SNP Links for Gene (Select 8650) - SNP

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Select item 14915793301.

rs1491579330 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 14:73385496 (GRCh38)
14:73852204 (GRCh37)
Canonical SPDI:: NC_000014.9:73385495:CT:
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00008/1 (ALFA)
-=0.00011/3 (TOMMO)
-=0.00074/46 (GnomAD)
HGVS:: NC_000014.9:g.73385496_73385497del, NC_000014.8:g.73852204_73852205del, NG_029061.2:g.78084_78085del

Select item 14915694892.

rs1491569489 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTTGTTTTTCTTTT,CTTTT,CTTTTTTTCTTTT [Show Flanks]
Chromosome:: 14:73353073 (GRCh38)
14:73819782 (GRCh37)
Canonical SPDI:: NC_000014.9:73353073:TTTT:TTTTCTTGTTTTTCTTTT,NC_000014.9:73353073:TTTT:TTTTCTTTT,NC_000014.9:73353073:TTTT:TTTTCTTTTTTTCTTTT
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTCTTTT=0./0 (ALFA)
TTTTCTTGTTTTTC=0.00009/2 (TOMMO)
TTTTC=0.0002/8 (GnomAD)
HGVS:: NC_000014.9:g.73353074_73353077T[4]CTTGTTTTTCTTTT[1], NC_000014.9:g.73353074_73353077T[4]CTTTT[1], NC_000014.9:g.73353074_73353077TTTTCTTT[2]T[1], NC_000014.8:g.73819782_73819785T[4]CTTGTTTTTCTTTT[1], NC_000014.8:g.73819782_73819785T[4]CTTTT[1], NC_000014.8:g.73819782_73819785TTTTCTTT[2]T[1], NG_029061.2:g.110504_110507A[4]GAAAAACAAGAAAA[1], NG_029061.2:g.110504_110507A[4]GAAAA[1], NG_029061.2:g.110504_110507AAAAGAAA[2]A[1]

Select item 14915674643.

rs1491567464 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 14:73387770 (GRCh38)
14:73854479 (GRCh37)
Canonical SPDI:: NC_000014.9:73387770:CC:CCC
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CCC=0./0 (ALFA)
C=0.000531/74 (GnomAD)
HGVS:: NC_000014.9:g.73387772dup, NC_000014.8:g.73854480dup, NG_029061.2:g.75810dup

Select item 14915539024.

rs1491553902 has merged into rs869074049 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAA>-,AA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 14:73389286 (GRCh38)
14:73855994 (GRCh37)
Canonical SPDI:: NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73389272:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000014.9:g.73389286_73389293del, NC_000014.9:g.73389288_73389293del, NC_000014.9:g.73389291_73389293del, NC_000014.9:g.73389292_73389293del, NC_000014.9:g.73389293del, NC_000014.9:g.73389293dup, NC_000014.9:g.73389292_73389293dup, NC_000014.9:g.73389291_73389293dup, NC_000014.9:g.73389290_73389293dup, NC_000014.9:g.73389289_73389293dup, NC_000014.9:g.73389288_73389293dup, NC_000014.9:g.73389287_73389293dup, NC_000014.9:g.73389286_73389293dup, NC_000014.9:g.73389285_73389293dup, NC_000014.9:g.73389284_73389293dup, NC_000014.9:g.73389283_73389293dup, NC_000014.9:g.73389282_73389293dup, NC_000014.9:g.73389281_73389293dup, NC_000014.9:g.73389280_73389293dup, NC_000014.9:g.73389279_73389293dup, NC_000014.9:g.73389278_73389293dup, NC_000014.9:g.73389277_73389293dup, NC_000014.9:g.73389276_73389293dup, NC_000014.9:g.73389275_73389293dup, NC_000014.9:g.73389274_73389293dup, NC_000014.9:g.73389273_73389293dup, NC_000014.9:g.73389293_73389294insAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.73389293_73389294insAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.73389293_73389294insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.73389293_73389294insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.73389293_73389294insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.73389293_73389294insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.73389293_73389294insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.73855994_73856001del, NC_000014.8:g.73855996_73856001del, NC_000014.8:g.73855999_73856001del, NC_000014.8:g.73856000_73856001del, NC_000014.8:g.73856001del, NC_000014.8:g.73856001dup, NC_000014.8:g.73856000_73856001dup, NC_000014.8:g.73855999_73856001dup, NC_000014.8:g.73855998_73856001dup, NC_000014.8:g.73855997_73856001dup, NC_000014.8:g.73855996_73856001dup, NC_000014.8:g.73855995_73856001dup, NC_000014.8:g.73855994_73856001dup, NC_000014.8:g.73855993_73856001dup, NC_000014.8:g.73855992_73856001dup, NC_000014.8:g.73855991_73856001dup, NC_000014.8:g.73855990_73856001dup, NC_000014.8:g.73855989_73856001dup, NC_000014.8:g.73855988_73856001dup, NC_000014.8:g.73855987_73856001dup, NC_000014.8:g.73855986_73856001dup, NC_000014.8:g.73855985_73856001dup, NC_000014.8:g.73855984_73856001dup, NC_000014.8:g.73855983_73856001dup, NC_000014.8:g.73855982_73856001dup, NC_000014.8:g.73855981_73856001dup, NC_000014.8:g.73856001_73856002insAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.73856001_73856002insAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.73856001_73856002insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.73856001_73856002insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.73856001_73856002insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.73856001_73856002insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.73856001_73856002insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029061.2:g.74301_74308del, NG_029061.2:g.74303_74308del, NG_029061.2:g.74306_74308del, NG_029061.2:g.74307_74308del, NG_029061.2:g.74308del, NG_029061.2:g.74308dup, NG_029061.2:g.74307_74308dup, NG_029061.2:g.74306_74308dup, NG_029061.2:g.74305_74308dup, NG_029061.2:g.74304_74308dup, NG_029061.2:g.74303_74308dup, NG_029061.2:g.74302_74308dup, NG_029061.2:g.74301_74308dup, NG_029061.2:g.74300_74308dup, NG_029061.2:g.74299_74308dup, NG_029061.2:g.74298_74308dup, NG_029061.2:g.74297_74308dup, NG_029061.2:g.74296_74308dup, NG_029061.2:g.74295_74308dup, NG_029061.2:g.74294_74308dup, NG_029061.2:g.74293_74308dup, NG_029061.2:g.74292_74308dup, NG_029061.2:g.74291_74308dup, NG_029061.2:g.74290_74308dup, NG_029061.2:g.74289_74308dup, NG_029061.2:g.74288_74308dup, NG_029061.2:g.74308_74309insTTTTTTTTTTTTTTTTTTTTTT, NG_029061.2:g.74308_74309insTTTTTTTTTTTTTTTTTTTTTTT, NG_029061.2:g.74308_74309insTTTTTTTTTTTTTTTTTTTTTTTT, NG_029061.2:g.74308_74309insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029061.2:g.74308_74309insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029061.2:g.74308_74309insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029061.2:g.74308_74309insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14915508345.

rs1491550834 [Homo sapiens]

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

Select item 14915242536.

rs1491524253 has merged into rs752154048 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 14:73445367 (GRCh38)
14:73912075 (GRCh37)
Canonical SPDI:: NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:73445354:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000014.9:g.73445367_73445396del, NC_000014.9:g.73445369_73445396del, NC_000014.9:g.73445370_73445396del, NC_000014.9:g.73445371_73445396del, NC_000014.9:g.73445372_73445396del, NC_000014.9:g.73445373_73445396del, NC_000014.9:g.73445374_73445396del, NC_000014.9:g.73445375_73445396del, NC_000014.9:g.73445376_73445396del, NC_000014.9:g.73445377_73445396del, NC_000014.9:g.73445378_73445396del, NC_000014.9:g.73445379_73445396del, NC_000014.9:g.73445380_73445396del, NC_000014.9:g.73445381_73445396del, NC_000014.9:g.73445382_73445396del, NC_000014.9:g.73445383_73445396del, NC_000014.9:g.73445384_73445396del, NC_000014.9:g.73445385_73445396del, NC_000014.9:g.73445386_73445396del, NC_000014.9:g.73445387_73445396del, NC_000014.9:g.73445388_73445396del, NC_000014.9:g.73445389_73445396del, NC_000014.9:g.73445390_73445396del, NC_000014.9:g.73445391_73445396del, NC_000014.9:g.73445392_73445396del, NC_000014.9:g.73445393_73445396del, NC_000014.9:g.73445394_73445396del, NC_000014.9:g.73445395_73445396del, NC_000014.9:g.73445396del, NC_000014.9:g.73445396dup, NC_000014.9:g.73445395_73445396dup, NC_000014.9:g.73445394_73445396dup, NC_000014.9:g.73445393_73445396dup, NC_000014.9:g.73445392_73445396dup, NC_000014.9:g.73445391_73445396dup, NC_000014.9:g.73445390_73445396dup, NC_000014.9:g.73445389_73445396dup, NC_000014.9:g.73445388_73445396dup, NC_000014.9:g.73445387_73445396dup, NC_000014.9:g.73445386_73445396dup, NC_000014.9:g.73445385_73445396dup, NC_000014.9:g.73445384_73445396dup, NC_000014.9:g.73445383_73445396dup, NC_000014.9:g.73445382_73445396dup, NC_000014.9:g.73445381_73445396dup, NC_000014.9:g.73445380_73445396dup, NC_000014.9:g.73445379_73445396dup, NC_000014.9:g.73445378_73445396dup, NC_000014.9:g.73445377_73445396dup, NC_000014.9:g.73445376_73445396dup, NC_000014.9:g.73445375_73445396dup, NC_000014.9:g.73445374_73445396dup, NC_000014.9:g.73445373_73445396dup, NC_000014.9:g.73445372_73445396dup, NC_000014.9:g.73445370_73445396dup, NC_000014.9:g.73445369_73445396dup, NC_000014.9:g.73445368_73445396dup, NC_000014.9:g.73445367_73445396dup, NC_000014.9:g.73445366_73445396dup, NC_000014.9:g.73445365_73445396dup, NC_000014.8:g.73912075_73912104del, NC_000014.8:g.73912077_73912104del, NC_000014.8:g.73912078_73912104del, NC_000014.8:g.73912079_73912104del, NC_000014.8:g.73912080_73912104del, NC_000014.8:g.73912081_73912104del, NC_000014.8:g.73912082_73912104del, NC_000014.8:g.73912083_73912104del, NC_000014.8:g.73912084_73912104del, NC_000014.8:g.73912085_73912104del, NC_000014.8:g.73912086_73912104del, NC_000014.8:g.73912087_73912104del, NC_000014.8:g.73912088_73912104del, NC_000014.8:g.73912089_73912104del, NC_000014.8:g.73912090_73912104del, NC_000014.8:g.73912091_73912104del, NC_000014.8:g.73912092_73912104del, NC_000014.8:g.73912093_73912104del, NC_000014.8:g.73912094_73912104del, NC_000014.8:g.73912095_73912104del, NC_000014.8:g.73912096_73912104del, NC_000014.8:g.73912097_73912104del, NC_000014.8:g.73912098_73912104del, NC_000014.8:g.73912099_73912104del, NC_000014.8:g.73912100_73912104del, NC_000014.8:g.73912101_73912104del, NC_000014.8:g.73912102_73912104del, NC_000014.8:g.73912103_73912104del, NC_000014.8:g.73912104del, NC_000014.8:g.73912104dup, NC_000014.8:g.73912103_73912104dup, NC_000014.8:g.73912102_73912104dup, NC_000014.8:g.73912101_73912104dup, NC_000014.8:g.73912100_73912104dup, NC_000014.8:g.73912099_73912104dup, NC_000014.8:g.73912098_73912104dup, NC_000014.8:g.73912097_73912104dup, NC_000014.8:g.73912096_73912104dup, NC_000014.8:g.73912095_73912104dup, NC_000014.8:g.73912094_73912104dup, NC_000014.8:g.73912093_73912104dup, NC_000014.8:g.73912092_73912104dup, NC_000014.8:g.73912091_73912104dup, NC_000014.8:g.73912090_73912104dup, NC_000014.8:g.73912089_73912104dup, NC_000014.8:g.73912088_73912104dup, NC_000014.8:g.73912087_73912104dup, NC_000014.8:g.73912086_73912104dup, NC_000014.8:g.73912085_73912104dup, NC_000014.8:g.73912084_73912104dup, NC_000014.8:g.73912083_73912104dup, NC_000014.8:g.73912082_73912104dup, NC_000014.8:g.73912081_73912104dup, NC_000014.8:g.73912080_73912104dup, NC_000014.8:g.73912078_73912104dup, NC_000014.8:g.73912077_73912104dup, NC_000014.8:g.73912076_73912104dup, NC_000014.8:g.73912075_73912104dup, NC_000014.8:g.73912074_73912104dup, NC_000014.8:g.73912073_73912104dup, NG_029061.2:g.18197_18226del, NG_029061.2:g.18199_18226del, NG_029061.2:g.18200_18226del, NG_029061.2:g.18201_18226del, NG_029061.2:g.18202_18226del, NG_029061.2:g.18203_18226del, NG_029061.2:g.18204_18226del, NG_029061.2:g.18205_18226del, NG_029061.2:g.18206_18226del, NG_029061.2:g.18207_18226del, NG_029061.2:g.18208_18226del, NG_029061.2:g.18209_18226del, NG_029061.2:g.18210_18226del, NG_029061.2:g.18211_18226del, NG_029061.2:g.18212_18226del, NG_029061.2:g.18213_18226del, NG_029061.2:g.18214_18226del, NG_029061.2:g.18215_18226del, NG_029061.2:g.18216_18226del, NG_029061.2:g.18217_18226del, NG_029061.2:g.18218_18226del, NG_029061.2:g.18219_18226del, NG_029061.2:g.18220_18226del, NG_029061.2:g.18221_18226del, NG_029061.2:g.18222_18226del, NG_029061.2:g.18223_18226del, NG_029061.2:g.18224_18226del, NG_029061.2:g.18225_18226del, NG_029061.2:g.18226del, NG_029061.2:g.18226dup, NG_029061.2:g.18225_18226dup, NG_029061.2:g.18224_18226dup, NG_029061.2:g.18223_18226dup, NG_029061.2:g.18222_18226dup, NG_029061.2:g.18221_18226dup, NG_029061.2:g.18220_18226dup, NG_029061.2:g.18219_18226dup, NG_029061.2:g.18218_18226dup, NG_029061.2:g.18217_18226dup, NG_029061.2:g.18216_18226dup, NG_029061.2:g.18215_18226dup, NG_029061.2:g.18214_18226dup, NG_029061.2:g.18213_18226dup, NG_029061.2:g.18212_18226dup, NG_029061.2:g.18211_18226dup, NG_029061.2:g.18210_18226dup, NG_029061.2:g.18209_18226dup, NG_029061.2:g.18208_18226dup, NG_029061.2:g.18207_18226dup, NG_029061.2:g.18206_18226dup, NG_029061.2:g.18205_18226dup, NG_029061.2:g.18204_18226dup, NG_029061.2:g.18203_18226dup, NG_029061.2:g.18202_18226dup, NG_029061.2:g.18200_18226dup, NG_029061.2:g.18199_18226dup, NG_029061.2:g.18198_18226dup, NG_029061.2:g.18197_18226dup, NG_029061.2:g.18196_18226dup, NG_029061.2:g.18195_18226dup

Select item 14915080967.

rs1491508096 has merged into rs551368866 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT [Show Flanks]
Chromosome:: 14:73406102 (GRCh38)
14:73872810 (GRCh37)
Canonical SPDI:: NC_000014.9:73406092:TTTTTTTTTTTTTTT:TTTTTTTTT,NC_000014.9:73406092:TTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000014.9:73406092:TTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000014.9:73406092:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:73406092:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:73406092:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:73406092:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:73406092:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:73406092:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:73406092:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
-=0.000011/3 (TOPMED)
TTT=0.202647/781 (ALSPAC)
TTT=0.208468/773 (TWINSUK)
T=0.375/15 (GENOME_DK)
HGVS:: NC_000014.9:g.73406102_73406107del, NC_000014.9:g.73406103_73406107del, NC_000014.9:g.73406104_73406107del, NC_000014.9:g.73406105_73406107del, NC_000014.9:g.73406106_73406107del, NC_000014.9:g.73406107del, NC_000014.9:g.73406107dup, NC_000014.9:g.73406106_73406107dup, NC_000014.9:g.73406105_73406107dup, NC_000014.9:g.73406104_73406107dup, NC_000014.8:g.73872810_73872815del, NC_000014.8:g.73872811_73872815del, NC_000014.8:g.73872812_73872815del, NC_000014.8:g.73872813_73872815del, NC_000014.8:g.73872814_73872815del, NC_000014.8:g.73872815del, NC_000014.8:g.73872815dup, NC_000014.8:g.73872814_73872815dup, NC_000014.8:g.73872813_73872815dup, NC_000014.8:g.73872812_73872815dup, NG_029061.2:g.57483_57488del, NG_029061.2:g.57484_57488del, NG_029061.2:g.57485_57488del, NG_029061.2:g.57486_57488del, NG_029061.2:g.57487_57488del, NG_029061.2:g.57488del, NG_029061.2:g.57488dup, NG_029061.2:g.57487_57488dup, NG_029061.2:g.57486_57488dup, NG_029061.2:g.57485_57488dup

Select item 14915020478.

rs1491502047 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CA [Show Flanks]
Chromosome:: 14:73372344 (GRCh38)
14:73839053 (GRCh37)
Canonical SPDI:: NC_000014.9:73372344:A:ACA
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACA=0./0 (ALFA)
AC=0.0006/23 (GnomAD)
HGVS:: NC_000014.9:g.73372345_73372346insCA, NC_000014.8:g.73839053_73839054insCA, NG_029061.2:g.91236_91237insGT

Select item 14915017949.

rs1491501794 [Homo sapiens]

Variant type:: DEL
Alleles:: GA>- [Show Flanks]
Chromosome:: 14:73313668 (GRCh38)
14:73780376 (GRCh37)
Canonical SPDI:: NC_000014.9:73313667:GA:
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000014.9:g.73313668_73313669del, NC_000014.8:g.73780376_73780377del, NG_029061.2:g.149912_149913del

Select item 149148384710.

rs1491483847 has merged into rs199628671 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAAAAAA [Show Flanks]
Chromosome:: 14:73328287 (GRCh38)
14:73794995 (GRCh37)
Canonical SPDI:: NC_000014.9:73328274:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000014.9:73328274:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000014.9:73328274:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:73328274:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:73328274:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000014.9:73328274:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000014.9:73328274:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000014.9:g.73328287_73328288del, NC_000014.9:g.73328288del, NC_000014.9:g.73328288dup, NC_000014.9:g.73328287_73328288dup, NC_000014.9:g.73328286_73328288dup, NC_000014.9:g.73328285_73328288dup, NC_000014.9:g.73328279_73328288dup, NC_000014.8:g.73794995_73794996del, NC_000014.8:g.73794996del, NC_000014.8:g.73794996dup, NC_000014.8:g.73794995_73794996dup, NC_000014.8:g.73794994_73794996dup, NC_000014.8:g.73794993_73794996dup, NC_000014.8:g.73794987_73794996dup, NG_029061.2:g.135305_135306del, NG_029061.2:g.135306del, NG_029061.2:g.135306dup, NG_029061.2:g.135305_135306dup, NG_029061.2:g.135304_135306dup, NG_029061.2:g.135303_135306dup, NG_029061.2:g.135297_135306dup

Select item 149145675911.

rs1491456759 [Homo sapiens]

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

Select item 149144967812.

rs1491449678 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 14:73367793 (GRCh38)
14:73834501 (GRCh37)
Canonical SPDI:: NC_000014.9:73367791:AGA:A
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.73367793_73367794del, NC_000014.8:g.73834501_73834502del, NG_029061.2:g.95788_95789del

Select item 149143495313.

rs1491434953 has merged into rs67252605 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA [Show Flanks]
Chromosome:: 14:73457055 (GRCh38)
14:73923762 (GRCh37)
Canonical SPDI:: NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAA,NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAA,NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAAAA,NC_000014.9:73457046:AAAAAAAAAA:AAAAAAAAAAAA
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
-=0.17192/774 (1000Genomes)
-=0.2/8 (GENOME_DK)
-=0.20865/931 (Estonian)
-=0.26537/984 (TWINSUK)
-=0.27089/1044 (ALSPAC)
-=0.29167/175 (NorthernSweden)
HGVS:: NC_000014.9:g.73457055_73457056del, NC_000014.9:g.73457056del, NC_000014.9:g.73457056dup, NC_000014.9:g.73457055_73457056dup, NC_000014.8:g.73923762_73923763del, NC_000014.8:g.73923763del, NC_000014.8:g.73923763dup, NC_000014.8:g.73923762_73923763dup, NG_029061.2:g.6533_6534del, NG_029061.2:g.6534del, NG_029061.2:g.6534dup, NG_029061.2:g.6533_6534dup

Select item 149142849914.

rs1491428499 [Homo sapiens]

Variant type:: INS
Alleles:: ->C,CTC [Show Flanks]
Chromosome:: 14:73437042 (GRCh38)
14:73903751 (GRCh37)
Canonical SPDI:: NC_000014.9:73437042::C,NC_000014.9:73437042::CTC
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTC=0./0 (ALFA)
CTC=0.000004/1 (TOPMED)
C=0.000143/4 (TOMMO)
HGVS:: NC_000014.9:g.73437042_73437043insC, NC_000014.9:g.73437042_73437043insCTC, NC_000014.8:g.73903750_73903751insC, NC_000014.8:g.73903750_73903751insCTC, NG_029061.2:g.26538_26539insG, NG_029061.2:g.26538_26539insGAG

Select item 149140042715.

rs1491400427 has merged into rs71112755 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTT>-,T,TT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:73437054 (GRCh38)
14:73903762 (GRCh37)
Canonical SPDI:: NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:73437041:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.73437054_73437062del, NC_000014.9:g.73437055_73437062del, NC_000014.9:g.73437056_73437062del, NC_000014.9:g.73437059_73437062del, NC_000014.9:g.73437060_73437062del, NC_000014.9:g.73437061_73437062del, NC_000014.9:g.73437062del, NC_000014.9:g.73437062dup, NC_000014.9:g.73437061_73437062dup, NC_000014.9:g.73437060_73437062dup, NC_000014.9:g.73437059_73437062dup, NC_000014.9:g.73437058_73437062dup, NC_000014.9:g.73437057_73437062dup, NC_000014.9:g.73437054_73437062dup, NC_000014.9:g.73437051_73437062dup, NC_000014.9:g.73437044_73437062dup, NC_000014.9:g.73437043_73437062dup, NC_000014.9:g.73437042_73437062dup, NC_000014.8:g.73903762_73903770del, NC_000014.8:g.73903763_73903770del, NC_000014.8:g.73903764_73903770del, NC_000014.8:g.73903767_73903770del, NC_000014.8:g.73903768_73903770del, NC_000014.8:g.73903769_73903770del, NC_000014.8:g.73903770del, NC_000014.8:g.73903770dup, NC_000014.8:g.73903769_73903770dup, NC_000014.8:g.73903768_73903770dup, NC_000014.8:g.73903767_73903770dup, NC_000014.8:g.73903766_73903770dup, NC_000014.8:g.73903765_73903770dup, NC_000014.8:g.73903762_73903770dup, NC_000014.8:g.73903759_73903770dup, NC_000014.8:g.73903752_73903770dup, NC_000014.8:g.73903751_73903770dup, NC_000014.8:g.73903750_73903770dup, NG_029061.2:g.26531_26539del, NG_029061.2:g.26532_26539del, NG_029061.2:g.26533_26539del, NG_029061.2:g.26536_26539del, NG_029061.2:g.26537_26539del, NG_029061.2:g.26538_26539del, NG_029061.2:g.26539del, NG_029061.2:g.26539dup, NG_029061.2:g.26538_26539dup, NG_029061.2:g.26537_26539dup, NG_029061.2:g.26536_26539dup, NG_029061.2:g.26535_26539dup, NG_029061.2:g.26534_26539dup, NG_029061.2:g.26531_26539dup, NG_029061.2:g.26528_26539dup, NG_029061.2:g.26521_26539dup, NG_029061.2:g.26520_26539dup, NG_029061.2:g.26519_26539dup

Select item 149138982116.

rs1491389821 has merged into rs60750268 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>-,ATAT [Show Flanks]
Chromosome:: 14:73440207 (GRCh38)
14:73906915 (GRCh37)
Canonical SPDI:: NC_000014.9:73440196:ATATATATATAT:ATATATATAT,NC_000014.9:73440196:ATATATATATAT:ATATATATATATAT
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATATATAT=0./0 (ALFA)
HGVS:: NC_000014.9:g.73440197AT[5], NC_000014.9:g.73440197AT[7], NC_000014.8:g.73906905AT[5], NC_000014.8:g.73906905AT[7], NG_029061.2:g.23373AT[5], NG_029061.2:g.23373AT[7]

Select item 149138968517.

rs1491389685 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: 14:73288558 (GRCh38)
14:73755266 (GRCh37)
Canonical SPDI:: NC_000014.9:73288556:ATA:A
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.01544/69 (ALFA)
-=0.00198/33 (TOMMO)
HGVS:: NC_000014.9:g.73288558_73288559del, NC_000014.8:g.73755266_73755267del, NG_029061.2:g.175023_175024del

Select item 149138626618.

rs1491386266 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTCT>-,CT [Show Flanks]
Chromosome:: 14:73294820 (GRCh38)
14:73761528 (GRCh37)
Canonical SPDI:: NC_000014.9:73294817:CTCTCT:CT,NC_000014.9:73294817:CTCTCT:CTCT
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.73294818CT[1], NC_000014.9:g.73294818CT[2], NC_000014.8:g.73761526CT[1], NC_000014.8:g.73761526CT[2], NG_029061.2:g.168758AG[1], NG_029061.2:g.168758AG[2]

Select item 149138613819.

rs1491386138 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 14:73391053 (GRCh38)
14:73857762 (GRCh37)
Canonical SPDI:: NC_000014.9:73391053:A:AA
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0.000498/7 (ALFA)
A=0.00088/233 (TOPMED)
A=0.001281/118 (GnomAD)
HGVS:: NC_000014.9:g.73391054dup, NC_000014.8:g.73857762dup, NG_029061.2:g.72527dup

Select item 149137670820.

rs1491376708 [Homo sapiens]

Variant type:: INS
Alleles:: ->CTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:73354839 (GRCh38)
14:73821548 (GRCh37)
Canonical SPDI:: NC_000014.9:73354839::CTTTTTTTTTTTT
Gene:: NUMB (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000014.9:g.73354839_73354840insCTTTTTTTTTTTT, NC_000014.8:g.73821547_73821548insCTTTTTTTTTTTT, NG_029061.2:g.108741_108742insAAAAAAAAAAAAG

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