Links from Gene
Items: 1 to 20 of 10875
1.
rs1491565533 has merged into rs59173540 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GTGTGTGTGTGTGTGTGTGT>-,GTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
[Show Flanks]
- Chromosome:
- 7:96996563
(GRCh38)
7:96625875
(GRCh37)
- Canonical SPDI:
- NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000007.14:96996548:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
- Gene:
- DLX6-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
GTGTGTGTGTGTGTGTGT=0./0
(
ALFA)
- HGVS:
NC_000007.14:g.96996549GT[7], NC_000007.14:g.96996549GT[9], NC_000007.14:g.96996549GT[11], NC_000007.14:g.96996549GT[12], NC_000007.14:g.96996549GT[13], NC_000007.14:g.96996549GT[14], NC_000007.14:g.96996549GT[15], NC_000007.14:g.96996549GT[16], NC_000007.14:g.96996549GT[18], NC_000007.14:g.96996549GT[19], NC_000007.14:g.96996549GT[20], NC_000007.14:g.96996549GT[21], NC_000007.14:g.96996549GT[22], NC_000007.14:g.96996549GT[23], NC_000007.14:g.96996549GT[24], NC_000007.14:g.96996549GT[25], NC_000007.14:g.96996549GT[26], NC_000007.14:g.96996549GT[27], NC_000007.14:g.96996549GT[28], NC_000007.13:g.96625861GT[7], NC_000007.13:g.96625861GT[9], NC_000007.13:g.96625861GT[11], NC_000007.13:g.96625861GT[12], NC_000007.13:g.96625861GT[13], NC_000007.13:g.96625861GT[14], NC_000007.13:g.96625861GT[15], NC_000007.13:g.96625861GT[16], NC_000007.13:g.96625861GT[18], NC_000007.13:g.96625861GT[19], NC_000007.13:g.96625861GT[20], NC_000007.13:g.96625861GT[21], NC_000007.13:g.96625861GT[22], NC_000007.13:g.96625861GT[23], NC_000007.13:g.96625861GT[24], NC_000007.13:g.96625861GT[25], NC_000007.13:g.96625861GT[26], NC_000007.13:g.96625861GT[27], NC_000007.13:g.96625861GT[28]
3.
rs1491460673 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- CC>-
[Show Flanks]
- Chromosome:
- 7:96996035
(GRCh38)
7:96625347
(GRCh37)
- Canonical SPDI:
- NC_000007.14:96996033:CCC:C
- Gene:
- DLX6-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0.00443/67
(
ALFA)
-=0.00114/75
(GnomAD)
-=0.00187/31
(TOMMO)
-=0.00769/14
(Korea1K)
- HGVS:
5.
rs1491286606 has merged into rs11266928 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- CCC>-,C,CC,CCCC,CCCCC,CCCCCC
[Show Flanks]
- Chromosome:
- 7:97015056
(GRCh38)
7:96644368
(GRCh37)
- Canonical SPDI:
- NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCC,NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCC,NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCC,NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCC,NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCCC,NC_000007.14:97015047:CCCCCCCCCCC:CCCCCCCCCCCCCC
- Gene:
- DLX6-AS1 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
CCCCCCCCCCCCCC=0./0
(
ALFA)
-=0.4056/1563
(ALSPAC)
CC=0.4895/1495
(1000Genomes)
- HGVS:
NC_000007.14:g.97015056_97015058del, NC_000007.14:g.97015057_97015058del, NC_000007.14:g.97015058del, NC_000007.14:g.97015058dup, NC_000007.14:g.97015057_97015058dup, NC_000007.14:g.97015056_97015058dup, NC_000007.13:g.96644368_96644370del, NC_000007.13:g.96644369_96644370del, NC_000007.13:g.96644370del, NC_000007.13:g.96644370dup, NC_000007.13:g.96644369_96644370dup, NC_000007.13:g.96644368_96644370dup
6.
rs1491244327 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- AA>-
[Show Flanks]
- Chromosome:
- 7:97006105
(GRCh38)
7:96635417
(GRCh37)
- Canonical SPDI:
- NC_000007.14:97006104:AA:
- Gene:
- DLX6 (Varview), DLX6-AS1 (Varview)
- Functional Consequence:
- frameshift_variant,coding_sequence_variant,intron_variant
- Validated:
- by frequency,by cluster
- MAF:
-=0.000106/2
(TOMMO)
-=0.000154/21
(GnomAD)
-=0.000781/5
(1000Genomes)
- HGVS:
7.
rs1491196302 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->A,T
[Show Flanks]
- Chromosome:
- 7:96996034
(GRCh38)
7:96625347
(GRCh37)
- Canonical SPDI:
- NC_000007.14:96996034::A,NC_000007.14:96996034::T
- Gene:
- DLX6-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by cluster
- MAF:
T=0.00037/6
(TOMMO)
- HGVS:
8.
rs1491166950 has merged into rs35152391 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GCGCGCGCGCGC>-,GC,GCGC,GCGCGC,GCGCGCGC,GCGCGCGCGC,GCGCGCGCGCGCGC,GCGCGCGCGCGCGCGC
[Show Flanks]
- Chromosome:
- 7:96999868
(GRCh38)
7:96629180
(GRCh37)
- Canonical SPDI:
- NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGC,NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGC,NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGC,NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGC,NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGC,NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGC,NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGC,NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGC
- Gene:
- DLX6-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
GCGCGC=0./0
(
ALFA)
GC=0.000015/4
(TOPMED)
- HGVS:
NC_000007.14:g.96999862GC[3], NC_000007.14:g.96999862GC[4], NC_000007.14:g.96999862GC[5], NC_000007.14:g.96999862GC[6], NC_000007.14:g.96999862GC[7], NC_000007.14:g.96999862GC[8], NC_000007.14:g.96999862GC[10], NC_000007.14:g.96999862GC[11], NC_000007.13:g.96629174GC[3], NC_000007.13:g.96629174GC[4], NC_000007.13:g.96629174GC[5], NC_000007.13:g.96629174GC[6], NC_000007.13:g.96629174GC[7], NC_000007.13:g.96629174GC[8], NC_000007.13:g.96629174GC[10], NC_000007.13:g.96629174GC[11]
9.
rs1491151060 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GC>-
[Show Flanks]
- Chromosome:
- 7:96981573
(GRCh38)
7:96610885
(GRCh37)
- Canonical SPDI:
- NC_000007.14:96981571:CGC:C
- Gene:
- DLX6-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0.000337/4
(
ALFA)
-=0.000142/2
(TOMMO)
-=0.000355/40
(GnomAD)
-=0.001645/3
(Korea1K)
- HGVS:
10.
rs1491135215 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->TCC
[Show Flanks]
- Chromosome:
- 7:97004939
(GRCh38)
7:96634252
(GRCh37)
- Canonical SPDI:
- NC_000007.14:97004939:CC:CCTCC
- Gene:
- DLX6 (Varview), DLX6-AS1 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,intron_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
CCTCC=0./0
(
ALFA)
CCT=0.00064/2
(GnomAD)
- HGVS:
12.
rs1491087012 has merged into rs71980200 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAA>-,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 7:96991909
(GRCh38)
7:96621221
(GRCh37)
- Canonical SPDI:
- NC_000007.14:96991900:AAAAAAAAAAAAAAA:AAAAAAAA,NC_000007.14:96991900:AAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000007.14:96991900:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000007.14:96991900:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000007.14:96991900:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000007.14:96991900:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000007.14:96991900:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000007.14:96991900:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000007.14:96991900:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000007.14:96991900:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000007.14:96991900:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:96991900:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- DLX6-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAA=0./0
(
ALFA)
-=0.000011/3
(TOPMED)
-=0.34984/1752
(1000Genomes)
- HGVS:
NC_000007.14:g.96991909_96991915del, NC_000007.14:g.96991912_96991915del, NC_000007.14:g.96991913_96991915del, NC_000007.14:g.96991914_96991915del, NC_000007.14:g.96991915del, NC_000007.14:g.96991915dup, NC_000007.14:g.96991914_96991915dup, NC_000007.14:g.96991913_96991915dup, NC_000007.14:g.96991912_96991915dup, NC_000007.14:g.96991911_96991915dup, NC_000007.14:g.96991903_96991915dup, NC_000007.14:g.96991902_96991915dup, NC_000007.13:g.96621221_96621227del, NC_000007.13:g.96621224_96621227del, NC_000007.13:g.96621225_96621227del, NC_000007.13:g.96621226_96621227del, NC_000007.13:g.96621227del, NC_000007.13:g.96621227dup, NC_000007.13:g.96621226_96621227dup, NC_000007.13:g.96621225_96621227dup, NC_000007.13:g.96621224_96621227dup, NC_000007.13:g.96621223_96621227dup, NC_000007.13:g.96621215_96621227dup, NC_000007.13:g.96621214_96621227dup
13.
rs1491027170 has merged into rs140062889 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- CACACACACACA>-,CA,CACA,CACACA,CACACACA,CACACACACA,CACACACACACACA,CACACACACACACACA,CACACACACACACACACA,CACACACACACACACACACA
[Show Flanks]
- Chromosome:
- 7:96990621
(GRCh38)
7:96619933
(GRCh37)
- Canonical SPDI:
- NC_000007.14:96990611:ACACACACACACACACACACA:ACACACACA,NC_000007.14:96990611:ACACACACACACACACACACA:ACACACACACA,NC_000007.14:96990611:ACACACACACACACACACACA:ACACACACACACA,NC_000007.14:96990611:ACACACACACACACACACACA:ACACACACACACACA,NC_000007.14:96990611:ACACACACACACACACACACA:ACACACACACACACACA,NC_000007.14:96990611:ACACACACACACACACACACA:ACACACACACACACACACA,NC_000007.14:96990611:ACACACACACACACACACACA:ACACACACACACACACACACACA,NC_000007.14:96990611:ACACACACACACACACACACA:ACACACACACACACACACACACACA,NC_000007.14:96990611:ACACACACACACACACACACA:ACACACACACACACACACACACACACA,NC_000007.14:96990611:ACACACACACACACACACACA:ACACACACACACACACACACACACACACA
- Gene:
- DLX6-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
ACACACACACA=0./0
(
ALFA)
-=0.11263/485
(1000Genomes)
- HGVS:
NC_000007.14:g.96990613CA[4], NC_000007.14:g.96990613CA[5], NC_000007.14:g.96990613CA[6], NC_000007.14:g.96990613CA[7], NC_000007.14:g.96990613CA[8], NC_000007.14:g.96990613CA[9], NC_000007.14:g.96990613CA[11], NC_000007.14:g.96990613CA[12], NC_000007.14:g.96990613CA[13], NC_000007.14:g.96990613CA[14], NC_000007.13:g.96619925CA[4], NC_000007.13:g.96619925CA[5], NC_000007.13:g.96619925CA[6], NC_000007.13:g.96619925CA[7], NC_000007.13:g.96619925CA[8], NC_000007.13:g.96619925CA[9], NC_000007.13:g.96619925CA[11], NC_000007.13:g.96619925CA[12], NC_000007.13:g.96619925CA[13], NC_000007.13:g.96619925CA[14]
14.
rs1491021208 has merged into rs34726035 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTT>-,T,TT,TTTT,TTTTT,TTTTTTTT
[Show Flanks]
- Chromosome:
- 7:96988008
(GRCh38)
7:96617320
(GRCh37)
- Canonical SPDI:
- NC_000007.14:96987994:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000007.14:96987994:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000007.14:96987994:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000007.14:96987994:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000007.14:96987994:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000007.14:96987994:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT
- Gene:
- DLX6-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTTT=0./0
(
ALFA)
-=0.23303/1167
(1000Genomes)
- HGVS:
NC_000007.14:g.96988008_96988010del, NC_000007.14:g.96988009_96988010del, NC_000007.14:g.96988010del, NC_000007.14:g.96988010dup, NC_000007.14:g.96988009_96988010dup, NC_000007.14:g.96988006_96988010dup, NC_000007.13:g.96617320_96617322del, NC_000007.13:g.96617321_96617322del, NC_000007.13:g.96617322del, NC_000007.13:g.96617322dup, NC_000007.13:g.96617321_96617322dup, NC_000007.13:g.96617318_96617322dup
15.
rs1490908392 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- G>-
[Show Flanks]
- Chromosome:
- 7:97007271
(GRCh38)
7:96636583
(GRCh37)
- Canonical SPDI:
- NC_000007.14:97007270:GG:G
- Gene:
- DLX6 (Varview), DLX6-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
GG=0./0
(
ALFA)
-=0.000007/1
(GnomAD)
-=0.000011/3
(TOPMED)
- HGVS:
16.
rs1490853857 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G,T
[Show Flanks]
- Chromosome:
- 7:96995945
(GRCh38)
7:96625257
(GRCh37)
- Canonical SPDI:
- NC_000007.14:96995944:C:G,NC_000007.14:96995944:C:T
- Gene:
- DLX6-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
G=0.000036/5
(GnomAD)
- HGVS:
17.
rs1490848434 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 7:96986159
(GRCh38)
7:96615471
(GRCh37)
- Canonical SPDI:
- NC_000007.14:96986158:T:C
- Gene:
- DLX6-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0.000108/2
(
ALFA)
C=0.000008/2
(TOPMED)
C=0.000014/2
(GnomAD)
C=0.000223/1
(Estonian)
- HGVS:
18.
rs1490831433 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 7:97014694
(GRCh38)
7:96644006
(GRCh37)
- Canonical SPDI:
- NC_000007.14:97014693:A:G
- Gene:
- DLX6-AS1 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
G=0.000035/1
(TOMMO)
G=0.000342/1
(KOREAN)
G=0.000546/1
(Korea1K)
- HGVS:
20.
rs1490770752 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 7:97001461
(GRCh38)
7:96630773
(GRCh37)
- Canonical SPDI:
- NC_000007.14:97001460:C:T
- Gene:
- DLX6-AS1 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000008/2
(TOPMED)
T=0.000014/2
(GnomAD)
- HGVS: