Variant #0000324553 (NC_000016.9:g.4744960T>C, NM_139170.2:c.-39791T>C (C16orf71))

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.4744960T>C
DNA change (hg38) g.4694959T>C
Published as NUDT16L1(NM_001193452.1):c.486T>C (p.(=))
ISCN -
DB-ID NUDT16L1_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) Retrieve
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     
MGRN1 NM_001142289.2 ?/. - c.*6051T>C r.(=) p.(=)
NUDT16L1 NM_032349.3 ?/. - c.416T>C r.(?) p.(Val139Ala)
ANKS3 NM_133450.3 ?/. - c.*1949A>G r.(=) p.(=)
C16orf71 NM_139170.2 ?/. - c.-39791T>C r.(?) p.(=)


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