Links from Gene
Items: 1 to 20 of 1000
2.
rs1491163654 has merged into rs1164353374 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 16:24666652
(GRCh38)
16:24677973
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000016.10:24666639:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
- HGVS:
NC_000016.10:g.24666652_24666669del, NC_000016.10:g.24666653_24666669del, NC_000016.10:g.24666654_24666669del, NC_000016.10:g.24666655_24666669del, NC_000016.10:g.24666656_24666669del, NC_000016.10:g.24666657_24666669del, NC_000016.10:g.24666658_24666669del, NC_000016.10:g.24666659_24666669del, NC_000016.10:g.24666660_24666669del, NC_000016.10:g.24666661_24666669del, NC_000016.10:g.24666662_24666669del, NC_000016.10:g.24666663_24666669del, NC_000016.10:g.24666664_24666669del, NC_000016.10:g.24666665_24666669del, NC_000016.10:g.24666666_24666669del, NC_000016.10:g.24666667_24666669del, NC_000016.10:g.24666668_24666669del, NC_000016.10:g.24666669del, NC_000016.10:g.24666669dup, NC_000016.10:g.24666668_24666669dup, NC_000016.10:g.24666667_24666669dup, NC_000016.10:g.24666666_24666669dup, NC_000016.10:g.24666665_24666669dup, NC_000016.10:g.24666664_24666669dup, NC_000016.10:g.24666663_24666669dup, NC_000016.10:g.24666662_24666669dup, NC_000016.10:g.24666661_24666669dup, NC_000016.10:g.24666660_24666669dup, NC_000016.9:g.24677973_24677990del, NC_000016.9:g.24677974_24677990del, NC_000016.9:g.24677975_24677990del, NC_000016.9:g.24677976_24677990del, NC_000016.9:g.24677977_24677990del, NC_000016.9:g.24677978_24677990del, NC_000016.9:g.24677979_24677990del, NC_000016.9:g.24677980_24677990del, NC_000016.9:g.24677981_24677990del, NC_000016.9:g.24677982_24677990del, NC_000016.9:g.24677983_24677990del, NC_000016.9:g.24677984_24677990del, NC_000016.9:g.24677985_24677990del, NC_000016.9:g.24677986_24677990del, NC_000016.9:g.24677987_24677990del, NC_000016.9:g.24677988_24677990del, NC_000016.9:g.24677989_24677990del, NC_000016.9:g.24677990del, NC_000016.9:g.24677990dup, NC_000016.9:g.24677989_24677990dup, NC_000016.9:g.24677988_24677990dup, NC_000016.9:g.24677987_24677990dup, NC_000016.9:g.24677986_24677990dup, NC_000016.9:g.24677985_24677990dup, NC_000016.9:g.24677984_24677990dup, NC_000016.9:g.24677983_24677990dup, NC_000016.9:g.24677982_24677990dup, NC_000016.9:g.24677981_24677990dup
3.
rs1491062622 has merged into rs1555486918 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AA>-,AAAA,AAAAAA,AAAAAAAA
[Show Flanks]
- Chromosome:
- 16:24664815
(GRCh38)
16:24676136
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24664812:AAAA:AA,NC_000016.10:24664812:AAAA:AAAAAA,NC_000016.10:24664812:AAAA:AAAAAAAA,NC_000016.10:24664812:AAAA:AAAAAAAAAA
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAA=0./0
(
ALFA)
AAAA=0.000016/2
(GnomAD_exomes)
-=0.000832/8
(ExAC)
- HGVS:
4.
rs1491017566 has merged into rs61045296 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AA>-,A,AAA
[Show Flanks]
- Chromosome:
- 16:24669499
(GRCh38)
16:24680820
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24669487:AAAAAAAAAAAAA:AAAAAAAAAAA,NC_000016.10:24669487:AAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:24669487:AAAAAAAAAAAAA:AAAAAAAAAAAAAA
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAAAAA=0./0
(
ALFA)
A=0.282149/1413
(1000Genomes)
A=0.340145/90033
(TOPMED)
A=0.426667/256
(NorthernSweden)
A=0.474831/1830
(ALSPAC)
A=0.488943/1813
(TWINSUK)
A=0.5/20
(GENOME_DK)
- HGVS:
5.
rs1490852084 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 16:24661414
(GRCh38)
16:24672735
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24661413:T:C
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- downstream_transcript_variant,500B_downstream_variant,intron_variant,genic_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:
6.
rs1490830628 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>T
[Show Flanks]
- Chromosome:
- 16:24664742
(GRCh38)
16:24676063
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24664741:A:T
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.000671/3
(
ALFA)
T=0.000022/3
(GnomAD)
T=0.00067/3
(Estonian)
- HGVS:
8.
rs1490362403 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A,C
[Show Flanks]
- Chromosome:
- 16:24661828
(GRCh38)
16:24673149
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24661827:G:A,NC_000016.10:24661827:G:C
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000007/1
(GnomAD)
- HGVS:
10.
rs1489872236 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 16:24662279
(GRCh38)
16:24673600
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24662278:G:A
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000008/2
(TOPMED)
A=0.000016/2
(GnomAD)
- HGVS:
12.
rs1489641087 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 16:24663271
(GRCh38)
16:24674592
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24663270:G:A
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0.000071/1
(
ALFA)
A=0.000004/1
(TOPMED)
- HGVS:
13.
rs1489573668 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C
[Show Flanks]
- Chromosome:
- 16:24661955
(GRCh38)
16:24673276
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24661954:G:C
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant,genic_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:
14.
rs1489187759 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- A>-
[Show Flanks]
- Chromosome:
- 16:24665990
(GRCh38)
16:24677311
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24665989:A:
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
-=0.000014/2
(GnomAD)
- HGVS:
15.
rs1489158576 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 16:24664971
(GRCh38)
16:24676292
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24664970:G:A
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0.000111/1
(
ALFA)
A=0.000007/1
(GnomAD_exomes)
- HGVS:
16.
rs1488933830 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>C,G
[Show Flanks]
- Chromosome:
- 16:24670722
(GRCh38)
16:24682043
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24670721:A:C,NC_000016.10:24670721:A:G
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
C=0.001638/3
(Korea1K)
- HGVS:
17.
rs1488026554 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>A
[Show Flanks]
- Chromosome:
- 16:24664319
(GRCh38)
16:24675640
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24664318:T:A
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0.000071/1
(
ALFA)
A=0.000015/4
(TOPMED)
- HGVS:
18.
rs1487880842 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>G
[Show Flanks]
- Chromosome:
- 16:24670127
(GRCh38)
16:24681448
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24670126:T:G
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000019/5
(TOPMED)
G=0.000021/3
(GnomAD)
- HGVS:
19.
rs1487290340 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 16:24667463
(GRCh38)
16:24678784
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24667462:A:G
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0.000071/1
(
ALFA)
G=0.000007/1
(GnomAD)
- HGVS:
20.
rs1486871952 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 16:24671215
(GRCh38)
16:24682536
(GRCh37)
- Canonical SPDI:
- NC_000016.10:24671214:A:G
- Gene:
- TNRC6A (Varview), LINC01567 (Varview)
- Functional Consequence:
- upstream_transcript_variant,genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
G=0.000007/1
(GnomAD)
- HGVS: