Variant #0000321922 (NC_000011.9:g.2182139T>C, INS(NM_000207.2):c.63A>G)

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.2182139T>C
DNA change (hg38) g.2160909T>C
Published as INS(NM_000207.2):c.63A>G (p.(Pro21=))
ISCN -
DB-ID INS_000006
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) 0.0014 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
INS NM_000207.2 -?/. - c.63A>G - r.(?) p.(Pro21=)
TH NM_000360.3 -?/. - c.*3324A>G - r.(=) p.(=)
IGF2 NM_000612.4 -?/. - c.-22687A>G - r.(?) p.(=)
INS-IGF2 NM_001042376.2 -?/. - c.63A>G - r.(?) p.(Pro21=)
TH NM_199292.2 -?/. - c.*3324A>G - r.(=) p.(=)