Links from Gene
Items: 1 to 20 of 1000
1.
rs1491542998 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->T
[Show Flanks]
- Chromosome:
- 11:57682913
(GRCh38)
11:57450386
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57682913:T:TT
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
TT=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS:
2.
rs1491513075 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- AA>-
[Show Flanks]
- Chromosome:
- 11:57700414
(GRCh38)
11:57467886
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57700413:AA:
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- 3_prime_UTR_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.000008/1
(GnomAD)
- HGVS:
3.
rs1491503057 has merged into rs34645509 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 11:57674326
(GRCh38)
11:57441798
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57674316:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTT=0./0
(
ALFA)
-=0.000008/2
(TOPMED)
T=0.197284/988
(1000Genomes)
T=0.475/19
(GENOME_DK)
- HGVS:
NC_000011.10:g.57674326_57674332del, NC_000011.10:g.57674329_57674332del, NC_000011.10:g.57674330_57674332del, NC_000011.10:g.57674331_57674332del, NC_000011.10:g.57674332del, NC_000011.10:g.57674332dup, NC_000011.10:g.57674331_57674332dup, NC_000011.10:g.57674330_57674332dup, NC_000011.10:g.57674329_57674332dup, NC_000011.10:g.57674328_57674332dup, NC_000011.10:g.57674327_57674332dup, NC_000011.10:g.57674326_57674332dup, NC_000011.10:g.57674325_57674332dup, NC_000011.10:g.57674324_57674332dup, NC_000011.10:g.57674323_57674332dup, NC_000011.10:g.57674322_57674332dup, NC_000011.10:g.57674321_57674332dup, NC_000011.10:g.57674320_57674332dup, NC_000011.10:g.57674319_57674332dup, NC_000011.10:g.57674318_57674332dup, NC_000011.10:g.57674317_57674332dup, NC_000011.10:g.57674332_57674333insTTTTTTTTTTTTTTTTT, NC_000011.10:g.57674332_57674333insTTTTTTTTTTTTTTTTTT, NC_000011.10:g.57674332_57674333insTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.57674332_57674333insTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.57674332_57674333insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.57441798_57441804del, NC_000011.9:g.57441801_57441804del, NC_000011.9:g.57441802_57441804del, NC_000011.9:g.57441803_57441804del, NC_000011.9:g.57441804del, NC_000011.9:g.57441804dup, NC_000011.9:g.57441803_57441804dup, NC_000011.9:g.57441802_57441804dup, NC_000011.9:g.57441801_57441804dup, NC_000011.9:g.57441800_57441804dup, NC_000011.9:g.57441799_57441804dup, NC_000011.9:g.57441798_57441804dup, NC_000011.9:g.57441797_57441804dup, NC_000011.9:g.57441796_57441804dup, NC_000011.9:g.57441795_57441804dup, NC_000011.9:g.57441794_57441804dup, NC_000011.9:g.57441793_57441804dup, NC_000011.9:g.57441792_57441804dup, NC_000011.9:g.57441791_57441804dup, NC_000011.9:g.57441790_57441804dup, NC_000011.9:g.57441789_57441804dup, NC_000011.9:g.57441804_57441805insTTTTTTTTTTTTTTTTT, NC_000011.9:g.57441804_57441805insTTTTTTTTTTTTTTTTTT, NC_000011.9:g.57441804_57441805insTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.57441804_57441805insTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.57441804_57441805insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
4.
rs1491478335 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- TT>-
[Show Flanks]
- Chromosome:
- 11:57700432
(GRCh38)
11:57467904
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57700431:TT:
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- 3_prime_UTR_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
-=0.000007/1
(GnomAD)
- HGVS:
6.
rs1491299857 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->A
[Show Flanks]
- Chromosome:
- 11:57700432
(GRCh38)
11:57467905
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57700432::A
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- 3_prime_UTR_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by cluster
- MAF:
A=0.000051/7
(GnomAD)
A=0.000156/1
(1000Genomes)
A=0.000212/4
(TOMMO)
- HGVS:
7.
rs1491257251 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- TC>-
[Show Flanks]
- Chromosome:
- 11:57667364
(GRCh38)
11:57434836
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57667363:TC:
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
-=0.00017/2
(
ALFA)
-=0.00011/3
(TOMMO)
- HGVS:
8.
rs1491224045 has merged into rs10561191 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTT>-,T,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 11:57689688
(GRCh38)
11:57457160
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTT=0./0
(
ALFA)
-=0.3874/1940
(1000Genomes)
- HGVS:
NC_000011.10:g.57689688_57689698del, NC_000011.10:g.57689689_57689698del, NC_000011.10:g.57689691_57689698del, NC_000011.10:g.57689692_57689698del, NC_000011.10:g.57689693_57689698del, NC_000011.10:g.57689695_57689698del, NC_000011.10:g.57689696_57689698del, NC_000011.10:g.57689697_57689698del, NC_000011.10:g.57689698del, NC_000011.10:g.57689698dup, NC_000011.10:g.57689697_57689698dup, NC_000011.10:g.57689696_57689698dup, NC_000011.10:g.57689695_57689698dup, NC_000011.10:g.57689691_57689698dup, NC_000011.9:g.57457160_57457170del, NC_000011.9:g.57457161_57457170del, NC_000011.9:g.57457163_57457170del, NC_000011.9:g.57457164_57457170del, NC_000011.9:g.57457165_57457170del, NC_000011.9:g.57457167_57457170del, NC_000011.9:g.57457168_57457170del, NC_000011.9:g.57457169_57457170del, NC_000011.9:g.57457170del, NC_000011.9:g.57457170dup, NC_000011.9:g.57457169_57457170dup, NC_000011.9:g.57457168_57457170dup, NC_000011.9:g.57457167_57457170dup, NC_000011.9:g.57457163_57457170dup
9.
rs1491150709 has merged into rs10561191 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTT>-,T,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 11:57689688
(GRCh38)
11:57457160
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:57689677:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTT=0./0
(
ALFA)
-=0.3874/1940
(1000Genomes)
- HGVS:
NC_000011.10:g.57689688_57689698del, NC_000011.10:g.57689689_57689698del, NC_000011.10:g.57689691_57689698del, NC_000011.10:g.57689692_57689698del, NC_000011.10:g.57689693_57689698del, NC_000011.10:g.57689695_57689698del, NC_000011.10:g.57689696_57689698del, NC_000011.10:g.57689697_57689698del, NC_000011.10:g.57689698del, NC_000011.10:g.57689698dup, NC_000011.10:g.57689697_57689698dup, NC_000011.10:g.57689696_57689698dup, NC_000011.10:g.57689695_57689698dup, NC_000011.10:g.57689691_57689698dup, NC_000011.9:g.57457160_57457170del, NC_000011.9:g.57457161_57457170del, NC_000011.9:g.57457163_57457170del, NC_000011.9:g.57457164_57457170del, NC_000011.9:g.57457165_57457170del, NC_000011.9:g.57457167_57457170del, NC_000011.9:g.57457168_57457170del, NC_000011.9:g.57457169_57457170del, NC_000011.9:g.57457170del, NC_000011.9:g.57457170dup, NC_000011.9:g.57457169_57457170dup, NC_000011.9:g.57457168_57457170dup, NC_000011.9:g.57457167_57457170dup, NC_000011.9:g.57457163_57457170dup
10.
rs1491126823 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- CT>-
[Show Flanks]
- Chromosome:
- 11:57684066
(GRCh38)
11:57451538
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57684065:CT:
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.000008/1
(GnomAD)
-=0.000071/1
(TOMMO)
- HGVS:
11.
rs1491101464 has merged into rs869200151 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AA>-,A
[Show Flanks]
- Chromosome:
- 11:57698150
(GRCh38)
11:57465622
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57698148:AAA:A,NC_000011.10:57698148:AAA:AA
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0.000337/4
(
ALFA)
-=0.000245/34
(GnomAD)
-=0.000248/4
(TOMMO)
- HGVS:
12.
rs1490879461 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G
[Show Flanks]
- Chromosome:
- 11:57694437
(GRCh38)
11:57461909
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57694436:C:G
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
G=0.00308/9
(KOREAN)
- HGVS:
13.
rs1490876050 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 11:57696870
(GRCh38)
11:57464342
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57696869:C:T
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- coding_sequence_variant,intron_variant,synonymous_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000007/1
(GnomAD)
T=0.000008/2
(TOPMED)
- HGVS:
14.
rs1490787469 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>T
[Show Flanks]
- Chromosome:
- 11:57687413
(GRCh38)
11:57454885
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57687412:A:T
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000008/2
(TOPMED)
- HGVS:
15.
rs1490764098 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- ATAG>-
[Show Flanks]
- Chromosome:
- 11:57683884
(GRCh38)
11:57451356
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57683883:ATAG:
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency
- MAF:
-=0.000007/1
(GnomAD)
- HGVS:
16.
rs1490754010 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 11:57671348
(GRCh38)
11:57438820
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57671347:C:T
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
T=0.000007/1
(GnomAD)
- HGVS:
17.
rs1490682612 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>T
[Show Flanks]
- Chromosome:
- 11:57670367
(GRCh38)
11:57437839
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57670366:A:T
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
T=0.000007/1
(GnomAD)
- HGVS:
18.
rs1490421145 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 11:57695932
(GRCh38)
11:57463404
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57695931:C:T
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- coding_sequence_variant,synonymous_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000007/1
(GnomAD)
- HGVS:
NC_000011.10:g.57695932C>T, NC_000011.9:g.57463404C>T, NM_015457.3:c.898C>T, NM_015457.2:c.898C>T, XM_011544901.2:c.898C>T, XM_011544901.1:c.898C>T, XM_011544899.2:c.898C>T, XM_011544899.1:c.898C>T, XM_011544900.2:c.898C>T, XM_011544900.1:c.898C>T, XM_047426724.1:c.898C>T
19.
rs1490403890 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>C
[Show Flanks]
- Chromosome:
- 11:57665870
(GRCh38)
11:57433342
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57665869:A:C
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000007/1
(GnomAD)
- HGVS:
20.
rs1490351502 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 11:57695019
(GRCh38)
11:57462491
(GRCh37)
- Canonical SPDI:
- NC_000011.10:57695018:T:C
- Gene:
- ZDHHC5 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0.000071/1
(
ALFA)
C=0.000014/2
(GnomAD)
C=0.000019/5
(TOPMED)
- HGVS: