Variant #0000563728 (NC_000017.10:g.79899044C>T, NM_006907.2:c.-4354G>A (PYCR1))

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.79899044C>T
DNA change (hg38) g.81941168C>T
Published as MYADML2(NM_001145113.2):c.574G>A (p.(Val192Met))
ISCN -
DB-ID MYADML2_000005
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) 0.00337 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     
MYADML2 NM_001145113.2 -?/. - c.574G>A r.(?) p.(Val192Met)
PYCR1 NM_006907.2 -?/. - c.-4354G>A r.(?) p.(=)


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