Variant #0000966296 (NC_000011.9:g.2169055G>C, NM_000207.2:c.*12027C>G (INS))

Chromosome 11
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.2169055G>C
DNA change (hg38) -
Published as INS-IGF2(NM_001042376.2):c.408-18C>G (p.(=))
ISCN -
DB-ID IGF2_000095
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) 0.00125 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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
INS NM_000207.2 -?/. - c.*12027C>G - r.(=) p.(=)
IGF2 NM_000612.4 -?/. - c.-9603C>G - r.(?) p.(=)
INS-IGF2 NM_001042376.2 -?/. - c.408-18C>G - r.(=) p.(=)


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