Variant #0000576622 (NC_000023.10:g.53449338dup, NC_000023.10(NM_006306.2):c.109+104dup (SMC1A))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.53449338dup
DNA change (hg38) g.53422386dup
Published as SMC1A(NM_006306.3):c.109+103dupC
ISCN -
DB-ID RIBC1_000008
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
RIBC1 NM_001031745.3 -/. - c.-705dup r.(?) p.(=)
SMC1A NM_006306.2 -/. - c.109+104dup r.(=) p.(=)


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