Links from Gene
Items: 1 to 20 of 11113
1.
rs1491580575 has merged into rs55660217 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- CACACACACA>-,CA,CACA,CACACA,CACACACA,CACACACACACA,CACACACACACACA,CACACACACACACACA,CACACACACACACACACA,CACACACACACACACACACA,CACACACACACACACACACACA
[Show Flanks]
- Chromosome:
- 5:99548518
(GRCh38)
5:98884222
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA,NC_000005.10:99548504:ACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
ACACACACACACACA=0./0
(
ALFA)
-=0./0
(KOREAN)
- HGVS:
NC_000005.10:g.99548506CA[6], NC_000005.10:g.99548506CA[7], NC_000005.10:g.99548506CA[8], NC_000005.10:g.99548506CA[9], NC_000005.10:g.99548506CA[10], NC_000005.10:g.99548506CA[12], NC_000005.10:g.99548506CA[13], NC_000005.10:g.99548506CA[14], NC_000005.10:g.99548506CA[15], NC_000005.10:g.99548506CA[16], NC_000005.10:g.99548506CA[17], NC_000005.9:g.98884210CA[6], NC_000005.9:g.98884210CA[7], NC_000005.9:g.98884210CA[8], NC_000005.9:g.98884210CA[9], NC_000005.9:g.98884210CA[10], NC_000005.9:g.98884210CA[12], NC_000005.9:g.98884210CA[13], NC_000005.9:g.98884210CA[14], NC_000005.9:g.98884210CA[15], NC_000005.9:g.98884210CA[16], NC_000005.9:g.98884210CA[17]
2.
rs1491541311 has merged into rs35601920 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TCTCTCTCTCTC>-,TC,TCTC,TCTCTC,TCTCTCTC,TCTCTCTCTC,TCTCTCTCTCTCTC,TCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC
[Show Flanks]
- Chromosome:
- 5:99575467
(GRCh38)
5:98911171
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC,NC_000005.10:99575453:CTCTCTCTCTCTCTCTCTCTCTCTC:CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
CTCTCTCTCTCTCTC=0./0
(
ALFA)
CT=0.2987/1496
(1000Genomes)
- HGVS:
NC_000005.10:g.99575455TC[6], NC_000005.10:g.99575455TC[7], NC_000005.10:g.99575455TC[8], NC_000005.10:g.99575455TC[9], NC_000005.10:g.99575455TC[10], NC_000005.10:g.99575455TC[11], NC_000005.10:g.99575455TC[13], NC_000005.10:g.99575455TC[14], NC_000005.10:g.99575455TC[15], NC_000005.10:g.99575455TC[16], NC_000005.10:g.99575455TC[17], NC_000005.10:g.99575455TC[18], NC_000005.10:g.99575455TC[19], NC_000005.10:g.99575455TC[20], NC_000005.10:g.99575455TC[21], NC_000005.10:g.99575455TC[22], NC_000005.10:g.99575455TC[23], NC_000005.9:g.98911159TC[6], NC_000005.9:g.98911159TC[7], NC_000005.9:g.98911159TC[8], NC_000005.9:g.98911159TC[9], NC_000005.9:g.98911159TC[10], NC_000005.9:g.98911159TC[11], NC_000005.9:g.98911159TC[13], NC_000005.9:g.98911159TC[14], NC_000005.9:g.98911159TC[15], NC_000005.9:g.98911159TC[16], NC_000005.9:g.98911159TC[17], NC_000005.9:g.98911159TC[18], NC_000005.9:g.98911159TC[19], NC_000005.9:g.98911159TC[20], NC_000005.9:g.98911159TC[21], NC_000005.9:g.98911159TC[22], NC_000005.9:g.98911159TC[23]
3.
rs1491529563 has merged into rs200616095 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ATATAT>-,ATAT,ATATATAT,ATATATATAT,ATATATATATAT,ATATATATTTTAAAATATATGTATTTTAAAATATATATATATATATATATATATAT
[Show Flanks]
- Chromosome:
- 5:99541635
(GRCh38)
5:98877339
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99541626:ATATATATATATAT:ATATATAT,NC_000005.10:99541626:ATATATATATATAT:ATATATATATAT,NC_000005.10:99541626:ATATATATATATAT:ATATATATATATATAT,NC_000005.10:99541626:ATATATATATATAT:ATATATATATATATATAT,NC_000005.10:99541626:ATATATATATATAT:ATATATATATATATATATAT,NC_000005.10:99541626:ATATATATATATAT:ATATATATATATATATTTTAAAATATATGTATTTTAAAATATATATATATATATATATATATAT
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
ATATATATATAT=0./0
(
ALFA)
AT=0.075/3
(GENOME_DK)
- HGVS:
NC_000005.10:g.99541627AT[4], NC_000005.10:g.99541627AT[6], NC_000005.10:g.99541627AT[8], NC_000005.10:g.99541627AT[9], NC_000005.10:g.99541627AT[10], NC_000005.10:g.99541627_99541640AT[8]TTTAAAATATATGTATTTTAAAATATATATATATATATATATATATAT[1], NC_000005.9:g.98877331AT[4], NC_000005.9:g.98877331AT[6], NC_000005.9:g.98877331AT[8], NC_000005.9:g.98877331AT[9], NC_000005.9:g.98877331AT[10], NC_000005.9:g.98877331_98877344AT[8]TTTAAAATATATGTATTTTAAAATATATATATATATATATATATATAT[1]
4.
rs1491418769 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->GT
[Show Flanks]
- Chromosome:
- 5:99541627
(GRCh38)
5:98877332
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99541627:T:TGT
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
TGT=0./0
(
ALFA)
TG=0.000004/1
(TOPMED)
- HGVS:
5.
rs1491369328 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->CA
[Show Flanks]
- Chromosome:
- 5:99536643
(GRCh38)
5:98872348
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99536643:CA:CACA
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
CACA=0.000084/1
(
ALFA)
CA=0.00015/21
(GnomAD)
CA=0.001734/29
(TOMMO)
- HGVS:
6.
rs1491229787 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- GC>-
[Show Flanks]
- Chromosome:
- 5:99536643
(GRCh38)
5:98872347
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99536642:GC:
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
-=0.000007/1
(GnomAD)
- HGVS:
7.
rs1491088698 has merged into rs369399517 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TATATA>-,TA,TATA,TATATATA,TATATATATA,TATATATATATA,TATATATATATATA,TATATATATATATATA
[Show Flanks]
- Chromosome:
- 5:99541674
(GRCh38)
5:98877378
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99541662:ATATATATATATATATA:ATATATATATA,NC_000005.10:99541662:ATATATATATATATATA:ATATATATATATA,NC_000005.10:99541662:ATATATATATATATATA:ATATATATATATATA,NC_000005.10:99541662:ATATATATATATATATA:ATATATATATATATATATA,NC_000005.10:99541662:ATATATATATATATATA:ATATATATATATATATATATA,NC_000005.10:99541662:ATATATATATATATATA:ATATATATATATATATATATATA,NC_000005.10:99541662:ATATATATATATATATA:ATATATATATATATATATATATATA,NC_000005.10:99541662:ATATATATATATATATA:ATATATATATATATATATATATATATA
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
ATATATATATATA=0./0
(
ALFA)
ATAT=0.21526/1078
(1000Genomes)
- HGVS:
NC_000005.10:g.99541664TA[5], NC_000005.10:g.99541664TA[6], NC_000005.10:g.99541664TA[7], NC_000005.10:g.99541664TA[9], NC_000005.10:g.99541664TA[10], NC_000005.10:g.99541664TA[11], NC_000005.10:g.99541664TA[12], NC_000005.10:g.99541664TA[13], NC_000005.9:g.98877368TA[5], NC_000005.9:g.98877368TA[6], NC_000005.9:g.98877368TA[7], NC_000005.9:g.98877368TA[9], NC_000005.9:g.98877368TA[10], NC_000005.9:g.98877368TA[11], NC_000005.9:g.98877368TA[12], NC_000005.9:g.98877368TA[13]
9.
rs1491014516 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AT>-
[Show Flanks]
- Chromosome:
- 5:99548585
(GRCh38)
5:98884289
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99548583:TAT:T
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
-=0.00018/3
(TOMMO)
- HGVS:
12.
rs1490829190 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C
[Show Flanks]
- Chromosome:
- 5:99564335
(GRCh38)
5:98900039
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99564334:G:C
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
C=0.000007/1
(GnomAD)
- HGVS:
13.
rs1490731579 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G,T
[Show Flanks]
- Chromosome:
- 5:99559598
(GRCh38)
5:98895302
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99559597:C:G,NC_000005.10:99559597:C:T
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000014/2
(GnomAD)
T=0.000068/18
(TOPMED)
T=0.000177/3
(TOMMO)
T=0.001092/2
(Korea1K)
- HGVS:
14.
rs1490680194 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>C
[Show Flanks]
- Chromosome:
- 5:99565386
(GRCh38)
5:98901090
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99565385:A:C
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
15.
rs1490645581 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 5:99546822
(GRCh38)
5:98882526
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99546821:T:C
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000008/2
(TOPMED)
C=0.000014/2
(GnomAD)
- HGVS:
16.
rs1490593110 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>A,C
[Show Flanks]
- Chromosome:
- 5:99558718
(GRCh38)
5:98894422
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99558717:T:A,NC_000005.10:99558717:T:C
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000029/4
(GnomAD)
- HGVS:
17.
rs1490589437 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>C,G
[Show Flanks]
- Chromosome:
- 5:99572568
(GRCh38)
5:98908272
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99572567:A:C,NC_000005.10:99572567:A:G
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000014/2
(GnomAD)
- HGVS:
20.
rs1490567363 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>G
[Show Flanks]
- Chromosome:
- 5:99560006
(GRCh38)
5:98895710
(GRCh37)
- Canonical SPDI:
- NC_000005.10:99560005:T:G
- Gene:
- LINC02113 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
- HGVS: