Links from Protein
Items: 1 to 20 of 208
1.
rs1490573451 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 9:21367957
(GRCh38)
9:21367956
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367956:C:T
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,synonymous_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.000071/1
(
ALFA)
T=0.000007/1
(GnomAD)
T=0.000008/2
(GnomAD_exomes)
T=0.000019/5
(TOPMED)
- HGVS:
2.
rs1484496229 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C
[Show Flanks]
- Chromosome:
- 9:21367548
(GRCh38)
9:21367547
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367547:G:C
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0.000071/1
(
ALFA)
C=0.000004/1
(GnomAD_exomes)
C=0.000015/2
(GnomAD)
- HGVS:
3.
rs1480480967 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 9:21367884
(GRCh38)
9:21367883
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367883:C:T
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency
- MAF:
T=0.000004/1
(GnomAD_exomes)
- HGVS:
4.
rs1478789687 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C
[Show Flanks]
- Chromosome:
- 9:21367526
(GRCh38)
9:21367525
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367525:G:C
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(GnomAD_exomes)
C=0.000004/1
(TOPMED)
- HGVS:
5.
rs1470582946 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>T
[Show Flanks]
- Chromosome:
- 9:21367796
(GRCh38)
9:21367795
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367795:A:T
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0.000071/1
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS:
6.
rs1460964713 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 9:21367493
(GRCh38)
9:21367492
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367492:A:G
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency
- MAF:
G=0.000004/1
(GnomAD_exomes)
- HGVS:
7.
rs1460383741 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>A
[Show Flanks]
- Chromosome:
- 9:21367809
(GRCh38)
9:21367808
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367808:C:A
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0.000096/2
(
ALFA)
A=0.000009/2
(GnomAD_exomes)
A=0.000053/14
(TOPMED)
A=0.000076/10
(GnomAD)
- HGVS:
8.
rs1453394744 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C
[Show Flanks]
- Chromosome:
- 9:21367777
(GRCh38)
9:21367776
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367776:G:C
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency
- MAF:
C=0.000005/1
(GnomAD_exomes)
- HGVS:
9.
rs1453253767 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A,C
[Show Flanks]
- Chromosome:
- 9:21367785
(GRCh38)
9:21367784
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367784:G:A,NC_000009.12:21367784:G:C
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
C=0.000005/1
(GnomAD_exomes)
A=0.000071/1
(TOMMO)
- HGVS:
10.
rs1446970246 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 9:21367747
(GRCh38)
9:21367746
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367746:G:A
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,synonymous_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000006/1
(GnomAD_exomes)
A=0.000008/2
(TOPMED)
- HGVS:
11.
rs1440021892 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 9:21367441
(GRCh38)
9:21367440
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367440:T:C
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,synonymous_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0.000111/1
(
ALFA)
C=0.000004/1
(GnomAD_exomes)
- HGVS:
12.
rs1433057670 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 9:21367618
(GRCh38)
9:21367617
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367617:T:C
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,synonymous_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000015/2
(GnomAD)
- HGVS:
13.
rs1430733590 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A,C
[Show Flanks]
- Chromosome:
- 9:21367996
(GRCh38)
9:21367995
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367995:G:A,NC_000009.12:21367995:G:C
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,synonymous_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
A=0.000004/1
(GnomAD_exomes)
C=0.000004/1
(TOPMED)
- HGVS:
14.
rs1428193830 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 9:21367529
(GRCh38)
9:21367528
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367528:C:T
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(GnomAD_exomes)
T=0.000004/1
(TOPMED)
- HGVS:
15.
rs1426723876 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 9:21367983
(GRCh38)
9:21367982
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367982:T:C
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by cluster
- MAF:
C=0.000008/2
(GnomAD_exomes)
C=0.000312/2
(1000Genomes)
- HGVS:
16.
rs1423583809 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C
[Show Flanks]
- Chromosome:
- 9:21367991
(GRCh38)
9:21367990
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367990:G:C
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000008/2
(GnomAD_exomes)
C=0.000008/2
(TOPMED)
C=0.000021/3
(GnomAD)
- HGVS:
17.
rs1420856369 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 9:21367667
(GRCh38)
9:21367666
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367666:T:C
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
18.
rs1417667831 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 9:21367748
(GRCh38)
9:21367747
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367747:A:G
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
- HGVS:
19.
rs1408803406 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C
[Show Flanks]
- Chromosome:
- 9:21367662
(GRCh38)
9:21367661
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367661:G:C
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0.000071/1
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
20.
rs1404774957 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 9:21367460
(GRCh38)
9:21367459
(GRCh37)
- Canonical SPDI:
- NC_000009.12:21367459:T:C
- Gene:
- IFNA13 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(GnomAD_exomes)
C=0.000004/1
(TOPMED)
C=0.000007/1
(GnomAD)
- HGVS: