Variant #0000537520 (NC_000009.11:g.139925599G>A, NC_000009.11(NM_207511.1):c.-1066-851G>A (C9orf139))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.139925599G>A
DNA change (hg38) g.137031147G>A
Published as FUT7(NM_004479.3):c.592C>T (p.(Arg198Trp))
ISCN -
DB-ID ABCA2_000015
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) 3.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FUT7 NM_004479.3 -?/. - c.592C>T r.(?) p.(Arg198Trp)
C9orf139 NM_207511.1 -?/. - c.-1066-851G>A r.(=) p.(=)
ABCA2 NM_212533.2 -?/. - c.-2275C>T r.(?) p.(=)


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