SNP Links for Gene (Select 7539) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 20 of 4007

<< First< Prev

Page of 201

Next >Last >>

Select item 14914147201.

rs1491414720 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->TATATATATACATATATATACACATATATATATATGTG
Chromosome:: no mapping
Canonical SPDI:

Select item 14913523372.

rs1491352337 has merged into rs552307250 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>-,TATA [Show Flanks]
Chromosome:: 9:113058577 (GRCh38)
9:115820857 (GRCh37)
Canonical SPDI:: NC_000009.12:113058567:ATATATATATA:ATATATATA,NC_000009.12:113058567:ATATATATATA:ATATATATATATA
Gene:: ZFP37 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATA=0.00012/2 (ALFA)
-=0.00055/1 (Korea1K)
AT=0.00679/34 (1000Genomes)
HGVS:: NC_000009.12:g.113058569TA[4], NC_000009.12:g.113058569TA[6], NC_000009.11:g.115820849TA[4], NC_000009.11:g.115820849TA[6], NG_047087.1:g.3215AT[4], NG_047087.1:g.3215AT[6]

Select item 14913144053.

rs1491314405 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CATTTA [Show Flanks]
Chromosome:: 9:113043142 (GRCh38)
9:115805423 (GRCh37)
Canonical SPDI:: NC_000009.12:113043142:TTACATTTA:TTACATTTACATTTA
Gene:: ZFP37 (Varview)
Functional Consequence:: coding_sequence_variant,inframe_insertion
Validated:: by frequency
MAF:: TTACAT=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.113043146_113043151dup, NC_000009.11:g.115805426_115805431dup, NG_047087.1:g.18644_18649dup, NM_003408.3:c.1470_1475dup, NM_003408.2:c.1470_1475dup, NM_003408.1:c.1470_1475dup, NM_001282515.2:c.1515_1520dup, NM_001282515.1:c.1515_1520dup, NM_001282518.2:c.1473_1478dup, NM_001282518.1:c.1473_1478dup, NP_003399.1:p.Lys490_Cys491dup, NP_001269444.1:p.Lys505_Cys506dup, NP_001269447.1:p.Lys491_Cys492dup

Select item 14912013804.

rs1491201380 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 9:113043142 (GRCh38)
9:115805422 (GRCh37)
Canonical SPDI:: NC_000009.12:113043141:AT:
Gene:: ZFP37 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000071/1 (ALFA)
-=0.000008/2 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.113043142_113043143del, NC_000009.11:g.115805422_115805423del, NG_047087.1:g.18649_18650del, NM_003408.3:c.1475_1476del, NM_003408.2:c.1475_1476del, NM_003408.1:c.1475_1476del, NM_001282515.2:c.1520_1521del, NM_001282515.1:c.1520_1521del, NM_001282518.2:c.1478_1479del, NM_001282518.1:c.1478_1479del, NP_003399.1:p.Asn492fs, NP_001269444.1:p.Asn507fs, NP_001269447.1:p.Asn493fs

Select item 14907995115.

rs1490799511 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:113056878 (GRCh38)
9:115819158 (GRCh37)
Canonical SPDI:: NC_000009.12:113056877:C:T
Gene:: ZFP37 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.113056878C>T, NC_000009.11:g.115819158C>T, NG_047087.1:g.4914G>A

Select item 14907438386.

rs1490743838 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:113057773 (GRCh38)
9:115820053 (GRCh37)
Canonical SPDI:: NC_000009.12:113057772:A:G
Gene:: ZFP37 (Varview)
Functional Consequence:: 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_000009.12:g.113057773A>G, NC_000009.11:g.115820053A>G, NG_047087.1:g.4019T>C

Select item 14906602297.

rs1490660229 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:113056230 (GRCh38)
9:115818510 (GRCh37)
Canonical SPDI:: NC_000009.12:113056229:A:G
Gene:: ZFP37 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD)
G=0.000106/2 (TOMMO)
G=0.000342/1 (KOREAN)
HGVS:: NC_000009.12:g.113056230A>G, NC_000009.11:g.115818510A>G, NG_047087.1:g.5562T>C

Select item 14905889568.

rs1490588956 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:113058141 (GRCh38)
9:115820421 (GRCh37)
Canonical SPDI:: NC_000009.12:113058140:C:T
Gene:: ZFP37 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.113058141C>T, NC_000009.11:g.115820421C>T, NG_047087.1:g.3651G>A

Select item 14905805929.

rs1490580592 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:113058542 (GRCh38)
9:115820822 (GRCh37)
Canonical SPDI:: NC_000009.12:113058541:A:G
Gene:: ZFP37 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.113058542A>G, NC_000009.11:g.115820822A>G, NG_047087.1:g.3250T>C

Select item 149051796610.

rs1490517966 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 9:113057381 (GRCh38)
9:115819661 (GRCh37)
Canonical SPDI:: NC_000009.12:113057380:G:A,NC_000009.12:113057380:G:C
Gene:: ZFP37 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.113057381G>A, NC_000009.12:g.113057381G>C, NC_000009.11:g.115819661G>A, NC_000009.11:g.115819661G>C, NG_047087.1:g.4411C>T, NG_047087.1:g.4411C>G

Select item 148994921911.

rs1489949219 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 9:113058721 (GRCh38)
9:115821001 (GRCh37)
Canonical SPDI:: NC_000009.12:113058720:A:C,NC_000009.12:113058720:A:G
Gene:: ZFP37 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000009.12:g.113058721A>C, NC_000009.12:g.113058721A>G, NC_000009.11:g.115821001A>C, NC_000009.11:g.115821001A>G, NG_047087.1:g.3071T>G, NG_047087.1:g.3071T>C

Select item 148986866812.

rs1489868668 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:113051764 (GRCh38)
9:115814044 (GRCh37)
Canonical SPDI:: NC_000009.12:113051763:T:A
Gene:: ZFP37 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.113051764T>A, NC_000009.11:g.115814044T>A, NG_047087.1:g.10028A>T

Select item 148984216213.

rs1489842162 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 9:113054933 (GRCh38)
9:115817213 (GRCh37)
Canonical SPDI:: NC_000009.12:113054932:C:A,NC_000009.12:113054932:C:T
Gene:: ZFP37 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000009.12:g.113054933C>A, NC_000009.12:g.113054933C>T, NC_000009.11:g.115817213C>A, NC_000009.11:g.115817213C>T, NG_047087.1:g.6859G>T, NG_047087.1:g.6859G>A

Select item 148974782014.

rs1489747820 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 9:113058448 (GRCh38)
9:115820728 (GRCh37)
Canonical SPDI:: NC_000009.12:113058447:A:C,NC_000009.12:113058447:A:G,NC_000009.12:113058447:A:T
Gene:: ZFP37 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000009.12:g.113058448A>C, NC_000009.12:g.113058448A>G, NC_000009.12:g.113058448A>T, NC_000009.11:g.115820728A>C, NC_000009.11:g.115820728A>G, NC_000009.11:g.115820728A>T, NG_047087.1:g.3344T>G, NG_047087.1:g.3344T>C, NG_047087.1:g.3344T>A

Select item 148956220615.

rs1489562206 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:113043454 (GRCh38)
9:115805734 (GRCh37)
Canonical SPDI:: NC_000009.12:113043453:G:A
Gene:: ZFP37 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.113043454G>A, NC_000009.11:g.115805734G>A, NG_047087.1:g.18338C>T, NM_003408.3:c.1164C>T, NM_003408.2:c.1164C>T, NM_003408.1:c.1164C>T, NM_001282515.2:c.1209C>T, NM_001282515.1:c.1209C>T, NM_001282518.2:c.1167C>T, NM_001282518.1:c.1167C>T

Select item 148955839316.

rs1489558393 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:113042938 (GRCh38)
9:115805218 (GRCh37)
Canonical SPDI:: NC_000009.12:113042937:G:A
Gene:: ZFP37 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.113042938G>A, NC_000009.11:g.115805218G>A, NG_047087.1:g.18854C>T, NM_003408.3:c.1680C>T, NM_003408.2:c.1680C>T, NM_003408.1:c.1680C>T, NM_001282515.2:c.1725C>T, NM_001282515.1:c.1725C>T, NM_001282518.2:c.1683C>T, NM_001282518.1:c.1683C>T

Select item 148948473017.

rs1489484730 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:113054630 (GRCh38)
9:115816910 (GRCh37)
Canonical SPDI:: NC_000009.12:113054629:T:C
Gene:: ZFP37 (Varview)
Functional Consequence:: intron_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_000009.12:g.113054630T>C, NC_000009.11:g.115816910T>C, NG_047087.1:g.7162A>G

Select item 148941817318.

rs1489418173 has merged into rs1262691243 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACA>-,CA [Show Flanks]
Chromosome:: 9:113058543 (GRCh38)
9:115820823 (GRCh37)
Canonical SPDI:: NC_000009.12:113058539:ACACACA:ACA,NC_000009.12:113058539:ACACACA:ACACA
Gene:: ZFP37 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACA=0./0 (ALFA)
HGVS:: NC_000009.12:g.113058541CA[1], NC_000009.12:g.113058541CA[2], NC_000009.11:g.115820821CA[1], NC_000009.11:g.115820821CA[2], NG_047087.1:g.3247GT[1], NG_047087.1:g.3247GT[2]

Select item 148938130019.

rs1489381300 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:113042837 (GRCh38)
9:115805117 (GRCh37)
Canonical SPDI:: NC_000009.12:113042836:G:T
Gene:: ZFP37 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.113042837G>T, NC_000009.11:g.115805117G>T, NG_047087.1:g.18955C>A, NM_003408.3:c.1781C>A, NM_003408.2:c.1781C>A, NM_003408.1:c.1781C>A, NM_001282515.2:c.1826C>A, NM_001282515.1:c.1826C>A, NM_001282518.2:c.1784C>A, NM_001282518.1:c.1784C>A, NP_003399.1:p.Ser594Tyr, NP_001269444.1:p.Ser609Tyr, NP_001269447.1:p.Ser595Tyr

Select item 148915799820.

rs1489157998 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:113050234 (GRCh38)
9:115812514 (GRCh37)
Canonical SPDI:: NC_000009.12:113050233:A:T
Gene:: ZFP37 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.113050234A>T, NC_000009.11:g.115812514A>T, NG_047087.1:g.11558T>A

<< First< Prev

Page of 201

Next >Last >>

Supplemental Content

Filters: Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

SNP Links for Gene (Select 7539) (4007)
SNP

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

dbSNP

Result Filters

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to: