Variant #0000966305 (NC_000011.9:g.2187270G>T, NM_000207.2:c.-4890C>A (INS))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2187270G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID TH_000077 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.-4890C>A - r.(?) p.(=)
TH NM_000360.3 +?/. - c.1066C>A - r.(?) p.(Leu356Met)
IGF2 NM_000612.4 +?/. - c.-27818C>A - r.(?) p.(=)
INS-IGF2 NM_001042376.2 +?/. - c.-4890C>A - r.(?) p.(=)
TH NM_199292.2 +?/. - c.1159C>A - r.(?) p.(Leu387Met)


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