939004del, NC_000014.8:g.103939004dup, NC_000014.8:g.103939003_103939004dup, NC_000014.8:g.103939002_103939004dup, NC_000014.8:g.103939001_103939004dup, NC_000014.8:g.103939000_103939004dup, NC_000014.8:g.103938999_103939004dup, NG_030339.2:g.92294_92304del, NG_030339.2:g.92299_92304del, NG_030339.2:g.92300_92304del, NG_030339.2:g.92301_92304del, NG_030339.2:g.92302_92304del, NG_030339.2:g.92303_92304del, NG_030339.2:g.92304del, NG_030339.2:g.92304dup, NG_030339.2:g.92303_92304dup, NG_030339.2:g.92302_92304dup, NG_030339.2:g.92301_92304dup, NG_030339.2:g.92300_92304dup, NG_030339.2:g.92299_92304dup

Select item 149139968815.

rs1491399688 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 14:103407555 (GRCh38)
14:103873893 (GRCh37)
Canonical SPDI:: NC_000014.9:103407555::A
Gene:: MARK3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00017/2 (ALFA)
A=0.00171/41 (GnomAD)
HGVS:: NC_000014.9:g.103407555_103407556insA, NC_000014.8:g.103873892_103873893insA, NG_030339.2:g.27192_27193insA

Select item 149139054816.

rs1491390548 has merged into rs71126011 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 14:103389953 (GRCh38)
14:103856290 (GRCh37)
Canonical SPDI:: NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:103389943:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MARK3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000014.9:g.103389953_103389966del, NC_000014.9:g.103389954_103389966del, NC_000014.9:g.103389955_103389966del, NC_000014.9:g.103389956_103389966del, NC_000014.9:g.103389957_103389966del, NC_000014.9:g.103389958_103389966del, NC_000014.9:g.103389959_103389966del, NC_000014.9:g.103389960_103389966del, NC_000014.9:g.103389961_103389966del, NC_000014.9:g.103389962_103389966del, NC_000014.9:g.103389963_103389966del, NC_000014.9:g.103389964_103389966del, NC_000014.9:g.103389965_103389966del, NC_000014.9:g.103389966del, NC_000014.9:g.103389966dup, NC_000014.9:g.103389965_103389966dup, NC_000014.9:g.103389964_103389966dup, NC_000014.9:g.103389963_103389966dup, NC_000014.9:g.103389962_103389966dup, NC_000014.9:g.103389961_103389966dup, NC_000014.9:g.103389960_103389966dup, NC_000014.8:g.103856290_103856303del, NC_000014.8:g.103856291_103856303del, NC_000014.8:g.103856292_103856303del, NC_000014.8:g.103856293_103856303del, NC_000014.8:g.103856294_103856303del, NC_000014.8:g.103856295_103856303del, NC_000014.8:g.103856296_103856303del, NC_000014.8:g.103856297_103856303del, NC_000014.8:g.103856298_103856303del, NC_000014.8:g.103856299_103856303del, NC_000014.8:g.103856300_103856303del, NC_000014.8:g.103856301_103856303del, NC_000014.8:g.103856302_103856303del, NC_000014.8:g.103856303del, NC_000014.8:g.103856303dup, NC_000014.8:g.103856302_103856303dup, NC_000014.8:g.103856301_103856303dup, NC_000014.8:g.103856300_103856303dup, NC_000014.8:g.103856299_103856303dup, NC_000014.8:g.103856298_103856303dup, NC_000014.8:g.103856297_103856303dup, NG_030339.2:g.9590_9603del, NG_030339.2:g.9591_9603del, NG_030339.2:g.9592_9603del, NG_030339.2:g.9593_9603del, NG_030339.2:g.9594_9603del, NG_030339.2:g.9595_9603del, NG_030339.2:g.9596_9603del, NG_030339.2:g.9597_9603del, NG_030339.2:g.9598_9603del, NG_030339.2:g.9599_9603del, NG_030339.2:g.9600_9603del, NG_030339.2:g.9601_9603del, NG_030339.2:g.9602_9603del, NG_030339.2:g.9603del, NG_030339.2:g.9603dup, NG_030339.2:g.9602_9603dup, NG_030339.2:g.9601_9603dup, NG_030339.2:g.9600_9603dup, NG_030339.2:g.9599_9603dup, NG_030339.2:g.9598_9603dup, NG_030339.2:g.9597_9603dup

Select item 149138418717.

rs1491384187 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 14:103399714 (GRCh38)
14:103866052 (GRCh37)
Canonical SPDI:: NC_000014.9:103399714::G
Gene:: MARK3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.00042/5 (ALFA)
G=0.00121/91 (GnomAD)
G=0.00154/26 (TOMMO)
HGVS:: NC_000014.9:g.103399714_103399715insG, NC_000014.8:g.103866051_103866052insG, NG_030339.2:g.19351_19352insG

Select item 149138057218.

rs1491380572 has merged into rs71126026 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTT>-,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:103452478 (GRCh38)
14:103918815 (GRCh37)
Canonical SPDI:: NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:103452471:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: MARK3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTT=0./0 (ALFA)
HGVS:: NC_000014.9:g.103452478_103452489del, NC_000014.9:g.103452482_103452489del, NC_000014.9:g.103452484_103452489del, NC_000014.9:g.103452485_103452489del, NC_000014.9:g.103452486_103452489del, NC_000014.9:g.103452487_103452489del, NC_000014.9:g.103452488_103452489del, NC_000014.9:g.103452489del, NC_000014.9:g.103452489dup, NC_000014.9:g.103452472_103452489T[19]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.103452488_103452489dup, NC_000014.9:g.103452472_103452489T[20]GTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.103452487_103452489dup, NC_000014.9:g.103452486_103452489dup, NC_000014.9:g.103452472_103452489T[22]GTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.103452485_103452489dup, NC_000014.9:g.103452484_103452489dup, NC_000014.9:g.103452483_103452489dup, NC_000014.9:g.103452482_103452489dup, NC_000014.9:g.103452481_103452489dup, NC_000014.9:g.103452480_103452489dup, NC_000014.9:g.103452479_103452489dup, NC_000014.9:g.103452478_103452489dup, NC_000014.9:g.103452477_103452489dup, NC_000014.9:g.103452476_103452489dup, NC_000014.9:g.103452475_103452489dup, NC_000014.9:g.103452474_103452489dup, NC_000014.9:g.103452473_103452489dup, NC_000014.9:g.103452472_103452489dup, NC_000014.9:g.103452489_103452490insTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.103452489_103452490insTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.103452489_103452490insTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.103452489_103452490insTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.103452489_103452490insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.103452489_103452490insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.103452489_103452490insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.103452489_103452490insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.103452489_103452490insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.103452489_103452490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.103452489_103452490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.103452489_103452490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.103452489_103452490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.103452489_103452490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.103918815_103918826del, NC_000014.8:g.103918819_103918826del, NC_000014.8:g.103918821_103918826del, NC_000014.8:g.103918822_103918826del, NC_000014.8:g.103918823_103918826del, NC_000014.8:g.103918824_103918826del, NC_000014.8:g.103918825_103918826del, NC_000014.8:g.103918826del, NC_000014.8:g.103918826dup, NC_000014.8:g.103918809_103918826T[19]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.103918825_103918826dup, NC_000014.8:g.103918809_103918826T[20]GTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.103918824_103918826dup, NC_000014.8:g.103918823_103918826dup, NC_000014.8:g.103918809_103918826T[22]GTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.103918822_103918826dup, NC_000014.8:g.103918821_103918826dup, NC_000014.8:g.103918820_103918826dup, NC_000014.8:g.103918819_103918826dup, NC_000014.8:g.103918818_103918826dup, NC_000014.8:g.103918817_103918826dup, NC_000014.8:g.103918816_103918826dup, NC_000014.8:g.103918815_103918826dup, NC_000014.8:g.103918814_103918826dup, NC_000014.8:g.103918813_103918826dup, NC_000014.8:g.103918812_103918826dup, NC_000014.8:g.103918811_103918826dup, NC_000014.8:g.103918810_103918826dup, NC_000014.8:g.103918809_103918826dup, NC_000014.8:g.103918826_103918827insTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.103918826_103918827insTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.103918826_103918827insTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.103918826_103918827insTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.103918826_103918827insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.103918826_103918827insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.103918826_103918827insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.103918826_103918827insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.103918826_103918827insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.103918826_103918827insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.103918826_103918827insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.103918826_103918827insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.103918826_103918827insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.103918826_103918827insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030339.2:g.72115_72126del, NG_030339.2:g.72119_72126del, NG_030339.2:g.72121_72126del, NG_030339.2:g.72122_72126del, NG_030339.2:g.72123_72126del, NG_030339.2:g.72124_72126del, NG_030339.2:g.72125_72126del, NG_030339.2:g.72126del, NG_030339.2:g.72126dup, NG_030339.2:g.72109_72126T[19]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_030339.2:g.72125_72126dup, NG_030339.2:g.72109_72126T[20]GTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_030339.2:g.72124_72126dup, NG_030339.2:g.72123_72126dup, NG_030339.2:g.72109_72126T[22]GTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_030339.2:g.72122_72126dup, NG_030339.2:g.72121_72126dup, NG_030339.2:g.72120_72126dup, NG_030339.2:g.72119_72126dup, NG_030339.2:g.72118_72126dup, NG_030339.2:g.72117_72126dup, NG_030339.2:g.72116_72126dup, NG_030339.2:g.72115_72126dup, NG_030339.2:g.72114_72126dup, NG_030339.2:g.72113_72126dup, NG_030339.2:g.72112_72126dup, NG_030339.2:g.72111_72126dup, NG_030339.2:g.72110_72126dup, NG_030339.2:g.72109_72126dup, NG_030339.2:g.72126_72127insTTTTTTTTTTTTTTTTTTT, NG_030339.2:g.72126_72127insTTTTTTTTTTTTTTTTTTTT, NG_030339.2:g.72126_72127insTTTTTTTTTTTTTTTTTTTTT, NG_030339.2:g.72126_72127insTTTTTTTTTTTTTTTTTTTTTTT, NG_030339.2:g.72126_72127insTTTTTTTTTTTTTTTTTTTTTTTT, NG_030339.2:g.72126_72127insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030339.2:g.72126_72127insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030339.2:g.72126_72127insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030339.2:g.72126_72127insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030339.2:g.72126_72127insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030339.2:g.72126_72127insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030339.2:g.72126_72127insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030339.2:g.72126_72127insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_030339.2:g.72126_72127insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149137226519.

rs1491372265 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 14:103501552 (GRCh38)
14:103967889 (GRCh37)
Canonical SPDI:: NC_000014.9:103501549:CTCT:CT
Gene:: MARK3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CTCT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.103501550CT[1], NC_000014.8:g.103967887CT[1], NG_030339.2:g.121187CT[1]

Select item 149136706220.

rs1491367062 [Homo sapiens]

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

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