Variant #0000255160 (NC_000007.13:g.150751367A>G, NM_003040.3:c.-5546A>G (SLC4A2))

Chromosome 7
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.150751367A>G
DNA change (hg38) g.151054280A>G
Published as CDK5(NM_004935.3):c.724T>C (p.Y242H)
ISCN -
DB-ID CDK5_000005
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
SLC4A2 NM_003040.3 -?/. - c.-5546A>G r.(?) p.(=)
ASIC3 NM_004769.3 -?/. - c.*1628A>G r.(=) p.(=)
CDK5 NM_004935.3 -?/. - c.724T>C r.(?) p.(Tyr242His)


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