SNP Links for Nucleotide (Select 158138499) - SNP

Links from Nucleotide

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Select item 14907456211.

rs1490745621 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 22:23400421 (GRCh38)
22:23742608 (GRCh37)
Canonical SPDI:: NC_000022.11:23400420:C:A
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000022.11:g.23400421C>A, NC_000022.10:g.23742608C>A, NT_187632.1:g.46379C>A, NR_003950.1:n.528G>T, NM_152509.1:c.-114G>T

Select item 14897960672.

rs1489796067 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 22:23393949 (GRCh38)
22:23736137 (GRCh37)
Canonical SPDI:: NC_000022.11:23393949:G:GG
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000022.11:g.23393950dup, NC_000022.10:g.23736137dup, NT_187632.1:g.39908dup, NR_003950.1:n.1297dup

Select item 14877593713.

rs1487759371 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 22:23402547 (GRCh38)
22:23744734 (GRCh37)
Canonical SPDI:: NC_000022.11:23402546:G:T
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000022.11:g.23402547G>T, NC_000022.10:g.23744734G>T, NT_187632.1:g.48505G>T, NR_003950.1:n.66C>A, NM_152509.1:c.-463C>A

Select item 14867515434.

rs1486751543 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 22:23391363 (GRCh38)
22:23733550 (GRCh37)
Canonical SPDI:: NC_000022.11:23391362:T:C
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000057/15 (TOPMED)
HGVS:: NC_000022.11:g.23391363T>C, NC_000022.10:g.23733550T>C, NT_187632.1:g.37321T>C, NR_003950.1:n.1790A>G, NM_152509.1:c.*406A>G

Select item 14864195205.

rs1486419520 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 22:23391414 (GRCh38)
22:23733601 (GRCh37)
Canonical SPDI:: NC_000022.11:23391413:G:A,NC_000022.11:23391413:G:T
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0./0 (KOREAN)
HGVS:: NC_000022.11:g.23391414G>A, NC_000022.11:g.23391414G>T, NC_000022.10:g.23733601G>A, NC_000022.10:g.23733601G>T, NT_187632.1:g.37372G>A, NT_187632.1:g.37372G>T, NR_003950.1:n.1739C>T, NR_003950.1:n.1739C>A, NM_152509.1:c.*355C>T, NM_152509.1:c.*355C>A

Select item 14863036416.

rs1486303641 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:23400326 (GRCh38)
22:23742513 (GRCh37)
Canonical SPDI:: NC_000022.11:23400325:C:T
Gene:: ZDHHC8P1 (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=0.000015/4 (TOPMED)
T=0.000035/1 (TOMMO)
T=0.000685/2 (KOREAN)
HGVS:: NC_000022.11:g.23400326C>T, NC_000022.10:g.23742513C>T, NT_187632.1:g.46284C>T, NR_003950.1:n.623G>A, NM_152509.1:c.-19G>A

Select item 14857309947.

rs1485730994 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 22:23402501 (GRCh38)
22:23744688 (GRCh37)
Canonical SPDI:: NC_000022.11:23402500:A:T
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000022.11:g.23402501A>T, NC_000022.10:g.23744688A>T, NT_187632.1:g.48459A>T, NR_003950.1:n.112T>A, NM_152509.1:c.-417T>A

Select item 14822743758.

rs1482274375 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:23402504 (GRCh38)
22:23744691 (GRCh37)
Canonical SPDI:: NC_000022.11:23402503:G:A
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000079/21 (TOPMED)
A=0.000122/17 (GnomAD)
HGVS:: NC_000022.11:g.23402504G>A, NC_000022.10:g.23744691G>A, NT_187632.1:g.48462G>A, NR_003950.1:n.109C>T, NM_152509.1:c.-420C>T

Select item 14821189689.

rs1482118968 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 22:23401908 (GRCh38)
22:23744095 (GRCh37)
Canonical SPDI:: NC_000022.11:23401907:G:A,NC_000022.11:23401907:G:T
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000022.11:g.23401908G>A, NC_000022.11:g.23401908G>T, NC_000022.10:g.23744095G>A, NC_000022.10:g.23744095G>T, NT_187632.1:g.47866G>A, NT_187632.1:g.47866G>T, NR_003950.1:n.298C>T, NR_003950.1:n.298C>A

Select item 148089089710.

rs1480890897 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 22:23391252 (GRCh38)
22:23733439 (GRCh37)
Canonical SPDI:: NC_000022.11:23391251:A:G
Gene:: ZDHHC8P1 (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_000022.11:g.23391252A>G, NC_000022.10:g.23733439A>G, NT_187632.1:g.37210A>G, NR_003950.1:n.1901T>C, NM_152509.1:c.*515T>C

Select item 147928341311.

rs1479283413 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:23399815 (GRCh38)
22:23742002 (GRCh37)
Canonical SPDI:: NC_000022.11:23399814:G:A
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000022.11:g.23399815G>A, NC_000022.10:g.23742002G>A, NT_187632.1:g.45773G>A, NR_003950.1:n.1134C>T, NM_152509.1:c.493C>T

Select item 147823598612.

rs1478235986 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 22:23402496 (GRCh38)
22:23744683 (GRCh37)
Canonical SPDI:: NC_000022.11:23402495:G:C
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000022.11:g.23402496G>C, NC_000022.10:g.23744683G>C, NT_187632.1:g.48454G>C, NR_003950.1:n.117C>G, NM_152509.1:c.-412C>G

Select item 147777199313.

rs1477771993 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 22:23394030 (GRCh38)
22:23736217 (GRCh37)
Canonical SPDI:: NC_000022.11:23394029:C:G
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.23394030C>G, NC_000022.10:g.23736217C>G, NT_187632.1:g.39988C>G, NR_003950.1:n.1217G>C

Select item 147529320414.

rs1475293204 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 22:23392773 (GRCh38)
22:23734960 (GRCh37)
Canonical SPDI:: NC_000022.11:23392772:G:A,NC_000022.11:23392772:G:C
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000022.11:g.23392773G>A, NC_000022.11:g.23392773G>C, NC_000022.10:g.23734960G>A, NC_000022.10:g.23734960G>C, NT_187632.1:g.38731G>A, NT_187632.1:g.38731G>C, NR_003950.1:n.1382C>T, NR_003950.1:n.1382C>G

Select item 147468076015.

rs1474680760 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 22:23391100 (GRCh38)
22:23733287 (GRCh37)
Canonical SPDI:: NC_000022.11:23391099:T:C
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000022.11:g.23391100T>C, NC_000022.10:g.23733287T>C, NT_187632.1:g.37058T>C, NR_003950.1:n.2053A>G, NM_152509.1:c.*667A>G

Select item 147451888516.

rs1474518885 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:23392753 (GRCh38)
22:23734940 (GRCh37)
Canonical SPDI:: NC_000022.11:23392752:G:A
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000026/7 (TOPMED)
A=0.000029/4 (GnomAD)
HGVS:: NC_000022.11:g.23392753G>A, NC_000022.10:g.23734940G>A, NT_187632.1:g.38711G>A, NR_003950.1:n.1402C>T

Select item 147441550717.

rs1474415507 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:23391339 (GRCh38)
22:23733526 (GRCh37)
Canonical SPDI:: NC_000022.11:23391338:C:T
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000026/7 (TOPMED)
T=0.000061/8 (GnomAD)
T=0.000106/2 (TOMMO)
T=0.000685/2 (KOREAN)
HGVS:: NC_000022.11:g.23391339C>T, NC_000022.10:g.23733526C>T, NT_187632.1:g.37297C>T, NR_003950.1:n.1814G>A, NM_152509.1:c.*428G>A

Select item 147419259018.

rs1474192590 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 22:23391165 (GRCh38)
22:23733352 (GRCh37)
Canonical SPDI:: NC_000022.11:23391164:C:A,NC_000022.11:23391164:C:T
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000022.11:g.23391165C>A, NC_000022.11:g.23391165C>T, NC_000022.10:g.23733352C>A, NC_000022.10:g.23733352C>T, NT_187632.1:g.37123C>A, NT_187632.1:g.37123C>T, NR_003950.1:n.1988G>T, NR_003950.1:n.1988G>A, NM_152509.1:c.*602G>T, NM_152509.1:c.*602G>A

Select item 147329037119.

rs1473290371 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 22:23400483 (GRCh38)
22:23742670 (GRCh37)
Canonical SPDI:: NC_000022.11:23400482:G:T
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.23400483G>T, NC_000022.10:g.23742670G>T, NT_187632.1:g.46441G>T, NR_003950.1:n.466C>A, NM_152509.1:c.-176C>A

Select item 147111905620.

rs1471119056 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 22:23399937 (GRCh38)
22:23742124 (GRCh37)
Canonical SPDI:: NC_000022.11:23399936:A:G
Gene:: ZDHHC8P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.23399937A>G, NC_000022.10:g.23742124A>G, NT_187632.1:g.45895A>G, NR_003950.1:n.1012T>C, NM_152509.1:c.371T>C

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