Variant #0000563848 (NC_000017.10:g.8701315G>A, NM_152599.3:c.1124C>T (MFSD6L))

Chromosome 17
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.8701315G>A
DNA change (hg38) g.8797997G>A
Published as MFSD6L(NM_152599.3):c.1124C>T (p.(Thr375Ile))
ISCN -
DB-ID MFSD6L_000010
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) 0.0032 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
PIK3R6 NM_001010855.2 -?/. - c.*5276C>T r.(=) p.(=)
MFSD6L NM_152599.3 -?/. - c.1124C>T r.(?) p.(Thr375Ile)


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