Variant #0000949641 (NC_000011.9:g.2185556G>A, NM_000207.2:c.-3176C>T (INS))

Chromosome 11
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.2185556G>A
DNA change (hg38) -
Published as TH(NM_000360.3):c.1401C>T (p.(Asp467=))
ISCN -
DB-ID IGF2_000094
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) 0.00663 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 2023-11-27 17:35:39 +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.-3176C>T - r.(?) p.(=)
TH NM_000360.3 -/. - c.1401C>T - r.(?) p.(=)
IGF2 NM_000612.4 -/. - c.-26104C>T - r.(?) p.(=)
INS-IGF2 NM_001042376.2 -/. - c.-3176C>T - r.(?) p.(=)
TH NM_199292.2 -/. - c.1494C>T - r.(?) p.(=)


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