http://identifiers.org/hco/18/GRCh38#31447760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20643308-C-A

31447760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 5 prime UTR variant
orthologous variants: 20643308-C-T

http://identifiers.org/hco/18/GRCh38#31447774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20643322-A-C

31447774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 5 prime UTR variant
orthologous variants: 20643322-A-G

31447774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 5 prime UTR variant
orthologous variants: 20643322-A-T

31447810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 5 prime UTR variant
orthologous variants: 20643364-A-G

http://identifiers.org/hco/18/GRCh38#31447889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20643443-C-A

31447908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense variant
orthologous variants: 20643462-G-A

31447908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense variant
orthologous variants: 20643462-G-T

31448015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20643568-A-G

31448234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20643761-T-G

31448486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20644025-A-G

31448490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20644029-G-A

31448644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20644170-T-G

31448654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20644177-G-A

31448654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20644177-G-C

31448693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20644210-C-T

31448782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20644272-G-A

31448790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20644280-C-G

31450035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20644902-T-C

31450062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20644918-G-T

31450066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20644923-T-C

31450101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20644957-G-A

31450101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20644957-G-T

http://identifiers.org/hco/18/GRCh38#31450122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20644979-C-A

31450225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20645063-T-C

31450325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20645136-G-T

31451105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20646661-C-T

31451162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20646717-G-C

31451181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20646736-A-G

http://identifiers.org/hco/18/GRCh38#31451202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20646755-A-C

http://identifiers.org/hco/18/GRCh38#31451245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20646802-C-A

31451604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20647134-A-G

31451703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20647240-T-C

31451703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20647240-T-G

31451860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20647394-G-A

31451974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20647503-T-C

31452137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20647658-G-A

31452837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20648378-A-G

31453103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20648601-C-T

31454299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron_variant, undefined
orthologous variants: 20650412-G-A

31454299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron_variant, undefined
orthologous variants: 20650412-G-T

31454464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron_variant, undefined
orthologous variants: 20650501-G-A

31454509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20650544-A-G

31455361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20651013-G-C

31455367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20651019-C-T

31455467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20651094-T-G

31456319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20652704-T-C

31456345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20652730-T-A

31456345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20652730-T-C

31456345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20652730-T-G

http://identifiers.org/hco/18/GRCh38#31456391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20652776-C-A

31456391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20652776-C-T

31456395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20652780-T-C

31456395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20652780-T-G

31456457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20652841-T-C

31456457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense variant
orthologous variants: 20652841-T-G

31456500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20652879-A-G

31456593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20652961-A-T

31456865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653424-A-T

31456907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653450-G-A

31456907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653450-G-C

31456907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653450-G-T

http://identifiers.org/hco/18/GRCh38#31456910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20653453-C-A

31456919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653463-G-A

31456920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653464-G-A

31456920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653464-G-C

31456929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653476-A-T

31456935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653482-A-T

http://identifiers.org/hco/18/GRCh38#31456938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20653485-C-A

31456960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653507-T-C

http://identifiers.org/hco/18/GRCh38#31456994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20653541-C-A

31456994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 20653541-C-T

31457019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20653566-G-A

31457019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense variant
orthologous variants: 20653566-G-T

31457170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653715-T-A

31457170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653715-T-C

http://identifiers.org/hco/18/GRCh38#31457201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20653747-C-A

31457201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653747-C-T

31457320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653873-T-C

31457369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653911-T-C

31457408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20653947-G-A

31457518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654043-A-G

31458011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654092-T-G

31458012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654093-T-G

http://identifiers.org/hco/18/GRCh38#31458029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20654110-C-A

31458029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654110-C-T

31458178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654249-C-T

31458226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654300-T-C

31458226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654300-T-G

31458249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654320-G-A

31458250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654321-G-T

31458301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654366-T-A

31458301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654366-T-C

31458303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654368-T-C

http://identifiers.org/hco/18/GRCh38#31458329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20654401-C-A

31458329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654401-C-T

31458345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654417-G-A

31458345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654417-G-T

31458350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654422-G-A

31458350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654422-G-T

31458380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654430-T-C

31458380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654430-T-G

31458385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654435-G-A

31458410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654458-G-A

31458411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654459-G-C

31458411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654459-G-T

31458429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654477-G-C

http://identifiers.org/hco/18/GRCh38#31458468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20654537-C-A

31458468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20654537-C-T

31458516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20654585-T-A

http://identifiers.org/hco/18/GRCh38#31458614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20654677-C-A

31458614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654677-C-T

http://identifiers.org/hco/18/GRCh38#31458649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20654702-C-A

31458649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654702-C-T

31458698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654747-G-A

31458698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654747-G-C

31458700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654749-A-G

31458714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654763-A-G

31458771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20654833-A-T

31459010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20655054-C-T

31459149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense variant
orthologous variants: 20655193-G-A

http://identifiers.org/hco/18/GRCh38#31459221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20655266-C-A

31459227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20655272-T-C

31459349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20655391-G-A

31459564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20655590-T-C

31459597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20655623-A-G

31459609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20655635-T-G

31459650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20655676-A-G

31459650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20655676-A-T

31459765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20656572-T-G

31459790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20656597-A-T

31459815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20656622-T-A

http://identifiers.org/hco/18/GRCh38#31459832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20656636-C-A

31459832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20656636-C-G

31460059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20656860-A-G

31460475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20657227-C-T

31460482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20657234-T-G

31460573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20657316-A-G

http://identifiers.org/hco/18/GRCh38#31460703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20657453-A-C

31460703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20657453-A-T

31460811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20657597-T-C

31460931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20657714-C-T

31461036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20657819-G-C

31461036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20657819-G-T

31461044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20657827-G-A

31461044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20657827-G-T

http://identifiers.org/hco/18/GRCh38#31461045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20657828-C-A

31461070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20657851-T-A

31461070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20657851-T-C

31461121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20657897-A-G

31461211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20658188-C-T

31461251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense variant
orthologous variants: 20658228-A-G

31461313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20658290-T-C

31461417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20658394-G-A

http://identifiers.org/hco/18/GRCh38#31461420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20658397-C-A

31461536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20658509-T-C

31461536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20658509-T-G

31461555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20658528-A-G

http://identifiers.org/hco/18/GRCh38#31461561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20658534-C-A

http://identifiers.org/hco/18/GRCh38#31461724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20658713-C-A

31461802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20658791-G-A

31461802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20658791-G-C

31461802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20658791-G-T

31461823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20658812-G-T

31461853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20658842-G-T

http://identifiers.org/hco/18/GRCh38#31461894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20658881-C-A

31462372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20659001-C-G

http://identifiers.org/hco/18/GRCh38#31462405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20659036-C-A

31462537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20659170-A-G

31463607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20660080-T-C

31463870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20660469-A-T

31463878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20660477-G-T

31463985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20660593-G-A

31463985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20660593-G-T

31464033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20660609-T-C

31464043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20660619-T-C

http://identifiers.org/hco/18/GRCh38#31464093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20660644-A-C

31464103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 20660654-T-A

31464202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense variant
orthologous variants: 20660753-G-A

31464411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20660959-T-C

http://identifiers.org/hco/18/GRCh38#31464497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20661038-A-C

31464680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20661201-G-A

31464714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20661235-A-G

31464730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20661247-A-G

31464733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20661250-A-G

31464736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20661253-A-G

31464824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20661358-T-C

31465094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20661818-C-T

31465310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 20662000-T-C

31465345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20662035-A-G

31465345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20662035-A-T

http://identifiers.org/hco/18/GRCh38#31465432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20662122-C-A

31465702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20662379-C-G

31465702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20662379-C-T

31465728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20662705-C-T

31465772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20662744-C-G

31465985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20663103-C-T

31466054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20663162-G-A

31466077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20663182-T-C

31466133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20663684-A-G

31466310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20663850-C-T

http://identifiers.org/hco/18/GRCh38#31466396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20663932-C-A

31466396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20663932-C-G

31466396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20663932-C-T

31466436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20663976-A-G

31466465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20664003-G-A

31466617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense variant
orthologous variants: 20664502-A-T

31466711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20664599-A-G

31466747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20664635-C-T

31466773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20664656-G-T

31466824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20664713-T-C

31466824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20664713-T-G

31466913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20664786-A-G

31467521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20664922-T-C

31467550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20664951-C-G

31467600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20664994-C-G

31467600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20664994-C-T

http://identifiers.org/hco/18/GRCh38#31467747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20665122-C-A

31467976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20665342-G-A

31468256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20665623-A-T

31468331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20665693-G-A

31468342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20665704-T-A

31468360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20665722-A-G

31468432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20665815-G-T

31468441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20665824-C-T

31468522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20665906-G-A

31469051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20666383-T-G

31469055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20666387-C-T

31469073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20666416-G-T

31469075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20666418-T-C

31469093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20666436-C-T

31469216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20666559-G-A

31469228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20666571-G-A

31469228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense variant
orthologous variants: 20666571-G-T

31469336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20666673-C-G

31469360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20666698-A-T

31469362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20666700-T-C

31469385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20666723-G-T

31469459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20666791-T-A

31469459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20666791-T-C

31469464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20666796-G-A

31469464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20666796-G-T

31469594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20667226-C-G

31469645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20667277-T-C

31469674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20667306-G-A

31469755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20667392-A-G

31469762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20667399-G-A

31469920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20667470-A-G

31470101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20667818-T-C

31470166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20667888-T-C

31470213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20667937-A-G

31470232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20667956-A-G

31471409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20668497-C-T

31471433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20668521-G-A

31471824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20669481-G-C

http://identifiers.org/hco/18/GRCh38#31471928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20669584-A-C

31471951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20669613-A-G

http://identifiers.org/hco/18/GRCh38#31472257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20669858-C-A

31472308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense variant
orthologous variants: 20669906-G-T

31472372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20669973-A-G

http://identifiers.org/hco/18/GRCh38#31472460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20670061-C-A

31472460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20670061-C-T

31472490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20670089-T-C

http://identifiers.org/hco/18/GRCh38#31472574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20670180-C-A

31472574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20670180-C-T

31472604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20670210-T-C

31472637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20670233-T-C

http://identifiers.org/hco/18/GRCh38#31472658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20670246-C-A

31472668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20670257-T-C

31474335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20671552-T-C

31474341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20671558-A-G

http://identifiers.org/hco/18/GRCh38#31474389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20671603-C-A

31474428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20671642-G-A

31474428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20671642-G-T

31474501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20671716-G-A

31474501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20671716-G-C

31474501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20671716-G-T

31475222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20672280-T-C

31475295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20672333-A-G

31475510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20672527-A-T

31475593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: intron variant
orthologous variants: 20672612-T-C

31475666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20672673-G-A

31475766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense variant
orthologous variants: 20672770-T-A

31475801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense variant
orthologous variants: 20672805-C-G

31475900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20672904-G-A

31475900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20672904-G-C

31475900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20672904-G-T

31476017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: synonymous variant
orthologous variants: 20673072-T-A

31476257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: missense variant
orthologous variants: 20673309-A-G

31476326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673379-A-G

31476357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673407-T-A

31476412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673456-G-A

31476412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673456-G-T

31476417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673461-A-T

31476435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673480-G-T

31476486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673538-T-A

http://identifiers.org/hco/18/GRCh38#31476525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20673574-C-A

31476525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673574-C-T

http://identifiers.org/hco/18/GRCh38#31476544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20673593-C-A

http://identifiers.org/hco/18/GRCh38#31476554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20673603-C-A

31476554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673603-C-T

31476575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673623-T-C

http://identifiers.org/hco/18/GRCh38#31476590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20673638-A-C

31476590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673638-A-G

31476600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673648-G-A

31476613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673668-G-T

31476653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673715-T-G

31477082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20673925-A-T

31477225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20674071-T-G

31477402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20674236-T-G

31477711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20674669-T-A

31477721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20674679-G-C

31477739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20674694-G-T

31477761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20674715-T-C

http://identifiers.org/hco/18/GRCh38#31477818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20674779-C-A

31477827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20674788-T-A

31477865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20674821-G-A

31478279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20675974-C-T

31478297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20675992-G-A

31478297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20675992-G-C

http://identifiers.org/hco/18/GRCh38#31478371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#20676069-C-A

31478371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20676069-C-T

31478380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20676078-C-T

31478484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20676335-T-C

31478634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3050
most severe consequence: 3 prime UTR variant
orthologous variants: 20676494-G-A