Variant #0000611526 (NC_000008.10:g.145638299C>G, NM_013291.2:c.-3641G>C (CPSF1))

Chromosome 8
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.145638299C>G
DNA change (hg38) g.144412915C>G
Published as SLC39A4(NM_017767.2):c.1584G>C (p.L528=), SLC39A4(NM_130849.4):c.1659G>C (p.L553=)
ISCN -
DB-ID CPSF1_000020 See all 2 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) 0.0025 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPSF1 NM_013291.2 -?/. - c.-3641G>C r.(?) p.(=)
SLC39A4 NM_017767.2 -?/. - c.1584G>C r.(?) p.(Leu528=)
SLC39A4 NM_130849.2 -?/. - c.1659G>C r.(?) p.(Leu553=)


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