Variant #0000325775 (NC_000017.10:g.79900165A>G, NM_006907.2:c.-5475T>C (PYCR1))

Chromosome 17
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.79900165A>G
DNA change (hg38) g.81942289A>G
Published as MYADML2(NM_001145113.2):c.-103+7T>C (p.(=))
ISCN -
DB-ID MYADML2_000004
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     
MYADML2 NM_001145113.2 ?/. - c.-103+7T>C r.(=) p.(=)
PYCR1 NM_006907.2 ?/. - c.-5475T>C r.(?) p.(=)


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