Variant #0000535643 (NC_000009.11:g.103046765G>C, NM_014425.3:c.1948G>C (INVS))

Chromosome 9
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.103046765G>C
DNA change (hg38) g.100284483G>C
Published as INVS(NM_001318381.1):c.1660G>C (p.A554P), INVS(NM_014425.3):c.1948G>C (p.(Ala650Pro)), INVS(NM_014425.5):c.1948G>C (p.A650P)
ISCN -
DB-ID INVS_000001 See all 8 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) 0.00402 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INVS NM_014425.3 -?/. - c.1948G>C r.(?) p.(Ala650Pro)
TEX10 NM_017746.3 -?/. - c.*17708C>G r.(=) p.(=)


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