Links from Gene
Items: 1 to 20 of 28462
1.
rs1491475481 has merged into rs72215351 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TA>-,TATA
[Show Flanks]
- Chromosome:
- 5:8411249
(GRCh38)
5:8411362
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8411247:ATA:A,NC_000005.10:8411247:ATA:ATATA
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0.097171/1587
(
ALFA)
-=0.003362/56
(TOMMO)
-=0.009279/17
(Korea1K)
-=0.083466/418
(1000Genomes)
-=0.086384/387
(Estonian)
-=0.092266/24422
(TOPMED)
-=0.094006/13061
(GnomAD)
-=0.115385/69
(NorthernSweden)
-=0.125/5
(GENOME_DK)
-=0.138038/532
(ALSPAC)
-=0.148297/148
(GoNL)
-=0.148598/551
(TWINSUK)
...more- HGVS:
2.
rs1491470453 has merged into rs11370658 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 5:8449471
(GRCh38)
5:8449584
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8449461:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTT=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
- HGVS:
NC_000005.10:g.8449471_8449479del, NC_000005.10:g.8449474_8449479del, NC_000005.10:g.8449475_8449479del, NC_000005.10:g.8449476_8449479del, NC_000005.10:g.8449477_8449479del, NC_000005.10:g.8449478_8449479del, NC_000005.10:g.8449479del, NC_000005.10:g.8449479dup, NC_000005.10:g.8449478_8449479dup, NC_000005.10:g.8449477_8449479dup, NC_000005.10:g.8449476_8449479dup, NC_000005.10:g.8449475_8449479dup, NC_000005.10:g.8449474_8449479dup, NC_000005.10:g.8449472_8449479dup, NC_000005.9:g.8449584_8449592del, NC_000005.9:g.8449587_8449592del, NC_000005.9:g.8449588_8449592del, NC_000005.9:g.8449589_8449592del, NC_000005.9:g.8449590_8449592del, NC_000005.9:g.8449591_8449592del, NC_000005.9:g.8449592del, NC_000005.9:g.8449592dup, NC_000005.9:g.8449591_8449592dup, NC_000005.9:g.8449590_8449592dup, NC_000005.9:g.8449589_8449592dup, NC_000005.9:g.8449588_8449592dup, NC_000005.9:g.8449587_8449592dup, NC_000005.9:g.8449585_8449592dup ...more
3.
rs1491449615 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->CA
[Show Flanks]
- Chromosome:
- 5:8419051
(GRCh38)
5:8419165
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8419051::CA
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
CA=0./0
(
ALFA)
CA=0.000018/2
(GnomAD)
- HGVS:
4.
rs1491402958 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->C
[Show Flanks]
- Chromosome:
- 5:8449462
(GRCh38)
5:8449576
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8449462::C
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0.000084/1
(
ALFA)
C=0.000008/2
(TOPMED)
C=0.000032/1
(GnomAD)
...more- HGVS:
6.
rs1491369743 has merged into rs71609187 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 5:8454949
(GRCh38)
5:8455062
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000005.10:8454938:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTT=0./0
(
ALFA)
-=0.00003/8
(TOPMED)
- HGVS:
NC_000005.10:g.8454949_8454961del, NC_000005.10:g.8454950_8454961del, NC_000005.10:g.8454951_8454961del, NC_000005.10:g.8454952_8454961del, NC_000005.10:g.8454953_8454961del, NC_000005.10:g.8454954_8454961del, NC_000005.10:g.8454955_8454961del, NC_000005.10:g.8454956_8454961del, NC_000005.10:g.8454957_8454961del, NC_000005.10:g.8454958_8454961del, NC_000005.10:g.8454959_8454961del, NC_000005.10:g.8454960_8454961del, NC_000005.10:g.8454961del, NC_000005.10:g.8454961dup, NC_000005.10:g.8454960_8454961dup, NC_000005.10:g.8454959_8454961dup, NC_000005.10:g.8454958_8454961dup, NC_000005.10:g.8454957_8454961dup, NC_000005.10:g.8454956_8454961dup, NC_000005.10:g.8454953_8454961dup, NC_000005.10:g.8454952_8454961dup, NC_000005.10:g.8454951_8454961dup, NC_000005.10:g.8454950_8454961dup, NC_000005.10:g.8454946_8454961dup, NC_000005.10:g.8454944_8454961dup, NC_000005.9:g.8455062_8455074del, NC_000005.9:g.8455063_8455074del, NC_000005.9:g.8455064_8455074del, NC_000005.9:g.8455065_8455074del, NC_000005.9:g.8455066_8455074del, NC_000005.9:g.8455067_8455074del, NC_000005.9:g.8455068_8455074del, NC_000005.9:g.8455069_8455074del, NC_000005.9:g.8455070_8455074del, NC_000005.9:g.8455071_8455074del, NC_000005.9:g.8455072_8455074del, NC_000005.9:g.8455073_8455074del, NC_000005.9:g.8455074del, NC_000005.9:g.8455074dup, NC_000005.9:g.8455073_8455074dup, NC_000005.9:g.8455072_8455074dup, NC_000005.9:g.8455071_8455074dup, NC_000005.9:g.8455070_8455074dup, NC_000005.9:g.8455069_8455074dup, NC_000005.9:g.8455066_8455074dup, NC_000005.9:g.8455065_8455074dup, NC_000005.9:g.8455064_8455074dup, NC_000005.9:g.8455063_8455074dup, NC_000005.9:g.8455059_8455074dup, NC_000005.9:g.8455057_8455074dup ...more
7.
rs1491364198 has merged into rs35855574 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA
[Show Flanks]
- Chromosome:
- 5:8376421
(GRCh38)
5:8376534
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAAAAA=0./0
(
ALFA)
AA=0.4764/2386
(1000Genomes)
- HGVS:
NC_000005.10:g.8376421_8376425del, NC_000005.10:g.8376422_8376425del, NC_000005.10:g.8376423_8376425del, NC_000005.10:g.8376424_8376425del, NC_000005.10:g.8376425del, NC_000005.10:g.8376425dup, NC_000005.10:g.8376424_8376425dup, NC_000005.9:g.8376534_8376538del, NC_000005.9:g.8376535_8376538del, NC_000005.9:g.8376536_8376538del, NC_000005.9:g.8376537_8376538del, NC_000005.9:g.8376538del, NC_000005.9:g.8376538dup, NC_000005.9:g.8376537_8376538dup ...more
8.
rs1491362868 has merged into rs1457624732 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GAGA>-,GA,GAGAGA
[Show Flanks]
- Chromosome:
- 5:8363771
(GRCh38)
5:8363884
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8363763:AGAGAGAGAGA:AGAGAGA,NC_000005.10:8363763:AGAGAGAGAGA:AGAGAGAGA,NC_000005.10:8363763:AGAGAGAGAGA:AGAGAGAGAGAGA
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AGAGAGAGA=0./0
(
ALFA)
AG=0.000007/1
(GnomAD)
- HGVS:
9.
rs1491295342 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TT>-
[Show Flanks]
- Chromosome:
- 5:8374841
(GRCh38)
5:8374954
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8374837:TTTTT:TTT
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
TTT=0./0
(
ALFA)
-=0.000007/1
(GnomAD)
- HGVS:
10.
rs1491285506 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- AA>-
[Show Flanks]
- Chromosome:
- 5:8363763
(GRCh38)
5:8363876
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8363762:AA:
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.000035/1
(TOMMO)
-=0.000086/12
(GnomAD)
...more- HGVS:
11.
rs1491279016 has merged into rs200025260 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GGGG>-,GG,GGGGGG
[Show Flanks]
- Chromosome:
- 5:8419114
(GRCh38)
5:8419227
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8419111:GGGGGG:GG,NC_000005.10:8419111:GGGGGG:GGGG,NC_000005.10:8419111:GGGGGG:GGGGGGGG
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
GGGGGGGG=0./0
(
ALFA)
GG=0.06133/1028
(TOMMO)
GG=0.12472/558
(Estonian)
GG=0.13333/80
(NorthernSweden)
GG=0.15/6
(GENOME_DK)
-=0.25454/981
(ALSPAC)
...more- HGVS:
12.
rs1491264710 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- CA>-
[Show Flanks]
- Chromosome:
- 5:8376408
(GRCh38)
5:8376521
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8376407:CA:
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0.01054/125
(
ALFA)
-=0.00071/12
(TOMMO)
- HGVS:
13.
rs1491249249 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->ATAATTTTATAATTGTATTAT
[Show Flanks]
- Chromosome:
- 5:8374838
(GRCh38)
5:8374952
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8374838:TTTTATAATTGTATTAT:TTTTATAATTGTATTATATAATTTTATAATTGTATTAT
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTATAATTGTATTATATAATTTTATAATTGTATTAT=0./0
(
ALFA)
TTTTATAATTGTATTATATAA=0.000007/1
(GnomAD)
TTTTATAATTGTATTATATAA=0.000011/3
(TOPMED)
...more- HGVS:
14.
rs1491248026 has merged into rs1301042503 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GTTT>-,GTTTAATTTGTTT
[Show Flanks]
- Chromosome:
- 5:8353892
(GRCh38)
5:8354005
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8353888:TTTGTTT:TTT,NC_000005.10:8353888:TTTGTTT:TTTGTTTAATTTGTTT
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTGTTTAATTTGTTT=0./0
(
ALFA)
- HGVS:
15.
rs1491148921 has merged into rs200025260 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GGGG>-,GG,GGGGGG
[Show Flanks]
- Chromosome:
- 5:8419114
(GRCh38)
5:8419227
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8419111:GGGGGG:GG,NC_000005.10:8419111:GGGGGG:GGGG,NC_000005.10:8419111:GGGGGG:GGGGGGGG
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
GGGGGGGG=0./0
(
ALFA)
GG=0.06133/1028
(TOMMO)
GG=0.12472/558
(Estonian)
GG=0.13333/80
(NorthernSweden)
GG=0.15/6
(GENOME_DK)
-=0.25454/981
(ALSPAC)
...more- HGVS:
17.
rs1491054905 has merged into rs34800047 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TT>-,T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 5:8400521
(GRCh38)
5:8400634
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000005.10:8400509:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTTTTTT=0./0
(
ALFA)
- HGVS:
NC_000005.10:g.8400521_8400522del, NC_000005.10:g.8400522del, NC_000005.10:g.8400522dup, NC_000005.10:g.8400521_8400522dup, NC_000005.10:g.8400520_8400522dup, NC_000005.10:g.8400519_8400522dup, NC_000005.10:g.8400518_8400522dup, NC_000005.10:g.8400516_8400522dup, NC_000005.10:g.8400512_8400522dup, NC_000005.9:g.8400634_8400635del, NC_000005.9:g.8400635del, NC_000005.9:g.8400635dup, NC_000005.9:g.8400634_8400635dup, NC_000005.9:g.8400633_8400635dup, NC_000005.9:g.8400632_8400635dup, NC_000005.9:g.8400631_8400635dup, NC_000005.9:g.8400629_8400635dup, NC_000005.9:g.8400625_8400635dup ...more
18.
rs1491042725 has merged into rs35736363 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ATATAT>-,AT,ATAT,ATATATAT,ATATATATAT,ATATATATATAT,ATATATATATATAT,ATATATATATATATAT,ATATATATATATATATAT,ATATATATATATATATATAT,ATATATATATATATATATATATAT,ATATATATATATATATATATATATAT
[Show Flanks]
- Chromosome:
- 5:8375420
(GRCh38)
5:8375533
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATAT,NC_000005.10:8375404:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATAT
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TATATATATATATATAT=0./0
(
ALFA)
TATATATATATATATATA=0.000004/1
(TOPMED)
- HGVS:
NC_000005.10:g.8375406AT[7], NC_000005.10:g.8375406AT[8], NC_000005.10:g.8375406AT[9], NC_000005.10:g.8375406AT[11], NC_000005.10:g.8375406AT[12], NC_000005.10:g.8375406AT[13], NC_000005.10:g.8375406AT[14], NC_000005.10:g.8375406AT[15], NC_000005.10:g.8375406AT[16], NC_000005.10:g.8375406AT[17], NC_000005.10:g.8375406AT[19], NC_000005.10:g.8375406AT[20], NC_000005.9:g.8375519AT[7], NC_000005.9:g.8375519AT[8], NC_000005.9:g.8375519AT[9], NC_000005.9:g.8375519AT[11], NC_000005.9:g.8375519AT[12], NC_000005.9:g.8375519AT[13], NC_000005.9:g.8375519AT[14], NC_000005.9:g.8375519AT[15], NC_000005.9:g.8375519AT[16], NC_000005.9:g.8375519AT[17], NC_000005.9:g.8375519AT[19], NC_000005.9:g.8375519AT[20] ...more
19.
rs1490992391 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G,T
[Show Flanks]
- Chromosome:
- 5:8425816
(GRCh38)
5:8425929
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8425815:A:G,NC_000005.10:8425815:A:T
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
G=0.000029/4
(GnomAD)
- HGVS:
20.
rs1490977582 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->T
[Show Flanks]
- Chromosome:
- 5:8427905
(GRCh38)
5:8428019
(GRCh37)
- Canonical SPDI:
- NC_000005.10:8427905:T:TT
- Gene:
- LINC02226 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TT=0./0
(
ALFA)
T=0.000014/2
(GnomAD)
T=0.000019/5
(TOPMED)
...more- HGVS: