SNP Links for Gene (Select 10863) - SNP

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Select item 14915777261.

rs1491577726 [Homo sapiens]

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

Select item 14914999292.

rs1491499929 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 8:24306364 (GRCh38)
8:24163878 (GRCh37)
Canonical SPDI:: NC_000008.11:24306364:T:TT
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000008.11:g.24306365dup, NC_000008.10:g.24163878dup, NG_029394.2:g.17299dup

Select item 14914011793.

rs1491401179 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 8:24355517 (GRCh38)
8:24213030 (GRCh37)
Canonical SPDI:: NC_000008.11:24355516:CT:
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,non_coding_transcript_variant,intron_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.24355517_24355518del, NC_000008.10:g.24213030_24213031del, NG_029394.2:g.66451_66452del, NM_014265.6:c.*1113_*1114del, NM_014265.5:c.*1113_*1114del, NR_130710.2:n.3588_3589del, NR_130710.1:n.3617_3618del, NM_001304351.2:c.*1113_*1114del, NM_001304351.1:c.*1113_*1114del, XM_005273380.5:c.*1171_*1172del, XM_005273380.4:c.*1171_*1172del, XM_005273380.3:c.*1171_*1172del, XM_005273380.2:c.*1171_*1172del, XM_006716273.4:c.*1113_*1114del, XM_006716273.3:c.*1113_*1114del, XM_006716273.2:c.*1113_*1114del, XM_011544368.4:c.*1171_*1172del, XM_011544368.3:c.*1171_*1172del, XM_011544368.2:c.*1171_*1172del, XM_011544368.1:c.*1171_*1172del, XM_011544367.4:c.*1113_*1114del, XM_011544367.3:c.*1113_*1114del, XM_011544367.2:c.*1113_*1114del, XM_011544367.1:c.*1113_*1114del, XM_011544371.4:c.*1113_*1114del, XM_011544371.3:c.*1113_*1114del, XM_011544371.2:c.*1113_*1114del, XM_011544371.1:c.*1113_*1114del, XM_017012974.3:c.*1090_*1091del, XM_017012974.2:c.*1090_*1091del, XM_017012974.1:c.*1090_*1091del, XM_017012975.3:c.*1113_*1114del, XM_017012975.2:c.*1113_*1114del, XM_017012975.1:c.*1113_*1114del, XM_047421272.1:c.*1113_*1114del, XM_047421273.1:c.*1113_*1114del, XM_047421274.1:c.*1113_*1114del

Select item 14913501944.

rs1491350194 has merged into rs757200200 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA [Show Flanks]
Chromosome:: 8:24305480 (GRCh38)
8:24162993 (GRCh37)
Canonical SPDI:: NC_000008.11:24305477:AAAA:AA,NC_000008.11:24305477:AAAA:AAA,NC_000008.11:24305477:AAAA:AAAAA
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAA=0./0 (ALFA)
A=0.00036/6 (TOMMO)
HGVS:: NC_000008.11:g.24305480_24305481del, NC_000008.11:g.24305481del, NC_000008.11:g.24305481dup, NC_000008.10:g.24162993_24162994del, NC_000008.10:g.24162994del, NC_000008.10:g.24162994dup, NG_029394.2:g.16414_16415del, NG_029394.2:g.16415del, NG_029394.2:g.16415dup

Select item 14913046815.

rs1491304681 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>- [Show Flanks]
Chromosome:: 8:24306355 (GRCh38)
8:24163868 (GRCh37)
Canonical SPDI:: NC_000008.11:24306353:AAA:A
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.002917/47 (ALFA)
-=0.003508/59 (TOMMO)
-=0.012938/1542 (GnomAD)
HGVS:: NC_000008.11:g.24306355_24306356del, NC_000008.10:g.24163868_24163869del, NG_029394.2:g.17289_17290del

Select item 14912585856.

rs1491258585 [Homo sapiens]

Variant type:: INS
Alleles:: ->T,TATATATATATATATATATATATATATATATTT,TATATATATATATATATATATATATATTT [Show Flanks]
Chromosome:: 8:24306354 (GRCh38)
8:24163868 (GRCh37)
Canonical SPDI:: NC_000008.11:24306354::T,NC_000008.11:24306354::TATATATATATATATATATATATATATATATTT,NC_000008.11:24306354::TATATATATATATATATATATATATATTT
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: T=0.00643/11 (Korea1K)
T=0.0073/30 (Estonian)
T=0.11006/1766 (TOMMO)
HGVS:: NC_000008.11:g.24306354_24306355insT, NC_000008.11:g.24306354_24306355insTATATATATATATATATATATATATATATATTT, NC_000008.11:g.24306354_24306355insTATATATATATATATATATATATATATTT, NC_000008.10:g.24163867_24163868insT, NC_000008.10:g.24163867_24163868insTATATATATATATATATATATATATATATATTT, NC_000008.10:g.24163867_24163868insTATATATATATATATATATATATATATTT, NG_029394.2:g.17288_17289insT, NG_029394.2:g.17288_17289insTATATATATATATATATATATATATATATATTT, NG_029394.2:g.17288_17289insTATATATATATATATATATATATATATTT

Select item 14912549697.

rs1491254969 has merged into rs5890146 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAATAAAAAAATATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGGAAAAAAAAAGAAATAATTGAAAGTTTATAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 8:24325884 (GRCh38)
8:24183397 (GRCh37)
Canonical SPDI:: NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAATAAAAAAATATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGGAAAAAAAAAGAAATAATTGAAAGTTTATAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:24325871:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000008.11:g.24325884_24325900del, NC_000008.11:g.24325885_24325900del, NC_000008.11:g.24325886_24325900del, NC_000008.11:g.24325887_24325900del, NC_000008.11:g.24325888_24325900del, NC_000008.11:g.24325889_24325900del, NC_000008.11:g.24325890_24325900del, NC_000008.11:g.24325891_24325900del, NC_000008.11:g.24325892_24325900del, NC_000008.11:g.24325893_24325900del, NC_000008.11:g.24325894_24325900del, NC_000008.11:g.24325895_24325900del, NC_000008.11:g.24325896_24325900del, NC_000008.11:g.24325897_24325900del, NC_000008.11:g.24325898_24325900del, NC_000008.11:g.24325899_24325900del, NC_000008.11:g.24325900del, NC_000008.11:g.24325900dup, NC_000008.11:g.24325899_24325900dup, NC_000008.11:g.24325898_24325900dup, NC_000008.11:g.24325896_24325900dup, NC_000008.11:g.24325895_24325900dup, NC_000008.11:g.24325894_24325900dup, NC_000008.11:g.24325893_24325900dup, NC_000008.11:g.24325892_24325900dup, NC_000008.11:g.24325891_24325900dup, NC_000008.11:g.24325890_24325900dup, NC_000008.11:g.24325889_24325900dup, NC_000008.11:g.24325888_24325900dup, NC_000008.11:g.24325887_24325900dup, NC_000008.11:g.24325886_24325900dup, NC_000008.11:g.24325885_24325900dup, NC_000008.11:g.24325884_24325900dup, NC_000008.11:g.24325883_24325900dup, NC_000008.11:g.24325882_24325900dup, NC_000008.11:g.24325881_24325900dup, NC_000008.11:g.24325880_24325900dup, NC_000008.11:g.24325879_24325900dup, NC_000008.11:g.24325878_24325900dup, NC_000008.11:g.24325877_24325900dup, NC_000008.11:g.24325876_24325900dup, NC_000008.11:g.24325875_24325900dup, NC_000008.11:g.24325874_24325900dup, NC_000008.11:g.24325873_24325900dup, NC_000008.11:g.24325872_24325900dup, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325900_24325901insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.11:g.24325872_24325900A[66]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000008.11:g.24325872_24325900A[64]TAA[2]A[5]TA[2]A[38], NC_000008.11:g.24325872_24325900A[55]GGAAAAAAAAAGAAATAATTGAAAGTTTATAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000008.11:g.24325872_24325900A[53]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000008.11:g.24325872_24325900A[30]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000008.11:g.24325872_24325900A[30]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000008.11:g.24325872_24325900A[30]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000008.10:g.24183397_24183413del, NC_000008.10:g.24183398_24183413del, NC_000008.10:g.24183399_24183413del, NC_000008.10:g.24183400_24183413del, NC_000008.10:g.24183401_24183413del, NC_000008.10:g.24183402_24183413del, NC_000008.10:g.24183403_24183413del, NC_000008.10:g.24183404_24183413del, NC_000008.10:g.24183405_24183413del, NC_000008.10:g.24183406_24183413del, NC_000008.10:g.24183407_24183413del, NC_000008.10:g.24183408_24183413del, NC_000008.10:g.24183409_24183413del, NC_000008.10:g.24183410_24183413del, NC_000008.10:g.24183411_24183413del, NC_000008.10:g.24183412_24183413del, NC_000008.10:g.24183413del, NC_000008.10:g.24183413dup, NC_000008.10:g.24183412_24183413dup, NC_000008.10:g.24183411_24183413dup, NC_000008.10:g.24183409_24183413dup, NC_000008.10:g.24183408_24183413dup, NC_000008.10:g.24183407_24183413dup, NC_000008.10:g.24183406_24183413dup, NC_000008.10:g.24183405_24183413dup, NC_000008.10:g.24183404_24183413dup, NC_000008.10:g.24183403_24183413dup, NC_000008.10:g.24183402_24183413dup, NC_000008.10:g.24183401_24183413dup, NC_000008.10:g.24183400_24183413dup, NC_000008.10:g.24183399_24183413dup, NC_000008.10:g.24183398_24183413dup, NC_000008.10:g.24183397_24183413dup, NC_000008.10:g.24183396_24183413dup, NC_000008.10:g.24183395_24183413dup, NC_000008.10:g.24183394_24183413dup, NC_000008.10:g.24183393_24183413dup, NC_000008.10:g.24183392_24183413dup, NC_000008.10:g.24183391_24183413dup, NC_000008.10:g.24183390_24183413dup, NC_000008.10:g.24183389_24183413dup, NC_000008.10:g.24183388_24183413dup, NC_000008.10:g.24183387_24183413dup, NC_000008.10:g.24183386_24183413dup, NC_000008.10:g.24183385_24183413dup, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183413_24183414insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.24183385_24183413A[66]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000008.10:g.24183385_24183413A[64]TAA[2]A[5]TA[2]A[38], NC_000008.10:g.24183385_24183413A[55]GGAAAAAAAAAGAAATAATTGAAAGTTTATAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000008.10:g.24183385_24183413A[53]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000008.10:g.24183385_24183413A[30]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000008.10:g.24183385_24183413A[30]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000008.10:g.24183385_24183413A[30]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029394.2:g.36818_36834del, NG_029394.2:g.36819_36834del, NG_029394.2:g.36820_36834del, NG_029394.2:g.36821_36834del, NG_029394.2:g.36822_36834del, NG_029394.2:g.36823_36834del, NG_029394.2:g.36824_36834del, NG_029394.2:g.36825_36834del, NG_029394.2:g.36826_36834del, NG_029394.2:g.36827_36834del, NG_029394.2:g.36828_36834del, NG_029394.2:g.36829_36834del, NG_029394.2:g.36830_36834del, NG_029394.2:g.36831_36834del, NG_029394.2:g.36832_36834del, NG_029394.2:g.36833_36834del, NG_029394.2:g.36834del, NG_029394.2:g.36834dup, NG_029394.2:g.36833_36834dup, NG_029394.2:g.36832_36834dup, NG_029394.2:g.36830_36834dup, NG_029394.2:g.36829_36834dup, NG_029394.2:g.36828_36834dup, NG_029394.2:g.36827_36834dup, NG_029394.2:g.36826_36834dup, NG_029394.2:g.36825_36834dup, NG_029394.2:g.36824_36834dup, NG_029394.2:g.36823_36834dup, NG_029394.2:g.36822_36834dup, NG_029394.2:g.36821_36834dup, NG_029394.2:g.36820_36834dup, NG_029394.2:g.36819_36834dup, NG_029394.2:g.36818_36834dup, NG_029394.2:g.36817_36834dup, NG_029394.2:g.36816_36834dup, NG_029394.2:g.36815_36834dup, NG_029394.2:g.36814_36834dup, NG_029394.2:g.36813_36834dup, NG_029394.2:g.36812_36834dup, NG_029394.2:g.36811_36834dup, NG_029394.2:g.36810_36834dup, NG_029394.2:g.36809_36834dup, NG_029394.2:g.36808_36834dup, NG_029394.2:g.36807_36834dup, NG_029394.2:g.36806_36834dup, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36834_36835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_029394.2:g.36806_36834A[66]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029394.2:g.36806_36834A[64]TAA[2]A[5]TA[2]A[38], NG_029394.2:g.36806_36834A[55]GGAAAAAAAAAGAAATAATTGAAAGTTTATAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029394.2:g.36806_36834A[53]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029394.2:g.36806_36834A[30]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029394.2:g.36806_36834A[30]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_029394.2:g.36806_36834A[30]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]

Select item 14912397288.

rs1491239728 has merged into rs71212527 [Homo sapiens]

Variant type:: DELINS
Alleles:: TGTGTGTGTG>-,TG,TGTG,TGTGTG,TGTGTGTG,TGTGTGTGTGTG,TGTGTGTGTGTGTG,TGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTG [Show Flanks]
Chromosome:: 8:24336051 (GRCh38)
8:24193564 (GRCh37)
Canonical SPDI:: NC_000008.11:24336039:GTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTG,NC_000008.11:24336039:GTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTG,NC_000008.11:24336039:GTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTG,NC_000008.11:24336039:GTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTG,NC_000008.11:24336039:GTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTG,NC_000008.11:24336039:GTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:24336039:GTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:24336039:GTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:24336039:GTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTG
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: intron_variant,3_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGTGTGTGTGTG=0./0 (ALFA)
HGVS:: NC_000008.11:g.24336041TG[5], NC_000008.11:g.24336041TG[6], NC_000008.11:g.24336041TG[7], NC_000008.11:g.24336041TG[8], NC_000008.11:g.24336041TG[9], NC_000008.11:g.24336041TG[11], NC_000008.11:g.24336041TG[12], NC_000008.11:g.24336041TG[13], NC_000008.11:g.24336041TG[14], NC_000008.10:g.24193554TG[5], NC_000008.10:g.24193554TG[6], NC_000008.10:g.24193554TG[7], NC_000008.10:g.24193554TG[8], NC_000008.10:g.24193554TG[9], NC_000008.10:g.24193554TG[11], NC_000008.10:g.24193554TG[12], NC_000008.10:g.24193554TG[13], NC_000008.10:g.24193554TG[14], NG_029394.2:g.46975TG[5], NG_029394.2:g.46975TG[6], NG_029394.2:g.46975TG[7], NG_029394.2:g.46975TG[8], NG_029394.2:g.46975TG[9], NG_029394.2:g.46975TG[11], NG_029394.2:g.46975TG[12], NG_029394.2:g.46975TG[13], NG_029394.2:g.46975TG[14], NM_021777.5:c.*344TG[5], NM_021777.5:c.*344TG[6], NM_021777.5:c.*344TG[7], NM_021777.5:c.*344TG[8], NM_021777.5:c.*344TG[9], NM_021777.5:c.*344TG[11], NM_021777.5:c.*344TG[12], NM_021777.5:c.*344TG[13], NM_021777.5:c.*344TG[14], NM_021777.4:c.*344TG[5], NM_021777.4:c.*344TG[6], NM_021777.4:c.*344TG[7], NM_021777.4:c.*344TG[8], NM_021777.4:c.*344TG[9], NM_021777.4:c.*344TG[11], NM_021777.4:c.*344TG[12], NM_021777.4:c.*344TG[13], NM_021777.4:c.*344TG[14], NM_021777.3:c.*344TG[5], NM_021777.3:c.*344TG[6], NM_021777.3:c.*344TG[7], NM_021777.3:c.*344TG[8], NM_021777.3:c.*344TG[9], NM_021777.3:c.*344TG[11], NM_021777.3:c.*344TG[12], NM_021777.3:c.*344TG[13], NM_021777.3:c.*344TG[14], NR_130709.2:n.1855TG[5], NR_130709.2:n.1855TG[6], NR_130709.2:n.1855TG[7], NR_130709.2:n.1855TG[8], NR_130709.2:n.1855TG[9], NR_130709.2:n.1855TG[11], NR_130709.2:n.1855TG[12], NR_130709.2:n.1855TG[13], NR_130709.2:n.1855TG[14], NR_130709.1:n.1884TG[5], NR_130709.1:n.1884TG[6], NR_130709.1:n.1884TG[7], NR_130709.1:n.1884TG[8], NR_130709.1:n.1884TG[9], NR_130709.1:n.1884TG[11], NR_130709.1:n.1884TG[12], NR_130709.1:n.1884TG[13], NR_130709.1:n.1884TG[14]

Select item 14912076919.

rs1491207691 [Homo sapiens]

Variant type:: INS
Alleles:: ->T,TATATATATATATATATATATATATT [Show Flanks]
Chromosome:: 8:24306362 (GRCh38)
8:24163876 (GRCh37)
Canonical SPDI:: NC_000008.11:24306362::T,NC_000008.11:24306362::TATATATATATATATATATATATATT
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: T=0.000181/3 (TOMMO)
T=0.003946/432 (GnomAD)
HGVS:: NC_000008.11:g.24306362_24306363insT, NC_000008.11:g.24306362_24306363insTATATATATATATATATATATATATT, NC_000008.10:g.24163875_24163876insT, NC_000008.10:g.24163875_24163876insTATATATATATATATATATATATATT, NG_029394.2:g.17296_17297insT, NG_029394.2:g.17296_17297insTATATATATATATATATATATATATT

Select item 149118349210.

rs1491183492 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>- [Show Flanks]
Chromosome:: 8:24306363 (GRCh38)
8:24163876 (GRCh37)
Canonical SPDI:: NC_000008.11:24306361:AAA:A
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000169/2 (ALFA)
-=0.000094/10 (GnomAD)
-=0.000107/2 (TOMMO)
HGVS:: NC_000008.11:g.24306363_24306364del, NC_000008.10:g.24163876_24163877del, NG_029394.2:g.17297_17298del

Select item 149113382511.

rs1491133825 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 8:24305477 (GRCh38)
8:24162990 (GRCh37)
Canonical SPDI:: NC_000008.11:24305476:TA:
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency
MAF:: -=0.000023/3 (GnomAD)
HGVS:: NC_000008.11:g.24305477_24305478del, NC_000008.10:g.24162990_24162991del, NG_029394.2:g.16411_16412del

Select item 149113039912.

rs1491130399 [Homo sapiens]

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

Select item 149107517613.

rs1491075176 has merged into rs10654023 [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,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 8:24305462 (GRCh38)
8:24162975 (GRCh37)
Canonical SPDI:: NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:24305451:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
TTTTTTTT=0./0 (GENOME_DK)
-=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.24305462_24305477del, NC_000008.11:g.24305463_24305477del, NC_000008.11:g.24305464_24305477del, NC_000008.11:g.24305465_24305477del, NC_000008.11:g.24305466_24305477del, NC_000008.11:g.24305467_24305477del, NC_000008.11:g.24305468_24305477del, NC_000008.11:g.24305469_24305477del, NC_000008.11:g.24305470_24305477del, NC_000008.11:g.24305471_24305477del, NC_000008.11:g.24305472_24305477del, NC_000008.11:g.24305473_24305477del, NC_000008.11:g.24305474_24305477del, NC_000008.11:g.24305475_24305477del, NC_000008.11:g.24305476_24305477del, NC_000008.11:g.24305477del, NC_000008.11:g.24305477dup, NC_000008.11:g.24305476_24305477dup, NC_000008.11:g.24305475_24305477dup, NC_000008.11:g.24305474_24305477dup, NC_000008.11:g.24305473_24305477dup, NC_000008.11:g.24305472_24305477dup, NC_000008.11:g.24305471_24305477dup, NC_000008.11:g.24305470_24305477dup, NC_000008.11:g.24305469_24305477dup, NC_000008.11:g.24305461_24305477dup, NC_000008.10:g.24162975_24162990del, NC_000008.10:g.24162976_24162990del, NC_000008.10:g.24162977_24162990del, NC_000008.10:g.24162978_24162990del, NC_000008.10:g.24162979_24162990del, NC_000008.10:g.24162980_24162990del, NC_000008.10:g.24162981_24162990del, NC_000008.10:g.24162982_24162990del, NC_000008.10:g.24162983_24162990del, NC_000008.10:g.24162984_24162990del, NC_000008.10:g.24162985_24162990del, NC_000008.10:g.24162986_24162990del, NC_000008.10:g.24162987_24162990del, NC_000008.10:g.24162988_24162990del, NC_000008.10:g.24162989_24162990del, NC_000008.10:g.24162990del, NC_000008.10:g.24162990dup, NC_000008.10:g.24162989_24162990dup, NC_000008.10:g.24162988_24162990dup, NC_000008.10:g.24162987_24162990dup, NC_000008.10:g.24162986_24162990dup, NC_000008.10:g.24162985_24162990dup, NC_000008.10:g.24162984_24162990dup, NC_000008.10:g.24162983_24162990dup, NC_000008.10:g.24162982_24162990dup, NC_000008.10:g.24162974_24162990dup, NG_029394.2:g.16396_16411del, NG_029394.2:g.16397_16411del, NG_029394.2:g.16398_16411del, NG_029394.2:g.16399_16411del, NG_029394.2:g.16400_16411del, NG_029394.2:g.16401_16411del, NG_029394.2:g.16402_16411del, NG_029394.2:g.16403_16411del, NG_029394.2:g.16404_16411del, NG_029394.2:g.16405_16411del, NG_029394.2:g.16406_16411del, NG_029394.2:g.16407_16411del, NG_029394.2:g.16408_16411del, NG_029394.2:g.16409_16411del, NG_029394.2:g.16410_16411del, NG_029394.2:g.16411del, NG_029394.2:g.16411dup, NG_029394.2:g.16410_16411dup, NG_029394.2:g.16409_16411dup, NG_029394.2:g.16408_16411dup, NG_029394.2:g.16407_16411dup, NG_029394.2:g.16406_16411dup, NG_029394.2:g.16405_16411dup, NG_029394.2:g.16404_16411dup, NG_029394.2:g.16403_16411dup, NG_029394.2:g.16395_16411dup

Select item 149100504614.

rs1491005046 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 8:24297169 (GRCh38)
8:24154682 (GRCh37)
Canonical SPDI:: NC_000008.11:24297167:TGT:T
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.000042/5 (GnomAD)
-=0.001132/19 (TOMMO)
-=0.001638/3 (Korea1K)
HGVS:: NC_000008.11:g.24297169_24297170del, NC_000008.10:g.24154682_24154683del, NG_029394.2:g.8103_8104del

Select item 149099466015.

rs1490994660 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GT [Show Flanks]
Chromosome:: 8:24340998 (GRCh38)
8:24198512 (GRCh37)
Canonical SPDI:: NC_000008.11:24340998:GTGT:GTGTGT
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGTGT=0.000071/1 (ALFA)
GT=0.000021/3 (GnomAD)
GT=0.000064/17 (TOPMED)
HGVS:: NC_000008.11:g.24340999GT[3], NC_000008.10:g.24198512GT[3], NG_029394.2:g.51933GT[3]

Select item 149095703016.

rs1490957030 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:24354740 (GRCh38)
8:24212253 (GRCh37)
Canonical SPDI:: NC_000008.11:24354739:G:A
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,non_coding_transcript_variant,intron_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000008.11:g.24354740G>A, NC_000008.10:g.24212253G>A, NG_029394.2:g.65674G>A, NM_014265.6:c.*336G>A, NM_014265.5:c.*336G>A, NM_014265.4:c.*336G>A, NR_130710.2:n.2811G>A, NR_130710.1:n.2840G>A, NM_001304351.2:c.*336G>A, NM_001304351.1:c.*336G>A, XM_005273380.5:c.*394G>A, XM_005273380.4:c.*394G>A, XM_005273380.3:c.*394G>A, XM_005273380.2:c.*394G>A, XM_005273380.1:c.*394G>A, XM_006716273.4:c.*336G>A, XM_006716273.3:c.*336G>A, XM_006716273.2:c.*336G>A, XM_006716273.1:c.*336G>A, XM_011544368.4:c.*394G>A, XM_011544368.3:c.*394G>A, XM_011544368.2:c.*394G>A, XM_011544368.1:c.*394G>A, XM_011544367.4:c.*336G>A, XM_011544367.3:c.*336G>A, XM_011544367.2:c.*336G>A, XM_011544367.1:c.*336G>A, XM_011544371.4:c.*336G>A, XM_011544371.3:c.*336G>A, XM_011544371.2:c.*336G>A, XM_011544371.1:c.*336G>A, XM_017012974.3:c.*313G>A, XM_017012974.2:c.*313G>A, XM_017012974.1:c.*313G>A, XM_017012975.3:c.*336G>A, XM_017012975.2:c.*336G>A, XM_017012975.1:c.*336G>A, XM_047421272.1:c.*336G>A, XM_047421273.1:c.*336G>A, XM_047421274.1:c.*336G>A, NM_021778.1:c.*332G>A

Select item 149090475917.

rs1490904759 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 8:24309355 (GRCh38)
8:24166868 (GRCh37)
Canonical SPDI:: NC_000008.11:24309354:A:C
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000043/6 (GnomAD)
HGVS:: NC_000008.11:g.24309355A>C, NC_000008.10:g.24166868A>C, NG_029394.2:g.20289A>C

Select item 149088935418.

rs1490889354 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:24306565 (GRCh38)
8:24164078 (GRCh37)
Canonical SPDI:: NC_000008.11:24306564:C:T
Gene:: ADAM28 (Varview), ADAM7-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.24306565C>T, NC_000008.10:g.24164078C>T, NG_029394.2:g.17499C>T

Select item 149076697819.

rs1490766978 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 8:24294583 (GRCh38)
8:24152096 (GRCh37)
Canonical SPDI:: NC_000008.11:24294582:C:G,NC_000008.11:24294582:C:T
Gene:: ADAM28 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.24294583C>G, NC_000008.11:g.24294583C>T, NC_000008.10:g.24152096C>G, NC_000008.10:g.24152096C>T, NG_029394.2:g.5517C>G, NG_029394.2:g.5517C>T

Select item 149073419320.

rs1490734193 [Homo sapiens]

Variant type:: DELINS
Alleles:: TC>- [Show Flanks]
Chromosome:: 8:24294865 (GRCh38)
8:24152378 (GRCh37)
Canonical SPDI:: NC_000008.11:24294860:TCTCTC:TCTC
Gene:: ADAM28 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TCTC=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.24294861TC[2], NC_000008.10:g.24152374TC[2], NG_029394.2:g.5795TC[2]

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