SNP Links for Nucleotide (Select 1236511455) - SNP

Links from Nucleotide

Items: 1 to 20 of 585

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Select item 14906945301.

rs1490694530 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 10:31317334 (GRCh38)
10:31606264 (GRCh37)
Canonical SPDI:: NC_000010.11:31317334:A:AA
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant,intron_variant
HGVS:: NC_000010.11:g.31317335dup, NC_000010.10:g.31606264dup, NG_017048.1:g.3164dup, NR_148977.1:n.1761dup, NR_148976.1:n.1573dup, NR_024284.1:n.1406dup, NR_148975.1:n.1371dup

Select item 14892433702.

rs1489243370 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:31318513 (GRCh38)
10:31607442 (GRCh37)
Canonical SPDI:: NC_000010.11:31318512:G:A
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.31318513G>A, NC_000010.10:g.31607442G>A, NG_017048.1:g.4342G>A, NM_001323638.2:c.-1349G>A, NM_001323638.1:c.-1349G>A, NM_001323643.2:c.-1009G>A, NM_001323643.1:c.-1009G>A, NR_024285.1:n.19G>A, NR_148977.1:n.583C>T, NR_148976.1:n.395C>T, NR_024284.1:n.228C>T, NR_148975.1:n.193C>T

Select item 14878213513.

rs1487821351 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:31319653 (GRCh38)
10:31608582 (GRCh37)
Canonical SPDI:: NC_000010.11:31319652:G:A
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000010.11:g.31319653G>A, NC_000010.10:g.31608582G>A, NG_017048.1:g.5482G>A, NR_148976.1:n.229C>T

Select item 14872894534.

rs1487289453 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 10:31317679 (GRCh38)
10:31606608 (GRCh37)
Canonical SPDI:: NC_000010.11:31317678:G:T
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.31317679G>T, NC_000010.10:g.31606608G>T, NG_017048.1:g.3508G>T, NR_148977.1:n.1417C>A, NR_148976.1:n.1229C>A, NR_024284.1:n.1062C>A, NR_148975.1:n.1027C>A

Select item 14860560405.

rs1486056040 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:31319787 (GRCh38)
10:31608716 (GRCh37)
Canonical SPDI:: NC_000010.11:31319786:G:A
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant,upstream_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_000010.11:g.31319787G>A, NC_000010.10:g.31608716G>A, NG_017048.1:g.5616G>A, NM_001323657.2:c.-1020G>A, NM_001323656.2:c.-1017G>A, NM_001323658.2:c.-859G>A, NR_148976.1:n.95C>T

Select item 14853279396.

rs1485327939 [Homo sapiens]

Variant type:: INS
Alleles:: ->TCTTCTACAT [Show Flanks]
Chromosome:: 10:31316689 (GRCh38)
10:31605619 (GRCh37)
Canonical SPDI:: NC_000010.11:31316689::TCTTCTACAT
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTTCTACAT=0./0 (ALFA)
TCTTCTACAT=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.31316689_31316690insTCTTCTACAT, NC_000010.10:g.31605618_31605619insTCTTCTACAT, NG_017048.1:g.2518_2519insTCTTCTACAT, NR_148977.1:n.2406_2407insATGTAGAAGA, NR_148976.1:n.2218_2219insATGTAGAAGA, NR_024284.1:n.2051_2052insATGTAGAAGA, NR_148975.1:n.2016_2017insATGTAGAAGA

Select item 14833309007.

rs1483330900 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 10:31317541 (GRCh38)
10:31606470 (GRCh37)
Canonical SPDI:: NC_000010.11:31317540:A:C
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000010.11:g.31317541A>C, NC_000010.10:g.31606470A>C, NG_017048.1:g.3370A>C, NR_148977.1:n.1555T>G, NR_148976.1:n.1367T>G, NR_024284.1:n.1200T>G, NR_148975.1:n.1165T>G

Select item 14828741188.

rs1482874118 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:31318422 (GRCh38)
10:31607351 (GRCh37)
Canonical SPDI:: NC_000010.11:31318421:G:A
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.31318422G>A, NC_000010.10:g.31607351G>A, NG_017048.1:g.4251G>A, NM_001323638.2:c.-1440G>A, NM_001323643.2:c.-1100G>A, NR_148977.1:n.674C>T, NR_148976.1:n.486C>T, NR_024284.1:n.319C>T, NR_148975.1:n.284C>T

Select item 14812711659.

rs1481271165 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:31316634 (GRCh38)
10:31605563 (GRCh37)
Canonical SPDI:: NC_000010.11:31316633:A:G
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_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_000010.11:g.31316634A>G, NC_000010.10:g.31605563A>G, NG_017048.1:g.2463A>G, NR_148977.1:n.2462T>C, NR_148976.1:n.2274T>C, NR_024284.1:n.2107T>C, NR_148975.1:n.2072T>C

Select item 147771595010.

rs1477715950 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 10:31318267 (GRCh38)
10:31607196 (GRCh37)
Canonical SPDI:: NC_000010.11:31318266:C:A,NC_000010.11:31318266:C:G
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000010.11:g.31318267C>A, NC_000010.11:g.31318267C>G, NC_000010.10:g.31607196C>A, NC_000010.10:g.31607196C>G, NG_017048.1:g.4096C>A, NG_017048.1:g.4096C>G, NR_148977.1:n.829G>T, NR_148977.1:n.829G>C, NR_148976.1:n.641G>T, NR_148976.1:n.641G>C, NR_024284.1:n.474G>T, NR_024284.1:n.474G>C, NR_148975.1:n.439G>T, NR_148975.1:n.439G>C

Select item 147708596611.

rs1477085966 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:31317335 (GRCh38)
10:31606264 (GRCh37)
Canonical SPDI:: NC_000010.11:31317334:A:G
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.31317335A>G, NC_000010.10:g.31606264A>G, NG_017048.1:g.3164A>G, NR_148977.1:n.1761T>C, NR_148976.1:n.1573T>C, NR_024284.1:n.1406T>C, NR_148975.1:n.1371T>C

Select item 147375553612.

rs1473755536 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 10:31318161 (GRCh38)
10:31607090 (GRCh37)
Canonical SPDI:: NC_000010.11:31318160:A:C
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_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_000010.11:g.31318161A>C, NC_000010.10:g.31607090A>C, NG_017048.1:g.3990A>C, NR_148977.1:n.935T>G, NR_148976.1:n.747T>G, NR_024284.1:n.580T>G, NR_148975.1:n.545T>G

Select item 147292756613.

rs1472927566 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 10:31318028 (GRCh38)
10:31606957 (GRCh37)
Canonical SPDI:: NC_000010.11:31318027:C:A
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.31318028C>A, NC_000010.10:g.31606957C>A, NG_017048.1:g.3857C>A, NR_148977.1:n.1068G>T, NR_148976.1:n.880G>T, NR_024284.1:n.713G>T, NR_148975.1:n.678G>T

Select item 147276605714.

rs1472766057 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:31317628 (GRCh38)
10:31606557 (GRCh37)
Canonical SPDI:: NC_000010.11:31317627:A:G
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000010.11:g.31317628A>G, NC_000010.10:g.31606557A>G, NG_017048.1:g.3457A>G, NR_148977.1:n.1468T>C, NR_148976.1:n.1280T>C, NR_024284.1:n.1113T>C, NR_148975.1:n.1078T>C

Select item 147187862115.

rs1471878621 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 10:31318254 (GRCh38)
10:31607183 (GRCh37)
Canonical SPDI:: NC_000010.11:31318253:G:A,NC_000010.11:31318253:G:C
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000010.11:g.31318254G>A, NC_000010.11:g.31318254G>C, NC_000010.10:g.31607183G>A, NC_000010.10:g.31607183G>C, NG_017048.1:g.4083G>A, NG_017048.1:g.4083G>C, NR_148977.1:n.842C>T, NR_148977.1:n.842C>G, NR_148976.1:n.654C>T, NR_148976.1:n.654C>G, NR_024284.1:n.487C>T, NR_024284.1:n.487C>G, NR_148975.1:n.452C>T, NR_148975.1:n.452C>G

Select item 147106980116.

rs1471069801 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 10:31319715 (GRCh38)
10:31608644 (GRCh37)
Canonical SPDI:: NC_000010.11:31319714:C:A,NC_000010.11:31319714:C:T
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000010.11:g.31319715C>A, NC_000010.11:g.31319715C>T, NC_000010.10:g.31608644C>A, NC_000010.10:g.31608644C>T, NG_017048.1:g.5544C>A, NG_017048.1:g.5544C>T, NR_148976.1:n.167G>T, NR_148976.1:n.167G>A

Select item 146979146817.

rs1469791468 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:31317015 (GRCh38)
10:31605944 (GRCh37)
Canonical SPDI:: NC_000010.11:31317014:T:C
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000212/4 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000399/56 (GnomAD)
C=0.000893/4 (Estonian)
HGVS:: NC_000010.11:g.31317015T>C, NC_000010.10:g.31605944T>C, NG_017048.1:g.2844T>C, NR_148977.1:n.2081A>G, NR_148976.1:n.1893A>G, NR_024284.1:n.1726A>G, NR_148975.1:n.1691A>G

Select item 146925116618.

rs1469251166 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:31319685 (GRCh38)
10:31608614 (GRCh37)
Canonical SPDI:: NC_000010.11:31319684:T:C
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.31319685T>C, NC_000010.10:g.31608614T>C, NG_017048.1:g.5514T>C, NR_148976.1:n.197A>G

Select item 146770679619.

rs1467706796 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:31316552 (GRCh38)
10:31605481 (GRCh37)
Canonical SPDI:: NC_000010.11:31316551:C:G
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000029/4 (GnomAD)
HGVS:: NC_000010.11:g.31316552C>G, NC_000010.10:g.31605481C>G, NG_017048.1:g.2381C>G, NR_148977.1:n.2544G>C, NR_148976.1:n.2356G>C, NR_024284.1:n.2189G>C, NR_148975.1:n.2154G>C

Select item 146671235120.

rs1466712351 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 10:31317141 (GRCh38)
10:31606071 (GRCh37)
Canonical SPDI:: NC_000010.11:31317141:AA:AAA
Gene:: ZEB1 (Varview), ZEB1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
HGVS:: NC_000010.11:g.31317143dup, NC_000010.10:g.31606072dup, NG_017048.1:g.2972dup, NR_148977.1:n.1954dup, NR_148976.1:n.1766dup, NR_024284.1:n.1599dup, NR_148975.1:n.1564dup

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