Variant #0000279820 (NC_000002.11:g.238455241C>T, NC_000002.11(NM_024101.5):c.1540-8C>T (MLPH))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.238455241C>T
DNA change (hg38) g.237546598C>T
Published as MLPH(NM_024101.5):c.1540-8C>T, MLPH(NM_024101.6):c.1540-8C>T (p.?), MLPH(NM_024101.7):c.1540-8C>T
ISCN -
DB-ID MLPH_000021 See all 3 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) 0.00305 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLPH NM_024101.5 -/. - c.1540-8C>T r.(=) p.(=)


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