SNP Links for Gene (Select 646951) - SNP

Links from Gene

Items: 1 to 20 of 5218

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Select item 14907218461.

rs1490721846 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 3:150884886 (GRCh38)
3:150602673 (GRCh37)
Canonical SPDI:: NC_000003.12:150884885:G:A,NC_000003.12:150884885:G:C
Gene:: MINDY4B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.150884886G>A, NC_000003.12:g.150884886G>C, NC_000003.11:g.150602673G>A, NC_000003.11:g.150602673G>C

Select item 14905474692.

rs1490547469 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:150883495 (GRCh38)
3:150601282 (GRCh37)
Canonical SPDI:: NC_000003.12:150883494:G:A
Gene:: MINDY4B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.150883495G>A, NC_000003.11:g.150601282G>A

Select item 14905036753.

rs1490503675 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 3:150877409 (GRCh38)
3:150595196 (GRCh37)
Canonical SPDI:: NC_000003.12:150877408:C:G
Gene:: MINDY4B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: G=0.0076/14 (Korea1K)
HGVS:: NC_000003.12:g.150877409C>G, NC_000003.11:g.150595196C>G

Select item 14902032484.

rs1490203248 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 3:150878913 (GRCh38)
3:150596700 (GRCh37)
Canonical SPDI:: NC_000003.12:150878912:A:C
Gene:: MINDY4B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000003.12:g.150878913A>C, NC_000003.11:g.150596700A>C

Select item 14901285945.

rs1490128594 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:150890202 (GRCh38)
3:150607989 (GRCh37)
Canonical SPDI:: NC_000003.12:150890201:C:T
Gene:: MINDY4B (Varview), LOC124909446 (Varview)
Functional Consequence:: intron_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=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.150890202C>T, NC_000003.11:g.150607989C>T

Select item 14899647006.

rs1489964700 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 3:150889673 (GRCh38)
3:150607460 (GRCh37)
Canonical SPDI:: NC_000003.12:150889672:G:C
Gene:: MINDY4B (Varview), LOC124909446 (Varview)
Functional Consequence:: intron_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=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.150889673G>C, NC_000003.11:g.150607460G>C

Select item 14898385357.

rs1489838535 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 3:150882176 (GRCh38)
3:150599963 (GRCh37)
Canonical SPDI:: NC_000003.12:150882175:T:G
Gene:: MINDY4B (Varview)
Functional Consequence:: intron_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_000003.12:g.150882176T>G, NC_000003.11:g.150599963T>G

Select item 14897909118.

rs1489790911 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:150877819 (GRCh38)
3:150595606 (GRCh37)
Canonical SPDI:: NC_000003.12:150877818:T:C
Gene:: MINDY4B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0./0 (GnomAD)
C=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.150877819T>C, NC_000003.11:g.150595606T>C

Select item 14896284159.

rs1489628415 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:150880215 (GRCh38)
3:150598002 (GRCh37)
Canonical SPDI:: NC_000003.12:150880214:T:C
Gene:: MINDY4B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000043/6 (GnomAD)
HGVS:: NC_000003.12:g.150880215T>C, NC_000003.11:g.150598002T>C

Select item 148962179510.

rs1489621795 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 3:150871093 (GRCh38)
3:150588880 (GRCh37)
Canonical SPDI:: NC_000003.12:150871092:C:G
Gene:: MINDY4B (Varview), SIAH2-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.150871093C>G, NC_000003.11:g.150588880C>G, NM_001351281.2:c.1335G>C, NM_001351281.1:c.504G>C, XR_007096130.1:n.1171C>G, NP_001338210.2:p.Lys445Asn

Select item 148958621911.

rs1489586219 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:150893053 (GRCh38)
3:150610840 (GRCh37)
Canonical SPDI:: NC_000003.12:150893052:C:T
Gene:: MINDY4B (Varview)
Functional Consequence:: 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_000003.12:g.150893053C>T, NC_000003.11:g.150610840C>T

Select item 148952213112.

rs1489522131 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:150874799 (GRCh38)
3:150592586 (GRCh37)
Canonical SPDI:: NC_000003.12:150874798:A:G
Gene:: MINDY4B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
HGVS:: NC_000003.12:g.150874799A>G, NC_000003.11:g.150592586A>G

Select item 148952147313.

rs1489521473 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 3:150879108 (GRCh38)
3:150596895 (GRCh37)
Canonical SPDI:: NC_000003.12:150879107:G:A,NC_000003.12:150879107:G:T
Gene:: MINDY4B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
T=0.000156/1 (1000Genomes)
HGVS:: NC_000003.12:g.150879108G>A, NC_000003.12:g.150879108G>T, NC_000003.11:g.150596895G>A, NC_000003.11:g.150596895G>T

Select item 148901211814.

rs1489012118 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 3:150890331 (GRCh38)
3:150608118 (GRCh37)
Canonical SPDI:: NC_000003.12:150890330:G:A,NC_000003.12:150890330:G:C
Gene:: MINDY4B (Varview), LOC124909446 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,upstream_transcript_variant,2KB_upstream_variant
HGVS:: NC_000003.12:g.150890331G>A, NC_000003.12:g.150890331G>C, NC_000003.11:g.150608118G>A, NC_000003.11:g.150608118G>C, NM_001351281.2:c.742C>T, NM_001351281.2:c.742C>G, NM_001351281.1:c.-90C>T, NM_001351281.1:c.-90C>G, NP_001338210.2:p.His248Tyr, NP_001338210.2:p.His248Asp

Select item 148893889015.

rs1488938890 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:150892390 (GRCh38)
3:150610177 (GRCh37)
Canonical SPDI:: NC_000003.12:150892389:A:G
Gene:: MINDY4B (Varview), LOC124909446 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000003.12:g.150892390A>G, NC_000003.11:g.150610177A>G, XR_007096131.1:n.646A>G

Select item 148888743016.

rs1488887430 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 3:150893379 (GRCh38)
3:150611166 (GRCh37)
Canonical SPDI:: NC_000003.12:150893378:A:G,NC_000003.12:150893378:A:T
Gene:: MINDY4B (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000003.12:g.150893379A>G, NC_000003.12:g.150893379A>T, NC_000003.11:g.150611166A>G, NC_000003.11:g.150611166A>T, NM_001351281.2:c.466T>C, NM_001351281.2:c.466T>A, NP_001338210.2:p.Ser156Pro, NP_001338210.2:p.Ser156Thr

Select item 148864500917.

rs1488645009 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:150873391 (GRCh38)
3:150591178 (GRCh37)
Canonical SPDI:: NC_000003.12:150873390:G:A
Gene:: MINDY4B (Varview), SIAH2-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.150873391G>A, NC_000003.11:g.150591178G>A, XR_007096130.1:n.3469G>A

Select item 148841671418.

rs1488416714 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:150870859 (GRCh38)
3:150588646 (GRCh37)
Canonical SPDI:: NC_000003.12:150870858:A:G
Gene:: MINDY4B (Varview), SIAH2-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,non_coding_transcript_variant,3_prime_UTR_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_000003.12:g.150870859A>G, NC_000003.11:g.150588646A>G, NM_001351281.2:c.*186T>C, XR_007096130.1:n.937A>G

Select item 148837479119.

rs1488374791 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 3:150885855 (GRCh38)
3:150603642 (GRCh37)
Canonical SPDI:: NC_000003.12:150885854:C:A,NC_000003.12:150885854:C:T
Gene:: MINDY4B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.150885855C>A, NC_000003.12:g.150885855C>T, NC_000003.11:g.150603642C>A, NC_000003.11:g.150603642C>T

Select item 148824629620.

rs1488246296 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:150893498 (GRCh38)
3:150611285 (GRCh37)
Canonical SPDI:: NC_000003.12:150893497:T:C
Gene:: MINDY4B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.150893498T>C, NC_000003.11:g.150611285T>C

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