64203697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336090-T-C

64203700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336093-G-C

64203700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336093-G-T

64203706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336099-A-G

64203721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336112-T-A

64203721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336112-T-C

http://identifiers.org/hco/1/GRCh38#64203736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100336127-A-C

64203736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336127-A-G

64203736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336127-A-T

http://identifiers.org/hco/1/GRCh38#64203746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100336137-C-A

64203746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336137-C-G

64203746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336137-C-T

64203763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336153-G-T

http://identifiers.org/hco/1/GRCh38#64203786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100336170-A-C

http://identifiers.org/hco/1/GRCh38#64203807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100336180-C-A

64203807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336180-C-G

64203807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336180-C-T

64203809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336182-G-A

64203809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336182-G-T

64203821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336193-G-A

64203840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336212-G-T

64203973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336318-G-A

64203973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336318-G-T

64203988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336333-A-G

64204026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100336364-A-G

64204151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100336479-T-G

64204666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100337167-A-G

64204674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100337175-T-C

64204734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100337235-G-A

64204966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100337473-G-A

64205461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100338314-A-G

64205511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100338577-T-G

64205539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100338653-T-C

http://identifiers.org/hco/1/GRCh38#64206085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100339174-A-C

64206227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100339303-T-C

64206318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100339395-A-T

64206532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100339556-A-G

64206543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100339567-T-C

http://identifiers.org/hco/1/GRCh38#64206629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100339647-C-A

64206629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100339647-C-T

64206759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100339974-T-C

64206789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100340004-T-A

64206789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100340004-T-C

http://identifiers.org/hco/1/GRCh38#64206807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100340022-C-A

64206821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100340036-T-C

http://identifiers.org/hco/1/GRCh38#64206859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100340074-A-C

64206859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100340074-A-G

64206918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100340167-A-G

64206923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100340172-T-A

64206923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100340172-T-C

64206952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100340198-A-G

http://identifiers.org/hco/1/GRCh38#64206968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100340214-C-A

64207293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100340491-G-C

64207300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100340498-G-A

64207656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100340954-T-A

64207656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100340954-T-C

64207689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100340981-T-A

64207689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100340981-T-C

64207791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100341070-A-G

64208301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100341543-G-A

64209037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100342309-T-C

64209058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100342329-C-T

64209082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100342355-T-C

64209111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100342381-A-G

64210618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100343740-G-A

64210618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100343740-G-C

64210618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100343740-G-T

64210653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100343773-T-A

64210656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100343776-T-C

64210656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100343776-T-G

64210758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100343860-T-C

64210848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100343996-G-T

64210909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100344167-T-C

64210935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100344193-G-C

64210946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100344204-T-C

64210947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100344205-T-C

64210947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100344205-T-G

64210979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100344238-G-A

http://identifiers.org/hco/1/GRCh38#64210987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100344247-C-A

64210987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100344247-C-T

64211114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100344360-G-T

64211374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100344597-T-C

64214720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100347216-A-G

64214736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100347229-A-G

64214745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100347238-T-C

64214745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100347238-T-G

64214746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100347239-A-T

http://identifiers.org/hco/1/GRCh38#64215328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100347505-A-C

64215337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100347513-T-G

64215349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100347524-T-C

64215352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100347527-G-A

64215352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100347527-G-T

64215382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100347557-G-T

64215420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100347595-G-T

64215440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100347961-A-G

64215492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100348022-G-T

http://identifiers.org/hco/1/GRCh38#64215597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100348106-C-A

64215870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100348333-T-C

64216046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100348486-A-G

64216332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100352151-A-G

64216380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100352199-T-C

64216546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100352343-C-T

64216549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100352346-G-T

64216966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100352731-C-G

64217442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100353998-T-C

64217457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100354013-C-T

64217873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100354936-A-T

64218187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100355266-C-T

64218295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100355363-G-C

64218302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100355370-G-A

64218487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100355542-A-G

64220134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100371272-A-G

64220235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100371335-G-A

64220463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100371492-G-A

64220712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100371734-G-A

64220712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100371734-G-C

64220712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100371734-G-T

http://identifiers.org/hco/1/GRCh38#64220745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100371766-A-C

64220745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100371766-A-G

64220748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100371769-T-A

64220748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100371769-T-G

http://identifiers.org/hco/1/GRCh38#64220821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100371841-C-A

64220821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100371841-C-G

64220821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100371841-C-T

64220878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100371897-G-A

64220879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100371898-T-C

http://identifiers.org/hco/1/GRCh38#64220982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100372003-C-A

64221005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100372032-T-A

http://identifiers.org/hco/1/GRCh38#64222116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100373141-A-C

64222315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100373354-A-G

64222482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100373508-G-A

64222625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100373649-G-A

64223028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100374515-C-T

64223077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100374639-T-G

64223691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100375290-T-G

http://identifiers.org/hco/1/GRCh38#64228279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100377613-C-A

64228474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100377787-A-G

64228497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100377810-G-A

64228552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100377866-G-C

http://identifiers.org/hco/1/GRCh38#64229337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100378033-A-C

64229337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100378033-A-G

http://identifiers.org/hco/1/GRCh38#64229972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100378593-A-C

64229981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100378602-G-A

64229981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100378602-G-T

64230131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100378742-T-C

64230169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100378815-C-T

http://identifiers.org/hco/1/GRCh38#64230319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100379046-C-A

64230326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100379053-C-G

64230326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100379053-C-T

64230884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100379588-A-G

64230884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100379588-A-T

64230947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100379647-G-A

64231038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100379737-G-T

64231113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100379801-G-A

64231133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100379821-A-G

64231422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100380104-A-G

64231528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100380226-A-G

64231795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100380511-C-T

64232253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100380945-C-T

64232256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100380948-T-C

64232256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100380948-T-G

64232265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100380957-T-C

64232327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381015-A-G

64232327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381015-A-T

http://identifiers.org/hco/1/GRCh38#64232495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100381365-A-C

64232532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381427-C-T

64232533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381428-A-G

64232689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381583-T-A

http://identifiers.org/hco/1/GRCh38#64232703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100381605-C-A

64232703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381605-C-T

64232747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381653-T-A

64232747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381653-T-C

http://identifiers.org/hco/1/GRCh38#64232786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100381697-C-A

64232786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100381697-C-G

64234096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100382381-C-T

64234219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100382485-G-A

64234219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100382485-G-C

64234336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100382598-C-T

64234365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100382627-T-C

64234584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100382835-A-G

64234622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100382873-T-G

http://identifiers.org/hco/1/GRCh38#64234954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100383190-A-C

64235046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100383266-A-T

64235262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100383485-C-G

64235438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100383660-A-G

64235601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100383827-C-G

64235777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100384003-A-G

64235835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100384065-T-C

64235922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100384154-A-G

64235936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100384169-G-A

64236065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100384301-G-A

64236065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100384301-G-C

http://identifiers.org/hco/1/GRCh38#64236404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100384594-C-A

64236408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100384598-A-G

64236720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100384915-T-A

64237141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100385306-A-G

64237170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100385334-T-C

http://identifiers.org/hco/1/GRCh38#64237268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100385440-C-A

http://identifiers.org/hco/1/GRCh38#64237271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100385443-C-A

64237271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100385443-C-T

64237386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100386316-C-G

64237472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100386395-C-T

64237519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100386442-C-T

64237761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100386683-G-A

64237998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100386898-A-G

64238137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100387030-G-T

64238161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100387053-T-C

64238689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100387363-T-C

64240106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100387616-A-T

64240175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100387681-G-A

64240179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100387686-A-G

64240183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100387690-A-G

64240362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100388092-T-A

64240411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100388153-T-C

64240569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100388310-T-C

64240931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100388576-C-T

64240977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100388625-G-T

64241429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100389089-C-T

64241553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100389212-A-G

64241553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100389212-A-T

64241565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100389224-T-A

64241565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100389224-T-G

http://identifiers.org/hco/1/GRCh38#64241768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100389414-A-C

64241768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100389414-A-G

64241819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100389468-G-C

http://identifiers.org/hco/1/GRCh38#64241849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100389493-C-A

64241849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100389493-C-T

64241859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100389503-G-A

64241859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100389503-G-T

64241884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100389526-G-T

http://identifiers.org/hco/1/GRCh38#64242628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100390575-C-A

64242797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100390679-C-T

64242820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100390702-T-C

http://identifiers.org/hco/1/GRCh38#64242851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100390733-C-A

64242979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100390839-C-T

64243013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100390874-C-G

64243013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100390874-C-T

http://identifiers.org/hco/1/GRCh38#64243046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100390907-A-C

64243046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100390907-A-G

64243376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100391237-T-C

64243537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100391647-G-T

64243560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100391674-T-A

64243568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100391682-C-T

64243630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100391839-T-C

64243765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100391973-A-G

http://identifiers.org/hco/1/GRCh38#64243811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100392025-A-C

64243909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100392096-G-T

64243947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100392134-G-A

64244012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100392197-T-C

http://identifiers.org/hco/1/GRCh38#64244092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100392279-C-A

64244142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100392327-T-C

64244217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100392387-A-T

64244594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100392685-C-T

64244638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100392721-G-T

64244688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100392768-C-T

64244735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100392813-C-T

64244750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100392830-G-A

64244771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100392845-G-A

64244799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100392874-G-A

64244854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100392913-A-G

64244970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100393013-G-A

64244970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100393013-G-T

64245206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100393243-T-G

64245553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100394386-T-C

64245727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100394540-C-G

64245751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100394565-C-T

64245832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100394607-C-T

64245888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100394654-A-G

64245894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100394660-G-A

http://identifiers.org/hco/1/GRCh38#64245911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100394677-C-A

64246034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100394763-A-G

64246166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100394889-C-T

64246193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100394915-T-C

64246448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100395215-A-G

64248216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100396999-C-T

64248225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100397008-T-G

64248424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100397150-A-G

http://identifiers.org/hco/1/GRCh38#64248463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100397188-A-C

64248469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100397194-C-T

64248477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100397202-G-A

64260480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100404242-A-T

64260526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100404304-T-C

64260552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100404326-T-A

64260569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100404339-A-G

64260624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 100404393-G-A

64260624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100404393-G-T

http://identifiers.org/hco/1/GRCh38#64260663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100404438-A-C

64260717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100404494-T-C

64261733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100405493-A-G

64261740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100405500-C-T

64261978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100405734-G-T

64266930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100406850-T-C

64266930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100406850-T-G

http://identifiers.org/hco/1/GRCh38#64266988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100406883-C-A

64266988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100406883-C-G

64267082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100406965-A-T

64267308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100407290-T-A

64267308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100407290-T-G