Variant #0000308449 (NC_000008.10:g.145641411G>A, NM_130849.2:c.257C>T (SLC39A4))

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.145641411G>A
DNA change (hg38) g.144416027G>A
Published as SLC39A4(NM_001280557.1):c.-2535C>T (p.(=)), SLC39A4(NM_017767.2):c.182C>T (p.P61L), SLC39A4(NM_130849.4):c.257C>T (p.P86L)
ISCN -
DB-ID SLC39A4_000012 See all 3 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) 0.00208 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 2018-01-15 20:58:59 +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     
SLC39A4 NM_017767.2 -?/. - c.182C>T r.(?) p.(Pro61Leu)
SLC39A4 NM_130849.2 -?/. - c.257C>T r.(?) p.(Pro86Leu)


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