SNP Links for Nucleotide (Select 223029496) - SNP

Links from Nucleotide

Items: 1 to 20 of 812

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Select item 14911072651.

rs1491107265 [Homo sapiens]

Variant type:: DEL
Alleles:: AG>- [Show Flanks]
Chromosome:: 15:30211729 (GRCh38)
15:30503932 (GRCh37)
Canonical SPDI:: NC_000015.10:30211728:AG:
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.30211729_30211730del, NC_000015.9:g.30503932_30503933del, NW_011332701.1:g.2384164_2384165del, NT_187660.1:g.2496648_2496649del, NR_026771.1:n.1449_1450del

Select item 14903591772.

rs1490359177 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 15:30196096 (GRCh38)
15:30488299 (GRCh37)
Canonical SPDI:: NC_000015.10:30196095:C:A,NC_000015.10:30196095:C:T
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000015.10:g.30196096C>A, NC_000015.10:g.30196096C>T, NC_000015.9:g.30488299C>A, NC_000015.9:g.30488299C>T, NW_011332701.1:g.2368532C>A, NW_011332701.1:g.2368532C>T, NT_187660.1:g.2481016C>A, NT_187660.1:g.2481016C>T, NR_026771.1:n.61C>A, NR_026771.1:n.61C>T

Select item 14894677973.

rs1489467797 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:30213453 (GRCh38)
15:30505656 (GRCh37)
Canonical SPDI:: NC_000015.10:30213452:A:G
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.30213453A>G, NC_000015.9:g.30505656A>G, NW_011332701.1:g.2385889A>G, NT_187660.1:g.2498373A>G, NR_026771.1:n.3173A>G

Select item 14892610444.

rs1489261044 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:30214457 (GRCh38)
15:30506660 (GRCh37)
Canonical SPDI:: NC_000015.10:30214456:C:T
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000037/5 (GnomAD)
HGVS:: NC_000015.10:g.30214457C>T, NC_000015.9:g.30506660C>T, NW_011332701.1:g.2386893C>T, NT_187660.1:g.2499377C>T, NR_026771.1:n.4177C>T

Select item 14892276895.

rs1489227689 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:30213114 (GRCh38)
15:30505317 (GRCh37)
Canonical SPDI:: NC_000015.10:30213113:C:T
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000022/3 (GnomAD)
HGVS:: NC_000015.10:g.30213114C>T, NC_000015.9:g.30505317C>T, NW_011332701.1:g.2385550C>T, NT_187660.1:g.2498034C>T, NR_026771.1:n.2834C>T

Select item 14890665646.

rs1489066564 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 15:30210578 (GRCh38)
15:30502781 (GRCh37)
Canonical SPDI:: NC_000015.10:30210577:C:G
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000015.10:g.30210578C>G, NC_000015.9:g.30502781C>G, NW_011332701.1:g.2383013C>G, NT_187660.1:g.2495497C>G, NR_026771.1:n.298C>G

Select item 14882496237.

rs1488249623 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATATGTATAT>- [Show Flanks]
Chromosome:: 15:30212685 (GRCh38)
15:30504888 (GRCh37)
Canonical SPDI:: NC_000015.10:30212677:TGTATATATATGTATAT:TGTATAT
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTATAT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.000016/2 (GnomAD)
HGVS:: NC_000015.10:g.30212685_30212694del, NC_000015.9:g.30504888_30504897del, NW_011332701.1:g.2385120_2385129del, NT_187660.1:g.2497604_2497613del, NR_026771.1:n.2405_2414del

Select item 14880987818.

rs1488098781 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:30210494 (GRCh38)
15:30502697 (GRCh37)
Canonical SPDI:: NC_000015.10:30210493:G:A
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
A=0.000022/3 (GnomAD_exomes)
HGVS:: NC_000015.10:g.30210494G>A, NC_000015.9:g.30502697G>A, NW_011332701.1:g.2382929G>A, NT_187660.1:g.2495413G>A, NR_026771.1:n.214G>A

Select item 14875128229.

rs1487512822 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 15:30212601 (GRCh38)
15:30504804 (GRCh37)
Canonical SPDI:: NC_000015.10:30212600:G:T
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000015.10:g.30212601G>T, NC_000015.9:g.30504804G>T, NW_011332701.1:g.2385036G>T, NT_187660.1:g.2497520G>T, NR_026771.1:n.2321G>T

Select item 148728248510.

rs1487282485 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 15:30210568 (GRCh38)
15:30502771 (GRCh37)
Canonical SPDI:: NC_000015.10:30210567:G:C
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000015.10:g.30210568G>C, NC_000015.9:g.30502771G>C, NW_011332701.1:g.2383003G>C, NT_187660.1:g.2495487G>C, NR_026771.1:n.288G>C

Select item 148724903711.

rs1487249037 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:30212159 (GRCh38)
15:30504362 (GRCh37)
Canonical SPDI:: NC_000015.10:30212158:G:A
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000084/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.30212159G>A, NC_000015.9:g.30504362G>A, NW_011332701.1:g.2384594G>A, NT_187660.1:g.2497078G>A, NR_026771.1:n.1879G>A

Select item 148664212712.

rs1486642127 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 15:30212907 (GRCh38)
15:30505110 (GRCh37)
Canonical SPDI:: NC_000015.10:30212906:G:C
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000015.10:g.30212907G>C, NC_000015.9:g.30505110G>C, NW_011332701.1:g.2385342G>C, NT_187660.1:g.2497826G>C, NR_026771.1:n.2627G>C

Select item 148663511013.

rs1486635110 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:30211127 (GRCh38)
15:30503330 (GRCh37)
Canonical SPDI:: NC_000015.10:30211126:C:T
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.00008/1 (ALFA)
HGVS:: NC_000015.10:g.30211127C>T, NC_000015.9:g.30503330C>T, NW_011332701.1:g.2383562C>T, NT_187660.1:g.2496046C>T, NR_026771.1:n.847C>T

Select item 148628127014.

rs1486281270 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:30211646 (GRCh38)
15:30503849 (GRCh37)
Canonical SPDI:: NC_000015.10:30211645:G:A
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.30211646G>A, NC_000015.9:g.30503849G>A, NW_011332701.1:g.2384081G>A, NT_187660.1:g.2496565G>A, NR_026771.1:n.1366G>A

Select item 148529873815.

rs1485298738 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 15:30211264 (GRCh38)
15:30503467 (GRCh37)
Canonical SPDI:: NC_000015.10:30211263:A:C
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.30211264A>C, NC_000015.9:g.30503467A>C, NW_011332701.1:g.2383699A>C, NT_187660.1:g.2496183A>C, NR_026771.1:n.984A>C

Select item 148402392416.

rs1484023924 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:30213691 (GRCh38)
15:30505894 (GRCh37)
Canonical SPDI:: NC_000015.10:30213690:C:T
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000015.10:g.30213691C>T, NC_000015.9:g.30505894C>T, NW_011332701.1:g.2386127C>T, NT_187660.1:g.2498611C>T, NR_026771.1:n.3411C>T

Select item 148338508017.

rs1483385080 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 15:30210664 (GRCh38)
15:30502867 (GRCh37)
Canonical SPDI:: NC_000015.10:30210663:C:A
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000015.10:g.30210664C>A, NC_000015.9:g.30502867C>A, NW_011332701.1:g.2383099C>A, NT_187660.1:g.2495583C>A, NR_026771.1:n.384C>A

Select item 148091950218.

rs1480919502 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:30211355 (GRCh38)
15:30503558 (GRCh37)
Canonical SPDI:: NC_000015.10:30211354:A:G
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000015.10:g.30211355A>G, NC_000015.9:g.30503558A>G, NW_011332701.1:g.2383790A>G, NT_187660.1:g.2496274A>G, NR_026771.1:n.1075A>G

Select item 148026452519.

rs1480264525 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 15:30213164 (GRCh38)
15:30505367 (GRCh37)
Canonical SPDI:: NC_000015.10:30213163:T:G
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.004468/53 (ALFA)
G=0.00619/825 (GnomAD)
G=0.007027/45 (1000Genomes)
HGVS:: NC_000015.10:g.30213164T>G, NC_000015.9:g.30505367T>G, NW_011332701.1:g.2385600T>G, NT_187660.1:g.2498084T>G, NR_026771.1:n.2884T>G

Select item 147946196420.

rs1479461964 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:30213653 (GRCh38)
15:30505856 (GRCh37)
Canonical SPDI:: NC_000015.10:30213652:G:A
Gene:: LINC02249 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.30213653G>A, NC_000015.9:g.30505856G>A, NW_011332701.1:g.2386089G>A, NT_187660.1:g.2498573G>A, NR_026771.1:n.3373G>A

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