SNP Links for Nucleotide (Select 373838739) - SNP

Links from Nucleotide

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Select item 14909276671.

rs1490927667 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 14:58645894 (GRCh38)
14:59112612 (GRCh37)
Canonical SPDI:: NC_000014.9:58645893:A:C
Gene:: DACT1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000031/1 (ALFA)
C=0.000012/3 (GnomAD_exomes)
C=0.000014/2 (GnomAD)
HGVS:: NC_000014.9:g.58645894A>C, NC_000014.8:g.59112612A>C, NG_032025.1:g.16827A>C, NM_016651.6:c.1271A>C, NM_016651.5:c.1271A>C, NM_001079520.2:c.1160A>C, NM_001079520.1:c.1160A>C, NR_046093.2:n.940A>C, NR_046093.1:n.933A>C, NR_165652.1:n.1352A>C, NR_165651.1:n.1320A>C, NR_046095.1:n.1241A>C, NR_165650.1:n.1051A>C, NP_057735.2:p.Lys424Thr, NP_001072988.1:p.Lys387Thr

Select item 14902623332.

rs1490262333 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:58646173 (GRCh38)
14:59112891 (GRCh37)
Canonical SPDI:: NC_000014.9:58646172:G:A
Gene:: DACT1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000014.9:g.58646173G>A, NC_000014.8:g.59112891G>A, NG_032025.1:g.17106G>A, NM_016651.6:c.1550G>A, NM_016651.5:c.1550G>A, NM_001079520.2:c.1439G>A, NM_001079520.1:c.1439G>A, NR_046093.2:n.1219G>A, NR_046093.1:n.1212G>A, NR_165652.1:n.1631G>A, NR_165651.1:n.1599G>A, NR_046095.1:n.1520G>A, NR_165650.1:n.1330G>A, NP_057735.2:p.Gly517Asp, NP_001072988.1:p.Gly480Asp

Select item 14898025273.

rs1489802527 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 14:58638860 (GRCh38)
14:59105578 (GRCh37)
Canonical SPDI:: NC_000014.9:58638859:G:T
Gene:: DACT1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000014.9:g.58638860G>T, NC_000014.8:g.59105578G>T, NG_032025.1:g.9793G>T, NR_165652.1:n.24G>T, NR_165651.1:n.24G>T, NR_046095.1:n.24G>T

Select item 14891145814.

rs1489114581 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 14:58647364 (GRCh38)
14:59114082 (GRCh37)
Canonical SPDI:: NC_000014.9:58647363:GG:G
Gene:: DACT1 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.58647365del, NC_000014.8:g.59114083del, NG_032025.1:g.18298del, NM_016651.6:c.*231del, NM_016651.5:c.*231del, NM_001079520.2:c.*231del, NM_001079520.1:c.*231del, NR_046093.2:n.2411del, NR_046093.1:n.2404del, NR_165652.1:n.2823del, NR_165651.1:n.2791del, NR_046095.1:n.2712del, NR_165650.1:n.2522del

Select item 14866313265.

rs1486631326 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 14:58645839 (GRCh38)
14:59112557 (GRCh37)
Canonical SPDI:: NC_000014.9:58645838:C:G,NC_000014.9:58645838:C:T
Gene:: DACT1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.58645839C>G, NC_000014.9:g.58645839C>T, NC_000014.8:g.59112557C>G, NC_000014.8:g.59112557C>T, NG_032025.1:g.16772C>G, NG_032025.1:g.16772C>T, NM_016651.6:c.1216C>G, NM_016651.6:c.1216C>T, NM_016651.5:c.1216C>G, NM_016651.5:c.1216C>T, NM_001079520.2:c.1105C>G, NM_001079520.2:c.1105C>T, NM_001079520.1:c.1105C>G, NM_001079520.1:c.1105C>T, NR_046093.2:n.885C>G, NR_046093.2:n.885C>T, NR_046093.1:n.878C>G, NR_046093.1:n.878C>T, NR_165652.1:n.1297C>G, NR_165652.1:n.1297C>T, NR_165651.1:n.1265C>G, NR_165651.1:n.1265C>T, NR_046095.1:n.1186C>G, NR_046095.1:n.1186C>T, NR_165650.1:n.996C>G, NR_165650.1:n.996C>T, NP_057735.2:p.Pro406Ala, NP_057735.2:p.Pro406Ser, NP_001072988.1:p.Pro369Ala, NP_001072988.1:p.Pro369Ser

Select item 14856150576.

rs1485615057 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 14:58647402 (GRCh38)
14:59114120 (GRCh37)
Canonical SPDI:: NC_000014.9:58647401:T:G
Gene:: DACT1 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000014.9:g.58647402T>G, NC_000014.8:g.59114120T>G, NG_032025.1:g.18335T>G, NM_016651.6:c.*268T>G, NM_016651.5:c.*268T>G, NM_001079520.2:c.*268T>G, NM_001079520.1:c.*268T>G, NR_046093.2:n.2448T>G, NR_046093.1:n.2441T>G, NR_165652.1:n.2860T>G, NR_165651.1:n.2828T>G, NR_046095.1:n.2749T>G, NR_165650.1:n.2559T>G

Select item 14840197957.

rs1484019795 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 14:58640861 (GRCh38)
14:59107579 (GRCh37)
Canonical SPDI:: NC_000014.9:58640860:T:A
Gene:: DACT1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.58640861T>A, NC_000014.8:g.59107579T>A, NG_032025.1:g.11794T>A, NM_016651.6:c.471T>A, NM_016651.5:c.471T>A, NM_001079520.2:c.471T>A, NM_001079520.1:c.471T>A, NR_046093.2:n.251T>A, NR_046093.1:n.244T>A, NR_165652.1:n.552T>A, NR_165651.1:n.631T>A, NR_046095.1:n.552T>A, NR_165650.1:n.251T>A

Select item 14834938388.

rs1483493838 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:58647247 (GRCh38)
14:59113965 (GRCh37)
Canonical SPDI:: NC_000014.9:58647246:A:G
Gene:: DACT1 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.58647247A>G, NC_000014.8:g.59113965A>G, NG_032025.1:g.18180A>G, NM_016651.6:c.*113A>G, NM_016651.5:c.*113A>G, NM_001079520.2:c.*113A>G, NM_001079520.1:c.*113A>G, NR_046093.2:n.2293A>G, NR_046093.1:n.2286A>G, NR_165652.1:n.2705A>G, NR_165651.1:n.2673A>G, NR_046095.1:n.2594A>G, NR_165650.1:n.2404A>G

Select item 14833604209.

rs1483360420 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:58646551 (GRCh38)
14:59113269 (GRCh37)
Canonical SPDI:: NC_000014.9:58646550:C:T
Gene:: DACT1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000014.9:g.58646551C>T, NC_000014.8:g.59113269C>T, NG_032025.1:g.17484C>T, NM_016651.6:c.1928C>T, NM_016651.5:c.1928C>T, NM_001079520.2:c.1817C>T, NM_001079520.1:c.1817C>T, NR_046093.2:n.1597C>T, NR_046093.1:n.1590C>T, NR_165652.1:n.2009C>T, NR_165651.1:n.1977C>T, NR_046095.1:n.1898C>T, NR_165650.1:n.1708C>T, NP_057735.2:p.Pro643Leu, NP_001072988.1:p.Pro606Leu

Select item 148334529510.

rs1483345295 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:58646379 (GRCh38)
14:59113097 (GRCh37)
Canonical SPDI:: NC_000014.9:58646378:C:T
Gene:: DACT1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.58646379C>T, NC_000014.8:g.59113097C>T, NG_032025.1:g.17312C>T, NM_016651.6:c.1756C>T, NM_016651.5:c.1756C>T, NM_001079520.2:c.1645C>T, NM_001079520.1:c.1645C>T, NR_046093.2:n.1425C>T, NR_046093.1:n.1418C>T, NR_165652.1:n.1837C>T, NR_165651.1:n.1805C>T, NR_046095.1:n.1726C>T, NR_165650.1:n.1536C>T, NP_057735.2:p.His586Tyr, NP_001072988.1:p.His549Tyr

Select item 148259675111.

rs1482596751 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 14:58639037 (GRCh38)
14:59105755 (GRCh37)
Canonical SPDI:: NC_000014.9:58639036:T:A,NC_000014.9:58639036:T:C
Gene:: DACT1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000014.9:g.58639037T>A, NC_000014.9:g.58639037T>C, NC_000014.8:g.59105755T>A, NC_000014.8:g.59105755T>C, NG_032025.1:g.9970T>A, NG_032025.1:g.9970T>C, NR_165652.1:n.201T>A, NR_165652.1:n.201T>C, NR_165651.1:n.201T>A, NR_165651.1:n.201T>C, NR_046095.1:n.201T>A, NR_046095.1:n.201T>C

Select item 148143795812.

rs1481437958 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:58646420 (GRCh38)
14:59113138 (GRCh37)
Canonical SPDI:: NC_000014.9:58646419:C:T
Gene:: DACT1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000014.9:g.58646420C>T, NC_000014.8:g.59113138C>T, NG_032025.1:g.17353C>T, NM_016651.6:c.1797C>T, NM_016651.5:c.1797C>T, NM_001079520.2:c.1686C>T, NM_001079520.1:c.1686C>T, NR_046093.2:n.1466C>T, NR_046093.1:n.1459C>T, NR_165652.1:n.1878C>T, NR_165651.1:n.1846C>T, NR_046095.1:n.1767C>T, NR_165650.1:n.1577C>T

Select item 148102206613.

rs1481022066 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 14:58646177 (GRCh38)
14:59112895 (GRCh37)
Canonical SPDI:: NC_000014.9:58646176:CCCCCC:CCCCC
Gene:: DACT1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,frameshift_variant
HGVS:: NC_000014.9:g.58646182del, NC_000014.8:g.59112900del, NG_032025.1:g.17115del, NM_016651.6:c.1559del, NM_016651.5:c.1559del, NM_001079520.2:c.1448del, NM_001079520.1:c.1448del, NR_046093.2:n.1228del, NR_046093.1:n.1221del, NR_165652.1:n.1640del, NR_165651.1:n.1608del, NR_046095.1:n.1529del, NR_165650.1:n.1339del, NP_057735.2:p.Pro520fs, NP_001072988.1:p.Pro483fs

Select item 148022197214.

rs1480221972 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACATA>- [Show Flanks]
Chromosome:: 14:58648241 (GRCh38)
14:59114959 (GRCh37)
Canonical SPDI:: NC_000014.9:58648237:ATAACATA:ATA
Gene:: DACT1 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATA=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000015/4 (TOPMED)
-=0.000071/1 (TOMMO)
HGVS:: NC_000014.9:g.58648241_58648245del, NC_000014.8:g.59114959_59114963del, NG_032025.1:g.19174_19178del, NM_016651.6:c.*1107_*1111del, NM_016651.5:c.*1107_*1111del, NM_001079520.2:c.*1107_*1111del, NM_001079520.1:c.*1107_*1111del, NR_046093.2:n.3287_3291del, NR_046093.1:n.3280_3284del, NR_165652.1:n.3699_3703del, NR_165651.1:n.3667_3671del, NR_046095.1:n.3588_3592del, NR_165650.1:n.3398_3402del

Select item 147881701915.

rs1478817019 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:58640770 (GRCh38)
14:59107488 (GRCh37)
Canonical SPDI:: NC_000014.9:58640769:A:G
Gene:: DACT1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_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_000014.9:g.58640770A>G, NC_000014.8:g.59107488A>G, NG_032025.1:g.11703A>G, NM_016651.6:c.380A>G, NM_016651.5:c.380A>G, NM_001079520.2:c.380A>G, NM_001079520.1:c.380A>G, NR_046093.2:n.160A>G, NR_046093.1:n.153A>G, NR_165652.1:n.461A>G, NR_165651.1:n.540A>G, NR_046095.1:n.461A>G, NR_165650.1:n.160A>G, NP_057735.2:p.Asn127Ser, NP_001072988.1:p.Asn127Ser

Select item 147871845816.

rs1478718458 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:58646619 (GRCh38)
14:59113337 (GRCh37)
Canonical SPDI:: NC_000014.9:58646618:G:A
Gene:: DACT1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.58646619G>A, NC_000014.8:g.59113337G>A, NG_032025.1:g.17552G>A, NM_016651.6:c.1996G>A, NM_016651.5:c.1996G>A, NM_001079520.2:c.1885G>A, NM_001079520.1:c.1885G>A, NR_046093.2:n.1665G>A, NR_046093.1:n.1658G>A, NR_165652.1:n.2077G>A, NR_165651.1:n.2045G>A, NR_046095.1:n.1966G>A, NR_165650.1:n.1776G>A, NP_057735.2:p.Val666Met, NP_001072988.1:p.Val629Met

Select item 147871718417.

rs1478717184 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 14:58647485 (GRCh38)
14:59114203 (GRCh37)
Canonical SPDI:: NC_000014.9:58647484:T:G
Gene:: DACT1 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.58647485T>G, NC_000014.8:g.59114203T>G, NG_032025.1:g.18418T>G, NM_016651.6:c.*351T>G, NM_016651.5:c.*351T>G, NM_001079520.2:c.*351T>G, NM_001079520.1:c.*351T>G, NR_046093.2:n.2531T>G, NR_046093.1:n.2524T>G, NR_165652.1:n.2943T>G, NR_165651.1:n.2911T>G, NR_046095.1:n.2832T>G, NR_165650.1:n.2642T>G

Select item 147826624218.

rs1478266242 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 14:58641720 (GRCh38)
14:59108438 (GRCh37)
Canonical SPDI:: NC_000014.9:58641719:C:G
Gene:: DACT1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000014.9:g.58641720C>G, NC_000014.8:g.59108438C>G, NG_032025.1:g.12653C>G, NM_016651.6:c.607C>G, NM_016651.5:c.607C>G, NM_001079520.2:c.607C>G, NM_001079520.1:c.607C>G, NR_046093.2:n.387C>G, NR_046093.1:n.380C>G, NR_165652.1:n.688C>G, NR_165651.1:n.767C>G, NR_046095.1:n.688C>G, NR_165650.1:n.387C>G, NP_057735.2:p.Leu203Val, NP_001072988.1:p.Leu203Val

Select item 147800329519.

rs1478003295 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 14:58646563 (GRCh38)
14:59113281 (GRCh37)
Canonical SPDI:: NC_000014.9:58646562:C:G,NC_000014.9:58646562:C:T
Gene:: DACT1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000014.9:g.58646563C>G, NC_000014.9:g.58646563C>T, NC_000014.8:g.59113281C>G, NC_000014.8:g.59113281C>T, NG_032025.1:g.17496C>G, NG_032025.1:g.17496C>T, NM_016651.6:c.1940C>G, NM_016651.6:c.1940C>T, NM_016651.5:c.1940C>G, NM_016651.5:c.1940C>T, NM_001079520.2:c.1829C>G, NM_001079520.2:c.1829C>T, NM_001079520.1:c.1829C>G, NM_001079520.1:c.1829C>T, NR_046093.2:n.1609C>G, NR_046093.2:n.1609C>T, NR_046093.1:n.1602C>G, NR_046093.1:n.1602C>T, NR_165652.1:n.2021C>G, NR_165652.1:n.2021C>T, NR_165651.1:n.1989C>G, NR_165651.1:n.1989C>T, NR_046095.1:n.1910C>G, NR_046095.1:n.1910C>T, NR_165650.1:n.1720C>G, NR_165650.1:n.1720C>T, NP_057735.2:p.Ala647Gly, NP_057735.2:p.Ala647Val, NP_001072988.1:p.Ala610Gly, NP_001072988.1:p.Ala610Val

Select item 147588651120.

rs1475886511 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:58645492 (GRCh38)
14:59112210 (GRCh37)
Canonical SPDI:: NC_000014.9:58645491:A:G
Gene:: DACT1 (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.58645492A>G, NC_000014.8:g.59112210A>G, NG_032025.1:g.16425A>G, NM_016651.6:c.869A>G, NM_016651.5:c.869A>G, NM_001079520.2:c.758A>G, NM_001079520.1:c.758A>G, NR_046093.2:n.538A>G, NR_046093.1:n.531A>G, NR_165652.1:n.950A>G, NR_165651.1:n.918A>G, NR_046095.1:n.839A>G, NR_165650.1:n.649A>G, NP_057735.2:p.Asn290Ser, NP_001072988.1:p.Asn253Ser

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