53497384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77701729-A-G

http://identifiers.org/hco/6/GRCh38#53497801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77701362-C-A

53497970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77701163-G-T

53498251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77701027-T-C

53498294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700985-G-A

53498294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700985-G-C

53498294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700985-G-T

53498301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700978-A-G

http://identifiers.org/hco/6/GRCh38#53498425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77700856-C-A

53498425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700856-C-T

53498640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700646-G-T

53498657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700630-G-A

53498657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700630-G-T

53498682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700608-T-C

53498683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700607-A-G

53498683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700607-A-T

http://identifiers.org/hco/6/GRCh38#53498686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77700604-C-A

53498686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700604-C-G

53498724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700571-G-A

53498724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700571-G-T

53498894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77700393-G-T

53498895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77700392-A-G

53499213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77700114-T-A

53499269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77700061-A-T

53499287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77700043-C-T

53499330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77700009-G-A

53499517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77699896-G-A

53499588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77699860-A-G

53500017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77699497-A-G

53500183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77699318-C-G

53500183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77699318-C-T

53500185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77699316-T-C

53500210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77699293-G-T

53500215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77699288-G-A

53500215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77699288-G-C

53500316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77699194-G-A

53500329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77699181-C-T

53500400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77699105-G-C

53500422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77699086-A-G

53502188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77697689-A-G

53502517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77697461-G-T

53502668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77697281-G-A

53502719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77697218-A-G

http://identifiers.org/hco/6/GRCh38#53505260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77695692-C-A

53505264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77695688-T-A

53505264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77695688-T-C

53505307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77695644-A-G

53505370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77695594-C-T

53505378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77695586-A-G

http://identifiers.org/hco/6/GRCh38#53505386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77695578-C-A

53505386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77695578-C-T

http://identifiers.org/hco/6/GRCh38#53505503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77695461-A-C

53505503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77695461-A-G

53505503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77695461-A-T

53505526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77695441-G-A

53505526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77695441-G-T

http://identifiers.org/hco/6/GRCh38#53505541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77695426-A-C

53505542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77695425-C-T

http://identifiers.org/hco/6/GRCh38#53505569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77695404-C-A

53505569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77695404-C-T

53505615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77695360-T-C

53505668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77695307-G-T

53505671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77695304-T-C

53505685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77695291-G-T

53506081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77694895-G-C

53506081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77694895-G-T

http://identifiers.org/hco/6/GRCh38#53506133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77694848-C-A

http://identifiers.org/hco/6/GRCh38#53506712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77694795-C-A

http://identifiers.org/hco/6/GRCh38#53506720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77694787-C-A

53506720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77694787-C-T

53507039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77694544-T-A

53507039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77694544-T-C

http://identifiers.org/hco/6/GRCh38#53507064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77694523-A-C

53507466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77694142-G-C

53507466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77694142-G-T

53507632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77693977-A-T

53508154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77693624-A-G

53508167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77693614-A-G

53508248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77693520-G-A

53508374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77693419-G-A

53508399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77693396-G-C

53508632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 77693109-G-T

53508771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77692979-A-G

53508816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77692947-C-T

http://identifiers.org/hco/6/GRCh38#53508819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77692944-A-C

53508819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77692944-A-T

53509094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77692748-T-A

53509094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77692748-T-C

53509144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77692720-A-G

53509167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77692697-T-C

53509311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77692556-G-T

http://identifiers.org/hco/6/GRCh38#53509325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77692542-A-C

53509394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77692485-T-A

53509394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77692485-T-G

53509467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77692425-T-C

53509510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77692399-A-G

53509522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77692387-A-G

53510020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77692216-A-G

53510020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77692216-A-T

http://identifiers.org/hco/6/GRCh38#53510101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77692143-A-C

53510146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77692102-T-C

53510163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77692092-G-A

53510196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77692050-A-G

53510277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77691977-G-T

53510755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77691551-C-T

http://identifiers.org/hco/6/GRCh38#53510965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77691280-C-A

53510965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77691280-C-T

53511397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77690772-T-C

http://identifiers.org/hco/6/GRCh38#53511589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77690568-A-C

53511653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77690498-C-T

53511756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77690376-T-A

53511756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77690376-T-C

53511756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77690376-T-G

53511822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77690329-T-C

53511857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77690302-T-C

53511908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77690242-G-C

53511908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77690242-G-T

53512630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77689899-G-A

53512693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77689841-A-G

http://identifiers.org/hco/6/GRCh38#53512734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77689804-C-A

53512774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77689766-G-A

53512876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77689693-C-T

http://identifiers.org/hco/6/GRCh38#53512963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77689606-C-A

53512963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77689606-C-G

53513557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77689259-C-T

53513563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77689253-G-T

53513585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77689236-G-A

53513588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77689233-G-A

53513588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77689233-G-T

53513684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77689139-G-T

53513686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77689137-G-A

53513766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77689052-G-A

53513766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77689052-G-T

53513883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 77688903-G-A

53513883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 77688903-G-T

http://identifiers.org/hco/6/GRCh38#53514018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77688801-C-A

http://identifiers.org/hco/6/GRCh38#53514058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77688760-A-C

53514058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77688760-A-G

53514172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77688678-C-T

53514180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77688671-C-T

53514289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77688562-T-C

53514298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77688553-G-A

53514298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77688553-G-C

53514426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77688430-T-C

53514516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77688345-C-T

http://identifiers.org/hco/6/GRCh38#53514535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77688331-A-C

53514535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77688331-A-G

53514573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77688298-A-T

53514605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77688266-T-C

http://identifiers.org/hco/6/GRCh38#53514609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77688262-C-A

53514609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77688262-C-G

53514610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77688261-T-A

53514610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77688261-T-C

53514639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77688243-G-A

53514639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77688243-G-T

53514898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77688030-C-T

53514977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77687982-G-A

http://identifiers.org/hco/6/GRCh38#53514989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77687970-C-A

53515005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77687955-A-G

53515037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77687913-C-T

53515195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77687783-G-A

53515596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77687272-G-C

53515793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77687126-A-G

53515820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77687097-A-G

53515842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77687079-A-G

53515848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77687073-T-A

53516285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77686743-T-A

53516288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77686740-C-G

53516288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77686740-C-T

53516302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77686725-G-A

53516302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77686725-G-T

53516337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77686689-G-A

http://identifiers.org/hco/6/GRCh38#53516482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77686563-C-A

53516647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77686435-C-T

53516835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77686260-A-G

53517474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77686030-A-T

http://identifiers.org/hco/6/GRCh38#53517520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77685993-C-A

53517539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77685974-T-C

53518657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77685512-C-T

53518698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77685476-T-C

http://identifiers.org/hco/6/GRCh38#53519043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77685156-C-A

53519081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77685119-C-T

53519412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77684854-T-C

53519418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77684839-C-T

http://identifiers.org/hco/6/GRCh38#53519431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77684817-A-C

53519861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77684610-C-T

53520013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77684473-C-T

53520014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77684472-C-T

http://identifiers.org/hco/6/GRCh38#53520142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77684371-A-C

53520142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77684371-A-G

53520673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683692-G-A

53520673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683692-G-T

53520678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683687-G-A

53520678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683687-G-C

53520678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683687-G-T

53520685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683680-G-A

53520685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683680-G-T

53520838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77683528-T-C

53520865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77683501-A-G

53520952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77683414-G-C

53521046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683322-G-T

53521057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683311-T-A

53521057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683311-T-C

53521061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683307-T-C

53521125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683255-C-T

http://identifiers.org/hco/6/GRCh38#53521129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77683252-A-C

53521129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683252-A-G

http://identifiers.org/hco/6/GRCh38#53521622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77683074-A-C

53521626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683070-G-A

53521649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77683047-G-A

53521740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77682963-G-A

53521776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77682934-A-G

53521980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77682822-A-T

http://identifiers.org/hco/6/GRCh38#53522299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77682575-C-A

53522390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77682501-A-G

53522502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77682384-T-C

53523016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77681749-T-C

53523158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77681611-C-G

53523276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77681482-A-G

53523298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77681458-G-T

53523421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77681332-A-G

53523502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77681187-T-C

53523596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77681093-T-C

53523596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77681093-T-G

53523898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77680605-T-C

53523907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77680596-G-A

http://identifiers.org/hco/6/GRCh38#53523936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77680567-C-A

53523936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77680567-C-T

53523978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77680534-C-T

53523980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77680532-G-T

53524003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77680510-C-T

53524135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77680370-G-A

53525021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77679648-G-A

53525359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77679384-G-A

53525722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77678304-T-C

53525740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77678285-A-G

53526234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77677844-C-G

http://identifiers.org/hco/6/GRCh38#53526271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77677808-C-A

53526271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77677808-C-T

53526939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77677468-C-T

53527037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77677355-A-G

53527281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77677189-C-T

http://identifiers.org/hco/6/GRCh38#53527346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77677134-C-A

53527714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77676762-G-T

53527826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77676662-T-A

53528625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77675455-T-C

53528658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77675422-T-C

53528725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77675346-T-C

53528729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77675342-G-C

53528873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77675220-C-T

53528895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77675198-A-T

http://identifiers.org/hco/6/GRCh38#53529097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77675084-C-A

53529450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77674603-T-C

http://identifiers.org/hco/6/GRCh38#53529625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77674494-C-A

53529694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77674425-C-G

53529846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77674296-T-C

53530184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77674065-C-T

53530675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77673660-G-A

53530991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77673424-G-A

53531158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77673277-T-A

53532402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77672488-A-G

53532642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77671785-A-G

53532846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77671596-T-C

53532986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77671474-C-T

53537416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77668257-T-C

http://identifiers.org/hco/6/GRCh38#53539284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77665470-A-C

53539310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77665444-A-G

53539581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77665170-T-A

53539581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77665170-T-C

53539633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77665109-T-C

53539805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77664809-C-T

53541236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77664671-A-G

53541285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77664628-G-T

53541307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77664609-G-A

53541307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77664609-G-C

53541352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77664565-G-A

53541353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77664564-T-C

53541905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77664083-T-C

53542165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77663907-A-T

53542365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77663724-G-A

53542414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77663671-T-A

53542414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77663671-T-C

53542434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77663647-C-T

53542495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77663581-G-A

53542496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77663580-G-A

53542566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77663520-T-A

53542566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77663520-T-G

53542567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77663519-G-A

53542642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77663461-G-A

53543139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77663296-C-T

http://identifiers.org/hco/6/GRCh38#53543349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77663112-C-A

53543421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77663045-G-C

53543468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77662996-T-C

53543605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77662871-T-G

53543749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77662752-T-C

53543816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77662702-T-C

53543820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77662698-T-C

http://identifiers.org/hco/6/GRCh38#53543881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77662659-A-C

53543933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77662609-C-T

53544235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77662354-G-A

http://identifiers.org/hco/6/GRCh38#53544380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77662296-C-A

http://identifiers.org/hco/6/GRCh38#53544381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77662295-C-A

53544381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77662295-C-G

53544381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77662295-C-T

53544384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77662292-G-A

53544512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 77662223-A-G

53544620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 77662115-G-A

53544620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 77662115-G-C

53544620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 77662115-G-T

http://identifiers.org/hco/6/GRCh38#53544996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#77661899-C-A

53544996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 77661899-C-T

53545122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: 77661791-G-A

53545122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: 77661791-G-T

53545186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77661716-A-G

53545221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77661682-T-A

53545693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77661031-T-G

53545729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77660993-G-A

53546057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77660685-C-T

53546199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77660403-T-C

53546316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77660302-T-C

53546521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77660092-G-A

53547013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77659248-C-T

53547038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77659242-C-T

http://identifiers.org/hco/6/GRCh38#53547490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77658594-A-C

53547766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77658380-T-G

53547787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77658367-G-C

http://identifiers.org/hco/6/GRCh38#53547943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#77658254-C-A

53547943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: 77658254-C-T

53547982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: 77658238-G-A

53547982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: 77658238-G-C

53547982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: 77658238-G-T

http://identifiers.org/hco/6/GRCh38#53547997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#77658221-C-A

53547997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: 77658221-C-T

http://identifiers.org/hco/6/GRCh38#53548003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#77658215-C-A

53548003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: 77658215-C-T

http://identifiers.org/hco/6/GRCh38#53548030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#77658184-C-A

53548030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: 77658184-C-T

http://identifiers.org/hco/6/GRCh38#53548031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#77658183-C-A

53548031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: 77658183-C-T

http://identifiers.org/hco/6/GRCh38#53548043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#77658172-C-A

53548043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: 77658172-C-T

53548085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 77658143-G-A

53548290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77658002-T-A

53548290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77658002-T-C

53548303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77657989-T-C

53548353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: 77657963-G-A

53548353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: 77657963-G-T

53548359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, undefined
orthologous variants: 77657957-A-G

53548599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77657787-G-C

53548657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77657727-C-G

53549179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77657172-G-A

53549184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77657167-G-A

53549184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77657167-G-C

53549853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77656540-C-T

53550023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron variant
orthologous variants: 77656366-T-C

53564474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77654155-A-G

53564545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77654105-G-T

53564980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77653566-G-T

53565009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77653538-T-A

http://identifiers.org/hco/6/GRCh38#53565044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77653504-A-C

53565045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77653503-C-T

53565057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77653478-T-C

53565237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77653309-T-C

53565238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77653308-A-T

53565400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77653154-C-T

53565454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77653100-G-C

53565492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77653089-G-A

53565516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77653065-T-C

http://identifiers.org/hco/6/GRCh38#53565551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77653030-C-A

53565615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77652958-T-C

53565774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77652720-A-G

53566462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77652146-T-G

http://identifiers.org/hco/6/GRCh38#53566544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77652107-A-C

53566621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77652048-C-T

53566772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77651967-C-T

53567109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77651692-T-A

53567807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77650720-G-A

53567842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77650686-A-T

53567939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77650589-G-A

53568025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77650504-T-C

53568098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77650452-G-C

53568690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77649944-A-G

53568980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77649586-C-T

53569214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77649370-T-C

53569276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77649306-A-G

53569479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 77649024-C-T

http://identifiers.org/hco/6/GRCh38#53569482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77649021-C-A

53569482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77649021-C-T

http://identifiers.org/hco/6/GRCh38#53569483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77649020-C-A

53569503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77649004-T-C

http://identifiers.org/hco/6/GRCh38#53569510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77648997-C-A

53569510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77648997-C-T

53569516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77648987-T-A

53571180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77648672-G-C

53571457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77648420-A-G

53583207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77647102-G-T

53583239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77647074-G-T

53584416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77634293-G-A

53584420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77634289-T-C

53584539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77634166-T-G

53584540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77634165-T-G

53587309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77633066-C-T

http://identifiers.org/hco/6/GRCh38#53587372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77632908-C-A

53587372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77632908-C-T

53587519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77632766-G-C

53587872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77632418-C-G

53600947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77624897-G-C

53601005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77624841-T-C

53601175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77624700-T-C

53601175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77624700-T-G

53601182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77624693-C-T

53601186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77624689-T-G

53601237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77624636-T-C

53601592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77624603-C-T

53601671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77624524-A-G

53601672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77624523-A-G

53601968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77623783-T-G

53601979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77623772-T-C

53601991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77623760-G-T

53601998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77623753-G-A

53601998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77623753-G-T

53602583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77622881-T-C

53603506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77622321-A-G

53603546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77622289-T-C

53603675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77621534-T-G

53603716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77621500-G-T

53603925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77621344-G-A

53604021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77621233-T-G

53604036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77621218-A-G

53604099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77621168-A-G

53604711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77620900-A-T

53604759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77620863-T-C

53604906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77620732-G-A

http://identifiers.org/hco/6/GRCh38#53604939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77620701-C-A

53605021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77620633-G-T

53609254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77619916-G-A

http://identifiers.org/hco/6/GRCh38#53609357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77619817-C-A

53610814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77619254-A-G

53610907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77619176-T-A

53610907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77619176-T-C

53610921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77619161-T-G

53611197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618929-C-T

53611396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618742-T-C

53611396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618742-T-G

53611404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618734-A-G

53611578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618561-G-C

53611589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618551-T-C

53611839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618253-T-C

53611931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77618012-G-C

53611965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77617974-T-C

53612892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77617081-A-G

http://identifiers.org/hco/6/GRCh38#53612945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77617029-A-C

53613018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77616894-G-A

53613347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77616585-C-T

53613495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77616425-G-A

53613776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77616163-T-C

53615521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77611778-A-G

53615555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77611748-T-A

53615555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4311
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77611748-T-C