http://identifiers.org/hco/21/GRCh38#38367757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95151505-A-C

38377947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95155057-T-C

http://identifiers.org/hco/21/GRCh38#38380243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95157507-C-A

38380268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95157532-G-A

38380291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95157555-G-A

38380291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95157555-G-T

38380295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95157559-C-T

http://identifiers.org/hco/21/GRCh38#38380501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95157737-C-A

38380513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95157748-G-T

http://identifiers.org/hco/21/GRCh38#38380520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95157755-C-A

38380557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95157775-A-G

38380560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95157778-G-T

38380588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95157801-T-C

38380598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95157811-G-A

http://identifiers.org/hco/21/GRCh38#38380601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95157814-C-A

38380749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95157988-G-T

38380761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95158000-A-G

38380797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95158036-T-C

38380817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95158056-T-C

38380822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95158061-T-C

http://identifiers.org/hco/21/GRCh38#38381048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95158651-C-A

38381048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95158651-C-T

38381096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95158696-G-A

38381096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95158696-G-C

38381123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95158724-T-C

http://identifiers.org/hco/21/GRCh38#38381129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95158730-C-A

38381129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95158730-C-G

38381129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95158730-C-T

38381213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95158810-A-G

38381219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95158816-C-T

38381226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95158823-T-C

38381246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95158847-C-T

38381413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95159008-G-T

38381616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95159637-A-T

38381653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95159674-C-T

38381719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95159730-G-A

38381719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95159730-G-T

38381872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95159872-G-A

38381872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95159872-G-T

38381956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95159960-A-G

38382377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95160421-T-C

38382378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95160422-G-A

38382378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95160422-G-T

38382401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95160446-A-G

38382424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95160470-C-T

http://identifiers.org/hco/21/GRCh38#38382494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95160530-C-A

38382505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95160541-T-C

38382615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95160623-A-G

38382696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95160822-T-C

38382709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95160835-G-T

38382830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95161078-G-A

38382830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95161078-G-T

38382831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95161079-C-T

38382925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95161184-G-A

38382925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95161184-G-T

38383301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95161567-T-C

38383308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95161574-T-C

38383352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95161614-T-A

38383352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95161614-T-C

38383460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 95161722-G-A

38383460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, undefined
orthologous variants: 95161722-G-T

38383535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 95161797-T-A

38383724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 95161986-A-G

38383783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, missense_variant
orthologous variants: 95162045-G-A

38383783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 95162045-G-T

38384046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95162270-T-A

38384046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95162270-T-C

38384046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95162270-T-G

38384242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95162446-G-A

38384479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95162699-T-C

38384564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95162782-G-C

38384636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95162848-G-A

38384761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95162975-T-C

http://identifiers.org/hco/21/GRCh38#38384801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95163015-C-A

http://identifiers.org/hco/21/GRCh38#38384812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95163026-C-A

38384925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95163128-C-T

38385134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95163906-T-A

38385287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95164207-G-T

38385328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95164247-G-T

38385390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95164311-T-C

http://identifiers.org/hco/21/GRCh38#38385402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95164323-C-A

38385458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95164379-A-G

38385571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95164487-C-T

38385574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95164490-T-C

38385721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95164636-C-T

38385768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95164682-C-T

38386029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95164961-T-C

38386142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95165083-A-G

38386595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95165498-G-A

38386608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95165510-T-C

38387792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95165853-A-G

38388003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95166048-G-A

38388106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95166164-C-T

38388122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95166180-G-T

38388358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95166394-T-C

38388509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95166641-T-G

38388595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95166770-G-A

38389165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95167240-A-G

38389373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95167448-G-C

38389484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95167554-A-G

38389606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95167929-G-A

38389920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95168276-T-C

38390014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95168372-C-T

http://identifiers.org/hco/21/GRCh38#38390226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95168589-A-C

38390244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95168595-T-A

38390501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95168944-C-T

38390556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95169089-C-T

38390633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95169180-C-G

38390967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95169488-A-G

38391094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95169597-T-C

http://identifiers.org/hco/21/GRCh38#38391147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95169611-C-A

http://identifiers.org/hco/21/GRCh38#38391179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95169642-C-A

38391179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95169642-C-G

38391179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95169642-C-T

38391190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95169653-C-T

38391191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95169654-T-G

38391620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95170121-T-C

38391631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95170153-G-A

38391631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95170153-G-T

http://identifiers.org/hco/21/GRCh38#38391648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95170170-C-A

38391648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron variant
orthologous variants: 95170170-C-T

38391705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95170227-T-C

38391758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95170290-T-G

http://identifiers.org/hco/21/GRCh38#38391763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95170295-C-A

38391767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95170299-A-G

http://identifiers.org/hco/21/GRCh38#38391830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95170349-C-A

38391830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95170349-C-T

38391846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95170371-G-A

38391846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95170371-G-T

38392155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95170638-T-C

38392186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95170669-A-G

38392333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95170815-G-A

38392333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95170815-G-T

http://identifiers.org/hco/21/GRCh38#38392383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95170861-C-A

38392383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95170861-C-G

38392383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95170861-C-T

38392496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95170970-A-G

38392496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95170970-A-T

38392583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95171027-G-A

38392583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95171027-G-T

38392905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95171676-C-T

http://identifiers.org/hco/21/GRCh38#38392970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95171741-C-A

38393018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95171787-G-C

38393201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95171960-G-A

38393298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95172049-A-G

38393392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95172143-A-G

38393455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95172359-A-G

38393582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95172588-G-T

38394246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95173217-C-T

38394647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95173450-T-C

http://identifiers.org/hco/21/GRCh38#38394650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95173453-C-A

38394748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95173558-T-C

38394828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95173651-T-C

38395353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95174145-A-G

http://identifiers.org/hco/21/GRCh38#38395658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95174420-C-A

38395747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95174511-G-A

http://identifiers.org/hco/21/GRCh38#38395833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95174590-C-A

38395940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95174678-G-A

38396069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95174744-A-G

38396839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95175470-G-C

38397028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95175581-G-A

38397288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95175793-G-A

38397673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95175830-G-A

38397892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95176022-G-A

38399111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95176753-C-T

38399128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95176775-C-T

38399166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95176803-G-A

38399166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95176803-G-T

38399412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95177019-T-G

38399724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95177330-G-A

38399819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95177404-T-C

38399901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95177472-C-T

38399921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95177506-G-A

38400077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95177658-G-A

38400077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95177658-G-T

http://identifiers.org/hco/21/GRCh38#38400150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95177732-C-A

38400273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95177851-G-T

http://identifiers.org/hco/21/GRCh38#38400284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95177862-A-C

38400290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95177868-C-T

http://identifiers.org/hco/21/GRCh38#38400331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95177893-C-A

38400331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95177893-C-T

38400390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95177979-G-A

38400394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95177983-T-C

http://identifiers.org/hco/21/GRCh38#38400484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#95178075-C-A

38400484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95178075-C-T

http://identifiers.org/hco/21/GRCh38#38400496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#95178085-C-A

38400496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 95178085-C-T

38400525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95178113-C-T

38400532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95178120-G-A

38400532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95178120-G-T

38400537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95178124-C-T

38400857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95178415-G-A

38401058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95178581-T-C

38401060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95178583-T-C

38401101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95178625-T-C

http://identifiers.org/hco/21/GRCh38#38401138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95178663-C-A

38401138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95178663-C-T

38401178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95178703-A-G

38401352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95178879-G-A

38401405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95178928-T-C

38401418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95178941-G-A

38401599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179117-T-G

38401606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179124-T-C

38401638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179156-G-A

38401725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179263-G-A

38401795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179340-C-T

38401876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179413-A-T

38401958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179490-G-A

38402121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179646-T-C

38402227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179741-T-C

38402231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179745-C-T

38402235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179749-G-A

38402494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179912-G-A

38402494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179912-G-T

38402523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179940-T-C

38402536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179953-C-T

38402544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179958-G-A

38402544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95179958-G-C

38402732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95180264-G-A

38402732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95180264-G-C

38402732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95180264-G-T

http://identifiers.org/hco/21/GRCh38#38402740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95180272-A-C

38402740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95180272-A-G

http://identifiers.org/hco/21/GRCh38#38402752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95180284-A-C

http://identifiers.org/hco/21/GRCh38#38402753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95180285-A-C

38402846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95180386-G-T

38402895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95180432-T-C

38403145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95180664-C-G

38403165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95180680-T-A

38403369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95180834-G-T

http://identifiers.org/hco/21/GRCh38#38403379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95180844-C-A

38403379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95180844-C-T

http://identifiers.org/hco/21/GRCh38#38403469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95180911-C-A

http://identifiers.org/hco/21/GRCh38#38403606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95181027-A-C

38403606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95181027-A-G

38403667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95181088-T-C

38403731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95181153-T-A

38403731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95181153-T-C

38403804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95181219-C-T

38403810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95181225-A-G

http://identifiers.org/hco/21/GRCh38#38403811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95181226-C-A

38409775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95182815-G-A

38409836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95182878-T-C

38410048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95183089-A-G

38410327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95183382-A-G

38410404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95183450-A-T

38410475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95183516-G-A

38410959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95184102-C-T

38411143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95184273-G-C

38415647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95185952-C-G

38415647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95185952-C-T

http://identifiers.org/hco/21/GRCh38#38415681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95185990-C-A

http://identifiers.org/hco/21/GRCh38#38415760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95186070-C-A

38415760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95186070-C-G

38415786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95186096-C-T

38415957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95186185-C-T

38415991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95186218-A-G

38416015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95186241-G-T

38416048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95186271-C-T

38416108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95186323-G-A

38416245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95186449-C-T

38416374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95186559-T-G

38416478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95186652-C-T

38416569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95186737-T-C

38416790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95186941-A-G

38417029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95187181-G-A

38417284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95187431-T-A

38417882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95187694-G-A

38419531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95188455-G-A

38419537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95188462-G-C

38419572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95188494-A-G

38419945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95188850-C-T

http://identifiers.org/hco/21/GRCh38#38420024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95188921-A-C

38420024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95188921-A-T

38420059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95188939-T-A

38420060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95188940-G-T

38420188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95189063-G-A

38420204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95189095-G-A

38420204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95189095-G-T

38420299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95189186-T-C

38420307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95189194-T-C

http://identifiers.org/hco/21/GRCh38#38420403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95189282-A-C

38420408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95189287-C-T

38420557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95189434-C-T

38420787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95189612-T-C

38420825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95189665-A-T

http://identifiers.org/hco/21/GRCh38#38420852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95189688-A-C

38420852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95189688-A-G

38420923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95189757-A-G

38420932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95189766-G-A

38420982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95189814-T-C

38421170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95189910-T-C

38421331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95190079-G-T

http://identifiers.org/hco/21/GRCh38#38421365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95190110-A-C

38421433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95190179-A-G

38421434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95190180-T-C

http://identifiers.org/hco/21/GRCh38#38421450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95190198-A-C

38421569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95190310-T-C

38421672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95190404-C-T

38423581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95190927-C-T

http://identifiers.org/hco/21/GRCh38#38424288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95191645-C-A

38424358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95191724-T-C

38424444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95191867-A-G

38424446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95191869-G-A

38424638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95192047-C-T

38424673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95192082-C-T

38424810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95192203-C-T

http://identifiers.org/hco/21/GRCh38#38425524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95192761-C-A

http://identifiers.org/hco/21/GRCh38#38425575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95192812-C-A

38425575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95192812-C-T

38425737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95192966-T-C

38425901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95193147-G-A

38425905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95193151-G-A

38426155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95193763-T-G

38426236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95193844-A-T

38426443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95194055-C-T

38426455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95194082-G-A

38433638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95197574-T-A

38433638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95197574-T-C

38433799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95197746-G-A

38433810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95197757-T-C

38433965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95197850-C-T

38434832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95199289-T-C

38434858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95199317-T-C

38434876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95199335-G-A

38435095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95199609-G-A

38435201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95199785-T-C

38435414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95200002-T-G

38435426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95200013-C-T

38435668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95200242-G-A

38435917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95200482-T-C

http://identifiers.org/hco/21/GRCh38#38437937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95204736-C-A

38437968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95204762-G-C

38438026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95204808-T-A

38438026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95204808-T-C

38438072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95204845-T-C

38438074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95204847-G-A

38438079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95204854-C-T

38438187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95204959-A-G

38438212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95204988-C-T

38438272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95205033-C-T

38438489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95205411-C-T

http://identifiers.org/hco/21/GRCh38#38438552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95205550-A-C

38438669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95205673-C-T

38438678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95205682-C-T

38438697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95205700-T-C

38438723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95205713-G-A

38438808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95205804-A-G

38438947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95205922-T-G

38439157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95206458-G-A

38439425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95206705-G-A

38439511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95206773-G-C

38439597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95206864-T-C

38444057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95209034-G-A

38444120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95209097-G-A

38444172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95209150-G-A

38444172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95209150-G-C

38444233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95209208-G-C

38444269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95209244-C-T

38444276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95209251-T-C

38444374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95209348-G-A

38444538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95209517-T-C

38444670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95210079-G-T

38444777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95210164-T-A

38444783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95210170-G-A

38444803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95210186-C-T

38445354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95210546-G-T

38445357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95210549-T-C

38445386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95210578-G-A

38445386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95210578-G-T

38445462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95210652-G-T

38445592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95210782-C-T

38445671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95210862-T-C

http://identifiers.org/hco/21/GRCh38#38445693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95210871-C-A

38445693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95210871-C-T

http://identifiers.org/hco/21/GRCh38#38445699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95210877-C-A

38445699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95210877-C-T

http://identifiers.org/hco/21/GRCh38#38445810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95211003-C-A

38445860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95211052-G-A

38446022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95211212-T-C

38446028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95211218-C-T

38446088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95211279-T-G

38446641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95211915-A-G

38446684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95211993-A-T

38446768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95212118-C-G

38446872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95212207-G-A

38447002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95212306-G-A

38447002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95212306-G-T

38447064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95212360-A-G

38447067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95212363-C-T

38447175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95212479-G-A

38447175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95212479-G-T

http://identifiers.org/hco/21/GRCh38#38447427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95212704-C-A

38447581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95212846-T-A

38447581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95212846-T-C

38447807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95213060-C-T

38447823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95213075-G-A

http://identifiers.org/hco/21/GRCh38#38447857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95213109-C-A

38447989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95213245-A-T

38448093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95213338-A-G

38448291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95213528-A-G

38448659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95214037-C-G

http://identifiers.org/hco/21/GRCh38#38448792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95214164-A-C

38448792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95214164-A-G

38449109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95214474-G-T

38449234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95214598-T-C

38449246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95214610-A-T

38449263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95214627-T-C

38450531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95216721-A-G

38450552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95216742-T-C

38450671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95216849-A-G

38451146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95217824-G-A

38451195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95217874-G-A

38451195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95217874-G-T

38451218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95217893-T-C

38451244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95217919-A-G

38451253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95217928-G-A

38451253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95217928-G-T

http://identifiers.org/hco/21/GRCh38#38451255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95217930-C-A

38451267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95217942-T-C

38451267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95217942-T-G

38451273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95217945-G-T

38451415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95218073-G-A

38451483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95218140-T-C

38451542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95218197-T-C

38451807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95218580-T-A

38451939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95218886-T-G

http://identifiers.org/hco/21/GRCh38#38452215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95219167-C-A

http://identifiers.org/hco/21/GRCh38#38452447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95219433-C-A

38452706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95219644-C-T

38454474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95222314-C-G

38454496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95222340-A-G

http://identifiers.org/hco/21/GRCh38#38454719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95222538-C-A

38454719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95222538-C-T

38454825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95222644-A-G

38454905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95222733-G-A

38455295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95223446-G-A

38455434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95223572-A-G

38455435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95223573-T-C

38455553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95223687-G-C

38455955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95224053-C-G

38455955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95224053-C-T

http://identifiers.org/hco/21/GRCh38#38456080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95224169-C-A

38456104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95224194-T-C

38456126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95224216-T-C

http://identifiers.org/hco/21/GRCh38#38456171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95224246-C-A

38456508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95224886-G-A

38456652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95225019-T-G

38456670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95225037-T-C

http://identifiers.org/hco/21/GRCh38#38456701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95225067-A-C

38457081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95225441-C-T

38457498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95225545-C-T

38457586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95225626-G-A

38457735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95225768-G-A

38457755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95225788-T-C

http://identifiers.org/hco/21/GRCh38#38457936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95225958-C-A

38458113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95226135-G-A

38458149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95226162-G-A

38458152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95226165-A-G

38458962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95226903-T-C

38459164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95227016-A-G

38459509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95227344-A-G

38459803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95227564-A-G

38460132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95227905-C-T

38460160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95227932-T-G

38460197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95227966-G-T

38460290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95228058-C-T

38460334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95228106-C-T

38460337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95228109-T-C

38460444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95228172-T-C

38460994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95228753-G-A

38461192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95228930-T-A

38461267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95229015-C-G

38461403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95229145-T-C

http://identifiers.org/hco/21/GRCh38#38461541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95229268-C-A

38461541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95229268-C-T

38461610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95229296-C-G

38461610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95229296-C-T

38469852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95230595-T-G

http://identifiers.org/hco/21/GRCh38#38470900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95230904-C-A

38470925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95230931-G-A

38470925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95230931-G-T

38471108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95231126-G-T

38471142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95231159-G-T

38471171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95231166-T-G

38471307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95231470-G-T

38471317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95231481-G-A

http://identifiers.org/hco/21/GRCh38#38471427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95231581-C-A

38471662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95231823-A-G

http://identifiers.org/hco/21/GRCh38#38471677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95231839-C-A

38471737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95231902-G-A

38471825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95231990-G-T

38471833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95231998-T-C

http://identifiers.org/hco/21/GRCh38#38471893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95232054-C-A

38471933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95232095-G-A

38472129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95232361-G-T

38472131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95232385-T-C

38472156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95232443-G-T

38472283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95232806-C-T

http://identifiers.org/hco/21/GRCh38#38472396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95232909-C-A

38472530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95232992-C-T

38472799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95233236-C-G

38472799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95233236-C-T

38473472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95237082-A-G

38473798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95237359-G-A

38473876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95237435-G-A

38473903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95237469-G-A

38473903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95237469-G-T

38474076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95237693-T-C

38474143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95237758-G-T

38474193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95237807-G-A

38474193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95237807-G-T

38474216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95237830-C-T

38474267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95237884-A-G

38475140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95238886-T-C

38475490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95239200-A-G

38475554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95239261-T-C

38475615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95239296-G-A

38475653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95239338-A-G

38475666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95239351-C-T

38475715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95239369-G-C

38475904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95239538-C-T

http://identifiers.org/hco/21/GRCh38#38476022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95239609-C-A

http://identifiers.org/hco/21/GRCh38#38476081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95239667-C-A

38476086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95239672-C-T

38476172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95239842-G-A

38476345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95240010-G-A

http://identifiers.org/hco/21/GRCh38#38476750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95240407-C-A

38476750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95240407-C-G

38476750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95240407-C-T

38476850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95240498-T-C

38476899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95240535-A-G

38476948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95240576-T-C

38477296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95240665-G-A

38477437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95240732-G-A

38477903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95241186-A-G

http://identifiers.org/hco/21/GRCh38#38478003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95241279-C-A

http://identifiers.org/hco/21/GRCh38#38478204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95241458-A-C

38478230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95241484-G-A

38478230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95241484-G-T

38478313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95241564-T-G

38478489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95241703-G-A

38478489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95241703-G-T

38478561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95241800-A-G

38478577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95241816-A-G

38478660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95241871-A-G

38478756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95242002-C-T

38478944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95242181-C-T

38479112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95242335-T-C

38479148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95242373-T-C

38479190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95242424-T-C

http://identifiers.org/hco/21/GRCh38#38479260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95242494-A-C

38479344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95242578-C-T

38479381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95242612-G-T

38480410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95242881-A-T

http://identifiers.org/hco/21/GRCh38#38480560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95243033-A-C

38480858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95243318-G-A

38480938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95243738-T-A

38481287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95244035-T-C

38481791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95245356-A-G

38481954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95245513-T-A

38481954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95245513-T-C

38483043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95246399-T-C

38483043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95246399-T-G

http://identifiers.org/hco/21/GRCh38#38483304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95246579-A-C

38483304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95246579-A-T

38483309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95246580-T-C

38483366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95246641-C-G

38483367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95246642-A-G

38483550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95246821-T-C

38487380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95248756-G-A

38487593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95248950-G-A

38487617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95248974-T-G

38487794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249108-G-A

38487835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249150-A-T

38487996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249327-T-C

38488036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249365-C-G

38488036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249365-C-T

38488195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249516-G-C

38488314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249599-G-A

38488379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249668-C-T

38488448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249734-C-T

38488546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249830-C-T

38488696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249957-A-G

38488714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95249977-C-T

38488927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95250139-T-C

38489290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95250540-C-T

38489360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95250620-G-A

38489545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95250792-A-G

http://identifiers.org/hco/21/GRCh38#38489699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95250920-C-A

38489760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95250979-T-G

38489998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95251293-G-A

38490067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95251447-G-A

38490157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95251522-T-G

http://identifiers.org/hco/21/GRCh38#38490234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95251597-C-A

38490234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95251597-C-T

38490337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95251654-G-A

38490535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95251794-G-A

38490593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95251840-C-G

38490593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95251840-C-T

38490641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95251877-T-C

38490886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95252096-T-C

http://identifiers.org/hco/21/GRCh38#38491102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95252264-A-C

38491102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95252264-A-G

38491611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95253364-A-G

38491963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95253964-C-T

38491983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95253988-A-T

38492269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254241-A-G

38492284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254256-T-A

38492367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254346-C-T

http://identifiers.org/hco/21/GRCh38#38492510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95254449-A-C

38492538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254479-G-A

38492613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254551-G-A

38492613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254551-G-T

http://identifiers.org/hco/21/GRCh38#38492726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95254641-C-A

38492726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254641-C-T

38492881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254766-C-T

38492889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254774-T-C

38492940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95254825-C-G

38493179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95255012-T-C

38493572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95255416-T-C

38493599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95255454-T-C

38493658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95255516-C-G

38493692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95255551-C-T

http://identifiers.org/hco/21/GRCh38#38493724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95255578-C-A

http://identifiers.org/hco/21/GRCh38#38493738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95255590-A-C

http://identifiers.org/hco/21/GRCh38#38493801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95255635-C-A

38495099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95256944-T-G

38495420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95257316-G-A

38495517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95257433-C-G

38495557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95257482-T-A

38495584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95257501-G-A

38495597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95257514-C-T

38495709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95257626-G-A

http://identifiers.org/hco/21/GRCh38#38495930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95257782-A-C

38495933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95257786-C-G

38495991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95257832-C-G

38496378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95258171-A-G

38496399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95258192-T-C

38497079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95258856-A-G

http://identifiers.org/hco/21/GRCh38#38497155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95258929-A-C

38497404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95259141-C-T

38497491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95259221-G-A

http://identifiers.org/hco/21/GRCh38#38497663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95259398-C-A

38497828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95259561-T-C

38497913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95259648-T-C

38497913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95259648-T-G

38497939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95259674-A-G

38497940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95259675-A-G

38498043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95259772-A-G

38499245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261113-A-T

38499265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261133-T-C

38499277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261145-T-C

38499330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261198-T-C

38499341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261209-G-A

38499370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261237-A-G

38499377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261244-C-T

38499489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261367-C-G

38499491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261369-A-G

38499524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261395-G-A

38499826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261702-A-G

38499831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261707-G-A

38499831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261707-G-C

38499831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261707-G-T

38499835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261711-G-T

38499859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261730-A-G

38499871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261742-A-G

38499906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95261777-G-C

38500249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262126-T-G

38500276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262152-G-A

38500338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262170-T-C

38500359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262190-A-T

38500373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262204-T-C

38500621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262336-T-A

38500719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262407-T-G

http://identifiers.org/hco/21/GRCh38#38500893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95262592-C-A

38500960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262675-A-G

38500978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262684-T-C

http://identifiers.org/hco/21/GRCh38#38501057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95262770-A-C

38501057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262770-A-G

38501512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262891-A-G

38501549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262924-C-T

38501621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262979-G-A

38501645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95262995-C-T

38501776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95263075-C-T

38501931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95263228-T-C

38502132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95263386-A-T

38502133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95263387-C-T

38503578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95264610-G-T

38503613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95264681-T-C

38503851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95264915-C-G

38503851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95264915-C-T

38503852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95264916-G-A

38503976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95265041-T-C

38504070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95265487-C-T

38504122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95265538-C-G

38504327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95265743-G-A

38504458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95265866-G-A

38504540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95266042-T-C

38504543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95266045-T-A

38504543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95266045-T-C

38504629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95266194-T-C

38504748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95266321-C-T

38504830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95266397-T-G

38504850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95266415-G-A

38505133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95266904-G-A

38505133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95266904-G-C

38505220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95266982-A-G

38505226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95266988-C-T

38505278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95267010-G-A

38505325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95267058-T-G

http://identifiers.org/hco/21/GRCh38#38505402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95267086-A-C

38505402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95267086-A-G

38505447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95267130-T-C

38505823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95267555-T-C

38505982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95267721-G-T

38508627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95268830-C-T

38508930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95269082-C-T

38508999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95269146-C-T

38509092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95269240-A-G

38509134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95269272-A-G

38509163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95269294-T-C

38509193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95269316-G-C

38509361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95269484-G-T

38509443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95269568-G-C

38509481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95269605-T-G

http://identifiers.org/hco/21/GRCh38#38509688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95269745-C-A

38509992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95270050-G-C

38510149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95270190-C-T

38510802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95270918-G-A

38511194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95271282-A-G

38522076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95279130-T-C

38522160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95279213-A-T

38522276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95279330-G-A

38522452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95279504-T-A

38522678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95279713-G-T

38522865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95279889-G-A

38522995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95280058-T-C

38523153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95280334-T-C

38523159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95280340-A-G

38523195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95280391-G-A

38523195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95280391-G-T

38523237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95280433-T-C

38523500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95281368-A-G

38523619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95281482-T-G

38523621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95281484-A-G

38523842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95281697-C-T

38523870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95281723-A-G

38524463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95282248-A-T

38524484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95282263-G-A

38524608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95282361-T-C

38525009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95282652-G-A

38525459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95283450-G-A

http://identifiers.org/hco/21/GRCh38#38525473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95283465-A-C

38525665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95283637-C-T

38526100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95284402-T-C

38526168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95284459-G-A

38526168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95284459-G-T

38526316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95284597-G-A

38527267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95285927-G-A

38527427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286073-T-C

38527630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286259-C-T

38527707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95286322-C-T

38528752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95287423-G-A

38528752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95287423-G-T

38531078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95291294-T-C

38531078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95291294-T-G

38531187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95291410-A-G

38531224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95291447-C-T

38531228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95291451-G-C

38531899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95292345-G-A

38532097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95292563-A-G

38532244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95292683-G-A

38532252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95292691-G-A

38532257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95292696-T-C

38532353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95292807-A-T

38532399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95292857-T-C

38532418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95292876-T-C

38532454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95292965-C-T

38532773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95293202-T-C

38532915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95293341-A-G

38533241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95293888-T-C

38533479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95294122-A-G

http://identifiers.org/hco/21/GRCh38#38533800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95294443-C-A

38533859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95294502-T-C

38533883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95294526-G-T

38534128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95295180-A-G

38534306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95295299-G-A

38534339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95295329-T-C

38534345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95295337-T-C

http://identifiers.org/hco/21/GRCh38#38534440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95295453-A-C

38534440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95295453-A-T

38534445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95295458-A-G

38534508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95295502-T-G

38534620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95295611-G-A

38534844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95295828-A-G

38535150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95295917-G-A

http://identifiers.org/hco/21/GRCh38#38535152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95295919-C-A

http://identifiers.org/hco/21/GRCh38#38535476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95296139-C-A

http://identifiers.org/hco/21/GRCh38#38535629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95296251-C-A

38535629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95296251-C-T

38535643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95296265-A-G

38535658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95296281-C-G

38535901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95296512-A-G

38540323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95298148-G-A

38540436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95298258-G-A

38540570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95298396-C-G

38540832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95298572-A-G

38541054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95298802-C-T

38541086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95298817-T-C

38541155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95298904-C-T

http://identifiers.org/hco/21/GRCh38#38541309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95299247-A-C

38541309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95299247-A-G

38541473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95299387-C-T

http://identifiers.org/hco/21/GRCh38#38541491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95299405-A-C

38542535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95300283-G-A

http://identifiers.org/hco/21/GRCh38#38542547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95300296-C-A

38542691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95300440-C-T

38542717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95300465-G-A

38542779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95300524-A-G

38542784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95300529-G-T

http://identifiers.org/hco/21/GRCh38#38542825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95300569-C-A

38542835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95300579-A-G

38542886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95300626-T-C

38545815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95302600-C-T

38545881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95302752-T-G

38546373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95303188-C-T

38546425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95303237-G-A

38546473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95303287-C-T

38546795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95303609-G-A

38546856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95303664-C-T

38547268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95304241-T-C

38547273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95304246-T-A

38547342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95304306-C-T

38547343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95304307-A-G

38547533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95304477-G-A

38547849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95305489-C-T

38547998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95305651-A-G

38548095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95305780-G-A

38548134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95305819-C-T

38548138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95305823-T-C

38548238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95305926-T-C

38548275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95305968-A-T

38548284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95305977-T-A

38548319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95306019-T-C

38549263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95306539-A-G

38549330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95306603-A-G

38549441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95306713-G-A

38549441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95306713-G-T

38549569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95306856-A-G

38549609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95306897-G-C

38549626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95306914-G-A

38549659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95306947-A-G

38549679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95306960-G-A

38549824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95307094-T-G

38549827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95307097-G-T

38549899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95307207-C-T

38549950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95307278-T-C

38549950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95307278-T-G

38549985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95307309-T-A

38549985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95307309-T-C

38550074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95307377-G-A

38550075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95307378-T-C

38550105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95307408-G-A

38550114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95307416-G-A

38558479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95308076-A-G

38558567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95308173-G-A

38558619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95308220-C-T

38559104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95308998-T-C

38559151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95309031-C-T

http://identifiers.org/hco/21/GRCh38#38559160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95309043-C-A

38559171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95309054-C-T

38559245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95309120-A-G

38559295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95309149-A-G

38559327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95309180-G-C

38559359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95309205-T-A

38559359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95309205-T-C

38559360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95309206-C-G

38559365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95309211-T-C

http://identifiers.org/hco/21/GRCh38#38559418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95309245-C-A

38559418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95309245-C-T

38561220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95318068-G-A

38561227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95318075-G-A

38561404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95318895-C-T

38561618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95319311-G-C

38561742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95319426-T-C

38561779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95319463-T-C

38561829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95319508-C-T

http://identifiers.org/hco/21/GRCh38#38561876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95319560-C-A

38562848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95320250-G-C

38563807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95322072-A-G

38564033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95322246-T-C

38564069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95322263-G-A

38571749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95324847-T-A

38571896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95324988-G-A

38572022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325107-T-C

38575532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325238-G-A

38575532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325238-G-T

38575564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325289-T-C

38575576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325303-T-C

38575650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325374-G-T

38575686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95325410-G-A

38575746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 95325472-G-A

38575794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325516-T-G

38575796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325518-T-C

38575797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325519-G-A

38575797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325519-G-C

38575797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325519-G-T

38575802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325524-T-A

38575802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325524-T-C

38575821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325543-G-A

38575821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325543-G-T

38575859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325578-A-G

38576014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95325723-T-C

38578850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95326745-G-C

38582123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95327044-T-C

38583117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95328440-G-A

38583175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95328496-C-G

38583246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95328565-G-C

38583296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95328603-T-C

38583313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95328618-G-A

38583372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95328676-C-T

38583736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95329774-A-G

38584242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95330233-C-T

38584273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95330265-T-C

38584569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95330527-A-G

38584864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95331143-G-A

38584864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95331143-G-C

http://identifiers.org/hco/21/GRCh38#38584905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95331184-C-A

http://identifiers.org/hco/21/GRCh38#38584972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95331250-C-A

38585050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95331317-T-A

38585068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95331340-G-A

38585223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95331462-T-C

38585259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95331494-T-C

38585351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95332259-A-G

38585403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95332315-T-C

38585717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95332590-A-G

38585729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95332602-G-T

38585792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95332657-C-T

38585822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95332688-C-G

38585925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95332802-G-A

38585955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95332831-G-A

38586162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95333045-A-T

38587901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95333517-T-C

38587955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95333572-T-C

38588128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95333754-G-C

38588170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95333803-T-A

http://identifiers.org/hco/21/GRCh38#38588255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95333888-C-A

38588255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95333888-C-G

38599942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95335185-A-G

38600193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95335391-C-T

38600197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95335395-T-G

38600339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95335502-C-T

38600721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95335838-A-T

38600743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95335859-C-T

http://identifiers.org/hco/21/GRCh38#38601969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95337935-C-A

38601982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95337948-A-G

38602000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95337966-A-G

http://identifiers.org/hco/21/GRCh38#38602038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95338003-C-A

38602038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95338003-C-T

http://identifiers.org/hco/21/GRCh38#38602141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95338103-A-C

38602141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95338103-A-G

38602606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95338248-A-G

38602743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95338380-A-G

38602828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95338451-C-T

38602841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95338464-A-G

38604282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95340630-T-C

38604408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95340757-A-G

38604481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95340825-T-G

38604698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95341268-T-C

38605005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95341551-G-A

38605304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95342368-G-A

38605305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95342369-C-G

38605390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95342452-T-A

38605390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95342452-T-C

38605773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95342974-G-C

http://identifiers.org/hco/21/GRCh38#38606361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95343198-C-A

38606766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95343483-G-A

38606799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95343523-C-T

http://identifiers.org/hco/21/GRCh38#38606954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95343689-C-A

http://identifiers.org/hco/21/GRCh38#38607180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95343962-C-A

38607180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95343962-C-T

38610637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95346180-G-A

38610704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95346237-A-G

38610704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95346237-A-T

38610773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95346307-T-C

http://identifiers.org/hco/21/GRCh38#38610850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95346382-A-C

38610986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95346520-G-A

38611111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95346645-G-A

38611247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95346741-C-T

38611254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95346748-C-G

38611386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95346888-A-G

38611388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95346890-C-T

http://identifiers.org/hco/21/GRCh38#38611452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95346953-C-A

38611461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95346962-G-C

38611777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95347230-C-T

38611782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95347235-C-T

38611863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95347281-C-T

38612016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95347427-A-T

38612142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95347545-A-T

38612285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95347652-T-C

38613129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95348567-G-A

38613202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95348658-A-G

http://identifiers.org/hco/21/GRCh38#38613350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95348781-A-C

38613608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95348961-C-T

38613731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349083-C-T

38613825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349172-C-T

38613886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349238-G-C

38613922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349276-G-A

38613964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349290-A-T

38614016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349342-G-A

38614029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349355-C-G

38614116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349410-A-G

38614216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349488-G-A

38614226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349498-G-T

38614245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349510-T-C

38614245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349510-T-G

38614628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349791-G-A

38615440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95350556-A-G

38615794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95350898-A-T

38615809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95350913-T-C

38616654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95351209-C-G

38616762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95351306-G-T

38617036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95351541-G-T

38617169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95351667-G-A

38617646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95352106-A-G

http://identifiers.org/hco/21/GRCh38#38617663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95352123-C-A

38618208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95352408-A-G

http://identifiers.org/hco/21/GRCh38#38618215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95352416-C-A

http://identifiers.org/hco/21/GRCh38#38618216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95352417-C-A

38618225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95352426-A-G

38618459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95352535-A-G

38618546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95352616-G-A

http://identifiers.org/hco/21/GRCh38#38618917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95352936-C-A

38618923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95352942-C-T

38619220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95353185-T-C

38619311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95353230-G-A

38619376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95353283-T-A

38619653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95353509-T-C

38619749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95353606-A-G

38619921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95353772-T-C

38619932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95353782-G-A

38619949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95353798-G-A

38620080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95353923-T-G

38620153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95353995-A-G

http://identifiers.org/hco/21/GRCh38#38620169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95354011-C-A

38620241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95354438-T-G

38620264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95354458-A-G

38620353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95354534-C-T

38620452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95354614-G-C

38620778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95354920-G-A

38620778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95354920-G-C

38620914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355023-A-G

38621090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355234-G-A

38621169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355337-A-G

38621210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355375-A-T

38621344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355555-C-T

38621383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355593-G-A

38621455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355674-G-A

38621617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355779-G-A

38621646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355804-G-T

38621842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355994-C-G

38621842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355994-C-T

38622062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95356213-G-A

38622062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95356213-G-C

38622178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95356302-T-G

38622214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95356335-C-T

http://identifiers.org/hco/21/GRCh38#38622329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95356412-A-C

38622386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95356508-C-T

http://identifiers.org/hco/21/GRCh38#38622437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95356558-C-A

38623445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95356808-A-G

38623536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95356872-G-A

38623556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95356894-C-T

38623761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95357132-C-T

38623781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95357152-G-A

38623810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95357170-G-A

38623852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95357219-C-T

38623869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95357235-G-T

38624098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95357426-C-T

38624163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95357467-C-G

38624168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95357472-C-T

http://identifiers.org/hco/21/GRCh38#38624185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95357489-C-A

38628354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95358326-C-G

http://identifiers.org/hco/21/GRCh38#38636395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95367788-C-A

38636395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95367788-C-G

38636468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95367871-A-G

38636537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95367943-T-C

38636579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95367984-A-G

38641976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95370142-T-C

38642081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95370234-A-G

38642306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95370452-G-C

http://identifiers.org/hco/21/GRCh38#38642316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95370462-A-C

38642339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95370485-A-G

38642404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95370560-T-C

38643344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95372886-A-T

38643379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95372920-G-A

38643379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95372920-G-T

38643492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95373021-G-C

38646441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95374062-T-C

38646609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95374227-C-T

38648342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95375493-T-C

38648391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95375545-A-G

38648659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95375761-C-T

38649033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376143-C-T

http://identifiers.org/hco/21/GRCh38#38649048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95376158-A-C

38649151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376251-A-G

38649382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376440-C-G

38649496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376545-T-G

38649538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376587-C-G

38649547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376596-T-A

38649547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376596-T-C

38649743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376862-C-G

38649898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95377201-C-T

38650160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95377434-C-G

http://identifiers.org/hco/21/GRCh38#38650250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95377520-A-C

38650573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95377602-G-A

38650885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95377831-A-G

38651111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378051-G-A

38651504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378537-G-A

38651719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378714-C-T

38651821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378762-C-T

38651855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378778-C-T

38651865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378788-A-G

38652006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378863-T-G

38652117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378963-G-A

38652209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95379062-C-T

38652219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95379072-C-T

38652228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95379081-C-T

38652587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95379365-G-T

38653458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380206-T-C

38653636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380373-C-T

38653678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380415-G-A

38653679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380416-G-A

38653821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380559-G-C

38653937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380669-C-T

38653972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380703-C-T

38654119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380852-T-C

38654123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380856-A-G

38654145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380878-G-A

38654177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380888-T-C

38654181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380892-T-C

38654204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380915-G-A

http://identifiers.org/hco/21/GRCh38#38654799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95381279-C-A

38654839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95381319-T-C

38654839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95381319-T-G

http://identifiers.org/hco/21/GRCh38#38654882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95381355-A-C

38654887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95381360-C-T

http://identifiers.org/hco/21/GRCh38#38655271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95381710-C-A

38655362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95381800-T-C

38655368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95381806-T-C

38655507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95381914-C-T

38655757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95382128-C-G

38656020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95382341-G-A

38656040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95382358-C-T

38656041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95382359-G-A

38656333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95382627-G-A

38656348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95382640-T-C

http://identifiers.org/hco/21/GRCh38#38656438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95382776-A-C

38656819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95383130-G-T

38656897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95383265-G-A

38657036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95383400-C-T

38657135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95383487-T-A

38657256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95383556-C-T

38657487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95383775-C-T

38658017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95384246-G-A

38658068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95384298-T-C

38658354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95384570-T-A

38658472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95384687-T-A

38658655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95384862-A-G

http://identifiers.org/hco/21/GRCh38#38658768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95384968-C-A

38658791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95384992-T-C

38658850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95385051-G-A

http://identifiers.org/hco/21/GRCh38#38658883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#95385084-C-A

38658989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95385189-T-G

38659379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95385550-G-A

38659430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95385586-G-A

38659636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95385750-T-C

38659705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95385810-C-T

38660580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95386364-G-T

38660626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95386400-G-A

38660626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95386400-G-T

38660939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95386674-G-A

38661458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95387172-G-C

38661458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95387172-G-T

38661495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3446
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95387207-G-A