Transcript #00007225 (NM_152701.3, ABCA13 gene)

Transcript name ATP-binding cassette, sub-family A (ABC1), member 13
Gene name ABCA13 (ATP binding cassette subfamily A member 13)
Chromosome 7
Transcript - NCBI ID NM_152701.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_689914.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2017-08-07 18:44:03 +02:00 (CEST)
Date last edited N/A


Variants

5116 entries on 52 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. c.-40T>C r.(=) p.(=)
./. c.-31G>A r.(=) p.(=)
./. c.-25T>G r.(=) p.(=)
./. c.-18G>C r.(=) p.(=)
./. c.-16G>A r.(=) p.(=)
./. c.-11G>T r.(=) p.(=)
./. c.-6G>A r.(=) p.(=)
./. c.-1C>T r.(=) p.(=)
./. c.6069delCinsG r.(?) p.(LeuSer2023=)
./. c.12975+5delGinsC r.spl? p.?
./. c.12975+43delCinsT r.(=) p.(=)
./. c.14745-12delCinsT r.(=) p.(=)
./. c.9860-43delCinsT r.(=) p.(=)
./. c.9860-43delCinsA r.(=) p.(=)
./. c.14854delAinsG r.(?) p.(Thr4952Ala)
./. c.9236delAinsG r.(?) p.(Lys3079Arg)
./. c.6293delCinsA r.(?) p.(Thr2098Asn)
./. c.8542delCinsG r.(?) p.(Leu2848Val)
./. c.14351delTinsC r.(?) p.(Met4784Thr)
./. c.11335+30delCinsA r.(=) p.(=)
./. c.12460-20delCinsT r.(=) p.(=)
./. c.4342delCinsT r.(?) p.(Leu1448Phe)
./. c.12460-19delGinsA r.(=) p.(=)
./. c.4347delTinsC r.(?) p.(CysSerSerAsnGly1449=)
./. c.1062+11delCinsG r.(=) p.(=)
./. c.12460-10delTinsC r.(=) p.(=)
./. c.1680delCinsA r.(?) p.(ValIle560=)
./. c.12460-10delTinsG r.(=) p.(=)
./. c.12460-8delTinsC r.(=) p.(=)
./. c.6456delGinsA r.(?) p.(GluSerSer2152=)
./. c.9999+17delGinsA r.(=) p.(=)
./. c.3435delCinsT r.(?) p.(HisCys1145=)
./. c.12492delGinsT r.(?) p.(Lys4164Asn)
./. c.2454delTinsC r.(?) p.(AsnLeu818=)
./. c.8727-28delAinsG r.(=) p.(=)
./. c.12492delGinsA r.(?) p.(LysLys4164=)
./. c.13183-10delCinsT r.(=) p.(=)
./. c.10689-49delAinsG r.(=) p.(=)
./. c.12565delTinsG r.(?) p.(Cys4189Gly)
./. c.1859delCinsT r.(?) p.(Ser620Phe)
./. c.7727delTinsA r.(?) p.(Leu2576Ter)
./. c.10689-24delGinsA r.(=) p.(=)
./. c.3507delGinsT r.(?) p.(Met1169Ile)
./. c.3507delGinsA r.(?) p.(Met1169Ile)
./. c.6723delCinsT r.(?) p.(IleLeu2241=)
./. c.13291delGinsA r.(?) p.(Gly4431Arg)
./. c.2638delGinsT r.(?) p.(Asp880Tyr)
./. c.8837-40delAinsG r.(=) p.(=)
./. c.12091delAinsG r.(?) p.(Thr4031Ala)
./. c.11518delCinsA r.(?) p.(Pro3840Thr)
./. c.14547delCinsT r.(?) p.(HisAlaAspLysPro4849=)
./. c.14547delCinsA r.(?) p.(His4849Gln)
./. c.8902delCinsT r.(?) p.(His2968Tyr)
./. c.9498delGinsA r.(?) p.(ValArg3166=)
./. c.5695delAinsG r.(?) p.(Ile1899Val)
./. c.2743delGinsA r.(?) p.(Glu915Lys)
./. c.14592delAinsG r.(?) p.(LysLeu4864=)
./. c.9517-30delAinsG r.(=) p.(=)
./. c.11614delGinsA r.(?) p.(Ala3872Thr)
./. c.11631delCinsT r.(?) p.(AsnGly3877=)
./. c.70-11delTinsA r.(=) p.(=)
./. c.13347-37delCinsT r.(=) p.(=)
./. c.12229-25delCinsT r.(=) p.(=)
./. c.12229-25delCinsA r.(=) p.(=)
./. c.164-2delAinsG r.spl? p.?
./. c.803delAinsG r.(?) p.(Asp268Gly)
./. c.14052-2delAinsG r.spl? p.?
./. c.14052-2delAinsC r.spl? p.?
./. c.2996delTinsC r.(?) p.(Ile999Thr)
./. c.3003delAinsG r.(?) p.(GlnPhe1001=)
./. c.14116delAinsC r.(?) p.(Lys4706Gln)
./. c.1A>C r.(?) p.(Met1?)
./. c.6G>A r.(?) p.(Gly2=)
./. c.9T>C r.(?) p.(His3=)
./. c.10G>A r.(?) p.(Ala4Thr)
./. c.12C>T r.(?) p.(Ala4=)
./. c.13G>A r.(?) p.(Gly5Arg)
./. c.13G>T r.(?) p.(Gly5Trp)
./. c.17G>A r.(?) p.(Cys6Tyr)
./. c.18C>A r.(?) p.(Cys6Ter)
./. c.20A>G r.(?) p.(Gln7Arg)
./. c.20_22del r.(?) p.(Gln7_Phe8delinsLeu)
./. c.21G>A r.(?) p.(Gln7=)
./. c.21G>C r.(?) p.(Gln7His)
./. c.24C>G r.(?) p.(Phe8Leu)
./. c.30C>T r.(?) p.(Ala10=)
./. c.31C>G r.(?) p.(Leu11Val)
./. c.48G>C r.(?) p.(Trp16Cys)
./. c.58C>T r.(?) p.(Leu20Phe)
./. c.68C>T r.(?) p.(Pro23Leu)
./. c.69G>A r.(?) p.(Pro23=)
./. c.69+3G>A r.spl? p.?
./. c.69+15T>G r.(=) p.(=)
./. c.69+22C>T r.(=) p.(=)
./. c.69+25T>C r.(=) p.(=)
./. c.69+32C>T r.(=) p.(=)
./. c.70-10_70-9del r.(=) p.(=)
./. c.70-9dup r.(=) p.(=)
./. c.71T>A r.(?) p.(Val24Asp)
./. c.73C>T r.(?) p.(Leu25Phe)
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