Links from Nucleotide
Items: 1 to 20 of 103
1.
rs1480252637 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 13:21872814
(GRCh38)
13:22446953
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21872813:T:C
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0.000142/2
(
ALFA)
C=0.000014/2
(GnomAD)
C=0.000023/6
(TOPMED)
...more- HGVS:
2.
rs1479791863 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 13:21873206
(GRCh38)
13:22447345
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21873205:T:C
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0./0
(GnomAD)
- HGVS:
3.
rs1478873231 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 13:21873075
(GRCh38)
13:22447214
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21873074:C:T
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000015/4
(TOPMED)
- HGVS:
4.
rs1471459211 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A,T
[Show Flanks]
- Chromosome:
- 13:21873059
(GRCh38)
13:22447198
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21873058:G:A,NC_000013.11:21873058:G:T
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS:
5.
rs1467376282 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 13:21873186
(GRCh38)
13:22447325
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21873185:G:T
- Gene:
- LINC00424 (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)
...more- HGVS:
7.
rs1464337513 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 13:21873062
(GRCh38)
13:22447201
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21873061:G:A
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.000014/2
(GnomAD)
...more- HGVS:
8.
rs1456028071 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C
[Show Flanks]
- Chromosome:
- 13:21872860
(GRCh38)
13:22446999
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21872859:G:C
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000007/1
(GnomAD)
- HGVS:
9.
rs1423138636 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>A,C
[Show Flanks]
- Chromosome:
- 13:21873084
(GRCh38)
13:22447223
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21873083:T:A,NC_000013.11:21873083:T:C
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
A=0.00006/1
(TOMMO)
...more- HGVS:
10.
rs1423101277 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A,T
[Show Flanks]
- Chromosome:
- 13:21872991
(GRCh38)
13:22447130
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21872990:G:A,NC_000013.11:21872990:G:T
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000007/1
(GnomAD)
- HGVS:
11.
rs1420839102 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C,T
[Show Flanks]
- Chromosome:
- 13:21872873
(GRCh38)
13:22447012
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21872872:G:C,NC_000013.11:21872872:G:T
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000008/2
(TOPMED)
C=0.000035/1
(TOMMO)
...more- HGVS:
13.
rs1386360612 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G
[Show Flanks]
- Chromosome:
- 13:21872888
(GRCh38)
13:22447027
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21872887:C:G
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
G=0.000007/1
(GnomAD)
- HGVS:
14.
rs1382635069 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>G
[Show Flanks]
- Chromosome:
- 13:21872875
(GRCh38)
13:22447014
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21872874:T:G
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000011/3
(TOPMED)
G=0.000021/3
(GnomAD)
...more- HGVS:
15.
rs1364688758 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>A,T
[Show Flanks]
- Chromosome:
- 13:21873030
(GRCh38)
13:22447169
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21873029:C:A,NC_000013.11:21873029:C:T
- Gene:
- LINC00424 (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=0.000071/1
(TOMMO)
...more- HGVS:
16.
rs1363032454 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->CCTT
[Show Flanks]
- Chromosome:
- 13:21872960
(GRCh38)
13:22447100
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21872960:T:TCCTT
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
TCCTT=0./0
(
ALFA)
TCCT=0.000008/2
(TOPMED)
- HGVS:
17.
rs1360070344 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A,T
[Show Flanks]
- Chromosome:
- 13:21873176
(GRCh38)
13:22447315
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21873175:G:A,NC_000013.11:21873175:G:T
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.000054/1
(
ALFA)
A=0.000015/4
(TOPMED)
A=0.000071/1
(TOMMO)
T=0.000223/1
(Estonian)
...more- HGVS:
18.
rs1358049790 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 13:21872857
(GRCh38)
13:22446996
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21872856:C:T
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0.000071/1
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS:
19.
rs1348576233 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>A
[Show Flanks]
- Chromosome:
- 13:21872825
(GRCh38)
13:22446964
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21872824:T:A
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
- HGVS:
20.
rs1348236997 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 13:21872937
(GRCh38)
13:22447076
(GRCh37)
- Canonical SPDI:
- NC_000013.11:21872936:G:T
- Gene:
- LINC00424 (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.000054/1
(
ALFA)
T=0.000004/1
(TOPMED)
T=0.000007/1
(GnomAD)
T=0.000223/1
(Estonian)
...more- HGVS: