76201944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 135835783-T-C

76201967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 135835808-G-A

76201967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 135835808-G-T

http://identifiers.org/hco/7/GRCh38#76201977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#135835818-C-A

76201977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 135835818-C-T

http://identifiers.org/hco/7/GRCh38#76202058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#135835885-C-A

76202058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 135835885-C-T

76202063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 135835890-G-A

76202088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, undefined
orthologous variants: 135835916-G-A

76202088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, undefined
orthologous variants: 135835916-G-C

76202088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, undefined
orthologous variants: 135835916-G-T

76202914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135836712-C-T

76203000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135836805-G-A

76203000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135836805-G-C

76203000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135836805-G-T

76203072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135836862-A-G

76203369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135837168-A-G

76203713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135837997-T-C

76203717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135838001-T-C

76203935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135838206-G-C

76203988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135838258-C-T

76203989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135838259-T-G

76204066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135838328-C-T

76204463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135838953-G-T

76204464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135838954-G-A

76204464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135838954-G-C

76204464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135838954-G-T

76204471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135838961-G-A

76205160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135840798-C-G

76205249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135840718-A-G

76205278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135840685-C-T

76205309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135840669-A-T

76205355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135840624-A-G

76206490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135841710-T-G

76206563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135841771-C-T

76206564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135841772-G-A

76206649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135841856-T-A

76206658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135841865-C-G

76206658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135841865-C-T

76206771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135841970-T-C

76206771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135841970-T-G

76208016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135844008-G-T

76208375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135844344-A-G

76208456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135844437-C-G

76209183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135844609-G-A

76209224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135844650-G-A

76209302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135844713-A-G

76209395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135844812-C-T

76210100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135845539-G-A

76210222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135845727-G-C

76211224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135847323-C-G

76211224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135847323-C-T

76211241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135847340-C-G

76211461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135847496-T-C

76211485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135847520-G-A

76211489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135847524-T-A

http://identifiers.org/hco/7/GRCh38#76211554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135847575-A-C

76211749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135847740-C-T

76211761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135847752-G-A

76214276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135849177-C-T

76214611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135849495-G-A

76214963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135850405-G-T

76215078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135850693-T-A

76215109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135850724-T-C

76215109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135850724-T-G

76215139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135850754-A-T

76215200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135850816-C-T

76216469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135851162-C-G

76216809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135851496-C-T

76216857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135851544-C-T

76216858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135851545-G-A

76219397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135853526-A-G

76220078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135853785-T-C

76220092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135853798-C-T

76220100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135853806-G-A

76220456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135854897-G-C

76220572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135854981-G-A

76220833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, undefined
orthologous variants: 135855254-A-G

76220989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135855402-A-G

http://identifiers.org/hco/7/GRCh38#76221029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#135855457-C-A

76221054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135855482-G-A

76221054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135855482-G-C

76221055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135855483-T-C

76229579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135857010-G-T

76232137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135859787-C-T

76232711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135860172-A-G

76232730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135860188-T-C

76234305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135861928-T-C

76234518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135862123-T-C

76234557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135862162-G-A

76234557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135862162-G-T

76234832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135863713-A-G

76234832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135863713-A-T

http://identifiers.org/hco/7/GRCh38#76234837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135863718-C-A

http://identifiers.org/hco/7/GRCh38#76234894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#135863759-C-A

http://identifiers.org/hco/7/GRCh38#76234914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135863779-C-A

76234914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135863779-C-G

76234914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135863779-C-T

76235090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135863927-G-T

76235097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 135863934-A-G

76235328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135864161-T-C

76235328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135864161-T-G

http://identifiers.org/hco/7/GRCh38#76235398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#135864250-C-A

76235398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135864250-C-G

76235398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135864250-C-T

76235418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135864268-G-C

76235418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135864268-G-T

76235435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135864280-G-A

76235435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135864280-G-T

http://identifiers.org/hco/7/GRCh38#76248366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135869387-C-A

76248366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135869387-C-T

http://identifiers.org/hco/7/GRCh38#76248367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135869388-C-A

76248367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135869388-C-G

76248367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135869388-C-T

76248368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135869389-A-G

76248368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135869389-A-T

76248369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135869390-G-T

76248415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135869403-A-G

http://identifiers.org/hco/7/GRCh38#76248421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135869408-A-C

76248421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135869408-A-G

http://identifiers.org/hco/7/GRCh38#76248426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135869413-A-C

76248426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135869413-A-G

76250880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135874989-T-C

76250927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135875030-G-C

76250930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135875033-A-G

76254674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135876825-G-C

76254722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135876883-A-G

http://identifiers.org/hco/7/GRCh38#76254906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135877045-A-C

76258082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135879909-G-A

76258193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135880061-G-C

76258236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135880111-G-A

76258317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135880188-G-A

76258317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135880188-G-C

76259766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135880902-G-A

http://identifiers.org/hco/7/GRCh38#76259768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135880904-C-A

76259768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135880904-C-T

http://identifiers.org/hco/7/GRCh38#76259769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135880905-C-A

76259769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135880905-C-T

76259840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135880982-G-A

76259840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135880982-G-T

http://identifiers.org/hco/7/GRCh38#76259888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135881018-C-A

76259888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135881018-C-T

http://identifiers.org/hco/7/GRCh38#76260086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135881216-A-C

http://identifiers.org/hco/7/GRCh38#76260249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135881366-C-A

76260249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135881366-C-T

76260430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135881452-T-G

http://identifiers.org/hco/7/GRCh38#76260783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135881659-C-A

76260783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135881659-C-T

http://identifiers.org/hco/7/GRCh38#76260844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135881716-C-A

76260844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135881716-C-G

76260844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135881716-C-T

76260937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135881810-G-A

76260937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135881810-G-C

76260937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135881810-G-T

76260984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135881856-C-T

http://identifiers.org/hco/7/GRCh38#76261018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135881890-C-A

76261018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135881890-C-T

http://identifiers.org/hco/7/GRCh38#76261224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135883107-A-C

76261224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135883107-A-G

76261224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135883107-A-T

76261296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135883170-T-A

76261296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135883170-T-C

76261296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135883170-T-G

http://identifiers.org/hco/7/GRCh38#76261297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135883171-C-A

76261297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135883171-C-G

76261297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135883171-C-T

76261342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135883212-G-A

76261342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135883212-G-C

http://identifiers.org/hco/7/GRCh38#76261346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135883216-C-A

76261423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135883292-G-C

http://identifiers.org/hco/7/GRCh38#76261718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135883561-C-A

76261718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135883561-C-T

http://identifiers.org/hco/7/GRCh38#76261897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135883702-C-A

76262067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135883864-C-G

76262089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135883886-T-G

76263065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, undefined
orthologous variants: 135884143-T-G

76263227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, undefined
orthologous variants: 135884288-C-T

76263354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, undefined
orthologous variants: 135884394-G-A

76263379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135884419-G-T

76264710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135884664-C-T

76264711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135884665-G-A

76264711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135884665-G-C

76264733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135884689-C-T

76264868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135884804-G-A

76264868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135884804-G-T

76264912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135884892-A-G

76265018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135885007-G-C

76265359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 135885294-G-A

76265359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 135885294-G-C

76265359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 135885294-G-T

76265409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense variant
orthologous variants: 135885344-T-A

76265559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135885475-A-G

76265559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135885475-A-T

76265608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135885508-T-C

76265608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135885508-T-G

76265663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135885566-G-A

76265663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135885566-G-T

76267270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: synonymous variant
orthologous variants: 135885904-G-A

76267270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense variant
orthologous variants: 135885904-G-T

http://identifiers.org/hco/7/GRCh38#76267419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135886053-C-A

76267419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense variant
orthologous variants: 135886053-C-T

http://identifiers.org/hco/7/GRCh38#76267520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135886163-C-A

76267520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, missense_variant
orthologous variants: 135886163-C-G

76267520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, stop_gained
orthologous variants: 135886163-C-T

76267655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886321-G-T

76267705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886370-G-A

76267705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886370-G-T

76267720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886385-G-A

76267720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886385-G-T

76267732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886394-G-C

76267732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886394-G-T

76267755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886418-A-G

76267824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886470-G-T

76267844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886485-G-T

http://identifiers.org/hco/7/GRCh38#76267853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135886498-C-A

76267853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886498-C-G

76268024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886612-C-G

76268024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886612-C-T

76268049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886637-G-T

http://identifiers.org/hco/7/GRCh38#76268060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135886648-C-A

http://identifiers.org/hco/7/GRCh38#76268069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135886657-C-A

76268069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886657-C-T

http://identifiers.org/hco/7/GRCh38#76268126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135886701-C-A

76268126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886701-C-T

http://identifiers.org/hco/7/GRCh38#76268164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135886745-C-A

76268205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886786-A-G

76268409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135886950-G-A

http://identifiers.org/hco/7/GRCh38#76268500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135887025-C-A

76268686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887210-A-G

76268688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887212-C-T

76268690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887214-G-A

76268690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887214-G-T

76268774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887301-G-C

76268774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887301-G-T

http://identifiers.org/hco/7/GRCh38#76268833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135887360-C-A

76268833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887360-C-T

76268853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887380-A-G

76268965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887458-G-T

http://identifiers.org/hco/7/GRCh38#76269038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135887531-C-A

76269038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887531-C-T

76269116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887624-T-C

76269122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887630-T-C

76269143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887650-G-A

76269143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887650-G-T

76269151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887658-A-G

http://identifiers.org/hco/7/GRCh38#76269201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135887718-C-A

76269258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887765-G-A

76269360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135887857-T-C

http://identifiers.org/hco/7/GRCh38#76269768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135888267-C-A

76269768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135888267-C-T

http://identifiers.org/hco/7/GRCh38#76269827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135888369-A-C

76269827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 135888369-A-T

http://identifiers.org/hco/7/GRCh38#76269867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135888404-C-A

76270031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135888560-G-A

76270031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135888560-G-T

76272855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135889388-C-G

76272947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135889466-G-A

76273007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135889525-C-G

76273007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135889525-C-T

76273055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135889564-C-T

76273139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135889598-T-C

76273237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135889644-C-G

76273651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135890070-C-T

76273686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135890105-C-T

http://identifiers.org/hco/7/GRCh38#76273698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135890117-C-A

76274021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135890510-C-T

76274029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135890518-A-G

76274074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135890559-T-C

76274254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135890719-C-T

76274275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135890741-G-A

76274275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135890741-G-T

76274307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135890774-G-T

76274319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135890786-G-A

76274560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135891005-A-G

http://identifiers.org/hco/7/GRCh38#76274630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135891075-A-C

76275228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135891336-A-G

76275257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135891363-G-T

76275294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135891398-G-C

76276875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135892638-G-C

76277114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135892805-T-C

http://identifiers.org/hco/7/GRCh38#76277258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135892934-C-A

76277419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135893084-C-T

76277523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135893192-G-A

76278397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135894122-G-A

76278441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135894149-C-T

76278758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135894431-T-G

76278759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135894432-G-A

76278823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135894494-T-C

76278988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135894740-C-G

76279242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135895179-G-C

76279242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135895179-G-T

76279246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135895183-G-A

http://identifiers.org/hco/7/GRCh38#76279583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135895521-C-A

76279782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135895719-T-C

http://identifiers.org/hco/7/GRCh38#76280113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135896045-A-C

76280196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135896174-C-T

76280352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135896375-G-C

http://identifiers.org/hco/7/GRCh38#76280765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135896791-A-C

76280765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135896791-A-T

76281356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135896939-T-C

76281378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135896963-T-C

http://identifiers.org/hco/7/GRCh38#76281503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135897080-C-A

76281503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: synonymous variant
orthologous variants: 135897080-C-T

76281646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense variant
orthologous variants: 135897223-G-A

76281653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: synonymous variant
orthologous variants: 135897230-T-A

76281653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: synonymous variant
orthologous variants: 135897230-T-C

76281653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: synonymous variant
orthologous variants: 135897230-T-G

76281689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: synonymous variant
orthologous variants: 135897266-G-A

76281689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: synonymous variant
orthologous variants: 135897266-G-C

76281689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: synonymous variant
orthologous variants: 135897266-G-T

http://identifiers.org/hco/7/GRCh38#76281753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135897324-C-A

76281753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense variant
orthologous variants: 135897324-C-G

76281753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense variant
orthologous variants: 135897324-C-T

http://identifiers.org/hco/7/GRCh38#76281785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135897356-C-A

76281785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: synonymous variant
orthologous variants: 135897356-C-T

http://identifiers.org/hco/7/GRCh38#76281840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135897395-A-C

76281840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron variant
orthologous variants: 135897395-A-G

http://identifiers.org/hco/7/GRCh38#76282629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135897667-C-A

76282629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135897667-C-T

76282709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135897743-G-A

76282709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135897743-G-C

76282709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135897743-G-T

76282888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135897923-G-A

76282888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135897923-G-T

http://identifiers.org/hco/7/GRCh38#76282932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135897980-C-A

76282932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135897980-C-T

76283087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135898134-G-A

76283087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135898134-G-T

76283122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898161-G-A

76283122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898161-G-C

76283122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898161-G-T

76283127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898166-T-C

http://identifiers.org/hco/7/GRCh38#76283137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135898177-C-A

76283137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898177-C-G

76283137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898177-C-T

76283147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898187-T-C

http://identifiers.org/hco/7/GRCh38#76283189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135898248-C-A

76283189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898248-C-T

76283192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898251-A-G

76283192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898251-A-T

76283381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898443-G-A

76283381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898443-G-T

76283397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898454-G-T

76283413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898470-G-A

76283413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898470-G-T

76283431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898480-T-C

http://identifiers.org/hco/7/GRCh38#76283450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135898499-C-A

76283450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898499-C-T

http://identifiers.org/hco/7/GRCh38#76283451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135898500-C-A

76283498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898548-T-A

76283498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898548-T-C

76283498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898548-T-G

http://identifiers.org/hco/7/GRCh38#76283562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135898612-C-A

http://identifiers.org/hco/7/GRCh38#76283700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135898756-C-A

76283700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898756-C-G

76283700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898756-C-T

76283710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135898766-T-C

76284710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135899844-C-G

http://identifiers.org/hco/7/GRCh38#76284806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135899949-C-A

http://identifiers.org/hco/7/GRCh38#76285464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135901762-C-A

76285464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135901762-C-T

76285504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135901789-G-A

76285504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135901789-G-C

76285504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135901789-G-T

76285519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135901804-A-G

http://identifiers.org/hco/7/GRCh38#76285713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135902032-C-A

76285713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135902032-C-T

76285726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: non_coding_transcript_exon_variant, stop_gained, synonymous_variant
orthologous variants: 135902045-C-T

http://identifiers.org/hco/7/GRCh38#76285933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135902250-C-A

76286241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135902590-T-A

76286241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135902590-T-C

76286937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135903283-A-G

http://identifiers.org/hco/7/GRCh38#76287016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135903344-A-C

76287016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135903344-A-G

76287052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135903378-G-A

http://identifiers.org/hco/7/GRCh38#76287088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#135903419-C-A

76287088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26729
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135903419-C-T