145858411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42118303-A-G

http://identifiers.org/hco/5/GRCh38#145858442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42118329-C-A

145858442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42118329-C-G

145858442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42118329-C-T

145858580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42118448-T-C

http://identifiers.org/hco/5/GRCh38#145858630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42118485-A-C

145858630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42118485-A-T

145858946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42118798-T-A

145859190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119005-G-A

145859190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119005-G-C

145859190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119005-G-T

http://identifiers.org/hco/5/GRCh38#145859192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42119007-C-A

145859192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119007-C-G

145859192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119007-C-T

145859233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119048-G-A

145859338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119154-C-G

145859338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119154-C-T

145859401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119235-T-C

145859516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119354-A-G

http://identifiers.org/hco/5/GRCh38#145859549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42119387-A-C

145859549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119387-A-G

145859549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119387-A-T

145859633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119472-G-A

145859633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119472-G-T

145859656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119496-G-A

145859670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119506-G-A

145859730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119571-G-A

145859730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 3 prime UTR variant
orthologous variants: 42119571-G-T

http://identifiers.org/hco/5/GRCh38#145859871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42119712-C-A

145859871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: synonymous variant
orthologous variants: 42119712-C-G

145859871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: synonymous variant
orthologous variants: 42119712-C-T

145859906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: missense variant
orthologous variants: 42119744-T-G

145859948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42119786-A-G

http://identifiers.org/hco/5/GRCh38#145859955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42119793-C-A

http://identifiers.org/hco/5/GRCh38#145859974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42119812-C-A

145859974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42119812-C-T

http://identifiers.org/hco/5/GRCh38#145859979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42119817-C-A

145859979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42119817-C-G

145860009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42119847-G-A

145860009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42119847-G-T

http://identifiers.org/hco/5/GRCh38#145860032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42119870-C-A

145860032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42119870-C-G

145860032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42119870-C-T

http://identifiers.org/hco/5/GRCh38#145860033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42119871-C-A

145860033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42119871-C-G

145860039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42119877-A-G

http://identifiers.org/hco/5/GRCh38#145860055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42119893-C-A

145860214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42120025-A-T

145860314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42120123-A-G

145860418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42120213-G-A

145860712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42120879-C-G

145860755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42120921-C-G

145861012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42121180-A-G

145861018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42121184-T-C

145861053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42121218-G-A

145861053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42121218-G-T

145861087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42121255-T-C

145861247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42121397-G-A

145861405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42121580-G-A

145861414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42121589-G-A

145862627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42121786-C-G

145862666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42121828-T-C

145862889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42122048-T-A

145863048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42122237-G-C

http://identifiers.org/hco/5/GRCh38#145863433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42122596-C-A

145863433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42122596-C-G

http://identifiers.org/hco/5/GRCh38#145863439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42122602-A-C

145863449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42122612-T-G

145863509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42122673-T-G

145863614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42122780-G-A

http://identifiers.org/hco/5/GRCh38#145864044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42123042-C-A

145864076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42123074-G-T

145864322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42123293-A-G

145864349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42123320-G-A

http://identifiers.org/hco/5/GRCh38#145864917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42123727-C-A

145864917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42123727-C-T

145864929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42123739-G-T

145864956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42123766-G-A

145864968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42123776-T-C

145865057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42123863-C-G

145865190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42123989-T-C

http://identifiers.org/hco/5/GRCh38#145865645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42124076-C-A

145865809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42124232-C-T

http://identifiers.org/hco/5/GRCh38#145865987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42124356-A-C

145865987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42124356-A-G

145866039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42124400-G-A

145866048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42124409-A-G

http://identifiers.org/hco/5/GRCh38#145866108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42124478-C-A

145866166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42124525-A-G

145866267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42124595-A-G

145866547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: missense variant
orthologous variants: 42124868-G-A

145866547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: missense variant
orthologous variants: 42124868-G-T

145866555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: synonymous variant
orthologous variants: 42124876-G-A

145866555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: missense variant
orthologous variants: 42124876-G-C

145866668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 5_prime_UTR_variant, stop_gained
orthologous variants: 42125010-G-A

145866668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 42125010-G-T

145866726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 5_prime_UTR_variant, splice_region_variant, synonymous_variant
orthologous variants: 42125068-G-A

145866726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 5_prime_UTR_variant, splice_region_variant, synonymous_variant
orthologous variants: 42125068-G-C

145866767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42125098-A-G

145866776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42125107-G-A

145866776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42125107-G-T

145866796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42125127-T-C

145866824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42125155-G-A

145866824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42125155-G-T

145866832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42125163-A-G

145866919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42125245-G-A

145866965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42125291-A-G

145866970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42125296-A-G

http://identifiers.org/hco/5/GRCh38#145867026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42125374-C-A

145867196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42125517-G-C

145867802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42126743-T-C

145867926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42126868-T-C

145868238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42127150-C-T

145868586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42127484-T-C

145868742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42127651-G-T

145868879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42127775-C-T

145869017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42127910-G-A

145869123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42127993-C-T

145869288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42128618-G-T

145869963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42129367-C-G

145870018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42129410-C-G

145870018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42129410-C-T

145870128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42129513-G-A

145870290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42129644-T-A

145870322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42129676-A-G

145870463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42129806-T-C

145870746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42130064-G-T

145871036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42130194-A-G

145871218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42130318-G-A

145871218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42130318-G-T

145871219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42130319-A-T

145871305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42130414-T-C

145871343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42130450-C-T

145871475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42130590-A-G

http://identifiers.org/hco/5/GRCh38#145871481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42130596-C-A

145871481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42130596-C-T

145871967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42131053-T-G

http://identifiers.org/hco/5/GRCh38#145872111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42131197-C-A

145872111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42131197-C-T

http://identifiers.org/hco/5/GRCh38#145872495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42131603-C-A

145872495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42131603-C-T

145872619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42131718-T-C

145872619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42131718-T-G

145872620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42131719-G-A

145872747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, missense_variant
orthologous variants: 42131846-C-G

145872769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, missense_variant
orthologous variants: 42131868-G-A

145872957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 42132056-A-T

http://identifiers.org/hco/5/GRCh38#145873319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42132412-A-C

145873980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42133027-T-C

145876796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42136283-C-T

145876987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42136459-A-G

145877205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42136671-A-G

http://identifiers.org/hco/5/GRCh38#145877272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42136738-C-A

145884146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42138581-A-G

145884249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42138687-G-A

145884249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42138687-G-T

145884390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42138824-G-C

145884799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42139186-T-G

145885213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42139546-A-T

http://identifiers.org/hco/5/GRCh38#145885357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42139659-C-A

145885549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42139863-C-T

145885637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42139970-T-C

145885805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42140134-G-C

145885805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42140134-G-T

145885889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42140211-C-T

145885899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42140221-A-G

http://identifiers.org/hco/5/GRCh38#145886107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42140410-C-A

http://identifiers.org/hco/5/GRCh38#145886152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42140450-A-C

http://identifiers.org/hco/5/GRCh38#145886316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42140611-C-A

145886316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42140611-C-G

145886316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42140611-C-T

145886381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42140675-G-A

145887511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42143024-C-T

145887680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42143183-G-A

145887680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42143183-G-C

145887840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42143394-T-C

145887872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42143585-A-G

145887980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42143694-A-G

145888110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42143891-G-A

145888390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42144292-A-G

145888417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42144319-G-A

145888417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42144319-G-T

145888692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42144614-T-C

145902814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42144695-A-T

145902860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42144749-A-G

145903260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42145110-G-A

http://identifiers.org/hco/5/GRCh38#145903364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42145176-A-C

http://identifiers.org/hco/5/GRCh38#145903497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42145296-C-A

145903497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42145296-C-G

145903516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42145315-T-C

145906035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42147287-T-G

145906090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42147348-G-A

145906152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42147407-C-G

145906436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42147694-A-T

145906739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42147964-G-A

145906776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42147994-T-G

145906902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42148142-A-T

145906926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42148166-T-C

145907087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42148313-A-T

145908185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42149913-G-A

145908221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42149949-T-C

145908226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42149961-A-G

145908226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42149961-A-T

145908651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42150372-T-G

145909074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42150760-C-T

145909219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42150882-G-A

145909434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42151119-G-A

145909480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42151165-T-C

145909536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42151218-G-C

145909639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42151321-A-G

145909763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42151428-C-T

145910097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42153033-G-A

145910176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42153114-A-T

145910200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42153134-A-G

145910284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42153216-C-T

145910864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42155332-G-A

145910920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42155364-G-A

145911188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42156190-G-A

145911206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42156208-C-G

145911206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42156208-C-T

145911312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42156308-A-G

145911322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42156318-G-A

145911322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42156318-G-C

145911491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42156449-T-C

145911526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42156484-T-A

145911631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42156571-A-G

145911670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42156604-C-T

145914081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42159462-G-A

145914133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42159514-G-A

145914840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42159894-G-A

145914887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42159935-G-C

145915070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42160102-G-A

145915075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42160107-C-G

145915075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42160107-C-T

145915134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42160156-T-G

145915750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42161574-A-G

145915793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42161607-G-A

145915870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42161677-C-T

145915873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42161680-A-G

http://identifiers.org/hco/5/GRCh38#145915942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42161748-C-A

http://identifiers.org/hco/5/GRCh38#145916049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42161883-C-A

145916049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42161883-C-G

145916179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42162026-A-G

145916269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42162121-G-C

http://identifiers.org/hco/5/GRCh38#145916291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42162143-A-C

145916493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42162343-G-A

145916576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42162412-G-A

145916652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42162475-T-C

145917069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42162832-T-G

145917086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42162862-G-T

145917159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42162919-G-C

145917487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42163231-C-G

145918321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42166302-G-T

http://identifiers.org/hco/5/GRCh38#145918516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42166525-C-A

145918535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42166545-T-C

145918860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42166841-G-A

145919007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42166999-C-T

145919051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42167039-A-G

145919198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42167168-G-T

145919241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42167211-T-C

145919367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42167776-T-C

145919449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42167842-T-A

145919470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42167883-C-T

145919750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42168160-A-G

145919759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42168165-A-T

145920018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42168437-G-A

145920018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42168437-G-T

145920281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42168653-A-G

145920304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42168677-T-G

145920312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42168689-C-T

145920464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42168793-T-C

145920474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42168803-T-C

145920679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42168984-G-A

145920732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42169038-C-T

145921057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42169363-T-C

145921086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42169392-C-T

145922028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42170243-G-A

145922120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42170328-A-G

145922332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42170499-T-G

145922529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42170669-A-T

145922901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42171257-G-C

145923361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42172340-A-G

145923493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42172473-T-C

http://identifiers.org/hco/5/GRCh38#145923527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42172509-C-A

145924356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42174762-G-A

145924452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42174956-T-G

145924903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42175386-G-A

145925012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42175489-G-C

145925606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42176125-G-T

145925709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42176226-T-C

145925750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42176265-T-A

145925833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42176343-T-C

145926009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42176521-T-C

145926042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42176552-A-G

145926126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42176627-G-C

145929557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42178496-C-T

145929576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42178512-A-G

145929822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42178690-C-G

145929994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42178842-T-C

145930004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42178852-A-G

145930476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42178943-T-A

145930522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42178988-C-T

http://identifiers.org/hco/5/GRCh38#145930815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42179292-C-A

145930904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42179374-C-T

145930965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42179414-T-C

145931493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42179617-C-T

145931501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 42179625-C-T

145931838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42179920-C-G

145931838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42179920-C-T

145931840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42179922-A-G

145931939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42180010-T-C

145932080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42180445-A-G

http://identifiers.org/hco/5/GRCh38#145932397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#42180707-C-A

145932678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42181045-C-T

145932697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42181054-C-T

145933102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42181338-G-A

145933139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42181364-T-A

145933335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42181536-C-T

145933409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42181588-G-C

145933414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42181589-C-T

145933656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42181837-T-C

145933773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42181956-C-T

145933884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42182064-A-G

145934119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42182269-C-T

145934231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42182375-T-C

145934269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42182905-T-C

145934304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42182944-T-C

145934462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42183278-G-A

145935680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron variant
orthologous variants: 42184730-T-C

145935779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42184826-A-G

145935896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42184925-T-A

145935907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42184938-G-A

145935907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42184938-G-T

145936034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42185044-T-A

145936081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42185091-G-A

145936628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42185574-G-A

145936628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42185574-G-T

145936630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42185576-G-A

145936658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42185601-G-T

145936737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42185670-A-G

145936766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42185693-G-A

145936766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42185693-G-T

145936821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42185774-G-A

145936821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33862
most severe consequence: intron_variant, undefined
orthologous variants: 42185774-G-T