200891057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136162266-G-A

200891057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136162266-G-C

200891057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136162266-G-T

http://identifiers.org/hco/1/GRCh38#200891098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136162225-C-A

200891098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136162225-C-G

200891098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136162225-C-T

200891126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136162197-A-G

200891126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136162197-A-T

http://identifiers.org/hco/1/GRCh38#200891167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136162174-C-A

200891167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136162174-C-T

200891200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136162141-T-C

200891257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136162084-G-A

200891257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136162084-G-T

200891299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136162042-T-A

200891299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136162042-T-C

200891299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136162042-T-G

http://identifiers.org/hco/1/GRCh38#200891345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136161996-C-A

200891345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136161996-C-T

200891356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136161985-G-A

200891356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136161985-G-T

200891384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5 prime UTR variant
orthologous variants: 136161957-A-G

http://identifiers.org/hco/1/GRCh38#200891433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136161908-C-A

200891433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 136161908-C-G

http://identifiers.org/hco/1/GRCh38#200891434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136161907-C-A

http://identifiers.org/hco/1/GRCh38#200891601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136161739-C-A

200891601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, missense_variant
orthologous variants: 136161739-C-T

http://identifiers.org/hco/1/GRCh38#200891641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136161699-C-A

200891717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136161625-T-A

200891738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136161604-A-G

200891738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136161604-A-T

http://identifiers.org/hco/1/GRCh38#200891759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136161573-C-A

200891759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136161573-C-T

200891787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136161546-G-A

200891803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136161530-G-T

200891888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136161446-G-T

200892203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136161155-T-C

200892247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136161130-T-C

200892317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136161060-G-T

http://identifiers.org/hco/1/GRCh38#200893220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136159993-C-A

200893354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136159862-A-G

200894018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136159245-C-T

200894055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136159208-G-A

200894088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136159172-C-T

200894298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136158990-A-T

200894432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136158583-G-A

200894530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136158499-A-G

200894573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136158434-G-T

200894678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136158340-G-A

200894678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136158340-G-C

200894678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136158340-G-T

200894689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136158329-G-A

200894689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136158329-G-T

http://identifiers.org/hco/1/GRCh38#200894691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136158327-C-A

200894691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136158327-C-T

200894718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136158301-T-C

200894778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136158248-G-A

200894800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136158226-T-C

200894870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136158154-T-C

200894947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 136158070-G-A

200894947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 136158070-G-T

200894948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 136158069-G-A

200894948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 136158069-G-T

http://identifiers.org/hco/1/GRCh38#200894960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136158057-C-A

200894960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 136158057-C-T

200894961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 136158056-T-C

200894961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 136158056-T-G

200895055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 136157957-T-A

200895055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 136157957-T-C

200895120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136157896-G-A

200895120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136157896-G-T

http://identifiers.org/hco/1/GRCh38#200895199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136157823-C-A

200895199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136157823-C-T

200895219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136157804-T-A

200895219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136157804-T-C

200895237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136157784-G-A

200895237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136157784-G-T

200895369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136157676-T-A

200895451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136157599-T-C

200895470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136157581-C-T

200895517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136157500-A-T

200895946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136157122-G-A

200895969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136157099-C-G

200896614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136156529-C-T

200896640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136156503-G-T

http://identifiers.org/hco/1/GRCh38#200896764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136156399-C-A

200896764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136156399-C-T

200896816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136156382-C-G

200896816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136156382-C-T

200897015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136156186-C-G

http://identifiers.org/hco/1/GRCh38#200897036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136156165-A-C

http://identifiers.org/hco/1/GRCh38#200897300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136155958-C-A

200897300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136155958-C-T

200897337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136155921-C-T

http://identifiers.org/hco/1/GRCh38#200898158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136155523-A-C

200898158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136155523-A-T

200898167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136155514-G-T

200898173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136155503-A-G

http://identifiers.org/hco/1/GRCh38#200898182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136155494-C-A

200898182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136155494-C-T

200898205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136155471-T-C

200898282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136155418-T-A

200898282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136155418-T-C

http://identifiers.org/hco/1/GRCh38#200898332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136155373-C-A

200898332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant, stop_gained
orthologous variants: 136155373-C-T

200898338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 136155367-G-A

200898377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 136155328-G-T

http://identifiers.org/hco/1/GRCh38#200898393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136155312-A-C

http://identifiers.org/hco/1/GRCh38#200898577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136155157-C-A

200898577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136155157-C-T

200898590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136155142-G-A

200898590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136155142-G-T

200898652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136155082-G-A

200899046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136154916-G-A

200899069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136154893-A-G

200899324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136154769-G-A

200899324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136154769-G-T

200899415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136154697-T-C

200899517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 136154596-G-A

http://identifiers.org/hco/1/GRCh38#200899619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136154490-A-C

200899619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136154490-A-G

http://identifiers.org/hco/1/GRCh38#200899644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136154465-C-A

200899644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136154465-C-G

http://identifiers.org/hco/1/GRCh38#200899687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136154442-C-A

200899687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136154442-C-T

200899713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136154420-T-C

200899747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136154387-T-A

200899747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136154387-T-C

http://identifiers.org/hco/1/GRCh38#200899898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136154244-A-C

200899978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136154164-G-C

200899978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136154164-G-T

http://identifiers.org/hco/1/GRCh38#200900046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136154088-C-A

200900046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136154088-C-T

http://identifiers.org/hco/1/GRCh38#200900054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136154062-C-A

http://identifiers.org/hco/1/GRCh38#200900248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136153858-C-A

200900248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136153858-C-T

200900295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136153828-G-C

http://identifiers.org/hco/1/GRCh38#200900691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136153499-C-A

200900691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136153499-C-T

200900806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136153390-T-C

200900836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136153380-T-A

200900854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136153364-G-A

200900854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136153364-G-T

200900866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136153354-G-T

http://identifiers.org/hco/1/GRCh38#200900875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136153345-C-A

200900875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136153345-C-T

http://identifiers.org/hco/1/GRCh38#200900889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136153335-C-A

200900889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136153335-C-T

http://identifiers.org/hco/1/GRCh38#200900924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136153307-C-A

200900924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136153307-C-T

http://identifiers.org/hco/1/GRCh38#200900952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136153279-C-A

200900952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 136153279-C-T

200901034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 136153197-C-T

200901066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 136153165-G-A

200901066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, stop_gained
orthologous variants: 136153165-G-T

200901171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136153060-G-A

200901171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136153060-G-C

200901171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136153060-G-T

http://identifiers.org/hco/1/GRCh38#200901196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136153038-A-C

200901250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136152994-T-C

http://identifiers.org/hco/1/GRCh38#200901255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136152989-C-A

200901255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136152989-C-T

http://identifiers.org/hco/1/GRCh38#200901294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136152933-C-A

200901380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136152870-C-T

200901553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136152749-C-G

200901621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136152695-G-A

200901895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136152483-C-G

200901927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136152456-G-A

200901935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136152448-A-G

200902531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136151958-G-A

200902531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136151958-G-T

200902752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136151776-C-G

200902983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136151544-G-T

200903001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136151526-T-C

200903082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136151445-A-G

200903855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136151273-T-A

200904020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136151107-T-A

200904439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136151002-T-C

200905086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136150401-A-G

200905658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136149986-C-T

200905795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136149917-C-G

200905795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136149917-C-T

200905969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136149751-G-A

200906145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136149600-T-C

http://identifiers.org/hco/1/GRCh38#200906194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136149559-C-A

200906228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136149526-T-C

200906614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136149456-A-G

200907703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136148983-A-G

200907703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136148983-A-T

200907721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136148961-T-C

200907765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136148919-T-C

200907848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136148847-G-A

200908068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136148652-G-T

http://identifiers.org/hco/1/GRCh38#200908171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136148563-C-A

200908171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136148563-C-T

200908257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136148478-G-A

200908257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136148478-G-T

200908347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136148388-T-C

200908385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, undefined
orthologous variants: 136148355-G-T

200908399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, undefined
orthologous variants: 136148341-G-T

200908446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136148306-T-C

200908446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136148306-T-G

http://identifiers.org/hco/1/GRCh38#200908474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136148278-C-A

200908474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron variant
orthologous variants: 136148278-C-T

200908765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136148042-C-G

200908828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 136147979-G-A

200908835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 136147972-G-A

200908835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 136147972-G-C

200908852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136147955-C-G

200908958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136147849-G-A

200908958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136147849-G-T

200908981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136147824-G-A

200909042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136147775-T-C

200909079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136147734-T-C

200909186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136147670-G-A

200909186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136147670-G-T

200909208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136147648-T-C

200909237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136147619-A-G

200909280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136147576-A-T

200909407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136147451-A-G

200909410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136147448-T-C

http://identifiers.org/hco/1/GRCh38#200909413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#136147445-C-A

200909413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136147445-C-T

200909530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136147348-T-G

http://identifiers.org/hco/1/GRCh38#200909539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136147339-C-A

200909539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136147339-C-T

200909676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136147244-T-C

200910341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136145415-T-G

200910431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136145334-T-C

http://identifiers.org/hco/1/GRCh38#200910878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136145129-C-A

200910918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136145089-A-T

200911308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136144309-G-A

200911308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136144309-G-T

http://identifiers.org/hco/1/GRCh38#200911532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136144097-A-C

200911556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136144073-G-A

200911556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136144073-G-T

http://identifiers.org/hco/1/GRCh38#200911829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136143800-C-A

200911829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense variant
orthologous variants: 136143800-C-T

200911832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense variant
orthologous variants: 136143797-C-T

http://identifiers.org/hco/1/GRCh38#200911895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136143734-C-A

200911895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: synonymous variant
orthologous variants: 136143734-C-T

200911968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136143661-G-A

200911968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136143661-G-T

http://identifiers.org/hco/1/GRCh38#200912060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136143569-C-A

200912060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136143569-C-T

200912126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136143503-C-T

200912141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136143488-C-T

200912250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136143448-G-A

200912250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136143448-G-T

200912630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136143080-A-G

http://identifiers.org/hco/1/GRCh38#200912751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136142990-A-C

200912751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136142990-A-G

200912964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136142706-G-A

200912985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136142686-T-G

200913478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136142213-G-T

http://identifiers.org/hco/1/GRCh38#200913506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136142185-C-A

200913506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136142185-C-T

http://identifiers.org/hco/1/GRCh38#200913508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136142183-C-A

http://identifiers.org/hco/1/GRCh38#200913543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136142148-A-C

200913556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136142135-T-C

200913638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136142043-C-T

200913754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136141927-T-C

200913754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136141927-T-G

200913755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136141926-T-C

200913836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136141853-G-A

200913932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136141758-G-A

200913932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136141758-G-T

200913968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136141739-A-G

200913969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136141738-G-A

http://identifiers.org/hco/1/GRCh38#200913972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136141735-C-A

200913972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136141735-C-G

http://identifiers.org/hco/1/GRCh38#200914020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136141704-C-A

200914050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136141681-G-A

200914050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136141681-G-T

200915537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136141470-G-A

http://identifiers.org/hco/1/GRCh38#200915540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136141467-C-A

200915540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136141467-C-T

200915581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136141416-G-A

200915581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136141416-G-T

http://identifiers.org/hco/1/GRCh38#200915585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136141409-C-A

200915585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136141409-C-T

200915627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25599
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136141363-A-G