SNP Links for Nucleotide (Select 209954658) - SNP

Links from Nucleotide

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Select item 14899533481.

rs1489953348 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 11:67791897 (GRCh38)
11:67559368 (GRCh37)
Canonical SPDI:: NC_000011.10:67791896:CCCCC:CCCC
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000011.10:g.67791901del, NC_000011.9:g.67559372del, NG_008772.2:g.6732del, NR_024249.1:n.1729del

Select item 14885428012.

rs1488542801 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 11:67792546 (GRCh38)
11:67560017 (GRCh37)
Canonical SPDI:: NC_000011.10:67792545:T:C,NC_000011.10:67792545:T:G
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.67792546T>C, NC_000011.10:g.67792546T>G, NC_000011.9:g.67560017T>C, NC_000011.9:g.67560017T>G, NG_008772.2:g.7377T>C, NG_008772.2:g.7377T>G, NR_024249.1:n.1080A>G, NR_024249.1:n.1080A>C

Select item 14867245303.

rs1486724530 [Homo sapiens]

Variant type:: DEL
Alleles:: CTC>- [Show Flanks]
Chromosome:: 11:67792395 (GRCh38)
11:67559866 (GRCh37)
Canonical SPDI:: NC_000011.10:67792394:CTC:
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.67792395_67792397del, NC_000011.9:g.67559866_67559868del, NG_008772.2:g.7226_7228del, NR_024249.1:n.1229_1231del

Select item 14866225304.

rs1486622530 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:67792397 (GRCh38)
11:67559868 (GRCh37)
Canonical SPDI:: NC_000011.10:67792396:C:G
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000021/3 (GnomAD)
G=0.000057/15 (TOPMED)
HGVS:: NC_000011.10:g.67792397C>G, NC_000011.9:g.67559868C>G, NG_008772.2:g.7228C>G, NR_024249.1:n.1229G>C

Select item 14857403585.

rs1485740358 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:67792730 (GRCh38)
11:67560201 (GRCh37)
Canonical SPDI:: NC_000011.10:67792729:G:A,NC_000011.10:67792729:G:T
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.67792730G>A, NC_000011.10:g.67792730G>T, NC_000011.9:g.67560201G>A, NC_000011.9:g.67560201G>T, NG_008772.2:g.7561G>A, NG_008772.2:g.7561G>T, NR_024249.1:n.896C>T, NR_024249.1:n.896C>A

Select item 14850880656.

rs1485088065 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:67792052 (GRCh38)
11:67559523 (GRCh37)
Canonical SPDI:: NC_000011.10:67792051:G:A,NC_000011.10:67792051:G:T
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00031/2 (1000Genomes)
HGVS:: NC_000011.10:g.67792052G>A, NC_000011.10:g.67792052G>T, NC_000011.9:g.67559523G>A, NC_000011.9:g.67559523G>T, NG_008772.2:g.6883G>A, NG_008772.2:g.6883G>T, NR_024249.1:n.1574C>T, NR_024249.1:n.1574C>A

Select item 14850358797.

rs1485035879 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:67792815 (GRCh38)
11:67560286 (GRCh37)
Canonical SPDI:: NC_000011.10:67792814:G:A
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000011.10:g.67792815G>A, NC_000011.9:g.67560286G>A, NG_008772.2:g.7646G>A, NR_024249.1:n.811C>T

Select item 14843198628.

rs1484319862 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:67803026 (GRCh38)
11:67570497 (GRCh37)
Canonical SPDI:: NC_000011.10:67803025:C:A,NC_000011.10:67803025:C:T
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.67803026C>A, NC_000011.10:g.67803026C>T, NC_000011.9:g.67570497C>A, NC_000011.9:g.67570497C>T, NR_024249.1:n.158G>T, NR_024249.1:n.158G>A

Select item 14840205669.

rs1484020566 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:67796705 (GRCh38)
11:67564176 (GRCh37)
Canonical SPDI:: NC_000011.10:67796704:G:A
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000011.10:g.67796705G>A, NC_000011.9:g.67564176G>A, NR_024249.1:n.311C>T

Select item 148333777910.

rs1483337779 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 11:67805308 (GRCh38)
11:67572779 (GRCh37)
Canonical SPDI:: NC_000011.10:67805307:C:A,NC_000011.10:67805307:C:G,NC_000011.10:67805307:C:T
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000006/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.67805308C>A, NC_000011.10:g.67805308C>G, NC_000011.10:g.67805308C>T, NC_000011.9:g.67572779C>A, NC_000011.9:g.67572779C>G, NC_000011.9:g.67572779C>T, NR_024249.1:n.29G>T, NR_024249.1:n.29G>C, NR_024249.1:n.29G>A

Select item 148219198211.

rs1482191982 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:67792271 (GRCh38)
11:67559742 (GRCh37)
Canonical SPDI:: NC_000011.10:67792270:A:T
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.67792271A>T, NC_000011.9:g.67559742A>T, NG_008772.2:g.7102A>T, NR_024249.1:n.1355T>A

Select item 148214922412.

rs1482149224 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 11:67793046 (GRCh38)
11:67560517 (GRCh37)
Canonical SPDI:: NC_000011.10:67793045:T:C,NC_000011.10:67793045:T:G
Gene:: FAM86C2P (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_000011.10:g.67793046T>C, NC_000011.10:g.67793046T>G, NC_000011.9:g.67560517T>C, NC_000011.9:g.67560517T>G, NG_008772.2:g.7877T>C, NG_008772.2:g.7877T>G, NR_024249.1:n.580A>G, NR_024249.1:n.580A>C

Select item 147978312513.

rs1479783125 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:67792302 (GRCh38)
11:67559773 (GRCh37)
Canonical SPDI:: NC_000011.10:67792301:G:A,NC_000011.10:67792301:G:T
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000029/4 (GnomAD)
HGVS:: NC_000011.10:g.67792302G>A, NC_000011.10:g.67792302G>T, NC_000011.9:g.67559773G>A, NC_000011.9:g.67559773G>T, NG_008772.2:g.7133G>A, NG_008772.2:g.7133G>T, NR_024249.1:n.1324C>T, NR_024249.1:n.1324C>A

Select item 147816376314.

rs1478163763 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:67803044 (GRCh38)
11:67570515 (GRCh37)
Canonical SPDI:: NC_000011.10:67803043:T:A
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.67803044T>A, NC_000011.9:g.67570515T>A, NR_024249.1:n.140A>T

Select item 147793657115.

rs1477936571 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:67805257 (GRCh38)
11:67572728 (GRCh37)
Canonical SPDI:: NC_000011.10:67805256:G:A,NC_000011.10:67805256:G:C
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.67805257G>A, NC_000011.10:g.67805257G>C, NC_000011.9:g.67572728G>A, NC_000011.9:g.67572728G>C, NR_024249.1:n.80C>T, NR_024249.1:n.80C>G

Select item 147757508016.

rs1477575080 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:67792416 (GRCh38)
11:67559887 (GRCh37)
Canonical SPDI:: NC_000011.10:67792415:C:T
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.67792416C>T, NC_000011.9:g.67559887C>T, NG_008772.2:g.7247C>T, NR_024249.1:n.1210G>A

Select item 147749711717.

rs1477497117 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 11:67793284 (GRCh38)
11:67560755 (GRCh37)
Canonical SPDI:: NC_000011.10:67793283:C:G,NC_000011.10:67793283:C:T
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000011.10:g.67793284C>G, NC_000011.10:g.67793284C>T, NC_000011.9:g.67560755C>G, NC_000011.9:g.67560755C>T, NG_008772.2:g.8115C>G, NG_008772.2:g.8115C>T, NR_024249.1:n.342G>C, NR_024249.1:n.342G>A

Select item 147630571418.

rs1476305714 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:67792456 (GRCh38)
11:67559927 (GRCh37)
Canonical SPDI:: NC_000011.10:67792455:C:T
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000084/1 (ALFA)
T=0.000087/23 (TOPMED)
T=0.000093/13 (GnomAD)
HGVS:: NC_000011.10:g.67792456C>T, NC_000011.9:g.67559927C>T, NG_008772.2:g.7287C>T, NR_024249.1:n.1170G>A

Select item 147532785119.

rs1475327851 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:67792807 (GRCh38)
11:67560278 (GRCh37)
Canonical SPDI:: NC_000011.10:67792806:C:T
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000011.10:g.67792807C>T, NC_000011.9:g.67560278C>T, NG_008772.2:g.7638C>T, NR_024249.1:n.819G>A

Select item 147515008620.

rs1475150086 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 11:67791899 (GRCh38)
11:67559370 (GRCh37)
Canonical SPDI:: NC_000011.10:67791898:C:A,NC_000011.10:67791898:C:G
Gene:: FAM86C2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.67791899C>A, NC_000011.10:g.67791899C>G, NC_000011.9:g.67559370C>A, NC_000011.9:g.67559370C>G, NG_008772.2:g.6730C>A, NG_008772.2:g.6730C>G, NR_024249.1:n.1727G>T, NR_024249.1:n.1727G>C

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