SNP Links for Gene (Select 9928) - SNP

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Select item 14915885391.

rs1491588539 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TAAAA [Show Flanks]
Chromosome:: 1:200594369 (GRCh38)
1:200563498 (GRCh37)
Canonical SPDI:: NC_000001.11:200594369:AAAA:AAAATAAAA
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000001.11:g.200594370_200594373A[4]TAAAA[1], NC_000001.10:g.200563498_200563501A[4]TAAAA[1], NG_042074.1:g.31362_31365T[4]ATTTT[1]

Select item 14915695542.

rs1491569554 [Homo sapiens]

Variant type:: DEL
Alleles:: CC>- [Show Flanks]
Chromosome:: 1:200567169 (GRCh38)
1:200536297 (GRCh37)
Canonical SPDI:: NC_000001.11:200567168:CC:
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: -=0.0054/21 (ALSPAC)
-=0.0067/25 (TWINSUK)
HGVS:: NC_000001.11:g.200567169_200567170del, NC_000001.10:g.200536297_200536298del, NG_042074.1:g.58565_58566del

Select item 14915606413.

rs1491560641 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 1:200575824 (GRCh38)
1:200544952 (GRCh37)
Canonical SPDI:: NC_000001.11:200575823:TA:
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.200575824_200575825del, NC_000001.10:g.200544952_200544953del, NG_042074.1:g.49910_49911del

Select item 14915575014.

rs1491557501 has merged into rs57476742 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTT>-,T,TT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:200593936 (GRCh38)
1:200563064 (GRCh37)
Canonical SPDI:: NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200593927:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000001.11:g.200593936_200593948del, NC_000001.11:g.200593937_200593948del, NC_000001.11:g.200593938_200593948del, NC_000001.11:g.200593945_200593948del, NC_000001.11:g.200593947_200593948del, NC_000001.11:g.200593948del, NC_000001.11:g.200593948dup, NC_000001.11:g.200593947_200593948dup, NC_000001.11:g.200593946_200593948dup, NC_000001.11:g.200593945_200593948dup, NC_000001.11:g.200593944_200593948dup, NC_000001.11:g.200593943_200593948dup, NC_000001.11:g.200593942_200593948dup, NC_000001.11:g.200593941_200593948dup, NC_000001.11:g.200593940_200593948dup, NC_000001.11:g.200593939_200593948dup, NC_000001.11:g.200593938_200593948dup, NC_000001.11:g.200593937_200593948dup, NC_000001.11:g.200593936_200593948dup, NC_000001.11:g.200593934_200593948dup, NC_000001.11:g.200593948_200593949insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200593948_200593949insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200593948_200593949insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200563064_200563076del, NC_000001.10:g.200563065_200563076del, NC_000001.10:g.200563066_200563076del, NC_000001.10:g.200563073_200563076del, NC_000001.10:g.200563075_200563076del, NC_000001.10:g.200563076del, NC_000001.10:g.200563076dup, NC_000001.10:g.200563075_200563076dup, NC_000001.10:g.200563074_200563076dup, NC_000001.10:g.200563073_200563076dup, NC_000001.10:g.200563072_200563076dup, NC_000001.10:g.200563071_200563076dup, NC_000001.10:g.200563070_200563076dup, NC_000001.10:g.200563069_200563076dup, NC_000001.10:g.200563068_200563076dup, NC_000001.10:g.200563067_200563076dup, NC_000001.10:g.200563066_200563076dup, NC_000001.10:g.200563065_200563076dup, NC_000001.10:g.200563064_200563076dup, NC_000001.10:g.200563062_200563076dup, NC_000001.10:g.200563076_200563077insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200563076_200563077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200563076_200563077insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042074.1:g.31795_31807del, NG_042074.1:g.31796_31807del, NG_042074.1:g.31797_31807del, NG_042074.1:g.31804_31807del, NG_042074.1:g.31806_31807del, NG_042074.1:g.31807del, NG_042074.1:g.31807dup, NG_042074.1:g.31806_31807dup, NG_042074.1:g.31805_31807dup, NG_042074.1:g.31804_31807dup, NG_042074.1:g.31803_31807dup, NG_042074.1:g.31802_31807dup, NG_042074.1:g.31801_31807dup, NG_042074.1:g.31800_31807dup, NG_042074.1:g.31799_31807dup, NG_042074.1:g.31798_31807dup, NG_042074.1:g.31797_31807dup, NG_042074.1:g.31796_31807dup, NG_042074.1:g.31795_31807dup, NG_042074.1:g.31793_31807dup, NG_042074.1:g.31807_31808insAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.31807_31808insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.31807_31808insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14913808225.

rs1491380822 has merged into rs66935478 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTT>-,T,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTCCTGGTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:200581772 (GRCh38)
1:200550900 (GRCh37)
Canonical SPDI:: NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTCCTGGTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200581761:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
-=0.35/14 (GENOME_DK)
HGVS:: NC_000001.11:g.200581772_200581784del, NC_000001.11:g.200581773_200581784del, NC_000001.11:g.200581776_200581784del, NC_000001.11:g.200581777_200581784del, NC_000001.11:g.200581778_200581784del, NC_000001.11:g.200581779_200581784del, NC_000001.11:g.200581780_200581784del, NC_000001.11:g.200581781_200581784del, NC_000001.11:g.200581782_200581784del, NC_000001.11:g.200581783_200581784del, NC_000001.11:g.200581784del, NC_000001.11:g.200581784dup, NC_000001.11:g.200581783_200581784dup, NC_000001.11:g.200581782_200581784dup, NC_000001.11:g.200581781_200581784dup, NC_000001.11:g.200581762_200581784T[27]CCTGGTCTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.11:g.200581780_200581784dup, NC_000001.11:g.200581779_200581784dup, NC_000001.11:g.200581778_200581784dup, NC_000001.11:g.200581777_200581784dup, NC_000001.11:g.200581776_200581784dup, NC_000001.11:g.200581772_200581784dup, NC_000001.11:g.200581771_200581784dup, NC_000001.11:g.200581767_200581784dup, NC_000001.11:g.200581762_200581784dup, NC_000001.10:g.200550900_200550912del, NC_000001.10:g.200550901_200550912del, NC_000001.10:g.200550904_200550912del, NC_000001.10:g.200550905_200550912del, NC_000001.10:g.200550906_200550912del, NC_000001.10:g.200550907_200550912del, NC_000001.10:g.200550908_200550912del, NC_000001.10:g.200550909_200550912del, NC_000001.10:g.200550910_200550912del, NC_000001.10:g.200550911_200550912del, NC_000001.10:g.200550912del, NC_000001.10:g.200550912dup, NC_000001.10:g.200550911_200550912dup, NC_000001.10:g.200550910_200550912dup, NC_000001.10:g.200550909_200550912dup, NC_000001.10:g.200550890_200550912T[27]CCTGGTCTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.10:g.200550908_200550912dup, NC_000001.10:g.200550907_200550912dup, NC_000001.10:g.200550906_200550912dup, NC_000001.10:g.200550905_200550912dup, NC_000001.10:g.200550904_200550912dup, NC_000001.10:g.200550900_200550912dup, NC_000001.10:g.200550899_200550912dup, NC_000001.10:g.200550895_200550912dup, NC_000001.10:g.200550890_200550912dup, NG_042074.1:g.43961_43973del, NG_042074.1:g.43962_43973del, NG_042074.1:g.43965_43973del, NG_042074.1:g.43966_43973del, NG_042074.1:g.43967_43973del, NG_042074.1:g.43968_43973del, NG_042074.1:g.43969_43973del, NG_042074.1:g.43970_43973del, NG_042074.1:g.43971_43973del, NG_042074.1:g.43972_43973del, NG_042074.1:g.43973del, NG_042074.1:g.43973dup, NG_042074.1:g.43972_43973dup, NG_042074.1:g.43971_43973dup, NG_042074.1:g.43970_43973dup, NG_042074.1:g.43951_43973A[24]GACCAGGAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_042074.1:g.43969_43973dup, NG_042074.1:g.43968_43973dup, NG_042074.1:g.43967_43973dup, NG_042074.1:g.43966_43973dup, NG_042074.1:g.43965_43973dup, NG_042074.1:g.43961_43973dup, NG_042074.1:g.43960_43973dup, NG_042074.1:g.43956_43973dup, NG_042074.1:g.43951_43973dup

Select item 14913747656.

rs1491374765 has merged into rs35647787 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAA>-,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:200610521 (GRCh38)
1:200579649 (GRCh37)
Canonical SPDI:: NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAAA=0./0 (ALFA)
AAA=0.000004/1 (TOPMED)
A=0.398762/1997 (1000Genomes)
HGVS:: NC_000001.11:g.200610521_200610530del, NC_000001.11:g.200610523_200610530del, NC_000001.11:g.200610525_200610530del, NC_000001.11:g.200610526_200610530del, NC_000001.11:g.200610527_200610530del, NC_000001.11:g.200610528_200610530del, NC_000001.11:g.200610529_200610530del, NC_000001.11:g.200610530del, NC_000001.11:g.200610530dup, NC_000001.11:g.200610528_200610530dup, NC_000001.11:g.200610523_200610530dup, NC_000001.10:g.200579649_200579658del, NC_000001.10:g.200579651_200579658del, NC_000001.10:g.200579653_200579658del, NC_000001.10:g.200579654_200579658del, NC_000001.10:g.200579655_200579658del, NC_000001.10:g.200579656_200579658del, NC_000001.10:g.200579657_200579658del, NC_000001.10:g.200579658del, NC_000001.10:g.200579658dup, NC_000001.10:g.200579656_200579658dup, NC_000001.10:g.200579651_200579658dup, NG_042074.1:g.15216_15225del, NG_042074.1:g.15218_15225del, NG_042074.1:g.15220_15225del, NG_042074.1:g.15221_15225del, NG_042074.1:g.15222_15225del, NG_042074.1:g.15223_15225del, NG_042074.1:g.15224_15225del, NG_042074.1:g.15225del, NG_042074.1:g.15225dup, NG_042074.1:g.15223_15225dup, NG_042074.1:g.15218_15225dup

Select item 14913462217.

rs1491346221 [Homo sapiens]

Variant type:: INS
Alleles:: ->TTTA [Show Flanks]
Chromosome:: 1:200574960 (GRCh38)
1:200544089 (GRCh37)
Canonical SPDI:: NC_000001.11:200574960::TTTA
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTTA=0.0002/1 (ALFA)
HGVS:: NC_000001.11:g.200574960_200574961insTTTA, NC_000001.10:g.200544088_200544089insTTTA, NG_042074.1:g.50774_50775insTAAA

Select item 14912967908.

rs1491296790 has merged into rs371729211 [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,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:200594380 (GRCh38)
1:200563508 (GRCh37)
Canonical SPDI:: NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000001.11:g.200594380_200594393del, NC_000001.11:g.200594381_200594393del, NC_000001.11:g.200594382_200594393del, NC_000001.11:g.200594383_200594393del, NC_000001.11:g.200594384_200594393del, NC_000001.11:g.200594385_200594393del, NC_000001.11:g.200594386_200594393del, NC_000001.11:g.200594387_200594393del, NC_000001.11:g.200594388_200594393del, NC_000001.11:g.200594389_200594393del, NC_000001.11:g.200594390_200594393del, NC_000001.11:g.200594391_200594393del, NC_000001.11:g.200594392_200594393del, NC_000001.11:g.200594393del, NC_000001.11:g.200594393dup, NC_000001.11:g.200594392_200594393dup, NC_000001.11:g.200594391_200594393dup, NC_000001.11:g.200594390_200594393dup, NC_000001.11:g.200594389_200594393dup, NC_000001.11:g.200594388_200594393dup, NC_000001.11:g.200594387_200594393dup, NC_000001.11:g.200594386_200594393dup, NC_000001.11:g.200594385_200594393dup, NC_000001.11:g.200594384_200594393dup, NC_000001.11:g.200594383_200594393dup, NC_000001.11:g.200594382_200594393dup, NC_000001.11:g.200594380_200594393dup, NC_000001.11:g.200594379_200594393dup, NC_000001.11:g.200594378_200594393dup, NC_000001.11:g.200594377_200594393dup, NC_000001.11:g.200594369_200594393A[27]TAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000001.10:g.200563508_200563521del, NC_000001.10:g.200563509_200563521del, NC_000001.10:g.200563510_200563521del, NC_000001.10:g.200563511_200563521del, NC_000001.10:g.200563512_200563521del, NC_000001.10:g.200563513_200563521del, NC_000001.10:g.200563514_200563521del, NC_000001.10:g.200563515_200563521del, NC_000001.10:g.200563516_200563521del, NC_000001.10:g.200563517_200563521del, NC_000001.10:g.200563518_200563521del, NC_000001.10:g.200563519_200563521del, NC_000001.10:g.200563520_200563521del, NC_000001.10:g.200563521del, NC_000001.10:g.200563521dup, NC_000001.10:g.200563520_200563521dup, NC_000001.10:g.200563519_200563521dup, NC_000001.10:g.200563518_200563521dup, NC_000001.10:g.200563517_200563521dup, NC_000001.10:g.200563516_200563521dup, NC_000001.10:g.200563515_200563521dup, NC_000001.10:g.200563514_200563521dup, NC_000001.10:g.200563513_200563521dup, NC_000001.10:g.200563512_200563521dup, NC_000001.10:g.200563511_200563521dup, NC_000001.10:g.200563510_200563521dup, NC_000001.10:g.200563508_200563521dup, NC_000001.10:g.200563507_200563521dup, NC_000001.10:g.200563506_200563521dup, NC_000001.10:g.200563505_200563521dup, NC_000001.10:g.200563497_200563521A[27]TAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_042074.1:g.31353_31366del, NG_042074.1:g.31354_31366del, NG_042074.1:g.31355_31366del, NG_042074.1:g.31356_31366del, NG_042074.1:g.31357_31366del, NG_042074.1:g.31358_31366del, NG_042074.1:g.31359_31366del, NG_042074.1:g.31360_31366del, NG_042074.1:g.31361_31366del, NG_042074.1:g.31362_31366del, NG_042074.1:g.31363_31366del, NG_042074.1:g.31364_31366del, NG_042074.1:g.31365_31366del, NG_042074.1:g.31366del, NG_042074.1:g.31366dup, NG_042074.1:g.31365_31366dup, NG_042074.1:g.31364_31366dup, NG_042074.1:g.31363_31366dup, NG_042074.1:g.31362_31366dup, NG_042074.1:g.31361_31366dup, NG_042074.1:g.31360_31366dup, NG_042074.1:g.31359_31366dup, NG_042074.1:g.31358_31366dup, NG_042074.1:g.31357_31366dup, NG_042074.1:g.31356_31366dup, NG_042074.1:g.31355_31366dup, NG_042074.1:g.31353_31366dup, NG_042074.1:g.31352_31366dup, NG_042074.1:g.31351_31366dup, NG_042074.1:g.31350_31366dup, NG_042074.1:g.31342_31366T[26]ATTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 14912829169.

rs1491282916 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:200610509 (GRCh38)
1:200579637 (GRCh37)
Canonical SPDI:: NC_000001.11:200610508:CA:
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00084/10 (ALFA)
HGVS:: NC_000001.11:g.200610509_200610510del, NC_000001.10:g.200579637_200579638del, NG_042074.1:g.15225_15226del

Select item 149127922610.

rs1491279226 has merged into rs371729211 [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,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:200594380 (GRCh38)
1:200563508 (GRCh37)
Canonical SPDI:: NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200594368:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000001.11:g.200594380_200594393del, NC_000001.11:g.200594381_200594393del, NC_000001.11:g.200594382_200594393del, NC_000001.11:g.200594383_200594393del, NC_000001.11:g.200594384_200594393del, NC_000001.11:g.200594385_200594393del, NC_000001.11:g.200594386_200594393del, NC_000001.11:g.200594387_200594393del, NC_000001.11:g.200594388_200594393del, NC_000001.11:g.200594389_200594393del, NC_000001.11:g.200594390_200594393del, NC_000001.11:g.200594391_200594393del, NC_000001.11:g.200594392_200594393del, NC_000001.11:g.200594393del, NC_000001.11:g.200594393dup, NC_000001.11:g.200594392_200594393dup, NC_000001.11:g.200594391_200594393dup, NC_000001.11:g.200594390_200594393dup, NC_000001.11:g.200594389_200594393dup, NC_000001.11:g.200594388_200594393dup, NC_000001.11:g.200594387_200594393dup, NC_000001.11:g.200594386_200594393dup, NC_000001.11:g.200594385_200594393dup, NC_000001.11:g.200594384_200594393dup, NC_000001.11:g.200594383_200594393dup, NC_000001.11:g.200594382_200594393dup, NC_000001.11:g.200594380_200594393dup, NC_000001.11:g.200594379_200594393dup, NC_000001.11:g.200594378_200594393dup, NC_000001.11:g.200594377_200594393dup, NC_000001.11:g.200594369_200594393A[27]TAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000001.10:g.200563508_200563521del, NC_000001.10:g.200563509_200563521del, NC_000001.10:g.200563510_200563521del, NC_000001.10:g.200563511_200563521del, NC_000001.10:g.200563512_200563521del, NC_000001.10:g.200563513_200563521del, NC_000001.10:g.200563514_200563521del, NC_000001.10:g.200563515_200563521del, NC_000001.10:g.200563516_200563521del, NC_000001.10:g.200563517_200563521del, NC_000001.10:g.200563518_200563521del, NC_000001.10:g.200563519_200563521del, NC_000001.10:g.200563520_200563521del, NC_000001.10:g.200563521del, NC_000001.10:g.200563521dup, NC_000001.10:g.200563520_200563521dup, NC_000001.10:g.200563519_200563521dup, NC_000001.10:g.200563518_200563521dup, NC_000001.10:g.200563517_200563521dup, NC_000001.10:g.200563516_200563521dup, NC_000001.10:g.200563515_200563521dup, NC_000001.10:g.200563514_200563521dup, NC_000001.10:g.200563513_200563521dup, NC_000001.10:g.200563512_200563521dup, NC_000001.10:g.200563511_200563521dup, NC_000001.10:g.200563510_200563521dup, NC_000001.10:g.200563508_200563521dup, NC_000001.10:g.200563507_200563521dup, NC_000001.10:g.200563506_200563521dup, NC_000001.10:g.200563505_200563521dup, NC_000001.10:g.200563497_200563521A[27]TAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_042074.1:g.31353_31366del, NG_042074.1:g.31354_31366del, NG_042074.1:g.31355_31366del, NG_042074.1:g.31356_31366del, NG_042074.1:g.31357_31366del, NG_042074.1:g.31358_31366del, NG_042074.1:g.31359_31366del, NG_042074.1:g.31360_31366del, NG_042074.1:g.31361_31366del, NG_042074.1:g.31362_31366del, NG_042074.1:g.31363_31366del, NG_042074.1:g.31364_31366del, NG_042074.1:g.31365_31366del, NG_042074.1:g.31366del, NG_042074.1:g.31366dup, NG_042074.1:g.31365_31366dup, NG_042074.1:g.31364_31366dup, NG_042074.1:g.31363_31366dup, NG_042074.1:g.31362_31366dup, NG_042074.1:g.31361_31366dup, NG_042074.1:g.31360_31366dup, NG_042074.1:g.31359_31366dup, NG_042074.1:g.31358_31366dup, NG_042074.1:g.31357_31366dup, NG_042074.1:g.31356_31366dup, NG_042074.1:g.31355_31366dup, NG_042074.1:g.31353_31366dup, NG_042074.1:g.31352_31366dup, NG_042074.1:g.31351_31366dup, NG_042074.1:g.31350_31366dup, NG_042074.1:g.31342_31366T[26]ATTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 149126251611.

rs1491262516 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 1:200575824 (GRCh38)
1:200544953 (GRCh37)
Canonical SPDI:: NC_000001.11:200575824:AAAAAA:AAAAAAA
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAA=0.000071/1 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.200575830dup, NC_000001.10:g.200544958dup, NG_042074.1:g.49910dup

Select item 149125637712.

rs1491256377 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AAGACTCTG [Show Flanks]
Chromosome:: 1:200564625 (GRCh38)
1:200533754 (GRCh37)
Canonical SPDI:: NC_000001.11:200564625:AAGACTCTG:AAGACTCTGAAGACTCTG
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AAGACTCTGAAGACTCTG=0./0 (ALFA)
AAGACTCTG=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.200564626_200564634dup, NC_000001.10:g.200533754_200533762dup, NG_042074.1:g.61101_61109dup

Select item 149116446913.

rs1491164469 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:200594368 (GRCh38)
1:200563496 (GRCh37)
Canonical SPDI:: NC_000001.11:200594367:CA:
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00194/23 (ALFA)
-=0.00589/81 (GnomAD)
HGVS:: NC_000001.11:g.200594368_200594369del, NC_000001.10:g.200563496_200563497del, NG_042074.1:g.31366_31367del

Select item 149110845114.

rs1491108451 has merged into rs993346438 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:200596901 (GRCh38)
1:200566029 (GRCh37)
Canonical SPDI:: NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200596888:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000001.11:g.200596901_200596913del, NC_000001.11:g.200596902_200596913del, NC_000001.11:g.200596903_200596913del, NC_000001.11:g.200596904_200596913del, NC_000001.11:g.200596905_200596913del, NC_000001.11:g.200596906_200596913del, NC_000001.11:g.200596907_200596913del, NC_000001.11:g.200596908_200596913del, NC_000001.11:g.200596909_200596913del, NC_000001.11:g.200596910_200596913del, NC_000001.11:g.200596911_200596913del, NC_000001.11:g.200596912_200596913del, NC_000001.11:g.200596913del, NC_000001.11:g.200596913dup, NC_000001.11:g.200596912_200596913dup, NC_000001.11:g.200596911_200596913dup, NC_000001.11:g.200596910_200596913dup, NC_000001.11:g.200596909_200596913dup, NC_000001.11:g.200596908_200596913dup, NC_000001.11:g.200596907_200596913dup, NC_000001.11:g.200596905_200596913dup, NC_000001.11:g.200596900_200596913dup, NC_000001.11:g.200596913_200596914insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.200596913_200596914insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200566029_200566041del, NC_000001.10:g.200566030_200566041del, NC_000001.10:g.200566031_200566041del, NC_000001.10:g.200566032_200566041del, NC_000001.10:g.200566033_200566041del, NC_000001.10:g.200566034_200566041del, NC_000001.10:g.200566035_200566041del, NC_000001.10:g.200566036_200566041del, NC_000001.10:g.200566037_200566041del, NC_000001.10:g.200566038_200566041del, NC_000001.10:g.200566039_200566041del, NC_000001.10:g.200566040_200566041del, NC_000001.10:g.200566041del, NC_000001.10:g.200566041dup, NC_000001.10:g.200566040_200566041dup, NC_000001.10:g.200566039_200566041dup, NC_000001.10:g.200566038_200566041dup, NC_000001.10:g.200566037_200566041dup, NC_000001.10:g.200566036_200566041dup, NC_000001.10:g.200566035_200566041dup, NC_000001.10:g.200566033_200566041dup, NC_000001.10:g.200566028_200566041dup, NC_000001.10:g.200566041_200566042insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.200566041_200566042insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042074.1:g.28834_28846del, NG_042074.1:g.28835_28846del, NG_042074.1:g.28836_28846del, NG_042074.1:g.28837_28846del, NG_042074.1:g.28838_28846del, NG_042074.1:g.28839_28846del, NG_042074.1:g.28840_28846del, NG_042074.1:g.28841_28846del, NG_042074.1:g.28842_28846del, NG_042074.1:g.28843_28846del, NG_042074.1:g.28844_28846del, NG_042074.1:g.28845_28846del, NG_042074.1:g.28846del, NG_042074.1:g.28846dup, NG_042074.1:g.28845_28846dup, NG_042074.1:g.28844_28846dup, NG_042074.1:g.28843_28846dup, NG_042074.1:g.28842_28846dup, NG_042074.1:g.28841_28846dup, NG_042074.1:g.28840_28846dup, NG_042074.1:g.28838_28846dup, NG_042074.1:g.28833_28846dup, NG_042074.1:g.28846_28847insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_042074.1:g.28846_28847insAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149109056815.

rs1491090568 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 1:200574960 (GRCh38)
1:200544088 (GRCh37)
Canonical SPDI:: NC_000001.11:200574959:TG:
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00042/5 (ALFA)
HGVS:: NC_000001.11:g.200574960_200574961del, NC_000001.10:g.200544088_200544089del, NG_042074.1:g.50774_50775del

Select item 149108393816.

rs1491083938 has merged into rs10643609 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:200561239 (GRCh38)
1:200530367 (GRCh37)
Canonical SPDI:: NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:200561229:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
-=0.2722/1363 (1000Genomes)
-=0.3/12 (GENOME_DK)
HGVS:: NC_000001.11:g.200561239_200561244del, NC_000001.11:g.200561240_200561244del, NC_000001.11:g.200561241_200561244del, NC_000001.11:g.200561242_200561244del, NC_000001.11:g.200561243_200561244del, NC_000001.11:g.200561244del, NC_000001.11:g.200561244dup, NC_000001.11:g.200561243_200561244dup, NC_000001.11:g.200561242_200561244dup, NC_000001.11:g.200561241_200561244dup, NC_000001.11:g.200561240_200561244dup, NC_000001.11:g.200561239_200561244dup, NC_000001.11:g.200561238_200561244dup, NC_000001.11:g.200561237_200561244dup, NC_000001.11:g.200561236_200561244dup, NC_000001.11:g.200561235_200561244dup, NC_000001.10:g.200530367_200530372del, NC_000001.10:g.200530368_200530372del, NC_000001.10:g.200530369_200530372del, NC_000001.10:g.200530370_200530372del, NC_000001.10:g.200530371_200530372del, NC_000001.10:g.200530372del, NC_000001.10:g.200530372dup, NC_000001.10:g.200530371_200530372dup, NC_000001.10:g.200530370_200530372dup, NC_000001.10:g.200530369_200530372dup, NC_000001.10:g.200530368_200530372dup, NC_000001.10:g.200530367_200530372dup, NC_000001.10:g.200530366_200530372dup, NC_000001.10:g.200530365_200530372dup, NC_000001.10:g.200530364_200530372dup, NC_000001.10:g.200530363_200530372dup, NG_042074.1:g.64500_64505del, NG_042074.1:g.64501_64505del, NG_042074.1:g.64502_64505del, NG_042074.1:g.64503_64505del, NG_042074.1:g.64504_64505del, NG_042074.1:g.64505del, NG_042074.1:g.64505dup, NG_042074.1:g.64504_64505dup, NG_042074.1:g.64503_64505dup, NG_042074.1:g.64502_64505dup, NG_042074.1:g.64501_64505dup, NG_042074.1:g.64500_64505dup, NG_042074.1:g.64499_64505dup, NG_042074.1:g.64498_64505dup, NG_042074.1:g.64497_64505dup, NG_042074.1:g.64496_64505dup

Select item 149105435617.

rs1491054356 has merged into rs79821962 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:200612010 (GRCh38)
1:200581138 (GRCh37)
Canonical SPDI:: NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:200612000:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
T=0.1692/310 (Korea1K)
T=0.3145/1575 (1000Genomes)
T=0.325/13 (GENOME_DK)
T=0.3278/196 (NorthernSweden)
T=0.3379/1253 (TWINSUK)
T=0.3415/1316 (ALSPAC)
HGVS:: NC_000001.11:g.200612010_200612011del, NC_000001.11:g.200612011del, NC_000001.11:g.200612011dup, NC_000001.11:g.200612010_200612011dup, NC_000001.11:g.200612009_200612011dup, NC_000001.11:g.200612008_200612011dup, NC_000001.11:g.200612007_200612011dup, NC_000001.11:g.200612006_200612011dup, NC_000001.11:g.200612005_200612011dup, NC_000001.11:g.200612004_200612011dup, NC_000001.11:g.200612001_200612011dup, NC_000001.11:g.200612011_200612012insTTTTTTTTTTTTT, NC_000001.11:g.200612011_200612012insTTTTTTTTTTTTTT, NC_000001.10:g.200581138_200581139del, NC_000001.10:g.200581139del, NC_000001.10:g.200581139dup, NC_000001.10:g.200581138_200581139dup, NC_000001.10:g.200581137_200581139dup, NC_000001.10:g.200581136_200581139dup, NC_000001.10:g.200581135_200581139dup, NC_000001.10:g.200581134_200581139dup, NC_000001.10:g.200581133_200581139dup, NC_000001.10:g.200581132_200581139dup, NC_000001.10:g.200581129_200581139dup, NC_000001.10:g.200581139_200581140insTTTTTTTTTTTTT, NC_000001.10:g.200581139_200581140insTTTTTTTTTTTTTT, NG_042074.1:g.13733_13734del, NG_042074.1:g.13734del, NG_042074.1:g.13734dup, NG_042074.1:g.13733_13734dup, NG_042074.1:g.13732_13734dup, NG_042074.1:g.13731_13734dup, NG_042074.1:g.13730_13734dup, NG_042074.1:g.13729_13734dup, NG_042074.1:g.13728_13734dup, NG_042074.1:g.13727_13734dup, NG_042074.1:g.13724_13734dup, NG_042074.1:g.13734_13735insAAAAAAAAAAAAA, NG_042074.1:g.13734_13735insAAAAAAAAAAAAAA

Select item 149099092218.

rs1490990922 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:200585184 (GRCh38)
1:200554312 (GRCh37)
Canonical SPDI:: NC_000001.11:200585183:A:G
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000071/1 (TOMMO)
G=0.003275/6 (Korea1K)
G=0.003422/10 (KOREAN)
HGVS:: NC_000001.11:g.200585184A>G, NC_000001.10:g.200554312A>G, NG_042074.1:g.40551T>C

Select item 149088105219.

rs1490881052 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:200602755 (GRCh38)
1:200571883 (GRCh37)
Canonical SPDI:: NC_000001.11:200602754:A:G
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000019/5 (TOPMED)
G=0.000021/3 (GnomAD)
G=0.000156/1 (1000Genomes)
HGVS:: NC_000001.11:g.200602755A>G, NC_000001.10:g.200571883A>G, NG_042074.1:g.22980T>C

Select item 149087901620.

rs1490879016 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:200570418 (GRCh38)
1:200539546 (GRCh37)
Canonical SPDI:: NC_000001.11:200570417:G:A
Gene:: KIF14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000001.11:g.200570418G>A, NC_000001.10:g.200539546G>A, NG_042074.1:g.55317C>T

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