Variant #0000607888 (NC_000002.11:g.27549576G>A, NM_002437.4:c.-3663C>T (MPV17))

Chromosome 2
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.27549576G>A
DNA change (hg38) g.27326709G>A
Published as GTF3C2(NM_001318909.1):c.2735C>T (p.S912F)
ISCN -
DB-ID MPV17_000020
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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GTF3C2 NM_001035521.1 -?/. - c.2702C>T r.(?) p.(Ser901Phe)
MPV17 NM_002437.4 -?/. - c.-3663C>T r.(?) p.(=)


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