Variant #0000537511 (NC_000009.11:g.139903412G>C, NM_207511.1:c.-20018G>C (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.139903412G>C
DNA change (hg38) g.137008960G>C
Published as ABCA2(NM_001606.5):c.6921C>G (p.A2307=)
ISCN -
DB-ID ABCA2_000006
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
C9orf139 NM_207511.1 -?/. - c.-20018G>C r.(?) p.(=)
ABCA2 NM_212533.2 -?/. - c.7011C>G r.(?) p.(Ala2337=)


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