SNP Links for Nucleotide (Select 336455092) - SNP

Links from Nucleotide

Items: 1 to 20 of 618

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Select item 14903382281.

rs1490338228 [Homo sapiens]

Variant type:: INS
Alleles:: ->GT [Show Flanks]
Chromosome:: 2:85826603 (GRCh38)
2:86053727 (GRCh37)
Canonical SPDI:: NC_000002.12:85826603::GT
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: GT=0.000078/11 (GnomAD)
HGVS:: NC_000002.12:g.85826603_85826604insGT, NC_000002.11:g.86053726_86053727insGT, NR_038888.1:n.2923_2924insGT

Select item 14880100122.

rs1488010012 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:85818320 (GRCh38)
2:86045443 (GRCh37)
Canonical SPDI:: NC_000002.12:85818319:G:T
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000002.12:g.85818320G>T, NC_000002.11:g.86045443G>T, NR_038888.1:n.239G>T

Select item 14866587363.

rs1486658736 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 2:85815319 (GRCh38)
2:86042442 (GRCh37)
Canonical SPDI:: NC_000002.12:85815318:A:C,NC_000002.12:85815318:A:G
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.00004/1 (TOMMO)
HGVS:: NC_000002.12:g.85815319A>C, NC_000002.12:g.85815319A>G, NC_000002.11:g.86042442A>C, NC_000002.11:g.86042442A>G, NR_038888.1:n.190A>C, NR_038888.1:n.190A>G

Select item 14861618024.

rs1486161802 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:85815171 (GRCh38)
2:86042294 (GRCh37)
Canonical SPDI:: NC_000002.12:85815170:G:T
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.85815171G>T, NC_000002.11:g.86042294G>T, NR_038888.1:n.42G>T

Select item 14849928665.

rs1484992866 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:85825429 (GRCh38)
2:86052552 (GRCh37)
Canonical SPDI:: NC_000002.12:85825428:G:A
Gene:: LOC284950 (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=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.85825429G>A, NC_000002.11:g.86052552G>A, NR_038888.1:n.1749G>A

Select item 14843196946.

rs1484319694 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:85826056 (GRCh38)
2:86053179 (GRCh37)
Canonical SPDI:: NC_000002.12:85826055:C:T
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.85826056C>T, NC_000002.11:g.86053179C>T, NR_038888.1:n.2376C>T

Select item 14826352067.

rs1482635206 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:85826255 (GRCh38)
2:86053378 (GRCh37)
Canonical SPDI:: NC_000002.12:85826254:C:T
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000002.12:g.85826255C>T, NC_000002.11:g.86053378C>T, NR_038888.1:n.2575C>T

Select item 14823720318.

rs1482372031 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 2:85824246 (GRCh38)
2:86051369 (GRCh37)
Canonical SPDI:: NC_000002.12:85824245:G:C
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.85824246G>C, NC_000002.11:g.86051369G>C, NR_038888.1:n.566G>C

Select item 14803587899.

rs1480358789 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 2:85826465 (GRCh38)
2:86053588 (GRCh37)
Canonical SPDI:: NC_000002.12:85826464:T:
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00005/7 (GnomAD)
-=0.000091/24 (TOPMED)
HGVS:: NC_000002.12:g.85826465del, NC_000002.11:g.86053588del, NR_038888.1:n.2785del

Select item 147847100710.

rs1478471007 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:85825118 (GRCh38)
2:86052241 (GRCh37)
Canonical SPDI:: NC_000002.12:85825117:C:T
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.85825118C>T, NC_000002.11:g.86052241C>T, NR_038888.1:n.1438C>T

Select item 147828656611.

rs1478286566 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:85825523 (GRCh38)
2:86052646 (GRCh37)
Canonical SPDI:: NC_000002.12:85825522:T:C
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000002.12:g.85825523T>C, NC_000002.11:g.86052646T>C, NR_038888.1:n.1843T>C

Select item 147791895512.

rs1477918955 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:85826253 (GRCh38)
2:86053376 (GRCh37)
Canonical SPDI:: NC_000002.12:85826252:T:C
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.85826253T>C, NC_000002.11:g.86053376T>C, NR_038888.1:n.2573T>C

Select item 147636741613.

rs1476367416 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:85824876 (GRCh38)
2:86051999 (GRCh37)
Canonical SPDI:: NC_000002.12:85824875:T:C
Gene:: LOC284950 (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=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.85824876T>C, NC_000002.11:g.86051999T>C, NR_038888.1:n.1196T>C

Select item 147520681914.

rs1475206819 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:85824067 (GRCh38)
2:86051190 (GRCh37)
Canonical SPDI:: NC_000002.12:85824066:C:T
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.85824067C>T, NC_000002.11:g.86051190C>T, NR_038888.1:n.387C>T

Select item 147422586215.

rs1474225862 [Homo sapiens]

Variant type:: DEL
Alleles:: TAC>- [Show Flanks]
Chromosome:: 2:85824659 (GRCh38)
2:86051782 (GRCh37)
Canonical SPDI:: NC_000002.12:85824658:TAC:
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.85824659_85824661del, NC_000002.11:g.86051782_86051784del, NR_038888.1:n.979_981del

Select item 147416976216.

rs1474169762 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:85824569 (GRCh38)
2:86051692 (GRCh37)
Canonical SPDI:: NC_000002.12:85824568:A:G
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.85824569A>G, NC_000002.11:g.86051692A>G, NR_038888.1:n.889A>G

Select item 147324914117.

rs1473249141 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:85825796 (GRCh38)
2:86052919 (GRCh37)
Canonical SPDI:: NC_000002.12:85825795:G:A
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.85825796G>A, NC_000002.11:g.86052919G>A, NR_038888.1:n.2116G>A

Select item 146513621118.

rs1465136211 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:85815175 (GRCh38)
2:86042298 (GRCh37)
Canonical SPDI:: NC_000002.12:85815174:G:A
Gene:: LOC284950 (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_000002.12:g.85815175G>A, NC_000002.11:g.86042298G>A, NR_038888.1:n.46G>A

Select item 146496548819.

rs1464965488 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:85815288 (GRCh38)
2:86042411 (GRCh37)
Canonical SPDI:: NC_000002.12:85815287:G:A
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0./0 (GnomAD)
HGVS:: NC_000002.12:g.85815288G>A, NC_000002.11:g.86042411G>A, NR_038888.1:n.159G>A

Select item 146258866120.

rs1462588661 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:85824050 (GRCh38)
2:86051173 (GRCh37)
Canonical SPDI:: NC_000002.12:85824049:C:T
Gene:: LOC284950 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.85824050C>T, NC_000002.11:g.86051173C>T, NR_038888.1:n.370C>T

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