Variant #0000576620 (NC_000023.10:g.53448866T>G, NC_000023.10(NM_006306.2):c.109+575A>C (SMC1A))

Chromosome X
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.53448866T>G
DNA change (hg38) -
Published as SMC1A(NM_001281463.1):c.22A>C (p.T8P)
ISCN -
DB-ID RIBC1_000007
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     
RIBC1 NM_001031745.3 -?/. - c.-1177T>G r.(?) p.(=)
SMC1A NM_006306.2 -?/. - c.109+575A>C r.(=) p.(=)


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