SNP Links for Nucleotide (Select 808154173) - SNP

Links from Nucleotide

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Select item 14907696631.

rs1490769663 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 18:54599180 (GRCh38)
18:52266411 (GRCh37)
Canonical SPDI:: NC_000018.10:54599179:T:A,NC_000018.10:54599179:T:C
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000018.10:g.54599180T>A, NC_000018.10:g.54599180T>C, NC_000018.9:g.52266411T>A, NC_000018.9:g.52266411T>C, XM_011525923.4:c.*1035T>A, XM_011525923.4:c.*1035T>C, XM_011525923.2:c.*1035T>A, XM_011525923.2:c.*1035T>C, NM_173629.3:c.*1035T>A, NM_173629.3:c.*1035T>C, NM_173629.2:c.*1035T>A, NM_173629.2:c.*1035T>C, NM_173629.1:c.*1035T>A, NM_173629.1:c.*1035T>C, XM_017025709.2:c.*1035T>A, XM_017025709.2:c.*1035T>C, XM_017025709.1:c.*1035T>A, XM_017025709.1:c.*1035T>C, NM_001307955.1:c.*1035T>A, NM_001307955.1:c.*1035T>C

Select item 14885845832.

rs1488584583 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CT [Show Flanks]
Chromosome:: 18:54598861 (GRCh38)
18:52266093 (GRCh37)
Canonical SPDI:: NC_000018.10:54598861:CTCTCTCTCT:CTCTCTCTCTCT
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTCTCTCTCTCT=0./0 (ALFA)
CT=0.000015/4 (TOPMED)
CT=0.000021/3 (GnomAD)
HGVS:: NC_000018.10:g.54598862CT[6], NC_000018.9:g.52266093CT[6], XM_011525923.4:c.*717CT[6], XM_011525923.2:c.*717CT[6], NM_173629.3:c.*717CT[6], NM_173629.2:c.*717CT[6], NM_173629.1:c.*717CT[6], XM_017025709.2:c.*717CT[6], XM_017025709.1:c.*717CT[6], NM_001307955.1:c.*717CT[6]

Select item 14865154703.

rs1486515470 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:54598279 (GRCh38)
18:52265510 (GRCh37)
Canonical SPDI:: NC_000018.10:54598278:C:T
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_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_000018.10:g.54598279C>T, NC_000018.9:g.52265510C>T, XM_011525923.4:c.*134C>T, XM_011525923.3:c.*134C>T, XM_011525923.2:c.*134C>T, XM_011525923.1:c.*134C>T, NM_173629.3:c.*134C>T, NM_173629.2:c.*134C>T, NM_173629.1:c.*134C>T, XM_017025709.2:c.*134C>T, XM_017025709.1:c.*134C>T, NM_001307955.1:c.*134C>T

Select item 14862714664.

rs1486271466 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 18:54591323 (GRCh38)
18:52258554 (GRCh37)
Canonical SPDI:: NC_000018.10:54591322:A:C
Gene:: DYNAP (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: C=0.000004/1 (GnomAD_exomes)
C=0.003275/6 (Korea1K)
HGVS:: NC_000018.10:g.54591323A>C, NC_000018.9:g.52258554A>C, XM_011525923.4:c.128A>C, XM_011525923.3:c.128A>C, XM_011525923.2:c.128A>C, XM_011525923.1:c.128A>C, NM_173629.3:c.41A>C, NM_173629.2:c.119A>C, NM_173629.1:c.119A>C, XM_017025709.2:c.128A>C, XM_017025709.1:c.128A>C, NM_001307955.1:c.128A>C, XP_011524225.1:p.His43Pro, NP_775900.2:p.His14Pro, XP_016881198.1:p.His43Pro, NP_001294884.1:p.His43Pro

Select item 14860850995.

rs1486085099 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:54598453 (GRCh38)
18:52265684 (GRCh37)
Canonical SPDI:: NC_000018.10:54598452:A:G
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.54598453A>G, NC_000018.9:g.52265684A>G, XM_011525923.4:c.*308A>G, XM_011525923.3:c.*308A>G, XM_011525923.2:c.*308A>G, XM_011525923.1:c.*308A>G, NM_173629.3:c.*308A>G, NM_173629.2:c.*308A>G, NM_173629.1:c.*308A>G, XM_017025709.2:c.*308A>G, XM_017025709.1:c.*308A>G, NM_001307955.1:c.*308A>G

Select item 14855368196.

rs1485536819 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 18:54598886 (GRCh38)
18:52266118 (GRCh37)
Canonical SPDI:: NC_000018.10:54598886:A:AA
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: AA=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.54598887dup, NC_000018.9:g.52266118dup, XM_011525923.4:c.*742dup, XM_011525923.2:c.*742dup, NM_173629.3:c.*742dup, NM_173629.2:c.*742dup, NM_173629.1:c.*742dup, XM_017025709.2:c.*742dup, XM_017025709.1:c.*742dup, NM_001307955.1:c.*742dup

Select item 14845608927.

rs1484560892 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 18:54599416 (GRCh38)
18:52266647 (GRCh37)
Canonical SPDI:: NC_000018.10:54599415:A:G,NC_000018.10:54599415:A:T
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000019/5 (TOPMED)
T=0.000156/1 (1000Genomes)
HGVS:: NC_000018.10:g.54599416A>G, NC_000018.10:g.54599416A>T, NC_000018.9:g.52266647A>G, NC_000018.9:g.52266647A>T, XM_011525923.4:c.*1271A>G, XM_011525923.4:c.*1271A>T, XM_011525923.2:c.*1271A>G, XM_011525923.2:c.*1271A>T, NM_173629.3:c.*1271A>G, NM_173629.3:c.*1271A>T, NM_173629.2:c.*1271A>G, NM_173629.2:c.*1271A>T, NM_173629.1:c.*1271A>G, NM_173629.1:c.*1271A>T, XM_017025709.2:c.*1271A>G, XM_017025709.2:c.*1271A>T, XM_017025709.1:c.*1271A>G, XM_017025709.1:c.*1271A>T, NM_001307955.1:c.*1271A>G, NM_001307955.1:c.*1271A>T

Select item 14793920158.

rs1479392015 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 18:54598585 (GRCh38)
18:52265816 (GRCh37)
Canonical SPDI:: NC_000018.10:54598584:T:A
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.54598585T>A, NC_000018.9:g.52265816T>A, XM_011525923.4:c.*440T>A, XM_011525923.2:c.*440T>A, NM_173629.3:c.*440T>A, NM_173629.2:c.*440T>A, NM_173629.1:c.*440T>A, XM_017025709.2:c.*440T>A, XM_017025709.1:c.*440T>A, NM_001307955.1:c.*440T>A

Select item 14753687739.

rs1475368773 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:54598998 (GRCh38)
18:52266229 (GRCh37)
Canonical SPDI:: NC_000018.10:54598997:A:G
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.54598998A>G, NC_000018.9:g.52266229A>G, XM_011525923.4:c.*853A>G, XM_011525923.2:c.*853A>G, NM_173629.3:c.*853A>G, NM_173629.2:c.*853A>G, NM_173629.1:c.*853A>G, XM_017025709.2:c.*853A>G, XM_017025709.1:c.*853A>G, NM_001307955.1:c.*853A>G

Select item 147462048510.

rs1474620485 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:54599112 (GRCh38)
18:52266343 (GRCh37)
Canonical SPDI:: NC_000018.10:54599111:A:G
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000054/1 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000021/3 (GnomAD)
G=0.000223/1 (Estonian)
HGVS:: NC_000018.10:g.54599112A>G, NC_000018.9:g.52266343A>G, XM_011525923.4:c.*967A>G, XM_011525923.2:c.*967A>G, NM_173629.3:c.*967A>G, NM_173629.2:c.*967A>G, NM_173629.1:c.*967A>G, XM_017025709.2:c.*967A>G, XM_017025709.1:c.*967A>G, NM_001307955.1:c.*967A>G

Select item 147186603611.

rs1471866036 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 18:54598272 (GRCh38)
18:52265503 (GRCh37)
Canonical SPDI:: NC_000018.10:54598271:C:A
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.54598272C>A, NC_000018.9:g.52265503C>A, XM_011525923.4:c.*127C>A, XM_011525923.3:c.*127C>A, XM_011525923.2:c.*127C>A, XM_011525923.1:c.*127C>A, NM_173629.3:c.*127C>A, NM_173629.2:c.*127C>A, NM_173629.1:c.*127C>A, XM_017025709.2:c.*127C>A, XM_017025709.1:c.*127C>A, NM_001307955.1:c.*127C>A

Select item 146972098812.

rs1469720988 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 18:54599406 (GRCh38)
18:52266637 (GRCh37)
Canonical SPDI:: NC_000018.10:54599405:C:G
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.54599406C>G, NC_000018.9:g.52266637C>G, XM_011525923.4:c.*1261C>G, XM_011525923.2:c.*1261C>G, NM_173629.3:c.*1261C>G, NM_173629.2:c.*1261C>G, NM_173629.1:c.*1261C>G, XM_017025709.2:c.*1261C>G, XM_017025709.1:c.*1261C>G, NM_001307955.1:c.*1261C>G

Select item 146898781113.

rs1468987811 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:54599164 (GRCh38)
18:52266395 (GRCh37)
Canonical SPDI:: NC_000018.10:54599163:G:A
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0.000084/1 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.54599164G>A, NC_000018.9:g.52266395G>A, XM_011525923.4:c.*1019G>A, XM_011525923.2:c.*1019G>A, NM_173629.3:c.*1019G>A, NM_173629.2:c.*1019G>A, NM_173629.1:c.*1019G>A, XM_017025709.2:c.*1019G>A, XM_017025709.1:c.*1019G>A, NM_001307955.1:c.*1019G>A

Select item 146792615914.

rs1467926159 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:54598579 (GRCh38)
18:52265810 (GRCh37)
Canonical SPDI:: NC_000018.10:54598578:A:G
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.54598579A>G, NC_000018.9:g.52265810A>G, XM_011525923.4:c.*434A>G, XM_011525923.3:c.*434A>G, XM_011525923.2:c.*434A>G, XM_011525923.1:c.*434A>G, NM_173629.3:c.*434A>G, NM_173629.2:c.*434A>G, NM_173629.1:c.*434A>G, XM_017025709.2:c.*434A>G, XM_017025709.1:c.*434A>G, NM_001307955.1:c.*434A>G

Select item 146757977015.

rs1467579770 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:54598116 (GRCh38)
18:52265347 (GRCh37)
Canonical SPDI:: NC_000018.10:54598115:A:G
Gene:: DYNAP (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.54598116A>G, NC_000018.9:g.52265347A>G, XM_011525923.4:c.613A>G, XM_011525923.3:c.613A>G, XM_011525923.2:c.613A>G, XM_011525923.1:c.613A>G, NM_173629.3:c.526A>G, NM_173629.2:c.604A>G, NM_173629.1:c.604A>G, XM_017025709.2:c.448A>G, XM_017025709.1:c.448A>G, NM_001307955.1:c.448A>G, XP_011524225.1:p.Ile205Val, NP_775900.2:p.Ile176Val, XP_016881198.1:p.Ile150Val, NP_001294884.1:p.Ile150Val

Select item 146466424416.

rs1464664244 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:54597947 (GRCh38)
18:52265178 (GRCh37)
Canonical SPDI:: NC_000018.10:54597946:C:T
Gene:: DYNAP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000018.10:g.54597947C>T, NC_000018.9:g.52265178C>T, XM_011525923.4:c.444C>T, XM_011525923.3:c.444C>T, XM_011525923.2:c.444C>T, XM_011525923.1:c.444C>T, NM_173629.3:c.357C>T, NM_173629.2:c.435C>T, NM_173629.1:c.435C>T, XM_017025709.2:c.279C>T, XM_017025709.1:c.279C>T, NM_001307955.1:c.279C>T

Select item 146460370417.

rs1464603704 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:54599017 (GRCh38)
18:52266248 (GRCh37)
Canonical SPDI:: NC_000018.10:54599016:A:G
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000432/8 (ALFA)
G=0.000015/4 (TOPMED)
G=0.000064/9 (GnomAD)
G=0.001786/8 (Estonian)
HGVS:: NC_000018.10:g.54599017A>G, NC_000018.9:g.52266248A>G, XM_011525923.4:c.*872A>G, XM_011525923.2:c.*872A>G, NM_173629.3:c.*872A>G, NM_173629.2:c.*872A>G, NM_173629.1:c.*872A>G, XM_017025709.2:c.*872A>G, XM_017025709.1:c.*872A>G, NM_001307955.1:c.*872A>G

Select item 146448822118.

rs1464488221 [Homo sapiens]

Variant type:: DEL
Alleles:: CGGCC>- [Show Flanks]
Chromosome:: 18:54597934 (GRCh38)
18:52265165 (GRCh37)
Canonical SPDI:: NC_000018.10:54597933:CGGCC:
Gene:: DYNAP (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.013/59 (ALFA)
HGVS:: NC_000018.10:g.54597934_54597938del, NC_000018.9:g.52265165_52265169del, XM_011525923.4:c.431_435del, XM_011525923.3:c.431_435del, XM_011525923.2:c.431_435del, XM_011525923.1:c.431_435del, NM_173629.3:c.344_348del, NM_173629.2:c.422_426del, NM_173629.1:c.422_426del, XM_017025709.2:c.266_270del, XM_017025709.1:c.266_270del, NM_001307955.1:c.266_270del, XP_011524225.1:p.Gly143_Ser144insTer, NP_775900.2:p.Gly114_Ser115insTer, XP_016881198.1:p.Gly88_Ser89insTer, NP_001294884.1:p.Gly88_Ser89insTer

Select item 146257664719.

rs1462576647 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:54599437 (GRCh38)
18:52266668 (GRCh37)
Canonical SPDI:: NC_000018.10:54599436:T:C
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_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_000018.10:g.54599437T>C, NC_000018.9:g.52266668T>C, XM_011525923.4:c.*1292T>C, XM_011525923.2:c.*1292T>C, NM_173629.3:c.*1292T>C, NM_173629.2:c.*1292T>C, NM_173629.1:c.*1292T>C, XM_017025709.2:c.*1292T>C, XM_017025709.1:c.*1292T>C, NM_001307955.1:c.*1292T>C

Select item 146153034220.

rs1461530342 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:54599079 (GRCh38)
18:52266310 (GRCh37)
Canonical SPDI:: NC_000018.10:54599078:A:G
Gene:: DYNAP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.54599079A>G, NC_000018.9:g.52266310A>G, XM_011525923.4:c.*934A>G, XM_011525923.2:c.*934A>G, NM_173629.3:c.*934A>G, NM_173629.2:c.*934A>G, NM_173629.1:c.*934A>G, XM_017025709.2:c.*934A>G, XM_017025709.1:c.*934A>G, NM_001307955.1:c.*934A>G

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