Links from Gene
Items: 1 to 20 of 1268
1.
rs1490444905 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>A
[Show Flanks]
- Chromosome:
- 5:133915752
(GRCh38)
5:133251443
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133915751:T:A
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.000007/1
(GnomAD)
- HGVS:
2.
rs1489664007 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 5:133916209
(GRCh38)
5:133251900
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133916208:C:T
- Gene:
- WSPAR (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:
3.
rs1489395218 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- G>-
[Show Flanks]
- Chromosome:
- 5:133915772
(GRCh38)
5:133251463
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133915771:G:
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
-=0./0
(
ALFA)
-=0.000007/1
(GnomAD)
-=0.000008/2
(TOPMED)
- HGVS:
4.
rs1489129632 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 5:133914852
(GRCh38)
5:133250543
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133914851:G:T
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS:
5.
rs1486198461 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A,C
[Show Flanks]
- Chromosome:
- 5:133913233
(GRCh38)
5:133248924
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133913232:G:A,NC_000005.10:133913232:G:C
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000014/2
(GnomAD)
- HGVS:
6.
rs1485419240 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>A
[Show Flanks]
- Chromosome:
- 5:133912731
(GRCh38)
5:133248422
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133912730:T:A
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
- HGVS:
7.
rs1485225292 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 5:133917499
(GRCh38)
5:133253190
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133917498:C:T
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- 500B_downstream_variant,downstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0.000071/1
(
ALFA)
T=0.000011/3
(TOPMED)
- HGVS:
8.
rs1485191527 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>A,G
[Show Flanks]
- Chromosome:
- 5:133914165
(GRCh38)
5:133249856
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133914164:T:A,NC_000005.10:133914164:T:G
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
- HGVS:
9.
rs1485143139 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 5:133913055
(GRCh38)
5:133248746
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133913054:T:C
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0.000071/1
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
10.
rs1484235977 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 5:133912506
(GRCh38)
5:133248197
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133912505:G:T
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0./0
(GnomAD)
T=0.000015/4
(TOPMED)
- HGVS:
11.
rs1483946962 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 5:133912993
(GRCh38)
5:133248684
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133912992:C:T
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000036/5
(GnomAD)
T=0.000064/17
(TOPMED)
T=0.000142/2
(TOMMO)
- HGVS:
12.
rs1483220939 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C
[Show Flanks]
- Chromosome:
- 5:133913137
(GRCh38)
5:133248828
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133913136:G:C
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
13.
rs1482711186 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AGGCCAGGT>-
[Show Flanks]
- Chromosome:
- 5:133911994
(GRCh38)
5:133247685
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133911991:GTAGGCCAGGT:GT
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa
- MAF:
GT=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
- HGVS:
14.
rs1482599093 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 5:133912819
(GRCh38)
5:133248510
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133912818:C:T
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000011/3
(TOPMED)
- HGVS:
15.
rs1481647382 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>A
[Show Flanks]
- Chromosome:
- 5:133917475
(GRCh38)
5:133253166
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133917474:T:A
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- downstream_transcript_variant,500B_downstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000007/1
(GnomAD)
A=0.000011/3
(TOPMED)
- HGVS:
16.
rs1481266620 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 5:133916072
(GRCh38)
5:133251763
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133916071:G:A
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.000007/1
(GnomAD)
- HGVS:
17.
rs1480393684 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 5:133913876
(GRCh38)
5:133249567
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133913875:C:T
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.000071/1
(
ALFA)
T=0.000007/1
(GnomAD)
T=0.000011/3
(TOPMED)
- HGVS:
18.
rs1479353392 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>A
[Show Flanks]
- Chromosome:
- 5:133914500
(GRCh38)
5:133250191
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133914499:C:A
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0.000071/1
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.000014/2
(GnomAD)
- HGVS:
19.
rs1477862673 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 5:133912625
(GRCh38)
5:133248316
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133912624:T:C
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
C=0.000007/1
(GnomAD)
- HGVS:
20.
rs1477625558 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 5:133915728
(GRCh38)
5:133251419
(GRCh37)
- Canonical SPDI:
- NC_000005.10:133915727:C:T
- Gene:
- WSPAR (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS: