Links from Gene
Items: 1 to 20 of 2832
1.
rs1490620337 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 3:129318413
(GRCh38)
3:129037256
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129318412:G:A
- Gene:
- H1-10-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000023/6
(TOPMED)
A=0.000318/5
(TOMMO)
A=0.000342/1
(KOREAN)
...more- HGVS:
3.
rs1490128691 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 3:129317917
(GRCh38)
3:129036760
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129317916:G:A
- Gene:
- H1-10 (Varview), H1-10-AS1 (Varview)
- Functional Consequence:
- intron_variant,upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0.000071/1
(
ALFA)
A=0.000029/4
(GnomAD)
A=0.00003/8
(TOPMED)
...more- HGVS:
4.
rs1490014223 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 3:129319229
(GRCh38)
3:129038072
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129319228:C:T
- Gene:
- H1-10-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
T=0.000014/2
(GnomAD)
...more- HGVS:
5.
rs1489910482 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 3:129324078
(GRCh38)
3:129042921
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129324077:G:A
- Gene:
- H1-10-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000014/2
(GnomAD)
A=0.000026/7
(TOPMED)
...more- HGVS:
6.
rs1489749715 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 3:129323270
(GRCh38)
3:129042113
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129323269:G:T
- Gene:
- H1-10-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.000071/1
(
ALFA)
T=0.000004/1
(TOPMED)
T=0.000007/1
(GnomAD)
...more- HGVS:
7.
rs1489452472 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C,T
[Show Flanks]
- Chromosome:
- 3:129316461
(GRCh38)
3:129035304
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129316460:G:C,NC_000003.12:129316460:G:T
- Gene:
- H1-10 (Varview), H1-10-AS1 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS:
8.
rs1489333478 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 3:129315897
(GRCh38)
3:129034740
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129315896:G:A
- Gene:
- H1-10 (Varview), H1-10-AS1 (Varview)
- Functional Consequence:
- coding_sequence_variant,upstream_transcript_variant,synonymous_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000014/2
(GnomAD)
- HGVS:
9.
rs1489285447 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>T
[Show Flanks]
- Chromosome:
- 3:129316786
(GRCh38)
3:129035629
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129316785:A:T
- Gene:
- H1-10 (Varview), H1-10-AS1 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000007/1
(GnomAD)
- HGVS:
11.
rs1488661297 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 3:129324268
(GRCh38)
3:129043111
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129324267:T:C
- Gene:
- H1-10-AS1 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000007/1
(GnomAD)
- HGVS:
12.
rs1488457348 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>G
[Show Flanks]
- Chromosome:
- 3:129316241
(GRCh38)
3:129035084
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129316240:T:G
- Gene:
- H1-10 (Varview), H1-10-AS1 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant,5_prime_UTR_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
G=0.000007/1
(GnomAD)
G=0.000177/3
(TOMMO)
...more- HGVS:
13.
rs1488442356 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 3:129323617
(GRCh38)
3:129042460
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129323616:G:A
- Gene:
- H1-10-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0./0
(
ALFA)
A=0.000008/2
(TOPMED)
- HGVS:
14.
rs1488031437 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 3:129323326
(GRCh38)
3:129042169
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129323325:C:T
- Gene:
- H1-10-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000008/2
(TOPMED)
- HGVS:
15.
rs1488002526 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 3:129322336
(GRCh38)
3:129041179
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129322335:G:A
- Gene:
- H1-10-AS1 (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)
...more- HGVS:
16.
rs1487980003 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 3:129316203
(GRCh38)
3:129035046
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129316202:G:A
- Gene:
- H1-10 (Varview), H1-10-AS1 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant,5_prime_UTR_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000023/6
(TOPMED)
A=0.000029/4
(GnomAD)
...more- HGVS:
17.
rs1487472236 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 3:129316081
(GRCh38)
3:129034924
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129316080:C:T
- Gene:
- H1-10 (Varview), H1-10-AS1 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant,5_prime_UTR_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.00003/2
(GnomAD)
- HGVS:
18.
rs1486065004 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- CTATAT>-
[Show Flanks]
- Chromosome:
- 3:129322421
(GRCh38)
3:129041264
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129322409:TATATCTATATCTATAT:TATATCTATAT
- Gene:
- H1-10-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TATATCTATAT=0.000071/1
(
ALFA)
-=0.000004/1
(TOPMED)
-=0.000015/2
(GnomAD)
...more- HGVS:
19.
rs1485826039 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 3:129319476
(GRCh38)
3:129038319
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129319475:C:T
- Gene:
- H1-10-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.000142/2
(
ALFA)
T=0.000014/2
(GnomAD)
T=0.000045/12
(TOPMED)
...more- HGVS:
20.
rs1485454192 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>C
[Show Flanks]
- Chromosome:
- 3:129314849
(GRCh38)
3:129033692
(GRCh37)
- Canonical SPDI:
- NC_000003.12:129314848:A:C
- Gene:
- H1-10 (Varview), H1-10-AS1 (Varview)
- Functional Consequence:
- upstream_transcript_variant,3_prime_UTR_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
C=0.000007/1
(GnomAD)
...more- HGVS: