http://identifiers.org/hco/1/GRCh38#1020130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281933-C-A

1020130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5 prime UTR variant
orthologous variants: 156281933-C-G

1020130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5 prime UTR variant
orthologous variants: 156281933-C-T

http://identifiers.org/hco/1/GRCh38#1020158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281899-C-A

1020158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5 prime UTR variant
orthologous variants: 156281899-C-T

http://identifiers.org/hco/1/GRCh38#1020159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281898-C-A

1020159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5 prime UTR variant
orthologous variants: 156281898-C-T

http://identifiers.org/hco/1/GRCh38#1020177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281871-C-A

1020177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156281871-C-G

1020177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156281871-C-T

http://identifiers.org/hco/1/GRCh38#1020182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281866-C-A

1020182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156281866-C-G

1020182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156281866-C-T

http://identifiers.org/hco/1/GRCh38#1020190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281852-C-A

1020190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 156281852-C-T

http://identifiers.org/hco/1/GRCh38#1020206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281836-C-A

1020206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156281836-C-T

1020235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 156281807-G-A

1020235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 156281807-G-C

1020235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 156281807-G-T

1020237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 156281805-G-A

1020237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 156281805-G-T

1020302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156281740-A-G

http://identifiers.org/hco/1/GRCh38#1020347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281695-C-A

1020347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156281695-C-T

http://identifiers.org/hco/1/GRCh38#1020377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281665-C-A

1020377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281665-C-T

http://identifiers.org/hco/1/GRCh38#1020381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281660-C-A

1020381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 156281660-C-T

http://identifiers.org/hco/1/GRCh38#1020383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281658-C-A

1020383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281658-C-T

1020421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281557-G-A

1020421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281557-G-C

1020421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281557-G-T

1020456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281522-C-T

http://identifiers.org/hco/1/GRCh38#1020457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281521-C-A

1020457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281521-C-G

1020457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281521-C-T

1020458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281520-G-A

1020458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281520-G-C

1020458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281520-G-T

http://identifiers.org/hco/1/GRCh38#1020461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281517-C-A

1020461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281517-C-G

1020461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281517-C-T

http://identifiers.org/hco/1/GRCh38#1020487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281490-C-A

1020487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281490-C-T

http://identifiers.org/hco/1/GRCh38#1020492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281485-C-A

1020492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281485-C-T

1020508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281468-G-A

1020508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281468-G-T

1020517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281459-G-A

1020517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281459-G-C

1020517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281459-G-T

http://identifiers.org/hco/1/GRCh38#1020534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281441-A-C

1020636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281321-T-C

1020660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281297-G-A

1020674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281283-C-T

1020694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281274-G-T

1020703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281265-G-T

1020763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281227-G-A

1020778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281215-G-C

1020815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281179-C-T

1020856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281143-G-T

http://identifiers.org/hco/1/GRCh38#1020858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156281141-C-A

1020858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281141-C-G

1020861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281138-G-A

1020861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281138-G-C

1020886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, undefined
orthologous variants: 156281111-C-T

1020910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, undefined
orthologous variants: 156281087-G-T

1020942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281072-G-A

1020957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281057-C-T

1020980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156281036-C-G

1021083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, undefined
orthologous variants: 156280953-G-A

1021083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, undefined
orthologous variants: 156280953-G-C

1021158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156280882-T-G

http://identifiers.org/hco/1/GRCh38#1021221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156280828-C-A

1021221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156280828-C-T

1021432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156280645-C-G

1021568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156280503-C-T

http://identifiers.org/hco/1/GRCh38#1021714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156280368-C-A

1021714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156280368-C-G

1021714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156280368-C-T

1021726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156280357-G-A

1022113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156280069-T-C

http://identifiers.org/hco/1/GRCh38#1022117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156280065-C-A

1022117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156280065-C-T

1022476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156279684-G-T

1022508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156279647-G-T

http://identifiers.org/hco/1/GRCh38#1022512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156279643-C-A

1022512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156279643-C-T

1022556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156279607-T-A

http://identifiers.org/hco/1/GRCh38#1022570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156279593-C-A

1022570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156279593-C-G

1022570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156279593-C-T

1022581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156279578-G-A

1022581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156279578-G-C

1022581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156279578-G-T

1022867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156279297-G-T

1022990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156279205-C-T

1023171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156279061-G-T

1023211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156279018-C-T

1023297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278921-G-A

1023336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278903-G-A

1023494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278794-C-T

1023513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278779-T-C

1023522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278770-C-G

1023522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278770-C-T

1023555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278717-G-A

1023703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278577-A-G

1023781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278500-G-A

1023781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278500-G-T

1023788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278492-G-A

1023872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278394-G-C

1023883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278383-G-A

http://identifiers.org/hco/1/GRCh38#1024045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156278249-A-C

1024048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278246-G-A

1024055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278240-C-T

1024071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278224-C-T

1024260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278084-C-T

1024294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278057-C-T

1024360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156278008-C-T

1024376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277992-G-C

1024471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277948-C-T

1024578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277926-C-T

1024744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277849-C-T

1024778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277826-G-A

1024784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277820-T-C

1024888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277719-C-T

1024906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277701-C-T

http://identifiers.org/hco/1/GRCh38#1025041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156277622-A-C

1025042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277621-A-T

1025049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277614-T-C

1025056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277607-G-A

http://identifiers.org/hco/1/GRCh38#1025137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156277541-A-C

1025210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277469-G-C

1025222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277457-C-T

1025298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277382-G-A

1025649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277077-T-A

1025649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277077-T-C

1025670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156277055-T-G

1025970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156276898-C-G

1025970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156276898-C-T

1026100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156276764-G-A

1026157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156276709-G-T

1026179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156276645-C-T

1026264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156276530-G-A

1026425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156276383-C-T

1026589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156276247-T-G

http://identifiers.org/hco/1/GRCh38#1026667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156276217-A-C

1026833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156276144-G-A

1026958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156276057-G-C

1027117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156275919-G-A

1027117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156275919-G-C

1027462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156275728-G-A

1027462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156275728-G-C

1027587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156275632-T-C

1027708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156275513-C-T

1031446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156273375-C-T

1031543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156273279-C-T

1031686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156273102-G-A

1031726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156273067-G-C

http://identifiers.org/hco/1/GRCh38#1031749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156273044-C-A

1032059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156272390-G-T

1032140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156272312-G-A

1032232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156272229-G-T

1032457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156272019-G-A

1032598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, undefined
orthologous variants: 156271896-T-C

1032844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, undefined
orthologous variants: 156271734-T-G

1032869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156271724-C-T

1033190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, undefined
orthologous variants: 156271447-G-T

1033291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156271353-C-G

1033643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156271077-G-A

1033643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156271077-G-C

1033688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156271036-C-T

1033700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156271024-C-G

1033700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156271024-C-T

1033806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156270918-G-C

http://identifiers.org/hco/1/GRCh38#1033832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156270892-C-A

1033864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156270859-C-G

1033864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156270859-C-T

1033865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156270858-C-G

1033958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156270751-G-A

1033958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156270751-G-T

1033984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156270723-T-G

1034016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270691-G-A

1034016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270691-G-C

1034016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270691-G-T

http://identifiers.org/hco/1/GRCh38#1034017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156270690-A-C

1034017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270690-A-G

1034028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270679-T-C

1034028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270679-T-G

1034029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270678-G-A

1034029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270678-G-T

http://identifiers.org/hco/1/GRCh38#1034038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156270672-C-A

1034038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270672-C-G

1034041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270669-G-A

http://identifiers.org/hco/1/GRCh38#1034060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156270650-C-A

1034060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270650-C-T

1034063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270616-G-A

http://identifiers.org/hco/1/GRCh38#1034109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156270573-C-A

1034109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270573-C-G

1034109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270573-C-T

1034229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270474-G-A

1034238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270463-G-C

1034292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270408-C-T

1034349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270352-T-G

http://identifiers.org/hco/1/GRCh38#1034350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156270351-C-A

1034350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270351-C-G

1034361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270340-C-T

1034409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270292-T-A

1034409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270292-T-C

1034431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270270-G-A

1034431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270270-G-T

1034463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270238-A-G

http://identifiers.org/hco/1/GRCh38#1034502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156270199-C-A

1034502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270199-C-G

1034510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270191-A-G

1034517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270184-A-G

1034527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270174-A-G

1034528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270173-G-A

1034535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156270166-G-A

http://identifiers.org/hco/1/GRCh38#1034652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156270057-C-A

1034652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 156270057-C-T

1034722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156269990-G-A

1034779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156269940-G-A

1034779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156269940-G-T

http://identifiers.org/hco/1/GRCh38#1034789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156269926-C-A

1034789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156269926-C-T

http://identifiers.org/hco/1/GRCh38#1034809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156269899-C-A

1034809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156269899-C-T

1034830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156269873-T-A

1034830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156269873-T-C

1034830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156269873-T-G

http://identifiers.org/hco/1/GRCh38#1034837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156269868-A-C

1034837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156269868-A-G

1034837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156269868-A-T

http://identifiers.org/hco/1/GRCh38#1034860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156269845-C-A

1034860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156269845-C-G

1034860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156269845-C-T

1034864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156269841-G-T

http://identifiers.org/hco/1/GRCh38#1034872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156269833-A-C

1034872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156269833-A-G

1034872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156269833-A-T

1034873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156269832-G-A

1034873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156269832-G-T

http://identifiers.org/hco/1/GRCh38#1034890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156269815-C-A

1034890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156269815-C-T

1034916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156269798-G-A

1034931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156269783-G-A

1034949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156269772-G-A

1034970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156269759-G-A

1034970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156269759-G-T

1035285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156269582-G-A

1035285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156269582-G-C

1035393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156269458-G-A

1035433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156269430-G-A

http://identifiers.org/hco/1/GRCh38#1035471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156269411-C-A

1035513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156269392-G-A

1035523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156269382-G-A

1035562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156269368-C-T

1035575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156269355-A-G

1035746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156269217-G-A

1035794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156269173-C-T

1035996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156269001-A-T

1036448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156268149-C-T

1036453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156268144-G-A

1036525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156268069-G-A

1036525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156268069-G-C

1036721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156267913-C-T

1036904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156267845-G-A

1036983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156267782-A-G

1037052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156267751-T-A

1037132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156267682-G-T

1037407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156267402-G-A

1037480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156267294-T-C

1037481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156267293-A-G

1037501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156267274-T-C

1037578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156267201-A-T

1037613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156267167-C-G

1037613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156267167-C-T

1037639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156267146-G-C

1037693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156267099-C-T

1037800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156266989-G-C

1037800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156266989-G-T

1038665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156266037-G-A

1038665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156266037-G-T

1038733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156265967-C-T

1038784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156265918-C-T

1039009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156265713-G-A

1039258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156265583-G-A

1039291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156265546-T-C

1039635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156265268-T-C

1039652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156265253-C-T

1039748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156265169-G-A

1039796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156265117-G-A

1039804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156265103-G-A

1039821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156265086-G-A

http://identifiers.org/hco/1/GRCh38#1040008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156264818-A-C

1040039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156264751-G-A

1040356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156264361-C-G

1040604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156264132-G-A

1040604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156264132-G-T

1040623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156264113-G-A

1040623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156264113-G-C

1040623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156264113-G-T

http://identifiers.org/hco/1/GRCh38#1040655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156264090-C-A

1040655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156264090-C-T

1040656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156264089-C-G

1040656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156264089-C-T

http://identifiers.org/hco/1/GRCh38#1040659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156264086-C-A

1040659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156264086-C-T

1040664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 156264064-G-C

1040664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 156264064-G-T

1040764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 156263964-G-A

1040764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 156263964-G-T

1040769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 156263959-G-A

1040769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 156263959-G-T

1040808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156263920-A-G

http://identifiers.org/hco/1/GRCh38#1040862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#156263866-C-A

1040862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 156263866-C-T

1040885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156263843-G-A

http://identifiers.org/hco/1/GRCh38#1041158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156263792-A-C

1041238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 156263712-G-A

1041238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 156263712-G-C

1041238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 156263712-G-T

1041244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 156263706-A-G

http://identifiers.org/hco/1/GRCh38#1041261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#156263689-C-A

1041261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 156263689-C-T

1041304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156263646-A-T

1041402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156263548-G-A

1041402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156263548-G-T

http://identifiers.org/hco/1/GRCh38#1041408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156263542-C-A

1041408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156263542-C-G

1041408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156263542-C-T

1041423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156263529-T-C

http://identifiers.org/hco/1/GRCh38#1041447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156263492-C-A

1041600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156263340-G-A

1041600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156263340-G-C

1041634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156263306-T-C

1041649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156263291-C-T

1041722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156263221-G-T

1041726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156263217-G-A

1041726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156263217-G-T

1041737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156263207-T-C

1041964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156263082-C-T

http://identifiers.org/hco/1/GRCh38#1042003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156263043-C-A

1042003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156263043-C-T

http://identifiers.org/hco/1/GRCh38#1042030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156263016-C-A

1042030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156263016-C-T

1042111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156262935-G-A

1042111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156262935-G-T

1042175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156262871-G-A

1042175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156262871-G-T

http://identifiers.org/hco/1/GRCh38#1042203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156262848-C-A

1042203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156262848-C-T

1042251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156262801-G-A

1042272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156262780-G-A

1042272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156262780-G-T

1042306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156262749-G-T

1042430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156262652-G-A

1042430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156262652-G-T

1042632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156262394-G-A

http://identifiers.org/hco/1/GRCh38#1043148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156261977-C-A

1043148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261977-C-G

1043148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261977-C-T

http://identifiers.org/hco/1/GRCh38#1043181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156261947-C-A

1043181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261947-C-T

1043182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261946-T-C

1043189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261939-G-A

1043189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261939-G-C

1043189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261939-G-T

http://identifiers.org/hco/1/GRCh38#1043193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156261937-C-A

1043193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261937-C-T

1043211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261919-G-T

1043212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261918-A-T

1043226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261909-G-A

1043271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156261864-T-C

1043339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 156261796-G-A

1043339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 156261796-G-C

1043339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 156261796-G-T

1043342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 156261793-C-T

1043352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156261783-C-T

1043412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156261723-T-C

1043432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 156261703-C-T

1043462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261673-G-A

1043477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261666-T-C

1043477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261666-T-G

1043478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261665-C-G

1043478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261665-C-T

1043490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261655-G-A

1043490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261655-G-T

1043503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261641-T-G

1043513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261630-C-T

1043531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 156261612-T-C

1043555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156261588-C-G

1043555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156261588-C-T

1043606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156261537-G-A

1043606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156261537-G-C

1043606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, stop_gained
orthologous variants: 156261537-G-T

1043636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156261507-G-A

1043636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156261507-G-T

1043642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156261501-G-A

1043642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156261501-G-T

1043666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156261477-T-A

1043720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156261423-G-A

1043720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156261423-G-C

1043745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261406-C-T

http://identifiers.org/hco/1/GRCh38#1043751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156261400-C-A

1043751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261400-C-T

1043795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261316-G-A

1043795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261316-G-T

http://identifiers.org/hco/1/GRCh38#1043808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156261304-C-A

1043808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261304-C-G

1043808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261304-C-T

1043900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156261212-C-T

1043918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156261194-T-A

1043918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156261194-T-C

1043918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156261194-T-G

1043930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156261182-G-A

1043930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156261182-G-C

1043930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156261182-G-T

http://identifiers.org/hco/1/GRCh38#1043957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156261155-C-A

1043957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156261155-C-T

1043963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156261149-G-A

1044011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156261101-C-T

1044030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 156261082-C-T

1044038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261075-G-A

1044038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261075-G-T

1044039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261074-C-T

1044045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261068-A-G

1044068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261045-G-A

1044089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156261027-T-C

1044156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156260960-G-A

http://identifiers.org/hco/1/GRCh38#1044165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156260951-C-A

1044207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156260909-G-A

1044326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 156260787-C-G

1044326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 156260787-C-T

1044350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156260763-G-A

1044350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156260763-G-C

1044358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156260755-T-C

1044370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156260743-T-C

1044371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156260742-G-A

1044386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156260727-C-G

1044415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156260698-G-A

1044415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156260698-G-C

1044455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156260657-G-A

1044455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156260657-G-C

1044455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156260657-G-T

1044478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156260643-G-A

1044478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156260643-G-C

1044478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156260643-G-T

1044642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156260340-T-C

http://identifiers.org/hco/1/GRCh38#1044656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156260312-C-A

1044675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156260290-C-T

1044720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156260210-C-T

1044874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156259962-T-C

1045080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156259758-G-A

1045080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156259758-G-C

1045080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156259758-G-T

1045085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156259753-G-A

1045085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156259753-G-T

1045093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156259740-A-G

1045098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156259735-G-T

1045138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156259695-G-A

1045143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156259689-C-G

1045143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156259689-C-T

1045247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156259585-G-A

1045288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156259544-G-A

1045297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156259535-C-G

1045297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156259535-C-T

1045394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156259440-G-A

1045394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156259440-G-C

1045686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156259214-G-A

1045689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156259211-C-T

1045703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156259197-C-T

1045722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156259178-T-A

1045722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156259178-T-C

1045828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156259074-G-A

1045828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156259074-G-C

http://identifiers.org/hco/1/GRCh38#1045859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156259043-C-A

1045861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156259041-G-A

1045898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156259001-C-T

1045946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156258951-C-T

1045955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156258944-G-A

1045955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156258944-G-C

1045973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156258926-C-T

1046008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156258891-G-A

1046008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156258891-G-C

1046020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156258879-G-A

1046020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156258879-G-C

1046020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156258879-G-T

http://identifiers.org/hco/1/GRCh38#1046053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156258846-C-A

1046111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156258788-G-A

1046140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156258757-A-G

1046193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156258704-G-A

1046193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156258704-G-C

1046272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 156258625-C-T

1046291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156258607-G-C

1046383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156258559-C-T

1046458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156258490-C-T

1046467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156258481-C-T

1046488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156258460-C-G

1046488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156258460-C-T

1046495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156258453-C-G

1046593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156258360-G-T

http://identifiers.org/hco/1/GRCh38#1046594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156258359-C-A

1046594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156258359-C-T

1046648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156258327-T-C

http://identifiers.org/hco/1/GRCh38#1046650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156258325-C-A

1046650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156258325-C-T

1046675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156258300-G-T

http://identifiers.org/hco/1/GRCh38#1046696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156258279-C-A

1046696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156258279-C-T

1046702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156258273-G-A

1046702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156258273-G-C

1046702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156258273-G-T

1046752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156258222-G-C

1046796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156258159-T-A

1046796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156258159-T-C

1046806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156258149-G-A

1046806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156258149-G-T

1046808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156258147-G-A

1046808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156258147-G-C

1046808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156258147-G-T

http://identifiers.org/hco/1/GRCh38#1046855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156258100-C-A

1046855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156258100-C-G

1046855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156258100-C-T

1046867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156258088-G-C

1046867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156258088-G-T

1046890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156258065-C-T

1046936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156258019-G-A

1046936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156258019-G-T

1046971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156257984-T-C

1046973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156257982-G-A

1046973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156257982-G-T

1046982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156257976-A-G

1046982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156257976-A-T

1047011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156257947-G-A

1047011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156257947-G-T

1047206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156257703-G-T

http://identifiers.org/hco/1/GRCh38#1047220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156257689-C-A

1047235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156257676-G-A

1047235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156257676-G-T

http://identifiers.org/hco/1/GRCh38#1047239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156257672-C-A

1047239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156257672-C-T

1047241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156257669-T-A

1047241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156257669-T-C

1047520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156257400-A-G

http://identifiers.org/hco/1/GRCh38#1047524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156257387-C-A

1047576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156257334-G-C

1047594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156257316-T-G

1047707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156257209-C-T

1047735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156257181-T-C

1047790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156257122-G-A

1047790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156257122-G-T

http://identifiers.org/hco/1/GRCh38#1047814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156257098-C-A

1047814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156257098-C-G

1047814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156257098-C-T

http://identifiers.org/hco/1/GRCh38#1047862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156257050-C-A

1047862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156257050-C-T

1047867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156257045-G-A

1047879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156257033-G-A

http://identifiers.org/hco/1/GRCh38#1047981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256926-A-C

1047981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156256926-A-G

1047981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156256926-A-T

http://identifiers.org/hco/1/GRCh38#1048051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256838-C-A

1048051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156256838-C-T

http://identifiers.org/hco/1/GRCh38#1048129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256763-A-C

1048129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156256763-A-G

http://identifiers.org/hco/1/GRCh38#1048137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256755-C-A

1048137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156256755-C-T

http://identifiers.org/hco/1/GRCh38#1048201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256691-C-A

1048201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156256691-C-T

http://identifiers.org/hco/1/GRCh38#1048254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256641-C-A

1048254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156256641-C-T

http://identifiers.org/hco/1/GRCh38#1048266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256629-C-A

1048266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156256629-C-G

1048266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: stop gained
orthologous variants: 156256629-C-T

http://identifiers.org/hco/1/GRCh38#1048278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256617-C-A

1048278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156256617-C-T

http://identifiers.org/hco/1/GRCh38#1048319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256576-C-A

1048319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156256576-C-T

1048343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156256552-G-A

1048343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156256552-G-T

1048394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156256501-G-A

1048394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156256501-G-T

1048868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 156256434-G-A

1048868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 156256434-G-T

http://identifiers.org/hco/1/GRCh38#1048869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256433-C-A

1048869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 156256433-C-T

1048887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156256415-G-A

1048887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156256415-G-T

http://identifiers.org/hco/1/GRCh38#1048944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256358-C-A

1048944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156256358-C-T

1049064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156256238-G-A

1049064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156256238-G-T

http://identifiers.org/hco/1/GRCh38#1049075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256226-A-C

1049075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156256226-A-G

1049075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156256226-A-T

1049083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156256218-G-A

1049083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156256218-G-C

1049083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156256218-G-T

http://identifiers.org/hco/1/GRCh38#1049093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256208-A-C

1049093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156256208-A-G

1049093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156256208-A-T

http://identifiers.org/hco/1/GRCh38#1049204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256104-C-A

1049204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156256104-C-G

1049204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156256104-C-T

http://identifiers.org/hco/1/GRCh38#1049219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256089-C-A

1049219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156256089-C-T

http://identifiers.org/hco/1/GRCh38#1049226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256082-C-A

http://identifiers.org/hco/1/GRCh38#1049243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256065-A-C

1049243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156256065-A-G

1049243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156256065-A-T

1049258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156256050-G-T

http://identifiers.org/hco/1/GRCh38#1049288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156256020-C-A

1049288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156256020-C-T

1049309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156255999-G-A

1049309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156255999-G-C

1049309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 156255999-G-T

1049378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156255930-C-T

1049384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156255924-G-A

1049449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 156255859-C-G

1049449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 156255859-C-T

1049493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255728-T-C

1049497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255722-G-A

1049497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255722-G-T

1049512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255697-G-C

1049512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255697-G-T

1049513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255696-G-A

1049513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255696-G-T

1049525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255678-G-T

1049530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255673-C-T

1049541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255662-G-A

1049558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 156255493-G-A

1049558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 156255493-G-T

1049687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156255364-G-T

1049690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156255361-G-A

1049690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: stop gained
orthologous variants: 156255361-G-T

1049696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156255355-G-A

1049696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156255355-G-C

1049696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156255355-G-T

http://identifiers.org/hco/1/GRCh38#1049702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156255349-C-A

1049702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156255349-C-T

1049711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156255340-C-T

http://identifiers.org/hco/1/GRCh38#1049809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156255242-C-A

1049809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255242-C-T

1049871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255190-C-G

1049958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156255113-G-A

1049997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156255074-C-T

1050013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156255058-C-T

1050047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255025-G-A

1050047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255025-G-T

1050051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255021-G-A

1050051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255021-G-T

1050060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255012-G-A

1050060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255012-G-C

1050060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255012-G-T

1050068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255004-G-A

1050068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255004-G-C

1050068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156255004-G-T

1050085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156254987-G-A

1050085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156254987-G-T

1050108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156254965-G-A

1050196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156254901-G-C

1050249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156254850-C-T

http://identifiers.org/hco/1/GRCh38#1050287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156254812-A-C

1050287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156254812-A-G

http://identifiers.org/hco/1/GRCh38#1050500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156254612-A-C

1050576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156254536-G-A

1050576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156254536-G-T

1050626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156254441-G-A

http://identifiers.org/hco/1/GRCh38#1050703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156254353-C-A

1050703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156254353-C-T

1050853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156254210-C-T

1050888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156254155-C-T

http://identifiers.org/hco/1/GRCh38#1050926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156254114-C-A

1050926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156254114-C-T

http://identifiers.org/hco/1/GRCh38#1051051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156253993-C-A

1051051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 156253993-C-G

1051051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 156253993-C-T

1051058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253986-T-C

1051085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253955-A-G

1051098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253942-G-A

1051098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253942-G-T

1051115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253926-G-A

1051115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253926-G-C

1051115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253926-G-T

1051128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253910-C-T

1051131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253907-T-A

http://identifiers.org/hco/1/GRCh38#1051151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156253887-A-C

1051151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253887-A-G

1051151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253887-A-T

1051168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253880-G-A

1051168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253880-G-T

http://identifiers.org/hco/1/GRCh38#1051185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156253866-A-C

1051185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253866-A-G

1051185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253866-A-T

1051214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253831-G-A

1051214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253831-G-T

1051224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253821-G-A

1051224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253821-G-C

1051224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253821-G-T

http://identifiers.org/hco/1/GRCh38#1051283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#156253761-C-A

1051283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, undefined
orthologous variants: 156253761-C-T

http://identifiers.org/hco/1/GRCh38#1051286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#156253758-C-A

1051286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, undefined
orthologous variants: 156253758-C-T

1051292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253752-G-A

1051292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253752-G-C

1051292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253752-G-T

1051328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253716-G-A

1051328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253716-G-T

http://identifiers.org/hco/1/GRCh38#1051329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156253715-C-A

1051329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253715-C-G

1051329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253715-C-T

1051338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253706-T-C

1051343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253701-T-A

1051343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253701-T-C

http://identifiers.org/hco/1/GRCh38#1051390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156253659-C-A

1051390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253659-C-T

1051409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253638-G-A

1051409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253638-G-C

1051409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253638-G-T

1051419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253615-G-A

1051419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253615-G-C

1051419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253615-G-T

1051427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253607-G-A

1051427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253607-G-T

1051437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253569-T-C

1051479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156253524-G-A

1051479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156253524-G-C

1051479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156253524-G-T

1051548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156253455-A-G

1051548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: synonymous variant
orthologous variants: 156253455-A-T

1051550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253453-G-A

1051550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253453-G-C

1051550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253453-G-T

1051583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253420-C-T

1051600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253403-G-A

1051610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253393-G-A

1051610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253393-G-T

1051680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253326-A-T

1051733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253270-G-T

1051790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense variant
orthologous variants: 156253213-G-A

http://identifiers.org/hco/1/GRCh38#1051828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156253160-C-A

1051828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253160-C-G

1051828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253160-C-T

1051831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253157-C-T

1051925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253072-C-G

1051925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253072-C-T

1051930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253067-C-G

1051930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron variant
orthologous variants: 156253067-C-T

1052009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156253008-A-G

1052009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156253008-A-T

1052204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252805-G-T

http://identifiers.org/hco/1/GRCh38#1052205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156252804-C-A

1052205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252804-C-T

1052267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252766-T-A

1052267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252766-T-C

1052267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252766-T-G

http://identifiers.org/hco/1/GRCh38#1052280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156252753-C-A

1052280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252753-C-G

http://identifiers.org/hco/1/GRCh38#1052312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156252745-C-A

1052312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252745-C-G

1052312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252745-C-T

1052313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252744-T-A

1052313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252744-T-C

1052313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252744-T-G

1052343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252714-G-T

1052352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252705-A-G

1052352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252705-A-T

1052940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252666-A-G

1053019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252585-A-G

1053020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252584-T-C

1053038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252565-G-A

1053038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252565-G-T

1053059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252553-G-A

1053420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252304-T-C

http://identifiers.org/hco/1/GRCh38#1053593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156252125-C-A

1053593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252125-C-T

1053665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252050-C-T

1053676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252039-G-A

1053676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252039-G-C

1053676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252039-G-T

http://identifiers.org/hco/1/GRCh38#1053698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156252014-C-A

1053698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252014-C-G

1053698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156252014-C-T

http://identifiers.org/hco/1/GRCh38#1053775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156251939-C-A

1053775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156251939-C-G

1053775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156251939-C-T

1053843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156251871-G-A

1053850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156251864-G-C

1053879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156251835-G-A

1053904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156251810-G-A

1053904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156251810-G-C

http://identifiers.org/hco/1/GRCh38#1053951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156251763-C-A

1054019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156251702-T-C

1054335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156251582-G-A

1054335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156251582-G-T

http://identifiers.org/hco/1/GRCh38#1054340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156251577-C-A

1054340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156251577-C-T

1054350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156251567-A-G

1054351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156251566-G-A

1054372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156251545-G-A

http://identifiers.org/hco/1/GRCh38#1054377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156251535-C-A

1054377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156251535-C-T

1054503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156251414-T-C

1054522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156251395-A-G

1054522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156251395-A-T

1054569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156251348-A-T

1054577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156251338-G-T

1054702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156251204-C-T

1054812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156251120-T-A

1054812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156251120-T-C

http://identifiers.org/hco/1/GRCh38#1055003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156250925-C-A

1055003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156250925-C-T

http://identifiers.org/hco/1/GRCh38#1055122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156250806-A-C

1055122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156250806-A-T

1055145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156250780-G-A

1055145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156250780-G-T

1055151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156250774-G-A

1055151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156250774-G-T

http://identifiers.org/hco/1/GRCh38#1055197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156250727-C-A

1055197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156250727-C-T

1055216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 156250709-G-A

1055216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 156250709-G-T

1055297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250603-T-C

1055303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250597-A-G

1055310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250590-A-T

1055418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250485-T-A

1055418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250485-T-C

1055418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250485-T-G

1055419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250484-G-A

1055419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250484-G-C

1055419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250484-G-T

http://identifiers.org/hco/1/GRCh38#1055521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156250360-C-A

1055521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250360-C-T

1055534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250348-G-A

1055661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250256-A-G

1055682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250235-C-T

http://identifiers.org/hco/1/GRCh38#1055693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156250220-C-A

1055708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250184-T-C

1055718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250168-T-C

http://identifiers.org/hco/1/GRCh38#1055807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156250080-A-C

http://identifiers.org/hco/1/GRCh38#1055817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156250070-C-A

1055817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250070-C-G

http://identifiers.org/hco/1/GRCh38#1055824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156250063-C-A

1055824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250063-C-T

1055841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250038-G-A

1055841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156250038-G-T

1055971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 329
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 156249919-C-T