167094227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165955333-G-A

167094244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165955317-T-G

http://identifiers.org/hco/1/GRCh38#167094265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165955298-C-A

167094265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165955298-C-T

http://identifiers.org/hco/1/GRCh38#167094314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165955252-C-A

167094314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165955252-C-T

167094334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165955229-T-C

167094399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165955164-G-A

167094399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165955164-G-T

167094452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165955110-C-T

167094565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165955017-G-A

167094565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165955017-G-T

167094641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165954934-G-A

167094643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165954932-G-A

167094722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165954890-G-A

167094722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165954890-G-T

http://identifiers.org/hco/1/GRCh38#167094760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165954837-C-A

167094760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165954837-C-T

http://identifiers.org/hco/1/GRCh38#167094763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165954834-A-C

http://identifiers.org/hco/1/GRCh38#167094764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165954833-C-A

167094764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165954833-C-T

http://identifiers.org/hco/1/GRCh38#167094775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165954821-C-A

167094907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant
orthologous variants: 165954689-G-A

167094907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant
orthologous variants: 165954689-G-T

167095100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165954583-C-T

167095101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165954582-T-C

167095178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165954523-G-A

167095848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165953947-T-G

167100600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165949721-T-G

167100931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165949385-G-A

167100951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165949373-A-G

167101270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165948700-G-A

167101320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165948650-C-T

167101850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165948378-G-A

167101874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165948355-A-T

http://identifiers.org/hco/1/GRCh38#167102015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165948219-A-C

167102059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165948173-T-C

167102148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165948085-G-A

167102153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165948080-G-C

167102158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165948075-G-A

167102320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165947876-A-T

167102404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165947797-C-T

167102430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165947771-C-T

167103119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165946977-T-C

167103465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165946653-T-C

167103553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165946570-A-G

http://identifiers.org/hco/1/GRCh38#167103661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165946471-C-A

167103661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165946471-C-T

167105511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165945616-A-G

167105559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165945569-C-G

167105683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165945411-C-T

167106055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165945079-T-C

167106168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165944720-C-T

167106316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165944570-T-C

167107436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165943942-A-G

167107436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165943942-A-T

167107483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165943897-T-C

167107676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165943710-T-A

167107676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165943710-T-C

167107776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165943599-G-A

167107951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165943434-A-T

167108274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165943140-G-A

167108303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165943119-T-C

167108343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165943091-T-G

167108413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165943020-A-G

167112044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165941056-T-C

167112111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165941240-C-G

167112148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165941200-C-T

167112275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165941056-T-A

167112407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165940916-C-T

167112551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165940786-A-G

http://identifiers.org/hco/1/GRCh38#167112665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165940669-C-A

167112861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165940481-C-T

167112907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165940440-T-A

167112907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165940440-T-C

167112917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165940432-T-G

167113109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165940270-C-T

167113240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165940153-G-A

167113240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165940153-G-C

167113244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165940149-A-G

167113278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165940124-G-C

167113488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939934-A-T

167113560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939842-T-C

167113616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939783-T-A

167113616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939783-T-C

167113616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939783-T-G

167113637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939764-G-T

167113654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939749-A-G

167113670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939734-T-A

http://identifiers.org/hco/1/GRCh38#167113688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165939713-C-A

167113688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939713-C-T

167113691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939710-G-T

167113964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939435-A-G

167114023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939366-A-T

167114024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939365-G-A

http://identifiers.org/hco/1/GRCh38#167114109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165939275-C-A

167114119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939265-C-T

167114146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939231-G-A

167114146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165939231-G-T

167117179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165937997-A-G

167117212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165937964-T-G

http://identifiers.org/hco/1/GRCh38#167117239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165937938-C-A

167117239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165937938-C-G

167117239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165937938-C-T

167117278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165937900-G-A

167117278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165937900-G-T

http://identifiers.org/hco/1/GRCh38#167117322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165937856-C-A

167117322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 165937856-C-T

167117459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant
orthologous variants: 165937719-C-T

167117483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant
orthologous variants: 165937695-G-A

167117567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 165937611-T-G

167117576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165937599-T-C

167117576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165937599-T-G

167117800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165937399-G-A

167118222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165937047-A-T

167118323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, undefined
orthologous variants: 165936941-G-A

167118422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165936853-C-T

http://identifiers.org/hco/1/GRCh38#167118595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165936691-C-A

167118743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165936569-A-G

167119126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165935858-G-T

167119286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, stop_gained
orthologous variants: 165935720-G-T

167119471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165935535-G-A

167119471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165935535-G-C

167119550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165935468-G-T

167119841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165935014-G-A

167119890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934975-G-A

167119903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934962-G-T

167120040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934814-A-G

167120523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934393-T-C

167120570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934347-G-A

167120817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934294-G-T

167120857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934259-T-C

167120857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934259-T-G

167120863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934253-T-C

167120863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934253-T-G

167120865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934251-T-C

167120865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934251-T-G

167120869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934247-T-C

167120869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934247-T-G

167120875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934241-T-C

167120875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934241-T-G

167120881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934235-T-C

167120881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934235-T-G

167120887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934229-C-G

167120887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934229-C-T

167120915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934227-T-G

167120919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934223-T-A

167120919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934223-T-G

167120928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934214-G-A

167120928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934214-G-T

167120931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934211-T-A

167120931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934211-T-C

167120931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934211-T-G

http://identifiers.org/hco/1/GRCh38#167120941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165934201-C-A

167120941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934201-C-T

http://identifiers.org/hco/1/GRCh38#167120949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165934193-C-A

167120949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934193-C-T

167120955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934187-T-A

167120955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934187-T-C

167120955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934187-T-G

167120993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165934149-C-T

167122533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165932515-G-A

167123307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165931252-T-C

http://identifiers.org/hco/1/GRCh38#167123346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165931209-C-A

167123392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165931158-C-G

167123417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165931133-G-A

167123417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165931133-G-C

167123448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165931112-G-A

167123448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165931112-G-T

167123504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165931067-T-C

167124296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165930908-T-G

167124325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165930881-G-A

167124595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165930612-G-T

167124618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165930589-G-A

167124850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929723-G-A

167124895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929684-G-C

167125154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929460-C-T

167125183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929431-G-A

167125183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929431-G-T

167125207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929414-A-G

167125269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929351-G-A

167125374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929259-G-A

167125490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929214-C-T

167125584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929128-G-C

167125587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929125-A-G

167125646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929078-A-G

167125646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929078-A-T

167125647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929077-G-A

167125647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929077-G-C

167125647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929077-G-T

http://identifiers.org/hco/1/GRCh38#167125648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165929076-C-A

167125648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929076-C-G

167125648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929076-C-T

http://identifiers.org/hco/1/GRCh38#167125649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165929075-C-A

167125649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929075-C-T

167125675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron variant
orthologous variants: 165929052-A-G

http://identifiers.org/hco/1/GRCh38#167126032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165928726-A-C

167126039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165928719-G-A

167126039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165928719-G-T

http://identifiers.org/hco/1/GRCh38#167126101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165928657-C-A

167126101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 165928657-C-T

167126149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165928609-A-G

167126205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 165928550-G-A

167126205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165928550-G-T

167126210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165928545-T-C

167126292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165928460-G-T

167126323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165928429-A-G

167126416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165928342-A-G

167126416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165928342-A-T

167126627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165928131-G-A

167126774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165927984-A-G

167126980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165927775-T-A

167127003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 165927752-A-G

http://identifiers.org/hco/1/GRCh38#167127130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165927625-C-A

167127157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165927598-A-G

167127239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165927549-C-G

167127356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165927432-T-G

167127476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165927321-G-A

167127486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 165927311-T-C

167127486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 165927311-T-G

167127512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165927285-A-T

167127541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165927256-A-G

167127847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 165926950-A-T

167128017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 165926780-C-T

167128090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165926707-G-A

167128307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165926493-G-A

167128318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165926482-G-A

167128318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165926482-G-T

167128481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165926319-G-A

167128481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165926319-G-C

167128603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165926197-G-A

167128603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 165926197-G-C

167128608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 165926192-A-G

167128609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 165926191-G-T

167128613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 165926173-G-T

167128628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 165926158-C-T

167128631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 165926155-T-C

http://identifiers.org/hco/1/GRCh38#167128757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165926048-C-A

167128757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165926048-C-T

http://identifiers.org/hco/1/GRCh38#167128833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165925985-C-A

167128833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165925985-C-G

http://identifiers.org/hco/1/GRCh38#167128846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165925975-C-A

167128846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165925975-C-T

http://identifiers.org/hco/1/GRCh38#167128852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165925969-C-A

167128852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165925969-C-G

167128852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165925969-C-T

http://identifiers.org/hco/1/GRCh38#167128902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165925899-C-A

167128902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165925899-C-G

167128902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165925899-C-T

167128981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165925849-A-T

167129072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25034
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165925756-T-C