SNP Links for Nucleotide (Select 633257804) - SNP

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Links from Nucleotide

Items: 1 to 20 of 844

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Select item 14914413381.

rs1491441338 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 21:38878449 (GRCh38)
21:40250373 (GRCh37)
Canonical SPDI:: NC_000021.9:38878447:ACA:A
Gene:: LOC400867 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.000021/3 (GnomAD)
HGVS:: NC_000021.9:g.38878449_38878450del, NC_000021.8:g.40250373_40250374del, NR_120405.1:n.2665_2666del, NM_001001692.1:c.*57_*58del

Select item 14909313592.

rs1490931359 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 21:38878067 (GRCh38)
21:40249991 (GRCh37)
Canonical SPDI:: NC_000021.9:38878066:C:G
Gene:: LOC400867 (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=0.000021/3 (GnomAD)
HGVS:: NC_000021.9:g.38878067C>G, NC_000021.8:g.40249991C>G, NR_120405.1:n.3047G>C, NM_001001692.1:c.*439G>C

Select item 14908798523.

rs1490879852 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:38879413 (GRCh38)
21:40251337 (GRCh37)
Canonical SPDI:: NC_000021.9:38879412:T:C
Gene:: LOC400867 (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_000021.9:g.38879413T>C, NC_000021.8:g.40251337T>C, NR_120405.1:n.1701A>G, NM_001001692.1:c.-496A>G

Select item 14908661844.

rs1490866184 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 21:38878585 (GRCh38)
21:40250510 (GRCh37)
Canonical SPDI:: NC_000021.9:38878585:A:AA
Gene:: LOC400867 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000021.9:g.38878586dup, NC_000021.8:g.40250510dup, NR_120405.1:n.2528dup, NM_001001692.1:c.331dup

Select item 14901143125.

rs1490114312 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 21:38879242 (GRCh38)
21:40251166 (GRCh37)
Canonical SPDI:: NC_000021.9:38879241:G:A
Gene:: LOC400867 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000021.9:g.38879242G>A, NC_000021.8:g.40251166G>A, NR_120405.1:n.1872C>T, NM_001001692.1:c.-326C>T

Select item 14883888786.

rs1488388878 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:38938351 (GRCh38)
21:40310275 (GRCh37)
Canonical SPDI:: NC_000021.9:38938350:T:C
Gene:: LOC400867 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000021.9:g.38938351T>C, NC_000021.8:g.40310275T>C, NR_120405.1:n.79A>G, NM_001001692.1:c.-2118A>G

Select item 14870616847.

rs1487061684 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:38877946 (GRCh38)
21:40249870 (GRCh37)
Canonical SPDI:: NC_000021.9:38877945:T:C
Gene:: LOC400867 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000021.9:g.38877946T>C, NC_000021.8:g.40249870T>C, NR_120405.1:n.3168A>G, NM_001001692.1:c.*560A>G

Select item 14857712438.

rs1485771243 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:38879604 (GRCh38)
21:40251528 (GRCh37)
Canonical SPDI:: NC_000021.9:38879603:A:G
Gene:: LOC400867 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000038/10 (TOPMED)
HGVS:: NC_000021.9:g.38879604A>G, NC_000021.8:g.40251528A>G, NR_120405.1:n.1510T>C, NM_001001692.1:c.-687T>C

Select item 14847820239.

rs1484782023 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:38877731 (GRCh38)
21:40249655 (GRCh37)
Canonical SPDI:: NC_000021.9:38877730:T:C
Gene:: LOC400867 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000021.9:g.38877731T>C, NC_000021.8:g.40249655T>C, NR_120405.1:n.3383A>G, NM_001001692.1:c.*775A>G

Select item 148331575510.

rs1483315755 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 21:38938417 (GRCh38)
21:40310341 (GRCh37)
Canonical SPDI:: NC_000021.9:38938416:C:G
Gene:: LOC400867 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000023/6 (TOPMED)
HGVS:: NC_000021.9:g.38938417C>G, NC_000021.8:g.40310341C>G, NR_120405.1:n.13G>C, NM_001001692.1:c.-2184G>C

Select item 148306730911.

rs1483067309 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:38880316 (GRCh38)
21:40252240 (GRCh37)
Canonical SPDI:: NC_000021.9:38880315:T:C
Gene:: LOC400867 (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_000021.9:g.38880316T>C, NC_000021.8:g.40252240T>C, NR_120405.1:n.798A>G, NM_001001692.1:c.-1399A>G

Select item 148206366012.

rs1482063660 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 21:38879029 (GRCh38)
21:40250953 (GRCh37)
Canonical SPDI:: NC_000021.9:38879028:A:C
Gene:: LOC400867 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000021.9:g.38879029A>C, NC_000021.8:g.40250953A>C, NR_120405.1:n.2085T>G, NM_001001692.1:c.-113T>G

Select item 148060599313.

rs1480605993 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:38938226 (GRCh38)
21:40310150 (GRCh37)
Canonical SPDI:: NC_000021.9:38938225:T:C
Gene:: LOC400867 (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=0.000008/2 (TOPMED)
HGVS:: NC_000021.9:g.38938226T>C, NC_000021.8:g.40310150T>C, NR_120405.1:n.204A>G, NM_001001692.1:c.-1993A>G

Select item 148021893614.

rs1480218936 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:38879051 (GRCh38)
21:40250975 (GRCh37)
Canonical SPDI:: NC_000021.9:38879050:T:C
Gene:: LOC400867 (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=0.000008/2 (TOPMED)
HGVS:: NC_000021.9:g.38879051T>C, NC_000021.8:g.40250975T>C, NR_120405.1:n.2063A>G, NM_001001692.1:c.-135A>G

Select item 147979432715.

rs1479794327 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 21:38879317 (GRCh38)
21:40251241 (GRCh37)
Canonical SPDI:: NC_000021.9:38879316:G:A
Gene:: LOC400867 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000021.9:g.38879317G>A, NC_000021.8:g.40251241G>A, NR_120405.1:n.1797C>T, NM_001001692.1:c.-401C>T

Select item 147923835616.

rs1479238356 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:38877690 (GRCh38)
21:40249614 (GRCh37)
Canonical SPDI:: NC_000021.9:38877689:A:G
Gene:: LOC400867 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000021.9:g.38877690A>G, NC_000021.8:g.40249614A>G, NR_120405.1:n.3424T>C, NM_001001692.1:c.*816T>C

Select item 147868902117.

rs1478689021 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 21:38937857 (GRCh38)
21:40309781 (GRCh37)
Canonical SPDI:: NC_000021.9:38937856:C:A
Gene:: LOC400867 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000021.9:g.38937857C>A, NC_000021.8:g.40309781C>A, NR_120405.1:n.573G>T, NM_001001692.1:c.-1624G>T

Select item 147859815818.

rs1478598158 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:38877720 (GRCh38)
21:40249644 (GRCh37)
Canonical SPDI:: NC_000021.9:38877719:T:C
Gene:: LOC400867 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00007/1 (TOMMO)
HGVS:: NC_000021.9:g.38877720T>C, NC_000021.8:g.40249644T>C, NR_120405.1:n.3394A>G, NM_001001692.1:c.*786A>G

Select item 147822971419.

rs1478229714 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:38879681 (GRCh38)
21:40251605 (GRCh37)
Canonical SPDI:: NC_000021.9:38879680:A:G
Gene:: LOC400867 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000023/6 (TOPMED)
HGVS:: NC_000021.9:g.38879681A>G, NC_000021.8:g.40251605A>G, NR_120405.1:n.1433T>C, NM_001001692.1:c.-764T>C

Select item 147788892920.

rs1477888929 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:38937987 (GRCh38)
21:40309911 (GRCh37)
Canonical SPDI:: NC_000021.9:38937986:A:G
Gene:: LOC400867 (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_000021.9:g.38937987A>G, NC_000021.8:g.40309911A>G, NR_120405.1:n.443T>C, NM_001001692.1:c.-1754T>C