Links from Nucleotide
Items: 1 to 20 of 917
1.
rs1491093943 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GA>-
[Show Flanks]
- Chromosome:
- 4:3587974
(GRCh38)
4:3589701
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3587972:AGA:A
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by cluster
- MAF:
-=0.00025/4
(ExAC)
- HGVS:
2.
rs1486124153 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 4:3576996
(GRCh38)
4:3578723
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3576995:A:G
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
- HGVS:
3.
rs1485427449 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G,T
[Show Flanks]
- Chromosome:
- 4:3590409
(GRCh38)
4:3592136
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3590408:C:G,NC_000004.12:3590408:C:T
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
- HGVS:
4.
rs1485075196 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>A,G
[Show Flanks]
- Chromosome:
- 4:3590088
(GRCh38)
4:3591815
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3590087:C:A,NC_000004.12:3590087:C:G
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
A=0.000342/1
(KOREAN)
- HGVS:
5.
rs1485061712 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>T
[Show Flanks]
- Chromosome:
- 4:3589119
(GRCh38)
4:3590846
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3589118:A:T
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0./0
(GnomAD)
- HGVS:
6.
rs1484718039 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G,T
[Show Flanks]
- Chromosome:
- 4:3589923
(GRCh38)
4:3591650
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3589922:C:G,NC_000004.12:3589922:C:T
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
G=0.00034/1
(KOREAN)
- HGVS:
8.
rs1484548759 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 4:3576977
(GRCh38)
4:3578704
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3576976:A:G
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
G=0.000015/4
(TOPMED)
- HGVS:
10.
rs1484080755 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 4:3590272
(GRCh38)
4:3591999
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3590271:G:T
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0.0002/1
(
ALFA)
T=0.0002/1
(Estonian)
- HGVS:
12.
rs1483100476 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 4:3590797
(GRCh38)
4:3592524
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3590796:C:T
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000021/3
(GnomAD)
T=0.00003/8
(TOPMED)
- HGVS:
13.
rs1482911779 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 4:3590901
(GRCh38)
4:3592628
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3590900:T:C
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000007/1
(GnomAD)
C=0.000008/2
(TOPMED)
- HGVS:
14.
rs1482734548 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>G
[Show Flanks]
- Chromosome:
- 4:3588938
(GRCh38)
4:3590665
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3588937:T:G
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0.000071/1
(
ALFA)
G=0.000007/1
(GnomAD)
G=0.000008/2
(TOPMED)
- HGVS:
15.
rs1482185847 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>T
[Show Flanks]
- Chromosome:
- 4:3589049
(GRCh38)
4:3590776
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3589048:A:T
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
T=0.000007/1
(GnomAD)
- HGVS:
18.
rs1479339765 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 4:3587907
(GRCh38)
4:3589634
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3587906:T:C
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0.000071/1
(
ALFA)
C=0.00003/8
(TOPMED)
C=0.000051/7
(GnomAD)
- HGVS:
19.
rs1478834478 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 4:3590780
(GRCh38)
4:3592507
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3590779:A:G
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0.000071/1
(
ALFA)
G=0.000007/1
(GnomAD)
G=0.000011/3
(TOPMED)
- HGVS:
20.
rs1478733024 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A,T
[Show Flanks]
- Chromosome:
- 4:3590539
(GRCh38)
4:3592266
(GRCh37)
- Canonical SPDI:
- NC_000004.12:3590538:G:A,NC_000004.12:3590538:G:T
- Gene:
- LINC00955 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0.000071/1
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS: