Variant #0000332930 (NC_000009.11:g.139906990C>T, NM_207511.1:c.-16440C>T (C9orf139))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.139906990C>T
DNA change (hg38) g.137012538C>T
Published as ABCA2(NM_001606.4):c.5134G>A (p.(Gly1712Ser)), ABCA2(NM_001606.5):c.5134G>A (p.G1712S), ABCA2(NM_212533.3):c.5224G>A (p.G1742S)
ISCN -
DB-ID ABCA2_000001 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00324 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C9orf139 NM_207511.1 ?/. - c.-16440C>T r.(?) p.(=)
ABCA2 NM_212533.2 ?/. - c.5224G>A r.(?) p.(Gly1742Ser)


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