Variant #0000324702 (NC_000016.9:g.29908193G>A, NM_012410.3:c.251C>T (SEZ6L2))

Chromosome 16
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.29908193G>A
DNA change (hg38) g.29896872G>A
Published as SEZ6L2(NM_001114099.2):c.251C>T (p.(Thr84Met))
ISCN -
DB-ID SEZ6L2_000002
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) 6.0E-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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEZ6L2 NM_012410.3 ?/. - c.251C>T r.(?) p.(Thr84Met)
KCTD13 NM_178863.3 ?/. - c.*10000C>T r.(=) p.(=)
ASPHD1 NM_181718.3 ?/. - c.-4100G>A r.(?) p.(=)


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