http://identifiers.org/hco/2/GRCh38#32628132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#75024781-A-C

32628134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, splice_donor_variant, undefined
orthologous variants: 75024783-G-A

32628134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, splice_donor_variant, undefined
orthologous variants: 75024783-G-T

32628158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75024807-G-T

32628165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75024814-A-G

32628255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75024881-C-G

32628255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75024881-C-T

32628272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75024898-G-C

32628272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75024898-G-T

32628366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 75024992-G-A

32630312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75025460-G-T

32630348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75025493-A-G

32630348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75025493-A-T

32630463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75025574-T-C

32630463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75025574-T-G

32630494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75025600-G-A

32630494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75025600-G-T

http://identifiers.org/hco/2/GRCh38#32630569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75025675-C-A

32630569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 75025675-C-T

32630573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 75025679-T-G

32631343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75026530-T-A

32631343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75026530-T-C

32631366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75026558-A-G

32631444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75026631-T-G

32631509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75026664-C-T

32632197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75027260-G-T

32632300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75027355-C-T

32632323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75027379-T-C

32633778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75027995-G-A

32633778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75027995-G-T

32633793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75028010-A-G

32633835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75028052-T-C

32633837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75028054-G-A

32633844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75028061-A-T

http://identifiers.org/hco/2/GRCh38#32633960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75028600-C-A

http://identifiers.org/hco/2/GRCh38#32640211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75031561-C-A

32640224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75031572-A-T

32640368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 75031711-C-G

32640368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 75031711-C-T

32640442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75031790-G-T

32640482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75031819-G-C

32640482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75031819-G-T

32640516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75031853-A-G

http://identifiers.org/hco/2/GRCh38#32640614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75031938-C-A

32641269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75032354-G-A

32644634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75033380-G-T

32644662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75033423-C-T

32647483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75035043-T-C

32649990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75036737-G-T

32650114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75036861-G-A

32650114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75036861-G-T

32650117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75036864-G-A

32650117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75036864-G-C

32650117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75036864-G-T

32650496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75038424-G-T

32650730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75038664-A-G

32650831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75038754-G-A

32650937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75038854-G-A

32651102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75039187-C-G

32651102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75039187-C-T

32651247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75039332-T-C

32651331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75039392-T-G

32652933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75041658-G-T

32653020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75041753-A-G

32653026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75041759-C-T

32653799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75042086-T-A

32653799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75042086-T-C

32653842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75042131-A-G

32653921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75042211-C-T

32657614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75044715-T-C

http://identifiers.org/hco/2/GRCh38#32657761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75044864-C-A

32657761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75044864-C-T

32657783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75044890-A-G

32658487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75045059-C-T

32658860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75046081-A-G

32664084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75046398-T-C

32664342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 75046632-G-A

32664400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 75046690-G-A

32664400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 75046690-G-C

32664496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75046785-T-G

32664526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75046818-G-A

32664526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75046818-G-T

32664708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75047249-C-T

32664801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75047353-T-G

32665383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049027-G-A

32665406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049048-T-A

http://identifiers.org/hco/2/GRCh38#32665935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75049257-C-A

32665938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049260-T-C

http://identifiers.org/hco/2/GRCh38#32665958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75049279-A-C

32665973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049294-G-A

32666077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049378-G-A

32666141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049442-T-G

32666183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049484-G-A

32666194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049495-A-G

32666379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049674-A-G

32666379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049674-A-T

32666446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049738-G-A

32666485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049777-T-C

http://identifiers.org/hco/2/GRCh38#32666492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75049784-C-A

32666492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049784-C-G

32666492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049784-C-T

32666497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049786-G-T

32666509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049798-G-A

32666509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049798-G-T

32666563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049840-A-T

32666587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049864-G-A

32666587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049864-G-C

32666613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75049890-T-C

32666672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 75049950-T-C

32667447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75051215-C-T

http://identifiers.org/hco/2/GRCh38#32667449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75051217-C-A

http://identifiers.org/hco/2/GRCh38#32672265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75054640-C-A

32672283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 75054658-C-G

32672289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 75054664-T-A

32672289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 75054664-T-C

http://identifiers.org/hco/2/GRCh38#32672534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75054891-C-A

http://identifiers.org/hco/2/GRCh38#32678728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75057939-C-A

http://identifiers.org/hco/2/GRCh38#32678795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75058003-A-C

32678795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75058003-A-G

http://identifiers.org/hco/2/GRCh38#32678960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75058162-C-A

32678960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75058162-C-T

http://identifiers.org/hco/2/GRCh38#32679052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75058294-C-A

32679052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75058294-C-T

32679198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75058570-A-G

32679213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75058585-G-A

32679293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75058660-G-C

32679662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75059458-T-A

32680022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75059497-G-C

32680064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75059538-A-G

32680099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75059567-T-C

32680181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75059647-A-G

32680181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75059647-A-T

32680340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75059793-T-G

32680407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75059870-T-A

http://identifiers.org/hco/2/GRCh38#32680647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75060100-C-A

http://identifiers.org/hco/2/GRCh38#32680840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75060306-A-C

32680882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75060330-C-T

32681194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75060619-C-G

32681194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75060619-C-T

32683310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75062319-A-G

http://identifiers.org/hco/2/GRCh38#32683311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75062320-C-A

32683350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75062359-T-C

32683439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75062681-G-A

http://identifiers.org/hco/2/GRCh38#32683571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75062863-C-A

32683571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75062863-C-G

32683593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75062885-G-A

32683600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75062892-G-A

32683604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75062896-C-T

32683700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75062985-A-G

32683733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75063018-G-A

32683738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75063023-A-G

http://identifiers.org/hco/2/GRCh38#32684488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75063174-C-A

32689394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75064230-G-A

32689447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75064288-T-C

32689744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75064679-A-G

32689836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75064770-T-C

32689900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75064848-G-T

32689907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75064855-G-T

32689909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75064857-A-T

32690537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75073638-C-T

32690596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75073695-A-T

32690730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75073819-A-T

32690789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75073876-T-C

32691712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75075086-C-G

32691775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75075150-C-T

32692066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75075408-G-C

32692066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75075408-G-T

32692380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75075592-T-C

32692414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75075626-G-C

32692583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75075796-T-C

32693314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75076450-T-C

32693765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75076873-C-G

32697466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75077078-T-A

http://identifiers.org/hco/2/GRCh38#32702844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75077275-C-A

32702844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 75077275-C-T

http://identifiers.org/hco/2/GRCh38#32702917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75077348-A-C

32702917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75077348-A-G

32702917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75077348-A-T

32703037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75077446-G-A

32703037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75077446-G-T

32711343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75077834-C-T

32711349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75077840-C-T

32712061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75078239-C-G

32712075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75078253-A-G

http://identifiers.org/hco/2/GRCh38#32712144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75078306-A-C

http://identifiers.org/hco/2/GRCh38#32712381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75078511-A-C

http://identifiers.org/hco/2/GRCh38#32729177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75080463-A-C

32729251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75080534-A-G

32729309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75080589-T-C

32729452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75080704-T-A

32730582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75081677-A-T

32731062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75081820-G-C

32731949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75082210-G-A

32731949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75082210-G-T

32731974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75082235-C-T

32732414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75082684-C-G

32732960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75083811-T-C

32733121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75083949-A-G

32733303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75084125-G-C

32733525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75084341-G-A

32733525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75084341-G-T

32733543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75084358-A-G

http://identifiers.org/hco/2/GRCh38#32733699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75084510-C-A

32733699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75084510-C-G

32733699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75084510-C-T

32733701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75084512-A-G

32733774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75084584-A-G

32733799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75084608-G-C

32733799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75084608-G-T

32733845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75084656-T-C

32733994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75084801-T-C

http://identifiers.org/hco/2/GRCh38#32734030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75084838-C-A

32734030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75084838-C-T

32734829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75085979-A-G

32735101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75086231-A-G

32735453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75086601-C-T

32735584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75086721-G-A

32735922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087076-C-G

32736124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087252-A-G

32736285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087385-C-T

32736390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087480-G-A

32736497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087591-C-T

32736595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087685-A-G

32736610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087700-A-G

32736849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087913-G-A

32736849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087913-G-T

32736856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087920-C-G

32736879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087939-T-G

32736880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087940-G-A

32736880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087940-G-C

http://identifiers.org/hco/2/GRCh38#32736923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75087983-C-A

32736923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087983-C-G

32736923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75087983-C-T

32736953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75088004-T-A

32736953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75088004-T-C

32737347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75088392-A-G

32738169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75089332-T-C

32738373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75089507-C-T

32738422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75089543-G-A

32738464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75089585-T-C

32738795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75089874-T-A

32739142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75090477-G-C

32739310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75090909-A-G

32739561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75091138-G-A

http://identifiers.org/hco/2/GRCh38#32739565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75091142-A-C

32739674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75091459-T-G

http://identifiers.org/hco/2/GRCh38#32739774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75091756-C-A

32740128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75092079-G-C

32740160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75092111-G-A

32740238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75092216-G-C

32740327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75092288-C-G

32741827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75092901-T-G

32741895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75092954-G-C

32742211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75093233-G-C

32742727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75093685-A-G

32742748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75093706-A-G

32742831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75093866-G-T

32743307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75094415-C-G

32743403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75094490-C-T

32745779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75094931-G-C

32745824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75094968-C-T

32746216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75095194-T-A

32746332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75095289-C-T

32746559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75095344-A-G

32746627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75095393-C-T

32746641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75095402-G-C

32746641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75095402-G-T

32746710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75095465-C-G

32746710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75095465-C-T

32747234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75096010-G-T

32747237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75096013-T-A

32747244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75096020-A-G

http://identifiers.org/hco/2/GRCh38#32749930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75096680-A-C

32749930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75096680-A-G

32750443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75097147-G-A

32750553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75097245-A-G

32750720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75100607-A-G

32750881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75100761-C-T

32750999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75100876-C-T

http://identifiers.org/hco/2/GRCh38#32751005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75100882-C-A

http://identifiers.org/hco/2/GRCh38#32751049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75100913-C-A

32751228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75101085-G-A

http://identifiers.org/hco/2/GRCh38#32751556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75101282-A-C

32751954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75101613-C-G

32752179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75101810-C-T

32752194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75101825-C-T

32752211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75101840-T-C

32752349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75101993-A-G

32752421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75102060-C-T

32752425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75102064-T-G

32752448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75102086-G-T

32752453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75102091-G-A

32752722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75102345-C-T

32752729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75102352-C-T

32752821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75102437-T-G

32752977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75102574-C-G

32752984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75102590-T-C

32753127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75102767-C-G

32753162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75102805-G-T

32753195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75102850-G-C

32753280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75102907-C-T

http://identifiers.org/hco/2/GRCh38#32753313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75102940-A-C

32753313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75102940-A-G

32753355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75102988-A-G

http://identifiers.org/hco/2/GRCh38#32753366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75102999-C-A

32753390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75103025-T-C

32755915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75103298-C-T

32755952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75103334-A-G

32755998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75103380-A-G

32756179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75103501-C-G

32756585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75103888-T-C

32758337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 75106224-A-G

32758384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75106271-T-C

32758502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 75106389-A-G

32758533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75106418-T-C

32758533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75106418-T-G

32759044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75106881-C-T

32762326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75111297-T-A

32762326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75111297-T-G

32762331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75111302-G-A

32762347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75111319-G-A

32762540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75111514-T-G

32762573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75111549-G-A

32763003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75111639-G-A

32763015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75111651-G-C

32763029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75111665-C-G

32763029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75111665-C-T

32763121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75111750-T-G

32763181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75111810-G-A

32763299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75111935-A-T

32763441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75112029-A-G

32763445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75112033-G-T

32763672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75112099-A-G

32763737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75112166-C-T

32763748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75112177-T-C

32763995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75112377-C-G

32764194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75112566-C-T

32768356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75113882-T-C

32768413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75113935-A-G

32768515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75114038-A-G

32768516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75114039-C-T

32768675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75114189-A-G

32769010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75114646-A-G

32769066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75114695-T-C

32769368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75114997-A-G

32769401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75115028-A-T

32769487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75115098-C-G

32769487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75115098-C-T

32769500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75115107-A-T

32769542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75115142-G-C

32769780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75115286-A-G

32769839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75115332-A-G

32770073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75115540-A-G

32770099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75115568-C-T

http://identifiers.org/hco/2/GRCh38#32770116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75115585-C-A

http://identifiers.org/hco/2/GRCh38#32770192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75115659-A-C

32770199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75115666-G-C

32770220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75115686-A-G

32770425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75115882-T-C

32770491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75115941-A-G

32770657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75116093-C-G

32770756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75116259-A-G

32771084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75116620-C-T

32771085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75116621-G-A

32771085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75116621-G-C

32771085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75116621-G-T

32771385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75116903-G-C

32771891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75117310-G-A

32771960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75117374-G-A

32772360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75117947-T-A

32772369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75117957-G-A

32772369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75117957-G-C

32772369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75117957-G-T

32772877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75118077-A-G

32773000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75118203-T-C

32773236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75118424-C-T

http://identifiers.org/hco/2/GRCh38#32773357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75118563-A-C

32773357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75118563-A-T

32773377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75118582-A-G

32773664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75119152-G-A

32774703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75127849-G-A

32774740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75127883-G-A

32774779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75127922-C-G

32774796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75127949-A-G

32774983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75128160-G-A

32775039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75128206-G-A

32775100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75128270-G-A

32776338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75135517-T-A

32776338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75135517-T-C

32776414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75135590-C-G

32776464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75135621-C-T

http://identifiers.org/hco/2/GRCh38#32777227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75135952-C-A

32777227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75135952-C-T

32777270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75135995-G-A

32777785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75136390-T-C

32777852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75136457-T-C

32777919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 75136524-C-T

32777930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 75136535-T-C

32777977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 75136582-C-G

32777977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 75136582-C-T

32782619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 75142321-A-G

32782710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75142412-G-C

32782710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75142412-G-T

32782723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75142425-A-G

32782744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75142444-T-A

32782744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75142444-T-C

32782975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75142661-T-C

32783241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75143430-G-A

32783513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75143694-A-G

32783523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75143704-T-C

32783539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75143721-G-A

32783660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75143821-A-G

32784040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75144086-T-C

32784101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75144140-G-C

32784933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75145239-A-T

32785043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75145350-T-G

32785191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75145502-G-A

32785458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75145740-C-G

32785527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75145806-A-G

32785613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75145893-T-G

32785668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75145955-G-A

32785668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75145955-G-T

32785680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75145967-C-T

32785950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75146144-C-G

32786026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75146184-G-T

http://identifiers.org/hco/2/GRCh38#32786101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75146243-A-C

32786101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75146243-A-T

32786109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75146251-C-G

32786176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75146264-C-G

32786176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75146264-C-T

32786493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75146487-A-G

32786523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75146516-A-G

32786523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75146516-A-T

http://identifiers.org/hco/2/GRCh38#32786823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75146794-A-C

32786851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75146820-T-A

32786851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75146820-T-G

http://identifiers.org/hco/2/GRCh38#32786898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75147208-C-A

32786898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75147208-C-T

http://identifiers.org/hco/2/GRCh38#32788630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75148533-A-C

32788838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75148809-G-T

32789207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75149195-G-T

32789346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75149355-C-T

32789619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75149567-G-A

32790054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75149695-G-C

http://identifiers.org/hco/2/GRCh38#32790122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75149813-A-C

32790122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75149813-A-G

http://identifiers.org/hco/2/GRCh38#32791065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75151435-C-A

http://identifiers.org/hco/2/GRCh38#32791203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75151581-C-A

32791439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75151755-G-A

32791462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75151777-G-A

32791520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75151836-A-G

32791656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75151930-A-G

32791694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75151969-T-C

32792077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75152166-G-A

32792139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75152217-A-G

32792880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75153315-T-C

32792900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75153335-T-C

32792994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75153423-G-T

32799479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75157984-A-G

http://identifiers.org/hco/2/GRCh38#32799559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75158056-A-C

32800831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75158669-C-T

http://identifiers.org/hco/2/GRCh38#32800918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75158751-A-C

32801080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75158951-G-A

32801317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75159163-T-G

32801407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75159235-C-T

32801442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75159260-C-T

32801570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75159387-G-C

32801652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75159463-G-A

32801750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75159561-C-T

32802177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75160243-A-G

32802261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75160325-A-G

32802558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75160539-A-G

32802635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75160587-C-G

32802757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75160698-T-A

32802790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75160730-T-G

32802823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75160762-C-T

32802919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75160825-A-G

32802974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75160871-T-A

32804893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75160989-G-A

32804896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75160992-A-G

32805135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75161185-T-G

32805143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75161190-G-A

32805272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75161280-G-A

32809428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75162345-G-T

32809573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75162490-C-T

http://identifiers.org/hco/2/GRCh38#32809579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75162496-A-C

32809579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75162496-A-G

32809601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75162517-G-C

32810559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75162988-T-C

32810782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75163172-A-T

32811242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75163626-G-C

32811321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75163704-G-T

32811598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75164175-T-A

32811598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75164175-T-C

32811880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75164434-G-A

http://identifiers.org/hco/2/GRCh38#32812172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75164700-C-A

http://identifiers.org/hco/2/GRCh38#32812353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75164863-C-A

32812353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75164863-C-G

32812353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75164863-C-T

32812677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 75165162-G-C

http://identifiers.org/hco/2/GRCh38#32812687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75165172-C-A

32812715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75165200-T-A

32812718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75165203-A-T

32812731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75165216-T-C

32812766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75165250-A-T

32812990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75165496-G-A

32812990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75165496-G-T

32813146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75165660-G-A

32813246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75165755-T-A

32813318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75165808-G-T

http://identifiers.org/hco/2/GRCh38#32813781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75166259-C-A

32813859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75166333-A-G

32814057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75166491-A-G

32816851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75168600-A-G

32817024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75168765-T-G

32817137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75168835-C-G

http://identifiers.org/hco/2/GRCh38#32817261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#75168904-A-C

32817261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75168904-A-G

32817386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75168982-A-G

32817410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169006-T-C

32817444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169028-A-G

32817444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169028-A-T

32817487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 75169071-G-A

32817487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 75169071-G-T

32817592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169176-T-C

32817592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169176-T-G

32817611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169193-T-C

32819693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169467-A-T

32819725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169498-C-T

32819770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169546-G-C

32819862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169622-C-T

32819883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169642-A-G

32819971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169710-G-A

32819995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169735-G-A

32820096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169841-C-G

32820098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169843-A-G

32820210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169948-G-C

32820240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75169965-C-T

32820579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75170116-C-T

32820713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75170214-G-A

32820713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75170214-G-C

32820734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75170242-T-C

32820740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75170248-T-C

32820740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75170248-T-G

32820779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75170296-T-C

32820792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75170308-T-C

32820798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75170314-T-C

32820935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25986
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75170448-T-C