Variant #0000298309 (NC_000008.10:g.145639726T>C, NM_013291.2:c.-5068A>G (CPSF1))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.145639726T>C
DNA change (hg38) g.144414342T>C
Published as SLC39A4(NM_017767.3):c.994A>G (p.T332A)
ISCN -
DB-ID SLC39A4_000007 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) 0.52038 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPSF1 NM_013291.2 -/. - c.-5068A>G r.(?) p.(=)
SLC39A4 NM_017767.2 -/. - c.994A>G r.(?) p.(Thr332Ala)
SLC39A4 NM_130849.2 -/. - c.1069A>G r.(?) p.(Thr357Ala)


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