Variant #0000605667 (NC_000001.10:g.3102991G>T, NM_022114.3:c.340G>T (PRDM16))

Chromosome 1
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.3102991G>T
DNA change (hg38) g.3186427G>T
Published as PRDM16(NM_022114.3):c.340G>T (p.V114L), PRDM16(NM_022114.4):c.340G>T (p.V114L)
ISCN -
DB-ID PRDM16_000290 See all 2 reported entries
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRDM16 NM_022114.3 -?/. - c.340G>T r.(?) p.(Val114Leu)


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