Variant #0000996069 (NC_000007.13:g.102296750C>G, NC_000007.13(NM_032959.5):c.*54+9774G>C (POLR2J2))

Chromosome 7
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.102296750C>G
DNA change (hg38) -
Published as SPDYE2B(NM_001166339.1):c.666C>G (p.(Asp222Glu))
ISCN -
DB-ID POLR2J2_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UPK3BL NM_001114403.2 -?/. - c.-13562G>C r.(?) p.(=)
SPDYE2B NM_001166339.1 -?/. - c.666C>G r.(?) p.(Asp222Glu)
POLR2J2 NM_032959.5 -?/. - c.*54+9774G>C r.(=) p.(=)


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