SNP Links for Gene (Select 152485) - SNP

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Select item 14915888781.

rs1491588878 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GA,TA [Show Flanks]
Chromosome:: 4:145856986 (GRCh38)
4:146778139 (GRCh37)
Canonical SPDI:: NC_000004.12:145856986:A:AGA,NC_000004.12:145856986:A:ATA
Gene:: ZNF827 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATA=0./0 (ALFA)
AG=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.145856987_145856988insGA, NC_000004.12:g.145856987_145856988insTA, NC_000004.11:g.146778139_146778140insGA, NC_000004.11:g.146778139_146778140insTA

Select item 14915832932.

rs1491583293 has merged into rs10605153 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAAAA>-,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,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,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 4:145781198 (GRCh38)
4:146702350 (GRCh37)
Canonical SPDI:: NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145781195:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ZNF827 (Varview), C4orf51 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
HGVS:: NC_000004.12:g.145781198_145781217del, NC_000004.12:g.145781202_145781217del, NC_000004.12:g.145781203_145781217del, NC_000004.12:g.145781204_145781217del, NC_000004.12:g.145781205_145781217del, NC_000004.12:g.145781206_145781217del, NC_000004.12:g.145781207_145781217del, NC_000004.12:g.145781209_145781217del, NC_000004.12:g.145781210_145781217del, NC_000004.12:g.145781211_145781217del, NC_000004.12:g.145781212_145781217del, NC_000004.12:g.145781214_145781217del, NC_000004.12:g.145781215_145781217del, NC_000004.12:g.145781216_145781217del, NC_000004.12:g.145781217del, NC_000004.12:g.145781217dup, NC_000004.12:g.145781216_145781217dup, NC_000004.12:g.145781215_145781217dup, NC_000004.12:g.145781214_145781217dup, NC_000004.12:g.145781213_145781217dup, NC_000004.12:g.145781212_145781217dup, NC_000004.12:g.145781211_145781217dup, NC_000004.12:g.145781210_145781217dup, NC_000004.12:g.145781209_145781217dup, NC_000004.12:g.145781208_145781217dup, NC_000004.12:g.145781207_145781217dup, NC_000004.12:g.145781206_145781217dup, NC_000004.12:g.145781205_145781217dup, NC_000004.12:g.145781204_145781217dup, NC_000004.12:g.145781203_145781217dup, NC_000004.12:g.145781202_145781217dup, NC_000004.12:g.145781201_145781217dup, NC_000004.12:g.145781200_145781217dup, NC_000004.12:g.145781199_145781217dup, NC_000004.12:g.145781198_145781217dup, NC_000004.12:g.145781197_145781217dup, NC_000004.12:g.145781196_145781217dup, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781217_145781218insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145781196_145781217A[56]CAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000004.12:g.145781196_145781217A[30]GAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000004.11:g.146702350_146702369del, NC_000004.11:g.146702354_146702369del, NC_000004.11:g.146702355_146702369del, NC_000004.11:g.146702356_146702369del, NC_000004.11:g.146702357_146702369del, NC_000004.11:g.146702358_146702369del, NC_000004.11:g.146702359_146702369del, NC_000004.11:g.146702361_146702369del, NC_000004.11:g.146702362_146702369del, NC_000004.11:g.146702363_146702369del, NC_000004.11:g.146702364_146702369del, NC_000004.11:g.146702366_146702369del, NC_000004.11:g.146702367_146702369del, NC_000004.11:g.146702368_146702369del, NC_000004.11:g.146702369del, NC_000004.11:g.146702369dup, NC_000004.11:g.146702368_146702369dup, NC_000004.11:g.146702367_146702369dup, NC_000004.11:g.146702366_146702369dup, NC_000004.11:g.146702365_146702369dup, NC_000004.11:g.146702364_146702369dup, NC_000004.11:g.146702363_146702369dup, NC_000004.11:g.146702362_146702369dup, NC_000004.11:g.146702361_146702369dup, NC_000004.11:g.146702360_146702369dup, NC_000004.11:g.146702359_146702369dup, NC_000004.11:g.146702358_146702369dup, NC_000004.11:g.146702357_146702369dup, NC_000004.11:g.146702356_146702369dup, NC_000004.11:g.146702355_146702369dup, NC_000004.11:g.146702354_146702369dup, NC_000004.11:g.146702353_146702369dup, NC_000004.11:g.146702352_146702369dup, NC_000004.11:g.146702351_146702369dup, NC_000004.11:g.146702350_146702369dup, NC_000004.11:g.146702349_146702369dup, NC_000004.11:g.146702348_146702369dup, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702369_146702370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146702348_146702369A[56]CAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000004.11:g.146702348_146702369A[30]GAAAAAAAAAAAAAAAAAAAAAAA[1]

Select item 14915662783.

rs1491566278 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CGTGTGTGTG [Show Flanks]
Chromosome:: 4:145930828 (GRCh38)
4:146851981 (GRCh37)
Canonical SPDI:: NC_000004.12:145930828:GTGTGTGTGCGTGTGTGTG:GTGTGTGTGCGTGTGTGTGCGTGTGTGTG
Gene:: ZNF827 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: GTGTGTGTGCGTGTGTGTGCGTGTGTGTG=0./0 (ALFA)
GTGTGTGTGC=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.145930838_145930847dup, NC_000004.11:g.146851990_146851999dup

Select item 14915115314.

rs1491511531 has merged into rs70956877 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACACACACACACACAC>-,ACAC,ACACAC,ACACACAC,ACACACACAC,ACACACACACAC,ACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC,ACACACACACACACACACACACAC,ACACACACACACACACACACACACAC,ACACACACACACACACACACACACACAC [Show Flanks]
Chromosome:: 4:145856995 (GRCh38)
4:146778147 (GRCh37)
Canonical SPDI:: NC_000004.12:145856985:CACACACACACACACACACACACAC:CACACACAC,NC_000004.12:145856985:CACACACACACACACACACACACAC:CACACACACACAC,NC_000004.12:145856985:CACACACACACACACACACACACAC:CACACACACACACAC,NC_000004.12:145856985:CACACACACACACACACACACACAC:CACACACACACACACAC,NC_000004.12:145856985:CACACACACACACACACACACACAC:CACACACACACACACACAC,NC_000004.12:145856985:CACACACACACACACACACACACAC:CACACACACACACACACACAC,NC_000004.12:145856985:CACACACACACACACACACACACAC:CACACACACACACACACACACAC,NC_000004.12:145856985:CACACACACACACACACACACACAC:CACACACACACACACACACACACACAC,NC_000004.12:145856985:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC,NC_000004.12:145856985:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC,NC_000004.12:145856985:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC,NC_000004.12:145856985:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACAC,NC_000004.12:145856985:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACAC
Gene:: ZNF827 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACACACACACAC=0./0 (ALFA)
HGVS:: NC_000004.12:g.145856987AC[4], NC_000004.12:g.145856987AC[6], NC_000004.12:g.145856987AC[7], NC_000004.12:g.145856987AC[8], NC_000004.12:g.145856987AC[9], NC_000004.12:g.145856987AC[10], NC_000004.12:g.145856987AC[11], NC_000004.12:g.145856987AC[13], NC_000004.12:g.145856987AC[14], NC_000004.12:g.145856987AC[15], NC_000004.12:g.145856987AC[16], NC_000004.12:g.145856987AC[17], NC_000004.12:g.145856987AC[18], NC_000004.11:g.146778139AC[4], NC_000004.11:g.146778139AC[6], NC_000004.11:g.146778139AC[7], NC_000004.11:g.146778139AC[8], NC_000004.11:g.146778139AC[9], NC_000004.11:g.146778139AC[10], NC_000004.11:g.146778139AC[11], NC_000004.11:g.146778139AC[13], NC_000004.11:g.146778139AC[14], NC_000004.11:g.146778139AC[15], NC_000004.11:g.146778139AC[16], NC_000004.11:g.146778139AC[17], NC_000004.11:g.146778139AC[18]

Select item 14915011265.

rs1491501126 has merged into rs763617063 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,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,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 4:145917712 (GRCh38)
4:146838864 (GRCh37)
Canonical SPDI:: NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145917700:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ZNF827 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
-=0.175/7 (GENOME_DK)
HGVS:: NC_000004.12:g.145917712_145917726del, NC_000004.12:g.145917713_145917726del, NC_000004.12:g.145917714_145917726del, NC_000004.12:g.145917715_145917726del, NC_000004.12:g.145917716_145917726del, NC_000004.12:g.145917717_145917726del, NC_000004.12:g.145917718_145917726del, NC_000004.12:g.145917719_145917726del, NC_000004.12:g.145917720_145917726del, NC_000004.12:g.145917721_145917726del, NC_000004.12:g.145917722_145917726del, NC_000004.12:g.145917723_145917726del, NC_000004.12:g.145917724_145917726del, NC_000004.12:g.145917725_145917726del, NC_000004.12:g.145917726del, NC_000004.12:g.145917726dup, NC_000004.12:g.145917725_145917726dup, NC_000004.12:g.145917724_145917726dup, NC_000004.12:g.145917723_145917726dup, NC_000004.12:g.145917722_145917726dup, NC_000004.12:g.145917721_145917726dup, NC_000004.12:g.145917720_145917726dup, NC_000004.12:g.145917719_145917726dup, NC_000004.12:g.145917718_145917726dup, NC_000004.12:g.145917717_145917726dup, NC_000004.12:g.145917716_145917726dup, NC_000004.12:g.145917715_145917726dup, NC_000004.12:g.145917714_145917726dup, NC_000004.12:g.145917713_145917726dup, NC_000004.12:g.145917712_145917726dup, NC_000004.12:g.145917711_145917726dup, NC_000004.12:g.145917710_145917726dup, NC_000004.12:g.145917709_145917726dup, NC_000004.12:g.145917708_145917726dup, NC_000004.12:g.145917707_145917726dup, NC_000004.12:g.145917706_145917726dup, NC_000004.12:g.145917705_145917726dup, NC_000004.12:g.145917704_145917726dup, NC_000004.12:g.145917703_145917726dup, NC_000004.12:g.145917702_145917726dup, NC_000004.12:g.145917701_145917726dup, NC_000004.12:g.145917726_145917727insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145917726_145917727insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145917726_145917727insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.145917701_145917726A[31]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000004.11:g.146838864_146838878del, NC_000004.11:g.146838865_146838878del, NC_000004.11:g.146838866_146838878del, NC_000004.11:g.146838867_146838878del, NC_000004.11:g.146838868_146838878del, NC_000004.11:g.146838869_146838878del, NC_000004.11:g.146838870_146838878del, NC_000004.11:g.146838871_146838878del, NC_000004.11:g.146838872_146838878del, NC_000004.11:g.146838873_146838878del, NC_000004.11:g.146838874_146838878del, NC_000004.11:g.146838875_146838878del, NC_000004.11:g.146838876_146838878del, NC_000004.11:g.146838877_146838878del, NC_000004.11:g.146838878del, NC_000004.11:g.146838878dup, NC_000004.11:g.146838877_146838878dup, NC_000004.11:g.146838876_146838878dup, NC_000004.11:g.146838875_146838878dup, NC_000004.11:g.146838874_146838878dup, NC_000004.11:g.146838873_146838878dup, NC_000004.11:g.146838872_146838878dup, NC_000004.11:g.146838871_146838878dup, NC_000004.11:g.146838870_146838878dup, NC_000004.11:g.146838869_146838878dup, NC_000004.11:g.146838868_146838878dup, NC_000004.11:g.146838867_146838878dup, NC_000004.11:g.146838866_146838878dup, NC_000004.11:g.146838865_146838878dup, NC_000004.11:g.146838864_146838878dup, NC_000004.11:g.146838863_146838878dup, NC_000004.11:g.146838862_146838878dup, NC_000004.11:g.146838861_146838878dup, NC_000004.11:g.146838860_146838878dup, NC_000004.11:g.146838859_146838878dup, NC_000004.11:g.146838858_146838878dup, NC_000004.11:g.146838857_146838878dup, NC_000004.11:g.146838856_146838878dup, NC_000004.11:g.146838855_146838878dup, NC_000004.11:g.146838854_146838878dup, NC_000004.11:g.146838853_146838878dup, NC_000004.11:g.146838878_146838879insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146838878_146838879insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146838878_146838879insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.146838853_146838878A[31]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], XM_011531635.3:c.-8610_-8596del, XM_011531635.3:c.-8609_-8596del, XM_011531635.3:c.-8608_-8596del, XM_011531635.3:c.-8607_-8596del, XM_011531635.3:c.-8606_-8596del, XM_011531635.3:c.-8605_-8596del, XM_011531635.3:c.-8604_-8596del, XM_011531635.3:c.-8603_-8596del, XM_011531635.3:c.-8602_-8596del, XM_011531635.3:c.-8601_-8596del, XM_011531635.3:c.-8600_-8596del, XM_011531635.3:c.-8599_-8596del, XM_011531635.3:c.-8598_-8596del, XM_011531635.3:c.-8597_-8596del, XM_011531635.3:c.-8596del, XM_011531635.3:c.-8596dup, XM_011531635.3:c.-8597_-8596dup, XM_011531635.3:c.-8598_-8596dup, XM_011531635.3:c.-8599_-8596dup, XM_011531635.3:c.-8600_-8596dup, XM_011531635.3:c.-8601_-8596dup, XM_011531635.3:c.-8602_-8596dup, XM_011531635.3:c.-8603_-8596dup, XM_011531635.3:c.-8604_-8596dup, XM_011531635.3:c.-8605_-8596dup, XM_011531635.3:c.-8606_-8596dup, XM_011531635.3:c.-8607_-8596dup, XM_011531635.3:c.-8608_-8596dup, XM_011531635.3:c.-8609_-8596dup, XM_011531635.3:c.-8610_-8596dup, XM_011531635.3:c.-8611_-8596dup, XM_011531635.3:c.-8612_-8596dup, XM_011531635.3:c.-8613_-8596dup, XM_011531635.3:c.-8614_-8596dup, XM_011531635.3:c.-8615_-8596dup, XM_011531635.3:c.-8616_-8596dup, XM_011531635.3:c.-8617_-8596dup, XM_011531635.3:c.-8618_-8596dup, XM_011531635.3:c.-8619_-8596dup, XM_011531635.3:c.-8620_-8596dup, XM_011531635.3:c.-8621_-8596dup, XM_011531635.3:c.-8596_-8595insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011531635.3:c.-8596_-8595insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011531635.3:c.-8596_-8595insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011531635.3:c.-8621_-8596T[29]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007769.2:c.-9369_-9355del, XM_017007769.2:c.-9368_-9355del, XM_017007769.2:c.-9367_-9355del, XM_017007769.2:c.-9366_-9355del, XM_017007769.2:c.-9365_-9355del, XM_017007769.2:c.-9364_-9355del, XM_017007769.2:c.-9363_-9355del, XM_017007769.2:c.-9362_-9355del, XM_017007769.2:c.-9361_-9355del, XM_017007769.2:c.-9360_-9355del, XM_017007769.2:c.-9359_-9355del, XM_017007769.2:c.-9358_-9355del, XM_017007769.2:c.-9357_-9355del, XM_017007769.2:c.-9356_-9355del, XM_017007769.2:c.-9355del, XM_017007769.2:c.-9355dup, XM_017007769.2:c.-9356_-9355dup, XM_017007769.2:c.-9357_-9355dup, XM_017007769.2:c.-9358_-9355dup, XM_017007769.2:c.-9359_-9355dup, XM_017007769.2:c.-9360_-9355dup, XM_017007769.2:c.-9361_-9355dup, XM_017007769.2:c.-9362_-9355dup, XM_017007769.2:c.-9363_-9355dup, XM_017007769.2:c.-9364_-9355dup, XM_017007769.2:c.-9365_-9355dup, XM_017007769.2:c.-9366_-9355dup, XM_017007769.2:c.-9367_-9355dup, XM_017007769.2:c.-9368_-9355dup, XM_017007769.2:c.-9369_-9355dup, XM_017007769.2:c.-9370_-9355dup, XM_017007769.2:c.-9371_-9355dup, XM_017007769.2:c.-9372_-9355dup, XM_017007769.2:c.-9373_-9355dup, XM_017007769.2:c.-9374_-9355dup, XM_017007769.2:c.-9375_-9355dup, XM_017007769.2:c.-9376_-9355dup, XM_017007769.2:c.-9377_-9355dup, XM_017007769.2:c.-9378_-9355dup, XM_017007769.2:c.-9379_-9355dup, XM_017007769.2:c.-9380_-9355dup, XM_017007769.2:c.-9355_-9354insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007769.2:c.-9355_-9354insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007769.2:c.-9355_-9354insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007769.2:c.-9380_-9355T[29]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 14914889356.

rs1491488935 has merged into rs1374403075 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>-,TATA [Show Flanks]
Chromosome:: 4:145793279 (GRCh38)
4:146714431 (GRCh37)
Canonical SPDI:: NC_000004.12:145793268:TATATATATATA:TATATATATA,NC_000004.12:145793268:TATATATATATA:TATATATATATATA
Gene:: ZNF827 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATATATA=0./0 (ALFA)
HGVS:: NC_000004.12:g.145793269TA[5], NC_000004.12:g.145793269TA[7], NC_000004.11:g.146714421TA[5], NC_000004.11:g.146714421TA[7]

Select item 14914648817.

rs1491464881 has merged into rs370427705 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 4:145938628 (GRCh38)
4:146859780 (GRCh37)
Canonical SPDI:: NC_000004.12:145938622:TTTTTTTTTTTTTTTT:TTTTT,NC_000004.12:145938622:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:145938622:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:145938622:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:145938622:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:145938622:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:145938622:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:145938622:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT
Gene:: ZNF827 (Varview)
Functional Consequence:: 5_prime_UTR_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
-=0.3/12 (GENOME_DK)
-=0.41713/2089 (1000Genomes)
HGVS:: NC_000004.12:g.145938628_145938638del, NC_000004.12:g.145938634_145938638del, NC_000004.12:g.145938636_145938638del, NC_000004.12:g.145938637_145938638del, NC_000004.12:g.145938638del, NC_000004.12:g.145938638dup, NC_000004.12:g.145938637_145938638dup, NC_000004.12:g.145938636_145938638dup, NC_000004.11:g.146859780_146859790del, NC_000004.11:g.146859786_146859790del, NC_000004.11:g.146859788_146859790del, NC_000004.11:g.146859789_146859790del, NC_000004.11:g.146859790del, NC_000004.11:g.146859790dup, NC_000004.11:g.146859789_146859790dup, NC_000004.11:g.146859788_146859790dup, NM_178835.5:c.-226_-216del, NM_178835.5:c.-220_-216del, NM_178835.5:c.-218_-216del, NM_178835.5:c.-217_-216del, NM_178835.5:c.-216del, NM_178835.5:c.-216dup, NM_178835.5:c.-217_-216dup, NM_178835.5:c.-218_-216dup, NM_178835.4:c.-226_-216del, NM_178835.4:c.-220_-216del, NM_178835.4:c.-218_-216del, NM_178835.4:c.-217_-216del, NM_178835.4:c.-216del, NM_178835.4:c.-216dup, NM_178835.4:c.-217_-216dup, NM_178835.4:c.-218_-216dup, XM_011531634.4:c.-226_-216del, XM_011531634.4:c.-220_-216del, XM_011531634.4:c.-218_-216del, XM_011531634.4:c.-217_-216del, XM_011531634.4:c.-216del, XM_011531634.4:c.-216dup, XM_011531634.4:c.-217_-216dup, XM_011531634.4:c.-218_-216dup, XM_017007768.3:c.-226_-216del, XM_017007768.3:c.-220_-216del, XM_017007768.3:c.-218_-216del, XM_017007768.3:c.-217_-216del, XM_017007768.3:c.-216del, XM_017007768.3:c.-216dup, XM_017007768.3:c.-217_-216dup, XM_017007768.3:c.-218_-216dup, XM_017007768.2:c.-226_-216del, XM_017007768.2:c.-220_-216del, XM_017007768.2:c.-218_-216del, XM_017007768.2:c.-217_-216del, XM_017007768.2:c.-216del, XM_017007768.2:c.-216dup, XM_017007768.2:c.-217_-216dup, XM_017007768.2:c.-218_-216dup, XM_017007768.1:c.-226_-216del, XM_017007768.1:c.-220_-216del, XM_017007768.1:c.-218_-216del, XM_017007768.1:c.-217_-216del, XM_017007768.1:c.-216del, XM_017007768.1:c.-216dup, XM_017007768.1:c.-217_-216dup, XM_017007768.1:c.-218_-216dup, XM_017007770.3:c.-226_-216del, XM_017007770.3:c.-220_-216del, XM_017007770.3:c.-218_-216del, XM_017007770.3:c.-217_-216del, XM_017007770.3:c.-216del, XM_017007770.3:c.-216dup, XM_017007770.3:c.-217_-216dup, XM_017007770.3:c.-218_-216dup, XM_017007770.2:c.-226_-216del, XM_017007770.2:c.-220_-216del, XM_017007770.2:c.-218_-216del, XM_017007770.2:c.-217_-216del, XM_017007770.2:c.-216del, XM_017007770.2:c.-216dup, XM_017007770.2:c.-217_-216dup, XM_017007770.2:c.-218_-216dup, XM_017007770.1:c.-226_-216del, XM_017007770.1:c.-220_-216del, XM_017007770.1:c.-218_-216del, XM_017007770.1:c.-217_-216del, XM_017007770.1:c.-216del, XM_017007770.1:c.-216dup, XM_017007770.1:c.-217_-216dup, XM_017007770.1:c.-218_-216dup, XM_017007775.3:c.-226_-216del, XM_017007775.3:c.-220_-216del, XM_017007775.3:c.-218_-216del, XM_017007775.3:c.-217_-216del, XM_017007775.3:c.-216del, XM_017007775.3:c.-216dup, XM_017007775.3:c.-217_-216dup, XM_017007775.3:c.-218_-216dup, XM_017007775.2:c.-226_-216del, XM_017007775.2:c.-220_-216del, XM_017007775.2:c.-218_-216del, XM_017007775.2:c.-217_-216del, XM_017007775.2:c.-216del, XM_017007775.2:c.-216dup, XM_017007775.2:c.-217_-216dup, XM_017007775.2:c.-218_-216dup, XM_017007775.1:c.-226_-216del, XM_017007775.1:c.-220_-216del, XM_017007775.1:c.-218_-216del, XM_017007775.1:c.-217_-216del, XM_017007775.1:c.-216del, XM_017007775.1:c.-216dup, XM_017007775.1:c.-217_-216dup, XM_017007775.1:c.-218_-216dup, XM_017007776.3:c.-226_-216del, XM_017007776.3:c.-220_-216del, XM_017007776.3:c.-218_-216del, XM_017007776.3:c.-217_-216del, XM_017007776.3:c.-216del, XM_017007776.3:c.-216dup, XM_017007776.3:c.-217_-216dup, XM_017007776.3:c.-218_-216dup, XM_017007776.2:c.-226_-216del, XM_017007776.2:c.-220_-216del, XM_017007776.2:c.-218_-216del, XM_017007776.2:c.-217_-216del, XM_017007776.2:c.-216del, XM_017007776.2:c.-216dup, XM_017007776.2:c.-217_-216dup, XM_017007776.2:c.-218_-216dup, XM_017007776.1:c.-226_-216del, XM_017007776.1:c.-220_-216del, XM_017007776.1:c.-218_-216del, XM_017007776.1:c.-217_-216del, XM_017007776.1:c.-216del, XM_017007776.1:c.-216dup, XM_017007776.1:c.-217_-216dup, XM_017007776.1:c.-218_-216dup, NM_001306215.2:c.-226_-216del, NM_001306215.2:c.-220_-216del, NM_001306215.2:c.-218_-216del, NM_001306215.2:c.-217_-216del, NM_001306215.2:c.-216del, NM_001306215.2:c.-216dup, NM_001306215.2:c.-217_-216dup, NM_001306215.2:c.-218_-216dup, NM_001306215.1:c.-226_-216del, NM_001306215.1:c.-220_-216del, NM_001306215.1:c.-218_-216del, NM_001306215.1:c.-217_-216del, NM_001306215.1:c.-216del, NM_001306215.1:c.-216dup, NM_001306215.1:c.-217_-216dup, NM_001306215.1:c.-218_-216dup, NM_001410850.1:c.-226_-216del, NM_001410850.1:c.-220_-216del, NM_001410850.1:c.-218_-216del, NM_001410850.1:c.-217_-216del, NM_001410850.1:c.-216del, NM_001410850.1:c.-216dup, NM_001410850.1:c.-217_-216dup, NM_001410850.1:c.-218_-216dup, XM_047449635.1:c.-226_-216del, XM_047449635.1:c.-220_-216del, XM_047449635.1:c.-218_-216del, XM_047449635.1:c.-217_-216del, XM_047449635.1:c.-216del, XM_047449635.1:c.-216dup, XM_047449635.1:c.-217_-216dup, XM_047449635.1:c.-218_-216dup, XM_047449640.1:c.-226_-216del, XM_047449640.1:c.-220_-216del, XM_047449640.1:c.-218_-216del, XM_047449640.1:c.-217_-216del, XM_047449640.1:c.-216del, XM_047449640.1:c.-216dup, XM_047449640.1:c.-217_-216dup, XM_047449640.1:c.-218_-216dup, XM_047449637.1:c.-226_-216del, XM_047449637.1:c.-220_-216del, XM_047449637.1:c.-218_-216del, XM_047449637.1:c.-217_-216del, XM_047449637.1:c.-216del, XM_047449637.1:c.-216dup, XM_047449637.1:c.-217_-216dup, XM_047449637.1:c.-218_-216dup, XM_047449638.1:c.-226_-216del, XM_047449638.1:c.-220_-216del, XM_047449638.1:c.-218_-216del, XM_047449638.1:c.-217_-216del, XM_047449638.1:c.-216del, XM_047449638.1:c.-216dup, XM_047449638.1:c.-217_-216dup, XM_047449638.1:c.-218_-216dup, XM_047449639.1:c.-226_-216del, XM_047449639.1:c.-220_-216del, XM_047449639.1:c.-218_-216del, XM_047449639.1:c.-217_-216del, XM_047449639.1:c.-216del, XM_047449639.1:c.-216dup, XM_047449639.1:c.-217_-216dup, XM_047449639.1:c.-218_-216dup

Select item 14914483118.

rs1491448311 has merged into rs1161382967 [Homo sapiens]

Variant type:: DELINS
Alleles:: TGTG>-,TG [Show Flanks]
Chromosome:: 4:145930834 (GRCh38)
4:146851986 (GRCh37)
Canonical SPDI:: NC_000004.12:145930827:TGTGTGTGTG:TGTGTG,NC_000004.12:145930827:TGTGTGTGTG:TGTGTGTG
Gene:: ZNF827 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTG=0./0 (ALFA)
-=0.000036/5 (GnomAD)
HGVS:: NC_000004.12:g.145930828TG[3], NC_000004.12:g.145930828TG[4], NC_000004.11:g.146851980TG[3], NC_000004.11:g.146851980TG[4]

Select item 14914394829.

rs1491439482 has merged into rs1330217552 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT [Show Flanks]
Chromosome:: 4:145857012 (GRCh38)
4:146778164 (GRCh37)
Canonical SPDI:: NC_000004.12:145857009:CTCT:CT,NC_000004.12:145857009:CTCT:CTCTCT
Gene:: ZNF827 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTCTCT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000156/1 (1000Genomes)
HGVS:: NC_000004.12:g.145857010CT[1], NC_000004.12:g.145857010CT[3], NC_000004.11:g.146778162CT[1], NC_000004.11:g.146778162CT[3]

Select item 149142566210.

rs1491425662 [Homo sapiens]

Variant type:: DEL
Alleles:: TC>- [Show Flanks]
Chromosome:: 4:145938937 (GRCh38)
4:146860089 (GRCh37)
Canonical SPDI:: NC_000004.12:145938936:TC:
Gene:: ZNF827 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.145938937_145938938del, NC_000004.11:g.146860089_146860090del, NM_178835.4:c.-531_-530del, NM_001306215.1:c.-531_-530del

Select item 149138484111.

rs1491384841 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 4:145872320 (GRCh38)
4:146793472 (GRCh37)
Canonical SPDI:: NC_000004.12:145872319:AA:
Gene:: ZNF827 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000178/25 (GnomAD)
-=0.000181/48 (TOPMED)
HGVS:: NC_000004.12:g.145872320_145872321del, NC_000004.11:g.146793472_146793473del

Select item 149138111012.

rs1491381110 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 4:145918332 (GRCh38)
4:146839484 (GRCh37)
Canonical SPDI:: NC_000004.12:145918331:CA:
Gene:: ZNF827 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.00666/79 (ALFA)
HGVS:: NC_000004.12:g.145918332_145918333del, NC_000004.11:g.146839484_146839485del

Select item 149136545313.

rs1491365453 has merged into rs34428145 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAAA>-,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 4:145918341 (GRCh38)
4:146839493 (GRCh37)
Canonical SPDI:: NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:145918332:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ZNF827 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAA=0./0 (ALFA)
-=0.1/4 (GENOME_DK)
HGVS:: NC_000004.12:g.145918341_145918359del, NC_000004.12:g.145918345_145918359del, NC_000004.12:g.145918346_145918359del, NC_000004.12:g.145918347_145918359del, NC_000004.12:g.145918348_145918359del, NC_000004.12:g.145918349_145918359del, NC_000004.12:g.145918350_145918359del, NC_000004.12:g.145918351_145918359del, NC_000004.12:g.145918352_145918359del, NC_000004.12:g.145918353_145918359del, NC_000004.12:g.145918354_145918359del, NC_000004.12:g.145918355_145918359del, NC_000004.12:g.145918356_145918359del, NC_000004.12:g.145918357_145918359del, NC_000004.12:g.145918358_145918359del, NC_000004.12:g.145918359del, NC_000004.12:g.145918359dup, NC_000004.12:g.145918358_145918359dup, NC_000004.12:g.145918357_145918359dup, NC_000004.12:g.145918356_145918359dup, NC_000004.12:g.145918355_145918359dup, NC_000004.12:g.145918354_145918359dup, NC_000004.12:g.145918353_145918359dup, NC_000004.12:g.145918352_145918359dup, NC_000004.12:g.145918351_145918359dup, NC_000004.12:g.145918350_145918359dup, NC_000004.12:g.145918347_145918359dup, NC_000004.12:g.145918345_145918359dup, NC_000004.12:g.145918343_145918359dup, NC_000004.12:g.145918342_145918359dup, NC_000004.12:g.145918337_145918359dup, NC_000004.11:g.146839493_146839511del, NC_000004.11:g.146839497_146839511del, NC_000004.11:g.146839498_146839511del, NC_000004.11:g.146839499_146839511del, NC_000004.11:g.146839500_146839511del, NC_000004.11:g.146839501_146839511del, NC_000004.11:g.146839502_146839511del, NC_000004.11:g.146839503_146839511del, NC_000004.11:g.146839504_146839511del, NC_000004.11:g.146839505_146839511del, NC_000004.11:g.146839506_146839511del, NC_000004.11:g.146839507_146839511del, NC_000004.11:g.146839508_146839511del, NC_000004.11:g.146839509_146839511del, NC_000004.11:g.146839510_146839511del, NC_000004.11:g.146839511del, NC_000004.11:g.146839511dup, NC_000004.11:g.146839510_146839511dup, NC_000004.11:g.146839509_146839511dup, NC_000004.11:g.146839508_146839511dup, NC_000004.11:g.146839507_146839511dup, NC_000004.11:g.146839506_146839511dup, NC_000004.11:g.146839505_146839511dup, NC_000004.11:g.146839504_146839511dup, NC_000004.11:g.146839503_146839511dup, NC_000004.11:g.146839502_146839511dup, NC_000004.11:g.146839499_146839511dup, NC_000004.11:g.146839497_146839511dup, NC_000004.11:g.146839495_146839511dup, NC_000004.11:g.146839494_146839511dup, NC_000004.11:g.146839489_146839511dup

Select item 149135087214.

rs1491350872 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 4:145781195 (GRCh38)
4:146702347 (GRCh37)
Canonical SPDI:: NC_000004.12:145781194:CA:
Gene:: ZNF827 (Varview), C4orf51 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
-=0.00095/21 (TOMMO)
HGVS:: NC_000004.12:g.145781195_145781196del, NC_000004.11:g.146702347_146702348del

Select item 149133643115.

rs1491336431 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 4:145793311 (GRCh38)
4:146714463 (GRCh37)
Canonical SPDI:: NC_000004.12:145793310:TT:
Gene:: ZNF827 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000004.12:g.145793311_145793312del, NC_000004.11:g.146714463_146714464del

Select item 149131725116.

rs1491317251 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 4:145793268 (GRCh38)
4:146714420 (GRCh37)
Canonical SPDI:: NC_000004.12:145793267:TT:
Gene:: ZNF827 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00001/1 (GnomAD)
HGVS:: NC_000004.12:g.145793268_145793269del, NC_000004.11:g.146714420_146714421del

Select item 149126429717.

rs1491264297 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,AA,T [Show Flanks]
Chromosome:: 4:145843223 (GRCh38)
4:146764376 (GRCh37)
Canonical SPDI:: NC_000004.12:145843223::A,NC_000004.12:145843223::AA,NC_000004.12:145843223::T
Gene:: ZNF827 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000004.12:g.145843223_145843224insA, NC_000004.12:g.145843223_145843224insAA, NC_000004.12:g.145843223_145843224insT, NC_000004.11:g.146764375_146764376insA, NC_000004.11:g.146764375_146764376insAA, NC_000004.11:g.146764375_146764376insT

Select item 149119872618.

rs1491198726 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATA,CATATAATATATATCTTATATATATTATATATATTAAATATATATCTTATATATTTAATA [Show Flanks]
Chromosome:: 4:145793311 (GRCh38)
4:146714464 (GRCh37)
Canonical SPDI:: NC_000004.12:145793311:TA:TAATA,NC_000004.12:145793311:TA:TACATATAATATATATCTTATATATATTATATATATTAAATATATATCTTATATATTTAATA
Gene:: ZNF827 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TAATA=0.00059/7 (ALFA)
TAA=0.00088/14 (TOMMO)
HGVS:: NC_000004.12:g.145793313_145793314insATA, NC_000004.12:g.145793313_145793314insCATATAATATATATCTTATATATATTATATATATTAAATATATATCTTATATATTTAATA, NC_000004.11:g.146714465_146714466insATA, NC_000004.11:g.146714465_146714466insCATATAATATATATCTTATATATATTATATATATTAAATATATATCTTATATATTTAATA

Select item 149116538619.

rs1491165386 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 4:145917700 (GRCh38)
4:146838852 (GRCh37)
Canonical SPDI:: NC_000004.12:145917699:CA:
Gene:: ZNF827 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000004.12:g.145917700_145917701del, NC_000004.11:g.146838852_146838853del, XM_011531635.3:c.-8596_-8595del, XM_017007769.2:c.-9355_-9354del

Select item 149115154620.

rs1491151546 [Homo sapiens]

Variant type:: DEL
Alleles:: GG>- [Show Flanks]
Chromosome:: 4:145843223 (GRCh38)
4:146764375 (GRCh37)
Canonical SPDI:: NC_000004.12:145843222:GG:
Gene:: ZNF827 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00023/1 (ALFA)
-=0.00001/1 (GnomAD)
HGVS:: NC_000004.12:g.145843223_145843224del, NC_000004.11:g.146764375_146764376del

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