SNP Links for Gene (Select 102) - SNP

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Select item 14915528131.

rs1491552813 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 15:58621156 (GRCh38)
15:58913356 (GRCh37)
Canonical SPDI:: NC_000015.10:58621156:GGGGG:GGGGGG
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGG=0.000071/1 (ALFA)
G=0./0 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000015.10:g.58621161dup, NC_000015.9:g.58913360dup, NG_033876.2:g.133551dup

Select item 14915500292.

rs1491550029 [Homo sapiens]

Variant type:: INS
Alleles:: ->T,TT [Show Flanks]
Chromosome:: 15:58727206 (GRCh38)
15:59019406 (GRCh37)
Canonical SPDI:: NC_000015.10:58727206::T,NC_000015.10:58727206::TT
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
HGVS:: NC_000015.10:g.58727206_58727207insT, NC_000015.10:g.58727206_58727207insTT, NC_000015.9:g.59019405_59019406insT, NC_000015.9:g.59019405_59019406insTT, NG_033876.2:g.27501_27502insA, NG_033876.2:g.27501_27502insAA

Select item 14915342963.

rs1491534296 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATTT,ATTTTATTT [Show Flanks]
Chromosome:: 15:58720405 (GRCh38)
15:59012605 (GRCh37)
Canonical SPDI:: NC_000015.10:58720405:TTT:TTTATTT,NC_000015.10:58720405:TTT:TTTATTTTATTT
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTTATTTTATTT=0./0 (ALFA)
TTTATTTTA=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.58720408_58720409insATTT, NC_000015.10:g.58720406_58720408TTTAT[2]TT[1], NC_000015.9:g.59012607_59012608insATTT, NC_000015.9:g.59012605_59012607TTTAT[2]TT[1], NG_033876.2:g.34302_34303insTAAA, NG_033876.2:g.34300_34302AAATA[2]AA[1]

Select item 14915071754.

rs1491507175 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 15:58698575 (GRCh38)
15:58990774 (GRCh37)
Canonical SPDI:: NC_000015.10:58698574:CA:
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: -=0.0051/19 (TWINSUK)
-=0.0101/39 (ALSPAC)
HGVS:: NC_000015.10:g.58698575_58698576del, NC_000015.9:g.58990774_58990775del, NG_033876.2:g.56132_56133del

Select item 14915060545.

rs1491506054 has merged into rs879811536 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTT>-,TTTT,TTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 15:58720409 (GRCh38)
15:59012608 (GRCh37)
Canonical SPDI:: NC_000015.10:58720404:TTTTTTTTTTTTTT:TTTT,NC_000015.10:58720404:TTTTTTTTTTTTTT:TTTTTTTT,NC_000015.10:58720404:TTTTTTTTTTTTTT:TTTTTTTTT,NC_000015.10:58720404:TTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000015.10:58720404:TTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000015.10:58720404:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:58720404:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000015.10:58720404:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000015.10:58720404:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTT=0./0 (ALFA)
-=0.000023/6 (TOPMED)
-=0.004376/8 (Korea1K)
HGVS:: NC_000015.10:g.58720409_58720418del, NC_000015.10:g.58720413_58720418del, NC_000015.10:g.58720414_58720418del, NC_000015.10:g.58720417_58720418del, NC_000015.10:g.58720418del, NC_000015.10:g.58720418dup, NC_000015.10:g.58720417_58720418dup, NC_000015.10:g.58720415_58720418dup, NC_000015.10:g.58720414_58720418dup, NC_000015.9:g.59012608_59012617del, NC_000015.9:g.59012612_59012617del, NC_000015.9:g.59012613_59012617del, NC_000015.9:g.59012616_59012617del, NC_000015.9:g.59012617del, NC_000015.9:g.59012617dup, NC_000015.9:g.59012616_59012617dup, NC_000015.9:g.59012614_59012617dup, NC_000015.9:g.59012613_59012617dup, NG_033876.2:g.34294_34303del, NG_033876.2:g.34298_34303del, NG_033876.2:g.34299_34303del, NG_033876.2:g.34302_34303del, NG_033876.2:g.34303del, NG_033876.2:g.34303dup, NG_033876.2:g.34302_34303dup, NG_033876.2:g.34300_34303dup, NG_033876.2:g.34299_34303dup

Select item 14914491206.

rs1491449120 has merged into rs60048171 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAACCCCTTTTCAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 15:58638621 (GRCh38)
15:58930820 (GRCh37)
Canonical SPDI:: NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58638614:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAACCCCTTTTCAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAA=0./0 (ALFA)
-=0.000008/2 (TOPMED)
AA=0.456869/2288 (1000Genomes)
AAAAAAAAAAAAAAAAAAAAAAAAAAAACCCCTTTTCAA=0.475/19 (GENOME_DK)
HGVS:: NC_000015.10:g.58638621_58638635del, NC_000015.10:g.58638623_58638635del, NC_000015.10:g.58638624_58638635del, NC_000015.10:g.58638625_58638635del, NC_000015.10:g.58638626_58638635del, NC_000015.10:g.58638627_58638635del, NC_000015.10:g.58638629_58638635del, NC_000015.10:g.58638632_58638635del, NC_000015.10:g.58638633_58638635del, NC_000015.10:g.58638634_58638635del, NC_000015.10:g.58638635del, NC_000015.10:g.58638635dup, NC_000015.10:g.58638634_58638635dup, NC_000015.10:g.58638633_58638635dup, NC_000015.10:g.58638632_58638635dup, NC_000015.10:g.58638631_58638635dup, NC_000015.10:g.58638630_58638635dup, NC_000015.10:g.58638628_58638635dup, NC_000015.10:g.58638627_58638635dup, NC_000015.10:g.58638626_58638635dup, NC_000015.10:g.58638625_58638635dup, NC_000015.10:g.58638624_58638635dup, NC_000015.10:g.58638623_58638635dup, NC_000015.10:g.58638618_58638635dup, NC_000015.10:g.58638617_58638635dup, NC_000015.10:g.58638635_58638636insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000015.10:g.58638615_58638635A[28]C[4]T[4]CAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000015.9:g.58930820_58930834del, NC_000015.9:g.58930822_58930834del, NC_000015.9:g.58930823_58930834del, NC_000015.9:g.58930824_58930834del, NC_000015.9:g.58930825_58930834del, NC_000015.9:g.58930826_58930834del, NC_000015.9:g.58930828_58930834del, NC_000015.9:g.58930831_58930834del, NC_000015.9:g.58930832_58930834del, NC_000015.9:g.58930833_58930834del, NC_000015.9:g.58930834del, NC_000015.9:g.58930834dup, NC_000015.9:g.58930833_58930834dup, NC_000015.9:g.58930832_58930834dup, NC_000015.9:g.58930831_58930834dup, NC_000015.9:g.58930830_58930834dup, NC_000015.9:g.58930829_58930834dup, NC_000015.9:g.58930827_58930834dup, NC_000015.9:g.58930826_58930834dup, NC_000015.9:g.58930825_58930834dup, NC_000015.9:g.58930824_58930834dup, NC_000015.9:g.58930823_58930834dup, NC_000015.9:g.58930822_58930834dup, NC_000015.9:g.58930817_58930834dup, NC_000015.9:g.58930816_58930834dup, NC_000015.9:g.58930834_58930835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000015.9:g.58930814_58930834A[28]C[4]T[4]CAAAAAAAAAAAAAAAAAAAAAAA[1], NG_033876.2:g.116079_116093del, NG_033876.2:g.116081_116093del, NG_033876.2:g.116082_116093del, NG_033876.2:g.116083_116093del, NG_033876.2:g.116084_116093del, NG_033876.2:g.116085_116093del, NG_033876.2:g.116087_116093del, NG_033876.2:g.116090_116093del, NG_033876.2:g.116091_116093del, NG_033876.2:g.116092_116093del, NG_033876.2:g.116093del, NG_033876.2:g.116093dup, NG_033876.2:g.116092_116093dup, NG_033876.2:g.116091_116093dup, NG_033876.2:g.116090_116093dup, NG_033876.2:g.116089_116093dup, NG_033876.2:g.116088_116093dup, NG_033876.2:g.116086_116093dup, NG_033876.2:g.116085_116093dup, NG_033876.2:g.116084_116093dup, NG_033876.2:g.116083_116093dup, NG_033876.2:g.116082_116093dup, NG_033876.2:g.116081_116093dup, NG_033876.2:g.116076_116093dup, NG_033876.2:g.116075_116093dup, NG_033876.2:g.116093_116094insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_033876.2:g.116073_116093T[23]GAAAAGGGGTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 14913937367.

rs1491393736 has merged into rs67378373 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 15:58647261 (GRCh38)
15:58939460 (GRCh37)
Canonical SPDI:: NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:58647248:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000015.10:g.58647261_58647278del, NC_000015.10:g.58647262_58647278del, NC_000015.10:g.58647263_58647278del, NC_000015.10:g.58647264_58647278del, NC_000015.10:g.58647265_58647278del, NC_000015.10:g.58647266_58647278del, NC_000015.10:g.58647267_58647278del, NC_000015.10:g.58647268_58647278del, NC_000015.10:g.58647269_58647278del, NC_000015.10:g.58647270_58647278del, NC_000015.10:g.58647271_58647278del, NC_000015.10:g.58647272_58647278del, NC_000015.10:g.58647273_58647278del, NC_000015.10:g.58647274_58647278del, NC_000015.10:g.58647275_58647278del, NC_000015.10:g.58647276_58647278del, NC_000015.10:g.58647277_58647278del, NC_000015.10:g.58647278del, NC_000015.10:g.58647278dup, NC_000015.10:g.58647277_58647278dup, NC_000015.10:g.58647276_58647278dup, NC_000015.10:g.58647275_58647278dup, NC_000015.10:g.58647274_58647278dup, NC_000015.10:g.58647273_58647278dup, NC_000015.10:g.58647272_58647278dup, NC_000015.10:g.58647271_58647278dup, NC_000015.10:g.58647270_58647278dup, NC_000015.10:g.58647269_58647278dup, NC_000015.10:g.58647268_58647278dup, NC_000015.10:g.58647267_58647278dup, NC_000015.10:g.58647266_58647278dup, NC_000015.10:g.58647249_58647278T[43]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000015.10:g.58647265_58647278dup, NC_000015.10:g.58647264_58647278dup, NC_000015.10:g.58647263_58647278dup, NC_000015.10:g.58647262_58647278dup, NC_000015.10:g.58647261_58647278dup, NC_000015.10:g.58647260_58647278dup, NC_000015.10:g.58647259_58647278dup, NC_000015.10:g.58647257_58647278dup, NC_000015.10:g.58647255_58647278dup, NC_000015.10:g.58647253_58647278dup, NC_000015.10:g.58647252_58647278dup, NC_000015.10:g.58647251_58647278dup, NC_000015.10:g.58647250_58647278dup, NC_000015.10:g.58647249_58647278dup, NC_000015.10:g.58647278_58647279insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.58647278_58647279insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.58647278_58647279insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.58647278_58647279insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.58647278_58647279insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.58647278_58647279insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.58647278_58647279insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.58647278_58647279insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.58647278_58647279insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.58647278_58647279insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.58647278_58647279insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.58647278_58647279insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.58647278_58647279insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.10:g.58647278_58647279insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.58939460_58939477del, NC_000015.9:g.58939461_58939477del, NC_000015.9:g.58939462_58939477del, NC_000015.9:g.58939463_58939477del, NC_000015.9:g.58939464_58939477del, NC_000015.9:g.58939465_58939477del, NC_000015.9:g.58939466_58939477del, NC_000015.9:g.58939467_58939477del, NC_000015.9:g.58939468_58939477del, NC_000015.9:g.58939469_58939477del, NC_000015.9:g.58939470_58939477del, NC_000015.9:g.58939471_58939477del, NC_000015.9:g.58939472_58939477del, NC_000015.9:g.58939473_58939477del, NC_000015.9:g.58939474_58939477del, NC_000015.9:g.58939475_58939477del, NC_000015.9:g.58939476_58939477del, NC_000015.9:g.58939477del, NC_000015.9:g.58939477dup, NC_000015.9:g.58939476_58939477dup, NC_000015.9:g.58939475_58939477dup, NC_000015.9:g.58939474_58939477dup, NC_000015.9:g.58939473_58939477dup, NC_000015.9:g.58939472_58939477dup, NC_000015.9:g.58939471_58939477dup, NC_000015.9:g.58939470_58939477dup, NC_000015.9:g.58939469_58939477dup, NC_000015.9:g.58939468_58939477dup, NC_000015.9:g.58939467_58939477dup, NC_000015.9:g.58939466_58939477dup, NC_000015.9:g.58939465_58939477dup, NC_000015.9:g.58939448_58939477T[43]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000015.9:g.58939464_58939477dup, NC_000015.9:g.58939463_58939477dup, NC_000015.9:g.58939462_58939477dup, NC_000015.9:g.58939461_58939477dup, NC_000015.9:g.58939460_58939477dup, NC_000015.9:g.58939459_58939477dup, NC_000015.9:g.58939458_58939477dup, NC_000015.9:g.58939456_58939477dup, NC_000015.9:g.58939454_58939477dup, NC_000015.9:g.58939452_58939477dup, NC_000015.9:g.58939451_58939477dup, NC_000015.9:g.58939450_58939477dup, NC_000015.9:g.58939449_58939477dup, NC_000015.9:g.58939448_58939477dup, NC_000015.9:g.58939477_58939478insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.58939477_58939478insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.58939477_58939478insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.58939477_58939478insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.58939477_58939478insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.58939477_58939478insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.58939477_58939478insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.58939477_58939478insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.58939477_58939478insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.58939477_58939478insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.58939477_58939478insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.58939477_58939478insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.58939477_58939478insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000015.9:g.58939477_58939478insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_033876.2:g.107442_107459del, NG_033876.2:g.107443_107459del, NG_033876.2:g.107444_107459del, NG_033876.2:g.107445_107459del, NG_033876.2:g.107446_107459del, NG_033876.2:g.107447_107459del, NG_033876.2:g.107448_107459del, NG_033876.2:g.107449_107459del, NG_033876.2:g.107450_107459del, NG_033876.2:g.107451_107459del, NG_033876.2:g.107452_107459del, NG_033876.2:g.107453_107459del, NG_033876.2:g.107454_107459del, NG_033876.2:g.107455_107459del, NG_033876.2:g.107456_107459del, NG_033876.2:g.107457_107459del, NG_033876.2:g.107458_107459del, NG_033876.2:g.107459del, NG_033876.2:g.107459dup, NG_033876.2:g.107458_107459dup, NG_033876.2:g.107457_107459dup, NG_033876.2:g.107456_107459dup, NG_033876.2:g.107455_107459dup, NG_033876.2:g.107454_107459dup, NG_033876.2:g.107453_107459dup, NG_033876.2:g.107452_107459dup, NG_033876.2:g.107451_107459dup, NG_033876.2:g.107450_107459dup, NG_033876.2:g.107449_107459dup, NG_033876.2:g.107448_107459dup, NG_033876.2:g.107447_107459dup, NG_033876.2:g.107430_107459A[41]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_033876.2:g.107446_107459dup, NG_033876.2:g.107445_107459dup, NG_033876.2:g.107444_107459dup, NG_033876.2:g.107443_107459dup, NG_033876.2:g.107442_107459dup, NG_033876.2:g.107441_107459dup, NG_033876.2:g.107440_107459dup, NG_033876.2:g.107438_107459dup, NG_033876.2:g.107436_107459dup, NG_033876.2:g.107434_107459dup, NG_033876.2:g.107433_107459dup, NG_033876.2:g.107432_107459dup, NG_033876.2:g.107431_107459dup, NG_033876.2:g.107430_107459dup, NG_033876.2:g.107459_107460insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_033876.2:g.107459_107460insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_033876.2:g.107459_107460insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_033876.2:g.107459_107460insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_033876.2:g.107459_107460insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_033876.2:g.107459_107460insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_033876.2:g.107459_107460insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_033876.2:g.107459_107460insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_033876.2:g.107459_107460insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_033876.2:g.107459_107460insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_033876.2:g.107459_107460insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_033876.2:g.107459_107460insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_033876.2:g.107459_107460insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_033876.2:g.107459_107460insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14913363348.

rs1491336334 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 15:58670213 (GRCh38)
15:58962413 (GRCh37)
Canonical SPDI:: NC_000015.10:58670213:GG:GGG
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGG=0.000071/1 (ALFA)
G=0.000026/7 (TOPMED)
G=0.000043/6 (GnomAD)
HGVS:: NC_000015.10:g.58670215dup, NC_000015.9:g.58962414dup, NG_033876.2:g.84494dup

Select item 14912983449.

rs1491298344 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CT,CTTCT [Show Flanks]
Chromosome:: 15:58691677 (GRCh38)
15:58983877 (GRCh37)
Canonical SPDI:: NC_000015.10:58691677:T:TCT,NC_000015.10:58691677:T:TCTTCT
Gene:: ADAM10 (Varview), HSP90AB4P (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TCTTCT=0./0 (ALFA)
HGVS:: NC_000015.10:g.58691678_58691679insCT, NC_000015.10:g.58691678_58691679insCTTCT, NC_000015.9:g.58983877_58983878insCT, NC_000015.9:g.58983877_58983878insCTTCT, NG_033876.2:g.63030_63031insGA, NG_033876.2:g.63030_63031insGAAGA, NR_073415.2:n.1930_1931insGA, NR_073415.2:n.1930_1931insGAAGA, NR_073415.1:n.1601_1602insGA, NR_073415.1:n.1601_1602insGAAGA

Select item 149129257210.

rs1491292572 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 15:58703311 (GRCh38)
15:58995511 (GRCh37)
Canonical SPDI:: NC_000015.10:58703311:C:CC
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0./0 (ALFA)
C=0.000015/2 (GnomAD)
C=0.000462/8 (TOMMO)
HGVS:: NC_000015.10:g.58703312dup, NC_000015.9:g.58995511dup, NG_033876.2:g.51396dup

Select item 149129037111.

rs1491290371 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GA [Show Flanks]
Chromosome:: 15:58688767 (GRCh38)
15:58980967 (GRCh37)
Canonical SPDI:: NC_000015.10:58688767:A:AGA
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AGA=0./0 (ALFA)
HGVS:: NC_000015.10:g.58688768_58688769insGA, NC_000015.9:g.58980967_58980968insGA, NG_033876.2:g.65940_65941insCT

Select item 149128996912.

rs1491289969 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 15:58638614 (GRCh38)
15:58930813 (GRCh37)
Canonical SPDI:: NC_000015.10:58638613:CA:
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.01416/168 (ALFA)
-=0.00483/135 (TOMMO)
HGVS:: NC_000015.10:g.58638614_58638615del, NC_000015.9:g.58930813_58930814del, NG_033876.2:g.116093_116094del

Select item 149121943013.

rs1491219430 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 15:58615277 (GRCh38)
15:58907477 (GRCh37)
Canonical SPDI:: NC_000015.10:58615277::G
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000015.10:g.58615277_58615278insG, NC_000015.9:g.58907476_58907477insG, NG_033876.2:g.139430_139431insC

Select item 149121790214.

rs1491217902 has merged into rs1420443728 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>-,CACA [Show Flanks]
Chromosome:: 15:58703316 (GRCh38)
15:58995515 (GRCh37)
Canonical SPDI:: NC_000015.10:58703310:ACACACA:ACACA,NC_000015.10:58703310:ACACACA:ACACACACA
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACACA=0./0 (ALFA)
HGVS:: NC_000015.10:g.58703312CA[2], NC_000015.10:g.58703312CA[4], NC_000015.9:g.58995511CA[2], NC_000015.9:g.58995511CA[4], NG_033876.2:g.51392GT[2], NG_033876.2:g.51392GT[4]

Select item 149118704415.

rs1491187044 [Homo sapiens]

Variant type:: DEL
Alleles:: AG>- [Show Flanks]
Chromosome:: 15:58670213 (GRCh38)
15:58962412 (GRCh37)
Canonical SPDI:: NC_000015.10:58670212:AG:
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.000071/1 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.58670213_58670214del, NC_000015.9:g.58962412_58962413del, NG_033876.2:g.84494_84495del

Select item 149118581616.

rs1491185816 has merged into rs780219725 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATATATATAT>-,AT,ATAT,ATATAT,ATATATAT,ATATATATATAT,ATATATATATATAT,ATATATATATATATAT,ATATATATATATATATAT,ATATATATATATATATATAT,ATATATATATATATATATATAT,ATATATATATATATATATATATAT,ATATATATATATATATATATATATAT,ATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATAT [Show Flanks]
Chromosome:: 15:58688778 (GRCh38)
15:58980977 (GRCh37)
Canonical SPDI:: NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000015.10:58688766:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATATAT=0./0 (ALFA)
HGVS:: NC_000015.10:g.58688768AT[5], NC_000015.10:g.58688768AT[6], NC_000015.10:g.58688768AT[7], NC_000015.10:g.58688768AT[8], NC_000015.10:g.58688768AT[9], NC_000015.10:g.58688768AT[11], NC_000015.10:g.58688768AT[12], NC_000015.10:g.58688768AT[13], NC_000015.10:g.58688768AT[14], NC_000015.10:g.58688768AT[15], NC_000015.10:g.58688768AT[16], NC_000015.10:g.58688768AT[17], NC_000015.10:g.58688768AT[18], NC_000015.10:g.58688768AT[19], NC_000015.10:g.58688768AT[20], NC_000015.10:g.58688768AT[21], NC_000015.10:g.58688768AT[22], NC_000015.10:g.58688768AT[23], NC_000015.10:g.58688768AT[24], NC_000015.10:g.58688768AT[25], NC_000015.10:g.58688768AT[26], NC_000015.10:g.58688768AT[27], NC_000015.10:g.58688768AT[28], NC_000015.10:g.58688768AT[29], NC_000015.9:g.58980967AT[5], NC_000015.9:g.58980967AT[6], NC_000015.9:g.58980967AT[7], NC_000015.9:g.58980967AT[8], NC_000015.9:g.58980967AT[9], NC_000015.9:g.58980967AT[11], NC_000015.9:g.58980967AT[12], NC_000015.9:g.58980967AT[13], NC_000015.9:g.58980967AT[14], NC_000015.9:g.58980967AT[15], NC_000015.9:g.58980967AT[16], NC_000015.9:g.58980967AT[17], NC_000015.9:g.58980967AT[18], NC_000015.9:g.58980967AT[19], NC_000015.9:g.58980967AT[20], NC_000015.9:g.58980967AT[21], NC_000015.9:g.58980967AT[22], NC_000015.9:g.58980967AT[23], NC_000015.9:g.58980967AT[24], NC_000015.9:g.58980967AT[25], NC_000015.9:g.58980967AT[26], NC_000015.9:g.58980967AT[27], NC_000015.9:g.58980967AT[28], NC_000015.9:g.58980967AT[29], NG_033876.2:g.65922TA[5], NG_033876.2:g.65922TA[6], NG_033876.2:g.65922TA[7], NG_033876.2:g.65922TA[8], NG_033876.2:g.65922TA[9], NG_033876.2:g.65922TA[11], NG_033876.2:g.65922TA[12], NG_033876.2:g.65922TA[13], NG_033876.2:g.65922TA[14], NG_033876.2:g.65922TA[15], NG_033876.2:g.65922TA[16], NG_033876.2:g.65922TA[17], NG_033876.2:g.65922TA[18], NG_033876.2:g.65922TA[19], NG_033876.2:g.65922TA[20], NG_033876.2:g.65922TA[21], NG_033876.2:g.65922TA[22], NG_033876.2:g.65922TA[23], NG_033876.2:g.65922TA[24], NG_033876.2:g.65922TA[25], NG_033876.2:g.65922TA[26], NG_033876.2:g.65922TA[27], NG_033876.2:g.65922TA[28], NG_033876.2:g.65922TA[29]

Select item 149118167317.

rs1491181673 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTT [Show Flanks]
Chromosome:: 15:58647249 (GRCh38)
15:58939449 (GRCh37)
Canonical SPDI:: NC_000015.10:58647249:TT:TTCTT
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTCTT=0.00034/4 (ALFA)
TTC=0.00061/8 (TOMMO)
TTC=0.01053/300 (GnomAD)
TTC=0.0635/103 (Korea1K)
HGVS:: NC_000015.10:g.58647251_58647252insCTT, NC_000015.9:g.58939450_58939451insCTT, NG_033876.2:g.107458_107459insGAA

Select item 149112998518.

rs1491129985 [Homo sapiens]

Variant type:: DEL
Alleles:: AG>- [Show Flanks]
Chromosome:: 15:58621156 (GRCh38)
15:58913355 (GRCh37)
Canonical SPDI:: NC_000015.10:58621155:AG:
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.58621156_58621157del, NC_000015.9:g.58913355_58913356del, NG_033876.2:g.133551_133552del

Select item 149111222119.

rs1491112221 has merged into rs35628107 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,A,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 15:58615287 (GRCh38)
15:58907486 (GRCh37)
Canonical SPDI:: NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000015.10:58615276:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
-=0.000011/3 (TOPMED)
A=0.401358/2010 (1000Genomes)
HGVS:: NC_000015.10:g.58615287_58615297del, NC_000015.10:g.58615288_58615297del, NC_000015.10:g.58615292_58615297del, NC_000015.10:g.58615293_58615297del, NC_000015.10:g.58615294_58615297del, NC_000015.10:g.58615295_58615297del, NC_000015.10:g.58615296_58615297del, NC_000015.10:g.58615297del, NC_000015.10:g.58615297dup, NC_000015.10:g.58615296_58615297dup, NC_000015.10:g.58615295_58615297dup, NC_000015.10:g.58615294_58615297dup, NC_000015.10:g.58615293_58615297dup, NC_000015.10:g.58615292_58615297dup, NC_000015.10:g.58615291_58615297dup, NC_000015.10:g.58615290_58615297dup, NC_000015.10:g.58615288_58615297dup, NC_000015.10:g.58615277_58615297A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000015.9:g.58907486_58907496del, NC_000015.9:g.58907487_58907496del, NC_000015.9:g.58907491_58907496del, NC_000015.9:g.58907492_58907496del, NC_000015.9:g.58907493_58907496del, NC_000015.9:g.58907494_58907496del, NC_000015.9:g.58907495_58907496del, NC_000015.9:g.58907496del, NC_000015.9:g.58907496dup, NC_000015.9:g.58907495_58907496dup, NC_000015.9:g.58907494_58907496dup, NC_000015.9:g.58907493_58907496dup, NC_000015.9:g.58907492_58907496dup, NC_000015.9:g.58907491_58907496dup, NC_000015.9:g.58907490_58907496dup, NC_000015.9:g.58907489_58907496dup, NC_000015.9:g.58907487_58907496dup, NC_000015.9:g.58907476_58907496A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_033876.2:g.139421_139431del, NG_033876.2:g.139422_139431del, NG_033876.2:g.139426_139431del, NG_033876.2:g.139427_139431del, NG_033876.2:g.139428_139431del, NG_033876.2:g.139429_139431del, NG_033876.2:g.139430_139431del, NG_033876.2:g.139431del, NG_033876.2:g.139431dup, NG_033876.2:g.139430_139431dup, NG_033876.2:g.139429_139431dup, NG_033876.2:g.139428_139431dup, NG_033876.2:g.139427_139431dup, NG_033876.2:g.139426_139431dup, NG_033876.2:g.139425_139431dup, NG_033876.2:g.139424_139431dup, NG_033876.2:g.139422_139431dup, NG_033876.2:g.139411_139431T[26]GTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 149104387120.

rs1491043871 has merged into rs199921945 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT,TTTTTT [Show Flanks]
Chromosome:: 15:58657899 (GRCh38)
15:58950098 (GRCh37)
Canonical SPDI:: NC_000015.10:58657888:TTTTTTTTTTTTT:TTTTTTTTTT,NC_000015.10:58657888:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000015.10:58657888:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000015.10:58657888:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000015.10:58657888:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:58657888:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
T=0.22444/1124 (1000Genomes)
T=0.25/10 (GENOME_DK)
HGVS:: NC_000015.10:g.58657899_58657901del, NC_000015.10:g.58657900_58657901del, NC_000015.10:g.58657901del, NC_000015.10:g.58657901dup, NC_000015.10:g.58657900_58657901dup, NC_000015.10:g.58657899_58657901dup, NC_000015.9:g.58950098_58950100del, NC_000015.9:g.58950099_58950100del, NC_000015.9:g.58950100del, NC_000015.9:g.58950100dup, NC_000015.9:g.58950099_58950100dup, NC_000015.9:g.58950098_58950100dup, NG_033876.2:g.96817_96819del, NG_033876.2:g.96818_96819del, NG_033876.2:g.96819del, NG_033876.2:g.96819dup, NG_033876.2:g.96818_96819dup, NG_033876.2:g.96817_96819dup

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