SNP Links for Gene (Select 3801) - SNP

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Select item 14915871181.

rs1491587118 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTT [Show Flanks]
Chromosome:: 16:57850466 (GRCh38)
16:57884371 (GRCh37)
Canonical SPDI:: NC_000016.10:57850466:TT:TTGTT
Gene:: KIFC3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TTGTT=0./0 (ALFA)
HGVS:: NC_000016.10:g.57850468_57850469insGTT, NC_000016.9:g.57884372_57884373insGTT

Select item 14915731442.

rs1491573144 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TAAAATAAAATAAAATAAAATAAAATAA [Show Flanks]
Chromosome:: 16:57860033 (GRCh38)
16:57893938 (GRCh37)
Canonical SPDI:: NC_000016.10:57860033:AA:AATAAAATAAAATAAAATAAAATAAAATAA
Gene:: KIFC3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency
MAF:: AATAAAATAAAATAAAATAAAATAAAAT=0.00025/18 (GnomAD)
HGVS:: NC_000016.10:g.57860035_57860036insTAAAATAAAATAAAATAAAATAAAATAA, NC_000016.9:g.57893939_57893940insTAAAATAAAATAAAATAAAATAAAATAA

Select item 14915572043.

rs1491557204 has merged into rs57102595 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 16:57857834 (GRCh38)
16:57891738 (GRCh37)
Canonical SPDI:: NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57857822:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: KIFC3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
TTTT=0.1975/761 (ALSPAC)
TTTT=0.2112/783 (TWINSUK)
HGVS:: NC_000016.10:g.57857834_57857844del, NC_000016.10:g.57857835_57857844del, NC_000016.10:g.57857836_57857844del, NC_000016.10:g.57857837_57857844del, NC_000016.10:g.57857838_57857844del, NC_000016.10:g.57857839_57857844del, NC_000016.10:g.57857840_57857844del, NC_000016.10:g.57857841_57857844del, NC_000016.10:g.57857842_57857844del, NC_000016.10:g.57857843_57857844del, NC_000016.10:g.57857844del, NC_000016.10:g.57857844dup, NC_000016.10:g.57857843_57857844dup, NC_000016.10:g.57857842_57857844dup, NC_000016.10:g.57857841_57857844dup, NC_000016.10:g.57857840_57857844dup, NC_000016.10:g.57857839_57857844dup, NC_000016.10:g.57857838_57857844dup, NC_000016.10:g.57857837_57857844dup, NC_000016.10:g.57857836_57857844dup, NC_000016.10:g.57857835_57857844dup, NC_000016.10:g.57857834_57857844dup, NC_000016.10:g.57857833_57857844dup, NC_000016.10:g.57857823_57857844T[34]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000016.10:g.57857832_57857844dup, NC_000016.10:g.57857830_57857844dup, NC_000016.10:g.57857829_57857844dup, NC_000016.10:g.57857828_57857844dup, NC_000016.10:g.57857826_57857844dup, NC_000016.9:g.57891738_57891748del, NC_000016.9:g.57891739_57891748del, NC_000016.9:g.57891740_57891748del, NC_000016.9:g.57891741_57891748del, NC_000016.9:g.57891742_57891748del, NC_000016.9:g.57891743_57891748del, NC_000016.9:g.57891744_57891748del, NC_000016.9:g.57891745_57891748del, NC_000016.9:g.57891746_57891748del, NC_000016.9:g.57891747_57891748del, NC_000016.9:g.57891748del, NC_000016.9:g.57891748dup, NC_000016.9:g.57891747_57891748dup, NC_000016.9:g.57891746_57891748dup, NC_000016.9:g.57891745_57891748dup, NC_000016.9:g.57891744_57891748dup, NC_000016.9:g.57891743_57891748dup, NC_000016.9:g.57891742_57891748dup, NC_000016.9:g.57891741_57891748dup, NC_000016.9:g.57891740_57891748dup, NC_000016.9:g.57891739_57891748dup, NC_000016.9:g.57891738_57891748dup, NC_000016.9:g.57891737_57891748dup, NC_000016.9:g.57891727_57891748T[34]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000016.9:g.57891736_57891748dup, NC_000016.9:g.57891734_57891748dup, NC_000016.9:g.57891733_57891748dup, NC_000016.9:g.57891732_57891748dup, NC_000016.9:g.57891730_57891748dup

Select item 14915550244.

rs1491555024 has merged into rs1182420410 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAAA [Show Flanks]
Chromosome:: 16:57860039 (GRCh38)
16:57893943 (GRCh37)
Canonical SPDI:: NC_000016.10:57860037:AAAA:A,NC_000016.10:57860037:AAAA:AA,NC_000016.10:57860037:AAAA:AAA,NC_000016.10:57860037:AAAA:AAAAAA
Gene:: KIFC3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000016.10:g.57860039_57860041del, NC_000016.10:g.57860040_57860041del, NC_000016.10:g.57860041del, NC_000016.10:g.57860040_57860041dup, NC_000016.9:g.57893943_57893945del, NC_000016.9:g.57893944_57893945del, NC_000016.9:g.57893945del, NC_000016.9:g.57893944_57893945dup

Select item 14915405665.

rs1491540566 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CAA [Show Flanks]
Chromosome:: 16:57860093 (GRCh38)
16:57893998 (GRCh37)
Canonical SPDI:: NC_000016.10:57860093:AA:AACAA
Gene:: KIFC3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: AACAA=0./0 (ALFA)
HGVS:: NC_000016.10:g.57860095_57860096insCAA, NC_000016.9:g.57893999_57894000insCAA

Select item 14915343376.

rs1491534337 [Homo sapiens]

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

Select item 14915307627.

rs1491530762 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TAAAATAAAATAAAATAAA [Show Flanks]
Chromosome:: 16:57860038 (GRCh38)
16:57893943 (GRCh37)
Canonical SPDI:: NC_000016.10:57860038:AAATAAAATAAAATAAAATAAA:AAATAAAATAAAATAAAATAAATAAAATAAAATAAAATAAA
Gene:: KIFC3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: AAATAAAATAAAATAAAAT=0.00411/397 (GnomAD)
HGVS:: NC_000016.10:g.57860042_57860060dup, NC_000016.9:g.57893946_57893964dup

Select item 14915130998.

rs1491513099 has merged into rs533115992 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 16:57811929 (GRCh38)
16:57845841 (GRCh37)
Canonical SPDI:: NC_000016.10:57811918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000016.10:57811918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000016.10:57811918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:57811918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:57811918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:57811918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000016.10:57811918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:57811918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000016.10:57811918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000016.10:57811918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000016.10:57811918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000016.10:57811918:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: KIFC3 (Varview), LOC388282 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
AA=0.1587/795 (1000Genomes)
HGVS:: NC_000016.10:g.57811929_57811936del, NC_000016.10:g.57811930_57811936del, NC_000016.10:g.57811931_57811936del, NC_000016.10:g.57811932_57811936del, NC_000016.10:g.57811933_57811936del, NC_000016.10:g.57811934_57811936del, NC_000016.10:g.57811935_57811936del, NC_000016.10:g.57811936del, NC_000016.10:g.57811936dup, NC_000016.10:g.57811935_57811936dup, NC_000016.10:g.57811934_57811936dup, NC_000016.10:g.57811930_57811936dup, NC_000016.9:g.57845841_57845848del, NC_000016.9:g.57845842_57845848del, NC_000016.9:g.57845843_57845848del, NC_000016.9:g.57845844_57845848del, NC_000016.9:g.57845845_57845848del, NC_000016.9:g.57845846_57845848del, NC_000016.9:g.57845847_57845848del, NC_000016.9:g.57845848del, NC_000016.9:g.57845848dup, NC_000016.9:g.57845847_57845848dup, NC_000016.9:g.57845846_57845848dup, NC_000016.9:g.57845842_57845848dup, NW_003871085.1:g.71820_71827del, NW_003871085.1:g.71821_71827del, NW_003871085.1:g.71822_71827del, NW_003871085.1:g.71823_71827del, NW_003871085.1:g.71824_71827del, NW_003871085.1:g.71825_71827del, NW_003871085.1:g.71826_71827del, NW_003871085.1:g.71827del, NW_003871085.1:g.71827dup, NW_003871085.1:g.71826_71827dup, NW_003871085.1:g.71825_71827dup, NW_003871085.1:g.71821_71827dup

Select item 14914968389.

rs1491496838 [Homo sapiens]

Variant type:: DEL
Alleles:: AC>- [Show Flanks]
Chromosome:: 16:57864184 (GRCh38)
16:57898088 (GRCh37)
Canonical SPDI:: NC_000016.10:57864183:AC:
Gene:: KIFC3 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: -=0.05/2 (GENOME_DK)
-=0.10791/60 (NorthernSweden)
-=0.15841/10777 (GnomAD)
-=0.20735/3426 (TOMMO)
HGVS:: NC_000016.10:g.57864184_57864185del, NC_000016.9:g.57898088_57898089del

Select item 149146468610.

rs1491464686 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 16:57854628 (GRCh38)
16:57888533 (GRCh37)
Canonical SPDI:: NC_000016.10:57854628:G:GG
Gene:: KIFC3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
HGVS:: NC_000016.10:g.57854629dup, NC_000016.9:g.57888533dup

Select item 149143025311.

rs1491430253 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TAAAATAAAATAAA [Show Flanks]
Chromosome:: 16:57860043 (GRCh38)
16:57893948 (GRCh37)
Canonical SPDI:: NC_000016.10:57860043:AAATAAAATAAAATAAA:AAATAAAATAAAATAAATAAAATAAAATAAA
Gene:: KIFC3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: AAATAAAATAAAAT=0.00185/193 (GnomAD)
HGVS:: NC_000016.10:g.57860047_57860060dup, NC_000016.9:g.57893951_57893964dup

Select item 149142461912.

rs1491424619 has merged into rs1400337211 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA,AAAAA,AAAAAAAAA [Show Flanks]
Chromosome:: 16:57780591 (GRCh38)
16:57814503 (GRCh37)
Canonical SPDI:: NC_000016.10:57780578:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:57780578:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:57780578:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000016.10:57780578:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:57780578:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000016.10:57780578:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA
Gene:: KIFC3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000016.10:g.57780591_57780592del, NC_000016.10:g.57780592del, NC_000016.10:g.57780592dup, NC_000016.10:g.57780591_57780592dup, NC_000016.10:g.57780590_57780592dup, NC_000016.10:g.57780586_57780592dup, NC_000016.9:g.57814503_57814504del, NC_000016.9:g.57814504del, NC_000016.9:g.57814504dup, NC_000016.9:g.57814503_57814504dup, NC_000016.9:g.57814502_57814504dup, NC_000016.9:g.57814498_57814504dup, NW_003871085.1:g.40482_40483del, NW_003871085.1:g.40483del, NW_003871085.1:g.40483dup, NW_003871085.1:g.40482_40483dup, NW_003871085.1:g.40481_40483dup, NW_003871085.1:g.40477_40483dup, XM_047434089.1:c.-1453_-1452del, XM_047434089.1:c.-1452del, XM_047434089.1:c.-1452dup, XM_047434089.1:c.-1453_-1452dup, XM_047434089.1:c.-1454_-1452dup, XM_047434089.1:c.-1458_-1452dup

Select item 149140889213.

rs1491408892 has merged into rs1377738930 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAAA,AAACAAAA [Show Flanks]
Chromosome:: 16:57860034 (GRCh38)
16:57893938 (GRCh37)
Canonical SPDI:: NC_000016.10:57860032:AAAA:A,NC_000016.10:57860032:AAAA:AA,NC_000016.10:57860032:AAAA:AAA,NC_000016.10:57860032:AAAA:AAAAAA,NC_000016.10:57860032:AAAA:AAAACAAAA
Gene:: KIFC3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.00004/1 (TOMMO)
HGVS:: NC_000016.10:g.57860034_57860036del, NC_000016.10:g.57860035_57860036del, NC_000016.10:g.57860036del, NC_000016.10:g.57860035_57860036dup, NC_000016.10:g.57860033_57860036A[4]CAAAA[1], NC_000016.9:g.57893938_57893940del, NC_000016.9:g.57893939_57893940del, NC_000016.9:g.57893940del, NC_000016.9:g.57893939_57893940dup, NC_000016.9:g.57893937_57893940A[4]CAAAA[1]

Select item 149138501114.

rs1491385011 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 16:57811918 (GRCh38)
16:57845830 (GRCh37)
Canonical SPDI:: NC_000016.10:57811917:CA:
Gene:: KIFC3 (Varview), LOC388282 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.05985/710 (ALFA)
-=0.00092/15 (TOMMO)
HGVS:: NC_000016.10:g.57811918_57811919del, NC_000016.9:g.57845830_57845831del, NW_003871085.1:g.71809_71810del

Select item 149138241315.

rs1491382413 has merged into rs55718589 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 16:57862208 (GRCh38)
16:57896112 (GRCh37)
Canonical SPDI:: NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:57862193:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: KIFC3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.2073/799 (ALSPAC)
T=0.396/1983 (1000Genomes)
T=0.4737/18 (GENOME_DK)
HGVS:: NC_000016.10:g.57862208_57862211del, NC_000016.10:g.57862209_57862211del, NC_000016.10:g.57862210_57862211del, NC_000016.10:g.57862211del, NC_000016.10:g.57862211dup, NC_000016.10:g.57862210_57862211dup, NC_000016.10:g.57862209_57862211dup, NC_000016.10:g.57862208_57862211dup, NC_000016.10:g.57862207_57862211dup, NC_000016.10:g.57862206_57862211dup, NC_000016.10:g.57862205_57862211dup, NC_000016.10:g.57862203_57862211dup, NC_000016.10:g.57862202_57862211dup, NC_000016.10:g.57862201_57862211dup, NC_000016.10:g.57862199_57862211dup, NC_000016.10:g.57862211_57862212insTTTTTTTTTTTTTTTTTTTTTTT, NC_000016.9:g.57896112_57896115del, NC_000016.9:g.57896113_57896115del, NC_000016.9:g.57896114_57896115del, NC_000016.9:g.57896115del, NC_000016.9:g.57896115dup, NC_000016.9:g.57896114_57896115dup, NC_000016.9:g.57896113_57896115dup, NC_000016.9:g.57896112_57896115dup, NC_000016.9:g.57896111_57896115dup, NC_000016.9:g.57896110_57896115dup, NC_000016.9:g.57896109_57896115dup, NC_000016.9:g.57896107_57896115dup, NC_000016.9:g.57896106_57896115dup, NC_000016.9:g.57896105_57896115dup, NC_000016.9:g.57896103_57896115dup, NC_000016.9:g.57896115_57896116insTTTTTTTTTTTTTTTTTTTTTTT

Select item 149137423516.

rs1491374235 has merged into rs398100201 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT [Show Flanks]
Chromosome:: 16:57857395 (GRCh38)
16:57891299 (GRCh37)
Canonical SPDI:: NC_000016.10:57857393:TCT:T,NC_000016.10:57857393:TCT:TCTCT
Gene:: KIFC3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.00004/1 (TOMMO)
-=0.00031/21 (GnomAD)
HGVS:: NC_000016.10:g.57857395_57857396del, NC_000016.10:g.57857395_57857396dup, NC_000016.9:g.57891299_57891300del, NC_000016.9:g.57891299_57891300dup

Select item 149137315917.

rs1491373159 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 16:57790077 (GRCh38)
16:57823990 (GRCh37)
Canonical SPDI:: NC_000016.10:57790077:C:CC
Gene:: KIFC3 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: CC=0./0 (ALFA)
HGVS:: NC_000016.10:g.57790078dup, NC_000016.9:g.57823990dup, NW_003871085.1:g.49969dup

Select item 149135996418.

rs1491359964 has merged into rs34278624 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAAAAAA [Show Flanks]
Chromosome:: 16:57855957 (GRCh38)
16:57889861 (GRCh37)
Canonical SPDI:: NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000016.10:57855945:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA
Gene:: KIFC3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
-=0.035/135 (ALSPAC)
HGVS:: NC_000016.10:g.57855957_57855960del, NC_000016.10:g.57855958_57855960del, NC_000016.10:g.57855959_57855960del, NC_000016.10:g.57855960del, NC_000016.10:g.57855960dup, NC_000016.10:g.57855959_57855960dup, NC_000016.10:g.57855954_57855960dup, NC_000016.9:g.57889861_57889864del, NC_000016.9:g.57889862_57889864del, NC_000016.9:g.57889863_57889864del, NC_000016.9:g.57889864del, NC_000016.9:g.57889864dup, NC_000016.9:g.57889863_57889864dup, NC_000016.9:g.57889858_57889864dup

Select item 149134894819.

rs1491348948 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>- [Show Flanks]
Chromosome:: 16:57823761 (GRCh38)
16:57857665 (GRCh37)
Canonical SPDI:: NC_000016.10:57823759:TTT:T
Gene:: KIFC3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00034/4 (ALFA)
-=0.00073/37 (GnomAD)
-=0.00751/125 (TOMMO)
HGVS:: NC_000016.10:g.57823761_57823762del, NC_000016.9:g.57857665_57857666del, NW_003871085.1:g.83652_83653del

Select item 149134345520.

rs1491343455 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 16:57780578 (GRCh38)
16:57814490 (GRCh37)
Canonical SPDI:: NC_000016.10:57780577:TA:
Gene:: KIFC3 (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000084/1 (ALFA)
-=0.000008/1 (GnomAD)
HGVS:: NC_000016.10:g.57780578_57780579del, NC_000016.9:g.57814490_57814491del, NW_003871085.1:g.40469_40470del, XM_047434089.1:c.-1452_-1451del

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