71929691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110397230-G-A

71929691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110397230-G-C

71929885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110397037-T-A

71929885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110397037-T-C

71929951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110396978-C-G

71930135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 110395894-C-T

http://identifiers.org/hco/16/GRCh38#71930273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110395785-C-A

71930273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110395785-C-T

71930288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110395767-T-C

71930399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110395679-C-T

71930454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110395629-G-C

71930464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110395624-T-A

71930464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110395624-T-C

71930464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110395624-T-G

71930545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110395570-G-C

http://identifiers.org/hco/16/GRCh38#71930570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110395546-C-A

71930570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110395546-C-T

71930578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110395538-A-G

71933269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110394431-G-A

71933283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110394417-G-T

71933345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110394371-G-A

71933345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110394371-G-T

71933346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110394370-T-G

http://identifiers.org/hco/16/GRCh38#71933362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110394354-C-A

71933362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110394354-C-G

71933362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110394354-C-T

71933367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110394330-T-A

http://identifiers.org/hco/16/GRCh38#71933405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110394292-A-C

71933405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110394292-A-G

71933405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110394292-A-T

71933426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: synonymous variant
orthologous variants: 110394252-T-C

71933430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110394248-T-A

71933430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110394248-T-G

71933475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110394203-A-G

71933592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110394097-T-C

71933665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110394030-T-C

71933780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393968-T-A

71933780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393968-T-G

71933826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393891-T-A

71933826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393891-T-C

71933834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393883-T-C

71934036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: stop gained
orthologous variants: 110393694-C-T

http://identifiers.org/hco/16/GRCh38#71934054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110393676-A-C

http://identifiers.org/hco/16/GRCh38#71934146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110393579-A-C

http://identifiers.org/hco/16/GRCh38#71934150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110393575-A-C

71934213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393515-G-A

71934213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393515-G-T

71934262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393474-T-A

http://identifiers.org/hco/16/GRCh38#71934263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110393473-A-C

71934263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393473-A-G

71934263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393473-A-T

71934264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393472-T-A

71934264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393472-T-C

71934379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393398-C-T

71934385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393392-G-C

71934484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393332-A-G

71934530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393294-C-G

http://identifiers.org/hco/16/GRCh38#71934735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110393035-C-A

71934735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393035-C-G

71934735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110393035-C-T

71935090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110392543-A-G

71935264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110392418-G-A

71935264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110392418-G-T

71935269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110392413-G-T

http://identifiers.org/hco/16/GRCh38#71935286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110392392-A-C

http://identifiers.org/hco/16/GRCh38#71935306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110392375-A-C

71935307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110392374-A-G

http://identifiers.org/hco/16/GRCh38#71935405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110392291-A-C

71935457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110392239-G-C

71935463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110392233-A-G

71935532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110392164-G-A

http://identifiers.org/hco/16/GRCh38#71935535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110392161-C-A

71935535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110392161-C-G

71935535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110392161-C-T

71937314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110391141-A-G

71937328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110391127-G-C

71937437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110391025-C-T

71937452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110391010-G-C

http://identifiers.org/hco/16/GRCh38#71937501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110390973-C-A

71937501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110390973-C-G

71937501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110390973-C-T

71937511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110390963-T-C

71937540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110390930-G-A

71937540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110390930-G-T

71937562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110390908-G-T

71937603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110390871-A-G

71939814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110389926-A-G

71942522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110383210-G-C

71942522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110383210-G-T

http://identifiers.org/hco/16/GRCh38#71942585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110383152-C-A

71942585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 110383152-C-T

71942654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant
orthologous variants: 110383091-G-C

71942682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant
orthologous variants: 110383059-C-G

71942716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant
orthologous variants: 110383033-G-C

http://identifiers.org/hco/16/GRCh38#71942759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/8/GRCm39#110382991-A-C

71942759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 110382991-A-G

71942768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 110382982-G-C

71942768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 110382982-G-T

71942874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110382891-T-C

71943014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: synonymous variant
orthologous variants: 110382751-G-A

71943014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: synonymous variant
orthologous variants: 110382751-G-C

71943014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: synonymous variant
orthologous variants: 110382751-G-T

71943048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110382717-G-A

71943882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110382379-T-A

71943882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110382379-T-C

71943882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110382379-T-G

http://identifiers.org/hco/16/GRCh38#71943941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110382332-C-A

71943941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110382332-C-G

71943941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110382332-C-T

71943998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110382279-G-A

71943998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110382279-G-T

71944044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 110382234-G-A

71944044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 110382234-G-C

71944122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110382159-A-T

71944152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 110382129-A-G

71944153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense_variant, splice_acceptor_variant
orthologous variants: 110382128-C-G

71944153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense_variant, splice_acceptor_variant, synonymous_variant
orthologous variants: 110382128-C-T

71944155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant, splice_region_variant, stop_gained
orthologous variants: 110382126-G-A

71944155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant, splice_region_variant, stop_gained
orthologous variants: 110382126-G-C

71944156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant, splice_region_variant, synonymous_variant
orthologous variants: 110382125-A-G

http://identifiers.org/hco/16/GRCh38#71944180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110382100-A-C

71944279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110382006-G-T

http://identifiers.org/hco/16/GRCh38#71944284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110382001-A-C

71944300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110381985-G-A

71944300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110381985-G-T

71944366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110381921-C-T

71944446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110381897-G-A

71944446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110381897-G-C

71944471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110381865-A-G

71944508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110381809-C-T

71946424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110377943-C-T

71946604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110377810-G-C

71946676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110377741-C-G

71946809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110377639-G-A

71946809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110377639-G-C

http://identifiers.org/hco/16/GRCh38#71947378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110377538-A-C

71947378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110377538-A-G

71947386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110377530-G-A

71947386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110377530-G-C

71947386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110377530-G-T

http://identifiers.org/hco/16/GRCh38#71947458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110377462-A-C

71947546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant
orthologous variants: 110377374-G-A

71947546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant
orthologous variants: 110377374-G-T

71947554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant
orthologous variants: 110377366-C-T

71947566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant
orthologous variants: 110377354-G-A

71947577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 110377343-T-C

71947638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110377281-A-G

http://identifiers.org/hco/16/GRCh38#71947654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110377265-A-C

71947654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110377265-A-G

71947654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110377265-A-T

71949760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110375391-G-A

71949760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110375391-G-T

71949793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110375358-T-A

71949847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110375304-G-A

71949892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110375259-A-G

71949983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110375168-C-T

71950009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110375142-G-A

71950009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110375142-G-C

71950067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110375088-G-C

71950067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110375088-G-T

71950073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110375082-G-A

71950073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110375082-G-T

71950169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 110374989-A-G

http://identifiers.org/hco/16/GRCh38#71950199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110374959-A-C

http://identifiers.org/hco/16/GRCh38#71950307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110374851-A-C

71950347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374808-G-A

71950347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374808-G-C

71950347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374808-G-T

71950370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374785-G-C

71950370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374785-G-T

71950376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374779-G-T

71950388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374767-A-G

71950407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374748-A-G

http://identifiers.org/hco/16/GRCh38#71950414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110374741-C-A

71950451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374709-G-A

71950451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374709-G-T

71950481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374681-G-C

71950498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374666-G-T

http://identifiers.org/hco/16/GRCh38#71950580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110374581-A-C

71950581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374580-G-A

http://identifiers.org/hco/16/GRCh38#71950633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110374538-C-A

71950671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374506-A-G

71950674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374503-G-A

71950693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374489-G-C

71950695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374487-A-G

71951453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374371-A-T

http://identifiers.org/hco/16/GRCh38#71951455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110374369-C-A

71951455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374369-C-T

71951495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374332-A-G

71951508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374315-T-A

71951508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374315-T-C

71951508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374315-T-G

71951628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 110374191-G-A

71951628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant
orthologous variants: 110374191-G-C

71951628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant
orthologous variants: 110374191-G-T

71951668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 110374151-C-G

71951677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 110374142-G-A

71951677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 110374142-G-C

71951677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 110374142-G-T

71951680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 110374139-T-C

71951755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374064-G-A

71951755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374064-G-C

71951755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374064-G-T

71951795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374023-G-C

71951795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110374023-G-T

71951962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110373861-A-G

71951984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110373837-C-G

71951984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110373837-C-T

http://identifiers.org/hco/16/GRCh38#71952157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110373673-A-C

71952158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110373672-C-T

http://identifiers.org/hco/16/GRCh38#71952189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110373644-C-A

71952191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110373642-T-C

71952191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110373642-T-G

http://identifiers.org/hco/16/GRCh38#71952894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110373603-C-A

71952894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 3_prime_UTR_variant, splice_region_variant, synonymous_variant
orthologous variants: 110373603-C-T

71952931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110373563-G-C

71952931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense_variant, stop_gained
orthologous variants: 110373563-G-T

71953037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant
orthologous variants: 110373460-T-C

http://identifiers.org/hco/16/GRCh38#71953103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110373394-A-C

71953103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110373394-A-G

71953103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110373394-A-T

71953108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110373389-T-A

71953108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110373389-T-C

http://identifiers.org/hco/16/GRCh38#71953161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110373369-C-A

71953172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110373357-T-A

71954117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110373109-T-C

71954149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110373077-A-G

71954230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense_variant, undefined
orthologous variants: 110372996-T-C

71954230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense_variant, undefined
orthologous variants: 110372996-T-G

http://identifiers.org/hco/16/GRCh38#71954271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110372955-C-A

71954326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, undefined
orthologous variants: 110372900-A-G

71954386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, undefined
orthologous variants: 110372661-G-C

71954386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, undefined
orthologous variants: 110372661-G-T

71954397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, undefined
orthologous variants: 110372194-A-T

71954408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110372183-T-C

71954439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110372152-G-A

71954439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110372152-G-C

71954439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110372152-G-T

71963274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110367473-A-G

71963315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: synonymous_variant, undefined
orthologous variants: 110367432-A-T

71963859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110367212-G-C

71963894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110367173-A-G

71963976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110367080-C-T

71967278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110365330-T-G

71967321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 110365287-A-G

71967325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110365283-G-A

71967325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110365283-G-C

http://identifiers.org/hco/16/GRCh38#71967343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110365265-A-C

71967343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110365265-A-G

71967382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110365226-G-A

71967382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110365226-G-T

71967388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110365220-A-G

71967439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110365194-G-A

71967439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110365194-G-T

71967450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110365183-T-C

71967880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110365082-A-G

71968105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110364876-G-T

71968108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110364873-T-A

71968108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110364873-T-C

71968109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110364872-G-T

71968120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110364863-A-G

http://identifiers.org/hco/16/GRCh38#71968143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110364841-C-A

71968143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110364841-C-T

71968269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110364739-T-C

71968275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110364733-C-G

71968275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110364733-C-T

71968293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110364711-C-T

71968461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110364550-A-G

71968477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110364537-G-A

71968478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110364536-C-T

http://identifiers.org/hco/16/GRCh38#71969781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110363136-C-A

71969781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110363136-C-T

http://identifiers.org/hco/16/GRCh38#71969886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110363039-C-A

71969886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110363039-C-G

71969886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110363039-C-T

71970026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110362899-A-G

71970043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: synonymous variant
orthologous variants: 110362882-G-A

71970124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110362801-C-G

71970124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110362801-C-T

71973237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110362107-G-T

http://identifiers.org/hco/16/GRCh38#71973243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110362101-C-A

71973243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110362101-C-T

71973284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110362069-A-G

71973405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: synonymous variant
orthologous variants: 110361957-G-A

71973405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110361957-G-T

http://identifiers.org/hco/16/GRCh38#71973406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110361956-C-A

71973406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110361956-C-T

71973421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110361941-G-A

71973596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110361767-T-A

71973596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110361767-T-C

71973622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110361744-G-C

71973622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110361744-G-T

http://identifiers.org/hco/16/GRCh38#71977236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110360031-C-A

71977236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 110360031-C-T

http://identifiers.org/hco/16/GRCh38#71977255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110360012-C-A

71977255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: synonymous variant
orthologous variants: 110360012-C-T

71977284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110359983-G-A

71977284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110359983-G-C

71977284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110359983-G-T

71977293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110359974-T-C

71977312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: synonymous variant
orthologous variants: 110359955-C-T

71977319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110359948-A-T

71977343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110359924-G-T

71977540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359766-G-A

71977540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359766-G-C

71977540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359766-G-T

71977565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359757-T-A

71977565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359757-T-C

http://identifiers.org/hco/16/GRCh38#71977591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110359731-C-A

71977591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359731-C-G

71977591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359731-C-T

71977592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359730-T-G

71977866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359578-C-T

71977914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359551-A-G

71978026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359466-A-G

71978052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359441-G-C

http://identifiers.org/hco/16/GRCh38#71978200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110359378-C-A

71978200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359378-C-T

71978202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359374-G-A

71978202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359374-G-C

71978202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359374-G-T

71978207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359369-A-G

71978208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359368-G-A

71978208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359368-G-T

71978209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110359367-A-G

71979606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110358562-T-C

71979729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110358089-G-A

71979729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110358089-G-T

71979760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110358059-C-G

71979760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110358059-C-T

71979762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110358057-G-C

71979762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110358057-G-T

71979838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110357981-G-A

71979838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: stop gained
orthologous variants: 110357981-G-T

http://identifiers.org/hco/16/GRCh38#71979850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110357969-A-C

71979862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110357957-G-A

71979892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110357927-G-A

71979892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110357927-G-C

71979910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 110357909-T-A

71979910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 110357909-T-C

71979933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110357890-G-A

71979933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110357890-G-C

http://identifiers.org/hco/16/GRCh38#71979978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110357845-A-C

71979992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110357831-C-T

71980065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: stop gained
orthologous variants: 110357754-G-A

71980065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110357754-G-T

71980153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110357666-A-G

71980153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110357666-A-T

http://identifiers.org/hco/16/GRCh38#71980230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110357605-C-A

71980230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110357605-C-G

71980230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110357605-C-T

71980232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110357603-G-C

71980232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110357603-G-T

71980262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110357574-G-A

71980275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110357561-T-A

71980275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110357561-T-C

71980286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110357551-G-A

http://identifiers.org/hco/16/GRCh38#71981100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110356411-C-A

71981271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110356253-G-A

71981704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110355815-C-T

http://identifiers.org/hco/16/GRCh38#71981955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110355540-A-C

71981955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110355540-A-G

71981992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110355504-A-G

71981992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110355504-A-T

71982013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110355485-A-T

71982018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110355480-G-A

71982018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110355480-G-C

71982018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110355480-G-T

http://identifiers.org/hco/16/GRCh38#71982032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110355469-C-A

71982060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 110355441-G-A

http://identifiers.org/hco/16/GRCh38#71982072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110355429-C-A

71982072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, missense_variant
orthologous variants: 110355429-C-T

71982085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 110355416-G-A

71983027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110354636-G-A

71983329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110354457-T-G

71983413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110354352-C-T

71986170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110351169-T-C

71986170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110351169-T-G

71986199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110351138-G-T

71986206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110351131-A-G

71986669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110349580-A-T

71990162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110348465-T-C

71990183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110348444-T-C

71990183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110348444-T-G

71990193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110348434-T-C

71990244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110348379-C-T

71990267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110348358-G-C

71990267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110348358-G-T

http://identifiers.org/hco/16/GRCh38#71990286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110348339-A-C

http://identifiers.org/hco/16/GRCh38#71990347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110348278-C-A

71990347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110348278-C-G

71990347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110348278-C-T

71993328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110347061-G-C

71993328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110347061-G-T

http://identifiers.org/hco/16/GRCh38#71993330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110347059-C-A

71993330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 110347059-C-T

71993331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 110347058-A-G

71993377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110347013-T-A

71993377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110347013-T-C

71993402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110346983-T-C

71998273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 110343090-A-T

71998299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: synonymous variant
orthologous variants: 110343064-G-A

71998299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110343064-G-C

71998734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110342667-A-G

71998816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110342598-T-A

71998924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110342493-T-A

71999040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110342234-G-A

71999048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110342226-G-C

71999073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110342180-C-T

71999080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110342159-G-T

71999142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110342015-C-G

71999209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110341948-T-C

71999256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110341908-G-A

71999556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110341576-G-T

71999560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110341558-T-A

71999600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110341533-A-G

71999600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110341533-A-T

http://identifiers.org/hco/16/GRCh38#71999671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110341466-C-A

71999671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: intron variant
orthologous variants: 110341466-C-T

71999704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110341433-T-A

71999704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110341433-T-C

71999900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110341237-C-G

71999900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110341237-C-T

71999915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110341222-C-G

71999915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110341222-C-T

71999925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: synonymous variant
orthologous variants: 110341200-A-G

71999961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: synonymous variant
orthologous variants: 110341164-T-C

71999961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: synonymous variant
orthologous variants: 110341164-T-G

71999968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: missense variant
orthologous variants: 110341157-T-A

71999998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 5 prime UTR variant
orthologous variants: 110341059-G-A

71999998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 5 prime UTR variant
orthologous variants: 110341059-G-C

72000006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 5 prime UTR variant
orthologous variants: 110341051-G-A

72000006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 5 prime UTR variant
orthologous variants: 110341051-G-T

72000013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 5 prime UTR variant
orthologous variants: 110341044-T-G

72000014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 5 prime UTR variant
orthologous variants: 110341043-T-C

72000096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 5 prime UTR variant
orthologous variants: 110340959-T-A

72000096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 5 prime UTR variant
orthologous variants: 110340959-T-C

72000191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21716
most severe consequence: 5 prime UTR variant
orthologous variants: 110340880-T-C