Variant #0000321462 (NC_000010.10:g.27447547G>C, NM_139312.2:c.-4408C>G (YME1L1))

Chromosome 10
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.27447547G>C
DNA change (hg38) g.27158618G>C
Published as MASTL(NM_001172303.1):c.256G>C (p.(Ala86Pro))
ISCN -
DB-ID MASTL_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     
MASTL NM_032844.3 ?/. - c.256G>C r.(?) p.(Ala86Pro)
YME1L1 NM_139312.2 ?/. - c.-4408C>G r.(?) p.(=)


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