SNP Links for Gene (Select 80232) - SNP

Links from Gene

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Select item 14915725531.

rs1491572553 [Homo sapiens]

Variant type:: DEL
Alleles:: GG>- [Show Flanks]
Chromosome:: 1:224410303 (GRCh38)
1:224598005 (GRCh37)
Canonical SPDI:: NC_000001.11:224410302:GG:
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000001.11:g.224410303_224410304del, NC_000001.10:g.224598005_224598006del, NG_047198.1:g.28996_28997del

Select item 14915253272.

rs1491525327 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ACCCCC [Show Flanks]
Chromosome:: 1:224433621 (GRCh38)
1:224621324 (GRCh37)
Canonical SPDI:: NC_000001.11:224433621:ACCCCC:ACCCCCACCCCC
Gene:: WDR26 (Varview), CNIH3 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACCCCCACCCCC=0./0 (ALFA)
ACCCCC=0.000004/1 (TOPMED)
ACCCCC=0.000018/1 (GnomAD)
HGVS:: NC_000001.11:g.224433622_224433627dup, NC_000001.10:g.224621324_224621329dup, NG_047198.1:g.5673_5678dup

Select item 14914571873.

rs1491457187 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:224410281 (GRCh38)
1:224597983 (GRCh37)
Canonical SPDI:: NC_000001.11:224410280:CA:
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000001.11:g.224410281_224410282del, NC_000001.10:g.224597983_224597984del, NG_047198.1:g.29018_29019del

Select item 14913852204.

rs1491385220 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 1:224385291 (GRCh38)
1:224572994 (GRCh37)
Canonical SPDI:: NC_000001.11:224385291:TTT:TTTT
Gene:: WDR26 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTT=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.224385294dup, NC_000001.10:g.224572996dup, NG_047198.1:g.54008dup, NM_025160.7:c.*4543dup, NM_025160.6:c.*4543dup, NM_001115113.3:c.*4543dup, NM_001115113.2:c.*4543dup, NM_001379403.1:c.*4543dup

Select item 14913562085.

rs1491356208 has merged into rs1394488602 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAGAAAAGAA>-,AAGAA,AAGAAAAGAAAAGAA,AAGAAAAGAAAAGAAAAGAA [Show Flanks]
Chromosome:: 1:224410317 (GRCh38)
1:224598019 (GRCh37)
Canonical SPDI:: NC_000001.11:224410303:GAAAAGAAAAGAAAAGAAAAGAA:GAAAAGAAAAGAA,NC_000001.11:224410303:GAAAAGAAAAGAAAAGAAAAGAA:GAAAAGAAAAGAAAAGAA,NC_000001.11:224410303:GAAAAGAAAAGAAAAGAAAAGAA:GAAAAGAAAAGAAAAGAAAAGAAAAGAA,NC_000001.11:224410303:GAAAAGAAAAGAAAAGAAAAGAA:GAAAAGAAAAGAAAAGAAAAGAAAAGAAAAGAA
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAAAAGAAAAGAAAAGAA=0./0 (ALFA)
-=0.00004/1 (TOMMO)
-=0.00078/5 (1000Genomes)
GAAAA=0.00167/1 (NorthernSweden)
HGVS:: NC_000001.11:g.224410307AAGAA[2], NC_000001.11:g.224410307AAGAA[3], NC_000001.11:g.224410307AAGAA[5], NC_000001.11:g.224410307AAGAA[6], NC_000001.10:g.224598009AAGAA[2], NC_000001.10:g.224598009AAGAA[3], NC_000001.10:g.224598009AAGAA[5], NC_000001.10:g.224598009AAGAA[6], NG_047198.1:g.28977TTTTC[2], NG_047198.1:g.28977TTTTC[3], NG_047198.1:g.28977TTTTC[5], NG_047198.1:g.28977TTTTC[6]

Select item 14913506776.

rs1491350677 has merged into rs1335487396 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATATATATATA>-,TA,TATA,TATATA,TATATATA,TATATATATA,TATATATATATATA,TATATATATATATATA,TATATATATATATATATA,TATATATATATATATATATA,TATATATATATATATATATATA,TATATATATATATATATATATATA,TATATATATATATATATATATATATA,TATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATA [Show Flanks]
Chromosome:: 1:224407161 (GRCh38)
1:224594863 (GRCh37)
Canonical SPDI:: NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:224407151:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATA
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATATATA=0./0 (ALFA)
HGVS:: NC_000001.11:g.224407153TA[4], NC_000001.11:g.224407153TA[5], NC_000001.11:g.224407153TA[6], NC_000001.11:g.224407153TA[7], NC_000001.11:g.224407153TA[8], NC_000001.11:g.224407153TA[9], NC_000001.11:g.224407153TA[11], NC_000001.11:g.224407153TA[12], NC_000001.11:g.224407153TA[13], NC_000001.11:g.224407153TA[14], NC_000001.11:g.224407153TA[15], NC_000001.11:g.224407153TA[16], NC_000001.11:g.224407153TA[17], NC_000001.11:g.224407153TA[18], NC_000001.11:g.224407153TA[19], NC_000001.11:g.224407153TA[20], NC_000001.11:g.224407153TA[21], NC_000001.11:g.224407153TA[22], NC_000001.11:g.224407153TA[23], NC_000001.11:g.224407153TA[24], NC_000001.11:g.224407153TA[25], NC_000001.11:g.224407153TA[26], NC_000001.11:g.224407153TA[28], NC_000001.10:g.224594855TA[4], NC_000001.10:g.224594855TA[5], NC_000001.10:g.224594855TA[6], NC_000001.10:g.224594855TA[7], NC_000001.10:g.224594855TA[8], NC_000001.10:g.224594855TA[9], NC_000001.10:g.224594855TA[11], NC_000001.10:g.224594855TA[12], NC_000001.10:g.224594855TA[13], NC_000001.10:g.224594855TA[14], NC_000001.10:g.224594855TA[15], NC_000001.10:g.224594855TA[16], NC_000001.10:g.224594855TA[17], NC_000001.10:g.224594855TA[18], NC_000001.10:g.224594855TA[19], NC_000001.10:g.224594855TA[20], NC_000001.10:g.224594855TA[21], NC_000001.10:g.224594855TA[22], NC_000001.10:g.224594855TA[23], NC_000001.10:g.224594855TA[24], NC_000001.10:g.224594855TA[25], NC_000001.10:g.224594855TA[26], NC_000001.10:g.224594855TA[28], NG_047198.1:g.32129AT[4], NG_047198.1:g.32129AT[5], NG_047198.1:g.32129AT[6], NG_047198.1:g.32129AT[7], NG_047198.1:g.32129AT[8], NG_047198.1:g.32129AT[9], NG_047198.1:g.32129AT[11], NG_047198.1:g.32129AT[12], NG_047198.1:g.32129AT[13], NG_047198.1:g.32129AT[14], NG_047198.1:g.32129AT[15], NG_047198.1:g.32129AT[16], NG_047198.1:g.32129AT[17], NG_047198.1:g.32129AT[18], NG_047198.1:g.32129AT[19], NG_047198.1:g.32129AT[20], NG_047198.1:g.32129AT[21], NG_047198.1:g.32129AT[22], NG_047198.1:g.32129AT[23], NG_047198.1:g.32129AT[24], NG_047198.1:g.32129AT[25], NG_047198.1:g.32129AT[26], NG_047198.1:g.32129AT[28]

Select item 14913468707.

rs1491346870 has merged into rs1331410813 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAA>-,A,AA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:224427121 (GRCh38)
1:224614823 (GRCh37)
Canonical SPDI:: NC_000001.11:224427104:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:224427104:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:224427104:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:224427104:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224427104:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224427104:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224427104:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224427104:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAAA=0./0 (ALFA)
A=0.00018/3 (TOMMO)
HGVS:: NC_000001.11:g.224427121_224427127del, NC_000001.11:g.224427122_224427127del, NC_000001.11:g.224427123_224427127del, NC_000001.11:g.224427127del, NC_000001.11:g.224427127dup, NC_000001.11:g.224427126_224427127dup, NC_000001.11:g.224427125_224427127dup, NC_000001.11:g.224427119_224427127dup, NC_000001.10:g.224614823_224614829del, NC_000001.10:g.224614824_224614829del, NC_000001.10:g.224614825_224614829del, NC_000001.10:g.224614829del, NC_000001.10:g.224614829dup, NC_000001.10:g.224614828_224614829dup, NC_000001.10:g.224614827_224614829dup, NC_000001.10:g.224614821_224614829dup, NG_047198.1:g.12189_12195del, NG_047198.1:g.12190_12195del, NG_047198.1:g.12191_12195del, NG_047198.1:g.12195del, NG_047198.1:g.12195dup, NG_047198.1:g.12194_12195dup, NG_047198.1:g.12193_12195dup, NG_047198.1:g.12187_12195dup

Select item 14913145818.

rs1491314581 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 1:224433621 (GRCh38)
1:224621323 (GRCh37)
Canonical SPDI:: NC_000001.11:224433620:TA:
Gene:: WDR26 (Varview), CNIH3 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by cluster
MAF:: -=0.00174/29 (TOMMO)
HGVS:: NC_000001.11:g.224433621_224433622del, NC_000001.10:g.224621323_224621324del, NG_047198.1:g.5678_5679del

Select item 14913090449.

rs1491309044 has merged into rs767368281 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:224401679 (GRCh38)
1:224589381 (GRCh37)
Canonical SPDI:: NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224401671:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000001.11:g.224401679_224401689del, NC_000001.11:g.224401688_224401689del, NC_000001.11:g.224401689del, NC_000001.11:g.224401689dup, NC_000001.11:g.224401688_224401689dup, NC_000001.11:g.224401687_224401689dup, NC_000001.11:g.224401686_224401689dup, NC_000001.11:g.224401685_224401689dup, NC_000001.11:g.224401684_224401689dup, NC_000001.11:g.224401683_224401689dup, NC_000001.11:g.224401682_224401689dup, NC_000001.11:g.224401681_224401689dup, NC_000001.11:g.224401680_224401689dup, NC_000001.11:g.224401679_224401689dup, NC_000001.11:g.224401678_224401689dup, NC_000001.11:g.224401677_224401689dup, NC_000001.11:g.224401676_224401689dup, NC_000001.11:g.224401675_224401689dup, NC_000001.11:g.224401674_224401689dup, NC_000001.11:g.224401673_224401689dup, NC_000001.11:g.224401672_224401689dup, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401689_224401690insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.224401672_224401689A[29]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000001.11:g.224401672_224401689A[29]TAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000001.10:g.224589381_224589391del, NC_000001.10:g.224589390_224589391del, NC_000001.10:g.224589391del, NC_000001.10:g.224589391dup, NC_000001.10:g.224589390_224589391dup, NC_000001.10:g.224589389_224589391dup, NC_000001.10:g.224589388_224589391dup, NC_000001.10:g.224589387_224589391dup, NC_000001.10:g.224589386_224589391dup, NC_000001.10:g.224589385_224589391dup, NC_000001.10:g.224589384_224589391dup, NC_000001.10:g.224589383_224589391dup, NC_000001.10:g.224589382_224589391dup, NC_000001.10:g.224589381_224589391dup, NC_000001.10:g.224589380_224589391dup, NC_000001.10:g.224589379_224589391dup, NC_000001.10:g.224589378_224589391dup, NC_000001.10:g.224589377_224589391dup, NC_000001.10:g.224589376_224589391dup, NC_000001.10:g.224589375_224589391dup, NC_000001.10:g.224589374_224589391dup, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589391_224589392insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224589374_224589391A[29]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000001.10:g.224589374_224589391A[29]TAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_047198.1:g.37618_37628del, NG_047198.1:g.37627_37628del, NG_047198.1:g.37628del, NG_047198.1:g.37628dup, NG_047198.1:g.37627_37628dup, NG_047198.1:g.37626_37628dup, NG_047198.1:g.37625_37628dup, NG_047198.1:g.37624_37628dup, NG_047198.1:g.37623_37628dup, NG_047198.1:g.37622_37628dup, NG_047198.1:g.37621_37628dup, NG_047198.1:g.37620_37628dup, NG_047198.1:g.37619_37628dup, NG_047198.1:g.37618_37628dup, NG_047198.1:g.37617_37628dup, NG_047198.1:g.37616_37628dup, NG_047198.1:g.37615_37628dup, NG_047198.1:g.37614_37628dup, NG_047198.1:g.37613_37628dup, NG_047198.1:g.37612_37628dup, NG_047198.1:g.37611_37628dup, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37628_37629insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_047198.1:g.37611_37628T[39]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_047198.1:g.37611_37628T[27]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 149129215710.

rs1491292157 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 1:224407172 (GRCh38)
1:224594874 (GRCh37)
Canonical SPDI:: NC_000001.11:224407171:AA:
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00006/5 (GnomAD)
HGVS:: NC_000001.11:g.224407172_224407173del, NC_000001.10:g.224594874_224594875del, NG_047198.1:g.32127_32128del

Select item 149121448011.

rs1491214480 [Homo sapiens]

Variant type:: INS
Alleles:: ->T,TAT,TATATATAT,TATATATATAT,TATATATATATATAT,TATATATATATATATAT,TATATATATATATATATAT,TATATATATATATATATATAT,TATATATATATATATATATATATAT,TATATATATATATATATATATATATAT,TATATATATATATATATATATATATATATG,TATATATATATATATATATATATATATG,TATATATATATATATATATATATG,TATATATATATATATATATATG,TATATATATATATATATATG,TATATATATATATATATG,TATATATATATATATG,TATATATATATATG,TATATATATATG,TATATATATG,TATATATG,TATATG,TG,TT [Show Flanks]
Chromosome:: 1:224407172 (GRCh38)
1:224594875 (GRCh37)
Canonical SPDI:: NC_000001.11:224407172::T,NC_000001.11:224407172::TAT,NC_000001.11:224407172::TATATATAT,NC_000001.11:224407172::TATATATATAT,NC_000001.11:224407172::TATATATATATATAT,NC_000001.11:224407172::TATATATATATATATAT,NC_000001.11:224407172::TATATATATATATATATAT,NC_000001.11:224407172::TATATATATATATATATATAT,NC_000001.11:224407172::TATATATATATATATATATATATAT,NC_000001.11:224407172::TATATATATATATATATATATATATAT,NC_000001.11:224407172::TATATATATATATATATATATATATATATG,NC_000001.11:224407172::TATATATATATATATATATATATATATG,NC_000001.11:224407172::TATATATATATATATATATATATG,NC_000001.11:224407172::TATATATATATATATATATATG,NC_000001.11:224407172::TATATATATATATATATATG,NC_000001.11:224407172::TATATATATATATATATG,NC_000001.11:224407172::TATATATATATATATG,NC_000001.11:224407172::TATATATATATATG,NC_000001.11:224407172::TATATATATATG,NC_000001.11:224407172::TATATATATG,NC_000001.11:224407172::TATATATG,NC_000001.11:224407172::TATATG,NC_000001.11:224407172::TG,NC_000001.11:224407172::TT
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATATATATATATATG=0./0 (ALFA)
TG=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.224407172_224407173insT, NC_000001.11:g.224407172_224407173insTAT, NC_000001.11:g.224407172_224407173insTATATATAT, NC_000001.11:g.224407172_224407173insTATATATATAT, NC_000001.11:g.224407172_224407173insTATATATATATATAT, NC_000001.11:g.224407172_224407173insTATATATATATATATAT, NC_000001.11:g.224407172_224407173insTATATATATATATATATAT, NC_000001.11:g.224407172_224407173insTATATATATATATATATATAT, NC_000001.11:g.224407172_224407173insTATATATATATATATATATATATAT, NC_000001.11:g.224407172_224407173insTATATATATATATATATATATATATAT, NC_000001.11:g.224407172_224407173insTATATATATATATATATATATATATATATG, NC_000001.11:g.224407172_224407173insTATATATATATATATATATATATATATG, NC_000001.11:g.224407172_224407173insTATATATATATATATATATATATG, NC_000001.11:g.224407172_224407173insTATATATATATATATATATATG, NC_000001.11:g.224407172_224407173insTATATATATATATATATATG, NC_000001.11:g.224407172_224407173insTATATATATATATATATG, NC_000001.11:g.224407172_224407173insTATATATATATATATG, NC_000001.11:g.224407172_224407173insTATATATATATATG, NC_000001.11:g.224407172_224407173insTATATATATATG, NC_000001.11:g.224407172_224407173insTATATATATG, NC_000001.11:g.224407172_224407173insTATATATG, NC_000001.11:g.224407172_224407173insTATATG, NC_000001.11:g.224407172_224407173insTG, NC_000001.11:g.224407172_224407173insTT, NC_000001.10:g.224594874_224594875insT, NC_000001.10:g.224594874_224594875insTAT, NC_000001.10:g.224594874_224594875insTATATATAT, NC_000001.10:g.224594874_224594875insTATATATATAT, NC_000001.10:g.224594874_224594875insTATATATATATATAT, NC_000001.10:g.224594874_224594875insTATATATATATATATAT, NC_000001.10:g.224594874_224594875insTATATATATATATATATAT, NC_000001.10:g.224594874_224594875insTATATATATATATATATATAT, NC_000001.10:g.224594874_224594875insTATATATATATATATATATATATAT, NC_000001.10:g.224594874_224594875insTATATATATATATATATATATATATAT, NC_000001.10:g.224594874_224594875insTATATATATATATATATATATATATATATG, NC_000001.10:g.224594874_224594875insTATATATATATATATATATATATATATG, NC_000001.10:g.224594874_224594875insTATATATATATATATATATATATG, NC_000001.10:g.224594874_224594875insTATATATATATATATATATATG, NC_000001.10:g.224594874_224594875insTATATATATATATATATATG, NC_000001.10:g.224594874_224594875insTATATATATATATATATG, NC_000001.10:g.224594874_224594875insTATATATATATATATG, NC_000001.10:g.224594874_224594875insTATATATATATATG, NC_000001.10:g.224594874_224594875insTATATATATATG, NC_000001.10:g.224594874_224594875insTATATATATG, NC_000001.10:g.224594874_224594875insTATATATG, NC_000001.10:g.224594874_224594875insTATATG, NC_000001.10:g.224594874_224594875insTG, NC_000001.10:g.224594874_224594875insTT, NG_047198.1:g.32127_32128insA, NG_047198.1:g.32127_32128insATA, NG_047198.1:g.32127_32128insATATATATA, NG_047198.1:g.32127_32128insATATATATATA, NG_047198.1:g.32127_32128insATATATATATATATA, NG_047198.1:g.32127_32128insATATATATATATATATA, NG_047198.1:g.32127_32128insATATATATATATATATATA, NG_047198.1:g.32127_32128insATATATATATATATATATATA, NG_047198.1:g.32127_32128insATATATATATATATATATATATATA, NG_047198.1:g.32127_32128insATATATATATATATATATATATATATA, NG_047198.1:g.32127_32128insCATATATATATATATATATATATATATATA, NG_047198.1:g.32127_32128insCATATATATATATATATATATATATATA, NG_047198.1:g.32127_32128insCATATATATATATATATATATATA, NG_047198.1:g.32127_32128insCATATATATATATATATATATA, NG_047198.1:g.32127_32128insCATATATATATATATATATA, NG_047198.1:g.32127_32128insCATATATATATATATATA, NG_047198.1:g.32127_32128insCATATATATATATATA, NG_047198.1:g.32127_32128insCATATATATATATA, NG_047198.1:g.32127_32128insCATATATATATA, NG_047198.1:g.32127_32128insCATATATATA, NG_047198.1:g.32127_32128insCATATATA, NG_047198.1:g.32127_32128insCATATA, NG_047198.1:g.32127_32128insCA, NG_047198.1:g.32127_32128insAA

Select item 149120933812.

rs1491209338 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 1:224385291 (GRCh38)
1:224572993 (GRCh37)
Canonical SPDI:: NC_000001.11:224385290:AT:
Gene:: WDR26 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000068/18 (TOPMED)
-=0.000071/10 (GnomAD)
HGVS:: NC_000001.11:g.224385291_224385292del, NC_000001.10:g.224572993_224572994del, NG_047198.1:g.54008_54009del, NM_025160.7:c.*4543_*4544del, NM_025160.6:c.*4543_*4544del, NM_001115113.3:c.*4543_*4544del, NM_001115113.2:c.*4543_*4544del, NM_001379403.1:c.*4543_*4544del

Select item 149117809213.

rs1491178092 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:224391363 (GRCh38)
1:224579065 (GRCh37)
Canonical SPDI:: NC_000001.11:224391362:CA:
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000001.11:g.224391363_224391364del, NC_000001.10:g.224579065_224579066del, NG_047198.1:g.47936_47937del

Select item 149115373514.

rs1491153735 has merged into rs869213487 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:224391371 (GRCh38)
1:224579073 (GRCh37)
Canonical SPDI:: NC_000001.11:224391363:AAAAAAAAAAAAAAAAAAAA:AAAAAAA,NC_000001.11:224391363:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:224391363:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:224391363:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:224391363:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:224391363:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:224391363:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:224391363:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:224391363:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224391363:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224391363:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224391363:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224391363:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:224391363:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAAAAA=0./0 (ALFA)
-=0.00056/1 (Korea1K)
-=0.11381/61 (NorthernSweden)
HGVS:: NC_000001.11:g.224391371_224391383del, NC_000001.11:g.224391375_224391383del, NC_000001.11:g.224391377_224391383del, NC_000001.11:g.224391378_224391383del, NC_000001.11:g.224391379_224391383del, NC_000001.11:g.224391381_224391383del, NC_000001.11:g.224391382_224391383del, NC_000001.11:g.224391383del, NC_000001.11:g.224391383dup, NC_000001.11:g.224391382_224391383dup, NC_000001.11:g.224391381_224391383dup, NC_000001.11:g.224391380_224391383dup, NC_000001.11:g.224391379_224391383dup, NC_000001.11:g.224391383_224391384insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.224579073_224579085del, NC_000001.10:g.224579077_224579085del, NC_000001.10:g.224579079_224579085del, NC_000001.10:g.224579080_224579085del, NC_000001.10:g.224579081_224579085del, NC_000001.10:g.224579083_224579085del, NC_000001.10:g.224579084_224579085del, NC_000001.10:g.224579085del, NC_000001.10:g.224579085dup, NC_000001.10:g.224579084_224579085dup, NC_000001.10:g.224579083_224579085dup, NC_000001.10:g.224579082_224579085dup, NC_000001.10:g.224579081_224579085dup, NC_000001.10:g.224579085_224579086insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_047198.1:g.47924_47936del, NG_047198.1:g.47928_47936del, NG_047198.1:g.47930_47936del, NG_047198.1:g.47931_47936del, NG_047198.1:g.47932_47936del, NG_047198.1:g.47934_47936del, NG_047198.1:g.47935_47936del, NG_047198.1:g.47936del, NG_047198.1:g.47936dup, NG_047198.1:g.47935_47936dup, NG_047198.1:g.47934_47936dup, NG_047198.1:g.47933_47936dup, NG_047198.1:g.47932_47936dup, NG_047198.1:g.47936_47937insTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149113543715.

rs1491135437 has merged into rs397983007 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTT>-,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:224410703 (GRCh38)
1:224598405 (GRCh37)
Canonical SPDI:: NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:224410694:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
TTTT=0.425/17 (GENOME_DK)
HGVS:: NC_000001.11:g.224410703_224410714del, NC_000001.11:g.224410705_224410714del, NC_000001.11:g.224410706_224410714del, NC_000001.11:g.224410708_224410714del, NC_000001.11:g.224410709_224410714del, NC_000001.11:g.224410710_224410714del, NC_000001.11:g.224410711_224410714del, NC_000001.11:g.224410712_224410714del, NC_000001.11:g.224410713_224410714del, NC_000001.11:g.224410714del, NC_000001.11:g.224410714dup, NC_000001.11:g.224410713_224410714dup, NC_000001.11:g.224410712_224410714dup, NC_000001.11:g.224410711_224410714dup, NC_000001.11:g.224410710_224410714dup, NC_000001.11:g.224410709_224410714dup, NC_000001.11:g.224410708_224410714dup, NC_000001.11:g.224410707_224410714dup, NC_000001.11:g.224410706_224410714dup, NC_000001.11:g.224410705_224410714dup, NC_000001.11:g.224410704_224410714dup, NC_000001.11:g.224410703_224410714dup, NC_000001.10:g.224598405_224598416del, NC_000001.10:g.224598407_224598416del, NC_000001.10:g.224598408_224598416del, NC_000001.10:g.224598410_224598416del, NC_000001.10:g.224598411_224598416del, NC_000001.10:g.224598412_224598416del, NC_000001.10:g.224598413_224598416del, NC_000001.10:g.224598414_224598416del, NC_000001.10:g.224598415_224598416del, NC_000001.10:g.224598416del, NC_000001.10:g.224598416dup, NC_000001.10:g.224598415_224598416dup, NC_000001.10:g.224598414_224598416dup, NC_000001.10:g.224598413_224598416dup, NC_000001.10:g.224598412_224598416dup, NC_000001.10:g.224598411_224598416dup, NC_000001.10:g.224598410_224598416dup, NC_000001.10:g.224598409_224598416dup, NC_000001.10:g.224598408_224598416dup, NC_000001.10:g.224598407_224598416dup, NC_000001.10:g.224598406_224598416dup, NC_000001.10:g.224598405_224598416dup, NG_047198.1:g.28594_28605del, NG_047198.1:g.28596_28605del, NG_047198.1:g.28597_28605del, NG_047198.1:g.28599_28605del, NG_047198.1:g.28600_28605del, NG_047198.1:g.28601_28605del, NG_047198.1:g.28602_28605del, NG_047198.1:g.28603_28605del, NG_047198.1:g.28604_28605del, NG_047198.1:g.28605del, NG_047198.1:g.28605dup, NG_047198.1:g.28604_28605dup, NG_047198.1:g.28603_28605dup, NG_047198.1:g.28602_28605dup, NG_047198.1:g.28601_28605dup, NG_047198.1:g.28600_28605dup, NG_047198.1:g.28599_28605dup, NG_047198.1:g.28598_28605dup, NG_047198.1:g.28597_28605dup, NG_047198.1:g.28596_28605dup, NG_047198.1:g.28595_28605dup, NG_047198.1:g.28594_28605dup

Select item 149112310716.

rs1491123107 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:224427104 (GRCh38)
1:224614806 (GRCh37)
Canonical SPDI:: NC_000001.11:224427103:CA:
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00022/19 (GnomAD)
HGVS:: NC_000001.11:g.224427104_224427105del, NC_000001.10:g.224614806_224614807del, NG_047198.1:g.12195_12196del

Select item 149109502517.

rs1491095025 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTATATATATAT [Show Flanks]
Chromosome:: 1:224407152 (GRCh38)
1:224594855 (GRCh37)
Canonical SPDI:: NC_000001.11:224407152:TATATATATAT:TATATATATATGTATATATATAT
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TATATATATATGTATATATATAT=0./0 (ALFA)
HGVS:: NC_000001.11:g.224407153_224407163TA[5]TGTATATATATAT[1], NC_000001.10:g.224594855_224594865TA[5]TGTATATATATAT[1], NG_047198.1:g.32137_32147AT[5]ACATATATATATA[1]

Select item 149106612718.

rs1491066127 [Homo sapiens]

Variant type:: INS
Alleles:: ->AC [Show Flanks]
Chromosome:: 1:224413207 (GRCh38)
1:224600910 (GRCh37)
Canonical SPDI:: NC_000001.11:224413207::AC
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AC=0./0 (ALFA)
HGVS:: NC_000001.11:g.224413207_224413208insAC, NC_000001.10:g.224600909_224600910insAC, NG_047198.1:g.26092_26093insGT

Select item 149105796819.

rs1491057968 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:224391384 (GRCh38)
1:224579086 (GRCh37)
Canonical SPDI:: NC_000001.11:224391382:ACA:A
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.11187/1327 (ALFA)
-=0.00577/438 (GnomAD)
HGVS:: NC_000001.11:g.224391384_224391385del, NC_000001.10:g.224579086_224579087del, NG_047198.1:g.47916_47917del

Select item 149102754220.

rs1491027542 [Homo sapiens]

Variant type:: DEL
Alleles:: AC>- [Show Flanks]
Chromosome:: 1:224413207 (GRCh38)
1:224600909 (GRCh37)
Canonical SPDI:: NC_000001.11:224413206:AC:
Gene:: WDR26 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: -=0.000035/1 (TOMMO)
-=0.000468/3 (1000Genomes)
-=0.000547/76 (GnomAD)
-=0.001092/2 (Korea1K)
HGVS:: NC_000001.11:g.224413207_224413208del, NC_000001.10:g.224600909_224600910del, NG_047198.1:g.26092_26093del

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