Variant #0000574314 (NC_000023.10:g.152988711_152988713del, NM_000033.3:c.-2011_-2009del (ABCD1))

Chromosome X
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.152988711_152988713del
DNA change (hg38) g.153723256_153723258del
Published as BCAP31(NM_001139457.2):c.190_192delTCT (p.S65del)
ISCN -
DB-ID BCAP31_000016 See all 2 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) 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 2020-07-21 13:28:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCD1 NM_000033.3 ?/. - c.-2011_-2009del r.(?) p.(=)
BCAP31 NM_001256447.1 ?/. - c.-12_-10del r.(?) p.(=)


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