Variant #0000609225 (NC_000004.11:g.52904401_52904402insGGC, NM_000232.4:c.26_27insCGC (SGCB))

Chromosome 4
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.52904401_52904402insGGC
DNA change (hg38) g.52038235_52038236insGGC
Published as -
ISCN -
DB-ID SGCB_000138
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCB NM_000232.4 -?/. - c.26_27insCGC r.(?) p.(Ala9dup)
LRRC66 NM_001024611.1 -?/. - c.-17936_-17935insCGC r.(?) p.(=)


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