Variant #0000534229 (NC_000008.10:g.145639157G>T, NM_013291.2:c.-4499C>A (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.145639157G>T
DNA change (hg38) g.144413773G>T
Published as SLC39A4(NM_017767.2):c.1321C>A (p.H441N)
ISCN -
DB-ID CPSF1_000016
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) 0.00024 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.-4499C>A r.(?) p.(=)
SLC39A4 NM_017767.2 -?/. - c.1321C>A r.(?) p.(His441Asn)
SLC39A4 NM_130849.2 -?/. - c.1396C>A r.(?) p.(His466Asn)


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