127623345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40585965-G-A

127623345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40585965-G-T

127623366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40585985-A-G

127623383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40586002-G-A

127623383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40586002-G-C

127623383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40586002-G-T

http://identifiers.org/hco/4/GRCh38#127623417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40586038-C-A

127623417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 40586038-C-T

http://identifiers.org/hco/4/GRCh38#127623460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40586081-C-A

http://identifiers.org/hco/4/GRCh38#127623538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40586126-C-A

127623538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40586126-C-G

127623538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40586126-C-T

127623834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40586318-T-C

127623894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40586374-C-T

127624177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40586587-A-G

127624280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40586683-C-T

127624635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40586973-A-G

127624817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40587159-G-A

127624860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40587200-A-G

127624889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40587226-G-A

127624889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40587226-G-T

127624987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40587320-C-G

127625043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40587365-A-T

http://identifiers.org/hco/4/GRCh38#127625082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40587404-C-A

127625083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40587405-T-C

127625552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40588060-A-G

127625561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40588069-A-G

127625605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40588113-C-G

127625712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40588166-A-G

http://identifiers.org/hco/4/GRCh38#127625912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40588342-C-A

127626064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40588461-T-C

127626074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40588471-G-A

127626525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40588924-G-C

127626583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40588960-C-T

127626853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40589477-C-T

127626899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40589523-A-G

127626988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40589589-G-C

127626999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40589600-T-G

127627193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40589896-C-G

127627214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40589917-A-G

http://identifiers.org/hco/4/GRCh38#127627225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40589928-C-A

127627225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40589928-C-T

127627328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40590046-G-A

127627365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40590107-T-A

127627733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40590441-G-A

127627817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40590526-A-G

127627872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40590585-T-C

127628514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40591268-G-A

127628514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40591268-G-C

127628524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40591278-T-C

127628756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40591510-C-T

127628791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40591547-G-A

127629244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40593082-A-G

127632269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40594479-A-T

127632796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, undefined
orthologous variants: 40594822-T-C

127632805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, undefined
orthologous variants: 40594831-A-G

127632805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, undefined
orthologous variants: 40594831-A-T

127632822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, undefined
orthologous variants: 40594832-G-A

127632822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, undefined
orthologous variants: 40594832-G-C

127632822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, undefined
orthologous variants: 40594832-G-T

127632831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40594841-A-G

http://identifiers.org/hco/4/GRCh38#127632866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40594851-C-A

127632866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron variant
orthologous variants: 40594851-C-T

127632888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, undefined
orthologous variants: 40594873-T-G

127632912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, undefined
orthologous variants: 40594897-G-A

http://identifiers.org/hco/4/GRCh38#127632938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#40594922-C-A

http://identifiers.org/hco/4/GRCh38#127632939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#40594923-C-A

127632939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, undefined
orthologous variants: 40594923-C-T

http://identifiers.org/hco/4/GRCh38#127632944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#40594926-C-A

127632944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: intron_variant, undefined
orthologous variants: 40594926-C-T

127632959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40594929-A-G

127632982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40594967-G-C

http://identifiers.org/hco/4/GRCh38#127632996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#40594975-A-C

127632996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40594975-A-G

127633028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40595006-C-G

127633045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 40595023-T-C

127633207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40595181-A-G

127633207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40595181-A-T

http://identifiers.org/hco/4/GRCh38#127633210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40595184-C-A

127633210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40595184-C-T

http://identifiers.org/hco/4/GRCh38#127633211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40595185-C-A

127633211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40595185-C-T

127633233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40595201-T-A

127633238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40595206-G-A

127633238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40595206-G-C

127633238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40595206-G-T

127633241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40595224-G-T

127633248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40595231-G-A

127633248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40595231-G-T

127633257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40595240-A-T

127633265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40595248-G-A

127633265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40595248-G-T

127633266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40595249-G-C

127633266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40595249-G-T

http://identifiers.org/hco/4/GRCh38#127633279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40595265-C-A

127633279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40595265-C-G

127633279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40595265-C-T

127633315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40595301-T-A

127633360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40595336-C-T

127633707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40595733-C-T

127634279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40596210-G-A

127634720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40596653-T-C

127634727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40596660-A-G

127634959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40596880-T-C

http://identifiers.org/hco/4/GRCh38#127635122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40597025-A-C

127635122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40597025-A-G

127635170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40597071-T-C

127635391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40597552-A-G

127635480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40597673-T-C

127635692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40597899-A-G

127635807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40597972-A-G

127635848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40598012-A-T

127635851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40598015-G-A

127635891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40598047-G-T

127635912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40598068-G-A

127636807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40598308-C-T

127636901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40598402-T-C

127636916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40598417-C-T

127637051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40598529-A-G

127637191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40598656-G-T

127638202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40602232-G-T

127638217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40602250-T-C

127638515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40602534-C-G

127638545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40602566-G-A

127638550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40602571-G-C

127638574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40602595-G-A

127638786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40602793-T-C

127638910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40602904-T-C

127638931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40602930-T-C

127638940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40602939-A-G

127639310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40603309-A-G

127641646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40603397-G-T

http://identifiers.org/hco/4/GRCh38#127642137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40605835-A-C

127642175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40605873-A-T

127642307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40606005-T-C

127642383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40606085-A-G

127642460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40606129-G-A

127642463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40606132-T-G

127642690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40606548-C-T

127643058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40606908-C-T

http://identifiers.org/hco/4/GRCh38#127643181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40607009-A-C

http://identifiers.org/hco/4/GRCh38#127643423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40608041-C-A

127643423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40608041-C-T

127643492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40608107-A-G

127643674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 40608298-C-T

127643693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 40608320-T-C

127643695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 40608322-T-A

127643695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 40608322-T-C

127643769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 40608396-A-G

127643769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 40608396-A-T

127643813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 40608440-A-G

http://identifiers.org/hco/4/GRCh38#127643824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40608451-A-C

127643866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 40608493-T-C

127643866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 40608493-T-G

127643877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 40608504-A-G

127643986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 40608613-T-C

http://identifiers.org/hco/4/GRCh38#127644079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40608705-C-A

http://identifiers.org/hco/4/GRCh38#127644206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40608808-A-C

127649919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40617094-A-G

127650040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40618151-G-A

127650114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40618212-A-T

127656550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40618604-A-G

127656573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40618630-T-A

127656573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40618630-T-C

127656589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40618646-T-A

127656821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40618869-G-A

127656821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40618869-G-T

127656842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40618890-G-T

127656947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40618996-C-G

127656947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40618996-C-T

127656976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40619023-A-G

127657004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40619051-C-T

http://identifiers.org/hco/4/GRCh38#127660287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40623435-A-C

127660350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40623493-G-A

127660419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40623555-A-G

127662690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40626141-T-A

127662784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40626218-T-C

127662876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40626311-C-G

127662940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40626371-G-A

127663007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40626439-G-A

127663028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40626456-T-A

127663261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40626698-A-T

127663355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40626951-T-C

http://identifiers.org/hco/4/GRCh38#127663361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40626957-C-A

127663361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40626957-C-G

127663361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40626957-C-T

127663363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40626983-T-C

http://identifiers.org/hco/4/GRCh38#127666959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40627841-A-C

http://identifiers.org/hco/4/GRCh38#127667103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40627968-A-C

127667400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40628248-G-C

127667531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40628372-A-G

127667785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40628605-T-G

127668237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40629028-A-G

127668241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40629032-C-G

127668314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40629088-A-G

127668568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40629315-G-A

http://identifiers.org/hco/4/GRCh38#127668598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40629342-A-C

127668845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40629466-G-A

127668902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40629521-G-A

127668902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40629521-G-T

127668949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40629574-T-G

127668966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40629586-G-T

127669162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 40629782-T-C

127669163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40629783-T-C

127669415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40630122-A-G

127669508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40630214-A-G

127670121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40630670-G-A

127672530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40632266-A-T

http://identifiers.org/hco/4/GRCh38#127672586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40632322-C-A

127672586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40632322-C-T

127672663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40632399-T-A

127672783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40632523-A-T

127673922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40633097-T-G

http://identifiers.org/hco/4/GRCh38#127674038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40633220-C-A

127674038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40633220-C-T

127674160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40633349-G-A

http://identifiers.org/hco/4/GRCh38#127674301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40633524-C-A

127674336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40633558-A-G

127674362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40633574-G-T

127684366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40633908-T-G

http://identifiers.org/hco/4/GRCh38#127684413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40633966-C-A

127684523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40634072-T-G

127684524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40634073-A-G

http://identifiers.org/hco/4/GRCh38#127684581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40634129-A-C

127684581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40634129-A-G

127684581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40634129-A-T

http://identifiers.org/hco/4/GRCh38#127685327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40635590-C-A

127685327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40635590-C-T

127685389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40635648-A-G

127685529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40635791-T-A

127685595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40635855-A-G

127685610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40635870-A-G

127685690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40635944-G-A

127685705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40635959-A-G

127685825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40636097-A-G

127685855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40636127-T-C

http://identifiers.org/hco/4/GRCh38#127686005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40636253-C-A

127686170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40636387-C-T

http://identifiers.org/hco/4/GRCh38#127686255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40636434-C-A

127686313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40636455-T-C

127686345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40636495-A-G

127686372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40636518-C-T

127686384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40636529-T-G

http://identifiers.org/hco/4/GRCh38#127686413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40636556-C-A

http://identifiers.org/hco/4/GRCh38#127686468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40636611-C-A

127686477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40636624-T-G

127686517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40636652-G-A

127686521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40636656-A-G

127686545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40636675-G-T

127686751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40636942-C-T

127686767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40636958-T-A

http://identifiers.org/hco/4/GRCh38#127686827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#40637014-A-C

127686827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40637014-A-G

127686848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40637034-T-C

127686875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40637061-G-T

127686952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40637132-T-C

127687102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40637302-G-A

127687161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40637361-G-T

127687166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40637366-A-G

http://identifiers.org/hco/4/GRCh38#127687352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40637552-C-A

127687352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40637552-C-T

127687593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40637706-G-C

127687593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40637706-G-T

127687608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40637721-C-G

127687664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40637773-T-C

127687787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 40637896-C-T

127687795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40637904-C-T

127687831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40637940-T-A

127687877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40637986-G-A

127687877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40637986-G-T

127687903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40638012-G-T

127688776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40639305-C-T

127688932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40639445-A-T

127689819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40640066-A-G

127698676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40641164-A-G

127698939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40641380-T-G

127699115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40641513-G-C

127699196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40641555-A-G

127699449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40641769-G-A

127699495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40641813-G-A

http://identifiers.org/hco/4/GRCh38#127699514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40641832-C-A

127699524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40641842-T-C

127699524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40641842-T-G

127699578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40641888-C-T

127699874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40642127-A-G

127699902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40642155-T-C

127699902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40642155-T-G

http://identifiers.org/hco/4/GRCh38#127700022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40642218-A-C

127700022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40642218-A-G

127700077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40642271-T-G

127700177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40642353-G-A

127700177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40642353-G-C

127700177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40642353-G-T

http://identifiers.org/hco/4/GRCh38#127700214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40642386-C-A

127700214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40642386-C-T

http://identifiers.org/hco/4/GRCh38#127700359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40642493-C-A

127700359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40642493-C-G

127700359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40642493-C-T

127700535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40642646-G-A

127703424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40644397-G-A

127703538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40644501-A-G

127703561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40644523-G-C

127704043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40644952-C-T

127704239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40645137-C-T

127704451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40645287-C-T

127705173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40645747-G-A

127705173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40645747-G-T

127705391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40645949-G-A

http://identifiers.org/hco/4/GRCh38#127705554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40646108-C-A

127705559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40646113-G-A

127705759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40646313-A-G

127706206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40646694-C-T

127706226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40646731-A-G

127706244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40646749-T-A

127706259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40646762-G-C

127706406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40646859-A-G

127706558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40647000-A-G

127706698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 40647140-A-T

127706736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 40647178-C-G

127706837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40647279-T-C

127706892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 40647331-A-G

http://identifiers.org/hco/4/GRCh38#127706933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40647372-C-A

127706933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40647372-C-T

127707578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40647709-G-A

127707763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40647870-A-G

127707763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40647870-A-T

127707831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40647950-C-T

127707972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648094-G-A

127707984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648106-C-G

127708401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648441-C-G

127708410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648450-C-T

127708455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648490-A-G

127708494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648520-T-C

127708509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648535-T-G

127708520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648546-A-G

http://identifiers.org/hco/4/GRCh38#127708533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40648559-C-A

127708645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40648665-A-G

127708645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 40648665-A-T

127708685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648705-T-A

http://identifiers.org/hco/4/GRCh38#127708701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40648721-C-A

127708701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648721-C-T

http://identifiers.org/hco/4/GRCh38#127708758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40648759-A-C

127708768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648769-G-T

127708788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648787-G-A

127708798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648797-G-A

127708798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648797-G-T

127708831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40648830-G-A

127709315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40649175-A-G

127709370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40649229-A-T

127709584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40649425-G-A

127710079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40650208-A-T

http://identifiers.org/hco/4/GRCh38#127710323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40650406-C-A

127710385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40650462-A-G

127710728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40651750-T-C

127710773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40651791-G-A

127710773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40651791-G-T

127710790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40651808-A-G

http://identifiers.org/hco/4/GRCh38#127710818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40651832-A-C

127710818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40651832-A-G

http://identifiers.org/hco/4/GRCh38#127710869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40651883-C-A

127711021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 40652022-T-G

127711188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40652123-T-C

http://identifiers.org/hco/4/GRCh38#127711200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40652134-C-A

127711265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40652155-T-C

http://identifiers.org/hco/4/GRCh38#127711357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40652237-C-A

127711357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40652237-C-T

127712361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40653159-A-G

127712447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40653239-T-C

http://identifiers.org/hco/4/GRCh38#127712490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40653276-A-C

127712498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40653284-C-G

127712587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40653354-A-G

127712743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40653494-G-T

127713887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40654020-G-A

127713887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40654020-G-T

127713888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40654021-T-C

127713888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40654021-T-G

http://identifiers.org/hco/4/GRCh38#127713891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40654024-C-A

127713891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40654024-C-T

127713897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40654030-T-G

127713905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40654038-G-A

127713945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 40654078-G-A

127713975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 40654108-G-A

127714007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40654140-A-G

127714039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 40654172-G-A

127714061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40654194-A-G

127714070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40654203-A-G

127714079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40654212-T-C

127714088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40654221-A-T

127714105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40654238-A-G

127714125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40654260-A-G

127714179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40654308-A-G

127714315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40654490-G-T

127714376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40654545-C-T

127715002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40655068-T-C

127715009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40655075-A-G

127715016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40655082-T-C

127715076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40655135-T-C

http://identifiers.org/hco/4/GRCh38#127716222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40655542-C-A

127716222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40655542-C-T

http://identifiers.org/hco/4/GRCh38#127716241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40655560-C-A

127716424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40655731-G-A

127716424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40655731-G-T

http://identifiers.org/hco/4/GRCh38#127716437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40655744-C-A

127716437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40655744-C-T

127716466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40655773-G-A

127716466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40655773-G-T

127716484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40655791-T-C

127716606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40655902-T-G

127716608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40655903-A-G

127716694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40655989-T-C

127716757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40656047-A-G

127716831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40656126-G-T

127716925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40656214-A-G

127723477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40656353-A-T

127723526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40656403-G-T

127724471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40656829-G-A

127724471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40656829-G-T

127724532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40656892-G-C

127724532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40656892-G-T

127724643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40656996-C-T

127724660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40657014-C-T

127724676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40657030-A-G

http://identifiers.org/hco/4/GRCh38#127724693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40657047-C-A

127724719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40657076-G-T

127725306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40657724-T-C

127725450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40657850-G-A

127725450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40657850-G-T

127725467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40657867-A-G

http://identifiers.org/hco/4/GRCh38#127725483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40657879-C-A

127725486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40657882-G-A

127725486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40657882-G-T

127725548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40657943-A-G

127725729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40658112-G-T

127725737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40658120-C-T

127725739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40658122-G-A

127725800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40658178-T-C

127725829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40658195-C-G

127725974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40658345-T-C

http://identifiers.org/hco/4/GRCh38#127726027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40658391-C-A

127726027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40658391-C-T

127726043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40658405-T-A

http://identifiers.org/hco/4/GRCh38#127726157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40658629-C-A

http://identifiers.org/hco/4/GRCh38#127726166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40658638-C-A

127726202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40658674-C-T

127726319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40658804-G-A

127726319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40658804-G-T

127726461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40658938-A-G

127726588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40659063-T-A

127726618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40659097-C-T

127726639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40659117-T-G

127726735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29239
most severe consequence: 3 prime UTR variant
orthologous variants: 40659210-G-C