http://identifiers.org/hco/9/GRCh38#130902551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31705258-C-A

130902551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705258-C-T

130902561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705268-G-A

130902561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705268-G-C

130902561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705268-G-T

130902707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705350-G-A

130902707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705350-G-T

http://identifiers.org/hco/9/GRCh38#130902785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31705393-C-A

130902785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705393-C-T

http://identifiers.org/hco/9/GRCh38#130902829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31705415-C-A

130902829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705415-C-T

130902881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705430-G-A

130902881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705430-G-T

http://identifiers.org/hco/9/GRCh38#130902940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31705500-C-A

130902940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705500-C-T

130902951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705511-C-T

130902959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705519-C-T

130903024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705545-C-T

130903135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705654-G-T

130903164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705666-A-G

130903267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705746-G-A

130903267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705746-G-T

130903376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705837-G-A

130903376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705837-G-T

130903404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705865-G-A

http://identifiers.org/hco/9/GRCh38#130903472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31705929-C-A

http://identifiers.org/hco/9/GRCh38#130903507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31705962-C-A

130903507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705962-C-T

http://identifiers.org/hco/9/GRCh38#130903508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31705963-C-A

130903508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705963-C-T

130903536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705980-G-A

130903536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705980-G-T

130903538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31705982-G-T

http://identifiers.org/hco/9/GRCh38#130903557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31706001-A-C

130903557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31706001-A-G

130903557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31706001-A-T

http://identifiers.org/hco/9/GRCh38#130903653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31706072-A-C

130903653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31706072-A-G

130903653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31706072-A-T

http://identifiers.org/hco/9/GRCh38#130903732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31706128-C-A

130903828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31706218-C-T

130903849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31706238-T-A

130903849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31706238-T-C

130903915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31706292-G-A

130903915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3 prime UTR variant
orthologous variants: 31706292-G-T

130903962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 31706340-G-A

130903962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 31706340-G-T

http://identifiers.org/hco/9/GRCh38#130904050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31706425-C-A

130904050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 31706425-C-T

130904051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 31706426-A-G

http://identifiers.org/hco/9/GRCh38#130904082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31706468-C-A

130904082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31706468-C-T

130904085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31706471-C-G

130904244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31706630-G-A

130904244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31706630-G-C

130904244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31706630-G-T

130904339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31706728-C-G

130904339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31706728-C-T

130904346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31706735-G-C

http://identifiers.org/hco/9/GRCh38#130904436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31706762-C-A

130904436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: 31706762-C-T

http://identifiers.org/hco/9/GRCh38#130904446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31706772-C-A

130904446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: 31706772-C-T

http://identifiers.org/hco/9/GRCh38#130904768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31707020-C-A

130905319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31707221-G-A

130905319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, stop_gained
orthologous variants: 31707221-G-T

130905340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31707242-A-G

130905349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 31707251-G-A

130905349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 31707251-G-C

130905418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 31707320-A-G

130905450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31707356-G-T

130905456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31707363-G-A

130905456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31707363-G-T

130905494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: 31707378-G-C

130905505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31707389-G-T

130905915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31708002-C-T

130905924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31708011-G-A

130907478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31709309-G-A

130907878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31709539-T-A

130907878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31709539-T-G

130908263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31709947-G-A

130908333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31710016-G-A

130908333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31710016-G-C

http://identifiers.org/hco/9/GRCh38#130908960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31710589-C-A

130909015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31710640-G-A

130909061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31710682-C-T

130911844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: synonymous variant
orthologous variants: 31711536-G-A

130911844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: synonymous variant
orthologous variants: 31711536-G-T

http://identifiers.org/hco/9/GRCh38#130911871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31711563-C-A

130911871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: synonymous variant
orthologous variants: 31711563-C-T

130911928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31711616-A-G

http://identifiers.org/hco/9/GRCh38#130911980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31711645-C-A

130911980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31711645-C-G

http://identifiers.org/hco/9/GRCh38#130911992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31711657-C-A

130911992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31711657-C-T

130912014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31711699-G-A

130912014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31711699-G-C

130912014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31711699-G-T

130912157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31711857-C-T

130912178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31711874-C-T

130912236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31711935-T-C

130912430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31712112-G-T

130912685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31712264-T-G

130912751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31712300-G-A

130913171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31712785-C-T

130913191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31712802-C-T

130913495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: 31713038-C-T

130913757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: 31713291-C-T

130913829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31713376-G-A

130913834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31713391-C-T

130914127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31713588-G-A

130914201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31713658-A-G

130914332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31713783-G-A

http://identifiers.org/hco/9/GRCh38#130916368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31715770-C-A

130916418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31715818-G-A

130916464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31715842-G-A

130917189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31716194-A-G

130917202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31716204-C-T

130917368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31716375-G-C

130917561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31716511-T-C

130917834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31716772-C-T

130917960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31716953-C-G

130918062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31717038-C-T

130918153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31717108-A-T

130918344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31717340-G-C

130918921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31717934-C-T

130919036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31718056-G-A

130919344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31718323-G-A

130919625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31718519-G-A

130919625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31718519-G-C

130919625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31718519-G-T

130919682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31718590-T-C

130920145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31719017-C-T

130920333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31719162-G-C

130920335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31719164-A-G

130920450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31719251-G-A

130920881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31719780-G-C

130921062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31719972-C-G

130921062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31719972-C-T

130921205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31720096-G-A

130921407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31720314-G-T

130921502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31720407-G-C

130921705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31720611-C-T

130921831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31720734-C-T

http://identifiers.org/hco/9/GRCh38#130921838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31720741-A-C

130921838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31720741-A-G

130921856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31720757-C-G

130921869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31720770-T-C

130921951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31720853-C-T

130921955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31720857-G-A

130921972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31720874-G-A

130922014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31720897-C-G

130922045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31720927-C-G

130922053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31720935-G-A

130923275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31723530-C-T

130923771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: synonymous variant
orthologous variants: 31723822-G-A

130923991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724045-G-A

130923991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724045-G-C

130923991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724045-G-T

130924007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724059-G-T

http://identifiers.org/hco/9/GRCh38#130924154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31724202-C-A

130924154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724202-C-G

130924154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724202-C-T

http://identifiers.org/hco/9/GRCh38#130924179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31724243-C-A

130924179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724243-C-T

130924213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724278-G-A

130924213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724278-G-T

130924217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724282-G-A

130924217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724282-G-T

http://identifiers.org/hco/9/GRCh38#130924218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31724283-C-A

130924218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724283-C-T

130924253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: synonymous_variant, undefined
orthologous variants: 31724317-G-A

130924253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: synonymous_variant, undefined
orthologous variants: 31724317-G-T

130924318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: missense variant
orthologous variants: 31724382-G-A

130924318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: synonymous variant
orthologous variants: 31724382-G-T

130924426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: 31724493-G-A

130924426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: 31724493-G-C

130924426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: 31724493-G-T

http://identifiers.org/hco/9/GRCh38#130924427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31724494-C-A

130924427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: 31724494-C-T

130924430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: 31724497-G-A

130924476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724518-G-T

130924673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724706-G-A

130924737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724823-G-A

130924801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31724873-G-A

130924908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31725041-C-T

130924909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31725042-G-A

130925046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31725207-G-T

130925150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31725305-T-G

http://identifiers.org/hco/9/GRCh38#130925261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31725419-C-A

130925322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31725477-C-T

130925337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31725492-G-A

130925439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31725574-C-T

130925540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31725627-G-A

130925680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31725736-C-T

130926071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31726101-T-C

130926157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31726158-C-T

130926168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31726161-G-T

130926416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31726390-A-G

130928419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31727114-C-T

130929039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31727692-G-C

130929079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31727765-C-T

130929104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31727789-T-A

130929362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31728058-G-C

130929452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31728126-G-T

http://identifiers.org/hco/9/GRCh38#130929461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31728135-C-A

130929461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31728135-C-G

130929509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31728179-G-A

130929509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31728179-G-T

130929511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31728181-A-G

130929511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31728181-A-T

130929705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 31728448-G-A

130929717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 31728460-C-G

http://identifiers.org/hco/9/GRCh38#130929803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31728540-C-A

130929803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 31728540-C-G

130929803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 31728540-C-T

130929896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 31728633-C-T

130929910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 31728647-G-A

130929918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 31728655-G-A

130929918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 31728655-G-T

130929944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 31728681-C-T

http://identifiers.org/hco/9/GRCh38#130929950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31728687-C-A

130929950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 31728687-C-G

130929950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 31728687-C-T

130929951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 31728688-G-A

130929951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 31728688-G-T

130930000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 31728737-G-A

130930000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 31728737-G-T

http://identifiers.org/hco/9/GRCh38#130930033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31728770-C-A

130930033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 31728770-C-T

130930198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31728918-G-A

130930198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31728918-G-C

130930198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31728918-G-T

130931131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31729107-C-T

130931935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31729591-C-G

130931935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31729591-C-T

130932038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31729697-G-C

130932961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: 31730858-G-A

http://identifiers.org/hco/9/GRCh38#130932971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31730868-C-A

130933302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31731169-G-C

130933462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31731310-G-T

130933582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31731393-G-A

130933848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron variant
orthologous variants: 31731558-G-T

130933857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31731567-T-C

130933857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31731567-T-G

130934005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31731697-A-G

130934047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31731740-G-A

130934047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31731740-G-T

130934240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31731887-C-T

130934358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31731959-G-C

130934358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31731959-G-T

130934387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31731979-T-C

130934419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31732011-G-A

130934490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31732072-C-T

130934667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31732260-G-A

130934746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31732323-C-G

130934785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31732349-C-T

130934829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31732396-T-A

130935331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31733131-C-G

130935455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31733240-G-A

130935484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31733269-C-T

130935599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31733377-G-A

130935995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31733667-G-A

130935995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31733667-G-C

http://identifiers.org/hco/9/GRCh38#130936188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31733817-C-A

130936188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31733817-C-T

130936270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31733876-G-A

130936270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31733876-G-T

130936290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31733877-G-A

130936290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31733877-G-C

130936290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31733877-G-T

130936375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31733933-A-G

130936395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31733952-A-G

130936526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31734007-G-A

130936526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31734007-G-T

130936566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31734053-G-C

130936683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31734145-G-A

130936683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31734145-G-T

130936954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31734368-G-T

130937019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31734412-A-G

130937099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31734477-G-A

130937425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31734748-T-G

130937489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31734792-G-C

130937496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31734799-T-C

130937761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31735061-G-A

130937761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31735061-G-C

130937797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31735094-C-T

130938063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31735339-G-A

130938063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31735339-G-T

130938110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31735396-C-T

130938384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31735644-G-A

130938384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31735644-G-T

130938515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31735702-T-C

130938584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31735771-G-A

130938584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31735771-G-T

130938623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31735810-G-A

130938623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31735810-G-T

130938625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31735812-G-A

130938625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31735812-G-C

130938625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31735812-G-T

130938690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31735855-G-A

130938690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31735855-G-T

130938713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31735878-G-A

130938713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31735878-G-T

130938849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31735998-G-A

http://identifiers.org/hco/9/GRCh38#130938951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31736078-C-A

130938951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31736078-C-G

130938951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31736078-C-T

http://identifiers.org/hco/9/GRCh38#130938981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31736108-C-A

130938981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31736108-C-T

http://identifiers.org/hco/9/GRCh38#130939115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31736196-C-A

130939115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31736196-C-T

130939184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31736261-T-A

130939281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31736307-T-C

130939464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31736409-G-A

130939475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31736422-C-T

130940091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31736827-C-T

130940132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31736874-G-A

130940132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31736874-G-C

130940379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31737097-G-A

130940381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31737099-A-G

130940394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31737111-G-A

130940394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31737111-G-C

130940636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31737327-G-A

130940702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25922
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31737410-A-G