Variant #0000861134 (NC_000008.10:g.145639182G>A, NM_013291.2:c.-4524C>T (CPSF1))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.145639182G>A
DNA change (hg38) -
Published as SLC39A4(NM_017767.2):c.1296C>T (p.S432=)
ISCN -
DB-ID CPSF1_000043
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_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     
CPSF1 NM_013291.2 ?/. - c.-4524C>T r.(?) p.(=)
SLC39A4 NM_017767.2 ?/. - c.1296C>T r.(?) p.(Ser432=)
SLC39A4 NM_130849.2 ?/. - c.1371C>T r.(?) p.(Ser457=)


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