77613178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56525909-G-A

77613178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56525909-G-T

77613180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56525912-T-C

77613181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56525913-T-C

77613334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56526065-C-T

77613577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56526302-G-A

77613577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56526302-G-T

77613580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56526305-G-A

77613580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56526305-G-T

77613721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56526445-T-C

77613781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56526509-G-A

77613781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56526509-G-C

77613781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56526509-G-T

http://identifiers.org/hco/15/GRCh38#77613869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56526589-A-C

77613869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56526589-A-G

77613869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56526589-A-T

77613948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56526648-T-A

77613948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56526648-T-C

77613948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56526648-T-G

77614203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56526902-G-A

77614449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56527148-G-A

77614539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56527238-G-A

77614539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56527238-G-T

77614668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56527367-C-G

77614896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56527595-C-T

77615609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56528308-G-C

77615609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56528308-G-T

77616368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528880-G-A

77616472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528907-C-T

77616543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56528950-G-A

77616607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529015-A-G

77616739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529131-G-A

77616927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529284-G-C

77617167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529486-G-A

77617293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529563-C-T

77617297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529567-T-G

77617304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529573-C-G

77617481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529713-C-T

77617561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529790-C-T

77617610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56529826-G-C

77618232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56530394-C-T

77619128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56530849-G-A

77619931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531517-G-A

77619951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531536-A-G

77619971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531556-C-T

77619996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531579-G-A

77620193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56531759-G-A

77620288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56531852-G-A

77620702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56532233-C-G

77620769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56532293-G-T

77620787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56532314-C-T

http://identifiers.org/hco/15/GRCh38#77621038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56532496-C-A

77621440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56532596-G-C

http://identifiers.org/hco/15/GRCh38#77621717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56532848-C-A

77621898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56533025-G-A

77622064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56533065-G-C

77622131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56533111-G-A

77622131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56533111-G-T

77622759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56533839-C-G

http://identifiers.org/hco/15/GRCh38#77622991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56533968-C-A

77623049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56534018-G-A

77623098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56534064-G-A

77623212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56534137-C-G

77623212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56534137-C-T

77623439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56534313-G-A

77624419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56534939-C-T

http://identifiers.org/hco/15/GRCh38#77624783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56535285-C-A

77624783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535285-C-G

77624783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535285-C-T

77624812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535315-C-G

77624841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535343-G-A

77625282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535660-T-C

77625414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56535900-G-A

77625560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536023-T-C

77625671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536168-G-A

http://identifiers.org/hco/15/GRCh38#77625697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56536194-C-A

http://identifiers.org/hco/15/GRCh38#77625991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56536411-C-A

77626013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536433-T-A

77626275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536654-G-C

77626442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56536816-A-G

77627277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537549-C-T

77627379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537648-C-G

77627811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56538067-G-T

http://identifiers.org/hco/15/GRCh38#77627814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#56538070-A-C

77627916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538180-G-A

77628160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538431-T-C

77628169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538440-T-A

77628169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538440-T-C

77628301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538554-A-T

77628564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538895-T-A

77628564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538895-T-C

77628651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538976-T-A

77628747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539243-G-A

77628854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539346-C-G

77628875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539365-G-A

77629153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539644-C-T

77629590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539985-C-T

77629629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540025-A-G

77630069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540370-G-T

77630482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56540570-A-G

77630559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56540653-C-G

77630559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56540653-C-T

77630567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56540661-G-C

77630621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56540740-G-A

77630910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56541029-C-T

77631043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56541128-C-T

77631193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56541267-G-A

77631500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56541575-G-A

http://identifiers.org/hco/15/GRCh38#77631639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56541719-C-A

77631639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56541719-C-T

77631814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56541902-C-T

http://identifiers.org/hco/15/GRCh38#77632250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56542298-C-A

77632250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56542298-C-T

77632304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56542353-G-A

77632304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56542353-G-T

http://identifiers.org/hco/15/GRCh38#77632348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56542397-C-A

77632348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56542397-C-T

77632409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56542453-T-C

77632409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56542453-T-G

http://identifiers.org/hco/15/GRCh38#77632555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56542598-C-A

77632555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56542598-C-G

77632555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56542598-C-T

77632610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56542653-G-A

77632610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56542653-G-T

77632622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56542665-T-A

77632622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56542665-T-C

77632708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56542763-C-T

77632720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 56542775-G-A

77633378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56543425-C-T

77633810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, undefined
orthologous variants: 56543924-C-T

77633829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, undefined
orthologous variants: 56543942-G-A

77634041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, undefined
orthologous variants: 56544135-A-G

http://identifiers.org/hco/15/GRCh38#77634418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#56544493-A-C

77634418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, undefined
orthologous variants: 56544493-A-G

77635826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56545756-G-T

77635835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56545765-C-T

77635872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56545802-C-T

77635876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56545806-A-G

77636108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56546180-T-C

77636787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56546872-C-T

http://identifiers.org/hco/15/GRCh38#77636797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56546900-C-A

http://identifiers.org/hco/15/GRCh38#77638295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56547336-C-A

77638295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56547336-C-G

77638987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56548112-T-C

77639055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56548190-T-C

77639172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56548237-A-T

77639297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56548356-G-T

77639528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56548584-G-A

77639657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56548709-G-C

77640188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56549183-T-C

77640220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56549213-A-G

77640263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56549300-G-A

77640273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56549310-T-C

77640355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56549360-G-A

77640363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56549368-G-C

77641350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56550224-G-C

http://identifiers.org/hco/15/GRCh38#77641670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56550544-C-A

77641690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56550564-T-C

http://identifiers.org/hco/15/GRCh38#77641762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56550632-C-A

77641762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56550632-C-G

77641762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56550632-C-T

77641956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56550769-G-T

77641957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56550770-G-A

77641957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56550770-G-T

77642041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56550842-G-A

77642542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56551179-C-T

77642947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56551498-C-T

http://identifiers.org/hco/15/GRCh38#77643002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56551556-A-C

77643224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56551852-T-C

77643278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56551919-C-G

77643885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56552368-A-G

77644438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56552867-C-T

77644447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56552876-A-G

77644510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56552947-G-A

77644867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553525-G-A

77645055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553690-G-A

77645186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553830-G-A

77645191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553836-G-A

http://identifiers.org/hco/15/GRCh38#77645223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56553892-C-A

77645223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553892-C-T

77645237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553906-C-T

77645271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56553950-T-C

77645582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554221-G-A

77645718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554350-C-G

77645718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554350-C-T

77645728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554360-G-A

77645728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554360-G-T

77645869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554494-G-A

77646108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554678-G-A

77646108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554678-G-T

77646159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554708-C-G

77646166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554715-G-C

77646251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56554804-C-G

http://identifiers.org/hco/15/GRCh38#77646470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56555029-C-A

77646527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56555101-G-T

77646576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56555137-G-A

77647034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56555511-G-A

77647128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56555551-C-T

77647145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56555568-C-T

77647328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56555758-G-A

77647336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56555765-A-G

77647380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56555892-G-A

77647455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56556095-G-T

77647464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56556104-G-A

77647640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56556407-G-A

77647734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56556498-A-G

77647871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56556609-G-A

77647993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56556728-C-T

77648037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56556760-G-A

77648076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56556774-G-A

77648076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56556774-G-T

http://identifiers.org/hco/15/GRCh38#77648084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56556782-C-A

77648261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56556938-G-A

77648478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56557051-C-T

http://identifiers.org/hco/15/GRCh38#77648490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56557063-A-C

77648490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56557063-A-G

http://identifiers.org/hco/15/GRCh38#77648495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56557068-C-A

http://identifiers.org/hco/15/GRCh38#77648520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56557093-C-A

77648584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56557126-T-C

77648817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56557349-G-A

77648817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56557349-G-T

77648819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56557351-G-A

77648837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56557369-G-A

77648837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56557369-G-T

77648869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56557401-C-T

77649384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56558088-G-T

77650560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559138-A-G

77651006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559474-G-C

77651006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559474-G-T

77651122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559872-T-A

77651134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56559896-T-C

77651465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56560223-C-G

77651708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56560788-G-T

77651732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56560812-G-T

77651859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56560929-G-A

http://identifiers.org/hco/15/GRCh38#77651954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56561018-C-A

77652001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56561063-T-C

77652095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56561126-A-G

77652275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56561305-G-T

http://identifiers.org/hco/15/GRCh38#77652297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56561324-C-A

77652795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56561634-C-T

77654207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56562749-G-A

77654390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56562913-G-T

77654438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56562961-C-G

77654574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56563079-G-A

77654713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56563163-C-T

77654870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56563304-T-C

77654870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56563304-T-G

77654968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56563396-A-G

77656043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56563800-C-T

77656372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56564099-C-T

77656502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56564227-C-T

77656564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56564289-G-A

77657371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56564998-G-A

77657573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56565193-C-T

77657592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56565210-G-T

77657601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56565219-C-T

77657976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56565578-G-A

77657980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56565582-G-A

77657980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56565582-G-C

77658082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56565661-G-A

77658209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56565786-C-T

http://identifiers.org/hco/15/GRCh38#77658752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56566156-C-A

77659083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56566282-G-C

77659154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56566321-C-T

77659413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56566575-C-G

77659413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56566575-C-T

77659754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56566865-T-A

77659873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56566966-T-C

77660211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567255-G-T

77660305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567295-G-T

77660313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567306-T-G

77660416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567399-C-G

77660416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56567399-C-T

77661079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56568224-C-G

http://identifiers.org/hco/15/GRCh38#77661201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56568313-C-A

http://identifiers.org/hco/15/GRCh38#77661972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56568894-C-A

77662035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56568936-G-A

77662388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56569225-G-A

77662619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56569304-T-C

77662758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56569434-C-T

77662963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56569548-G-C

77662977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56569562-G-A

77663327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56569867-G-A

77664006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570316-C-T

77664007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570317-G-A

77664154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570457-T-C

77664156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570459-T-C

77664157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570460-G-A

77664160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570463-T-C

77664164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570467-T-C

77664487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570736-A-G

77664528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570771-G-A

77664528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56570771-G-C

77664867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56571008-C-T

77664969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56571091-C-T

77665422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56571476-T-G

77665432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56571487-G-C

77665742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56571739-C-T

http://identifiers.org/hco/15/GRCh38#77665925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56571909-C-A

77665925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56571909-C-T

77666439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56572282-C-T

77666507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56572367-G-A

http://identifiers.org/hco/15/GRCh38#77666710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56572549-A-C

http://identifiers.org/hco/15/GRCh38#77666760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56572577-C-A

http://identifiers.org/hco/15/GRCh38#77666768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56572585-A-C

77666905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56573059-G-T

77666961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56573115-A-G

77666997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56573148-C-T

77667076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56573220-G-A

77667168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56573281-G-A

77667168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56573281-G-T

77667343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56573439-G-A

77667378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56573474-G-A

http://identifiers.org/hco/15/GRCh38#77667379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56573475-C-A

http://identifiers.org/hco/15/GRCh38#77667406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56573499-C-A

77667432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56573514-G-A

77667528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56573616-G-T

77667539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56573627-T-C

http://identifiers.org/hco/15/GRCh38#77667551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56573637-C-A

77667551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56573637-C-T

http://identifiers.org/hco/15/GRCh38#77667588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56573658-C-A

77667588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56573658-C-T

77667714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56573780-A-G

77667734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56573799-C-T

77667808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56573859-G-C

http://identifiers.org/hco/15/GRCh38#77668014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56573989-C-A

77668014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56573989-C-T

77668034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56574015-G-A

77668034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56574015-G-T

77668115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56574072-G-A

77668214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56574147-G-A

77668214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56574147-G-T

77668964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56574778-C-G

77669807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56575407-T-C

77669887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56575485-C-G

77669916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56575520-T-C

77670068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56575663-C-G

77670180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56575724-G-T

http://identifiers.org/hco/15/GRCh38#77670375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56575896-C-A

77670392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56575914-G-A

77670651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56576104-C-T

77670807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56576221-G-A

77671289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56576563-G-A

77671405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56576588-G-A

77671509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56576691-C-G

77671585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56576726-C-T

77672084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56577138-C-T

http://identifiers.org/hco/15/GRCh38#77672194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56577209-A-C

77672729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56577646-T-C

77672908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56577809-C-T

77672966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56577858-G-A

http://identifiers.org/hco/15/GRCh38#77673323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56578523-A-C

77673522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56578668-C-T

http://identifiers.org/hco/15/GRCh38#77673652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56578771-C-A

77673881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56579003-C-T

77673964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56579082-C-G

http://identifiers.org/hco/15/GRCh38#77674076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56579159-A-C

http://identifiers.org/hco/15/GRCh38#77674983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56579935-A-C

77675096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56580049-C-G

77675282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56580224-C-T

77675629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56580591-G-C

77675762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56580661-A-G

77675968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56580842-G-A

77676602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56581371-T-C

http://identifiers.org/hco/15/GRCh38#77676995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56581620-C-A

77677012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56581635-A-G

77677017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56581640-G-A

77677017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56581640-G-C

77677017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56581640-G-T

77677018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56581641-T-C

77677072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56581689-G-A

77677072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: 56581689-G-T

http://identifiers.org/hco/15/GRCh38#77677078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56581695-C-A

77677107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56581725-G-A

77677107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56581725-G-T

77677123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56581741-G-A

77677123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56581741-G-T

77677141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56581760-T-C

http://identifiers.org/hco/15/GRCh38#77677154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56581773-C-A

http://identifiers.org/hco/15/GRCh38#77677207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56581826-A-C

http://identifiers.org/hco/15/GRCh38#77677261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56581862-C-A

77677261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56581862-C-T

http://identifiers.org/hco/15/GRCh38#77677271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56581872-C-A

77677271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56581872-C-T

http://identifiers.org/hco/15/GRCh38#77677322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56581913-C-A

77677322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56581913-C-T

77677478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56582054-C-T

77677830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56582382-T-A

77677856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56582401-T-A

77677856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56582401-T-C

77677987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56582520-T-C

77678123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56582593-G-T

77678137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56582603-C-T

77678775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56583200-C-G

77678864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56583284-A-G

77678891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56583303-T-C

77678892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56583304-T-C

77679668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56584011-G-A

77680087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56584247-A-G

http://identifiers.org/hco/15/GRCh38#77680929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56585169-A-C

77680930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56585170-A-G

77680937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56585177-G-A

77681058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56585303-G-C

77681438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586393-C-T

77681546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586490-G-T

77681558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586502-T-C

77681558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586502-T-G

77681563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586507-T-G

77681834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586737-T-C

77681967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586856-C-T

77682030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56586916-C-T

77682228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56587100-G-T

77682483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56587375-T-A

77682549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56587440-T-A

77682640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56587516-T-G

77682646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56587524-T-C

77682680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56587553-C-T

77682770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56587599-G-A

77682846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56587670-G-A

77682846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56587670-G-T

77683396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56588202-C-G

77683406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56588214-A-G

77683563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56588369-C-T

77683584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56588393-T-C

77683717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56588545-G-T

77684060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56588706-G-A

77684303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56588846-T-C

77684473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56589012-C-T

77688707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56590638-G-A

77688835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56590765-G-A

77689528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56591167-T-C

77689597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56591225-A-G

77690029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56591572-C-G

77690146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56591706-T-G

77690326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56591910-C-T

77690522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56592070-T-C

77690568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56592117-G-A

77690568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56592117-G-C

77690610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56592286-G-T

77690613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56592289-T-A

77690613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56592289-T-C

http://identifiers.org/hco/15/GRCh38#77690721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56592405-C-A

77690721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 56592405-C-T

77690733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56592417-G-A

77690745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56592429-G-A

77690745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56592429-G-T

77690763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56592447-T-C

77690763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56592447-T-G

http://identifiers.org/hco/15/GRCh38#77690765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56592449-C-A

77690884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56592548-G-A

77690884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56592548-G-T

77690915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56592579-G-A

77690933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56592597-A-G

http://identifiers.org/hco/15/GRCh38#77692412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56593195-C-A

77692412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56593195-C-T

http://identifiers.org/hco/15/GRCh38#77692463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56593247-C-A

77692592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56593369-T-G

http://identifiers.org/hco/15/GRCh38#77692645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56593418-C-A

77692840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56593523-C-T

77693208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56593644-T-C

77693300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56593741-G-A

77693651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56594088-C-T

77694181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56596078-C-T

77694626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56596434-T-C

http://identifiers.org/hco/15/GRCh38#77695692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56596558-C-A

77695692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56596558-C-T

77695931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56596833-G-T

77696352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56597246-C-T

77696516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56597379-T-C

77697366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56598088-C-T

77697625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56598354-G-C

77698526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56599224-C-T

77698745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56599409-G-A

77698765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56599429-C-T

77698789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56599438-T-G

77698837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56599487-T-G

77699091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56599653-C-G

77699240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56599792-C-T

77699785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56599853-T-C

77700079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56600092-G-T

77700085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56600098-G-T

77700245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56600232-C-G

77700422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56600394-A-G

77700597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56600989-G-A

77700676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56601055-A-G

77701324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56601199-G-C

http://identifiers.org/hco/15/GRCh38#77701500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56601367-A-C

77702020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56601439-G-A

http://identifiers.org/hco/15/GRCh38#77703622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56601877-C-A

77703674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56601925-G-A

77704176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56603183-T-C

77704603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56603337-G-A

77704686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56603418-C-T

77704706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56603437-G-C

77704735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56603467-A-G

77705540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56604218-C-T

77705653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56604293-G-A

77705764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56604359-G-C

http://identifiers.org/hco/15/GRCh38#77705891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56604480-C-A

77706656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56605174-T-A

77706656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56605174-T-C

77706666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56605184-C-T

77706684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56605202-A-G

http://identifiers.org/hco/15/GRCh38#77706752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56605255-A-C

77706835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56605322-T-A

77707229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56605551-G-A

77707250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56605563-G-A

77707250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56605563-G-T

http://identifiers.org/hco/15/GRCh38#77707393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56605667-C-A

77707393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 56605667-C-T

http://identifiers.org/hco/15/GRCh38#77707641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56605891-C-A

77707641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56605891-C-T

77707693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56605941-C-T

77708241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56606470-T-C

77709522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56607311-G-A

77709545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56607333-T-G

77709622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56607407-C-T

http://identifiers.org/hco/15/GRCh38#77710427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56608437-C-A

77710498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56608510-G-C

http://identifiers.org/hco/15/GRCh38#77710621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56608632-A-C

77710690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56608695-T-C

77711412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56609329-C-G

77711467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56609385-G-A

77711698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56609686-A-T

http://identifiers.org/hco/15/GRCh38#77711724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56609714-A-C

77713406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56610480-A-G

http://identifiers.org/hco/15/GRCh38#77713612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56610652-C-A

77713765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56610785-C-T

77713855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56610870-G-A

77713905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56610915-T-C

http://identifiers.org/hco/15/GRCh38#77714023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56611016-C-A

77714023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56611016-C-T

http://identifiers.org/hco/15/GRCh38#77714403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56611377-C-A

77714403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56611377-C-T

77714408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56611382-C-T

http://identifiers.org/hco/15/GRCh38#77714475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56611441-C-A

77714558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56611566-T-C

77714800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56611878-G-A

http://identifiers.org/hco/15/GRCh38#77714871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56611946-C-A

77714871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56611946-C-G

77714871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56611946-C-T

77714987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612059-T-C

77715003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612075-C-T

77715252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612278-G-A

77715254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612280-G-A

77715456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612450-C-T

77715762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56612766-C-T

77715773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56612777-T-A

77716028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56612946-G-A

77716594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56613445-C-T

77716595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56613446-T-C

77716618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56613471-A-G

77716641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56613493-C-T

77716749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56613560-G-C

77716897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56613707-C-T

77716910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56613718-A-G

77717044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56613840-A-G

77717047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56613843-T-G

77717162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56613976-T-C

77718286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56614890-G-A

77718751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56615206-C-T

77718912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56615337-T-C

77718940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56615365-G-A

77719424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56615971-C-T

http://identifiers.org/hco/15/GRCh38#77719753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56616271-C-A

http://identifiers.org/hco/15/GRCh38#77719762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56616280-A-C

77720385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616751-T-A

77720410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56616777-T-G

77720780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617141-C-T

http://identifiers.org/hco/15/GRCh38#77720838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56617187-C-A

77721214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617493-G-A

77721235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617520-T-C

77721440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617702-C-T

77721497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617759-G-A

77721497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617759-G-T

77721613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617863-T-C

77721613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56617863-T-G

77721764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618020-T-C

77721767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618023-G-A

77721793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618043-G-A

http://identifiers.org/hco/15/GRCh38#77721895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56618136-A-C

77722663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56618890-T-C

http://identifiers.org/hco/15/GRCh38#77722856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56619186-C-A

77722902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619229-G-A

http://identifiers.org/hco/15/GRCh38#77722903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56619230-C-A

77723002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619312-G-A

77723026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619363-T-C

77723192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619451-A-G

77723417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619674-G-A

77723451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619699-C-G

77723451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619699-C-T

77723491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619736-G-A

77723825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619982-G-A

77723825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619982-G-C

77723825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56619982-G-T

77723865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620021-G-A

77723919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620072-A-G

77723957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620107-A-G

77724030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620179-G-A

77724449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620545-C-T

77724556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620628-C-G

77724754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620762-T-G

77724764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620772-C-T

http://identifiers.org/hco/15/GRCh38#77724948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56620916-C-A

77724948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620916-C-G

77724996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56620962-T-A

77725046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56621008-T-G

77725094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56621052-T-C

77729220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56623893-C-T

77729267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56623924-G-C

77729354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56623983-T-C

77729687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56624387-G-A

77729687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56624387-G-T

77729798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56624497-T-C

77729884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56624551-T-A

77729946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56624616-T-C

77730150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56625108-G-A

77730399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

77730712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

77730745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

77731040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

77731148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

77731337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56628720-G-A

77731356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56628745-C-T

http://identifiers.org/hco/15/GRCh38#77731381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56628769-C-A

77731575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56628918-G-A

77731635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56628943-C-G

77731774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56629065-G-A

77732243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56629390-C-T

77732447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56629580-G-A

77732447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56629580-G-T

77732753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56629867-T-C

http://identifiers.org/hco/15/GRCh38#77732979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#56630064-C-A

77732979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56630064-C-T

77733078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56630161-T-G

77733105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56630183-C-T

77733256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56630323-G-A

77733661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56630584-T-C

77733859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56630763-C-T

77733991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56630885-T-C

77734080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56631001-G-A

77734470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631224-C-T

77734738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631422-G-A

http://identifiers.org/hco/15/GRCh38#77734805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56631483-A-C

77734836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631499-C-T

http://identifiers.org/hco/15/GRCh38#77734964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56631570-C-A

77734964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631570-C-T

77735006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56631592-A-G

http://identifiers.org/hco/15/GRCh38#77735115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56631681-C-A

77735313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631847-G-A

77735350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631880-G-A

77735350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56631880-G-T

http://identifiers.org/hco/15/GRCh38#77735578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56632107-C-A

77735578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56632107-C-G

http://identifiers.org/hco/15/GRCh38#77735614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56632155-C-A

77735752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56632271-G-A

http://identifiers.org/hco/15/GRCh38#77735759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56632278-C-A

77736243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56632796-T-A

77736245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56632798-T-C

77736580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56633007-T-C

77736806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56633170-A-G

77736935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56633279-G-A

77737068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56633391-A-G

77737165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56633481-T-A

77737194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56633506-C-G

77737337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56633774-G-A

77737337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56633774-G-C

77737378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56633797-C-T

77737449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56633857-G-A

77737483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56633891-G-A

77737575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56633953-C-T

77737852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56634179-G-C

77737974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56634310-G-C

77738426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56634686-T-G

http://identifiers.org/hco/15/GRCh38#77738986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56635072-C-A

77739731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56635779-A-G

77740182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56636163-T-C

77741487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56636519-C-T

77741570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56636585-G-A

77741598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56636596-C-T

77741748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56636718-G-A

77741928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56636842-G-A

77742077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56636925-G-A

http://identifiers.org/hco/15/GRCh38#77742260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56637081-C-A

77742447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56637192-T-A

77742478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56637223-G-A

77742601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56637322-C-T

77742940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56637608-T-G

77743204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56637935-A-G

77743431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56638140-C-G

77743603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56638287-T-C

77743603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56638287-T-G

77743796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56638518-G-A

77743801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56638523-T-G

77744045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56638740-A-G

http://identifiers.org/hco/15/GRCh38#77744089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56638782-C-A

77746362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56639712-C-G

77746578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56639909-G-A

77746827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56640145-C-T

77746949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56640290-G-A

77746976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56640316-G-A

77747015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56640356-G-A

77747056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56640384-T-C

77747187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56640651-G-T

77747234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56640694-C-T

http://identifiers.org/hco/15/GRCh38#77747445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56640876-A-C

77747449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56640880-C-T

77747992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56641333-C-G

77747992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56641333-C-T

77748003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56641344-T-C

77748087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56641409-G-T

http://identifiers.org/hco/15/GRCh38#77748416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56641734-C-A

http://identifiers.org/hco/15/GRCh38#77749275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56641989-C-A

77749462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56642115-A-G

77749465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56642117-G-A

77749557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56642217-C-T

77749815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56642483-G-C

77749855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56642535-G-C

77750121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56642905-G-C

77750424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56643164-G-A

77750441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56643181-C-T

77750593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56643314-G-A

77751141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56643891-G-A

77751249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56643943-A-T

http://identifiers.org/hco/15/GRCh38#77751251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56643945-C-A

http://identifiers.org/hco/15/GRCh38#77751276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56643970-A-C

77751532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56644173-G-T

77752085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56644600-A-T

http://identifiers.org/hco/15/GRCh38#77752196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56644632-C-A

77752196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56644632-C-T

77752227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56644660-C-T

77752399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56644819-G-A

http://identifiers.org/hco/15/GRCh38#77752469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56644889-C-A

77752469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56644889-C-T

77752947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56645280-A-G

http://identifiers.org/hco/15/GRCh38#77753031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56645345-C-A

77753372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56645665-T-C

http://identifiers.org/hco/15/GRCh38#77753388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#56645681-A-C

77753411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56645700-G-A

77753423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56645710-C-T

77753557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56645818-T-C

77753590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56645851-G-A

http://identifiers.org/hco/15/GRCh38#77754125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56646376-A-C

77754204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646447-A-G

77754225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646468-A-G

77754233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646476-G-T

77754254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646497-G-A

77754258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646501-A-G

77754640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646878-T-G

77754693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56646931-C-G

77754830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56647039-C-T

http://identifiers.org/hco/15/GRCh38#77754879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56647082-C-A

77754879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56647082-C-G

77754879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56647082-C-T

77755116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56647295-C-T

77755331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56647508-C-T

77755894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648052-T-A

77755894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648052-T-C

77756129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648252-C-T

77756237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648304-C-T

http://identifiers.org/hco/15/GRCh38#77756358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56648400-C-A

77756358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648400-C-G

77756493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648516-C-G

http://identifiers.org/hco/15/GRCh38#77756594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56648613-A-C

77756594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648613-A-G

http://identifiers.org/hco/15/GRCh38#77756706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56648713-C-A

77756706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648713-C-T

77756813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648813-G-T

77756846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648848-A-G

http://identifiers.org/hco/15/GRCh38#77756859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56648861-C-A

77756989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648964-T-C

77757000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56648978-C-T

77757493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56649087-G-T

77757518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56649110-C-T

77757585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56649172-A-G

77757744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56649343-G-A

77757812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56649412-T-C

77757836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56649450-G-A

77757895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56649502-G-A

77757895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56649502-G-T

77758142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56649979-G-A

77758194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650030-G-C

77758342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650158-C-T

77758589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650355-C-G

77758619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650381-T-C

77758724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650487-A-G

77758815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650606-G-T

77758816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650607-A-G

http://identifiers.org/hco/15/GRCh38#77758864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56650650-A-C

77759175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650983-A-G

77759183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56650991-G-A

77759206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56651014-C-G

77759206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56651014-C-T

77759544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56651315-G-A

77759888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56651652-G-A

77759892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56651656-G-A

77759896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56651660-G-A

77759949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56651688-G-A

77759968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56651707-G-A

77759977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56651713-G-A

77759977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56651713-G-T

77760090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56651792-C-T

77760091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56651793-G-A

http://identifiers.org/hco/15/GRCh38#77760151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56651859-A-C

77760151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56651859-A-G

77761435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56652274-T-G

77761627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56652466-C-T

http://identifiers.org/hco/15/GRCh38#77761729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56652562-A-C

77761945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56652765-T-C

77762316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56653124-C-T

77762803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56653325-G-A

77763556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56654019-C-T

77763700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56654148-A-T

77764012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56654478-G-C

http://identifiers.org/hco/15/GRCh38#77764181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56654647-C-A

77764181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56654647-C-T

77764600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56655013-T-C

77764612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56655025-C-T

77764681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56655110-G-A

77764686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56655115-A-G

77764811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56655212-C-G

77764826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56655226-T-G

77765021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56655416-G-A

77766010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56656251-T-C

77766071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56656312-T-C

77767511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56658764-G-A

77767515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56658766-C-G

77767717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56658987-G-A

77767717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56658987-G-C

77767873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659145-C-G

77767910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659182-A-G

77768211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659465-G-A

77768326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659582-A-G

77768403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659655-C-T

77768659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56659897-G-A

77769371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56660579-T-C

77769431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56660631-C-T

http://identifiers.org/hco/15/GRCh38#77769485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56660685-A-C

77769614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56660811-G-A

77769614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56660811-G-C

77769849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661020-T-C

77769859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661030-G-A

77769859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661030-G-T

77769938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661070-T-G

77769972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661104-T-C

77770117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661225-G-C

http://identifiers.org/hco/15/GRCh38#77770164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56661271-C-A

77770164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661271-C-T

77771381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661444-G-A

77771506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661561-C-T

http://identifiers.org/hco/15/GRCh38#77771533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56661587-A-C

http://identifiers.org/hco/15/GRCh38#77771839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56661751-C-A

77771889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661803-G-A

77771889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56661803-G-C

77772187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662004-C-G

77772187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662004-C-T

http://identifiers.org/hco/15/GRCh38#77772220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56662038-C-A

http://identifiers.org/hco/15/GRCh38#77772246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56662056-C-A

http://identifiers.org/hco/15/GRCh38#77772250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56662060-C-A

77772417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662179-A-G

77772418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662180-T-A

77772420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662183-C-G

77772588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662321-G-A

77772588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662321-G-T

77773032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662751-G-A

77773258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56662968-T-C

http://identifiers.org/hco/15/GRCh38#77773529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56663202-C-A

77773599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56663270-G-T

http://identifiers.org/hco/15/GRCh38#77773625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56663295-C-A

77773739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56663375-T-C

77774332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56663751-C-T

77774363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56663773-C-T

77774563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56663980-C-T

77774569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56663986-C-T

77775003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56664361-G-A

77775010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56664368-G-A

77775280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56664541-C-T

77775300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56664559-A-G

http://identifiers.org/hco/15/GRCh38#77775679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56664867-C-A

77775837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56665036-G-A

77775887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56665087-G-A

77775887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56665087-G-T

77776006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56665215-G-A

http://identifiers.org/hco/15/GRCh38#77776251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56665468-C-A

77776414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56665636-G-A

77776674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56665805-A-G

77776718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56665839-A-G

77780188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56667654-G-A

77780279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56667729-G-A

http://identifiers.org/hco/15/GRCh38#77780481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56667895-A-C

77780595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56668009-T-C

77780772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56668419-T-C

77780774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56668421-C-T

77780786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56668450-C-T

77780856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56668521-A-G

77781168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56668781-T-C

77781596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56669147-T-C

77781788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56669308-G-A

77781831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56669361-G-A

77782210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56669748-C-T

77782314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56669836-A-G

77784437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56671780-C-T

77784792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56672121-G-T

http://identifiers.org/hco/15/GRCh38#77785047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#56672335-C-A

77785047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 56672335-C-T

77785112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56672400-G-A

http://identifiers.org/hco/15/GRCh38#77785122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#56672409-C-A

77785615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56672850-C-T

77785710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56672957-C-T

77785883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56673128-G-A

77786157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56673838-G-A

77786404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674009-C-G

77786451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674043-T-G

77786701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674288-G-C

77786820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674411-G-A

77786834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674426-G-T

http://identifiers.org/hco/15/GRCh38#77787013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56674570-C-A

77787013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56674570-C-T

http://identifiers.org/hco/15/GRCh38#77787135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56674670-C-A

77787135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674670-C-T

77787200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56674719-C-T

http://identifiers.org/hco/15/GRCh38#77787207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56674726-C-A

77787227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56674746-C-T

77787323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674768-C-T

77787327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674772-G-A

http://identifiers.org/hco/15/GRCh38#77787339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56674784-A-C

77787339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674784-A-G

http://identifiers.org/hco/15/GRCh38#77787366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56674819-C-A

77787366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674819-C-T

77787398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56674862-G-A

77788081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56675420-G-A

77788081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56675420-G-T

http://identifiers.org/hco/15/GRCh38#77788397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56675640-C-A

http://identifiers.org/hco/15/GRCh38#77788527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56675745-C-A

http://identifiers.org/hco/15/GRCh38#77788562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56675782-C-A

77790119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56677600-C-T

http://identifiers.org/hco/15/GRCh38#77790135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56677614-A-C

77790262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56677751-C-T

77790284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56677773-A-G

77790430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56677893-A-T

77790695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56678039-C-T

77790710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56678052-G-A

77790710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56678052-G-C

77790710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56678052-G-T

77791307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56679150-A-G

77791361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56679210-G-T

77791378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56679227-G-A

77791542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56679366-G-A

77791573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56679391-G-A

77791783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56679790-G-A

77791783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56679790-G-T

77792150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56680119-T-C

77792188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56680142-G-A

77792188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56680142-G-C

77792454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56680351-T-C

77792528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56680396-C-T

77792578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56680433-T-G

77792849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56680682-G-A

http://identifiers.org/hco/15/GRCh38#77792953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56680735-A-C

77793213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56680887-G-A

77793213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56680887-G-C

77794112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56681723-G-A

77795283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56682211-A-G

http://identifiers.org/hco/15/GRCh38#77795370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56682297-C-A

77795370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56682297-C-T

77795389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56682316-G-C

77795523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56682446-C-T

77795676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56682598-C-T

77796157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56683025-G-A

77796157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56683025-G-T

77796287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56683075-T-C

77796458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56683226-A-G

77796688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56683431-T-C

77796695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56683434-C-T

77797347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56683798-G-A

77797818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56684175-G-C

77798032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56684368-G-A

77798171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56684507-G-T

77798225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56684562-G-A

77798267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56684607-C-T

77798629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56684956-G-A

77798629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56684956-G-T

77798702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56685015-G-A

77799022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56685234-A-T

77799036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56685245-A-G

77799071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56685276-T-G

77799894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56686567-G-T

77799965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56686637-G-A

77800300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56686924-C-T

77800585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56687175-A-T

77801035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56687619-T-C

77801278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56687870-A-G

77801318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56687910-T-A

77801347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56687939-G-A

77801462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56688033-C-T

77801501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56688072-G-C

77801524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56688107-G-A

http://identifiers.org/hco/15/GRCh38#77801833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56688362-A-C

77802069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56688522-G-A

77802083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56688536-G-A

77802162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56688606-T-G

77802221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56688641-G-A

77802293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56688704-T-C

77802309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56688719-C-G

77802558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56689045-C-G

77802754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56689255-G-A

http://identifiers.org/hco/15/GRCh38#77802880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56689643-C-A

http://identifiers.org/hco/15/GRCh38#77802928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56689768-C-A

77802968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56689808-C-G

77803034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56689863-G-C

77803055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56689886-G-A

77803058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56689889-T-C

77803196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56690014-T-G

77803225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56690041-C-G

http://identifiers.org/hco/15/GRCh38#77803263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56690076-A-C

77803949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56690152-C-G

77803972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56690176-G-T

77803977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56690181-G-A

77804168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56690340-T-C

77804261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56690424-G-A

77804261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56690424-G-C

77804643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56690769-G-T

77804701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56690813-C-G

77804840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56690943-C-T

77804883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56690974-G-A

77804901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56690992-G-T

77804920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56691015-T-C

77805329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56691397-C-G

77805329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56691397-C-T

77805693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56691623-T-C

77805954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56691802-C-T

77806058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56691904-T-A

77806120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56691969-T-C

77806131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56691980-G-A

77806131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56691980-G-T

77806149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56691998-C-T

77806270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56692118-C-T

77806316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56692164-A-G

77806412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56692269-G-A

77806425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56692282-G-A

77806425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56692282-G-C

http://identifiers.org/hco/15/GRCh38#77806483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56692320-C-A

77806483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56692320-C-T

http://identifiers.org/hco/15/GRCh38#77806741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56692549-C-A

77806827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56692621-C-G

http://identifiers.org/hco/15/GRCh38#77806917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56692711-C-A

77806936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56692730-G-T

77806996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56692770-T-A

77806996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56692770-T-C

http://identifiers.org/hco/15/GRCh38#77807062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56692826-C-A

77807446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56693153-T-C

77807511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56693216-T-C

77807685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56693369-G-A

77807817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56693505-G-A

77807826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56693514-G-A

77808401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56693936-T-G

77808410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56693945-C-T

77808506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56693993-C-T

77808584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56694063-G-A

77808944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56694352-A-G

77809107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56694503-G-A

77809254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56694613-C-T

77809269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56694628-C-T

77809347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56694692-C-T

77809632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56694895-G-A

77809762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56694968-C-T

77809775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56694978-C-T

77809907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56695085-C-T

77810056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56695199-A-G

77810165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56695270-C-G

77811103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56695510-G-A

77811103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56695510-G-C

77811176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56695583-C-T

77811428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56695861-C-G

77811562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56699414-G-T

http://identifiers.org/hco/15/GRCh38#77811578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56699399-C-A

77811578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56699399-C-T

77811926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56696224-A-T

77811971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56696261-C-G

77812419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56696650-T-C

77812472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56696702-G-A

77812694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56696899-C-T

77812944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56697144-G-A

77812944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56697144-G-T

77813489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56697367-G-A

77813489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56697367-G-C

77813489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56697367-G-T

77813524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56697376-T-C

77813740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56697575-G-A

http://identifiers.org/hco/15/GRCh38#77813749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56697584-C-A

77813749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56697584-C-T

http://identifiers.org/hco/15/GRCh38#77814330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56698052-C-A

77814471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56698605-C-G

77814787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56698921-C-T

77814869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56699001-G-A

77815012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56699138-G-C

77815191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56699317-C-T

77815324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56699439-A-G

77815344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56699459-G-A

http://identifiers.org/hco/15/GRCh38#77815359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56699475-A-C

77815685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56699710-G-A

77815685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56699710-G-C

http://identifiers.org/hco/15/GRCh38#77815753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56699891-C-A

77815771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56699919-G-A

77816546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56700712-G-C

77817288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56701454-G-C

77817424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56701578-C-T

77817485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56701620-G-C

77817485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56701620-G-T

77817806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56701998-C-T

77817880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56702065-G-A

77818192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56702343-G-C

http://identifiers.org/hco/15/GRCh38#77818463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56702444-C-A

77818463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56702444-C-T

77818751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56702753-C-T

77818814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56702813-T-C

77818994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56702994-G-A

77819117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56703121-G-A

77819117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56703121-G-T

77819201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56703205-A-G

77819221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56703224-G-A

77819221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56703224-G-C

77819221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56703224-G-T

77819247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56703250-G-T

http://identifiers.org/hco/15/GRCh38#77819268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56703271-C-A

77819268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56703271-C-T

http://identifiers.org/hco/15/GRCh38#77819336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#56703339-C-A

77819336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 56703339-C-T

77819373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56703376-C-T

77819375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56703378-C-G

77819375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56703378-C-T

77819416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56703419-G-A

77819435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 56703438-A-G

77819707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56703759-C-T

77819726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56703779-G-T

77819746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56703799-C-T

77819770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56703823-C-T

77819902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56703934-G-A

77819902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56703934-G-T

77819992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56704017-T-C

77820053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 56704076-G-A

77820069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56704092-G-A

77820069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56704092-G-C

77820069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56704092-G-T

http://identifiers.org/hco/15/GRCh38#77820421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#56704392-C-A

77820452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56704431-G-T

77820697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56704679-G-T

77820851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56704769-G-A

77820851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21205
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56704769-G-T