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Select item 14915568821.

rs1491556882 [Homo sapiens]

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

Select item 14915549842.

rs1491554984 has merged into rs1165441029 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,T,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 19:38923229 (GRCh38)
19:39413869 (GRCh37)
Canonical SPDI:: NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:38923219:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000019.10:g.38923229_38923239del, NC_000019.10:g.38923230_38923239del, NC_000019.10:g.38923231_38923239del, NC_000019.10:g.38923233_38923239del, NC_000019.10:g.38923234_38923239del, NC_000019.10:g.38923235_38923239del, NC_000019.10:g.38923236_38923239del, NC_000019.10:g.38923237_38923239del, NC_000019.10:g.38923238_38923239del, NC_000019.10:g.38923239del, NC_000019.10:g.38923239dup, NC_000019.10:g.38923238_38923239dup, NC_000019.10:g.38923237_38923239dup, NC_000019.10:g.38923236_38923239dup, NC_000019.10:g.38923235_38923239dup, NC_000019.10:g.38923234_38923239dup, NC_000019.10:g.38923233_38923239dup, NC_000019.10:g.38923232_38923239dup, NC_000019.10:g.38923229_38923239dup, NC_000019.9:g.39413869_39413879del, NC_000019.9:g.39413870_39413879del, NC_000019.9:g.39413871_39413879del, NC_000019.9:g.39413873_39413879del, NC_000019.9:g.39413874_39413879del, NC_000019.9:g.39413875_39413879del, NC_000019.9:g.39413876_39413879del, NC_000019.9:g.39413877_39413879del, NC_000019.9:g.39413878_39413879del, NC_000019.9:g.39413879del, NC_000019.9:g.39413879dup, NC_000019.9:g.39413878_39413879dup, NC_000019.9:g.39413877_39413879dup, NC_000019.9:g.39413876_39413879dup, NC_000019.9:g.39413875_39413879dup, NC_000019.9:g.39413874_39413879dup, NC_000019.9:g.39413873_39413879dup, NC_000019.9:g.39413872_39413879dup, NC_000019.9:g.39413869_39413879dup, NG_031865.1:g.12667_12677del, NG_031865.1:g.12668_12677del, NG_031865.1:g.12669_12677del, NG_031865.1:g.12671_12677del, NG_031865.1:g.12672_12677del, NG_031865.1:g.12673_12677del, NG_031865.1:g.12674_12677del, NG_031865.1:g.12675_12677del, NG_031865.1:g.12676_12677del, NG_031865.1:g.12677del, NG_031865.1:g.12677dup, NG_031865.1:g.12676_12677dup, NG_031865.1:g.12675_12677dup, NG_031865.1:g.12674_12677dup, NG_031865.1:g.12673_12677dup, NG_031865.1:g.12672_12677dup, NG_031865.1:g.12671_12677dup, NG_031865.1:g.12670_12677dup, NG_031865.1:g.12667_12677dup, NW_014040929.1:g.332901_332911del, NW_014040929.1:g.332902_332911del, NW_014040929.1:g.332903_332911del, NW_014040929.1:g.332905_332911del, NW_014040929.1:g.332906_332911del, NW_014040929.1:g.332907_332911del, NW_014040929.1:g.332908_332911del, NW_014040929.1:g.332909_332911del, NW_014040929.1:g.332910_332911del, NW_014040929.1:g.332911del, NW_014040929.1:g.332911dup, NW_014040929.1:g.332910_332911dup, NW_014040929.1:g.332909_332911dup, NW_014040929.1:g.332908_332911dup, NW_014040929.1:g.332907_332911dup, NW_014040929.1:g.332906_332911dup, NW_014040929.1:g.332905_332911dup, NW_014040929.1:g.332904_332911dup, NW_014040929.1:g.332901_332911dup

Select item 14915266353.

rs1491526635 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 19:38920686 (GRCh38)
19:39411327 (GRCh37)
Canonical SPDI:: NC_000019.10:38920686::A
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NC_000019.10:g.38920686_38920687insA, NC_000019.9:g.39411326_39411327insA, NG_031865.1:g.15210_15211insT, NW_014040929.1:g.330358_330359insA

Select item 14915231634.

rs1491523163 has merged into rs142895480 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACACACA>-,CA,CACA,CACACA,CACACACACA [Show Flanks]
Chromosome:: 19:38920944 (GRCh38)
19:39411584 (GRCh37)
Canonical SPDI:: NC_000019.10:38920938:ACACACACACACA:ACACA,NC_000019.10:38920938:ACACACACACACA:ACACACA,NC_000019.10:38920938:ACACACACACACA:ACACACACA,NC_000019.10:38920938:ACACACACACACA:ACACACACACA,NC_000019.10:38920938:ACACACACACACA:ACACACACACACACA
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACA=0./0 (ALFA)
AC=0.3017/461 (Korea1K)
-=0.325/13 (GENOME_DK)
AC=0.3846/2463 (1000Genomes)
-=0.44504/251 (NorthernSweden)
AC=0.46785/6207 (TOMMO)
HGVS:: NC_000019.10:g.38920940CA[2], NC_000019.10:g.38920940CA[3], NC_000019.10:g.38920940CA[4], NC_000019.10:g.38920940CA[5], NC_000019.10:g.38920940CA[7], NC_000019.9:g.39411580CA[2], NC_000019.9:g.39411580CA[3], NC_000019.9:g.39411580CA[4], NC_000019.9:g.39411580CA[5], NC_000019.9:g.39411580CA[7], NG_031865.1:g.14947GT[2], NG_031865.1:g.14947GT[3], NG_031865.1:g.14947GT[4], NG_031865.1:g.14947GT[5], NG_031865.1:g.14947GT[7], NW_014040929.1:g.330612CA[2], NW_014040929.1:g.330612CA[3], NW_014040929.1:g.330612CA[4], NW_014040929.1:g.330612CA[5], NW_014040929.1:g.330612CA[7]

Select item 14914138695.

rs1491413869 [Homo sapiens]

Variant type:: DEL
Alleles:: CG>- [Show Flanks]
Chromosome:: 19:38920686 (GRCh38)
19:39411326 (GRCh37)
Canonical SPDI:: NC_000019.10:38920685:CG:
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000021/3 (GnomAD)
HGVS:: NC_000019.10:g.38920686_38920687del, NC_000019.9:g.39411326_39411327del, NG_031865.1:g.15210_15211del, NW_014040929.1:g.330358_330359del

Select item 14913168056.

rs1491316805 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTT [Show Flanks]
Chromosome:: 19:38923220 (GRCh38)
19:39413861 (GRCh37)
Canonical SPDI:: NC_000019.10:38923220:TT:TTCTT
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTCTT=0.00455/54 (ALFA)
TTC=0.01717/605 (GnomAD)
HGVS:: NC_000019.10:g.38923222_38923223insCTT, NC_000019.9:g.39413862_39413863insCTT, NG_031865.1:g.12676_12677insGAA, NW_014040929.1:g.332894_332895insCTT

Select item 14912827667.

rs1491282766 has merged into rs1307012207 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>-,CACA,CACAGACACA [Show Flanks]
Chromosome:: 19:38921086 (GRCh38)
19:39411726 (GRCh37)
Canonical SPDI:: NC_000019.10:38921084:ACA:A,NC_000019.10:38921084:ACA:ACACA,NC_000019.10:38921084:ACA:ACACAGACACA
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACAGACACA=0./0 (ALFA)
ACACAGAC=0.000004/1 (TOPMED)
AC=0.000051/7 (GnomAD)
HGVS:: NC_000019.10:g.38921086_38921087del, NC_000019.10:g.38921086_38921087dup, NC_000019.10:g.38921085_38921087AC[2]AGACACA[1], NC_000019.9:g.39411726_39411727del, NC_000019.9:g.39411726_39411727dup, NC_000019.9:g.39411725_39411727AC[2]AGACACA[1], NG_031865.1:g.14811_14812del, NG_031865.1:g.14811_14812dup, NG_031865.1:g.14810_14812TG[2]TCTGTGT[1], NW_014040929.1:g.330758_330759del, NW_014040929.1:g.330758_330759dup, NW_014040929.1:g.330757_330759AC[2]AGACACA[1]

Select item 14912804978.

rs1491280497 [Homo sapiens]

Variant type:: INS
Alleles:: ->T [Show Flanks]
Chromosome:: 19:38928417 (GRCh38)
19:39419058 (GRCh37)
Canonical SPDI:: NC_000019.10:38928417::T
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.00016/2 (GnomAD)
HGVS:: NC_000019.10:g.38928417_38928418insT, NC_000019.9:g.39419057_39419058insT, NG_031865.1:g.7479_7480insA, NG_029222.1:g.2710_2711insT, NW_014040929.1:g.338089_338090insT

Select item 14911972789.

rs1491197278 has merged into rs57463198 [Homo sapiens]

Variant type:: DELINS
Alleles:: CCCCCCCCCC>-,CCCCCCC,CCCCCCCC,CCCCCCCCC,CCCCCCCCCCC,CCCCCCCCCCCC [Show Flanks]
Chromosome:: 19:38928417 (GRCh38)
19:39419057 (GRCh37)
Canonical SPDI:: NC_000019.10:38928415:CCCCCCCCCCC:C,NC_000019.10:38928415:CCCCCCCCCCC:CCCCCCCC,NC_000019.10:38928415:CCCCCCCCCCC:CCCCCCCCC,NC_000019.10:38928415:CCCCCCCCCCC:CCCCCCCCCC,NC_000019.10:38928415:CCCCCCCCCCC:CCCCCCCCCCCC,NC_000019.10:38928415:CCCCCCCCCCC:CCCCCCCCCCCCC
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CCCCCCCC=0./0 (ALFA)
C=0.1717/860 (1000Genomes)
C=0.35/14 (GENOME_DK)
HGVS:: NC_000019.10:g.38928417_38928426del, NC_000019.10:g.38928424_38928426del, NC_000019.10:g.38928425_38928426del, NC_000019.10:g.38928426del, NC_000019.10:g.38928426dup, NC_000019.10:g.38928425_38928426dup, NC_000019.9:g.39419057_39419066del, NC_000019.9:g.39419064_39419066del, NC_000019.9:g.39419065_39419066del, NC_000019.9:g.39419066del, NC_000019.9:g.39419066dup, NC_000019.9:g.39419065_39419066dup, NG_031865.1:g.7472_7481del, NG_031865.1:g.7479_7481del, NG_031865.1:g.7480_7481del, NG_031865.1:g.7481del, NG_031865.1:g.7481dup, NG_031865.1:g.7480_7481dup, NG_029222.1:g.2710_2719del, NG_029222.1:g.2717_2719del, NG_029222.1:g.2718_2719del, NG_029222.1:g.2719del, NG_029222.1:g.2719dup, NG_029222.1:g.2718_2719dup, NW_014040929.1:g.338089_338098del, NW_014040929.1:g.338096_338098del, NW_014040929.1:g.338097_338098del, NW_014040929.1:g.338098del, NW_014040929.1:g.338098dup, NW_014040929.1:g.338097_338098dup

Select item 149112386910.

rs1491123869 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GACAGACACACAGATACACGGA [Show Flanks]
Chromosome:: 19:38920665 (GRCh38)
19:39411306 (GRCh37)
Canonical SPDI:: NC_000019.10:38920665:GAGACAGACACACAGATACACGGA:GAGACAGACACACAGATACACGGAGACAGACACACAGATACACGGA
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GAGACAGACACACAGATACACGGAGACAGACACACAGATACACGGA=0./0 (ALFA)
GAGACAGACACACAGATACACG=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.38920668_38920689dup, NC_000019.9:g.39411308_39411329dup, NG_031865.1:g.15210_15231dup, NW_014040929.1:g.330340_330361dup

Select item 149110802411.

rs1491108024 has merged into rs369390554 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 19:38932157 (GRCh38)
19:39422797 (GRCh37)
Canonical SPDI:: NC_000019.10:38932148:AAAAAAAAAAAAAA:AAAAAAAA,NC_000019.10:38932148:AAAAAAAAAAAAAA:AAAAAAAAA,NC_000019.10:38932148:AAAAAAAAAAAAAA:AAAAAAAAAA,NC_000019.10:38932148:AAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000019.10:38932148:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:38932148:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:38932148:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:38932148:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:38932148:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:38932148:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MRPS12 (Varview), SARS2 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
-=0.05132/257 (1000Genomes)
HGVS:: NC_000019.10:g.38932157_38932162del, NC_000019.10:g.38932158_38932162del, NC_000019.10:g.38932159_38932162del, NC_000019.10:g.38932160_38932162del, NC_000019.10:g.38932161_38932162del, NC_000019.10:g.38932162del, NC_000019.10:g.38932162dup, NC_000019.10:g.38932161_38932162dup, NC_000019.10:g.38932162_38932163insAAAAAAAAAAAAAAAAAA, NC_000019.10:g.38932162_38932163insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.39422797_39422802del, NC_000019.9:g.39422798_39422802del, NC_000019.9:g.39422799_39422802del, NC_000019.9:g.39422800_39422802del, NC_000019.9:g.39422801_39422802del, NC_000019.9:g.39422802del, NC_000019.9:g.39422802dup, NC_000019.9:g.39422801_39422802dup, NC_000019.9:g.39422802_39422803insAAAAAAAAAAAAAAAAAA, NC_000019.9:g.39422802_39422803insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031865.1:g.3743_3748del, NG_031865.1:g.3744_3748del, NG_031865.1:g.3745_3748del, NG_031865.1:g.3746_3748del, NG_031865.1:g.3747_3748del, NG_031865.1:g.3748del, NG_031865.1:g.3748dup, NG_031865.1:g.3747_3748dup, NG_031865.1:g.3748_3749insTTTTTTTTTTTTTTTTTT, NG_031865.1:g.3748_3749insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_029222.1:g.6450_6455del, NG_029222.1:g.6451_6455del, NG_029222.1:g.6452_6455del, NG_029222.1:g.6453_6455del, NG_029222.1:g.6454_6455del, NG_029222.1:g.6455del, NG_029222.1:g.6455dup, NG_029222.1:g.6454_6455dup, NG_029222.1:g.6455_6456insAAAAAAAAAAAAAAAAAA, NG_029222.1:g.6455_6456insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_014040929.1:g.341829_341834del, NW_014040929.1:g.341830_341834del, NW_014040929.1:g.341831_341834del, NW_014040929.1:g.341832_341834del, NW_014040929.1:g.341833_341834del, NW_014040929.1:g.341834del, NW_014040929.1:g.341834dup, NW_014040929.1:g.341833_341834dup, NW_014040929.1:g.341834_341835insAAAAAAAAAAAAAAAAAA, NW_014040929.1:g.341834_341835insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149109908612.

rs1491099086 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 19:38920668 (GRCh38)
19:39411308 (GRCh37)
Canonical SPDI:: NC_000019.10:38920664:AGAGA:AGA
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGA=0./0 (ALFA)
-=0.000021/3 (GnomAD)
-=0.000042/11 (TOPMED)
-=0.000241/4 (TOMMO)
-=0.001092/2 (Korea1K)
HGVS:: NC_000019.10:g.38920666GA[1], NC_000019.9:g.39411306GA[1], NG_031865.1:g.15229CT[1], NW_014040929.1:g.330338GA[1]

Select item 149087686313.

rs1490876863 has merged into rs142895480 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACACACA>-,CA,CACA,CACACA,CACACACACA [Show Flanks]
Chromosome:: 19:38920944 (GRCh38)
19:39411584 (GRCh37)
Canonical SPDI:: NC_000019.10:38920938:ACACACACACACA:ACACA,NC_000019.10:38920938:ACACACACACACA:ACACACA,NC_000019.10:38920938:ACACACACACACA:ACACACACA,NC_000019.10:38920938:ACACACACACACA:ACACACACACA,NC_000019.10:38920938:ACACACACACACA:ACACACACACACACA
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACA=0./0 (ALFA)
AC=0.3017/461 (Korea1K)
-=0.325/13 (GENOME_DK)
AC=0.3846/2463 (1000Genomes)
-=0.44504/251 (NorthernSweden)
AC=0.46785/6207 (TOMMO)
HGVS:: NC_000019.10:g.38920940CA[2], NC_000019.10:g.38920940CA[3], NC_000019.10:g.38920940CA[4], NC_000019.10:g.38920940CA[5], NC_000019.10:g.38920940CA[7], NC_000019.9:g.39411580CA[2], NC_000019.9:g.39411580CA[3], NC_000019.9:g.39411580CA[4], NC_000019.9:g.39411580CA[5], NC_000019.9:g.39411580CA[7], NG_031865.1:g.14947GT[2], NG_031865.1:g.14947GT[3], NG_031865.1:g.14947GT[4], NG_031865.1:g.14947GT[5], NG_031865.1:g.14947GT[7], NW_014040929.1:g.330612CA[2], NW_014040929.1:g.330612CA[3], NW_014040929.1:g.330612CA[4], NW_014040929.1:g.330612CA[5], NW_014040929.1:g.330612CA[7]

Select item 149082371714.

rs1490823717 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:38927042 (GRCh38)
19:39417682 (GRCh37)
Canonical SPDI:: NC_000019.10:38927041:T:C
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.38927042T>C, NC_000019.9:g.39417682T>C, NG_031865.1:g.8855A>G, NG_029222.1:g.1335T>C, NW_014040929.1:g.336714T>C

Select item 149076453615.

rs1490764536 has merged into rs796941097 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>-,AA,AAA,AAAA [Show Flanks]
Chromosome:: 19:38919126 (GRCh38)
19:39409766 (GRCh37)
Canonical SPDI:: NC_000019.10:38919125:AAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:38919125:AAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:38919125:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:38919125:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
AAA=0.000004/1 (TOPMED)
-=0.002089/35 (TOMMO)
HGVS:: NC_000019.10:g.38919138del, NC_000019.10:g.38919138dup, NC_000019.10:g.38919137_38919138dup, NC_000019.10:g.38919136_38919138dup, NC_000019.9:g.39409778del, NC_000019.9:g.39409778dup, NC_000019.9:g.39409777_39409778dup, NC_000019.9:g.39409776_39409778dup, NG_031865.1:g.16771del, NG_031865.1:g.16771dup, NG_031865.1:g.16770_16771dup, NG_031865.1:g.16769_16771dup, NW_014040929.1:g.328810del, NW_014040929.1:g.328810dup, NW_014040929.1:g.328809_328810dup, NW_014040929.1:g.328808_328810dup

Select item 149060193816.

rs1490601938 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:38926710 (GRCh38)
19:39417350 (GRCh37)
Canonical SPDI:: NC_000019.10:38926709:C:T
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.38926710C>T, NC_000019.9:g.39417350C>T, NG_031865.1:g.9187G>A, NG_029222.1:g.1003C>T, NW_014040929.1:g.336382C>T

Select item 149045846717.

rs1490458467 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 19:38923238 (GRCh38)
19:39413879 (GRCh37)
Canonical SPDI:: NC_000019.10:38923238::G
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000016/2 (GnomAD)
HGVS:: NC_000019.10:g.38923238_38923239insG, NC_000019.9:g.39413878_39413879insG, NG_031865.1:g.12658_12659insC, NW_014040929.1:g.332910_332911insG

Select item 149044717318.

rs1490447173 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:38921365 (GRCh38)
19:39412005 (GRCh37)
Canonical SPDI:: NC_000019.10:38921364:A:G
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.38921365A>G, NC_000019.9:g.39412005A>G, NG_031865.1:g.14532T>C, NW_014040929.1:g.331037A>G

Select item 149033281919.

rs1490332819 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:38927473 (GRCh38)
19:39418113 (GRCh37)
Canonical SPDI:: NC_000019.10:38927472:T:C
Gene:: SARS2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000342/1 (KOREAN)
HGVS:: NC_000019.10:g.38927473T>C, NC_000019.9:g.39418113T>C, NG_031865.1:g.8424A>G, NG_029222.1:g.1766T>C, NW_014040929.1:g.337145T>C

Select item 149025875020.

rs1490258750 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:38915117 (GRCh38)
19:39405757 (GRCh37)
Canonical SPDI:: NC_000019.10:38915116:G:A
Gene:: SARS2 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.38915117G>A, NC_000019.9:g.39405757G>A, NG_031865.1:g.20780C>T, NW_014040929.1:g.324789G>A

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