SNP Links for Gene (Select 158586) - SNP

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Select item 14909618301.

rs1490961830 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:57590079 (GRCh38)
X:57616512 (GRCh37)
Canonical SPDI:: NC_000023.11:57590078:G:A
Gene:: ZXDB (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.57590079G>A, NC_000023.10:g.57616512G>A

Select item 14908796912.

rs1490879691 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:57592298 (GRCh38)
X:57618731 (GRCh37)
Canonical SPDI:: NC_000023.11:57592297:G:A
Gene:: ZXDB (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000023.11:g.57592298G>A, NC_000023.10:g.57618731G>A, NM_007157.4:c.250G>A, NM_007157.3:c.250G>A, NP_009088.1:p.Gly84Ser

Select item 14903356793.

rs1490335679 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:57593338 (GRCh38)
X:57619771 (GRCh37)
Canonical SPDI:: NC_000023.11:57593337:C:G
Gene:: ZXDB (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.57593338C>G, NC_000023.10:g.57619771C>G, NM_007157.4:c.1290C>G, NM_007157.3:c.1290C>G

Select item 14896733304.

rs1489673330 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:57592521 (GRCh38)
X:57618954 (GRCh37)
Canonical SPDI:: NC_000023.11:57592520:C:T
Gene:: ZXDB (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.57592521C>T, NC_000023.10:g.57618954C>T, NM_007157.4:c.473C>T, NM_007157.3:c.473C>T, NP_009088.1:p.Ala158Val

Select item 14895143865.

rs1489514386 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:57591772 (GRCh38)
X:57618205 (GRCh37)
Canonical SPDI:: NC_000023.11:57591771:C:T
Gene:: ZXDB (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000019/2 (GnomAD)
T=0.000034/9 (TOPMED)
T=0.000045/1 (TOMMO)
HGVS:: NC_000023.11:g.57591772C>T, NC_000023.10:g.57618205C>T

Select item 14890372556.

rs1489037255 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: X:57593535 (GRCh38)
X:57619968 (GRCh37)
Canonical SPDI:: NC_000023.11:57593534:C:A,NC_000023.11:57593534:C:T
Gene:: ZXDB (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.57593535C>A, NC_000023.11:g.57593535C>T, NC_000023.10:g.57619968C>A, NC_000023.10:g.57619968C>T, NM_007157.4:c.1487C>A, NM_007157.4:c.1487C>T, NM_007157.3:c.1487C>A, NM_007157.3:c.1487C>T, NP_009088.1:p.Thr496Lys, NP_009088.1:p.Thr496Met

Select item 14888942177.

rs1488894217 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:57591956 (GRCh38)
X:57618389 (GRCh37)
Canonical SPDI:: NC_000023.11:57591955:T:C
Gene:: ZXDB (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000285/4 (ALFA)
C=0.000076/20 (TOPMED)
C=0.000115/12 (GnomAD)
HGVS:: NC_000023.11:g.57591956T>C, NC_000023.10:g.57618389T>C, NM_007157.3:c.-93T>C

Select item 14878687288.

rs1487868728 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:57595762 (GRCh38)
X:57622195 (GRCh37)
Canonical SPDI:: NC_000023.11:57595761:A:G
Gene:: ZXDB (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.57595762A>G, NC_000023.10:g.57622195A>G, NM_007157.4:c.*1302A>G, NM_007157.3:c.*1302A>G

Select item 14868413299.

rs1486841329 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:57593794 (GRCh38)
X:57620227 (GRCh37)
Canonical SPDI:: NC_000023.11:57593793:A:G
Gene:: ZXDB (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
HGVS:: NC_000023.11:g.57593794A>G, NC_000023.10:g.57620227A>G, NM_007157.4:c.1746A>G, NM_007157.3:c.1746A>G

Select item 148590641810.

rs1485906418 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:57597404 (GRCh38)
X:57623837 (GRCh37)
Canonical SPDI:: NC_000023.11:57597403:C:T
Gene:: ZXDB (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.57597404C>T, NC_000023.10:g.57623837C>T, NM_007157.4:c.*2944C>T, NM_007157.3:c.*2944C>T

Select item 148518088311.

rs1485180883 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:57595288 (GRCh38)
X:57621721 (GRCh37)
Canonical SPDI:: NC_000023.11:57595287:T:C
Gene:: ZXDB (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0.0004/2 (ALFA)
HGVS:: NC_000023.11:g.57595288T>C, NC_000023.10:g.57621721T>C, NM_007157.4:c.*828T>C, NM_007157.3:c.*828T>C

Select item 148489232812.

rs1484892328 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:57592584 (GRCh38)
X:57619017 (GRCh37)
Canonical SPDI:: NC_000023.11:57592583:G:T
Gene:: ZXDB (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_000023.11:g.57592584G>T, NC_000023.10:g.57619017G>T, NM_007157.4:c.536G>T, NM_007157.3:c.536G>T, NP_009088.1:p.Arg179Leu

Select item 148481656513.

rs1484816565 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:57597454 (GRCh38)
X:57623887 (GRCh37)
Canonical SPDI:: NC_000023.11:57597453:A:G
Gene:: ZXDB (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.57597454A>G, NC_000023.10:g.57623887A>G, NM_007157.4:c.*2994A>G, NM_007157.3:c.*2994A>G

Select item 148446628014.

rs1484466280 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: X:57597812 (GRCh38)
X:57624245 (GRCh37)
Canonical SPDI:: NC_000023.11:57597811:T:A,NC_000023.11:57597811:T:C
Gene:: ZXDB (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000023.11:g.57597812T>A, NC_000023.11:g.57597812T>C, NC_000023.10:g.57624245T>A, NC_000023.10:g.57624245T>C

Select item 148439119915.

rs1484391199 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:57592147 (GRCh38)
X:57618580 (GRCh37)
Canonical SPDI:: NC_000023.11:57592146:C:T
Gene:: ZXDB (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.57592147C>T, NC_000023.10:g.57618580C>T, NM_007157.4:c.99C>T, NM_007157.3:c.99C>T

Select item 148409380416.

rs1484093804 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:57596805 (GRCh38)
X:57623238 (GRCh37)
Canonical SPDI:: NC_000023.11:57596804:C:G
Gene:: ZXDB (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.57596805C>G, NC_000023.10:g.57623238C>G, NM_007157.4:c.*2345C>G, NM_007157.3:c.*2345C>G

Select item 148378379517.

rs1483783795 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: X:57593315 (GRCh38)
X:57619748 (GRCh37)
Canonical SPDI:: NC_000023.11:57593314:C:A,NC_000023.11:57593314:C:T
Gene:: ZXDB (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.57593315C>A, NC_000023.11:g.57593315C>T, NC_000023.10:g.57619748C>A, NC_000023.10:g.57619748C>T, NM_007157.4:c.1267C>A, NM_007157.4:c.1267C>T, NM_007157.3:c.1267C>A, NM_007157.3:c.1267C>T, NP_009088.1:p.Leu423Met

Select item 148350219318.

rs1483502193 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: X:57595263 (GRCh38)
X:57621697 (GRCh37)
Canonical SPDI:: NC_000023.11:57595263:TTT:TTTT
Gene:: ZXDB (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: TTTT=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.57595266dup, NC_000023.10:g.57621699dup, NM_007157.4:c.*806dup, NM_007157.3:c.*806dup

Select item 148345488219.

rs1483454882 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:57592817 (GRCh38)
X:57619250 (GRCh37)
Canonical SPDI:: NC_000023.11:57592816:G:A
Gene:: ZXDB (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.57592817G>A, NC_000023.10:g.57619250G>A, NM_007157.4:c.769G>A, NM_007157.3:c.769G>A, NP_009088.1:p.Gly257Ser

Select item 148335657420.

rs1483356574 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: X:57593891 (GRCh38)
X:57620324 (GRCh37)
Canonical SPDI:: NC_000023.11:57593890:C:A
Gene:: ZXDB (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000023.11:g.57593891C>A, NC_000023.10:g.57620324C>A, NM_007157.4:c.1843C>A, NM_007157.3:c.1843C>A, NP_009088.1:p.Pro615Thr

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