SNP Links for Nucleotide (Select 211904170) - SNP

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Select item 14915359961.

rs1491535996 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACA>-,CACACA [Show Flanks]
Chromosome:: 11:35162903 (GRCh38)
11:35184450 (GRCh37)
Canonical SPDI:: NC_000011.10:35162894:CACACACACACA:CACACACA,NC_000011.10:35162894:CACACACACACA:CACACACACACACA
Gene:: CD44 (Varview), SNORD164 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACACACACACACA=0./0 (ALFA)
HGVS:: NC_000011.10:g.35162895CA[4], NC_000011.10:g.35162895CA[7], NC_000011.9:g.35184442CA[4], NC_000011.9:g.35184442CA[7], NG_008937.1:g.29026CA[4], NG_008937.1:g.29026CA[7]

Select item 14915355892.

rs1491535589 has merged into rs35217950 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,TT,TTTTTT [Show Flanks]
Chromosome:: 11:35167272 (GRCh38)
11:35188819 (GRCh37)
Canonical SPDI:: NC_000011.10:35167270:TTTTT:T,NC_000011.10:35167270:TTTTT:TTT,NC_000011.10:35167270:TTTTT:TTTTTTT
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
TT=0.000015/2 (GnomAD)
HGVS:: NC_000011.10:g.35167272_35167275del, NC_000011.10:g.35167274_35167275del, NC_000011.10:g.35167274_35167275dup, NC_000011.9:g.35188819_35188822del, NC_000011.9:g.35188821_35188822del, NC_000011.9:g.35188821_35188822dup, NG_008937.1:g.33403_33406del, NG_008937.1:g.33405_33406del, NG_008937.1:g.33405_33406dup

Select item 14915331383.

rs1491533138 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 11:35181874 (GRCh38)
11:35203422 (GRCh37)
Canonical SPDI:: NC_000011.10:35181874::A
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000011.10:g.35181874_35181875insA, NC_000011.9:g.35203421_35203422insA, NG_008937.1:g.48005_48006insA

Select item 14915216574.

rs1491521657 has merged into rs57790931 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGTGTGTGTGTGTGT>-,GT,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
Chromosome:: 11:35211690 (GRCh38)
11:35233237 (GRCh37)
Canonical SPDI:: NC_000011.10:35211674:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT,NC_000011.10:35211674:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT,NC_000011.10:35211674:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT,NC_000011.10:35211674:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT,NC_000011.10:35211674:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT,NC_000011.10:35211674:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT,NC_000011.10:35211674:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000011.10:35211674:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000011.10:35211674:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000011.10:35211674:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000011.10:35211674:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000011.10:35211674:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Gene:: CD44 (Varview), CD44-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGTGTGTGTGT=0./0 (ALFA)
-=0.184/709 (ALSPAC)
-=0.3265/1635 (1000Genomes)
HGVS:: NC_000011.10:g.35211676GT[7], NC_000011.10:g.35211676GT[8], NC_000011.10:g.35211676GT[9], NC_000011.10:g.35211676GT[10], NC_000011.10:g.35211676GT[11], NC_000011.10:g.35211676GT[12], NC_000011.10:g.35211676GT[13], NC_000011.10:g.35211676GT[14], NC_000011.10:g.35211676GT[16], NC_000011.10:g.35211676GT[17], NC_000011.10:g.35211676GT[18], NC_000011.10:g.35211676GT[20], NC_000011.9:g.35233223GT[7], NC_000011.9:g.35233223GT[8], NC_000011.9:g.35233223GT[9], NC_000011.9:g.35233223GT[10], NC_000011.9:g.35233223GT[11], NC_000011.9:g.35233223GT[12], NC_000011.9:g.35233223GT[13], NC_000011.9:g.35233223GT[14], NC_000011.9:g.35233223GT[16], NC_000011.9:g.35233223GT[17], NC_000011.9:g.35233223GT[18], NC_000011.9:g.35233223GT[20], NG_008937.1:g.77807GT[7], NG_008937.1:g.77807GT[8], NG_008937.1:g.77807GT[9], NG_008937.1:g.77807GT[10], NG_008937.1:g.77807GT[11], NG_008937.1:g.77807GT[12], NG_008937.1:g.77807GT[13], NG_008937.1:g.77807GT[14], NG_008937.1:g.77807GT[16], NG_008937.1:g.77807GT[17], NG_008937.1:g.77807GT[18], NG_008937.1:g.77807GT[20]

Select item 14914985865.

rs1491498586 [Homo sapiens]

Variant type:: DELINS
Alleles:: TG>- [Show Flanks]
Chromosome:: 11:35206669 (GRCh38)
11:35228216 (GRCh37)
Canonical SPDI:: NC_000011.10:35206667:GTG:G
Gene:: CD44 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.00051/6 (ALFA)
-=0.00091/55 (GnomAD)
HGVS:: NC_000011.10:g.35206669_35206670del, NC_000011.9:g.35228216_35228217del, NG_008937.1:g.72800_72801del

Select item 14914701636.

rs1491470163 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 11:35211674 (GRCh38)
11:35233221 (GRCh37)
Canonical SPDI:: NC_000011.10:35211673:AT:
Gene:: CD44 (Varview), CD44-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.0001/7 (GnomAD)
HGVS:: NC_000011.10:g.35211674_35211675del, NC_000011.9:g.35233221_35233222del, NG_008937.1:g.77805_77806del

Select item 14914667587.

rs1491466758 has merged into rs1485501959 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATATATAT>-,ATATAT,ATATATATAT [Show Flanks]
Chromosome:: 11:35181674 (GRCh38)
11:35203221 (GRCh37)
Canonical SPDI:: NC_000011.10:35181669:ATATATATATAT:ATAT,NC_000011.10:35181669:ATATATATATAT:ATATATATAT,NC_000011.10:35181669:ATATATATATAT:ATATATATATATAT
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATATATAT=0./0 (ALFA)
-=0.00991/18 (Korea1K)
HGVS:: NC_000011.10:g.35181670AT[2], NC_000011.10:g.35181670AT[5], NC_000011.10:g.35181670AT[7], NC_000011.9:g.35203217AT[2], NC_000011.9:g.35203217AT[5], NC_000011.9:g.35203217AT[7], NG_008937.1:g.47801AT[2], NG_008937.1:g.47801AT[5], NG_008937.1:g.47801AT[7]

Select item 14914533448.

rs1491453344 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATATATATTTAT>-,ATATATATTTATATATATATTTAT [Show Flanks]
Chromosome:: 11:35181686 (GRCh38)
11:35203233 (GRCh37)
Canonical SPDI:: NC_000011.10:35181670:TATATATATATTTATATATATATTTAT:TATATATATATTTAT,NC_000011.10:35181670:TATATATATATTTATATATATATTTAT:TATATATATATTTATATATATATTTATATATATATTTAT
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATATTTATATATATATTTATATATATATTTAT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.00006/1 (TOMMO)
TATATATATATT=0.000076/9 (GnomAD)
HGVS:: NC_000011.10:g.35181674ATATATATTTAT[1], NC_000011.10:g.35181674ATATATATTTAT[3], NC_000011.9:g.35203221ATATATATTTAT[1], NC_000011.9:g.35203221ATATATATTTAT[3], NG_008937.1:g.47805ATATATATTTAT[1], NG_008937.1:g.47805ATATATATTTAT[3]

Select item 14914416129.

rs1491441612 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 11:35181874 (GRCh38)
11:35203421 (GRCh37)
Canonical SPDI:: NC_000011.10:35181873:TT:
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00015/11 (GnomAD)
HGVS:: NC_000011.10:g.35181874_35181875del, NC_000011.9:g.35203421_35203422del, NG_008937.1:g.48005_48006del

Select item 149141689910.

rs1491416899 [Homo sapiens]

Variant type:: DELINS
Alleles:: GG>- [Show Flanks]
Chromosome:: 11:35223507 (GRCh38)
11:35245054 (GRCh37)
Canonical SPDI:: NC_000011.10:35223505:GGG:G
Gene:: CD44 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,downstream_transcript_variant,intron_variant
Validated:: by frequency
MAF:: -=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.35223507_35223508del, NC_000011.9:g.35245054_35245055del, NG_008937.1:g.89638_89639del

Select item 149140380611.

rs1491403806 has merged into rs55982807 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATATATATA>-,TATA,TATATA,TATATATA,TATATATATATA,TATATATATATATA,TATATATATATATATA,TATATATATATATATATA [Show Flanks]
Chromosome:: 11:35222608 (GRCh38)
11:35244155 (GRCh37)
Canonical SPDI:: NC_000011.10:35222598:ATATATATATATATATATA:ATATATATA,NC_000011.10:35222598:ATATATATATATATATATA:ATATATATATATA,NC_000011.10:35222598:ATATATATATATATATATA:ATATATATATATATA,NC_000011.10:35222598:ATATATATATATATATATA:ATATATATATATATATA,NC_000011.10:35222598:ATATATATATATATATATA:ATATATATATATATATATATA,NC_000011.10:35222598:ATATATATATATATATATA:ATATATATATATATATATATATA,NC_000011.10:35222598:ATATATATATATATATATA:ATATATATATATATATATATATATA,NC_000011.10:35222598:ATATATATATATATATATA:ATATATATATATATATATATATATATA
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATATATATA=0./0 (ALFA)
-=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.35222600TA[4], NC_000011.10:g.35222600TA[6], NC_000011.10:g.35222600TA[7], NC_000011.10:g.35222600TA[8], NC_000011.10:g.35222600TA[10], NC_000011.10:g.35222600TA[11], NC_000011.10:g.35222600TA[12], NC_000011.10:g.35222600TA[13], NC_000011.9:g.35244147TA[4], NC_000011.9:g.35244147TA[6], NC_000011.9:g.35244147TA[7], NC_000011.9:g.35244147TA[8], NC_000011.9:g.35244147TA[10], NC_000011.9:g.35244147TA[11], NC_000011.9:g.35244147TA[12], NC_000011.9:g.35244147TA[13], NG_008937.1:g.88731TA[4], NG_008937.1:g.88731TA[6], NG_008937.1:g.88731TA[7], NG_008937.1:g.88731TA[8], NG_008937.1:g.88731TA[10], NG_008937.1:g.88731TA[11], NG_008937.1:g.88731TA[12], NG_008937.1:g.88731TA[13], NM_001202557.2:c.*222TA[4], NM_001202557.2:c.*222TA[6], NM_001202557.2:c.*222TA[7], NM_001202557.2:c.*222TA[8], NM_001202557.2:c.*222TA[10], NM_001202557.2:c.*222TA[11], NM_001202557.2:c.*222TA[12], NM_001202557.2:c.*222TA[13], NM_001202557.1:c.*222TA[4], NM_001202557.1:c.*222TA[6], NM_001202557.1:c.*222TA[7], NM_001202557.1:c.*222TA[8], NM_001202557.1:c.*222TA[10], NM_001202557.1:c.*222TA[11], NM_001202557.1:c.*222TA[12], NM_001202557.1:c.*222TA[13]

Select item 149139589612.

rs1491395896 has merged into rs371766266 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>-,TATA [Show Flanks]
Chromosome:: 11:35181953 (GRCh38)
11:35203500 (GRCh37)
Canonical SPDI:: NC_000011.10:35181945:ATATATATA:ATATATA,NC_000011.10:35181945:ATATATATA:ATATATATATA
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATATA=0.01458/213 (ALFA)
-=0.00004/1 (TOMMO)
AT=0.04872/244 (1000Genomes)
HGVS:: NC_000011.10:g.35181947TA[3], NC_000011.10:g.35181947TA[5], NC_000011.9:g.35203494TA[3], NC_000011.9:g.35203494TA[5], NG_008937.1:g.48078TA[3], NG_008937.1:g.48078TA[5]

Select item 149134572213.

rs1491345722 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 11:35175865 (GRCh38)
11:35197413 (GRCh37)
Canonical SPDI:: NC_000011.10:35175865:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000011.10:g.35175866_35175883T[30]GTTTTTTTTTTTTTTTTTT[1], NC_000011.9:g.35197413_35197430T[30]GTTTTTTTTTTTTTTTTTT[1], NG_008937.1:g.41997_42014T[30]GTTTTTTTTTTTTTTTTTT[1]

Select item 149133080814.

rs1491330808 has merged into rs1247958127 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA [Show Flanks]
Chromosome:: 11:35181935 (GRCh38)
11:35203482 (GRCh37)
Canonical SPDI:: NC_000011.10:35181933:AAA:A,NC_000011.10:35181933:AAA:AA,NC_000011.10:35181933:AAA:AAAA
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
HGVS:: NC_000011.10:g.35181935_35181936del, NC_000011.10:g.35181936del, NC_000011.10:g.35181936dup, NC_000011.9:g.35203482_35203483del, NC_000011.9:g.35203483del, NC_000011.9:g.35203483dup, NG_008937.1:g.48066_48067del, NG_008937.1:g.48067del, NG_008937.1:g.48067dup

Select item 149132926015.

rs1491329260 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 11:35181945 (GRCh38)
11:35203492 (GRCh37)
Canonical SPDI:: NC_000011.10:35181944:AA:
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00037/6 (ALFA)
-=0.00011/2 (TOMMO)
-=0.00066/51 (GnomAD)
-=0.00406/26 (1000Genomes)
HGVS:: NC_000011.10:g.35181945_35181946del, NC_000011.9:g.35203492_35203493del, NG_008937.1:g.48076_48077del

Select item 149124620116.

rs1491246201 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATATATATAAATATTATATATTATATATAAATTT>-,TATATATATAAATATTATATATTATATATAAATTTTATATATATAAATATTATATATTATATATAAATTT [Show Flanks]
Chromosome:: 11:35181960 (GRCh38)
11:35203507 (GRCh37)
Canonical SPDI:: NC_000011.10:35181946:TATATATAAATTTTATATATATAAATATTATATATTATATATAAATTT:TATATATAAATTT,NC_000011.10:35181946:TATATATAAATTTTATATATATAAATATTATATATTATATATAAATTT:TATATATAAATTTTATATATATAAATATTATATATTATATATAAATTTTATATATATAAATATTATATATTATATATAAATTT
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATAAATTTTATATATATAAATATTATATATTATATATAAATTTTATATATATAAATATTATATATTATATATAAATTT=0./0 (ALFA)
TATATATAAATTTTATATATATAAATATTATATAT=0.05681/943 (TOMMO)
TATATATAAATTTTATATATATAAATATTATATAT=0.05833/91 (Korea1K)
HGVS:: NC_000011.10:g.35181960_35181994del, NC_000011.10:g.35181960_35181994dup, NC_000011.9:g.35203507_35203541del, NC_000011.9:g.35203507_35203541dup, NG_008937.1:g.48091_48125del, NG_008937.1:g.48091_48125dup

Select item 149123785017.

rs1491237850 has merged into rs71457374 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,TT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 11:35175873 (GRCh38)
11:35197420 (GRCh37)
Canonical SPDI:: NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35175864:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
-=0.000034/9 (TOPMED)
HGVS:: NC_000011.10:g.35175873_35175883del, NC_000011.10:g.35175875_35175883del, NC_000011.10:g.35175877_35175883del, NC_000011.10:g.35175879_35175883del, NC_000011.10:g.35175880_35175883del, NC_000011.10:g.35175881_35175883del, NC_000011.10:g.35175882_35175883del, NC_000011.10:g.35175883del, NC_000011.10:g.35175883dup, NC_000011.10:g.35175882_35175883dup, NC_000011.10:g.35175881_35175883dup, NC_000011.10:g.35175880_35175883dup, NC_000011.10:g.35175879_35175883dup, NC_000011.10:g.35175878_35175883dup, NC_000011.10:g.35175876_35175883dup, NC_000011.9:g.35197420_35197430del, NC_000011.9:g.35197422_35197430del, NC_000011.9:g.35197424_35197430del, NC_000011.9:g.35197426_35197430del, NC_000011.9:g.35197427_35197430del, NC_000011.9:g.35197428_35197430del, NC_000011.9:g.35197429_35197430del, NC_000011.9:g.35197430del, NC_000011.9:g.35197430dup, NC_000011.9:g.35197429_35197430dup, NC_000011.9:g.35197428_35197430dup, NC_000011.9:g.35197427_35197430dup, NC_000011.9:g.35197426_35197430dup, NC_000011.9:g.35197425_35197430dup, NC_000011.9:g.35197423_35197430dup, NG_008937.1:g.42004_42014del, NG_008937.1:g.42006_42014del, NG_008937.1:g.42008_42014del, NG_008937.1:g.42010_42014del, NG_008937.1:g.42011_42014del, NG_008937.1:g.42012_42014del, NG_008937.1:g.42013_42014del, NG_008937.1:g.42014del, NG_008937.1:g.42014dup, NG_008937.1:g.42013_42014dup, NG_008937.1:g.42012_42014dup, NG_008937.1:g.42011_42014dup, NG_008937.1:g.42010_42014dup, NG_008937.1:g.42009_42014dup, NG_008937.1:g.42007_42014dup

Select item 149115437218.

rs1491154372 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 11:35199935 (GRCh38)
11:35221483 (GRCh37)
Canonical SPDI:: NC_000011.10:35199935::G
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.35199935_35199936insG, NC_000011.9:g.35221482_35221483insG, NG_008937.1:g.66066_66067insG

Select item 149113160519.

rs1491131605 has merged into rs60509735 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTATTTTTTTAATTTTTTTTGTATTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTATTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 11:35199946 (GRCh38)
11:35221493 (GRCh37)
Canonical SPDI:: NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTAATTTTTTTTGTATTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:35199934:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
TTTTT=0.3201/1603 (1000Genomes)
-=0.425/17 (GENOME_DK)
HGVS:: NC_000011.10:g.35199946_35199961del, NC_000011.10:g.35199948_35199961del, NC_000011.10:g.35199949_35199961del, NC_000011.10:g.35199950_35199961del, NC_000011.10:g.35199951_35199961del, NC_000011.10:g.35199952_35199961del, NC_000011.10:g.35199953_35199961del, NC_000011.10:g.35199954_35199961del, NC_000011.10:g.35199955_35199961del, NC_000011.10:g.35199956_35199961del, NC_000011.10:g.35199957_35199961del, NC_000011.10:g.35199958_35199961del, NC_000011.10:g.35199959_35199961del, NC_000011.10:g.35199960_35199961del, NC_000011.10:g.35199961del, NC_000011.10:g.35199961dup, NC_000011.10:g.35199960_35199961dup, NC_000011.10:g.35199935_35199961T[29]ATTTTTTTAATTTTTTTTGTATTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000011.10:g.35199959_35199961dup, NC_000011.10:g.35199958_35199961dup, NC_000011.10:g.35199935_35199961T[31]ATTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000011.10:g.35199957_35199961dup, NC_000011.10:g.35199956_35199961dup, NC_000011.10:g.35199955_35199961dup, NC_000011.10:g.35199954_35199961dup, NC_000011.10:g.35199953_35199961dup, NC_000011.10:g.35199952_35199961dup, NC_000011.10:g.35199951_35199961dup, NC_000011.10:g.35199950_35199961dup, NC_000011.10:g.35199949_35199961dup, NC_000011.10:g.35199948_35199961dup, NC_000011.10:g.35199947_35199961dup, NC_000011.10:g.35199935_35199961T[42]CCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000011.10:g.35199945_35199961dup, NC_000011.10:g.35199943_35199961dup, NC_000011.10:g.35199941_35199961dup, NC_000011.10:g.35199940_35199961dup, NC_000011.10:g.35199939_35199961dup, NC_000011.10:g.35199938_35199961dup, NC_000011.10:g.35199935_35199961T[51]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000011.10:g.35199961_35199962insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.35221493_35221508del, NC_000011.9:g.35221495_35221508del, NC_000011.9:g.35221496_35221508del, NC_000011.9:g.35221497_35221508del, NC_000011.9:g.35221498_35221508del, NC_000011.9:g.35221499_35221508del, NC_000011.9:g.35221500_35221508del, NC_000011.9:g.35221501_35221508del, NC_000011.9:g.35221502_35221508del, NC_000011.9:g.35221503_35221508del, NC_000011.9:g.35221504_35221508del, NC_000011.9:g.35221505_35221508del, NC_000011.9:g.35221506_35221508del, NC_000011.9:g.35221507_35221508del, NC_000011.9:g.35221508del, NC_000011.9:g.35221508dup, NC_000011.9:g.35221507_35221508dup, NC_000011.9:g.35221482_35221508T[29]ATTTTTTTAATTTTTTTTGTATTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000011.9:g.35221506_35221508dup, NC_000011.9:g.35221505_35221508dup, NC_000011.9:g.35221482_35221508T[31]ATTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000011.9:g.35221504_35221508dup, NC_000011.9:g.35221503_35221508dup, NC_000011.9:g.35221502_35221508dup, NC_000011.9:g.35221501_35221508dup, NC_000011.9:g.35221500_35221508dup, NC_000011.9:g.35221499_35221508dup, NC_000011.9:g.35221498_35221508dup, NC_000011.9:g.35221497_35221508dup, NC_000011.9:g.35221496_35221508dup, NC_000011.9:g.35221495_35221508dup, NC_000011.9:g.35221494_35221508dup, NC_000011.9:g.35221482_35221508T[42]CCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000011.9:g.35221492_35221508dup, NC_000011.9:g.35221490_35221508dup, NC_000011.9:g.35221488_35221508dup, NC_000011.9:g.35221487_35221508dup, NC_000011.9:g.35221486_35221508dup, NC_000011.9:g.35221485_35221508dup, NC_000011.9:g.35221482_35221508T[51]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000011.9:g.35221508_35221509insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_008937.1:g.66077_66092del, NG_008937.1:g.66079_66092del, NG_008937.1:g.66080_66092del, NG_008937.1:g.66081_66092del, NG_008937.1:g.66082_66092del, NG_008937.1:g.66083_66092del, NG_008937.1:g.66084_66092del, NG_008937.1:g.66085_66092del, NG_008937.1:g.66086_66092del, NG_008937.1:g.66087_66092del, NG_008937.1:g.66088_66092del, NG_008937.1:g.66089_66092del, NG_008937.1:g.66090_66092del, NG_008937.1:g.66091_66092del, NG_008937.1:g.66092del, NG_008937.1:g.66092dup, NG_008937.1:g.66091_66092dup, NG_008937.1:g.66066_66092T[29]ATTTTTTTAATTTTTTTTGTATTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_008937.1:g.66090_66092dup, NG_008937.1:g.66089_66092dup, NG_008937.1:g.66066_66092T[31]ATTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_008937.1:g.66088_66092dup, NG_008937.1:g.66087_66092dup, NG_008937.1:g.66086_66092dup, NG_008937.1:g.66085_66092dup, NG_008937.1:g.66084_66092dup, NG_008937.1:g.66083_66092dup, NG_008937.1:g.66082_66092dup, NG_008937.1:g.66081_66092dup, NG_008937.1:g.66080_66092dup, NG_008937.1:g.66079_66092dup, NG_008937.1:g.66078_66092dup, NG_008937.1:g.66066_66092T[42]CCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_008937.1:g.66076_66092dup, NG_008937.1:g.66074_66092dup, NG_008937.1:g.66072_66092dup, NG_008937.1:g.66071_66092dup, NG_008937.1:g.66070_66092dup, NG_008937.1:g.66069_66092dup, NG_008937.1:g.66066_66092T[51]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_008937.1:g.66092_66093insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149112650420.

rs1491126504 [Homo sapiens]

Variant type:: INS
Alleles:: ->G,GAATATATAG,T,TAG,TAGAATATATAG,TAGAATATATAT,TATAATATATAG,TATAATATATAT,TATGAATTATATATAATATATATTATATATTATATATTATATATATG,TATTATATATATATATATATTATATATATAGAATATATAG,TATTATATATATATATTATATTATATATAGAATATATAG,TATTATATATATATATTATATTATATATATAGAATATATAG,TATTATATATTATATATTATAATATATATATAGAATATATAG,TATTATATATTATATATTATAATATATATATATTATATATATATATTATATTATATATATAGAATATATAG,TATTATATATTATATATTATAATATATATATATTATATATATATATTATATTATATATATATAATATATAG,TATTATATATTATATATTATATATAGAATATATAG,TG,TTATATTATATAGATAGAATATATAG,TTATTTTATATATATAGAATATATAT [Show Flanks]
Chromosome:: 11:35181934 (GRCh38)
11:35203482 (GRCh37)
Canonical SPDI:: NC_000011.10:35181934::G,NC_000011.10:35181934::GAATATATAG,NC_000011.10:35181934::T,NC_000011.10:35181934::TAG,NC_000011.10:35181934::TAGAATATATAG,NC_000011.10:35181934::TAGAATATATAT,NC_000011.10:35181934::TATAATATATAG,NC_000011.10:35181934::TATAATATATAT,NC_000011.10:35181934::TATGAATTATATATAATATATATTATATATTATATATTATATATATG,NC_000011.10:35181934::TATTATATATATATATATATTATATATATAGAATATATAG,NC_000011.10:35181934::TATTATATATATATATTATATTATATATAGAATATATAG,NC_000011.10:35181934::TATTATATATATATATTATATTATATATATAGAATATATAG,NC_000011.10:35181934::TATTATATATTATATATTATAATATATATATAGAATATATAG,NC_000011.10:35181934::TATTATATATTATATATTATAATATATATATATTATATATATATATTATATTATATATATAGAATATATAG,NC_000011.10:35181934::TATTATATATTATATATTATAATATATATATATTATATATATATATTATATTATATATATATAATATATAG,NC_000011.10:35181934::TATTATATATTATATATTATATATAGAATATATAG,NC_000011.10:35181934::TG,NC_000011.10:35181934::TTATATTATATAGATAGAATATATAG,NC_000011.10:35181934::TTATTTTATATATATAGAATATATAT
Gene:: CD44 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAATATATAG=0./0 (ALFA)
G=0.00018/3 (TOMMO)
HGVS:: NC_000011.10:g.35181934_35181935insG, NC_000011.10:g.35181934_35181935insGAATATATAG, NC_000011.10:g.35181934_35181935insT, NC_000011.10:g.35181934_35181935insTAG, NC_000011.10:g.35181934_35181935insTAGAATATATAG, NC_000011.10:g.35181934_35181935insTAGAATATATAT, NC_000011.10:g.35181934_35181935insTATAATATATAG, NC_000011.10:g.35181934_35181935insTATAATATATAT, NC_000011.10:g.35181934_35181935insTATGAATTATATATAATATATATTATATATTATATATTATATATATG, NC_000011.10:g.35181934_35181935insTATTATATATATATATATATTATATATATAGAATATATAG, NC_000011.10:g.35181934_35181935insTATTATATATATATATTATATTATATATAGAATATATAG, NC_000011.10:g.35181934_35181935insTATTATATATATATATTATATTATATATATAGAATATATAG, NC_000011.10:g.35181934_35181935insTATTATATATTATATATTATAATATATATATAGAATATATAG, NC_000011.10:g.35181934_35181935insTATTATATATTATATATTATAATATATATATATTATATATATATATTATATTATATATATAGAATATATAG, NC_000011.10:g.35181934_35181935insTATTATATATTATATATTATAATATATATATATTATATATATATATTATATTATATATATATAATATATAG, NC_000011.10:g.35181934_35181935insTATTATATATTATATATTATATATAGAATATATAG, NC_000011.10:g.35181934_35181935insTG, NC_000011.10:g.35181934_35181935insTTATATTATATAGATAGAATATATAG, NC_000011.10:g.35181934_35181935insTTATTTTATATATATAGAATATATAT, NC_000011.9:g.35203481_35203482insG, NC_000011.9:g.35203481_35203482insGAATATATAG, NC_000011.9:g.35203481_35203482insT, NC_000011.9:g.35203481_35203482insTAG, NC_000011.9:g.35203481_35203482insTAGAATATATAG, NC_000011.9:g.35203481_35203482insTAGAATATATAT, NC_000011.9:g.35203481_35203482insTATAATATATAG, NC_000011.9:g.35203481_35203482insTATAATATATAT, NC_000011.9:g.35203481_35203482insTATGAATTATATATAATATATATTATATATTATATATTATATATATG, NC_000011.9:g.35203481_35203482insTATTATATATATATATATATTATATATATAGAATATATAG, NC_000011.9:g.35203481_35203482insTATTATATATATATATTATATTATATATAGAATATATAG, NC_000011.9:g.35203481_35203482insTATTATATATATATATTATATTATATATATAGAATATATAG, NC_000011.9:g.35203481_35203482insTATTATATATTATATATTATAATATATATATAGAATATATAG, NC_000011.9:g.35203481_35203482insTATTATATATTATATATTATAATATATATATATTATATATATATATTATATTATATATATAGAATATATAG, NC_000011.9:g.35203481_35203482insTATTATATATTATATATTATAATATATATATATTATATATATATATTATATTATATATATATAATATATAG, NC_000011.9:g.35203481_35203482insTATTATATATTATATATTATATATAGAATATATAG, NC_000011.9:g.35203481_35203482insTG, NC_000011.9:g.35203481_35203482insTTATATTATATAGATAGAATATATAG, NC_000011.9:g.35203481_35203482insTTATTTTATATATATAGAATATATAT, NG_008937.1:g.48065_48066insG, NG_008937.1:g.48065_48066insGAATATATAG, NG_008937.1:g.48065_48066insT, NG_008937.1:g.48065_48066insTAG, NG_008937.1:g.48065_48066insTAGAATATATAG, NG_008937.1:g.48065_48066insTAGAATATATAT, NG_008937.1:g.48065_48066insTATAATATATAG, NG_008937.1:g.48065_48066insTATAATATATAT, NG_008937.1:g.48065_48066insTATGAATTATATATAATATATATTATATATTATATATTATATATATG, NG_008937.1:g.48065_48066insTATTATATATATATATATATTATATATATAGAATATATAG, NG_008937.1:g.48065_48066insTATTATATATATATATTATATTATATATAGAATATATAG, NG_008937.1:g.48065_48066insTATTATATATATATATTATATTATATATATAGAATATATAG, NG_008937.1:g.48065_48066insTATTATATATTATATATTATAATATATATATAGAATATATAG, NG_008937.1:g.48065_48066insTATTATATATTATATATTATAATATATATATATTATATATATATATTATATTATATATATAGAATATATAG, NG_008937.1:g.48065_48066insTATTATATATTATATATTATAATATATATATATTATATATATATATTATATTATATATATATAATATATAG, NG_008937.1:g.48065_48066insTATTATATATTATATATTATATATAGAATATATAG, NG_008937.1:g.48065_48066insTG, NG_008937.1:g.48065_48066insTTATATTATATAGATAGAATATATAG, NG_008937.1:g.48065_48066insTTATTTTATATATATAGAATATATAT

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