59372803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70114699-T-C

59372803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70114699-T-G

http://identifiers.org/hco/15/GRCh38#59372849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70114653-C-A

59372849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70114653-C-G

59372849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70114653-C-T

59372861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70114639-G-A

59372861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70114639-G-T

http://identifiers.org/hco/15/GRCh38#59372863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70114637-C-A

59372863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70114637-C-G

59373064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70114437-G-A

59373064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70114437-G-T

http://identifiers.org/hco/15/GRCh38#59373065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70114436-C-A

59373148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70114352-A-G

59373150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70114350-A-G

59373229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70114272-T-G

59373234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70114267-G-A

59376950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70109503-A-T

59377058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70109388-A-G

59378128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, undefined
orthologous variants: 70108809-G-A

59378142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, undefined
orthologous variants: 70108795-A-T

59378231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70108706-C-G

http://identifiers.org/hco/15/GRCh38#59378241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70108695-C-A

59378330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70108241-A-T

59378342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70108229-A-G

59380918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70106415-C-T

59380923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70106410-T-G

59380924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70106409-C-T

59381021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70106308-A-G

59382007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70104024-C-T

59382022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70104009-G-C

59382106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70103925-G-A

59382176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70103862-C-G

59382176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70103862-C-T

59382240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70103839-T-C

59382255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70103824-C-G

59382279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70103800-A-G

59388813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70097531-A-G

59388914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70097423-A-G

59388915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70097422-C-T

59388921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70097416-C-G

59389005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70097371-A-T

59389838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70097014-G-T

59389921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70096931-G-A

59389921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70096931-G-T

59389953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70096901-C-T

59393280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70093146-G-A

59393282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70093144-G-T

59395819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70090638-T-C

59395849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70090609-T-C

http://identifiers.org/hco/15/GRCh38#59397396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70089469-A-C

59397593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70089283-C-G

59397826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70089045-G-A

59398301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70088573-G-A

59400417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70088008-A-G

http://identifiers.org/hco/15/GRCh38#59400459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70087968-C-A

59400459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70087968-C-T

59400643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70087794-T-C

59400780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70087676-G-A

59402204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70086647-A-G

59402204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70086647-A-T

59402213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70086638-G-A

59402294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5 prime UTR variant
orthologous variants: 70086554-T-A

59402294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5 prime UTR variant
orthologous variants: 70086554-T-C

59402308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5 prime UTR variant
orthologous variants: 70086540-G-C

59402308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5 prime UTR variant
orthologous variants: 70086540-G-T

59402367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70086516-A-G

http://identifiers.org/hco/15/GRCh38#59402388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70086496-C-A

59402388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70086496-C-G

59402445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70086442-T-C

59403309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70082214-A-T

59405711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70078192-C-T

59406077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70076707-A-G

59406077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70076707-A-T

59406106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70076678-G-A

59406190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70076602-C-T

59406289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70076259-A-G

59406289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70076259-A-T

59406323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70076245-T-C

59406324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70076244-A-G

59406487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70076110-C-T

59406656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70075950-A-G

59406746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70075853-C-T

59409122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70075306-G-A

59409133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70075293-G-T

59409213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70075214-C-G

59409213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70075214-C-T

http://identifiers.org/hco/15/GRCh38#59409219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70075208-C-A

59409219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70075208-C-G

59409247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70075165-C-G

59409328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70075081-G-T

59409419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70074997-T-C

59409478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70074940-T-A

http://identifiers.org/hco/15/GRCh38#59409656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70074802-A-C

59409656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70074802-A-G

59413082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, undefined
orthologous variants: 70071380-G-A

59413296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70071200-T-C

59413507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70070004-C-T

59413624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70069896-A-G

59416186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70068863-A-G

59416200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70068850-A-G

59416320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70068721-C-T

59416341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70068699-T-C

59416349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70068691-C-T

59416383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70068656-G-T

59416397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70068642-C-T

http://identifiers.org/hco/15/GRCh38#59416401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70068638-A-C

59416454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70068593-C-T

59416512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70068550-T-G

59416581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70068504-T-A

59416703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70068381-A-G

59416927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70067894-C-T

59417031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70067773-A-T

59417034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70067770-A-T

59417075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70067732-A-G

59417137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70067670-A-T

59419493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70066747-A-G

59420085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70066282-A-T

59420231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70066139-G-A

59420231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70066139-G-C

59420246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70066126-C-T

59420354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70066028-G-A

59420354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70066028-G-T

59421029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, undefined
orthologous variants: 70065149-T-A

59421029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, undefined
orthologous variants: 70065149-T-C

59421044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, undefined
orthologous variants: 70065134-T-C

http://identifiers.org/hco/15/GRCh38#59421590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70064869-C-A

59421590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70064869-C-T

59421640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70064823-G-A

59429769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70059607-A-G

http://identifiers.org/hco/15/GRCh38#59429954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70059446-A-C

59429959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70059441-G-A

59429959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70059441-G-T

59430082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70059363-A-T

59430139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70059314-C-T

59430450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70058964-G-C

59430562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70058848-T-C

http://identifiers.org/hco/15/GRCh38#59430587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70058818-A-C

59430683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70058721-A-T

59431062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70058414-G-C

59431062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70058414-G-T

59431735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70058291-G-A

59433325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70056435-G-A

59433326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70056434-T-A

59433473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70056280-G-A

59433561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70054469-T-C

59433785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70054265-G-A

59435764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70051490-C-T

59435882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70051368-C-T

59436017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70051269-A-G

59436111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70051031-T-C

59436147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70050994-G-A

59436402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70050830-G-T

59436528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70050703-G-A

59436559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70050673-A-G

59437266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70049565-G-A

59437370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70049455-C-T

59437467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70049369-C-T

59437559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70049288-T-A

59437572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70049281-G-A

59437886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70048958-G-A

59437935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70048917-G-A

59437935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70048917-G-T

http://identifiers.org/hco/15/GRCh38#59438023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#70048832-C-A

http://identifiers.org/hco/15/GRCh38#59438234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70048641-C-A

59438320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70048547-T-A

59438320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70048547-T-C

59438337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70048530-G-T

59438403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70048438-G-A

59438403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70048438-G-T

http://identifiers.org/hco/15/GRCh38#59438600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70048239-C-A

59438600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70048239-C-T

59438659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70048182-T-C

59438659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70048182-T-G

59438932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70047938-G-T

59438943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70047927-G-T

59439059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70047811-A-G

59439429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70047257-C-T

59439580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70047111-T-C

59439682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70047018-T-C

59439909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70046811-T-C

http://identifiers.org/hco/15/GRCh38#59439924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70046796-C-A

59439924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70046796-C-T

http://identifiers.org/hco/15/GRCh38#59439927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70046794-C-A

59439927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70046794-C-T

http://identifiers.org/hco/15/GRCh38#59439949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70046772-A-C

59439949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 70046772-A-T

59439951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 70046770-G-T

http://identifiers.org/hco/15/GRCh38#59439960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70046749-C-A

59439960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70046749-C-T

59439975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70046734-G-A

http://identifiers.org/hco/15/GRCh38#59440055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70046679-C-A

59440061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70046672-C-G

59440061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70046672-C-T

http://identifiers.org/hco/15/GRCh38#59440105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70046648-C-A

59440475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70046077-C-T

59440497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70046058-C-T

http://identifiers.org/hco/15/GRCh38#59440669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70045884-A-C

59440709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70045844-G-A

59440709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70045844-G-T

59440734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70045820-C-G

59440949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70045464-T-C

59441018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70045255-T-C

59441169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70045115-C-G

59441382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70044918-C-G

59441504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70044668-G-A

59441603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70044583-G-T

59441618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70044568-T-C

59441733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70044477-G-A

59441805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70044433-C-G

59441805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70044433-C-T

59441834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70044409-C-G

http://identifiers.org/hco/15/GRCh38#59441887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70044355-C-A

59441926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70044325-G-A

59441991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70044286-A-G

59442186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70044115-G-A

http://identifiers.org/hco/15/GRCh38#59444507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70041775-C-A

http://identifiers.org/hco/15/GRCh38#59444543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70041739-A-C

59444723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70041558-A-T

59444995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70039967-T-A

59445008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70039954-C-T

http://identifiers.org/hco/15/GRCh38#59445042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70039916-A-C

59445042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70039916-A-G

59445045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70039913-T-C

59445076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70039898-G-T

59445092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70039882-T-C

59445184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70039808-G-A

http://identifiers.org/hco/15/GRCh38#59445232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70039766-C-A

59445232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70039766-C-G

59445232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70039766-C-T

59445259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70039739-G-A

59445556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70039426-A-G

59445565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70039417-T-C

59445581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70039401-A-G

59445641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70039342-A-G

59445671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70039312-T-C

59445720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70039262-G-C

59445772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70039191-A-G

59445943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70039015-G-A

59446044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70038223-A-G

59446090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70038177-G-A

59446111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70038156-C-T

59446132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70038135-G-T

59446171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70038096-C-T

59446509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70037327-A-G

59446584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70037253-A-G

59446621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70037217-G-A

59446621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70037217-G-T

http://identifiers.org/hco/15/GRCh38#59446626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70037212-C-A

59446626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70037212-C-G

59446639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70037194-A-G

59446775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70037064-G-A

59446788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70037051-A-G

59446830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70037003-T-C

59447046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70036791-G-A

59447213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70036467-G-A

59447213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70036467-G-T

59447314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70036357-T-C

59447314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70036357-T-G

59447376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70036323-C-T

59447466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70036228-G-A

59447626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70036102-A-G

59447712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70036031-T-C

59455478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70035174-A-T

59455526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70035129-T-C

59455533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70035122-C-G

59458027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70034156-T-C

59458770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70033338-T-A

59458770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70033338-T-C

59458770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70033338-T-G

59458960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70033160-A-T

59458977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70033143-C-T

59459033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70033115-G-A

59459033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70033115-G-C

59459033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70033115-G-T

http://identifiers.org/hco/15/GRCh38#59459038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70033110-C-A

59459666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70032740-G-A

http://identifiers.org/hco/15/GRCh38#59459669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70032737-A-C

59459713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70032696-A-G

59459722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70032687-G-A

59459722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70032687-G-C

59459829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70032580-T-A

59459829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70032580-T-C

59459829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70032580-T-G

59459862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70032551-T-G

59459863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70032550-G-A

59459863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70032550-G-C

59459863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70032550-G-T

http://identifiers.org/hco/15/GRCh38#59459922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70032488-C-A

59459922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70032488-C-T

59460216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70032194-G-C

59460216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70032194-G-T

59460227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70032183-G-A

59460289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70032121-A-G

59460289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70032121-A-T

59460330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70029756-T-G

http://identifiers.org/hco/15/GRCh38#59460506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70029580-A-C

59460506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70029580-A-G

59460596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70029491-C-G

59460616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70029471-G-A

59460979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70029041-C-T

http://identifiers.org/hco/15/GRCh38#59475675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70026872-A-C

59478975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70023938-T-A

http://identifiers.org/hco/15/GRCh38#59479093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70023836-C-A

http://identifiers.org/hco/15/GRCh38#59479099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70023830-C-A

59479099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70023830-C-T

59479188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70023746-T-A

59479213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70023721-G-A

59480061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70022748-A-G

59480161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70022599-A-G

59480225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70022560-G-A

59480270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70022529-T-C

http://identifiers.org/hco/15/GRCh38#59480288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70022511-C-A

59480963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70021883-C-T

59481448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70021742-A-G

59482808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, undefined
orthologous variants: 70019964-A-G

59482820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, undefined
orthologous variants: 70019952-A-G

59491820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70018209-G-A

59491840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70018189-C-T

59492122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70017934-T-A

59492122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70017934-T-C

59492137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70017919-T-A

59492137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70017919-T-C

59492137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70017919-T-G

59492174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70017743-G-C

59492223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70017702-G-A

59492395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70017532-T-C

http://identifiers.org/hco/15/GRCh38#59492429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70016918-C-A

59492503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70016866-T-A

59492503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70016866-T-G

59492504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70016865-A-G

http://identifiers.org/hco/15/GRCh38#59492509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70016861-C-A

59492509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70016861-C-T

http://identifiers.org/hco/15/GRCh38#59492524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70016846-C-A

59492524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70016846-C-T

59492961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron_variant, undefined
orthologous variants: 70016195-T-C

59493264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70015356-C-G

59493264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70015356-C-T

59493284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70015336-C-T

59493880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70014696-G-A

59493880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70014696-G-T

59493962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70014595-G-C

59494097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70014472-A-G

59494120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70014452-T-G

59494153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70014422-A-G

59494316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70014280-G-C

59494494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70013365-T-C

59494685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70013102-A-T

http://identifiers.org/hco/15/GRCh38#59494864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70012919-C-A

http://identifiers.org/hco/15/GRCh38#59495002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70012823-C-A

http://identifiers.org/hco/15/GRCh38#59507155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70010281-C-A

59507155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70010281-C-G

59507375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70010068-G-A

59507375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70010068-G-T

59507376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70010067-G-A

59507416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70010024-T-A

59507416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70010024-T-G

59507444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70009996-C-G

59507451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70009989-G-A

59507451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70009989-G-T

59508400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70007996-G-A

59508459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70007938-G-A

59508737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70006592-T-G

59508789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70006547-G-T

59508805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70006531-C-G

59508830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70006509-A-T

59508836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70006503-T-C

http://identifiers.org/hco/15/GRCh38#59508932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70006405-A-C

59508956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: missense variant
orthologous variants: 70006381-C-G

59508956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: missense variant
orthologous variants: 70006381-C-T

http://identifiers.org/hco/15/GRCh38#59508973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70006364-A-C

59509023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70006318-G-A

http://identifiers.org/hco/15/GRCh38#59509029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70006312-C-A

59509047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70006296-T-C

59509069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70006040-T-C

59513044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70004220-T-A

59513405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70003733-C-T

59514260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70003518-A-G

59514260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70003518-A-T

http://identifiers.org/hco/15/GRCh38#59514443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70003312-C-A

http://identifiers.org/hco/15/GRCh38#59514509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70003261-C-A

59514879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70002013-C-T

59515309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70001888-G-A

http://identifiers.org/hco/15/GRCh38#59515315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70001882-C-A

59515438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70001787-C-G

59515756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70001541-G-T

http://identifiers.org/hco/15/GRCh38#59516538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#70001066-C-A

59516538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70001066-C-G

59516538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70001066-C-T

59516632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70000976-T-C

59516885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70000733-T-C

59517070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70000459-G-A

59517077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 70000452-C-T

http://identifiers.org/hco/15/GRCh38#59521176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#69998248-C-A

59521176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: intron variant
orthologous variants: 69998248-C-T

http://identifiers.org/hco/15/GRCh38#59521431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#69997996-C-A

59521431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69997996-C-T

59521463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69997964-T-G

59521721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69997738-G-T

http://identifiers.org/hco/15/GRCh38#59521726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#69997721-A-C

59521998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69997423-T-C

59522297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69997103-C-G

59522297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69997103-C-T

59522413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69996978-T-G

59522515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69996876-G-A

59522620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69996781-C-T

59522687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69996710-A-G

http://identifiers.org/hco/15/GRCh38#59522704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#69996694-C-A

http://identifiers.org/hco/15/GRCh38#59523032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#69996325-A-C

59523149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69996214-G-A

http://identifiers.org/hco/15/GRCh38#59523209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#69996156-C-A

59523209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69996156-C-T

59523225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69996141-T-C

59523403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69995953-G-T

http://identifiers.org/hco/15/GRCh38#59523411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#69995930-C-A

59523411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28379
most severe consequence: 3 prime UTR variant
orthologous variants: 69995930-C-T