Variant #0000545655 (NC_000011.9:g.71932628G>C, NM_001567.3:c.-3401G>C (INPPL1))

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.71932628G>C
DNA change (hg38) g.72221584G>C
Published as FOLR2(NM_000803.4):c.590G>C (p.(Ser197Thr))
ISCN -
DB-ID FOLR2_000002
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_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)     

RNA change     

Protein     
FOLR2 NM_000803.4 -?/. - c.590G>C r.(?) p.(Ser197Thr)
INPPL1 NM_001567.3 -?/. - c.-3401G>C r.(?) p.(=)
PHOX2A NM_005169.3 -?/. - c.*18165C>G r.(=) p.(=)


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