Variant #0000543450 (NC_000011.9:g.2170413G>A, NM_000207.2:c.*10669C>T (INS))

Chromosome 11
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.2170413G>A
DNA change (hg38) g.2149183G>A
Published as INS-IGF2(NM_001042376.2):c.350C>T (p.(Pro117Leu))
ISCN -
DB-ID IGF2_000037
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
INS NM_000207.2 ?/. - c.*10669C>T - r.(=) p.(=)
IGF2 NM_000612.4 ?/. - c.-10961C>T - r.(?) p.(=)
INS-IGF2 NM_001042376.2 ?/. - c.350C>T - r.(?) p.(Pro117Leu)


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