Variant #0000556317 (NC_000015.9:g.94943149G>C, NC_000015.9(NM_018349.3):c.1891-1G>C (MCTP2))

Chromosome 15
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.94943149G>C
DNA change (hg38) g.94399920G>C
Published as MCTP2(NM_001159643.1):c.1891-1G>C (p.?), MCTP2(NM_018349.3):c.1891-1G>C
ISCN -
DB-ID MCTP2_000007 See all 2 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) 3.0E-5 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 2020-07-07 10:32:47 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MCTP2 NM_018349.3 ?/. - c.1891-1G>C r.spl? p.?


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