53089671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415532-C-G

53089685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415518-A-G

53089720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415499-G-C

53089720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415499-G-T

53089752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415467-G-A

53089752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415467-G-T

53089753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415466-C-T

http://identifiers.org/hco/3/GRCh38#53089806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30415416-C-A

53089806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415416-C-T

53089843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415375-T-C

53089844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415374-T-C

53089955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415281-A-G

53089972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415264-A-T

53089973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415263-G-A

53089973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415263-G-T

http://identifiers.org/hco/3/GRCh38#53089974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30415262-C-A

53089974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415262-C-T

53089975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415261-A-G

http://identifiers.org/hco/3/GRCh38#53089981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30415255-A-C

53089999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415237-T-C

53090096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415151-A-G

53090112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415135-T-C

http://identifiers.org/hco/3/GRCh38#53090151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30415101-C-A

53090151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415101-C-T

53090204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415047-T-A

53090204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415047-T-C

http://identifiers.org/hco/3/GRCh38#53090208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30415043-C-A

53090208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30415043-C-T

53090257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30414993-G-A

53090257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30414993-G-T

53090273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30414977-G-T

53090294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30414956-C-T

53090312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30414938-C-T

53090319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30414931-G-A

http://identifiers.org/hco/3/GRCh38#53090349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30414905-C-A

53090431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30414823-G-T

53090485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30414770-G-T

53090632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30414113-T-G

53090755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30413987-G-T

http://identifiers.org/hco/3/GRCh38#53090806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30413933-C-A

53090806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30413933-C-T

53090867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30413873-G-T

53090875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30413865-T-C

53090887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30413853-A-G

53090887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30413853-A-T

53090927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30413814-T-C

53091212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30413540-T-G

53091276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30413485-G-A

53091276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30413485-G-T

http://identifiers.org/hco/3/GRCh38#53091417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30412965-C-A

53091451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30412931-G-C

53091451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30412931-G-T

53091506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30412878-G-T

53091722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30412714-G-A

53091727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30412709-T-C

53091771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30412682-T-G

http://identifiers.org/hco/3/GRCh38#53091854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30412613-A-C

http://identifiers.org/hco/3/GRCh38#53091859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30412608-C-A

53091859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30412608-C-T

53091891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30412576-G-T

53092110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30412336-T-C

53092115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30412331-C-T

http://identifiers.org/hco/3/GRCh38#53092131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30412226-C-A

53092131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30412226-C-T

53092146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30412209-G-A

53092146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30412209-G-T

53092280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30412021-G-A

53092280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30412021-G-T

53092320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30411959-A-G

http://identifiers.org/hco/3/GRCh38#53092322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30411957-C-A

53092322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30411957-C-T

53092428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 30411850-G-C

53092429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 30411849-G-A

53092673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30411624-G-A

53092673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30411624-G-T

53092828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30411241-T-A

53092909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30411012-A-G

53093245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410713-C-T

53098200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30406681-C-T

53098328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30406556-T-C

53098432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30406479-C-T

53098499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30406412-G-A

53098526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30406364-G-C

53098527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30406363-G-A

53098853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30406044-A-G

http://identifiers.org/hco/3/GRCh38#53099257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30404933-C-A

53099263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404928-G-A

53099263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404928-G-T

53099405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30404787-G-A

53099541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404663-A-T

53099565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404639-G-A

53100227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404299-A-G

53100300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404224-C-T

53103071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30402146-G-T

53103169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30402065-T-A

53103169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30402065-T-C

http://identifiers.org/hco/3/GRCh38#53103364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30401881-C-A

53103364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30401881-C-T

http://identifiers.org/hco/3/GRCh38#53103424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30401814-C-A

http://identifiers.org/hco/3/GRCh38#53103443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30401795-A-C

53103530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30401709-G-T

53103630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30401613-T-C

http://identifiers.org/hco/3/GRCh38#53103670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30401575-A-C

http://identifiers.org/hco/3/GRCh38#53103673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30401572-C-A

53103673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30401572-C-T

53103697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30401548-A-G

http://identifiers.org/hco/3/GRCh38#53103702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30401543-C-A

53103702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30401543-C-T

53103717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30401531-A-G

53103717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30401531-A-T

53103746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30401503-T-C

53103756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30401493-G-A

53103757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30401492-G-T

53103916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30401367-G-A

53104084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30401199-A-G

http://identifiers.org/hco/3/GRCh38#53104150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30401132-C-A

53104150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30401132-C-G

53104300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30401022-G-A

53104506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30400897-G-C

53105405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30400009-C-T

53105433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30399986-A-G

53105526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30399893-C-T

53105536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30399885-G-A

53105589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30399837-G-A

53105589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30399837-G-C

53105698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30399747-C-T

53106495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30399068-G-A

53106629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30398934-C-G

53106665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30398911-G-A

53106874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30398800-A-G

53106902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30398774-T-A

53106913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30398758-T-C

53107373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30398195-G-A

53107395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30398173-C-T

53107761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30398116-T-C

53109346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30397154-C-T

53109381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30397120-T-C

53109450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30397058-C-T

53111718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30396313-T-A

53111718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30396313-T-C

53111756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30396277-C-G

53111756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30396277-C-T

53111767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30396274-G-T

53111816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30396221-G-T

http://identifiers.org/hco/3/GRCh38#53111876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30396157-A-C

53111982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30396069-G-T

53112059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30396002-G-A

53112059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30396002-G-C

53112059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30396002-G-T

53113754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30394404-A-G

53113837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30394344-G-A

53113837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30394344-G-C

53114007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30394190-G-A

53114036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30394162-G-C

53114168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30394045-C-T

53114263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30393774-C-T

http://identifiers.org/hco/3/GRCh38#53114707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30393398-A-C

53114772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30393331-A-G

53114777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30393326-G-A

53114782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30393321-G-A

53114849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30393263-T-G

53115624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30391878-A-G

53115808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30391708-G-A

53116172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30391408-T-C

53116222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30391374-A-G

53117305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30390693-G-C

53117376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30390572-G-A

http://identifiers.org/hco/3/GRCh38#53117401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30390485-A-C

53117401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30390485-A-G

53117494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30390392-G-A

53117581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30390360-C-T

53118478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30389915-T-C

53118803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30389622-C-G

53119771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30388867-G-A

53119771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30388867-G-T

53119840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30388799-G-A

53119840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30388799-G-T

http://identifiers.org/hco/3/GRCh38#53120085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30388556-C-A

http://identifiers.org/hco/3/GRCh38#53120148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30388500-C-A

53120148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30388500-C-T

53121249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30385546-G-A

http://identifiers.org/hco/3/GRCh38#53121317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30385478-A-C

53121604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30385211-T-C

53121777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30385056-T-A

53121777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30385056-T-C

53121821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30385014-T-C

53121852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30384991-A-G

53121887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30384956-T-A

53121917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30384928-C-T

53122347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30383439-C-T

53122605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30383182-A-G

53122918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30382916-T-C

53122974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30382858-C-T

53123000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30382832-C-T

53123215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30382658-T-C

http://identifiers.org/hco/3/GRCh38#53123576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30382397-C-A

53123576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30382397-C-T

53123749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 30382243-G-A

53123796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30382196-G-A

53123796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30382196-G-C

53123796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30382196-G-T

53124144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30381653-A-G

53124210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30381587-C-T

53124438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30381357-T-C

53125107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30381131-A-G

53125444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380802-C-G

53125444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380802-C-T

53125502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380741-G-C

53125597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380644-G-C

http://identifiers.org/hco/3/GRCh38#53125774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30380480-C-A

53125789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380466-T-C

53125811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380444-T-C

53125870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380388-A-G

53126009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380258-G-A

53126025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380246-T-A

53126064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380210-C-T

http://identifiers.org/hco/3/GRCh38#53126066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30380208-A-C

53126066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380208-A-G

53126092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380182-T-A

53126378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379865-T-A

53126378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379865-T-C

53126419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379764-T-C

53126419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379764-T-G

53126626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379585-C-T

53127930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30378828-T-A

53128035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30378649-C-T

53129463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30377148-C-G

http://identifiers.org/hco/3/GRCh38#53130187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30376533-C-A

53130187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30376533-C-T

53130223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30376504-G-A

53130223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30376504-G-T

53130227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30376500-G-A

53130282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30376487-G-A

53130282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30376487-G-T

53130307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30376462-T-C

53130325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30376444-G-A

53130325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30376444-G-C

53130325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30376444-G-T

53130449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30220
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 30376321-T-G