SNP Links for Gene (Select 102724768) - SNP

Links from Gene

Items: 1 to 20 of 11850

<< First< Prev

Page of 593

Next >Last >>

Select item 14915728131.

rs1491572813 has merged into rs148635546 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGGGG>-,G,GG,GGG,GGGG,GGGGGG,GGGGGGG [Show Flanks]
Chromosome:: 10:59032754 (GRCh38)
10:60792514 (GRCh37)
Canonical SPDI:: NC_000010.11:59032747:GGGGGGGGGGG:GGGGGG,NC_000010.11:59032747:GGGGGGGGGGG:GGGGGGG,NC_000010.11:59032747:GGGGGGGGGGG:GGGGGGGG,NC_000010.11:59032747:GGGGGGGGGGG:GGGGGGGGG,NC_000010.11:59032747:GGGGGGGGGGG:GGGGGGGGGG,NC_000010.11:59032747:GGGGGGGGGGG:GGGGGGGGGGGG,NC_000010.11:59032747:GGGGGGGGGGG:GGGGGGGGGGGGG
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGGG=0./0 (ALFA)
GGG=0.00759/38 (1000Genomes)
HGVS:: NC_000010.11:g.59032754_59032758del, NC_000010.11:g.59032755_59032758del, NC_000010.11:g.59032756_59032758del, NC_000010.11:g.59032757_59032758del, NC_000010.11:g.59032758del, NC_000010.11:g.59032758dup, NC_000010.11:g.59032757_59032758dup, NC_000010.10:g.60792514_60792518del, NC_000010.10:g.60792515_60792518del, NC_000010.10:g.60792516_60792518del, NC_000010.10:g.60792517_60792518del, NC_000010.10:g.60792518del, NC_000010.10:g.60792518dup, NC_000010.10:g.60792517_60792518dup

Select item 14915727292.

rs1491572729 [Homo sapiens]

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

Select item 14914102133.

rs1491410213 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 10:59048638 (GRCh38)
10:60808398 (GRCh37)
Canonical SPDI:: NC_000010.11:59048637:AT:
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000010.11:g.59048638_59048639del, NC_000010.10:g.60808398_60808399del

Select item 14913889074.

rs1491388907 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>- [Show Flanks]
Chromosome:: 10:59058696 (GRCh38)
10:60818456 (GRCh37)
Canonical SPDI:: NC_000010.11:59058694:TTT:T
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000084/1 (ALFA)
-=0.000071/1 (TOMMO)
-=0.000137/18 (GnomAD)
HGVS:: NC_000010.11:g.59058696_59058697del, NC_000010.10:g.60818456_60818457del

Select item 14913320965.

rs1491332096 has merged into rs112984989 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:59048650 (GRCh38)
10:60808410 (GRCh37)
Canonical SPDI:: NC_000010.11:59048638:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:59048638:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:59048638:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:59048638:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:59048638:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:59048638:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:59048638:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:59048638:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000010.11:g.59048650_59048654del, NC_000010.11:g.59048653_59048654del, NC_000010.11:g.59048654del, NC_000010.11:g.59048654dup, NC_000010.11:g.59048653_59048654dup, NC_000010.11:g.59048652_59048654dup, NC_000010.11:g.59048651_59048654dup, NC_000010.11:g.59048639_59048654dup, NC_000010.10:g.60808410_60808414del, NC_000010.10:g.60808413_60808414del, NC_000010.10:g.60808414del, NC_000010.10:g.60808414dup, NC_000010.10:g.60808413_60808414dup, NC_000010.10:g.60808412_60808414dup, NC_000010.10:g.60808411_60808414dup, NC_000010.10:g.60808399_60808414dup

Select item 14912912286.

rs1491291228 has merged into rs969870842 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAA>-,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:59066098 (GRCh38)
10:60825858 (GRCh37)
Canonical SPDI:: NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:59066088:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LOC102724768 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.59066098_59066113del, NC_000010.11:g.59066101_59066113del, NC_000010.11:g.59066102_59066113del, NC_000010.11:g.59066103_59066113del, NC_000010.11:g.59066104_59066113del, NC_000010.11:g.59066105_59066113del, NC_000010.11:g.59066107_59066113del, NC_000010.11:g.59066108_59066113del, NC_000010.11:g.59066109_59066113del, NC_000010.11:g.59066110_59066113del, NC_000010.11:g.59066111_59066113del, NC_000010.11:g.59066112_59066113del, NC_000010.11:g.59066113del, NC_000010.11:g.59066113dup, NC_000010.11:g.59066112_59066113dup, NC_000010.11:g.59066111_59066113dup, NC_000010.11:g.59066110_59066113dup, NC_000010.11:g.59066109_59066113dup, NC_000010.11:g.59066108_59066113dup, NC_000010.11:g.59066107_59066113dup, NC_000010.11:g.59066106_59066113dup, NC_000010.11:g.59066096_59066113dup, NC_000010.10:g.60825858_60825873del, NC_000010.10:g.60825861_60825873del, NC_000010.10:g.60825862_60825873del, NC_000010.10:g.60825863_60825873del, NC_000010.10:g.60825864_60825873del, NC_000010.10:g.60825865_60825873del, NC_000010.10:g.60825867_60825873del, NC_000010.10:g.60825868_60825873del, NC_000010.10:g.60825869_60825873del, NC_000010.10:g.60825870_60825873del, NC_000010.10:g.60825871_60825873del, NC_000010.10:g.60825872_60825873del, NC_000010.10:g.60825873del, NC_000010.10:g.60825873dup, NC_000010.10:g.60825872_60825873dup, NC_000010.10:g.60825871_60825873dup, NC_000010.10:g.60825870_60825873dup, NC_000010.10:g.60825869_60825873dup, NC_000010.10:g.60825868_60825873dup, NC_000010.10:g.60825867_60825873dup, NC_000010.10:g.60825866_60825873dup, NC_000010.10:g.60825856_60825873dup, XR_428752.5:n.986_1001del, XR_428752.5:n.989_1001del, XR_428752.5:n.990_1001del, XR_428752.5:n.991_1001del, XR_428752.5:n.992_1001del, XR_428752.5:n.993_1001del, XR_428752.5:n.995_1001del, XR_428752.5:n.996_1001del, XR_428752.5:n.997_1001del, XR_428752.5:n.998_1001del, XR_428752.5:n.999_1001del, XR_428752.5:n.1000_1001del, XR_428752.5:n.1001del, XR_428752.5:n.1001dup, XR_428752.5:n.1000_1001dup, XR_428752.5:n.999_1001dup, XR_428752.5:n.998_1001dup, XR_428752.5:n.997_1001dup, XR_428752.5:n.996_1001dup, XR_428752.5:n.995_1001dup, XR_428752.5:n.994_1001dup, XR_428752.5:n.984_1001dup

Select item 14912300967.

rs1491230096 has merged into rs71467055 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTCTCTCTCTCTCTCTCTCTCTCTCTCT>-,CT,CTCT,CTCTCT,CTCTCTCT,CTCTCTCTCT,CTCTCTCTCTCT,CTCTCTCTCTCTCT,CTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT [Show Flanks]
Chromosome:: 10:59058668 (GRCh38)
10:60818428 (GRCh37)
Canonical SPDI:: NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000010.11:59058648:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTCTCTCTCTCTCTCTCTCT=0./0 (ALFA)
HGVS:: NC_000010.11:g.59058650CT[9], NC_000010.11:g.59058650CT[10], NC_000010.11:g.59058650CT[11], NC_000010.11:g.59058650CT[12], NC_000010.11:g.59058650CT[13], NC_000010.11:g.59058650CT[14], NC_000010.11:g.59058650CT[15], NC_000010.11:g.59058650CT[16], NC_000010.11:g.59058650CT[17], NC_000010.11:g.59058650CT[18], NC_000010.11:g.59058650CT[19], NC_000010.11:g.59058650CT[20], NC_000010.11:g.59058650CT[21], NC_000010.11:g.59058650CT[22], NC_000010.11:g.59058650CT[24], NC_000010.11:g.59058650CT[25], NC_000010.11:g.59058650CT[26], NC_000010.11:g.59058650CT[27], NC_000010.11:g.59058650CT[28], NC_000010.11:g.59058650CT[29], NC_000010.11:g.59058650CT[30], NC_000010.11:g.59058650CT[31], NC_000010.11:g.59058650CT[32], NC_000010.11:g.59058650CT[33], NC_000010.11:g.59058650CT[34], NC_000010.11:g.59058650CT[35], NC_000010.11:g.59058650CT[36], NC_000010.11:g.59058650CT[37], NC_000010.10:g.60818410CT[9], NC_000010.10:g.60818410CT[10], NC_000010.10:g.60818410CT[11], NC_000010.10:g.60818410CT[12], NC_000010.10:g.60818410CT[13], NC_000010.10:g.60818410CT[14], NC_000010.10:g.60818410CT[15], NC_000010.10:g.60818410CT[16], NC_000010.10:g.60818410CT[17], NC_000010.10:g.60818410CT[18], NC_000010.10:g.60818410CT[19], NC_000010.10:g.60818410CT[20], NC_000010.10:g.60818410CT[21], NC_000010.10:g.60818410CT[22], NC_000010.10:g.60818410CT[24], NC_000010.10:g.60818410CT[25], NC_000010.10:g.60818410CT[26], NC_000010.10:g.60818410CT[27], NC_000010.10:g.60818410CT[28], NC_000010.10:g.60818410CT[29], NC_000010.10:g.60818410CT[30], NC_000010.10:g.60818410CT[31], NC_000010.10:g.60818410CT[32], NC_000010.10:g.60818410CT[33], NC_000010.10:g.60818410CT[34], NC_000010.10:g.60818410CT[35], NC_000010.10:g.60818410CT[36], NC_000010.10:g.60818410CT[37]

Select item 14912210838.

rs1491221083 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 10:59066089 (GRCh38)
10:60825850 (GRCh37)
Canonical SPDI:: NC_000010.11:59066089::G
Gene:: LOC102724768 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.00008/1 (ALFA)
HGVS:: NC_000010.11:g.59066089_59066090insG, NC_000010.10:g.60825849_60825850insG, XR_428752.5:n.977_978insG

Select item 14911071379.

rs1491107137 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ACTC [Show Flanks]
Chromosome:: 10:59058649 (GRCh38)
10:60818410 (GRCh37)
Canonical SPDI:: NC_000010.11:59058649:CTC:CTCACTC
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CTCACTC=0./0 (ALFA)
HGVS:: NC_000010.11:g.59058652_59058653insACTC, NC_000010.10:g.60818412_60818413insACTC

Select item 149103224310.

rs1491032243 has merged into rs59432228 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:59026818 (GRCh38)
10:60786578 (GRCh37)
Canonical SPDI:: NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:59026805:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000010.11:g.59026818_59026833del, NC_000010.11:g.59026819_59026833del, NC_000010.11:g.59026820_59026833del, NC_000010.11:g.59026821_59026833del, NC_000010.11:g.59026822_59026833del, NC_000010.11:g.59026823_59026833del, NC_000010.11:g.59026824_59026833del, NC_000010.11:g.59026825_59026833del, NC_000010.11:g.59026826_59026833del, NC_000010.11:g.59026827_59026833del, NC_000010.11:g.59026828_59026833del, NC_000010.11:g.59026829_59026833del, NC_000010.11:g.59026830_59026833del, NC_000010.11:g.59026831_59026833del, NC_000010.11:g.59026832_59026833del, NC_000010.11:g.59026833del, NC_000010.11:g.59026833dup, NC_000010.11:g.59026832_59026833dup, NC_000010.11:g.59026831_59026833dup, NC_000010.11:g.59026830_59026833dup, NC_000010.11:g.59026829_59026833dup, NC_000010.11:g.59026828_59026833dup, NC_000010.11:g.59026827_59026833dup, NC_000010.10:g.60786578_60786593del, NC_000010.10:g.60786579_60786593del, NC_000010.10:g.60786580_60786593del, NC_000010.10:g.60786581_60786593del, NC_000010.10:g.60786582_60786593del, NC_000010.10:g.60786583_60786593del, NC_000010.10:g.60786584_60786593del, NC_000010.10:g.60786585_60786593del, NC_000010.10:g.60786586_60786593del, NC_000010.10:g.60786587_60786593del, NC_000010.10:g.60786588_60786593del, NC_000010.10:g.60786589_60786593del, NC_000010.10:g.60786590_60786593del, NC_000010.10:g.60786591_60786593del, NC_000010.10:g.60786592_60786593del, NC_000010.10:g.60786593del, NC_000010.10:g.60786593dup, NC_000010.10:g.60786592_60786593dup, NC_000010.10:g.60786591_60786593dup, NC_000010.10:g.60786590_60786593dup, NC_000010.10:g.60786589_60786593dup, NC_000010.10:g.60786588_60786593dup, NC_000010.10:g.60786587_60786593dup

Select item 149098161311.

rs1490981613 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 10:59063371 (GRCh38)
10:60823131 (GRCh37)
Canonical SPDI:: NC_000010.11:59063370:T:A
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000010.11:g.59063371T>A, NC_000010.10:g.60823131T>A

Select item 149094128512.

rs1490941285 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 10:59012868 (GRCh38)
10:60772628 (GRCh37)
Canonical SPDI:: NC_000010.11:59012864:AGAGA:AGA
Gene:: LOC102724768 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: AGA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.59012866GA[1], NC_000010.10:g.60772626GA[1]

Select item 149090353113.

rs1490903531 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:59037772 (GRCh38)
10:60797532 (GRCh37)
Canonical SPDI:: NC_000010.11:59037771:A:G
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.59037772A>G, NC_000010.10:g.60797532A>G

Select item 149083145414.

rs1490831454 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 10:59021918 (GRCh38)
10:60781678 (GRCh37)
Canonical SPDI:: NC_000010.11:59021917:T:A
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000026/7 (TOPMED)
HGVS:: NC_000010.11:g.59021918T>A, NC_000010.10:g.60781678T>A

Select item 149072064715.

rs1490720647 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:59048512 (GRCh38)
10:60808272 (GRCh37)
Canonical SPDI:: NC_000010.11:59048511:G:A
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.59048512G>A, NC_000010.10:g.60808272G>A

Select item 149065613616.

rs1490656136 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:59021316 (GRCh38)
10:60781076 (GRCh37)
Canonical SPDI:: NC_000010.11:59021315:C:T
Gene:: LOC102724768 (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.59021316C>T, NC_000010.10:g.60781076C>T

Select item 149062820817.

rs1490628208 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:59037335 (GRCh38)
10:60797095 (GRCh37)
Canonical SPDI:: NC_000010.11:59037334:T:C
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000010.11:g.59037335T>C, NC_000010.10:g.60797095T>C

Select item 149057645518.

rs1490576455 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:59029031 (GRCh38)
10:60788791 (GRCh37)
Canonical SPDI:: NC_000010.11:59029030:T:C
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: C=0.000029/4 (GnomAD)
HGVS:: NC_000010.11:g.59029031T>C, NC_000010.10:g.60788791T>C

Select item 149049236419.

rs1490492364 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 10:59064653 (GRCh38)
10:60824413 (GRCh37)
Canonical SPDI:: NC_000010.11:59064652:GGG:GG
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.59064655del, NC_000010.10:g.60824415del

Select item 149048039520.

rs1490480395 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:59044007 (GRCh38)
10:60803767 (GRCh37)
Canonical SPDI:: NC_000010.11:59044006:A:G
Gene:: LOC102724768 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.59044007A>G, NC_000010.10:g.60803767A>G

<< First< Prev

Page of 593

Next >Last >>

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 11850

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity