SNP Links for Nucleotide (Select 312261204) - SNP

Links from Nucleotide

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Select item 14915709541.

rs1491570954 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:97586136 (GRCh38)
10:99345893 (GRCh37)
Canonical SPDI:: NC_000010.11:97586135:CA:
Gene:: HOGA1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000010.11:g.97586136_97586137del, NC_000010.10:g.99345893_99345894del, NG_027922.1:g.6792_6793del

Select item 14915606722.

rs1491560672 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:97593029 (GRCh38)
10:99352786 (GRCh37)
Canonical SPDI:: NC_000010.11:97593028:CA:
Gene:: HOGA1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00067/8 (ALFA)
HGVS:: NC_000010.11:g.97593029_97593030del, NC_000010.10:g.99352786_99352787del, NG_027922.1:g.13685_13686del

Select item 14915134783.

rs1491513478 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 10:97588199 (GRCh38)
10:99347956 (GRCh37)
Canonical SPDI:: NC_000010.11:97588197:TCT:T
Gene:: HOGA1 (Varview), C10orf62 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.001293/21 (ALFA)
-=0.000061/1 (TOMMO)
-=0.001093/7 (1000Genomes)
-=0.001337/157 (GnomAD)
-=0.003834/7 (Korea1K)
HGVS:: NC_000010.11:g.97588199_97588200del, NC_000010.10:g.99347956_99347957del, NG_027922.1:g.8855_8856del

Select item 14914909204.

rs1491490920 has merged into rs60230634 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:97606139 (GRCh38)
10:99365896 (GRCh37)
Canonical SPDI:: NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97606128:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: HOGA1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
A=0.375/3 (KOREAN)
HGVS:: NC_000010.11:g.97606139_97606151del, NC_000010.11:g.97606142_97606151del, NC_000010.11:g.97606143_97606151del, NC_000010.11:g.97606144_97606151del, NC_000010.11:g.97606145_97606151del, NC_000010.11:g.97606146_97606151del, NC_000010.11:g.97606147_97606151del, NC_000010.11:g.97606148_97606151del, NC_000010.11:g.97606149_97606151del, NC_000010.11:g.97606150_97606151del, NC_000010.11:g.97606151del, NC_000010.11:g.97606151dup, NC_000010.11:g.97606150_97606151dup, NC_000010.11:g.97606149_97606151dup, NC_000010.11:g.97606148_97606151dup, NC_000010.11:g.97606147_97606151dup, NC_000010.11:g.97606146_97606151dup, NC_000010.11:g.97606145_97606151dup, NC_000010.11:g.97606144_97606151dup, NC_000010.11:g.97606143_97606151dup, NC_000010.11:g.97606142_97606151dup, NC_000010.11:g.97606141_97606151dup, NC_000010.11:g.97606140_97606151dup, NC_000010.11:g.97606139_97606151dup, NC_000010.11:g.97606138_97606151dup, NC_000010.11:g.97606137_97606151dup, NC_000010.11:g.97606134_97606151dup, NC_000010.11:g.97606133_97606151dup, NC_000010.11:g.97606132_97606151dup, NC_000010.10:g.99365896_99365908del, NC_000010.10:g.99365899_99365908del, NC_000010.10:g.99365900_99365908del, NC_000010.10:g.99365901_99365908del, NC_000010.10:g.99365902_99365908del, NC_000010.10:g.99365903_99365908del, NC_000010.10:g.99365904_99365908del, NC_000010.10:g.99365905_99365908del, NC_000010.10:g.99365906_99365908del, NC_000010.10:g.99365907_99365908del, NC_000010.10:g.99365908del, NC_000010.10:g.99365908dup, NC_000010.10:g.99365907_99365908dup, NC_000010.10:g.99365906_99365908dup, NC_000010.10:g.99365905_99365908dup, NC_000010.10:g.99365904_99365908dup, NC_000010.10:g.99365903_99365908dup, NC_000010.10:g.99365902_99365908dup, NC_000010.10:g.99365901_99365908dup, NC_000010.10:g.99365900_99365908dup, NC_000010.10:g.99365899_99365908dup, NC_000010.10:g.99365898_99365908dup, NC_000010.10:g.99365897_99365908dup, NC_000010.10:g.99365896_99365908dup, NC_000010.10:g.99365895_99365908dup, NC_000010.10:g.99365894_99365908dup, NC_000010.10:g.99365891_99365908dup, NC_000010.10:g.99365890_99365908dup, NC_000010.10:g.99365889_99365908dup, NG_027922.1:g.26795_26807del, NG_027922.1:g.26798_26807del, NG_027922.1:g.26799_26807del, NG_027922.1:g.26800_26807del, NG_027922.1:g.26801_26807del, NG_027922.1:g.26802_26807del, NG_027922.1:g.26803_26807del, NG_027922.1:g.26804_26807del, NG_027922.1:g.26805_26807del, NG_027922.1:g.26806_26807del, NG_027922.1:g.26807del, NG_027922.1:g.26807dup, NG_027922.1:g.26806_26807dup, NG_027922.1:g.26805_26807dup, NG_027922.1:g.26804_26807dup, NG_027922.1:g.26803_26807dup, NG_027922.1:g.26802_26807dup, NG_027922.1:g.26801_26807dup, NG_027922.1:g.26800_26807dup, NG_027922.1:g.26799_26807dup, NG_027922.1:g.26798_26807dup, NG_027922.1:g.26797_26807dup, NG_027922.1:g.26796_26807dup, NG_027922.1:g.26795_26807dup, NG_027922.1:g.26794_26807dup, NG_027922.1:g.26793_26807dup, NG_027922.1:g.26790_26807dup, NG_027922.1:g.26789_26807dup, NG_027922.1:g.26788_26807dup

Select item 14914782825.

rs1491478282 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TG [Show Flanks]
Chromosome:: 10:97613408 (GRCh38)
10:99373166 (GRCh37)
Canonical SPDI:: NC_000010.11:97613408:TG:TGTG
Validated:: by frequency,by alfa
MAF:: TGTG=0./0 (ALFA)
TG=0.00003/8 (TOPMED)
HGVS:: NC_000010.11:g.97613409_97613410dup, NC_000010.10:g.99373166_99373167dup, NG_027922.1:g.34065_34066dup

Select item 14913616946.

rs1491361694 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 10:97613408 (GRCh38)
10:99373165 (GRCh37)
Canonical SPDI:: NC_000010.11:97613407:AT:
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.97613408_97613409del, NC_000010.10:g.99373165_99373166del, NG_027922.1:g.34064_34065del

Select item 14912960587.

rs1491296058 [Homo sapiens]

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

Select item 14912871928.

rs1491287192 [Homo sapiens]

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

Select item 14912521539.

rs1491252153 has merged into rs1169191059 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,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,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:97593041 (GRCh38)
10:99352798 (GRCh37)
Canonical SPDI:: NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97593029:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAA
Gene:: HOGA1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.97593041_97593051del, NC_000010.11:g.97593042_97593051del, NC_000010.11:g.97593043_97593051del, NC_000010.11:g.97593044_97593051del, NC_000010.11:g.97593045_97593051del, NC_000010.11:g.97593046_97593051del, NC_000010.11:g.97593047_97593051del, NC_000010.11:g.97593048_97593051del, NC_000010.11:g.97593049_97593051del, NC_000010.11:g.97593050_97593051del, NC_000010.11:g.97593051del, NC_000010.11:g.97593051dup, NC_000010.11:g.97593050_97593051dup, NC_000010.11:g.97593049_97593051dup, NC_000010.11:g.97593048_97593051dup, NC_000010.11:g.97593047_97593051dup, NC_000010.11:g.97593046_97593051dup, NC_000010.11:g.97593045_97593051dup, NC_000010.11:g.97593044_97593051dup, NC_000010.11:g.97593043_97593051dup, NC_000010.11:g.97593042_97593051dup, NC_000010.11:g.97593041_97593051dup, NC_000010.11:g.97593040_97593051dup, NC_000010.11:g.97593039_97593051dup, NC_000010.11:g.97593038_97593051dup, NC_000010.11:g.97593037_97593051dup, NC_000010.11:g.97593036_97593051dup, NC_000010.11:g.97593035_97593051dup, NC_000010.11:g.97593034_97593051dup, NC_000010.11:g.97593033_97593051dup, NC_000010.11:g.97593032_97593051dup, NC_000010.11:g.97593031_97593051dup, NC_000010.11:g.97593030_97593051dup, NC_000010.11:g.97593051_97593052insAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.97593051_97593052insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.97593051_97593052insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.97593051_97593052insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.97593051_97593052insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.97593051_97593052insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.97593051_97593052insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.97593051_97593052insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.97593051_97593052insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.97593051_97593052insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.97593051_97593052insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.97593051_97593052insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.97593051_97593052insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.97593051_97593052insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.97593030_97593051A[39]CAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000010.10:g.99352798_99352808del, NC_000010.10:g.99352799_99352808del, NC_000010.10:g.99352800_99352808del, NC_000010.10:g.99352801_99352808del, NC_000010.10:g.99352802_99352808del, NC_000010.10:g.99352803_99352808del, NC_000010.10:g.99352804_99352808del, NC_000010.10:g.99352805_99352808del, NC_000010.10:g.99352806_99352808del, NC_000010.10:g.99352807_99352808del, NC_000010.10:g.99352808del, NC_000010.10:g.99352808dup, NC_000010.10:g.99352807_99352808dup, NC_000010.10:g.99352806_99352808dup, NC_000010.10:g.99352805_99352808dup, NC_000010.10:g.99352804_99352808dup, NC_000010.10:g.99352803_99352808dup, NC_000010.10:g.99352802_99352808dup, NC_000010.10:g.99352801_99352808dup, NC_000010.10:g.99352800_99352808dup, NC_000010.10:g.99352799_99352808dup, NC_000010.10:g.99352798_99352808dup, NC_000010.10:g.99352797_99352808dup, NC_000010.10:g.99352796_99352808dup, NC_000010.10:g.99352795_99352808dup, NC_000010.10:g.99352794_99352808dup, NC_000010.10:g.99352793_99352808dup, NC_000010.10:g.99352792_99352808dup, NC_000010.10:g.99352791_99352808dup, NC_000010.10:g.99352790_99352808dup, NC_000010.10:g.99352789_99352808dup, NC_000010.10:g.99352788_99352808dup, NC_000010.10:g.99352787_99352808dup, NC_000010.10:g.99352808_99352809insAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.99352808_99352809insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.99352808_99352809insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.99352808_99352809insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.99352808_99352809insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.99352808_99352809insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.99352808_99352809insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.99352808_99352809insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.99352808_99352809insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.99352808_99352809insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.99352808_99352809insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.99352808_99352809insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.99352808_99352809insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.99352808_99352809insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.99352787_99352808A[39]CAAAAAAAAAAAAAAAAAAAAAAA[1], NG_027922.1:g.13697_13707del, NG_027922.1:g.13698_13707del, NG_027922.1:g.13699_13707del, NG_027922.1:g.13700_13707del, NG_027922.1:g.13701_13707del, NG_027922.1:g.13702_13707del, NG_027922.1:g.13703_13707del, NG_027922.1:g.13704_13707del, NG_027922.1:g.13705_13707del, NG_027922.1:g.13706_13707del, NG_027922.1:g.13707del, NG_027922.1:g.13707dup, NG_027922.1:g.13706_13707dup, NG_027922.1:g.13705_13707dup, NG_027922.1:g.13704_13707dup, NG_027922.1:g.13703_13707dup, NG_027922.1:g.13702_13707dup, NG_027922.1:g.13701_13707dup, NG_027922.1:g.13700_13707dup, NG_027922.1:g.13699_13707dup, NG_027922.1:g.13698_13707dup, NG_027922.1:g.13697_13707dup, NG_027922.1:g.13696_13707dup, NG_027922.1:g.13695_13707dup, NG_027922.1:g.13694_13707dup, NG_027922.1:g.13693_13707dup, NG_027922.1:g.13692_13707dup, NG_027922.1:g.13691_13707dup, NG_027922.1:g.13690_13707dup, NG_027922.1:g.13689_13707dup, NG_027922.1:g.13688_13707dup, NG_027922.1:g.13687_13707dup, NG_027922.1:g.13686_13707dup, NG_027922.1:g.13707_13708insAAAAAAAAAAAAAAAAAAAAAAA, NG_027922.1:g.13707_13708insAAAAAAAAAAAAAAAAAAAAAAAA, NG_027922.1:g.13707_13708insAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027922.1:g.13707_13708insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027922.1:g.13707_13708insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027922.1:g.13707_13708insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027922.1:g.13707_13708insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027922.1:g.13707_13708insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027922.1:g.13707_13708insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027922.1:g.13707_13708insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027922.1:g.13707_13708insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027922.1:g.13707_13708insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027922.1:g.13707_13708insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027922.1:g.13707_13708insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027922.1:g.13686_13707A[39]CAAAAAAAAAAAAAAAAAAAAAAA[1]

Select item 149124025510.

rs1491240255 has merged into rs869251889 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGT>-,GT,GTGTGT,GTGTGTGT [Show Flanks]
Chromosome:: 10:97588381 (GRCh38)
10:99348138 (GRCh37)
Canonical SPDI:: NC_000010.11:97588369:TGTGTGTGTGTGTGT:TGTGTGTGTGT,NC_000010.11:97588369:TGTGTGTGTGTGTGT:TGTGTGTGTGTGT,NC_000010.11:97588369:TGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT,NC_000010.11:97588369:TGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT
Gene:: HOGA1 (Varview), C10orf62 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGTGTGT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
TG=0.000142/2 (TOMMO)
HGVS:: NC_000010.11:g.97588371GT[5], NC_000010.11:g.97588371GT[6], NC_000010.11:g.97588371GT[8], NC_000010.11:g.97588371GT[9], NC_000010.10:g.99348128GT[5], NC_000010.10:g.99348128GT[6], NC_000010.10:g.99348128GT[8], NC_000010.10:g.99348128GT[9], NG_027922.1:g.9027GT[5], NG_027922.1:g.9027GT[6], NG_027922.1:g.9027GT[8], NG_027922.1:g.9027GT[9]

Select item 149121294211.

rs1491212942 has merged into rs1221596544 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:97588210 (GRCh38)
10:99347967 (GRCh37)
Canonical SPDI:: NC_000010.11:97588199:TTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000010.11:97588199:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:97588199:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:97588199:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:97588199:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:97588199:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:97588199:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:97588199:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:97588199:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:97588199:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:97588199:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:97588199:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: HOGA1 (Varview), C10orf62 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
-=0.1091/55 (NorthernSweden)
HGVS:: NC_000010.11:g.97588210_97588215del, NC_000010.11:g.97588213_97588215del, NC_000010.11:g.97588214_97588215del, NC_000010.11:g.97588215del, NC_000010.11:g.97588215dup, NC_000010.11:g.97588214_97588215dup, NC_000010.11:g.97588213_97588215dup, NC_000010.11:g.97588212_97588215dup, NC_000010.11:g.97588211_97588215dup, NC_000010.11:g.97588210_97588215dup, NC_000010.11:g.97588200_97588215T[22]GTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000010.11:g.97588200_97588215dup, NC_000010.10:g.99347967_99347972del, NC_000010.10:g.99347970_99347972del, NC_000010.10:g.99347971_99347972del, NC_000010.10:g.99347972del, NC_000010.10:g.99347972dup, NC_000010.10:g.99347971_99347972dup, NC_000010.10:g.99347970_99347972dup, NC_000010.10:g.99347969_99347972dup, NC_000010.10:g.99347968_99347972dup, NC_000010.10:g.99347967_99347972dup, NC_000010.10:g.99347957_99347972T[22]GTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000010.10:g.99347957_99347972dup, NG_027922.1:g.8866_8871del, NG_027922.1:g.8869_8871del, NG_027922.1:g.8870_8871del, NG_027922.1:g.8871del, NG_027922.1:g.8871dup, NG_027922.1:g.8870_8871dup, NG_027922.1:g.8869_8871dup, NG_027922.1:g.8868_8871dup, NG_027922.1:g.8867_8871dup, NG_027922.1:g.8866_8871dup, NG_027922.1:g.8856_8871T[22]GTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_027922.1:g.8856_8871dup

Select item 149116763612.

rs1491167636 has merged into rs574023517 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:97586150 (GRCh38)
10:99345907 (GRCh37)
Canonical SPDI:: NC_000010.11:97586136:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:97586136:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:97586136:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:97586136:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:97586136:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:97586136:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:97586136:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:97586136:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:97586136:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: HOGA1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAAAAAA=0./0 (ALFA)
-=0.3874/1493 (ALSPAC)
HGVS:: NC_000010.11:g.97586150_97586153del, NC_000010.11:g.97586151_97586153del, NC_000010.11:g.97586152_97586153del, NC_000010.11:g.97586153del, NC_000010.11:g.97586153dup, NC_000010.11:g.97586152_97586153dup, NC_000010.11:g.97586151_97586153dup, NC_000010.11:g.97586149_97586153dup, NC_000010.11:g.97586145_97586153dup, NC_000010.10:g.99345907_99345910del, NC_000010.10:g.99345908_99345910del, NC_000010.10:g.99345909_99345910del, NC_000010.10:g.99345910del, NC_000010.10:g.99345910dup, NC_000010.10:g.99345909_99345910dup, NC_000010.10:g.99345908_99345910dup, NC_000010.10:g.99345906_99345910dup, NC_000010.10:g.99345902_99345910dup, NG_027922.1:g.6806_6809del, NG_027922.1:g.6807_6809del, NG_027922.1:g.6808_6809del, NG_027922.1:g.6809del, NG_027922.1:g.6809dup, NG_027922.1:g.6808_6809dup, NG_027922.1:g.6807_6809dup, NG_027922.1:g.6805_6809dup, NG_027922.1:g.6801_6809dup

Select item 149098577913.

rs1490985779 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 10:97601797 (GRCh38)
10:99361554 (GRCh37)
Canonical SPDI:: NC_000010.11:97601796:G:A,NC_000010.11:97601796:G:C
Gene:: HOGA1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
C=0.000248/4 (TOMMO)
HGVS:: NC_000010.11:g.97601797G>A, NC_000010.11:g.97601797G>C, NC_000010.10:g.99361554G>A, NC_000010.10:g.99361554G>C, NG_027922.1:g.22453G>A, NG_027922.1:g.22453G>C

Select item 149096361214.

rs1490963612 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:97587944 (GRCh38)
10:99347701 (GRCh37)
Canonical SPDI:: NC_000010.11:97587943:G:A
Gene:: HOGA1 (Varview), C10orf62 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.97587944G>A, NC_000010.10:g.99347701G>A, NG_027922.1:g.8600G>A

Select item 149077077315.

rs1490770773 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:97610640 (GRCh38)
10:99370397 (GRCh37)
Canonical SPDI:: NC_000010.11:97610639:A:G
Gene:: HOGA1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.00003/8 (TOPMED)
G=0.000036/5 (GnomAD)
HGVS:: NC_000010.11:g.97610640A>G, NC_000010.10:g.99370397A>G, NG_027922.1:g.31296A>G

Select item 149042171516.

rs1490421715 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:97583702 (GRCh38)
10:99343459 (GRCh37)
Canonical SPDI:: NC_000010.11:97583701:C:T
Gene:: ANKRD2 (Varview), HOGA1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.97583702C>T, NC_000010.10:g.99343459C>T, NG_027922.1:g.4358C>T, NG_034079.1:g.16262C>T, NM_020349.4:c.1060C>T, NM_020349.3:c.1060C>T, NM_020349.2:c.1060C>T, NM_001129981.3:c.961C>T, NM_001129981.2:c.961C>T, NM_001129981.1:c.961C>T, NM_001291219.3:c.880C>T, NM_001291219.2:c.880C>T, NM_001291219.1:c.1219C>T, NM_001291218.2:c.1318C>T, NM_001291218.1:c.1318C>T, NM_001346793.2:c.979C>T, NM_001346793.1:c.979C>T, NM_001346797.1:c.880C>T, NP_065082.2:p.Pro354Ser, NP_001123453.1:p.Pro321Ser, NP_001278148.2:p.Pro294Ser, NP_001278147.1:p.Pro440Ser, NP_001333722.1:p.Pro327Ser

Select item 149031971417.

rs1490319714 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 10:97580166 (GRCh38)
10:99339923 (GRCh37)
Canonical SPDI:: NC_000010.11:97580165:A:T
Gene:: ANKRD2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.97580166A>T, NC_000010.10:g.99339923A>T, NG_027922.1:g.822A>T, NG_034079.1:g.12726A>T

Select item 149011562018.

rs1490115620 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 10:97610768 (GRCh38)
10:99370525 (GRCh37)
Canonical SPDI:: NC_000010.11:97610767:C:G,NC_000010.11:97610767:C:T
Gene:: HOGA1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000034/9 (TOPMED)
G=0.000035/1 (TOMMO)
HGVS:: NC_000010.11:g.97610768C>G, NC_000010.11:g.97610768C>T, NC_000010.10:g.99370525C>G, NC_000010.10:g.99370525C>T, NG_027922.1:g.31424C>G, NG_027922.1:g.31424C>T

Select item 148998937819.

rs1489989378 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 10:97611325 (GRCh38)
10:99371083 (GRCh37)
Canonical SPDI:: NC_000010.11:97611325:A:AA
Gene:: HOGA1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
A=0.000546/1 (Korea1K)
HGVS:: NC_000010.11:g.97611326dup, NC_000010.10:g.99371083dup, NG_027922.1:g.31982dup

Select item 148996801220.

rs1489968012 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:97613802 (GRCh38)
10:99373559 (GRCh37)
Canonical SPDI:: NC_000010.11:97613801:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.97613802G>A, NC_000010.10:g.99373559G>A, NG_027922.1:g.34458G>A

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