Variant #0000320768 (NC_000001.10:g.43852328C>T, NM_015284.3:c.-3312C>T (SZT2))

Chromosome 1
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.43852328C>T
DNA change (hg38) g.43386657C>T
Published as MED8(NM_001001653.2):c.158G>A (p.(Ser53Asn))
ISCN -
DB-ID MED8_000001
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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
SZT2 NM_015284.3 ?/. - c.-3312C>T r.(?) p.(=)
HYI NM_031207.5 ?/. - c.*64653G>A r.(=) p.(=)
MED8 NM_052877.3 ?/. - c.425G>A r.(?) p.(Ser142Asn)


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