Variant #0000801464 (NC_000004.11:g.113568347T>C, C4orf21(NM_018392.4):c.-10407A>G)

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.113568347T>C
DNA change (hg38) -
Published as LARP7(NM_001267039.1):c.668-8T>C
ISCN -
DB-ID LARP7_000014
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) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LARP7 NM_016648.2 -?/. - c.647-8T>C r.(=) p.(=)
C4orf21 NM_018392.4 -?/. - c.-10407A>G r.(?) p.(=)