http://identifiers.org/hco/8/GRCh38#26514051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67148503-A-C

26514051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 67148503-A-G

26514051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 67148503-A-T

26514055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 67148499-G-A

26514055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 67148499-G-T

26514127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5 prime UTR variant
orthologous variants: 67148433-G-C

26514127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5 prime UTR variant
orthologous variants: 67148433-G-T

http://identifiers.org/hco/8/GRCh38#26514296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67148262-C-A

26514305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5 prime UTR variant
orthologous variants: 67148253-C-T

26514530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: missense variant
orthologous variants: 67148026-C-G

26514530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: missense variant
orthologous variants: 67148026-C-T

26514539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: missense variant
orthologous variants: 67148017-G-A

26514539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: missense variant
orthologous variants: 67148017-G-C

26514715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67147860-G-A

26514715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67147860-G-T

26514719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67147856-G-A

26514719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67147856-G-C

26514719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67147856-G-T

http://identifiers.org/hco/8/GRCh38#26514727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67147848-C-A

26514727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67147848-C-T

http://identifiers.org/hco/8/GRCh38#26515259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67147305-C-A

26515749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67146832-C-T

26516537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67145489-G-A

26516777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67145259-G-A

26516970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67145093-G-T

26519632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67141242-C-T

26519658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67141215-T-C

26519697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67141177-T-C

26519928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67140951-A-G

26520825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67140275-G-A

26520934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67140213-A-G

26521904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67139253-C-T

http://identifiers.org/hco/8/GRCh38#26522824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67138443-A-C

26522824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67138443-A-G

26523149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67138088-A-G

26523202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67138035-T-A

http://identifiers.org/hco/8/GRCh38#26523451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67137821-C-A

26530375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67135972-G-C

26531083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67130897-A-T

26531300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67130677-G-A

26531381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67130603-A-G

26531536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67130487-A-G

26531653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67130436-G-A

26531750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67130379-A-G

26531873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67130306-G-A

26532101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67130075-G-C

26532266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67129942-T-G

26532328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67129889-G-T

26535259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67125467-G-T

26535401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67125328-T-C

26535584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67124925-C-G

26535639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67124878-T-A

http://identifiers.org/hco/8/GRCh38#26537345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67121024-A-C

26537407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67120936-T-G

26537416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67120927-C-T

26537481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67120863-A-T

26537638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67120594-G-T

26537650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67120581-T-C

http://identifiers.org/hco/8/GRCh38#26537689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67120533-C-A

26537689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67120533-C-T

26538053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67120173-A-G

26538059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67120167-G-T

26538239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67119988-G-A

26538351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67119881-G-C

26564392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67113697-C-T

26570271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67111937-A-T

26570374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67111827-A-G

26570409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67111792-G-A

26570409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67111792-G-T

26570410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67111791-G-T

26570466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67111737-C-T

26570955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67111435-G-A

26571152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67111250-T-G

26571224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67111181-G-A

26571541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67110884-T-C

26571559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67110866-G-A

26571882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67110565-C-T

26571895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67110553-C-T

26572043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67110426-T-C

26572116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67110347-C-G

http://identifiers.org/hco/8/GRCh38#26572168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#67110293-A-C

26572227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67110244-C-T

26572335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67110128-G-A

http://identifiers.org/hco/8/GRCh38#26573165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67109494-A-C

26573188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67109476-G-A

26573188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67109476-G-C

26573205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67109454-G-A

26573205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67109454-G-T

26573249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67109399-G-A

26573249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67109399-G-C

26574294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67108952-G-T

26574296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67108950-G-T

http://identifiers.org/hco/8/GRCh38#26574297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67108949-C-A

26574297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67108949-C-T

26574318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67108932-G-A

26575388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67108566-G-A

26575496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67108466-T-C

26575532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67108420-G-A

26575825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67108152-G-A

26575877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67108098-C-T

26576168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67107448-T-C

26576186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67107433-T-C

26576186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67107433-T-G

26576246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67107373-A-T

26576352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67107253-T-A

http://identifiers.org/hco/8/GRCh38#26576648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67107021-A-C

26576886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67106873-C-T

http://identifiers.org/hco/8/GRCh38#26577053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#67106743-C-A

26577053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67106743-C-T

26577088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67106700-T-C

http://identifiers.org/hco/8/GRCh38#26577203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#67106660-C-A

26577203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67106660-C-G

26577203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67106660-C-T

http://identifiers.org/hco/8/GRCh38#26577269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#67106646-A-C

26577269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67106646-A-G

26577346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 67106626-G-A

26577346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 67106626-G-T

26577721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67106299-G-A

26577721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67106299-G-T

http://identifiers.org/hco/8/GRCh38#26577814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#67106214-C-A

26577814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67106214-C-T

26578044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 67106008-T-G

http://identifiers.org/hco/8/GRCh38#26578187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67105889-A-C

26578187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 67105889-A-G

26578199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 67105874-C-T

http://identifiers.org/hco/8/GRCh38#26578681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67105408-C-A

26578681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67105408-C-G

26578681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67105408-C-T

http://identifiers.org/hco/8/GRCh38#26578688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67105401-A-C

26579089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67105061-C-G

26579161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67104977-G-A

26579660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67104527-C-G

26579660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67104527-C-T

26580013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67104183-G-A

26580602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67103681-G-T

26581055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67103214-G-A

26581722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67102870-G-T

26581731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67102861-G-T

26581765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67102829-T-A

26581765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67102829-T-C

26581809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67102785-T-G

26581836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67102758-T-C

http://identifiers.org/hco/8/GRCh38#26581901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67102692-C-A

26581901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67102692-C-T

http://identifiers.org/hco/8/GRCh38#26581908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67102685-C-A

26581908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67102685-C-T

26581926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67102661-T-C

http://identifiers.org/hco/8/GRCh38#26581975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67102611-C-A

26581975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 67102611-C-T

26582023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 67102563-T-C

26582064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 67102522-G-A

26582064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 67102522-G-C

26582074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67102459-A-T

26582082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67102451-A-G

26582097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67102420-T-C

26582156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67102282-T-C

26582220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67102220-G-A

26582701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67101554-C-T

26583137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67101121-T-C

26583326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67100708-T-C

26583583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67100443-C-T

http://identifiers.org/hco/8/GRCh38#26583692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67100213-C-A

26583709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67100196-G-A

26583709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67100196-G-C

26583709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67100196-G-T

26583779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67100124-C-T

26583923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: missense variant
orthologous variants: 67099980-T-C

26584003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67099902-T-A

26584008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67099897-G-A

26584053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67099852-G-A

26584113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67099800-T-A

26584113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67099800-T-G

26584118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67099795-A-G

26584385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67099574-T-G

26584616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67099507-T-C

26584764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67099380-C-G

26584970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67099119-C-T

26585174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67098925-C-T

26585398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67098751-C-G

26585436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67098715-G-A

26585540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67098657-G-T

26586303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67098060-G-A

26586303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67098060-G-C

26586400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67098023-C-T

26586427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67097997-C-T

26586450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67097958-C-T

26586505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67097908-C-G

26586505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67097908-C-T

26586613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67097809-C-G

26586613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67097809-C-T

26587282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67097097-A-G

26587364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67097039-C-T

26587552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67096880-T-A

26587573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67096862-C-T

26587593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67096837-A-G

26587626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67096805-G-A

26587626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67096805-G-C

26587764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67096640-C-T

26589062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67095443-C-T

26589085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67095423-C-T

http://identifiers.org/hco/8/GRCh38#26589128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67095371-C-A

26589128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67095371-C-G

26589128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67095371-C-T

26589147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67095355-C-G

26589158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67095351-C-G

26589343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67095195-G-A

http://identifiers.org/hco/8/GRCh38#26589404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67095141-C-A

26589404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67095141-C-G

26589404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67095141-C-T

26589823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67094795-G-A

http://identifiers.org/hco/8/GRCh38#26589827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67094791-C-A

26589928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67094723-A-G

26589928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67094723-A-T

26590060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67094614-C-T

http://identifiers.org/hco/8/GRCh38#26590271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67094413-C-A

26590314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67094370-T-A

26590314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67094370-T-C

26590796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67094196-G-A

http://identifiers.org/hco/8/GRCh38#26591073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67094056-C-A

26591255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67093870-T-A

26592838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67093368-T-G

26593955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67092358-G-A

26594345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67091965-T-C

26594454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67091869-C-T

26594608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67091256-T-C

26594662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67091189-C-T

http://identifiers.org/hco/8/GRCh38#26594844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67091019-A-C

26595469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67090940-A-G

26595855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67090549-C-T

26595924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67090514-G-A

26596051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67090406-T-C

26596323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67090234-T-G

26596660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67089956-C-T

http://identifiers.org/hco/8/GRCh38#26596756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67089795-C-A

26596756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67089795-C-G

26596756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67089795-C-T

26597231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67089220-G-A

26598084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67088727-T-C

26598084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67088727-T-G

26598115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67088685-G-A

26598285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67088523-G-T

26598372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67088459-T-G

26608493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67085592-A-G

26608562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67085514-C-T

26608672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67085432-C-T

26609004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67085077-G-A

26610006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67083643-C-T

26610201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67083436-T-C

26611040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67082650-C-T

26611137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67082553-G-T

26611293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67082482-G-T

26611429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67082364-C-T

26611556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67082259-G-C

26611556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67082259-G-T

26611649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67082160-A-G

26611910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67081905-G-C

26612080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67081765-C-G

26612097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67081748-C-G

26612097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67081748-C-T

26612295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67081573-T-C

26612332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67081531-G-A

26612352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67081511-T-G

26612968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67079271-G-A

26613152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67079090-G-A

26613253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67078999-C-T

26613261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67078991-C-G

26613352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67078923-G-A

26613491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67078818-G-T

26613584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67078721-G-A

26613733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67078625-C-T

26613801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67078554-A-G

26617623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67078002-A-G

26617668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67077949-G-A

26617733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67077904-A-G

26617808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67077848-G-A

26619058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67076791-A-G

26619188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67076672-T-G

26619479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67076409-A-G

26619491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67076397-T-C

26619491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67076397-T-G

26619507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67076381-T-A

26619507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67076381-T-C

http://identifiers.org/hco/8/GRCh38#26619539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67076356-C-A

26619539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67076356-C-T

26619555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67076340-A-G

http://identifiers.org/hco/8/GRCh38#26619665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67076259-C-A

26622256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67073371-A-G

26622989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67072934-C-G

26622989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67072934-C-T

26622998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67072925-G-T

26623188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67072703-A-G

26623715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67072215-G-A

http://identifiers.org/hco/8/GRCh38#26623738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67072192-C-A

26623738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67072192-C-G

26623738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67072192-C-T

26623740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67072190-T-C

26623748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67072183-C-T

http://identifiers.org/hco/8/GRCh38#26623773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67072160-C-A

26623781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67072153-G-A

http://identifiers.org/hco/8/GRCh38#26623868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67072064-C-A

http://identifiers.org/hco/8/GRCh38#26623974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67071983-C-A

26623974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67071983-C-G

26623974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67071983-C-T

26623986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67071971-C-T

26624000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67071957-G-T

26624169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67071797-A-G

26624343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67071653-T-G

26624344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67071652-T-C

26624344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67071652-T-G

26624345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67071651-C-T

http://identifiers.org/hco/8/GRCh38#26624430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67071625-C-A

http://identifiers.org/hco/8/GRCh38#26624431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67071624-C-A

26624431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67071624-C-G

26625368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67069842-A-T

26625401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67069808-G-C

26625770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67069463-C-G

26625770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67069463-C-T

26626474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67067556-T-A

http://identifiers.org/hco/8/GRCh38#26626478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67067552-C-A

26626478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67067552-C-T

http://identifiers.org/hco/8/GRCh38#26626512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67067515-C-A

26626512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67067515-C-T

26626523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67067504-G-A

26626523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67067504-G-C

26626523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67067504-G-T

26626593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67067454-A-G

26626593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67067454-A-T

26626758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67067285-G-A

26626758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67067285-G-T

26626885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67067175-T-C

26626905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67067155-G-A

26627029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67067032-G-C

http://identifiers.org/hco/8/GRCh38#26627077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67066999-C-A

26627077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066999-C-T

26627198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066904-C-T

26627314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066790-C-T

26627431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066680-G-A

http://identifiers.org/hco/8/GRCh38#26627432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67066679-C-A

26627432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066679-C-G

26627432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066679-C-T

26627436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066675-G-T

26627501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066644-G-A

26627685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066467-T-C

http://identifiers.org/hco/8/GRCh38#26627730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67066425-C-A

26627750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066406-G-A

26627750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066406-G-T

26627767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066390-G-A

http://identifiers.org/hco/8/GRCh38#26627786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67066371-C-A

26627786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066371-C-G

26627786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066371-C-T

26627825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066333-G-A

26627825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066333-G-T

http://identifiers.org/hco/8/GRCh38#26627830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67066328-A-C

http://identifiers.org/hco/8/GRCh38#26627833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67066325-C-A

http://identifiers.org/hco/8/GRCh38#26627859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67066299-C-A

http://identifiers.org/hco/8/GRCh38#26627902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67066256-A-C

26627957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066202-C-G

26627957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066202-C-T

26627965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066194-G-A

26627965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066194-G-T

26627969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066190-A-G

26627978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066181-C-T

26627982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066177-G-T

26627998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066161-C-T

26628029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066132-G-A

26628029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066132-G-C

26628029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066132-G-T

26628081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066082-G-C

26628081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67066082-G-T

26631754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67065248-C-G

26631762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67065240-C-G

26631762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67065240-C-T

26631791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67065210-G-A

26631799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67065202-T-C

26631855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67065159-C-T

26631857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67065157-C-T

26631951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67065055-G-T

26631958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67065048-A-G

http://identifiers.org/hco/8/GRCh38#26631998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67065003-C-A

26632032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67064969-C-T

26632104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67064891-C-G

26632247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67064753-C-T

26632248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67064752-G-A

26632300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67064709-C-T

26632317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67064695-A-G

http://identifiers.org/hco/8/GRCh38#26632330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67064682-A-C

26632331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67064681-G-T

26632965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67063684-G-T

26633024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67063628-C-G

26633025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67063627-C-T

26633089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67063558-T-C

26633466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67063242-C-T

26634028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67063017-C-G

http://identifiers.org/hco/8/GRCh38#26634062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67062984-C-A

26634075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67062971-T-G

26634662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67062006-G-A

26634662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67062006-G-C

26634843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67061849-A-G

26634909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67061783-T-G

26634925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67061770-G-A

http://identifiers.org/hco/8/GRCh38#26634931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67061764-A-C

26634931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67061764-A-G

26635369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67061366-G-T

26635706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67061047-T-C

26635706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67061047-T-G

26636042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67060772-A-G

http://identifiers.org/hco/8/GRCh38#26636374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67060277-A-C

26636374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67060277-A-G

26636374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67060277-A-T

26636476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67060170-A-G

26637440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67059614-T-C

http://identifiers.org/hco/8/GRCh38#26637456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67059599-A-C

26637456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67059599-A-G

26637461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67059594-T-A

26637597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059469-G-T

26637610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059456-G-A

26637610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059456-G-T

26637617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059449-T-C

26637668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059397-G-A

26637668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059397-G-T

26637675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059390-A-G

26637686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059379-T-C

26637688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059377-T-G

26637746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059320-A-G

26637766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059313-T-C

http://identifiers.org/hco/8/GRCh38#26637783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67059299-C-A

26637783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059299-C-G

http://identifiers.org/hco/8/GRCh38#26637790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67059292-C-A

26637790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059292-C-T

26637800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059282-G-A

26637800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059282-G-T

26637904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059195-A-G

26637918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059180-C-T

26637972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059143-G-T

26637979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67059136-G-T

26638315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67058939-A-G

26638386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67058894-C-T

26638853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67058205-G-A

http://identifiers.org/hco/8/GRCh38#26638855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67058203-C-A

26638855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67058203-C-T

26638885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67058175-G-T

26639239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67057816-G-C

26639414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67057572-A-G

26639626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67057374-T-C

26639847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67057143-A-T

26639867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67057123-C-T

26639988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67056447-A-G

http://identifiers.org/hco/8/GRCh38#26640185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67056273-A-C

26640185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67056273-A-G

26640262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67056197-G-T

26640334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67056113-A-G

26640566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67055888-G-A

26640591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67055831-T-G

26640804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67055535-C-T

26641113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67055091-T-C

26641212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67055008-G-A

26641379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67054875-C-T

http://identifiers.org/hco/8/GRCh38#26642259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67054077-C-A

26642349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67053900-G-T

26642583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67053654-C-T

26642738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67053501-T-A

26642915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67053364-G-A

26642915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67053364-G-T

26642930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67053349-T-C

26642947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67053332-G-A

26642947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67053332-G-T

26642957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67053322-G-A

26642957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67053322-G-T

26642986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67053300-A-G

26643107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67053260-T-A

26643107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67053260-T-G

http://identifiers.org/hco/8/GRCh38#26643166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67053243-A-C

26643271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67053192-T-C

26643277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67053186-T-G

26643279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67053184-T-C

26643279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67053184-T-G

26643301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67053165-T-C

26643369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67053099-G-A

26643369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67053099-G-T

26643410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67053061-G-A

26643626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67052848-A-G

26643655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67052819-T-C

http://identifiers.org/hco/8/GRCh38#26643706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67052771-C-A

http://identifiers.org/hco/8/GRCh38#26643715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67052762-C-A

26643715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67052762-C-T

26643785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67052694-A-G

26643830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67052645-G-A

26643874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67052612-G-A

26643874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67052612-G-C

26643874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67052612-G-T

26643890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67052596-G-C

26643890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67052596-G-T

26643903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67052583-A-G

26643904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67052582-G-A

26643904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67052582-G-T

26643906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67052580-A-G

26647744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: synonymous variant
orthologous variants: 67050629-C-T

26647843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67050535-A-G

26647876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67050519-G-A

26647921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67050477-G-A

26647921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67050477-G-T

26648149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67050038-G-A

26648149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67050038-G-C

26648151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67050036-G-C

26648363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67049869-C-G

26648409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67049836-T-C

http://identifiers.org/hco/8/GRCh38#26648501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67049774-C-A

26648535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67049745-G-A

26648881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67049597-G-A

26648933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67049561-C-T

26648969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67049533-G-A

26649074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67049455-A-G

26649122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67049412-A-T

26649159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67049376-C-T

26649190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67049344-A-G

26649284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67049256-A-G

26649321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67049219-G-A

26649715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67048505-C-T

26649946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67048091-A-G

26650202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67047917-G-C

26650430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67047754-T-G

26650508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67047675-G-C

26650597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67047583-T-A

26650859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67047242-C-T

http://identifiers.org/hco/8/GRCh38#26651595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67046363-A-C

26651672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67046293-C-T

26651673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67046292-G-A

26651864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67046140-T-C

26651864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67046140-T-G

26652200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67045544-G-A

26652200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67045544-G-C

26652200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67045544-G-T

26652247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67045498-T-G

http://identifiers.org/hco/8/GRCh38#26652353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67045392-C-A

26652392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: missense variant
orthologous variants: 67045353-C-G

26652665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67045128-G-C

26652695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67045094-C-T

26652817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67044974-G-A

26652817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67044974-G-T

26652889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67044869-A-G

http://identifiers.org/hco/8/GRCh38#26653096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67044674-C-A

26653096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67044674-C-T

26653158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67044609-C-T

26653159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67044608-C-T

26653364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: missense variant
orthologous variants: 67044395-C-T

26653404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 67044355-T-C

26653404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 67044355-T-G

26653428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron variant
orthologous variants: 67044327-C-T

26655583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67042916-T-A

26655583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, undefined
orthologous variants: 67042916-T-C

26655608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 67042890-C-T

http://identifiers.org/hco/8/GRCh38#26655709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#67042789-C-A

26655709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 67042789-C-T

26655858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042653-T-A

26655858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042653-T-G

26655915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042596-T-C

26655915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042596-T-G

26655963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042550-G-A

26655963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042550-G-T

26655988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042525-T-A

26655988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042525-T-C

26655989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042524-G-T

http://identifiers.org/hco/8/GRCh38#26656030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67042477-C-A

26656144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042376-G-A

26656144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042376-G-T

http://identifiers.org/hco/8/GRCh38#26656171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67042348-A-C

26656171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042348-A-G

26656171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042348-A-T

26656357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042176-G-A

26656357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042176-G-T

26656458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042085-T-C

26656522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042028-G-C

26656559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67042009-T-C

http://identifiers.org/hco/8/GRCh38#26656713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67041830-C-A

26656765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67041782-G-A

http://identifiers.org/hco/8/GRCh38#26656773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67041774-C-A

26656773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67041774-C-T

26656794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67041753-A-G

26656807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67041741-C-T

26656840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67041702-A-G

26656931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67041650-G-T

http://identifiers.org/hco/8/GRCh38#26656983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67041600-C-A

26656983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67041600-C-T

26657130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67041432-G-T

26657136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67041426-G-T

26657229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67041346-A-T

http://identifiers.org/hco/8/GRCh38#26657244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67041331-C-A

26657244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67041331-C-T

http://identifiers.org/hco/8/GRCh38#26657273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67041290-C-A

26657418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67041146-G-A

http://identifiers.org/hco/8/GRCh38#26657807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67040699-C-A

26658076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67040410-A-G

26658076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67040410-A-T

26658146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67040340-C-T

26658147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67040339-G-A

26658147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3014
most severe consequence: 3 prime UTR variant
orthologous variants: 67040339-G-T