SNP Links for Gene (Select 221241) - SNP

Links from Gene

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Select item 14914856471.

rs1491485647 has merged into rs11338483 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT [Show Flanks]
Chromosome:: 18:64148417 (GRCh38)
18:61815651 (GRCh37)
Canonical SPDI:: NC_000018.10:64148407:TTTTTTTTTTTTT:TTTTTTTTT,NC_000018.10:64148407:TTTTTTTTTTTTT:TTTTTTTTTT,NC_000018.10:64148407:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000018.10:64148407:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000018.10:64148407:TTTTTTTTTTTTT:TTTTTTTTTTTTTT
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
TTT=0.289/87 (1000Genomes)
HGVS:: NC_000018.10:g.64148417_64148420del, NC_000018.10:g.64148418_64148420del, NC_000018.10:g.64148419_64148420del, NC_000018.10:g.64148420del, NC_000018.10:g.64148420dup, NC_000018.9:g.61815651_61815654del, NC_000018.9:g.61815652_61815654del, NC_000018.9:g.61815653_61815654del, NC_000018.9:g.61815654del, NC_000018.9:g.61815654dup

Select item 14914648892.

rs1491464889 [Homo sapiens]

Variant type:: INS
Alleles:: ->AG,G [Show Flanks]
Chromosome:: 18:64141077 (GRCh38)
18:61808312 (GRCh37)
Canonical SPDI:: NC_000018.10:64141077::AG,NC_000018.10:64141077::G
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000018.10:g.64141077_64141078insAG, NC_000018.10:g.64141077_64141078insG, NC_000018.9:g.61808311_61808312insAG, NC_000018.9:g.61808311_61808312insG

Select item 14913311013.

rs1491331101 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 18:64148407 (GRCh38)
18:61815641 (GRCh37)
Canonical SPDI:: NC_000018.10:64148406:AT:
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000018.10:g.64148407_64148408del, NC_000018.9:g.61815641_61815642del

Select item 14913289264.

rs1491328926 has merged into rs34096602 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACACACA>-,CA,CACA,CACACA,CACACACACA,CACACACACACA,CACACACACACACA,CACACACACACACACA,CACACACACACACACACA,CACACACACACACACACACA [Show Flanks]
Chromosome:: 18:64137863 (GRCh38)
18:61805097 (GRCh37)
Canonical SPDI:: NC_000018.10:64137847:ACACACACACACACACACACACA:ACACACACACACACA,NC_000018.10:64137847:ACACACACACACACACACACACA:ACACACACACACACACA,NC_000018.10:64137847:ACACACACACACACACACACACA:ACACACACACACACACACA,NC_000018.10:64137847:ACACACACACACACACACACACA:ACACACACACACACACACACA,NC_000018.10:64137847:ACACACACACACACACACACACA:ACACACACACACACACACACACACA,NC_000018.10:64137847:ACACACACACACACACACACACA:ACACACACACACACACACACACACACA,NC_000018.10:64137847:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACA,NC_000018.10:64137847:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA,NC_000018.10:64137847:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA,NC_000018.10:64137847:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACACACACACACA=0./0 (ALFA)
-=0.000045/12 (TOPMED)
HGVS:: NC_000018.10:g.64137849CA[7], NC_000018.10:g.64137849CA[8], NC_000018.10:g.64137849CA[9], NC_000018.10:g.64137849CA[10], NC_000018.10:g.64137849CA[12], NC_000018.10:g.64137849CA[13], NC_000018.10:g.64137849CA[14], NC_000018.10:g.64137849CA[15], NC_000018.10:g.64137849CA[16], NC_000018.10:g.64137849CA[17], NC_000018.9:g.61805083CA[7], NC_000018.9:g.61805083CA[8], NC_000018.9:g.61805083CA[9], NC_000018.9:g.61805083CA[10], NC_000018.9:g.61805083CA[12], NC_000018.9:g.61805083CA[13], NC_000018.9:g.61805083CA[14], NC_000018.9:g.61805083CA[15], NC_000018.9:g.61805083CA[16], NC_000018.9:g.61805083CA[17]

Select item 14912697365.

rs1491269736 [Homo sapiens]

Variant type:: INS
Alleles:: ->T [Show Flanks]
Chromosome:: 18:64141053 (GRCh38)
18:61808288 (GRCh37)
Canonical SPDI:: NC_000018.10:64141053::T
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
HGVS:: NC_000018.10:g.64141053_64141054insT, NC_000018.9:g.61808287_61808288insT

Select item 14912154346.

rs1491215434 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATTAT,TAT [Show Flanks]
Chromosome:: 18:64143572 (GRCh38)
18:61810807 (GRCh37)
Canonical SPDI:: NC_000018.10:64143572:TAT:TATATTAT,NC_000018.10:64143572:TAT:TATTAT
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATTAT=0./0 (ALFA)
TAT=0.06356/818 (TOMMO)
TAT=0.09974/152 (Korea1K)
HGVS:: NC_000018.10:g.64143573_64143575TA[2]TTAT[1], NC_000018.10:g.64143573_64143575dup, NC_000018.9:g.61810807_61810809TA[2]TTAT[1], NC_000018.9:g.61810807_61810809dup

Select item 14911686797.

rs1491168679 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 18:64141051 (GRCh38)
18:61808286 (GRCh37)
Canonical SPDI:: NC_000018.10:64141051:T:TT
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
T=0.00007/3 (GnomAD)
T=0.00205/34 (TOMMO)
HGVS:: NC_000018.10:g.64141052dup, NC_000018.9:g.61808286dup

Select item 14911569278.

rs1491156927 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: 18:64141052 (GRCh38)
18:61808286 (GRCh37)
Canonical SPDI:: NC_000018.10:64141050:ATA:A
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000018.10:g.64141052_64141053del, NC_000018.9:g.61808286_61808287del

Select item 14911556389.

rs1491155638 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>- [Show Flanks]
Chromosome:: 18:64143574 (GRCh38)
18:61810808 (GRCh37)
Canonical SPDI:: NC_000018.10:64143571:ATAT:AT
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: ATAT=0.00084/10 (ALFA)
HGVS:: NC_000018.10:g.64143572AT[1], NC_000018.9:g.61810806AT[1]

Select item 149114169110.

rs1491141691 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 18:64141077 (GRCh38)
18:61808311 (GRCh37)
Canonical SPDI:: NC_000018.10:64141076:AT:
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000018.10:g.64141077_64141078del, NC_000018.9:g.61808311_61808312del

Select item 149112925411.

rs1491129254 has merged into rs34175314 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,A,AAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 18:64141061 (GRCh38)
18:61808295 (GRCh37)
Canonical SPDI:: NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:64141052:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000018.10:g.64141061_64141077del, NC_000018.10:g.64141062_64141077del, NC_000018.10:g.64141064_64141077del, NC_000018.10:g.64141068_64141077del, NC_000018.10:g.64141070_64141077del, NC_000018.10:g.64141071_64141077del, NC_000018.10:g.64141072_64141077del, NC_000018.10:g.64141073_64141077del, NC_000018.10:g.64141074_64141077del, NC_000018.10:g.64141075_64141077del, NC_000018.10:g.64141076_64141077del, NC_000018.10:g.64141077del, NC_000018.10:g.64141077dup, NC_000018.10:g.64141076_64141077dup, NC_000018.10:g.64141075_64141077dup, NC_000018.10:g.64141074_64141077dup, NC_000018.10:g.64141073_64141077dup, NC_000018.10:g.64141072_64141077dup, NC_000018.10:g.64141071_64141077dup, NC_000018.10:g.64141070_64141077dup, NC_000018.10:g.64141069_64141077dup, NC_000018.10:g.64141063_64141077dup, NC_000018.10:g.64141055_64141077dup, NC_000018.9:g.61808295_61808311del, NC_000018.9:g.61808296_61808311del, NC_000018.9:g.61808298_61808311del, NC_000018.9:g.61808302_61808311del, NC_000018.9:g.61808304_61808311del, NC_000018.9:g.61808305_61808311del, NC_000018.9:g.61808306_61808311del, NC_000018.9:g.61808307_61808311del, NC_000018.9:g.61808308_61808311del, NC_000018.9:g.61808309_61808311del, NC_000018.9:g.61808310_61808311del, NC_000018.9:g.61808311del, NC_000018.9:g.61808311dup, NC_000018.9:g.61808310_61808311dup, NC_000018.9:g.61808309_61808311dup, NC_000018.9:g.61808308_61808311dup, NC_000018.9:g.61808307_61808311dup, NC_000018.9:g.61808306_61808311dup, NC_000018.9:g.61808305_61808311dup, NC_000018.9:g.61808304_61808311dup, NC_000018.9:g.61808303_61808311dup, NC_000018.9:g.61808297_61808311dup, NC_000018.9:g.61808289_61808311dup

Select item 149100295912.

rs1491002959 has merged into rs58215196 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGTGTGTGTGTGTGTGTGTGTGTGT>-,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
Chromosome:: 18:64118842 (GRCh38)
18:61786076 (GRCh37)
Canonical SPDI:: NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000018.10:64118824:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGTGTGTGTGTGTGT=0./0 (ALFA)
HGVS:: NC_000018.10:g.64118826GT[8], NC_000018.10:g.64118826GT[10], NC_000018.10:g.64118826GT[11], NC_000018.10:g.64118826GT[12], NC_000018.10:g.64118826GT[13], NC_000018.10:g.64118826GT[14], NC_000018.10:g.64118826GT[15], NC_000018.10:g.64118826GT[16], NC_000018.10:g.64118826GT[17], NC_000018.10:g.64118826GT[18], NC_000018.10:g.64118826GT[19], NC_000018.10:g.64118826GT[20], NC_000018.10:g.64118826GT[22], NC_000018.10:g.64118826GT[23], NC_000018.10:g.64118826GT[24], NC_000018.10:g.64118826GT[25], NC_000018.9:g.61786060GT[8], NC_000018.9:g.61786060GT[10], NC_000018.9:g.61786060GT[11], NC_000018.9:g.61786060GT[12], NC_000018.9:g.61786060GT[13], NC_000018.9:g.61786060GT[14], NC_000018.9:g.61786060GT[15], NC_000018.9:g.61786060GT[16], NC_000018.9:g.61786060GT[17], NC_000018.9:g.61786060GT[18], NC_000018.9:g.61786060GT[19], NC_000018.9:g.61786060GT[20], NC_000018.9:g.61786060GT[22], NC_000018.9:g.61786060GT[23], NC_000018.9:g.61786060GT[24], NC_000018.9:g.61786060GT[25]

Select item 149088476713.

rs1490884767 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:64091243 (GRCh38)
18:61758477 (GRCh37)
Canonical SPDI:: NC_000018.10:64091242:T:C
Gene:: LINC00305 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000021/3 (GnomAD)
HGVS:: NC_000018.10:g.64091243T>C, NC_000018.9:g.61758477T>C

Select item 149085676314.

rs1490856763 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:64085906 (GRCh38)
18:61753140 (GRCh37)
Canonical SPDI:: NC_000018.10:64085905:G:A
Gene:: LINC00305 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.64085906G>A, NC_000018.9:g.61753140G>A

Select item 149085329515.

rs1490853295 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 18:64143463 (GRCh38)
18:61810697 (GRCh37)
Canonical SPDI:: NC_000018.10:64143462:G:C
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.64143463G>C, NC_000018.9:g.61810697G>C

Select item 149084666216.

rs1490846662 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:64129545 (GRCh38)
18:61796779 (GRCh37)
Canonical SPDI:: NC_000018.10:64129544:C:T
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000015/4 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000018.10:g.64129545C>T, NC_000018.9:g.61796779C>T

Select item 149079939917.

rs1490799399 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 18:64126936 (GRCh38)
18:61794170 (GRCh37)
Canonical SPDI:: NC_000018.10:64126935:TTTT:TTT
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.64126939del, NC_000018.9:g.61794173del

Select item 149074559618.

rs1490745596 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAGAGGCCT>- [Show Flanks]
Chromosome:: 18:64110170 (GRCh38)
18:61777404 (GRCh37)
Canonical SPDI:: NC_000018.10:64110166:CCTGAGAGGCCT:CCT
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CCT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.64110170_64110178del, NC_000018.9:g.61777404_61777412del

Select item 149071997319.

rs1490719973 [Homo sapiens]

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

Select item 149065113920.

rs1490651139 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 18:64107296 (GRCh38)
18:61774530 (GRCh37)
Canonical SPDI:: NC_000018.10:64107295:T:C,NC_000018.10:64107295:T:G
Gene:: LINC00305 (Varview), LINC01924 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000018.10:g.64107296T>C, NC_000018.10:g.64107296T>G, NC_000018.9:g.61774530T>C, NC_000018.9:g.61774530T>G

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