129576498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26795130-G-C

129576598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26795029-T-C

129576640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26795013-C-T

129577019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26794623-T-C

129577245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26794375-T-C

http://identifiers.org/hco/6/GRCh38#129577350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26794270-C-A

129577350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26794270-C-T

129577587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26794035-A-T

129577598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26794024-T-A

129577694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26793943-G-A

129577869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26793772-G-A

129577921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26793725-A-G

129578067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26793618-C-G

129578142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26793541-A-G

129578187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26793386-G-A

129578187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26793386-G-T

129578188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26793385-G-T

129578189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26793384-A-G

http://identifiers.org/hco/6/GRCh38#129578300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26793275-C-A

129578340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26793237-T-C

http://identifiers.org/hco/6/GRCh38#129578354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26793227-C-A

129578366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26793215-A-G

129578406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3 prime UTR variant
orthologous variants: 26793177-G-T

129578421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26793161-A-G

129578541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26793062-T-A

129578541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26793062-T-G

129578580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26793023-G-A

129578580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26793023-G-C

129578622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26792982-G-A

129578622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26792982-G-T

http://identifiers.org/hco/6/GRCh38#129579934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26792571-C-A

129579934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26792571-C-G

129579998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26792505-A-G

129580164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26792354-T-C

http://identifiers.org/hco/6/GRCh38#129580168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26792350-C-A

129580168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26792350-C-G

129580347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26792179-A-G

129580533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26792041-T-G

129580567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26792009-A-G

129581562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26791733-A-G

129581616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26791673-G-A

http://identifiers.org/hco/6/GRCh38#129581660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26791629-C-A

129581660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26791629-C-T

129581687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26791599-G-A

129581687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26791599-G-T

129581740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26791551-T-C

129581840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26791448-G-T

129582285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26791058-C-T

http://identifiers.org/hco/6/GRCh38#129582291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26791052-A-C

129582533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26790868-T-C

129582562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26790839-T-C

http://identifiers.org/hco/6/GRCh38#129582590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26790813-A-C

129582598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26790805-G-A

129582844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26790601-A-G

129583391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26789413-T-C

129583489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26789326-G-A

http://identifiers.org/hco/6/GRCh38#129583851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26788971-C-A

129583851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26788971-C-T

129583854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26788965-T-A

129583854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26788965-T-C

129583854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26788965-T-G

http://identifiers.org/hco/6/GRCh38#129583882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26788940-A-C

129583882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26788940-A-T

129583923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26788825-G-A

129583923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26788825-G-C

129583923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26788825-G-T

129583941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26788781-G-A

129583941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26788781-G-C

129584407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26788305-A-T

129584650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26788076-T-C

129584650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26788076-T-G

129584683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26788043-T-G

129585060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787689-T-G

129585072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787674-A-T

129585414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787587-G-A

129585447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787555-A-G

129585466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787536-T-C

129585508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787505-T-C

129585596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787468-C-T

129585739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787434-C-T

129585847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787400-A-G

129585958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787358-T-A

129585968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787348-A-G

129585998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787329-T-C

129586074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787255-G-C

129586218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787077-G-A

129586258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26787036-A-G

129586692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26786645-A-G

129586798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26786541-C-T

129587392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26782068-C-T

129587441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26782022-C-T

129590246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781972-G-A

129590288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781936-T-G

129590335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781894-C-G

129590354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781875-C-G

129590354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781875-C-T

129590415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781857-C-T

129590446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781826-A-G

129590507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781759-G-C

129590515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781749-A-G

129590532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781732-G-T

129590653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781623-T-C

129590835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781485-A-G

129590931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781399-T-C

129590933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781397-C-T

http://identifiers.org/hco/6/GRCh38#129590949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26781391-A-C

129591011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781351-A-T

129591012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781350-G-C

http://identifiers.org/hco/6/GRCh38#129591082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26781278-A-C

129591114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781246-C-T

129591212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781150-C-T

129591219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26781143-C-T

129591862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26773597-G-A

129591887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26773573-T-C

129591947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26773510-T-C

129591991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26773471-A-G

http://identifiers.org/hco/6/GRCh38#129592065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26773403-A-C

129592065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26773403-A-G

http://identifiers.org/hco/6/GRCh38#129592081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26773387-C-A

129592284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26773187-G-C

129592330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26773141-A-G

129592371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26773118-C-T

http://identifiers.org/hco/6/GRCh38#129592438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26773078-C-A

129592438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26773078-C-G

129592542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26772994-G-T

129592716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26772851-G-A

129593867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26772274-G-A

129594732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26771748-A-G

129594851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26771636-A-G

http://identifiers.org/hco/6/GRCh38#129594869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26771620-C-A

129594869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26771620-C-T

129595001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26771502-T-C

129595178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26771340-T-G

129595301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26771108-A-G

129595375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26771037-G-A

129598355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26766859-G-A

http://identifiers.org/hco/6/GRCh38#129598598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26766624-A-C

129598615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26766603-T-C

129598741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26766498-C-T

129598916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26766150-G-A

129598916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26766150-G-T

129598922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26766144-G-A

129598922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26766144-G-T

129598925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26766141-G-A

129598925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26766141-G-T

129598928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26766138-G-A

129598928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26766138-G-T

129598931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26766135-G-A

129598931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26766135-G-T

129598948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26766118-G-A

129598948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26766118-G-T

129598956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26766110-G-A

129598956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26766110-G-T

129599014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26766020-A-G

129599097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26765951-G-T

129599131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26765917-T-C

129599178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26765903-A-G

129599193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26765889-A-G

129599193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26765889-A-T

129599250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26765832-T-C

129599322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26765760-T-C

129599352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26765730-G-A

129599352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26765730-G-T

129599360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26765722-T-C

129599381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26765669-A-G

129599639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26765413-A-G

129599643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26765409-C-T

http://identifiers.org/hco/6/GRCh38#129599791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26765246-C-A

129599810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26765227-T-C

129600086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26764943-G-A

129600219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26764790-C-T

129600298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26764713-T-C

129600355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26764653-G-C

129600560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26764463-A-T

http://identifiers.org/hco/6/GRCh38#129600593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26764426-C-A

129600593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26764426-C-T

129600926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26763701-T-A

129601098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26761693-G-A

129601129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26761684-C-T

129601145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26761667-T-C

129601171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26761641-A-G

129601947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26761295-T-C

http://identifiers.org/hco/6/GRCh38#129602037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26761212-C-A

http://identifiers.org/hco/6/GRCh38#129602095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26761157-A-C

129602165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26761093-G-T

129602171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26761088-A-G

129602191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26761068-C-T

129602280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26760973-T-C

129602462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26760765-G-A

129603754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26759453-T-C

129603998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26759231-A-T

129604033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26759197-C-G

129604033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26759197-C-T

129604507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26758757-A-T

129604550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26758715-G-A

129604597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26758695-T-C

129604739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26758575-G-C

129604790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26758535-G-A

129604790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26758535-G-T

http://identifiers.org/hco/6/GRCh38#129604851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26758474-C-A

129604875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26758453-A-G

129605050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26758049-G-C

129605672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26756974-A-G

129605692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26756953-C-T

129605752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26756889-A-T

http://identifiers.org/hco/6/GRCh38#129605792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26756849-A-C

129606001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26756645-A-G

129606008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26756638-T-C

129606051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26756591-G-A

129606051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26756591-G-T

129606392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26756249-G-A

129606550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26756120-G-A

http://identifiers.org/hco/6/GRCh38#129606827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26755838-A-C

129607100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26755788-T-A

129607295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26755655-T-A

129607375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26755571-A-T

129607643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26755285-G-T

http://identifiers.org/hco/6/GRCh38#129607769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26755169-C-A

129607769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26755169-C-T

http://identifiers.org/hco/6/GRCh38#129607778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26755161-C-A

http://identifiers.org/hco/6/GRCh38#129607807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26755132-C-A

129607807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26755132-C-T

129607849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26755087-A-G

129608021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26754916-T-A

129608021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26754916-T-G

129608027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26754910-T-C

129608028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26754909-T-G

129608099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26754849-A-G

129608099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26754849-A-T

http://identifiers.org/hco/6/GRCh38#129608155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26754793-C-A

129608155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26754793-C-T

http://identifiers.org/hco/6/GRCh38#129608214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26754735-A-C

http://identifiers.org/hco/6/GRCh38#129608754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26754226-C-A

129608754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26754226-C-T

http://identifiers.org/hco/6/GRCh38#129608891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26753987-A-C

129608896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26753982-T-G

129608947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26753941-G-A

http://identifiers.org/hco/6/GRCh38#129608948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26753940-C-A

129609002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26753896-G-A

129609219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26753788-G-C

129609219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26753788-G-T

129611240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26753507-C-T

129611473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26753293-T-C

129611514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26753253-A-G

129611514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26753253-A-T

129611600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26753161-C-G

129611600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26753161-C-T

129611619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26753142-A-G

129611834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26752933-A-T

129612016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26752756-A-T

129612191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26752433-G-T

129612192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26752432-T-A

129612256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26752301-G-C

129612300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26752261-T-C

129612454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26752094-T-C

129612564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26751987-G-A

129612736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26751812-T-C

129612765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26751785-T-C

129613380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26751525-A-T

129613401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26751505-T-C

129613407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26751499-T-A

129613576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26751346-A-T

129613630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26751293-T-A

http://identifiers.org/hco/6/GRCh38#129613963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26750894-A-C

129614250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26750567-T-C

129614780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26750286-G-A

129614780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26750286-G-T

http://identifiers.org/hco/6/GRCh38#129615257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26749786-A-C

129615257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26749786-A-G

129615257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26749786-A-T

129615294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26749728-A-G

129615384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26749586-G-A

129615451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26749505-A-G

129615562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26749405-T-C

129615639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26749330-C-G

129615657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26749315-T-C

129616144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26748828-T-C

129616175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26748795-A-G

129616390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26748592-T-C

129616968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26748126-A-G

129616973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26748121-A-G

129617131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26747864-G-A

129617368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26747609-G-A

129617388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26747589-T-C

129617464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26747538-G-A

129617707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26747272-C-G

129617856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26747018-G-C

129618021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26746860-G-A

129618280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26746430-C-T

129618317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26746398-A-T

129618493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26746227-T-C

129618493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26746227-T-G

129618620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26746131-G-A

129618761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26746006-A-G

129619800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26745612-C-T

129619895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26745529-G-A

129619909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26745517-A-G

129620021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26745409-T-C

129620471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26745248-A-G

129620761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26745034-G-A

129620761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26745034-G-C

129620795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26745000-G-A

129620795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26745000-G-C

http://identifiers.org/hco/6/GRCh38#129620813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26744987-A-C

129620815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26744985-A-G

129620869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26744918-C-G

http://identifiers.org/hco/6/GRCh38#129620922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26744859-C-A

129620922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26744859-C-T

http://identifiers.org/hco/6/GRCh38#129621292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26744459-C-A

129621292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26744459-C-T

129621744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26743498-G-A

129621867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26743373-G-A

129621883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26743360-C-T

129621955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26743304-T-C

129622153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26743150-C-T

129622499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26742607-G-A

129622630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26742462-T-A

129622630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26742462-T-G

129622686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26742404-C-T

129623095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26742300-A-G

129623117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26742278-G-T

129623319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26742073-G-A

129623466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26741947-G-A

129624097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26741349-G-A

129624219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26741228-G-A

129627614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26738698-G-A

http://identifiers.org/hco/6/GRCh38#129627736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26738600-A-C

129627785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26738558-T-A

129627794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26738549-A-G

129627884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26738464-G-T

129628034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26738292-T-C

129628170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26738171-A-G

129628247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26738098-G-A

129628504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26737716-G-C

129628729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26737528-G-T

129628743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26737516-G-A

129628941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26737068-A-G

129628960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26737049-T-A

129628960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26737049-T-C

129629115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26736900-G-A

129629116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26736899-G-A

129629119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26736896-C-T

129629371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: synonymous variant
orthologous variants: 26736711-G-A

129629385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: stop gained
orthologous variants: 26736697-G-A

129629462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26736620-G-A

129629509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26736564-G-T

129629618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26736471-G-C

129629618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26736471-G-T

http://identifiers.org/hco/6/GRCh38#129629773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26736321-C-A

129629895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26736201-G-T

129630402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26735737-T-C

129630402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26735737-T-G

http://identifiers.org/hco/6/GRCh38#129630586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26734897-C-A

129630941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26734578-T-A

129631217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26734327-G-C

129631256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26734292-C-T

129631267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26734281-T-C

129631291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26734256-C-G

129631312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26734235-G-A

http://identifiers.org/hco/6/GRCh38#129631426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26734123-A-C

129631426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26734123-A-G

http://identifiers.org/hco/6/GRCh38#129631717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26733410-A-C

129631863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26733288-T-G

129632054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26732920-T-C

129632091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26732890-T-C

http://identifiers.org/hco/6/GRCh38#129632102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26732879-C-A

http://identifiers.org/hco/6/GRCh38#129632143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26732463-C-A

http://identifiers.org/hco/6/GRCh38#129632342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26732298-C-A

129632498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26732143-C-G

129632655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26731986-T-C

129632828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26731724-A-G

129633453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26731347-G-A

129633453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26731347-G-T

129633685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26731228-G-C

129633829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26731103-C-T

http://identifiers.org/hco/6/GRCh38#129633978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26730988-C-A

129633978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26730988-C-T

http://identifiers.org/hco/6/GRCh38#129634021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26730952-A-C

129634021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26730952-A-G

129634103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 26730870-A-G

http://identifiers.org/hco/6/GRCh38#129634124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26730849-C-A

http://identifiers.org/hco/6/GRCh38#129634150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26730821-C-A

129634229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26730739-G-A

129634229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26730739-G-T

129634471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26730537-A-G

129634540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26730478-T-A

129634694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26730340-A-G

129634696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26730338-G-T

129634788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26730262-T-A

129634964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26728743-G-T

129635012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26728683-G-A

129635021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26728676-C-T

http://identifiers.org/hco/6/GRCh38#129635080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26728654-A-C

129635170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26728568-A-G

129635594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26728124-T-C

129635668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26728051-C-T

129635910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26727824-G-C

129636309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26727414-G-A

129636354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26727370-C-T

129636455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26727255-C-T

http://identifiers.org/hco/6/GRCh38#129636993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26726779-A-C

129637906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26726582-G-A

129638156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26726334-C-T

129638234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26726258-G-A

129638258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26726235-C-T

http://identifiers.org/hco/6/GRCh38#129638286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26726212-C-A

129638286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26726212-C-T

129638354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26726144-C-T

129638375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26726123-A-T

http://identifiers.org/hco/6/GRCh38#129638434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26726064-A-C

129638596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26725902-G-A

http://identifiers.org/hco/6/GRCh38#129638636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26725862-C-A

129638636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26725862-C-T

129638643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26725843-G-C

129638675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26725811-A-G

http://identifiers.org/hco/6/GRCh38#129638735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26725748-C-A

129638736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26725747-A-T

http://identifiers.org/hco/6/GRCh38#129638780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26725703-A-C

129638895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26725587-G-A

129638953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26725529-C-T

129639083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26725402-G-A

129639129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26725359-T-A

129639143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26725345-A-T

129639179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26725304-G-C

129639232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26725253-T-A

129639232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26725253-T-C

129639274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26725197-A-T

129639318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26724542-T-A

129639465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26724422-A-T

129639911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26724042-A-G

129639975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26723982-G-A

129640014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26723980-C-T

129640048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26723918-A-T

http://identifiers.org/hco/6/GRCh38#129640060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26723906-A-C

129640060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26723906-A-G

129640347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26723602-C-T

129640575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26723405-T-C

http://identifiers.org/hco/6/GRCh38#129640868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26723013-A-C

129640882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26723003-T-C

129640903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26722982-A-G

129640935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26722950-T-C

129641146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26722724-A-G

129641181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26722693-A-G

129641263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26722618-A-T

http://identifiers.org/hco/6/GRCh38#129641314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26722563-C-A

129641314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26722563-C-G

129641314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26722563-C-T

129641371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26722504-A-G

129641388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26722487-T-A

129641640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26722269-G-C

129641640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26722269-G-T

129641697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26722212-G-A

129641697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26722212-G-C

129641697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26722212-G-T

129641923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: missense variant
orthologous variants: 26722018-A-G

129642019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: splice acceptor variant
orthologous variants: 26721925-C-T

129642021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26721923-G-A

129642021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26721923-G-C

129642110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26721840-T-A

129642110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26721840-T-G

http://identifiers.org/hco/6/GRCh38#129643115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26720964-A-C

http://identifiers.org/hco/6/GRCh38#129643997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26720444-A-C

129643999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26720442-G-T

129644095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26720221-C-T

129644117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26720208-G-A

129644267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26720052-G-C

129644359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26719973-A-G

129644401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26719944-A-T

129644626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26719695-C-T

129644888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26719439-T-C

129644912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26719415-C-T

129644936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26719392-C-G

129645082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26719257-T-C

129645443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26718904-T-C

129646769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26718001-C-T

129646916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26717857-T-C

129647037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26717738-T-G

129647122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26717649-A-G

129647267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26717511-T-G

129648625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26714399-G-C

129650897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26712568-G-A

129650899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26712566-T-C

129650992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26712464-T-A

129650992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26712464-T-C

129651006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26712453-G-A

129651159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26712289-C-T

129651243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26712247-C-G

129651607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26711888-C-G

129651624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26711871-G-T

129651651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26711835-C-G

129651668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26711817-C-G

http://identifiers.org/hco/6/GRCh38#129651729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26711741-C-A

129651775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26711695-G-C

http://identifiers.org/hco/6/GRCh38#129651889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26711600-A-C

129651975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26711478-T-G

129651979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26711474-A-G

129651991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26711464-G-A

129651993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26711462-G-A

129652073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26711326-C-T

129652139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26711235-C-T

http://identifiers.org/hco/6/GRCh38#129652298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26711109-C-A

129652304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26711103-T-C

129652391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26711013-C-T

129652936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26710012-A-G

129652936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26710012-A-T

129653064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26709914-A-G

129653078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26709904-T-A

129653078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26709904-T-C

129653154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26709835-G-A

129653348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26709656-A-G

129653348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26709656-A-T

129653450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26709585-C-T

129653546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26709280-C-T

129654729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26706746-C-T

129654962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26706545-G-T

http://identifiers.org/hco/6/GRCh38#129655023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26706485-C-A

129655023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26706485-C-T

http://identifiers.org/hco/6/GRCh38#129655812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26705537-C-A

http://identifiers.org/hco/6/GRCh38#129655927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26705134-A-C

129655979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26705074-A-G

http://identifiers.org/hco/6/GRCh38#129656010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26705043-A-C

129656144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26704910-G-A

129656727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26704670-C-G

129656727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26704670-C-T

http://identifiers.org/hco/6/GRCh38#129657051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26704248-A-C

129657051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26704248-A-G

129657108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26704202-T-C

http://identifiers.org/hco/6/GRCh38#129657773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26703520-C-A

129657996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26703309-C-T

http://identifiers.org/hco/6/GRCh38#129658250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26703060-C-A

129658250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26703060-C-T

129658390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26702886-T-A

129658391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26702885-T-A

http://identifiers.org/hco/6/GRCh38#129658466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26702801-C-A

129658568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26702708-G-A

129658684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26702140-T-C

129659234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26701710-T-C

http://identifiers.org/hco/6/GRCh38#129659420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26701544-C-A

129659420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26701544-C-T

129660900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26699720-G-A

129660903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26699717-T-A

129660968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26699653-G-A

129660968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26699653-G-T

129661264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26699383-G-A

129661344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26699182-T-A

129661344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26699182-T-G

129661350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26699177-T-A

129661473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26699014-C-T

http://identifiers.org/hco/6/GRCh38#129661502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26698984-C-A

129661502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26698984-C-T

http://identifiers.org/hco/6/GRCh38#129661531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26698955-C-A

129661853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26698636-C-T

129662006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26698396-C-T

129662151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26698231-T-C

http://identifiers.org/hco/6/GRCh38#129662154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26698228-A-C

129662261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26698123-C-T

129662613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26697787-G-A

129662613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26697787-G-T

129662760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26697563-G-A

129662973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26697344-A-G

129662979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26697338-T-G

129662986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26697331-G-A

http://identifiers.org/hco/6/GRCh38#129663451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26696751-C-A

129663451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26696751-C-G

129663451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26696751-C-T

129666696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26693168-A-T

129666729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26693143-G-C

http://identifiers.org/hco/6/GRCh38#129666785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26693088-C-A

129666830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26693039-G-T

129666944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26692930-T-C

129667069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26692823-C-T

http://identifiers.org/hco/6/GRCh38#129667134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26692771-A-C

129667284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26692492-G-C

129667316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26692460-A-T

129667795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26691952-G-T

http://identifiers.org/hco/6/GRCh38#129667956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26691784-C-A

129668085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26691542-A-T

129668103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26691524-A-G

129668133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26691497-G-A

http://identifiers.org/hco/6/GRCh38#129668238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26691407-C-A

http://identifiers.org/hco/6/GRCh38#129668314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26691351-A-C

129668348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26691318-A-G

129668350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26691316-T-A

http://identifiers.org/hco/6/GRCh38#129668354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26691312-C-A

129668480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26691233-C-T

http://identifiers.org/hco/6/GRCh38#129668481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26691232-A-C

129668481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26691232-A-G

129668518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26691190-C-T

129668740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26690984-A-G

129668862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26690872-T-C

129668885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26690855-C-T

129668974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26690774-C-T

129669512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26690472-G-A

http://identifiers.org/hco/6/GRCh38#129669522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26690462-A-C

129669522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26690462-A-G

129669533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26690451-C-G

http://identifiers.org/hco/6/GRCh38#129669575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26690388-C-A

129669575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26690388-C-T

http://identifiers.org/hco/6/GRCh38#129669609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26690354-A-C

129669629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26690339-T-C

129669870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26690046-T-A

129669870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26690046-T-C

129669975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26689968-T-C

129670118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26689821-C-G

129670350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26689589-G-A

129670404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26689545-G-A

129670404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26689545-G-T

129670605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26689341-T-A

129670623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26689323-T-C

129671028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26687415-G-A

129671111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26687335-T-C

129671285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26687170-T-C

129671285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26687170-T-G

129672565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26686691-A-G

129672760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26686494-T-C

129672817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26686430-A-G

129672985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26686280-T-G

129673035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26686192-C-T

129673257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26685975-T-C

129673305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26685934-A-G

129673305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26685934-A-T

129673829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26685337-C-T

129673851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26685315-G-A

129674051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26685020-T-G

129674120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26684957-A-G

129674159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26684918-C-G

129674159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26684918-C-T

129674342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26684726-G-A

129677633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26683237-G-C

129677756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26683103-C-T

129677812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26683057-T-C

129677876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26682995-C-T

129677994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26682773-A-G

129678082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26682649-A-G

129678125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26682614-G-C

http://identifiers.org/hco/6/GRCh38#129678141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26682598-A-C

129678305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26682427-G-A

http://identifiers.org/hco/6/GRCh38#129678326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26682399-C-A

129678326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26682399-C-T

129678388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26682314-T-C

129678429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26682277-G-A

129678462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26682199-A-G

129678497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26682131-A-G

129678790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26681683-A-G

http://identifiers.org/hco/6/GRCh38#129679052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26681452-C-A

129679073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26681436-A-G

129679616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26680893-C-G

129679701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26680808-G-A

129680027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26680500-A-G

129680097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26680434-T-C

129680200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26680343-G-C

129680325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26680177-T-C

129680393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26680117-G-A

129680393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26680117-G-T

http://identifiers.org/hco/6/GRCh38#129680465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26680034-C-A

129680465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26680034-C-G

129680483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26680019-A-G

129681234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26679437-T-C

129681311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26679370-C-T

129681439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26679260-T-G

http://identifiers.org/hco/6/GRCh38#129681519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26679170-A-C

129681858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26678871-C-T

http://identifiers.org/hco/6/GRCh38#129682402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26677983-C-A

129682467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26677905-T-C

129683606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26676263-A-G

129683692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26676183-T-G

129684037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26675879-C-T

129684370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26675528-G-T

129684579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26675332-A-G

129684717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26675134-T-A

129684717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26675134-T-G

129685820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26673468-T-C

129686222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26673147-G-A

129686285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26673124-C-T

129686493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26672932-G-A

129687199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26672630-G-A

129687254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26672560-T-A

http://identifiers.org/hco/6/GRCh38#129687272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26672542-A-C

129687887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26671971-G-A

129687906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26671951-G-A

129687952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26671896-C-G

129687978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26671871-C-T

129688041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26671808-T-C

129688067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26671791-G-A

129688095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26671764-A-G

129688808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26671333-G-A

http://identifiers.org/hco/6/GRCh38#129688899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26671246-A-C

129688949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26671205-A-G

http://identifiers.org/hco/6/GRCh38#129689614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26670727-A-C

129689631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26670709-A-G

http://identifiers.org/hco/6/GRCh38#129689666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26670675-A-C

129689738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26670610-G-A

129689738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26670610-G-C

129690013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26670378-T-C

129690190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26670235-T-G

129690241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26670190-G-A

129690390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26670045-A-T

129690478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26669957-C-T

129690485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26669948-T-G

129690517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26669920-G-C

129690531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26669906-T-C

129690890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26669590-T-C

129691125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26669317-A-G

129691209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26669260-A-G

129691229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26669235-C-T

129691236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26669228-C-G

129691334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26669079-C-T

129691335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26669078-G-A

129691335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26669078-G-C

129691381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26668905-A-G

129691469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26668656-C-G

129691590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26668537-T-C

129691633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26668468-C-T

129691645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26668456-C-T

129691655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26668446-C-T

129692135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26668202-C-T

129692192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26668154-A-T

129692313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26668037-C-T

129692501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26667849-T-C

129692771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26667594-T-C

129692804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26667561-T-C

129693242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26667136-G-C

http://identifiers.org/hco/6/GRCh38#129693459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26666960-A-C

129693522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26666899-C-T

129693602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26666825-C-T

129693664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26666779-T-C

129693957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26666522-A-G

129693975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26666504-G-A

129694345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26666147-C-T

129694451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26666100-A-G

129694452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26666099-G-A

129694534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26666011-T-A

129694661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26665853-A-G

129694661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26665853-A-T

129694701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26665801-C-G

129694871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26665419-G-A

129694871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26665419-G-T

129694962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26665211-A-G

129695382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26664856-T-G

129695454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26664800-C-T

129695561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26664695-T-C

129695675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26664422-A-T

129695944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26662106-T-G

129696026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26662007-G-A

129696073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26661953-A-G

129696209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26661816-T-C

129696240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26661785-A-G

129696279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26661746-G-A

129697516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26660972-G-C

129697516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26660972-G-T

129697530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26660958-G-A

129697545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26660943-C-G

129697557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26660928-G-A

129697557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26660928-G-C

129697703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26660786-G-T

129697754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26660742-C-T

129698004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26660497-C-T

129698315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26659038-G-C

http://identifiers.org/hco/6/GRCh38#129698450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26658896-C-A

129698450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26658896-C-T

129698494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26658852-T-C

129698526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26658827-T-C

129699438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26657552-A-G

129699471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26657512-G-A

129699608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26657405-T-C

129699691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26657322-A-G

129699862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26657172-G-A

129699914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26657122-C-T

http://identifiers.org/hco/6/GRCh38#129700382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26656585-A-C

129700630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26656350-A-G

129701349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26656301-A-G

129701372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26656277-C-G

129701439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26656214-C-T

http://identifiers.org/hco/6/GRCh38#129702044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26655562-C-A

129702412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26655258-A-G

129702531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26655156-A-G

129702595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26655081-C-G

129702595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26655081-C-T

129702695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26654996-A-G

129703145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26654878-T-A

129703156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26654867-G-C

http://identifiers.org/hco/6/GRCh38#129703700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26654566-C-A

129703700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26654566-C-T

129703873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26654406-G-A

http://identifiers.org/hco/6/GRCh38#129703895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26654377-A-C

129703940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26654338-A-T

129704316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26654040-G-C

129704393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26653959-C-T

129704494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26653831-C-T

129704517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26653808-C-T

129704739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26653572-T-C

129704860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26653481-A-G

129705002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26653352-C-G

129705277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26652734-T-C

129705823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26651730-A-T

129706075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26651557-A-G

129706371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26651255-T-C

129706474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26651145-T-G

129707979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26650668-C-T

129708277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26650375-C-T

129708279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26650373-A-T

129708375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26650275-T-G

129708437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26650215-A-G

129708502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26650147-A-T

http://identifiers.org/hco/6/GRCh38#129708503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26650146-C-A

129708531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26650118-A-G

http://identifiers.org/hco/6/GRCh38#129708537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26650112-A-C

http://identifiers.org/hco/6/GRCh38#129709021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26649661-C-A

129709286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26649423-A-G

129709718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron variant
orthologous variants: 26648977-A-G

http://identifiers.org/hco/6/GRCh38#129709917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#26648783-C-A

129709917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26648783-C-G

129709917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26648783-C-T

129709920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26648780-G-T

http://identifiers.org/hco/6/GRCh38#129709985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#26648716-A-C

129709985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26648716-A-G

129709989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21035
most severe consequence: intron_variant, undefined
orthologous variants: 26648712-G-A