---
-
allele_string: G/A
assembly_name: GRCh38
colocated_variants:
-
allele_string: G/A
end: 1647710
frequencies:
A:
af: '0.0002'
afr: 0
amr: 0
eas: 0
eur: 0
gnomadg: '6.564e-06'
gnomadg_afr: 0
gnomadg_ami: 0
gnomadg_amr: 0
gnomadg_asj: 0
gnomadg_eas: 0
gnomadg_fin: 0
gnomadg_mid: 0
gnomadg_nfe: 0
gnomadg_remaining: 0
gnomadg_sas: '0.0002069'
sas: '0.001'
id: rs543148494
seq_region_name: 20
start: 1647710
strand: 1
end: 1647710
id: rs543148494
input: rs543148494
most_severe_consequence: non_coding_transcript_exon_variant
seq_region_name: 20
start: 1647710
strand: 1
transcript_consequences:
-
biotype: protein_coding
consequence_terms:
- intron_variant
gene_id: ENSG00000089012
gene_symbol: SIRPG
gene_symbol_source: HGNC
hgnc_id: HGNC:15757
impact: MODIFIER
strand: -1
transcript_id: ENST00000216927
variant_allele: A
-
biotype: protein_coding
consequence_terms:
- intron_variant
gene_id: ENSG00000089012
gene_symbol: SIRPG
gene_symbol_source: HGNC
hgnc_id: HGNC:15757
impact: MODIFIER
strand: -1
transcript_id: ENST00000303415
variant_allele: A
-
biotype: protein_coding
consequence_terms:
- intron_variant
gene_id: ENSG00000089012
gene_symbol: SIRPG
gene_symbol_source: HGNC
hgnc_id: HGNC:15757
impact: MODIFIER
strand: -1
transcript_id: ENST00000344103
variant_allele: A
-
biotype: protein_coding
consequence_terms:
- intron_variant
gene_id: ENSG00000089012
gene_symbol: SIRPG
gene_symbol_source: HGNC
hgnc_id: HGNC:15757
impact: MODIFIER
strand: -1
transcript_id: ENST00000381580
variant_allele: A
-
biotype: protein_coding
consequence_terms:
- intron_variant
gene_id: ENSG00000089012
gene_symbol: SIRPG
gene_symbol_source: HGNC
hgnc_id: HGNC:15757
impact: MODIFIER
strand: -1
transcript_id: ENST00000381583
variant_allele: A
-
biotype: lncRNA
cdna_end: 2033
cdna_start: 2033
consequence_terms:
- non_coding_transcript_exon_variant
gene_id: ENSG00000237914
gene_symbol: SIRPG-AS1
gene_symbol_source: HGNC
hgnc_id: HGNC:51229
impact: MODIFIER
strand: 1
transcript_id: ENST00000456177
variant_allele: A