SNP Links for Gene (Select 252884) - SNP

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Select item 14913060021.

rs1491306002 has merged into rs1201077158 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,AA,AAA,AAAAA,AAAAAA [Show Flanks]
Chromosome:: 18:35375307 (GRCh38)
18:32955271 (GRCh37)
Canonical SPDI:: NC_000018.10:35375304:AAAAAA:AA,NC_000018.10:35375304:AAAAAA:AAAA,NC_000018.10:35375304:AAAAAA:AAAAA,NC_000018.10:35375304:AAAAAA:AAAAAAA,NC_000018.10:35375304:AAAAAA:AAAAAAAA
Gene:: ZNF396 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
AA=0.00011/3 (TOMMO)
HGVS:: NC_000018.10:g.35375307_35375310del, NC_000018.10:g.35375309_35375310del, NC_000018.10:g.35375310del, NC_000018.10:g.35375310dup, NC_000018.10:g.35375309_35375310dup, NC_000018.9:g.32955271_32955274del, NC_000018.9:g.32955273_32955274del, NC_000018.9:g.32955274del, NC_000018.9:g.32955274dup, NC_000018.9:g.32955273_32955274dup

Select item 14911215562.

rs1491121556 has merged into rs374405615 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,TTT,TTTTTT [Show Flanks]
Chromosome:: 18:35368484 (GRCh38)
18:32948448 (GRCh37)
Canonical SPDI:: NC_000018.10:35368480:TTTTT:TTT,NC_000018.10:35368480:TTTTT:TTTTTT,NC_000018.10:35368480:TTTTT:TTTTTTTTT
Gene:: ZNF396 (Varview)
Functional Consequence:: 3_prime_UTR_variant,intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
TTTT=0.00134/42 (ExAC)
HGVS:: NC_000018.10:g.35368484_35368485del, NC_000018.10:g.35368485dup, NC_000018.10:g.35368482_35368485dup, NC_000018.9:g.32948448_32948449del, NC_000018.9:g.32948449dup, NC_000018.9:g.32948446_32948449dup, XM_006722432.4:c.*733_*734del, XM_006722432.4:c.*734dup, XM_006722432.4:c.*731_*734dup, XM_006722432.3:c.*733_*734del, XM_006722432.3:c.*734dup, XM_006722432.3:c.*731_*734dup, XM_017025687.2:c.*733_*734del, XM_017025687.2:c.*734dup, XM_017025687.2:c.*731_*734dup, XM_017025687.1:c.*733_*734del, XM_017025687.1:c.*734dup, XM_017025687.1:c.*731_*734dup, NM_001322290.2:c.*733_*734del, NM_001322290.2:c.*734dup, NM_001322290.2:c.*731_*734dup, NM_001322290.1:c.*733_*734del, NM_001322290.1:c.*734dup, NM_001322290.1:c.*731_*734dup, NM_001322286.2:c.*733_*734del, NM_001322286.2:c.*734dup, NM_001322286.2:c.*731_*734dup, NM_001322286.1:c.*733_*734del, NM_001322286.1:c.*734dup, NM_001322286.1:c.*731_*734dup

Select item 14910180273.

rs1491018027 has merged into rs35532616 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 18:35370516 (GRCh38)
18:32950480 (GRCh37)
Canonical SPDI:: NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:35370504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ZNF396 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000018.10:g.35370516_35370530del, NC_000018.10:g.35370517_35370530del, NC_000018.10:g.35370518_35370530del, NC_000018.10:g.35370519_35370530del, NC_000018.10:g.35370520_35370530del, NC_000018.10:g.35370521_35370530del, NC_000018.10:g.35370522_35370530del, NC_000018.10:g.35370523_35370530del, NC_000018.10:g.35370524_35370530del, NC_000018.10:g.35370525_35370530del, NC_000018.10:g.35370526_35370530del, NC_000018.10:g.35370527_35370530del, NC_000018.10:g.35370528_35370530del, NC_000018.10:g.35370529_35370530del, NC_000018.10:g.35370530del, NC_000018.10:g.35370530dup, NC_000018.10:g.35370529_35370530dup, NC_000018.10:g.35370528_35370530dup, NC_000018.10:g.35370527_35370530dup, NC_000018.10:g.35370526_35370530dup, NC_000018.10:g.35370525_35370530dup, NC_000018.10:g.35370524_35370530dup, NC_000018.10:g.35370523_35370530dup, NC_000018.10:g.35370521_35370530dup, NC_000018.9:g.32950480_32950494del, NC_000018.9:g.32950481_32950494del, NC_000018.9:g.32950482_32950494del, NC_000018.9:g.32950483_32950494del, NC_000018.9:g.32950484_32950494del, NC_000018.9:g.32950485_32950494del, NC_000018.9:g.32950486_32950494del, NC_000018.9:g.32950487_32950494del, NC_000018.9:g.32950488_32950494del, NC_000018.9:g.32950489_32950494del, NC_000018.9:g.32950490_32950494del, NC_000018.9:g.32950491_32950494del, NC_000018.9:g.32950492_32950494del, NC_000018.9:g.32950493_32950494del, NC_000018.9:g.32950494del, NC_000018.9:g.32950494dup, NC_000018.9:g.32950493_32950494dup, NC_000018.9:g.32950492_32950494dup, NC_000018.9:g.32950491_32950494dup, NC_000018.9:g.32950490_32950494dup, NC_000018.9:g.32950489_32950494dup, NC_000018.9:g.32950488_32950494dup, NC_000018.9:g.32950487_32950494dup, NC_000018.9:g.32950485_32950494dup

Select item 14910036744.

rs1491003674 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:35372918 (GRCh38)
18:32952882 (GRCh37)
Canonical SPDI:: NC_000018.10:35372917:G:A
Gene:: ZNF396 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.35372918G>A, NC_000018.9:g.32952882G>A

Select item 14901862005.

rs1490186200 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 18:35372239 (GRCh38)
18:32952203 (GRCh37)
Canonical SPDI:: NC_000018.10:35372238:A:G,NC_000018.10:35372238:A:T
Gene:: ZNF396 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.35372239A>G, NC_000018.10:g.35372239A>T, NC_000018.9:g.32952203A>G, NC_000018.9:g.32952203A>T

Select item 14894455996.

rs1489445599 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:35378018 (GRCh38)
18:32957982 (GRCh37)
Canonical SPDI:: NC_000018.10:35378017:C:T
Gene:: ZNF396 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000018.10:g.35378018C>T, NC_000018.9:g.32957982C>T

Select item 14893814057.

rs1489381405 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 18:35366662 (GRCh38)
18:32946626 (GRCh37)
Canonical SPDI:: NC_000018.10:35366661:C:G
Gene:: ZNF396 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_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_000018.10:g.35366662C>G, NC_000018.9:g.32946626C>G

Select item 14890155258.

rs1489015525 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 18:35378506 (GRCh38)
18:32958470 (GRCh37)
Canonical SPDI:: NC_000018.10:35378505:TTTTT:TTTT
Gene:: ZNF396 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTT=0./0 (ALFA)
-=0.000014/2 (GnomAD)
-=0.000023/6 (TOPMED)
HGVS:: NC_000018.10:g.35378510del, NC_000018.9:g.32958474del

Select item 14880019559.

rs1488001955 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 18:35378383 (GRCh38)
18:32958347 (GRCh37)
Canonical SPDI:: NC_000018.10:35378382:G:T
Gene:: ZNF396 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.35378383G>T, NC_000018.9:g.32958347G>T

Select item 148765883510.

rs1487658835 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 18:35369752 (GRCh38)
18:32949716 (GRCh37)
Canonical SPDI:: NC_000018.10:35369751:C:G
Gene:: ZNF396 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.35369752C>G, NC_000018.9:g.32949716C>G

Select item 148728030811.

rs1487280308 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 18:35372864 (GRCh38)
18:32952828 (GRCh37)
Canonical SPDI:: NC_000018.10:35372863:C:G
Gene:: ZNF396 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000029/4 (GnomAD)
HGVS:: NC_000018.10:g.35372864C>G, NC_000018.9:g.32952828C>G

Select item 148704216412.

rs1487042164 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 18:35367514 (GRCh38)
18:32947478 (GRCh37)
Canonical SPDI:: NC_000018.10:35367513:G:A,NC_000018.10:35367513:G:T
Gene:: ZNF396 (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
A=0.000071/1 (TOMMO)
A=0.000546/1 (Korea1K)
A=0.001027/3 (KOREAN)
HGVS:: NC_000018.10:g.35367514G>A, NC_000018.10:g.35367514G>T, NC_000018.9:g.32947478G>A, NC_000018.9:g.32947478G>T, XM_006722432.4:c.*1701C>T, XM_006722432.4:c.*1701C>A, NM_145756.3:c.*837C>T, NM_145756.3:c.*837C>A, NM_145756.2:c.*837C>T, NM_145756.2:c.*837C>A, XM_017025687.2:c.*1701C>T, XM_017025687.2:c.*1701C>A, NM_001322290.2:c.*1701C>T, NM_001322290.2:c.*1701C>A, NM_001322290.1:c.*1701C>T, NM_001322290.1:c.*1701C>A, NM_001322286.2:c.*1701C>T, NM_001322286.2:c.*1701C>A, NM_001322286.1:c.*1701C>T, NM_001322286.1:c.*1701C>A, XM_024451138.2:c.*837C>T, XM_024451138.2:c.*837C>A, XM_017025689.2:c.*837C>T, XM_017025689.2:c.*837C>A

Select item 148681319913.

rs1486813199 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 18:35372142 (GRCh38)
18:32952106 (GRCh37)
Canonical SPDI:: NC_000018.10:35372141:C:A,NC_000018.10:35372141:C:T
Gene:: ZNF396 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.35372142C>A, NC_000018.10:g.35372142C>T, NC_000018.9:g.32952106C>A, NC_000018.9:g.32952106C>T

Select item 148641592214.

rs1486415922 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:35376242 (GRCh38)
18:32956206 (GRCh37)
Canonical SPDI:: NC_000018.10:35376241:T:C
Gene:: ZNF396 (Varview)
Functional Consequence:: intron_variant,5_prime_UTR_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_000018.10:g.35376242T>C, NC_000018.9:g.32956206T>C, XM_006722432.4:c.-188A>G, XM_006722432.3:c.-188A>G, XM_006722432.2:c.-188A>G, XM_006722432.1:c.-188A>G, XM_017025687.2:c.-188A>G, XM_017025687.1:c.-188A>G

Select item 148634980915.

rs1486349809 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: 18:35371335 (GRCh38)
18:32951299 (GRCh37)
Canonical SPDI:: NC_000018.10:35371333:ATA:A
Gene:: ZNF396 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.35371335_35371336del, NC_000018.9:g.32951299_32951300del

Select item 148604649216.

rs1486046492 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 18:35368729 (GRCh38)
18:32948693 (GRCh37)
Canonical SPDI:: NC_000018.10:35368728:G:A,NC_000018.10:35368728:G:C,NC_000018.10:35368728:G:T
Gene:: ZNF396 (Varview)
Functional Consequence:: intron_variant,3_prime_UTR_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000018.10:g.35368729G>A, NC_000018.10:g.35368729G>C, NC_000018.10:g.35368729G>T, NC_000018.9:g.32948693G>A, NC_000018.9:g.32948693G>C, NC_000018.9:g.32948693G>T, XM_006722432.4:c.*486C>T, XM_006722432.4:c.*486C>G, XM_006722432.4:c.*486C>A, XM_006722432.3:c.*486C>T, XM_006722432.3:c.*486C>G, XM_006722432.3:c.*486C>A, XM_006722432.2:c.*486C>T, XM_006722432.2:c.*486C>G, XM_006722432.2:c.*486C>A, XM_006722432.1:c.*486C>T, XM_006722432.1:c.*486C>G, XM_006722432.1:c.*486C>A, XM_017025687.2:c.*486C>T, XM_017025687.2:c.*486C>G, XM_017025687.2:c.*486C>A, XM_017025687.1:c.*486C>T, XM_017025687.1:c.*486C>G, XM_017025687.1:c.*486C>A, NM_001322290.2:c.*486C>T, NM_001322290.2:c.*486C>G, NM_001322290.2:c.*486C>A, NM_001322290.1:c.*486C>T, NM_001322290.1:c.*486C>G, NM_001322290.1:c.*486C>A, NM_001322286.2:c.*486C>T, NM_001322286.2:c.*486C>G, NM_001322286.2:c.*486C>A, NM_001322286.1:c.*486C>T, NM_001322286.1:c.*486C>G, NM_001322286.1:c.*486C>A

Select item 148583715017.

rs1485837150 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:35376632 (GRCh38)
18:32956596 (GRCh37)
Canonical SPDI:: NC_000018.10:35376631:C:T
Gene:: ZNF396 (Varview)
Functional Consequence:: intron_variant,5_prime_UTR_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_000018.10:g.35376632C>T, NC_000018.9:g.32956596C>T, XM_006722432.4:c.-578G>A, XM_006722432.3:c.-578G>A, XM_017025687.2:c.-453G>A, XM_017025687.1:c.-453G>A, NM_001322290.2:c.-309G>A, NM_001322290.1:c.-309G>A, XM_024451138.2:c.-309G>A, XM_024451138.1:c.-309G>A

Select item 148561146218.

rs1485611462 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 18:35376202 (GRCh38)
18:32956166 (GRCh37)
Canonical SPDI:: NC_000018.10:35376201:C:A,NC_000018.10:35376201:C:T
Gene:: ZNF396 (Varview)
Functional Consequence:: intron_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.35376202C>A, NC_000018.10:g.35376202C>T, NC_000018.9:g.32956166C>A, NC_000018.9:g.32956166C>T, XM_006722432.4:c.-148G>T, XM_006722432.4:c.-148G>A, XM_006722432.3:c.-148G>T, XM_006722432.3:c.-148G>A, XM_006722432.2:c.-148G>T, XM_006722432.2:c.-148G>A, XM_006722432.1:c.-148G>T, XM_006722432.1:c.-148G>A, XM_017025687.2:c.-148G>T, XM_017025687.2:c.-148G>A, XM_017025687.1:c.-148G>T, XM_017025687.1:c.-148G>A

Select item 148527561419.

rs1485275614 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 18:35373950 (GRCh38)
18:32953914 (GRCh37)
Canonical SPDI:: NC_000018.10:35373949:G:T
Gene:: ZNF396 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.000111/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.35373950G>T, NC_000018.9:g.32953914G>T, XM_006722432.4:c.343C>A, XM_006722432.3:c.343C>A, XM_006722432.2:c.343C>A, XM_006722432.1:c.343C>A, NM_145756.3:c.343C>A, NM_145756.2:c.343C>A, XM_017025687.2:c.343C>A, XM_017025687.1:c.343C>A, NM_001322290.2:c.343C>A, NM_001322290.1:c.343C>A, NM_001322286.2:c.343C>A, NM_001322286.1:c.343C>A, XM_024451138.2:c.343C>A, XM_024451138.1:c.343C>A, XM_017025689.2:c.343C>A, XM_017025689.1:c.343C>A, NM_001322291.2:c.343C>A, NM_001322291.1:c.343C>A, XP_006722495.1:p.His115Asn, NP_665699.1:p.His115Asn, XP_016881176.1:p.His115Asn, NP_001309219.1:p.His115Asn, NP_001309215.1:p.His115Asn, XP_024306906.1:p.His115Asn, XP_016881178.1:p.His115Asn, NP_001309220.1:p.His115Asn

Select item 148522711920.

rs1485227119 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 18:35366492 (GRCh38)
18:32946456 (GRCh37)
Canonical SPDI:: NC_000018.10:35366491:G:T
Gene:: ZNF396 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.35366492G>T, NC_000018.9:g.32946456G>T

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