SNP Links for Nucleotide (Select 148833516) - SNP

Links from Nucleotide

Items: 1 to 20 of 437

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Select item 14891542191.

rs1489154219 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:33624348 (GRCh38)
9:33624346 (GRCh37)
Canonical SPDI:: NC_000009.12:33624347:G:C
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.33624348G>C, NC_000009.11:g.33624346G>C, NG_001337.2:g.17888G>C, NR_003573.1:n.124G>C

Select item 14875106792.

rs1487510679 [Homo sapiens]

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

Select item 14839784843.

rs1483978484 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:33624660 (GRCh38)
9:33624658 (GRCh37)
Canonical SPDI:: NC_000009.12:33624659:T:C
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.33624660T>C, NC_000009.11:g.33624658T>C, NG_001337.2:g.18200T>C, NR_003573.1:n.436T>C

Select item 14836488694.

rs1483648869 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 9:33625121 (GRCh38)
9:33625119 (GRCh37)
Canonical SPDI:: NC_000009.12:33625120:C:G,NC_000009.12:33625120:C:T
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.33625121C>G, NC_000009.12:g.33625121C>T, NC_000009.11:g.33625119C>G, NC_000009.11:g.33625119C>T, NG_001337.2:g.18661C>G, NG_001337.2:g.18661C>T, NR_003573.1:n.897C>G, NR_003573.1:n.897C>T

Select item 14822669465.

rs1482266946 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 9:33624572 (GRCh38)
9:33624570 (GRCh37)
Canonical SPDI:: NC_000009.12:33624571:T:G
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.33624572T>G, NC_000009.11:g.33624570T>G, NG_001337.2:g.18112T>G, NR_003573.1:n.348T>G

Select item 14810248416.

rs1481024841 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:33624387 (GRCh38)
9:33624385 (GRCh37)
Canonical SPDI:: NC_000009.12:33624386:T:A
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.33624387T>A, NC_000009.11:g.33624385T>A, NG_001337.2:g.17927T>A, NR_003573.1:n.163T>A

Select item 14788163277.

rs1478816327 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:33625356 (GRCh38)
9:33625354 (GRCh37)
Canonical SPDI:: NC_000009.12:33625355:T:C
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.33625356T>C, NC_000009.11:g.33625354T>C, NG_001337.2:g.18896T>C, NR_003573.1:n.1132T>C

Select item 14767771258.

rs1476777125 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:33624405 (GRCh38)
9:33624403 (GRCh37)
Canonical SPDI:: NC_000009.12:33624404:A:G
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.33624405A>G, NC_000009.11:g.33624403A>G, NG_001337.2:g.17945A>G, NR_003573.1:n.181A>G

Select item 14765384129.

rs1476538412 [Homo sapiens]

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

Select item 147380523910.

rs1473805239 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:33624295 (GRCh38)
9:33624293 (GRCh37)
Canonical SPDI:: NC_000009.12:33624294:C:G
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000009.12:g.33624295C>G, NC_000009.11:g.33624293C>G, NG_001337.2:g.17835C>G, NR_003573.1:n.71C>G

Select item 147356646311.

rs1473566463 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:33624781 (GRCh38)
9:33624779 (GRCh37)
Canonical SPDI:: NC_000009.12:33624780:C:T
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.33624781C>T, NC_000009.11:g.33624779C>T, NG_001337.2:g.18321C>T, NR_003573.1:n.557C>T

Select item 147169812212.

rs1471698122 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:33624450 (GRCh38)
9:33624448 (GRCh37)
Canonical SPDI:: NC_000009.12:33624449:T:C
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.33624450T>C, NC_000009.11:g.33624448T>C, NG_001337.2:g.17990T>C, NR_003573.1:n.226T>C

Select item 146678335513.

rs1466783355 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:33625248 (GRCh38)
9:33625246 (GRCh37)
Canonical SPDI:: NC_000009.12:33625247:C:T
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.33625248C>T, NC_000009.11:g.33625246C>T, NG_001337.2:g.18788C>T, NR_003573.1:n.1024C>T

Select item 146594670714.

rs1465946707 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 9:33625339 (GRCh38)
9:33625337 (GRCh37)
Canonical SPDI:: NC_000009.12:33625338:C:G,NC_000009.12:33625338:C:T
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.33625339C>G, NC_000009.12:g.33625339C>T, NC_000009.11:g.33625337C>G, NC_000009.11:g.33625337C>T, NG_001337.2:g.18879C>G, NG_001337.2:g.18879C>T, NR_003573.1:n.1115C>G, NR_003573.1:n.1115C>T

Select item 146514337615.

rs1465143376 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:33625377 (GRCh38)
9:33625375 (GRCh37)
Canonical SPDI:: NC_000009.12:33625376:G:A
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.33625377G>A, NC_000009.11:g.33625375G>A, NG_001337.2:g.18917G>A, NR_003573.1:n.1153G>A

Select item 146378920116.

rs1463789201 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:33624912 (GRCh38)
9:33624910 (GRCh37)
Canonical SPDI:: NC_000009.12:33624911:G:A
Gene:: ANXA2P2 (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=0.000019/5 (TOPMED)
HGVS:: NC_000009.12:g.33624912G>A, NC_000009.11:g.33624910G>A, NG_001337.2:g.18452G>A, NR_003573.1:n.688G>A

Select item 145924926217.

rs1459249262 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:33624237 (GRCh38)
9:33624235 (GRCh37)
Canonical SPDI:: NC_000009.12:33624236:C:T
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000009.12:g.33624237C>T, NC_000009.11:g.33624235C>T, NG_001337.2:g.17777C>T, NR_003573.1:n.13C>T

Select item 145811368518.

rs1458113685 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:33624299 (GRCh38)
9:33624297 (GRCh37)
Canonical SPDI:: NC_000009.12:33624298:G:A
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.33624299G>A, NC_000009.11:g.33624297G>A, NG_001337.2:g.17839G>A, NR_003573.1:n.75G>A

Select item 145576892619.

rs1455768926 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:33624590 (GRCh38)
9:33624588 (GRCh37)
Canonical SPDI:: NC_000009.12:33624589:C:T
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.33624590C>T, NC_000009.11:g.33624588C>T, NG_001337.2:g.18130C>T, NR_003573.1:n.366C>T

Select item 145297334120.

rs1452973341 [Homo sapiens]

Variant type:: DEL
Alleles:: GCGAC>- [Show Flanks]
Chromosome:: 9:33625247 (GRCh38)
9:33625245 (GRCh37)
Canonical SPDI:: NC_000009.12:33625246:GCGAC:
Gene:: ANXA2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000011/3 (TOPMED)
HGVS:: NC_000009.12:g.33625247_33625251del, NC_000009.11:g.33625245_33625249del, NG_001337.2:g.18787_18791del, NR_003573.1:n.1023_1027del

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