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Select item 14915602151.

rs1491560215 has merged into rs11314810 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAA>-,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 14:100272300 (GRCh38)
14:100738637 (GRCh37)
Canonical SPDI:: NC_000014.9:100272295:AAAAAAAAAAAAAA:AAAA,NC_000014.9:100272295:AAAAAAAAAAAAAA:AAAAAAAAAA,NC_000014.9:100272295:AAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000014.9:100272295:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000014.9:100272295:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000014.9:100272295:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:100272295:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:100272295:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
-=0.0589/227 (ALSPAC)
A=0.2867/1436 (1000Genomes)
HGVS:: NC_000014.9:g.100272300_100272309del, NC_000014.9:g.100272306_100272309del, NC_000014.9:g.100272307_100272309del, NC_000014.9:g.100272308_100272309del, NC_000014.9:g.100272309del, NC_000014.9:g.100272309dup, NC_000014.9:g.100272308_100272309dup, NC_000014.9:g.100272303_100272309dup, NC_000014.8:g.100738637_100738646del, NC_000014.8:g.100738643_100738646del, NC_000014.8:g.100738644_100738646del, NC_000014.8:g.100738645_100738646del, NC_000014.8:g.100738646del, NC_000014.8:g.100738646dup, NC_000014.8:g.100738645_100738646dup, NC_000014.8:g.100738640_100738646dup, NG_046908.1:g.38536_38545del, NG_046908.1:g.38542_38545del, NG_046908.1:g.38543_38545del, NG_046908.1:g.38544_38545del, NG_046908.1:g.38545del, NG_046908.1:g.38545dup, NG_046908.1:g.38544_38545dup, NG_046908.1:g.38539_38545dup

Select item 14915240722.

rs1491524072 has merged into rs55649674 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 14:100270274 (GRCh38)
14:100736611 (GRCh37)
Canonical SPDI:: NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:100270262:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
AAA=0.475/19 (GENOME_DK)
HGVS:: NC_000014.9:g.100270274_100270290del, NC_000014.9:g.100270275_100270290del, NC_000014.9:g.100270277_100270290del, NC_000014.9:g.100270278_100270290del, NC_000014.9:g.100270279_100270290del, NC_000014.9:g.100270280_100270290del, NC_000014.9:g.100270281_100270290del, NC_000014.9:g.100270282_100270290del, NC_000014.9:g.100270283_100270290del, NC_000014.9:g.100270284_100270290del, NC_000014.9:g.100270285_100270290del, NC_000014.9:g.100270286_100270290del, NC_000014.9:g.100270287_100270290del, NC_000014.9:g.100270288_100270290del, NC_000014.9:g.100270289_100270290del, NC_000014.9:g.100270290del, NC_000014.9:g.100270290dup, NC_000014.8:g.100736611_100736627del, NC_000014.8:g.100736612_100736627del, NC_000014.8:g.100736614_100736627del, NC_000014.8:g.100736615_100736627del, NC_000014.8:g.100736616_100736627del, NC_000014.8:g.100736617_100736627del, NC_000014.8:g.100736618_100736627del, NC_000014.8:g.100736619_100736627del, NC_000014.8:g.100736620_100736627del, NC_000014.8:g.100736621_100736627del, NC_000014.8:g.100736622_100736627del, NC_000014.8:g.100736623_100736627del, NC_000014.8:g.100736624_100736627del, NC_000014.8:g.100736625_100736627del, NC_000014.8:g.100736626_100736627del, NC_000014.8:g.100736627del, NC_000014.8:g.100736627dup, NG_046908.1:g.36510_36526del, NG_046908.1:g.36511_36526del, NG_046908.1:g.36513_36526del, NG_046908.1:g.36514_36526del, NG_046908.1:g.36515_36526del, NG_046908.1:g.36516_36526del, NG_046908.1:g.36517_36526del, NG_046908.1:g.36518_36526del, NG_046908.1:g.36519_36526del, NG_046908.1:g.36520_36526del, NG_046908.1:g.36521_36526del, NG_046908.1:g.36522_36526del, NG_046908.1:g.36523_36526del, NG_046908.1:g.36524_36526del, NG_046908.1:g.36525_36526del, NG_046908.1:g.36526del, NG_046908.1:g.36526dup

Select item 14914912113.

rs1491491211 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GT [Show Flanks]
Chromosome:: 14:100249749 (GRCh38)
14:100716087 (GRCh37)
Canonical SPDI:: NC_000014.9:100249749:T:TGT
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGT=0./0 (ALFA)
TG=0.000004/1 (TOPMED)
TG=0.000015/1 (GnomAD)
HGVS:: NC_000014.9:g.100249750_100249751insGT, NC_000014.8:g.100716087_100716088insGT, NG_046908.1:g.15986_15987insGT

Select item 14914791144.

rs1491479114 has merged into rs869267099 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 14:100249760 (GRCh38)
14:100716097 (GRCh37)
Canonical SPDI:: NC_000014.9:100249758:TGT:T
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.15419/1829 (ALFA)
-=0.00411/149 (GnomAD)
-=0.00553/42 (TOMMO)
-=0.22789/845 (TWINSUK)
-=0.2356/908 (ALSPAC)
HGVS:: NC_000014.9:g.100249760_100249761del, NC_000014.8:g.100716097_100716098del, NG_046908.1:g.15996_15997del

Select item 14913766245.

rs1491376624 has merged into rs57119106 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,TT,TTT,TTTT,TTTTTT,TTTTTTGTTTTTTTTTTTTTTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:100249755 (GRCh38)
14:100716092 (GRCh37)
Canonical SPDI:: NC_000014.9:100249748:TTTTTTTTTTT:TTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100249748:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000014.9:g.100249755_100249759del, NC_000014.9:g.100249757_100249759del, NC_000014.9:g.100249758_100249759del, NC_000014.9:g.100249759del, NC_000014.9:g.100249759dup, NC_000014.9:g.100249749_100249759T[12]GTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.100249758_100249759dup, NC_000014.9:g.100249757_100249759dup, NC_000014.9:g.100249756_100249759dup, NC_000014.9:g.100249755_100249759dup, NC_000014.9:g.100249754_100249759dup, NC_000014.9:g.100249753_100249759dup, NC_000014.9:g.100249752_100249759dup, NC_000014.9:g.100249751_100249759dup, NC_000014.9:g.100249750_100249759dup, NC_000014.9:g.100249749_100249759dup, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.100249759_100249760insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100716092_100716096del, NC_000014.8:g.100716094_100716096del, NC_000014.8:g.100716095_100716096del, NC_000014.8:g.100716096del, NC_000014.8:g.100716096dup, NC_000014.8:g.100716086_100716096T[12]GTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.100716095_100716096dup, NC_000014.8:g.100716094_100716096dup, NC_000014.8:g.100716093_100716096dup, NC_000014.8:g.100716092_100716096dup, NC_000014.8:g.100716091_100716096dup, NC_000014.8:g.100716090_100716096dup, NC_000014.8:g.100716089_100716096dup, NC_000014.8:g.100716088_100716096dup, NC_000014.8:g.100716087_100716096dup, NC_000014.8:g.100716086_100716096dup, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100716096_100716097insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_046908.1:g.15991_15995del, NG_046908.1:g.15993_15995del, NG_046908.1:g.15994_15995del, NG_046908.1:g.15995del, NG_046908.1:g.15995dup, NG_046908.1:g.15985_15995T[12]GTTTTTTTTTTTTTTTTTT[1], NG_046908.1:g.15994_15995dup, NG_046908.1:g.15993_15995dup, NG_046908.1:g.15992_15995dup, NG_046908.1:g.15991_15995dup, NG_046908.1:g.15990_15995dup, NG_046908.1:g.15989_15995dup, NG_046908.1:g.15988_15995dup, NG_046908.1:g.15987_15995dup, NG_046908.1:g.15986_15995dup, NG_046908.1:g.15985_15995dup, NG_046908.1:g.15995_15996insTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_046908.1:g.15995_15996insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14913596646.

rs1491359664 [Homo sapiens]

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

Select item 14912967627.

rs1491296762 has merged into rs10694000 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTT>-,TTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:100248124 (GRCh38)
14:100714461 (GRCh37)
Canonical SPDI:: NC_000014.9:100248121:TTTTTTTTTTTTTT:TT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248121:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
HGVS:: NC_000014.9:g.100248124_100248135del, NC_000014.9:g.100248128_100248135del, NC_000014.9:g.100248131_100248135del, NC_000014.9:g.100248132_100248135del, NC_000014.9:g.100248133_100248135del, NC_000014.9:g.100248134_100248135del, NC_000014.9:g.100248135del, NC_000014.9:g.100248135dup, NC_000014.9:g.100248134_100248135dup, NC_000014.9:g.100248133_100248135dup, NC_000014.9:g.100248132_100248135dup, NC_000014.9:g.100248131_100248135dup, NC_000014.9:g.100248130_100248135dup, NC_000014.9:g.100248129_100248135dup, NC_000014.9:g.100248128_100248135dup, NC_000014.9:g.100248127_100248135dup, NC_000014.9:g.100248126_100248135dup, NC_000014.9:g.100248125_100248135dup, NC_000014.9:g.100248124_100248135dup, NC_000014.9:g.100248123_100248135dup, NC_000014.9:g.100248135_100248136insTTTTTTTTTTTTTTTT, NC_000014.9:g.100248135_100248136insTTTTTTTTTTTTTTTTT, NC_000014.9:g.100248135_100248136insTTTTTTTTTTTTTTTTTT, NC_000014.9:g.100248135_100248136insTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.100248135_100248136insTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100714461_100714472del, NC_000014.8:g.100714465_100714472del, NC_000014.8:g.100714468_100714472del, NC_000014.8:g.100714469_100714472del, NC_000014.8:g.100714470_100714472del, NC_000014.8:g.100714471_100714472del, NC_000014.8:g.100714472del, NC_000014.8:g.100714472dup, NC_000014.8:g.100714471_100714472dup, NC_000014.8:g.100714470_100714472dup, NC_000014.8:g.100714469_100714472dup, NC_000014.8:g.100714468_100714472dup, NC_000014.8:g.100714467_100714472dup, NC_000014.8:g.100714466_100714472dup, NC_000014.8:g.100714465_100714472dup, NC_000014.8:g.100714464_100714472dup, NC_000014.8:g.100714463_100714472dup, NC_000014.8:g.100714462_100714472dup, NC_000014.8:g.100714461_100714472dup, NC_000014.8:g.100714460_100714472dup, NC_000014.8:g.100714472_100714473insTTTTTTTTTTTTTTTT, NC_000014.8:g.100714472_100714473insTTTTTTTTTTTTTTTTT, NC_000014.8:g.100714472_100714473insTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100714472_100714473insTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100714472_100714473insTTTTTTTTTTTTTTTTTTTTTTT, NG_046908.1:g.14360_14371del, NG_046908.1:g.14364_14371del, NG_046908.1:g.14367_14371del, NG_046908.1:g.14368_14371del, NG_046908.1:g.14369_14371del, NG_046908.1:g.14370_14371del, NG_046908.1:g.14371del, NG_046908.1:g.14371dup, NG_046908.1:g.14370_14371dup, NG_046908.1:g.14369_14371dup, NG_046908.1:g.14368_14371dup, NG_046908.1:g.14367_14371dup, NG_046908.1:g.14366_14371dup, NG_046908.1:g.14365_14371dup, NG_046908.1:g.14364_14371dup, NG_046908.1:g.14363_14371dup, NG_046908.1:g.14362_14371dup, NG_046908.1:g.14361_14371dup, NG_046908.1:g.14360_14371dup, NG_046908.1:g.14359_14371dup, NG_046908.1:g.14371_14372insTTTTTTTTTTTTTTTT, NG_046908.1:g.14371_14372insTTTTTTTTTTTTTTTTT, NG_046908.1:g.14371_14372insTTTTTTTTTTTTTTTTTT, NG_046908.1:g.14371_14372insTTTTTTTTTTTTTTTTTTT, NG_046908.1:g.14371_14372insTTTTTTTTTTTTTTTTTTTTTTT

Select item 14912246848.

rs1491224684 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CG,TG [Show Flanks]
Chromosome:: 14:100241979 (GRCh38)
14:100708317 (GRCh37)
Canonical SPDI:: NC_000014.9:100241979:G:GCG,NC_000014.9:100241979:G:GTG
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTG=0./0 (ALFA)
GT=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.100241980_100241981insCG, NC_000014.9:g.100241980_100241981insTG, NC_000014.8:g.100708317_100708318insCG, NC_000014.8:g.100708317_100708318insTG, NG_046908.1:g.8216_8217insCG, NG_046908.1:g.8216_8217insTG

Select item 14912091679.

rs1491209167 has merged into rs1196714660 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT [Show Flanks]
Chromosome:: 14:100254787 (GRCh38)
14:100721124 (GRCh37)
Canonical SPDI:: NC_000014.9:100254775:TTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000014.9:100254775:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:100254775:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:100254775:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:100254775:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:100254775:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:100254775:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000014.9:g.100254787_100254790del, NC_000014.9:g.100254788_100254790del, NC_000014.9:g.100254789_100254790del, NC_000014.9:g.100254790del, NC_000014.9:g.100254790dup, NC_000014.9:g.100254789_100254790dup, NC_000014.9:g.100254788_100254790dup, NC_000014.8:g.100721124_100721127del, NC_000014.8:g.100721125_100721127del, NC_000014.8:g.100721126_100721127del, NC_000014.8:g.100721127del, NC_000014.8:g.100721127dup, NC_000014.8:g.100721126_100721127dup, NC_000014.8:g.100721125_100721127dup, NG_046908.1:g.21023_21026del, NG_046908.1:g.21024_21026del, NG_046908.1:g.21025_21026del, NG_046908.1:g.21026del, NG_046908.1:g.21026dup, NG_046908.1:g.21025_21026dup, NG_046908.1:g.21024_21026dup

Select item 149110537210.

rs1491105372 [Homo sapiens]

Variant type:: DEL
Alleles:: GT>- [Show Flanks]
Chromosome:: 14:100249748 (GRCh38)
14:100716085 (GRCh37)
Canonical SPDI:: NC_000014.9:100249747:GT:
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000014.9:g.100249748_100249749del, NC_000014.8:g.100716085_100716086del, NG_046908.1:g.15984_15985del

Select item 149104412911.

rs1491044129 has merged into rs11415073 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:100248691 (GRCh38)
14:100715028 (GRCh37)
Canonical SPDI:: NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100248679:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
T=0.225/9 (GENOME_DK)
HGVS:: NC_000014.9:g.100248691_100248702del, NC_000014.9:g.100248692_100248702del, NC_000014.9:g.100248693_100248702del, NC_000014.9:g.100248694_100248702del, NC_000014.9:g.100248695_100248702del, NC_000014.9:g.100248696_100248702del, NC_000014.9:g.100248698_100248702del, NC_000014.9:g.100248699_100248702del, NC_000014.9:g.100248700_100248702del, NC_000014.9:g.100248701_100248702del, NC_000014.9:g.100248702del, NC_000014.9:g.100248702dup, NC_000014.9:g.100248701_100248702dup, NC_000014.9:g.100248700_100248702dup, NC_000014.9:g.100248699_100248702dup, NC_000014.9:g.100248698_100248702dup, NC_000014.9:g.100248697_100248702dup, NC_000014.9:g.100248696_100248702dup, NC_000014.9:g.100248695_100248702dup, NC_000014.9:g.100248694_100248702dup, NC_000014.9:g.100248693_100248702dup, NC_000014.9:g.100248692_100248702dup, NC_000014.9:g.100248691_100248702dup, NC_000014.9:g.100248689_100248702dup, NC_000014.9:g.100248686_100248702dup, NC_000014.8:g.100715028_100715039del, NC_000014.8:g.100715029_100715039del, NC_000014.8:g.100715030_100715039del, NC_000014.8:g.100715031_100715039del, NC_000014.8:g.100715032_100715039del, NC_000014.8:g.100715033_100715039del, NC_000014.8:g.100715035_100715039del, NC_000014.8:g.100715036_100715039del, NC_000014.8:g.100715037_100715039del, NC_000014.8:g.100715038_100715039del, NC_000014.8:g.100715039del, NC_000014.8:g.100715039dup, NC_000014.8:g.100715038_100715039dup, NC_000014.8:g.100715037_100715039dup, NC_000014.8:g.100715036_100715039dup, NC_000014.8:g.100715035_100715039dup, NC_000014.8:g.100715034_100715039dup, NC_000014.8:g.100715033_100715039dup, NC_000014.8:g.100715032_100715039dup, NC_000014.8:g.100715031_100715039dup, NC_000014.8:g.100715030_100715039dup, NC_000014.8:g.100715029_100715039dup, NC_000014.8:g.100715028_100715039dup, NC_000014.8:g.100715026_100715039dup, NC_000014.8:g.100715023_100715039dup, NG_046908.1:g.14927_14938del, NG_046908.1:g.14928_14938del, NG_046908.1:g.14929_14938del, NG_046908.1:g.14930_14938del, NG_046908.1:g.14931_14938del, NG_046908.1:g.14932_14938del, NG_046908.1:g.14934_14938del, NG_046908.1:g.14935_14938del, NG_046908.1:g.14936_14938del, NG_046908.1:g.14937_14938del, NG_046908.1:g.14938del, NG_046908.1:g.14938dup, NG_046908.1:g.14937_14938dup, NG_046908.1:g.14936_14938dup, NG_046908.1:g.14935_14938dup, NG_046908.1:g.14934_14938dup, NG_046908.1:g.14933_14938dup, NG_046908.1:g.14932_14938dup, NG_046908.1:g.14931_14938dup, NG_046908.1:g.14930_14938dup, NG_046908.1:g.14929_14938dup, NG_046908.1:g.14928_14938dup, NG_046908.1:g.14927_14938dup, NG_046908.1:g.14925_14938dup, NG_046908.1:g.14922_14938dup

Select item 149097518912.

rs1490975189 has merged into rs869125410 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:100244331 (GRCh38)
14:100710668 (GRCh37)
Canonical SPDI:: NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:100244320:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000014.9:g.100244331_100244343del, NC_000014.9:g.100244334_100244343del, NC_000014.9:g.100244335_100244343del, NC_000014.9:g.100244336_100244343del, NC_000014.9:g.100244337_100244343del, NC_000014.9:g.100244338_100244343del, NC_000014.9:g.100244339_100244343del, NC_000014.9:g.100244340_100244343del, NC_000014.9:g.100244341_100244343del, NC_000014.9:g.100244342_100244343del, NC_000014.9:g.100244343del, NC_000014.9:g.100244343dup, NC_000014.9:g.100244342_100244343dup, NC_000014.9:g.100244341_100244343dup, NC_000014.9:g.100244340_100244343dup, NC_000014.9:g.100244339_100244343dup, NC_000014.9:g.100244338_100244343dup, NC_000014.9:g.100244337_100244343dup, NC_000014.9:g.100244336_100244343dup, NC_000014.9:g.100244335_100244343dup, NC_000014.9:g.100244334_100244343dup, NC_000014.9:g.100244333_100244343dup, NC_000014.9:g.100244327_100244343dup, NC_000014.9:g.100244343_100244344insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.100710668_100710680del, NC_000014.8:g.100710671_100710680del, NC_000014.8:g.100710672_100710680del, NC_000014.8:g.100710673_100710680del, NC_000014.8:g.100710674_100710680del, NC_000014.8:g.100710675_100710680del, NC_000014.8:g.100710676_100710680del, NC_000014.8:g.100710677_100710680del, NC_000014.8:g.100710678_100710680del, NC_000014.8:g.100710679_100710680del, NC_000014.8:g.100710680del, NC_000014.8:g.100710680dup, NC_000014.8:g.100710679_100710680dup, NC_000014.8:g.100710678_100710680dup, NC_000014.8:g.100710677_100710680dup, NC_000014.8:g.100710676_100710680dup, NC_000014.8:g.100710675_100710680dup, NC_000014.8:g.100710674_100710680dup, NC_000014.8:g.100710673_100710680dup, NC_000014.8:g.100710672_100710680dup, NC_000014.8:g.100710671_100710680dup, NC_000014.8:g.100710670_100710680dup, NC_000014.8:g.100710664_100710680dup, NC_000014.8:g.100710680_100710681insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_046908.1:g.10567_10579del, NG_046908.1:g.10570_10579del, NG_046908.1:g.10571_10579del, NG_046908.1:g.10572_10579del, NG_046908.1:g.10573_10579del, NG_046908.1:g.10574_10579del, NG_046908.1:g.10575_10579del, NG_046908.1:g.10576_10579del, NG_046908.1:g.10577_10579del, NG_046908.1:g.10578_10579del, NG_046908.1:g.10579del, NG_046908.1:g.10579dup, NG_046908.1:g.10578_10579dup, NG_046908.1:g.10577_10579dup, NG_046908.1:g.10576_10579dup, NG_046908.1:g.10575_10579dup, NG_046908.1:g.10574_10579dup, NG_046908.1:g.10573_10579dup, NG_046908.1:g.10572_10579dup, NG_046908.1:g.10571_10579dup, NG_046908.1:g.10570_10579dup, NG_046908.1:g.10569_10579dup, NG_046908.1:g.10563_10579dup, NG_046908.1:g.10579_10580insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149084919813.

rs1490849198 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 14:100274129 (GRCh38)
14:100740466 (GRCh37)
Canonical SPDI:: NC_000014.9:100274128:C:A,NC_000014.9:100274128:C:G
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000021/3 (GnomAD)
A=0.000045/12 (TOPMED)
HGVS:: NC_000014.9:g.100274129C>A, NC_000014.9:g.100274129C>G, NC_000014.8:g.100740466C>A, NC_000014.8:g.100740466C>G, NG_046908.1:g.40365C>A, NG_046908.1:g.40365C>G

Select item 149083912514.

rs1490839125 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:100275677 (GRCh38)
14:100742014 (GRCh37)
Canonical SPDI:: NC_000014.9:100275676:A:G
Gene:: YY1 (Varview), MIR6764 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.100275677A>G, NC_000014.8:g.100742014A>G, NG_046908.1:g.41913A>G

Select item 149078645815.

rs1490786458 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:100276883 (GRCh38)
14:100743220 (GRCh37)
Canonical SPDI:: NC_000014.9:100276882:A:G
Gene:: YY1 (Varview), MIR6764 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.100276883A>G, NC_000014.8:g.100743220A>G, NG_046908.1:g.43119A>G

Select item 149067832716.

rs1490678327 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 14:100243662 (GRCh38)
14:100709999 (GRCh37)
Canonical SPDI:: NC_000014.9:100243661:G:C
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.100243662G>C, NC_000014.8:g.100709999G>C, NG_046908.1:g.9898G>C

Select item 149067638017.

rs1490676380 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:100276223 (GRCh38)
14:100742560 (GRCh37)
Canonical SPDI:: NC_000014.9:100276222:T:C
Gene:: YY1 (Varview), MIR6764 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000014.9:g.100276223T>C, NC_000014.8:g.100742560T>C, NG_046908.1:g.42459T>C

Select item 149064894318.

rs1490648943 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:100263968 (GRCh38)
14:100730305 (GRCh37)
Canonical SPDI:: NC_000014.9:100263967:A:G
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
HGVS:: NC_000014.9:g.100263968A>G, NC_000014.8:g.100730305A>G, NG_046908.1:g.30204A>G

Select item 149051421919.

rs1490514219 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:100244039 (GRCh38)
14:100710376 (GRCh37)
Canonical SPDI:: NC_000014.9:100244038:C:T
Gene:: YY1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.100244039C>T, NC_000014.8:g.100710376C>T, NG_046908.1:g.10275C>T

Select item 149044083420.

rs1490440834 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:100238877 (GRCh38)
14:100705214 (GRCh37)
Canonical SPDI:: NC_000014.9:100238876:T:C
Gene:: YY1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.100238877T>C, NC_000014.8:g.100705214T>C, NG_046908.1:g.5113T>C, NM_003403.4:c.-368T>C

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