Variant #0001055530 (NC_000016.9:g.30386188G>A, NC_000016.9(NM_013292.3):c.3+7G>A (MYLPF))

Chromosome 16
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.30386188G>A
DNA change (hg38) -
Published as MYLPF(NM_013292.5):c.3+7G>A
ISCN -
DB-ID MYLPF_000015
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) 0.00013 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYLPF NM_013292.3 -?/. - c.3+7G>A r.(=) p.(=)
TBC1D10B NM_015527.3 -?/. - c.-4684C>T r.(?) p.(=)
SEPT1 NM_052838.4 -?/. - c.*3567C>T r.(=) p.(=)
ZNF48 NM_152652.2 -?/. - c.-20928G>A r.(?) p.(=)


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