Variant #0000862940 (NC_000012.11:g.21652503A>G, NM_002907.3:c.2T>C (RECQL))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.21652503A>G
DNA change (hg38) -
Published as RECQL(NM_002907.4):c.2T>C (p.M1?)
ISCN -
DB-ID RECQL_000301 See all 4 reported entries
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) 0.00036 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +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     
RECQL NM_002907.3 +?/. - c.2T>C r.(?) p.(Met1?)
GOLT1B NM_016072.4 +?/. - c.-2355A>G r.(?) p.(=)
PYROXD1 NM_024854.3 +?/. - c.*30815A>G r.(=) p.(=)


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