30378967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 5 prime UTR variant
orthologous variants: 76737804-G-A

30378967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 5 prime UTR variant
orthologous variants: 76737804-G-C

30378967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 5 prime UTR variant
orthologous variants: 76737804-G-T

30378994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense variant
orthologous variants: 76737777-G-A

30378994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense variant
orthologous variants: 76737777-G-C

30378994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense variant
orthologous variants: 76737777-G-T

http://identifiers.org/hco/17/GRCh38#30379063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: stop_gained, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#76737690-C-A

30379063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, undefined
orthologous variants: 76737690-C-T

30379211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: synonymous variant
orthologous variants: 76737545-C-G

30379211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: synonymous variant
orthologous variants: 76737545-C-T

30379338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense variant
orthologous variants: 76737436-G-C

30379338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense variant
orthologous variants: 76737436-G-T

http://identifiers.org/hco/17/GRCh38#30379743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#76737031-C-A

30379743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76737031-C-T

30379751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76737023-G-A

30379751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76737023-G-T

30379764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76737009-T-A

30379764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76737009-T-C

30379782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736990-T-C

http://identifiers.org/hco/17/GRCh38#30379853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76736914-C-A

30379853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736914-C-T

30379863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736904-G-A

30379863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736904-G-T

http://identifiers.org/hco/17/GRCh38#30379865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76736902-A-C

30379865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736902-A-G

30379865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736902-A-T

30379875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736892-G-A

30379875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736892-G-T

http://identifiers.org/hco/17/GRCh38#30380145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76736651-C-A

30380192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736576-T-A

30380192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736576-T-C

30380192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736576-T-G

30380229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76736543-A-G

30380275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76736514-A-G

30380278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76736511-G-A

30380278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76736511-G-T

30380303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76736488-G-A

30380303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76736488-G-T

http://identifiers.org/hco/17/GRCh38#30380429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76736369-A-C

30380493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76736324-T-G

30380543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76736268-G-A

http://identifiers.org/hco/17/GRCh38#30380552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76736242-C-A

30380554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76736240-T-C

http://identifiers.org/hco/17/GRCh38#30380656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76736118-C-A

30380656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736118-C-T

30380665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736108-A-G

http://identifiers.org/hco/17/GRCh38#30380720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76736062-C-A

http://identifiers.org/hco/17/GRCh38#30380721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76736061-C-A

30380721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736061-C-T

30381174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76735391-G-A

30381187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76735379-A-G

30382280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76734082-G-A

30382709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76733690-G-A

30383020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76733471-C-T

http://identifiers.org/hco/17/GRCh38#30383164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76733347-A-C

30383683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76732987-A-G

30383721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76732949-A-G

30384410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76732246-A-T

30384778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76731956-G-T

30384849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76731731-G-T

30384891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76731604-T-C

30384891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76731604-T-G

http://identifiers.org/hco/17/GRCh38#30384935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76731515-C-A

30384935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76731515-C-G

30384935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76731515-C-T

30385122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76731326-G-A

30385215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76731233-G-A

30385215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76731233-G-T

30385227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76731221-G-A

30385227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76731221-G-C

30385539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76730970-C-T

30385659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76730887-C-T

30386440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76730239-T-G

30389346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76727832-C-T

30389499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76727693-C-T

30389513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76727679-G-T

30390487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76727004-A-T

30390508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76726984-G-A

30390700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76726800-T-C

30390700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76726800-T-G

30390832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76726678-C-T

30391175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76726260-A-G

30391175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76726260-A-T

30392502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76718480-G-A

30392676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76718211-G-A

30394209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76717228-G-A

30394209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76717228-G-C

30394433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76717067-C-T

30394475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76717022-T-C

30394606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76716943-G-A

30395180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76715908-A-T

30395498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, undefined
orthologous variants: 76715593-G-A

30395649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76715420-G-A

30395688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76715382-G-T

http://identifiers.org/hco/17/GRCh38#30395752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#76715335-C-A

30395770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76715323-A-T

http://identifiers.org/hco/17/GRCh38#30396459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76714103-C-A

30396556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76714007-A-G

http://identifiers.org/hco/17/GRCh38#30398081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76713489-A-C

30399053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76712545-C-T

30399297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76712389-G-T

30399312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76712375-T-C

30399312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76712375-T-G

30399363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76712345-T-C

30399503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76712252-G-A

30403154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76710675-A-G

http://identifiers.org/hco/17/GRCh38#30403156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76710673-C-A

30403156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76710673-C-T

30403222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76710609-G-A

30403260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76710600-A-T

30403347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76710574-T-A

30404933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76709720-A-G

30405002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76709652-A-G

30406313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76708891-T-C

30406370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76708826-T-C

30406419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76708559-T-C

30406672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76708302-T-C

30406675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76708299-T-C

30406679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76708293-C-G

30420588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76706008-T-C

30420588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76706008-T-G

30420653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76705942-A-G

30420655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76705940-G-A

http://identifiers.org/hco/17/GRCh38#30420710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76705866-C-A

30420731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76705845-A-G

http://identifiers.org/hco/17/GRCh38#30420747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76705834-A-C

30420747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76705834-A-G

30420752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76705829-T-C

30420969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense variant
orthologous variants: 76705609-A-G

30420969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense variant
orthologous variants: 76705609-A-T

30421049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76705529-C-T

30421085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76705498-T-G

30421088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76705495-T-C

30421485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76704897-G-A

30421577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76704678-A-G

30421787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: stop gained
orthologous variants: 76704353-C-T

30422012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76704172-T-C

30422217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76703986-C-G

30422702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense variant
orthologous variants: 76703527-G-C

30422714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense variant
orthologous variants: 76703515-G-A

30423043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76703189-A-G

30423363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76702849-C-T

http://identifiers.org/hco/17/GRCh38#30423453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76702760-C-A

30423453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76702760-C-T

30423640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense variant
orthologous variants: 76702576-A-G

30423640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense variant
orthologous variants: 76702576-A-T

30424584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76701223-G-A

30424674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76701151-T-C

30425782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76699978-A-G

30425821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76699939-A-G

30425866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76699891-A-G

http://identifiers.org/hco/17/GRCh38#30427259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76699818-C-A

30427259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76699818-C-T

30427344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76699744-T-C

30427378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76699709-T-C

30427582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76699507-A-G

30427594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76699495-T-C

30427697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76699389-G-A

30427697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76699389-G-T

http://identifiers.org/hco/17/GRCh38#30427787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76699275-A-C

30427787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76699275-A-T

30431761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76696919-T-C

30431822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense variant
orthologous variants: 76696859-A-T

http://identifiers.org/hco/17/GRCh38#30431911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76696791-C-A

30431911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76696791-C-T

http://identifiers.org/hco/17/GRCh38#30431958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76696758-C-A

30431958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76696758-C-T

30432200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76696527-G-A

30433261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76694777-G-A

30433645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76694111-C-T

30438169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76693867-C-T

http://identifiers.org/hco/17/GRCh38#30438841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76693296-C-A

30438841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76693296-C-G

30438841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76693296-C-T

http://identifiers.org/hco/17/GRCh38#30438842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76693295-C-A

30438842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76693295-C-T

30438879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76693255-T-C

30439050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76693083-A-G

30439152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692987-A-T

30439171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692968-T-A

30439236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692908-T-C

30439251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692893-G-A

30439307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692842-T-G

http://identifiers.org/hco/17/GRCh38#30442358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76692556-A-C

30442358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76692556-A-G

http://identifiers.org/hco/17/GRCh38#30442397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76692517-C-A

30442412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76692502-G-A

30442472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692443-A-G

30442473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692442-T-A

30442473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692442-T-C

30442473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692442-T-G

30442482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692435-T-A

30442500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692417-T-G

30442530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692377-G-T

30442575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76692162-T-C

30442810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691958-T-C

30442890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691877-G-A

30443046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691764-A-G

30443046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691764-A-T

30443047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691763-T-A

30443075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691735-G-A

30443190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691593-C-T

30443540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76691035-A-T

30443651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76690932-G-T

30443661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76690922-A-T

30443676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76690907-G-A

30443676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76690907-G-T

http://identifiers.org/hco/17/GRCh38#30443690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76690894-C-A

30443690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76690894-C-G

30443690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76690894-C-T

30443697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76690887-T-C

30443862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76690722-G-A

30443988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690597-T-C

http://identifiers.org/hco/17/GRCh38#30444010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76690586-A-C

30444021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690575-T-C

30444089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690507-G-A

30444089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690507-G-C

30444089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690507-G-T

30444090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690506-A-G

30444090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690506-A-T

http://identifiers.org/hco/17/GRCh38#30444110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76690400-C-A

30444110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76690400-C-T

30444798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76689664-C-T

30445132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76689339-C-T

30445157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76689314-G-A

30445602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76688812-G-T

30445644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76688769-T-C

30445670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76688749-G-A

30445670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron variant
orthologous variants: 76688749-G-T

30445716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76688703-A-G

30445716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76688703-A-T

30445806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76688613-G-A

30445806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76688613-G-T

30445881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 76688538-G-T

30445953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76688472-T-C

30445965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76688460-T-C

30446049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76688381-T-C

30446049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76688381-T-G

30446059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76688371-G-T

http://identifiers.org/hco/17/GRCh38#30446073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76688357-C-A

30446085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76688345-T-C

30446116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76688310-G-A

30446116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76688310-G-T

30447410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76688238-A-G

30447436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76688212-G-T

30447506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76688144-C-G

30447513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76688137-A-G

30447962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76687661-G-T

30447965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76687658-C-T

30448516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76687262-A-T

30448518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76687260-A-G

30448540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76687238-T-A

30448614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76687163-A-G

30448782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76687012-G-A

30449407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76686814-A-T

30449521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76686490-T-G

30449883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76686131-T-C

30449925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76686088-G-A

30449990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76686019-C-T

30450500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76685852-T-G

30450999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76685698-G-A

30451179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76685519-A-G

30451606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76683797-A-G

30451610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76683793-A-T

30451651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76683754-G-A

30451651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76683754-G-C

30451828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76683578-T-C

30451898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76683511-G-A

30451898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76683511-G-T

30451938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76683471-G-T

30451941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76683468-T-A

30451941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76683468-T-C

30451950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76683459-G-A

30451950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76683459-G-C

30452013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76683396-T-C

30452331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76683021-T-G

30452394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76682971-C-T

http://identifiers.org/hco/17/GRCh38#30455285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76682868-C-A

30455419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76682739-G-A

30455461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76682697-G-A

30455507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76682651-G-A

http://identifiers.org/hco/17/GRCh38#30455597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76682559-C-A

30455607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76682549-T-C

30455611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76682545-A-G

30455659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76682500-C-T

30455660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76682499-C-T

30455740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76682419-T-A

http://identifiers.org/hco/17/GRCh38#30455759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76682400-A-C

30455759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76682400-A-G

30455936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76682244-T-C

30455958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76682222-T-G

30456216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76681955-T-C

30456366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76681804-T-C

30456384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76681791-T-C

30456425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76681753-G-A

30456953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76681548-G-T

30456954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76681547-G-A

30460007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76679119-C-T

30460237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76678898-A-G

30460274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76678857-C-T

30460278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76678853-T-C

30460966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76677395-C-T

30460967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76677394-G-A

30461059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76677320-G-A

30461059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76677320-G-C

30461059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76677320-G-T

30461063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76677316-C-G

30461158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76677248-G-T

30461329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76677061-A-G

http://identifiers.org/hco/17/GRCh38#30461417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76676973-A-C

30461417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76676973-A-G

30461726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76676327-A-G

30462027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 76675878-G-A

30462027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 76675878-G-T

http://identifiers.org/hco/17/GRCh38#30462101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76675809-A-C

30462101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76675809-A-T

30462112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76675798-T-A

http://identifiers.org/hco/17/GRCh38#30462144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76675766-A-C

30462144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76675766-A-G

30462230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76675678-G-A

30462492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76675189-T-C

30462590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76675096-T-A

30462590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76675096-T-C

http://identifiers.org/hco/17/GRCh38#30462613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76675074-C-A

30462613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76675074-C-T

30463281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76674969-A-G

30463743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76674534-G-A

30463743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76674534-G-T

http://identifiers.org/hco/17/GRCh38#30464562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76673256-C-A

30464562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76673256-C-G

30464579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76673243-G-A

30464579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76673243-G-T

30464695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 76673127-G-C

30464906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 76672918-G-T

30465248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76672558-G-T

30465260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76672545-C-G

http://identifiers.org/hco/17/GRCh38#30465295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76672510-C-A

30465538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76672265-G-T

30465834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76671983-T-C

30465880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76671937-G-A

30465880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76671937-G-T

http://identifiers.org/hco/17/GRCh38#30465925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76671897-C-A

30465925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76671897-C-T

30466181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76671636-A-G

30466386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76671451-G-T

30466673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76671164-G-T

30467110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76670735-G-A

30467338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76670513-G-A

30467366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76670486-G-T

30467384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76670471-A-G

30467512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76670362-T-C

http://identifiers.org/hco/17/GRCh38#30467539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76670334-C-A

30467539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76670334-C-T

30467580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76670295-T-A

30468049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76669832-G-A

30468089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76669792-A-G

30468405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76669519-C-T

30468420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76669505-G-T

30468469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76669461-C-T

30468585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76669346-A-G

30468856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76669077-C-G

30468983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76668943-G-T

30469020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76668898-T-G

30469040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76668877-A-G

http://identifiers.org/hco/17/GRCh38#30469082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76668836-C-A

30469162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76668756-G-T

30469348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76668599-A-G

30469481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76668478-A-G

30469658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76668307-T-C

http://identifiers.org/hco/17/GRCh38#30469668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76668297-C-A

30469722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76668247-T-C

http://identifiers.org/hco/17/GRCh38#30469791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#76668204-C-A

30469889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2301
most severe consequence: 3 prime UTR variant
orthologous variants: 76668132-T-G