Variant #0000968378 (NC_000016.9:g.4744206C>A, NM_139170.2:c.-40545C>A (C16orf71))

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.4744206C>A
DNA change (hg38) -
Published as NUDT16L1(NM_001193452.1):c.381C>A (p.(Ile127=))
ISCN -
DB-ID ANKS3_000021
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) 0.00041 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 2024-02-26 20:06:56 +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     
MGRN1 NM_001142289.2 -?/. - c.*5297C>A r.(=) p.(=)
NUDT16L1 NM_032349.3 -?/. - c.381C>A r.(?) p.(=)
ANKS3 NM_133450.3 -?/. - c.*2703G>T r.(=) p.(=)
C16orf71 NM_139170.2 -?/. - c.-40545C>A r.(?) p.(=)


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