SNP Links for Nucleotide (Select 649572491) - SNP

Links from Nucleotide

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Select item 14830069771.

rs1483006977 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:72873079 (GRCh38)
9:75487995 (GRCh37)
Canonical SPDI:: NC_000009.12:72873078:A:G
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000009.12:g.72873079A>G, NC_000009.11:g.75487995A>G, NR_121120.1:n.171T>C, NR_121180.1:n.171T>C, NR_121181.1:n.119T>C

Select item 14825064672.

rs1482506467 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:72872231 (GRCh38)
9:75487147 (GRCh37)
Canonical SPDI:: NC_000009.12:72872230:C:T
Gene:: LINC01474 (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_000009.12:g.72872231C>T, NC_000009.11:g.75487147C>T, NR_121120.1:n.224G>A, NR_121180.1:n.224G>A, NR_121181.1:n.172G>A

Select item 14667728133.

rs1466772813 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:72871870 (GRCh38)
9:75486786 (GRCh37)
Canonical SPDI:: NC_000009.12:72871869:A:G
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.72871870A>G, NC_000009.11:g.75486786A>G, NR_121120.1:n.497T>C, NR_121180.1:n.493T>C, NR_121181.1:n.441T>C

Select item 14588994974.

rs1458899497 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 9:72871811 (GRCh38)
9:75486727 (GRCh37)
Canonical SPDI:: NC_000009.12:72871810:G:A,NC_000009.12:72871810:G:T
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000009.12:g.72871811G>A, NC_000009.12:g.72871811G>T, NC_000009.11:g.75486727G>A, NC_000009.11:g.75486727G>T, NR_121120.1:n.556C>T, NR_121120.1:n.556C>A, NR_121180.1:n.552C>T, NR_121180.1:n.552C>A, NR_121181.1:n.500C>T, NR_121181.1:n.500C>A

Select item 14529084885.

rs1452908488 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:72871991 (GRCh38)
9:75486907 (GRCh37)
Canonical SPDI:: NC_000009.12:72871990:T:C
Gene:: LINC01474 (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=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.72871991T>C, NC_000009.11:g.75486907T>C, NR_121120.1:n.376A>G, NR_121180.1:n.372A>G, NR_121181.1:n.320A>G

Select item 14525567826.

rs1452556782 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:72871982 (GRCh38)
9:75486898 (GRCh37)
Canonical SPDI:: NC_000009.12:72871981:A:G
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.72871982A>G, NC_000009.11:g.75486898A>G, NR_121120.1:n.385T>C, NR_121180.1:n.381T>C, NR_121181.1:n.329T>C

Select item 14335112157.

rs1433511215 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 9:72871794 (GRCh38)
9:75486710 (GRCh37)
Canonical SPDI:: NC_000009.12:72871793:GG:G
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0.000071/1 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.72871795del, NC_000009.11:g.75486711del, NR_121120.1:n.573del, NR_121180.1:n.569del, NR_121181.1:n.517del

Select item 14243792458.

rs1424379245 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:72872111 (GRCh38)
9:75487027 (GRCh37)
Canonical SPDI:: NC_000009.12:72872110:G:A
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.72872111G>A, NC_000009.11:g.75487027G>A, NR_121120.1:n.344C>T, NR_121180.1:n.344C>T, NR_121181.1:n.292C>T

Select item 14161322069.

rs1416132206 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:72872208 (GRCh38)
9:75487124 (GRCh37)
Canonical SPDI:: NC_000009.12:72872207:G:A
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.72872208G>A, NC_000009.11:g.75487124G>A, NR_121120.1:n.247C>T, NR_121180.1:n.247C>T, NR_121181.1:n.195C>T

Select item 141380013010.

rs1413800130 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:72872226 (GRCh38)
9:75487142 (GRCh37)
Canonical SPDI:: NC_000009.12:72872225:T:C
Gene:: LINC01474 (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=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.72872226T>C, NC_000009.11:g.75487142T>C, NR_121120.1:n.229A>G, NR_121180.1:n.229A>G, NR_121181.1:n.177A>G

Select item 140906208511.

rs1409062085 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 9:72872211 (GRCh38)
9:75487127 (GRCh37)
Canonical SPDI:: NC_000009.12:72872210:T:A,NC_000009.12:72872210:T:C
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.72872211T>A, NC_000009.12:g.72872211T>C, NC_000009.11:g.75487127T>A, NC_000009.11:g.75487127T>C, NR_121120.1:n.244A>T, NR_121120.1:n.244A>G, NR_121180.1:n.244A>T, NR_121180.1:n.244A>G, NR_121181.1:n.192A>T, NR_121181.1:n.192A>G

Select item 140904191612.

rs1409041916 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:72873144 (GRCh38)
9:75488060 (GRCh37)
Canonical SPDI:: NC_000009.12:72873143:C:A
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.72873144C>A, NC_000009.11:g.75488060C>A, NR_121120.1:n.106G>T, NR_121180.1:n.106G>T, NR_121181.1:n.54G>T

Select item 139906497413.

rs1399064974 [Homo sapiens]

Variant type:: INS
Alleles:: ->CT [Show Flanks]
Chromosome:: 9:72872146 (GRCh38)
9:75487063 (GRCh37)
Canonical SPDI:: NC_000009.12:72872146::CT
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: CT=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.72872146_72872147insCT, NC_000009.11:g.75487062_75487063insCT, NR_121120.1:n.308_309insAG, NR_121180.1:n.308_309insAG, NR_121181.1:n.256_257insAG

Select item 138415698114.

rs1384156981 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:72874074 (GRCh38)
9:75488990 (GRCh37)
Canonical SPDI:: NC_000009.12:72874073:G:A
Gene:: LINC01474 (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_000009.12:g.72874074G>A, NC_000009.11:g.75488990G>A, NR_121120.1:n.36C>T, NR_121180.1:n.36C>T, NR_121181.1:n.36C>T

Select item 136633576415.

rs1366335764 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 9:72871935 (GRCh38)
9:75486851 (GRCh37)
Canonical SPDI:: NC_000009.12:72871934:G:A,NC_000009.12:72871934:G:T
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.72871935G>A, NC_000009.12:g.72871935G>T, NC_000009.11:g.75486851G>A, NC_000009.11:g.75486851G>T, NR_121120.1:n.432C>T, NR_121120.1:n.432C>A, NR_121180.1:n.428C>T, NR_121180.1:n.428C>A, NR_121181.1:n.376C>T, NR_121181.1:n.376C>A

Select item 136503238716.

rs1365032387 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:72871918 (GRCh38)
9:75486834 (GRCh37)
Canonical SPDI:: NC_000009.12:72871917:T:C
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000009.12:g.72871918T>C, NC_000009.11:g.75486834T>C, NR_121120.1:n.449A>G, NR_121180.1:n.445A>G, NR_121181.1:n.393A>G

Select item 136342108417.

rs1363421084 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 9:72874082 (GRCh38)
9:75488998 (GRCh37)
Canonical SPDI:: NC_000009.12:72874081:G:C,NC_000009.12:72874081:G:T
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000009.12:g.72874082G>C, NC_000009.12:g.72874082G>T, NC_000009.11:g.75488998G>C, NC_000009.11:g.75488998G>T, NR_121120.1:n.28C>G, NR_121120.1:n.28C>A, NR_121180.1:n.28C>G, NR_121180.1:n.28C>A, NR_121181.1:n.28C>G, NR_121181.1:n.28C>A

Select item 135848179318.

rs1358481793 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:72872202 (GRCh38)
9:75487118 (GRCh37)
Canonical SPDI:: NC_000009.12:72872201:C:T
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
HGVS:: NC_000009.12:g.72872202C>T, NC_000009.11:g.75487118C>T, NR_121120.1:n.253G>A, NR_121180.1:n.253G>A, NR_121181.1:n.201G>A

Select item 135826601219.

rs1358266012 [Homo sapiens]

Variant type:: INS
Alleles:: ->GAGT [Show Flanks]
Chromosome:: 9:72872144 (GRCh38)
9:75487061 (GRCh37)
Canonical SPDI:: NC_000009.12:72872144::GAGT
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: GAGT=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.72872144_72872145insGAGT, NC_000009.11:g.75487060_75487061insGAGT, NR_121120.1:n.310_311insACTC, NR_121180.1:n.310_311insACTC, NR_121181.1:n.258_259insACTC

Select item 135500737120.

rs1355007371 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:72873153 (GRCh38)
9:75488069 (GRCh37)
Canonical SPDI:: NC_000009.12:72873152:T:C
Gene:: LINC01474 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
HGVS:: NC_000009.12:g.72873153T>C, NC_000009.11:g.75488069T>C, NR_121120.1:n.97A>G, NR_121180.1:n.97A>G, NR_121181.1:n.45A>G

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