Variant #0000888227 (NC_000008.10:g.145638215G>A, NM_013291.2:c.-3557C>T (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.145638215G>A
DNA change (hg38) -
Published as SLC39A4(NM_017767.2):c.1668C>T (p.V556=), SLC39A4(NM_130849.4):c.1743C>T (p.V581=)
ISCN -
DB-ID CPSF1_000009 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) 0.00073 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPSF1 NM_013291.2 -?/. - c.-3557C>T r.(?) p.(=)
SLC39A4 NM_017767.2 -?/. - c.1668C>T r.(?) p.(Val556=)
SLC39A4 NM_130849.2 -?/. - c.1743C>T r.(?) p.(Val581=)


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