48244333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87350749-G-A

48244333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87350749-G-C

48244333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87350749-G-T

http://identifiers.org/hco/16/GRCh38#48244365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87350788-C-A

48244365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87350788-C-T

48244458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87350881-C-T

48244463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87350886-C-T

48244535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87350958-C-T

http://identifiers.org/hco/16/GRCh38#48244614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87351037-C-A

48244614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 87351037-C-T

48244633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351056-T-C

48244655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351071-G-A

48244655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351071-G-T

48244664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351076-T-C

http://identifiers.org/hco/16/GRCh38#48244684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87351092-A-C

48244684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351092-A-G

48244900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87351289-G-A

48244972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87351358-G-A

48245037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351413-G-A

48245037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351413-G-T

48245041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351417-C-T

48245065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351441-T-C

48245101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351467-A-T

48245119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351484-C-T

48245157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351523-C-G

48245157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351523-C-T

48245183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351550-T-C

48245209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351571-G-A

48245251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351613-C-T

48245354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351720-G-C

48245376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351744-C-T

48245459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351806-C-T

48245467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351814-C-T

48245606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87351922-G-A

http://identifiers.org/hco/16/GRCh38#48245679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87352006-A-C

http://identifiers.org/hco/16/GRCh38#48245866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87352297-C-A

48245866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87352297-C-T

48246329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87352669-A-G

48247101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87354799-A-T

48247152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87354852-C-G

48247152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87354852-C-T

48247288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87354959-G-A

48247288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87354959-G-T

48247325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87354995-T-C

48248494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87356037-G-A

48249039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87356429-A-G

48249180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87356524-G-T

48249237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87356581-T-C

48249320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87356677-T-C

48252086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87357972-A-G

48252393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87358275-C-T

http://identifiers.org/hco/16/GRCh38#48252416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87358296-C-A

48252667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87358553-C-T

48253113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87358977-T-C

48253142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87359007-A-G

48253175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87359040-T-C

48255021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87359713-A-G

48255037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87359727-G-A

48255382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87360037-T-G

http://identifiers.org/hco/16/GRCh38#48256521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87360409-C-A

48256592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87360479-T-C

48258561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87361369-G-T

48258576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87361384-G-A

48258576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87361384-G-C

48258576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87361384-G-T

48258577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87361385-T-C

48258589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87361397-A-G

48258629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 87361436-T-C

48261024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87362433-A-T

48261067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87362466-A-G

48261373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87362989-G-A

48261486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 87363169-T-G

http://identifiers.org/hco/16/GRCh38#48261645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87363894-C-A

48261682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87363929-A-G

http://identifiers.org/hco/16/GRCh38#48261716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87363963-C-A

48261716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87363963-C-T

48261761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87364004-C-G

http://identifiers.org/hco/16/GRCh38#48261766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87364009-C-A

48261785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87364028-G-A

48262662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87364429-G-A

48262662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87364429-G-T

48262703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87364454-A-G

48262718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87364469-T-C

48262921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87364670-A-G

http://identifiers.org/hco/16/GRCh38#48262923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87364672-C-A

48262964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87364744-G-A

48262964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87364744-G-C

48262964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87364744-G-T

48269537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87367236-C-T

48270007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87368161-A-G

48270041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87368195-G-A

48270116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87368270-G-C

48270134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87368288-G-A

48270134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87368288-G-T

48270161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87368315-T-C

48270497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87368488-G-C

48270499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87368490-G-A

48270746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87368718-A-G

48270812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87368785-A-T

48271266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87368871-A-T

48271620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87369202-T-C

48271652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87369233-G-A

48271674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87369257-G-T

48271738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87369394-T-G

48271913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87369556-G-A

48273247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87369811-T-C

48273426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87369983-A-G

48273689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87370153-T-C

http://identifiers.org/hco/16/GRCh38#48273700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87370165-A-C

48273763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87371052-G-A

48273898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87371184-A-G

48274111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87371381-G-A

48274676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87373160-A-G

48274676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87373160-A-T

48275112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87375414-C-G

48275540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87375741-C-T

48275751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87376689-G-A

48275989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87376996-G-A

48276022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87377033-T-G

http://identifiers.org/hco/16/GRCh38#48276310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87378110-A-C

48276570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87378357-C-T

48276660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87378432-T-C

48276726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87378467-A-G

48277389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87378855-T-C

48277389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87378855-T-G

48277489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87378955-G-A

48277517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87378978-G-T

48277550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87379008-A-G

48277598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87379056-A-G

48277599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87379057-T-G

48277669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87379110-T-C

48278150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87379626-C-G

48278231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87379690-G-A

48278259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87379717-T-A

48278364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87379818-C-T

48278435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87379874-G-A

48287413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87389210-A-T

48287628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87389392-G-A

48287786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87389553-C-T

48288043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87389783-G-C

48288062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87389802-A-G

http://identifiers.org/hco/16/GRCh38#48295018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87391519-C-A

48295525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87391874-G-A

48295760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87392076-C-T

48295938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87392256-T-G

http://identifiers.org/hco/16/GRCh38#48296173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87392477-A-C

48296192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87392494-A-G

48296199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87392501-G-A

48296237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87392539-G-A

48296250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87392553-A-G

48296250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87392553-A-T

http://identifiers.org/hco/16/GRCh38#48298129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87393654-A-C

http://identifiers.org/hco/16/GRCh38#48298315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87393832-A-C

48298385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87393904-T-A

48298418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87393930-T-A

48298419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87393931-A-G

48299221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87393977-C-T

48299271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87394027-C-G

48299612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87394292-A-T

48299645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87394324-G-A

48299726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87394405-A-G

48299808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87394489-G-C

48299808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87394489-G-T

http://identifiers.org/hco/16/GRCh38#48299813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87394494-A-C

48299813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87394494-A-G

48299928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87394701-T-C

http://identifiers.org/hco/16/GRCh38#48300235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87395151-A-C

48300281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87395197-A-G

http://identifiers.org/hco/16/GRCh38#48300598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87395587-A-C

48300793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87395769-A-G

48300891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87395836-G-A

48300896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87395841-G-T

48300918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87395868-G-A

48301166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87396090-A-G

48302769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87399173-T-G

48302770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87399174-T-C

48302776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87399180-A-G

48303034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87399435-G-A

48303132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87399526-G-T

48303298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87399690-G-A

48303298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87399690-G-C

48303389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87399780-T-C

http://identifiers.org/hco/16/GRCh38#48303411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87399802-C-A

48303411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87399802-C-T

http://identifiers.org/hco/16/GRCh38#48303413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87399804-C-A

48303422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87399813-C-T

http://identifiers.org/hco/16/GRCh38#48303438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87399828-C-A

48303438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87399828-C-T

48303446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87399840-T-A

48304793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87400634-G-T

http://identifiers.org/hco/16/GRCh38#48304949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87400783-C-A

48305091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87400867-C-T

48305126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87400901-G-A

48305157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87400930-G-A

48305243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87401007-T-C

48305683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87401388-C-T

48305707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87401410-T-C

48305711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87401414-C-T

48305781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87401475-T-G

48305782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87401476-G-C

48305859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87401543-A-G

48306318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87401955-T-G

48306857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87402901-G-A

48307195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87403179-T-C

http://identifiers.org/hco/16/GRCh38#48307248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87403222-A-C

48307248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87403222-A-G

48307448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87403408-G-A

48307490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87403456-A-G

48315207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87403529-A-G

48316014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87404332-T-C

48316014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87404332-T-G

http://identifiers.org/hco/16/GRCh38#48316226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87404560-C-A

48316226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87404560-C-T

48316229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87404563-A-T

48316267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87404592-A-G

48316304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87404620-G-A

48316324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87404644-T-A

http://identifiers.org/hco/16/GRCh38#48316449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87404778-C-A

48316488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87404802-G-A

48316516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87404825-G-A

http://identifiers.org/hco/16/GRCh38#48316981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87405263-C-A

48317046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87405327-A-T

48317050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87405331-A-G

48317074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87405354-C-T

48317083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87405364-T-A

48317129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87405392-T-G

48317410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87412076-T-C

48317641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87412296-T-A

48317643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87412298-T-C

48317900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87412531-A-G

http://identifiers.org/hco/16/GRCh38#48318527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87413205-A-C

48318535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87413213-T-G

48320377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87417359-A-G

48320402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87417383-T-C

48320493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87417480-G-C

48320865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87418517-A-G

http://identifiers.org/hco/16/GRCh38#48321411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87418656-C-A

48321411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87418656-C-T

48323684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87419417-G-T

48323776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87419492-G-T

48334165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87435514-T-C

48334991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87435803-C-T

48335219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87436075-G-T

48335718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87436464-A-G

48336338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87437174-C-G

48345599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87439065-T-C

48345599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87439065-T-G

48345668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87439126-G-C

48345668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87439126-G-T

48347155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87439652-A-T

http://identifiers.org/hco/16/GRCh38#48347756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87440209-C-A

48347756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87440209-C-T

48347780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87440234-G-A

48347780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87440234-G-T

48347858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87440297-T-A

48347858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87440297-T-C

48347947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87440376-T-C

48348329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87440761-T-G

48348373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87440795-T-C

48348400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87440829-T-A

48348400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87440829-T-C

48348410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87440836-A-T

48348417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87440843-T-C

48348837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87440950-T-C

48351534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87442829-G-T

48351536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87442831-T-C

48351536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87442831-T-G

48351546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87442841-T-C

48351546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87442841-T-G

48351564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87442859-T-C

48351564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87442859-T-G

48351568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87442863-T-A

48351622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87442919-G-A

48351622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87442919-G-T

http://identifiers.org/hco/16/GRCh38#48351634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87442931-A-C

48351634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87442931-A-G

http://identifiers.org/hco/16/GRCh38#48351641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87442938-A-C

48351864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443138-G-T

http://identifiers.org/hco/16/GRCh38#48351875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87443149-C-A

48351978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443239-A-T

48351990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443251-G-T

http://identifiers.org/hco/16/GRCh38#48351995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87443257-A-C

48352020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443280-G-A

48352069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443317-T-A

48352132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443351-A-G

48352136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443355-C-T

48352167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443390-G-A

48352167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443390-G-T

http://identifiers.org/hco/16/GRCh38#48352169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87443394-A-C

48352169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443394-A-G

48352221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443531-G-A

48352221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443531-G-C

48352752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443777-G-A

48352794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443819-G-A

48352794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443819-G-T

48352900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87443919-T-C

http://identifiers.org/hco/16/GRCh38#48353003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87444027-C-A

48353003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87444027-C-G

48353003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87444027-C-T

http://identifiers.org/hco/16/GRCh38#48356286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87446792-C-A

http://identifiers.org/hco/16/GRCh38#48356376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87446864-A-C

48356653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87447115-A-G

48357666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87448040-A-T

http://identifiers.org/hco/16/GRCh38#48357887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87448265-A-C

48360190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87450170-G-C

48360647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87450680-G-A

http://identifiers.org/hco/16/GRCh38#48360818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87450865-C-A

48360876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87450916-C-T

48361201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87451264-G-A

48361201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87451264-G-T

http://identifiers.org/hco/16/GRCh38#48361230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87451293-C-A

48361230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87451293-C-T

48361361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87451419-A-G

http://identifiers.org/hco/16/GRCh38#48361785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/8/GRCm39#87451839-C-A

48361785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87451839-C-G

48361785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87451839-C-T

48361943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87451997-A-G

http://identifiers.org/hco/16/GRCh38#48362000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87452054-A-C

48362000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87452054-A-G

48362030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87452084-A-G

http://identifiers.org/hco/16/GRCh38#48362042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87452096-C-A

48362042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87452096-C-G

48362042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87452096-C-T

48362049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87452103-G-A

48362051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87452105-A-G

48362092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87452146-C-G

48362106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87452160-G-T

48362202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87452256-C-T

48362233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87452287-G-A

48362420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87452474-A-T

http://identifiers.org/hco/16/GRCh38#48362507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87452569-A-C

48362507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87452569-A-G

48362517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87452579-T-C

http://identifiers.org/hco/16/GRCh38#48362596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#87452673-A-C

48362596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87452673-A-G

48362602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87452679-T-A

48362602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87452679-T-C

48362651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87452728-G-T

48362708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87452798-T-C

48362708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20598
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87452798-T-G