SNP Links for Nucleotide (Select 702777836) - SNP

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Links from Nucleotide

Items: 1 to 20 of 131

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Select item 14894409241.

rs1489440924 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:23980159 (GRCh38)
22:24322350 (GRCh37)
Canonical SPDI:: NC_000022.11:23980158:G:A
Gene:: DDT (Varview), GSTT2 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000022.11:g.23980159G>A, NT_187633.1:g.216525G>A, NC_000022.10:g.24322350G>A, NM_000854.4:c.-39G>A, NM_000854.3:c.-39G>A, NR_126445.2:n.26G>A, NR_126445.1:n.132G>A, NR_126446.1:n.132G>A, NR_126442.1:n.132G>A, NM_001302670.1:c.-39G>A

Select item 14813318922.

rs1481331892 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:23982892 (GRCh38)
22:24325083 (GRCh37)
Canonical SPDI:: NC_000022.11:23982891:G:A
Gene:: GSTT2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.23982892G>A, NT_187633.1:g.219258G>A, NC_000022.10:g.24325083G>A, NM_000854.4:c.373G>A, NM_000854.3:c.373G>A, NR_126445.2:n.437G>A, NR_126445.1:n.543G>A, NR_126446.1:n.647G>A, NR_126442.1:n.577G>A, NM_001302670.1:c.373G>A

Select item 14766353183.

rs1476635318 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 22:23982760 (GRCh38)
22:24324951 (GRCh37)
Canonical SPDI:: NC_000022.11:23982759:T:C
Gene:: GSTT2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.23982760T>C, NT_187633.1:g.219126T>C, NC_000022.10:g.24324951T>C, NM_000854.4:c.333T>C, NM_000854.3:c.333T>C, NR_126445.2:n.397T>C, NR_126445.1:n.503T>C, NR_126446.1:n.607T>C, NR_126442.1:n.537T>C, NM_001302670.1:c.333T>C

Select item 14734423714.

rs1473442371 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 22:23980073 (GRCh38)
22:24322264 (GRCh37)
Canonical SPDI:: NC_000022.11:23980072:G:C
Gene:: DDT (Varview), GSTT2 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.00792/94 (ALFA)
C=0.04197/70 (GnomAD)
HGVS:: NC_000022.11:g.23980073G>C, NT_187633.1:g.216439G>C, NC_000022.10:g.24322264G>C, NM_000854.4:c.-125G>C, NR_126446.1:n.46G>C, NR_126442.1:n.46G>C, NM_001302670.1:c.-125G>C

Select item 14581159495.

rs1458115949 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:23983398 (GRCh38)
22:24325589 (GRCh37)
Canonical SPDI:: NC_000022.11:23983397:C:T
Gene:: GSTT2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000022.11:g.23983398C>T, NT_187633.1:g.219764C>T, NC_000022.10:g.24325589C>T, NM_000854.4:c.527C>T, NM_000854.3:c.527C>T, NR_126445.2:n.591C>T, NR_126445.1:n.697C>T, NR_126446.1:n.759C>T, NR_126442.1:n.689C>T, NM_001302670.1:c.485C>T

Select item 14571034376.

rs1457103437 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 22:23980971 (GRCh38)
22:24323162 (GRCh37)
Canonical SPDI:: NC_000022.11:23980970:T:C
Gene:: DDT (Varview), GSTT2 (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.23980971T>C, NT_187633.1:g.217337T>C, NC_000022.10:g.24323162T>C, NM_000854.4:c.136T>C, NM_000854.3:c.136T>C, NR_126445.2:n.200T>C, NR_126445.1:n.306T>C, NR_126446.1:n.410T>C, NR_126442.1:n.410T>C, NM_001302670.1:c.136T>C

Select item 14446869437.

rs1444686943 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:23980952 (GRCh38)
22:24323143 (GRCh37)
Canonical SPDI:: NC_000022.11:23980951:G:A
Gene:: DDT (Varview), GSTT2 (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000022.11:g.23980952G>A, NT_187633.1:g.217318G>A, NC_000022.10:g.24323143G>A, NM_000854.4:c.117G>A, NM_000854.3:c.117G>A, NR_126445.2:n.181G>A, NR_126445.1:n.287G>A, NR_126446.1:n.391G>A, NR_126442.1:n.391G>A, NM_001302670.1:c.117G>A

Select item 14307310698.

rs1430731069 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:23983431 (GRCh38)
22:24325622 (GRCh37)
Canonical SPDI:: NC_000022.11:23983430:G:A
Gene:: GSTT2 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000022.11:g.23983431G>A, NT_187633.1:g.219797G>A, NC_000022.10:g.24325622G>A, NM_000854.4:c.560G>A, NM_000854.3:c.560G>A, NR_126445.2:n.624G>A, NR_126445.1:n.730G>A, NR_126446.1:n.792G>A, NR_126442.1:n.722G>A, NM_001302670.1:c.518G>A

Select item 14279981639.

rs1427998163 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:23982667 (GRCh38)
22:24324858 (GRCh37)
Canonical SPDI:: NC_000022.11:23982666:G:A
Gene:: GSTT2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000022.11:g.23982667G>A, NT_187633.1:g.219033G>A, NC_000022.10:g.24324858G>A, NM_000854.4:c.240G>A, NM_000854.3:c.240G>A, NR_126445.2:n.304G>A, NR_126445.1:n.410G>A, NR_126446.1:n.514G>A, NM_001302670.1:c.240G>A

Select item 142373308210.

rs1423733082 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 22:23982633 (GRCh38)
22:24324824 (GRCh37)
Canonical SPDI:: NC_000022.11:23982632:C:A
Gene:: GSTT2 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000022.11:g.23982633C>A, NT_187633.1:g.218999C>A, NC_000022.10:g.24324824C>A, NM_000854.4:c.206C>A, NM_000854.3:c.206C>A, NR_126445.2:n.270C>A, NR_126445.1:n.376C>A, NR_126446.1:n.480C>A, NM_001302670.1:c.206C>A

Select item 142043477411.

rs1420434774 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:23980960 (GRCh38)
22:24323151 (GRCh37)
Canonical SPDI:: NC_000022.11:23980959:G:A
Gene:: DDT (Varview), GSTT2 (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.23980960G>A, NT_187633.1:g.217326G>A, NC_000022.10:g.24323151G>A, NM_000854.4:c.125G>A, NM_000854.3:c.125G>A, NR_126445.2:n.189G>A, NR_126445.1:n.295G>A, NR_126446.1:n.399G>A, NR_126442.1:n.399G>A, NM_001302670.1:c.125G>A

Select item 142027648512.

rs1420276485 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:23980985 (GRCh38)
22:24323176 (GRCh37)
Canonical SPDI:: NC_000022.11:23980984:C:T
Gene:: DDT (Varview), GSTT2 (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,upstream_transcript_variant
HGVS:: NC_000022.11:g.23980985C>T, NT_187633.1:g.217351C>T, NC_000022.10:g.24323176C>T, NM_000854.4:c.150C>T, NM_000854.3:c.150C>T, NR_126445.2:n.214C>T, NR_126445.1:n.320C>T, NR_126446.1:n.424C>T, NR_126442.1:n.424C>T, NM_001302670.1:c.150C>T

Select item 141681444013.

rs1416814440 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:23983747 (GRCh38)
22:24325938 (GRCh37)
Canonical SPDI:: NC_000022.11:23983746:C:T
Gene:: GSTT2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000022.11:g.23983747C>T, NT_187633.1:g.220113C>T, NC_000022.10:g.24325938C>T, NM_000854.4:c.*141C>T, NM_000854.3:c.*141C>T, NR_126445.2:n.940C>T, NR_126445.1:n.1046C>T, NR_126446.1:n.1108C>T, NR_126442.1:n.1038C>T, NM_001302670.1:c.*141C>T

Select item 140683974214.

rs1406839742 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 22:23981015 (GRCh38)
22:24323206 (GRCh37)
Canonical SPDI:: NC_000022.11:23981014:T:C
Gene:: DDT (Varview), GSTT2 (Varview)
Functional Consequence:: upstream_transcript_variant,non_coding_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000036/9 (GnomAD_exomes)
HGVS:: NC_000022.11:g.23981015T>C, NT_187633.1:g.217381T>C, NC_000022.10:g.24323206T>C, NM_000854.4:c.180T>C, NM_000854.3:c.180T>C, NR_126445.2:n.244T>C, NR_126445.1:n.350T>C, NR_126446.1:n.454T>C, NR_126442.1:n.454T>C, NM_001302670.1:c.180T>C

Select item 139506277215.

rs1395062772 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:23983574 (GRCh38)
22:24325765 (GRCh37)
Canonical SPDI:: NC_000022.11:23983573:G:A
Gene:: GSTT2 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000022.11:g.23983574G>A, NT_187633.1:g.219940G>A, NC_000022.10:g.24325765G>A, NM_000854.4:c.703G>A, NM_000854.3:c.703G>A, NR_126445.2:n.767G>A, NR_126445.1:n.873G>A, NR_126446.1:n.935G>A, NR_126442.1:n.865G>A, NM_001302670.1:c.661G>A

Select item 138341836616.

rs1383418366 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:23980044 (GRCh38)
22:24322235 (GRCh37)
Canonical SPDI:: NC_000022.11:23980043:C:T
Gene:: DDT (Varview), GSTT2 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000022.11:g.23980044C>T, NT_187633.1:g.216410C>T, NC_000022.10:g.24322235C>T, NM_000854.4:c.-154C>T, NR_126446.1:n.17C>T, NR_126442.1:n.17C>T, NM_001302670.1:c.-154C>T