Links from Gene
Items: 1 to 20 of 1785
2.
rs1490914991 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C
[Show Flanks]
- Chromosome:
- 15:82519319
(GRCh38)
15:82803732
(GRCh37)
- Canonical SPDI:
- NC_000015.10:82519318:G:C
- Gene:
- GOLGA6L17P (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
3.
rs1490428468 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C
[Show Flanks]
- Chromosome:
- 15:82518826
(GRCh38)
15:82803239
(GRCh37)
- Canonical SPDI:
- NC_000015.10:82518825:G:C
- Gene:
- GOLGA6L17P (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
4.
rs1490377246 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 15:82519660
(GRCh38)
15:82804073
(GRCh37)
- Canonical SPDI:
- NC_000015.10:82519659:C:T
- Gene:
- GOLGA6L17P (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000023/6
(TOPMED)
T=0.000814/23
(TOMMO)
T=0.000898/1
(Korea1K)
- HGVS:
5.
rs1490302230 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 15:82526106
(GRCh38)
15:82810552
(GRCh37)
- Canonical SPDI:
- NC_000015.10:82526105:G:A
- Gene:
- GOLGA6L17P (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
G=0.5/1
(SGDP_PRJ)
- HGVS:
6.
rs1489887674 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 15:82519357
(GRCh38)
15:82803770
(GRCh37)
- Canonical SPDI:
- NC_000015.10:82519356:C:T
- Gene:
- GOLGA6L17P (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0.000169/2
(
ALFA)
T=0.000018/2
(GnomAD)
- HGVS:
7.
rs1489861656 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>C
[Show Flanks]
- Chromosome:
- 15:82519432
(GRCh38)
15:82803845
(GRCh37)
- Canonical SPDI:
- NC_000015.10:82519431:A:C
- Gene:
- GOLGA6L17P (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
C=0.000008/1
(GnomAD)
- HGVS:
8.
rs1489823252 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C,G
[Show Flanks]
- Chromosome:
- 15:82524963
(GRCh38)
15:82809408
(GRCh37)
- Canonical SPDI:
- NC_000015.10:82524962:T:C,NC_000015.10:82524962:T:G
- Gene:
- GOLGA6L17P (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0./0
(GnomAD)
- HGVS:
9.
rs1489809901 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 15:82525780
(GRCh38)
15:82810226
(GRCh37)
- Canonical SPDI:
- NC_000015.10:82525779:A:G
- Gene:
- GOLGA6L17P (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
G=0.000007/1
(GnomAD)
- HGVS:
10.
rs1489687919 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 15:82518104
(GRCh38)
15:82802517
(GRCh37)
- Canonical SPDI:
- NC_000015.10:82518103:G:T
- Gene:
- GOLGA6L17P (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0.00944/112
(
ALFA)
T=0.00053/4
(TOMMO)
- HGVS:
14.
rs1488668263 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 15:82521248
(GRCh38)
15:82805660
(GRCh37)
- Canonical SPDI:
- NC_000015.10:82521247:C:T
- Gene:
- GOLGA6L17P (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000011/3
(TOPMED)
- HGVS:
15.
rs1488227431 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>A,T
[Show Flanks]
- Chromosome:
- 15:82521993
(GRCh38)
15:82806405
(GRCh37)
- Canonical SPDI:
- NC_000015.10:82521992:C:A,NC_000015.10:82521992:C:T
- Gene:
- GOLGA6L17P (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.00001/1
(GnomAD)
T=0.00015/4
(TOMMO)
- HGVS:
17.
rs1488027498 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 15:82521467
(GRCh38)
15:82805879
(GRCh37)
- Canonical SPDI:
- NC_000015.10:82521466:A:G
- Gene:
- GOLGA6L17P (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0.00607/72
(
ALFA)
G=0.0004/11
(TOMMO)
G=0.00047/3
(1000Genomes)
G=0.00051/8
(GnomAD)
- HGVS:
19.
rs1487541657 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 15:82526791
(GRCh38)
15:82811199
(GRCh37)
- Canonical SPDI:
- NC_000015.10:82526790:G:T
- Gene:
- GOLGA6L17P (Varview)
- Functional Consequence:
- downstream_transcript_variant,500B_downstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000007/1
(GnomAD)
T=0.000045/12
(TOPMED)
T=0.000312/2
(1000Genomes)
- HGVS:
20.
rs1487447267 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 15:82523163
(GRCh38)
15:82807575
(GRCh37)
- Canonical SPDI:
- NC_000015.10:82523162:A:G
- Gene:
- GOLGA6L17P (Varview)
- Functional Consequence:
- non_coding_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0.010201/121
(
ALFA)
G=0.002498/16
(1000Genomes)
G=0.00893/1035
(GnomAD)
- HGVS: