143390317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42334572-T-G

143390494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42334707-A-G

143390616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42334824-T-A

143390616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42334824-T-C

143390707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42334916-G-A

143390707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42334916-G-T

143390739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42334949-T-C

http://identifiers.org/hco/7/GRCh38#143390755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42334968-C-A

143390755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42334968-C-T

143390810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42334998-A-G

143390810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42334998-A-T

143390875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42335083-G-A

143390875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42335083-G-T

143390899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42335107-T-G

143391017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42335216-G-A

143391017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42335216-G-T

143391138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42335366-G-A

143391138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42335366-G-T

143391207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42335457-G-C

143391207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42335457-G-T

http://identifiers.org/hco/7/GRCh38#143391230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42335480-C-A

143391230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42335480-C-T

http://identifiers.org/hco/7/GRCh38#143391265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42335517-C-A

143391265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42335517-C-T

143391291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42335544-A-G

143391306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42335556-T-C

143391448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42335681-G-C

143391599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42335843-C-G

143391698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42335948-A-G

143391721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42335971-G-A

143391721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42335971-G-C

143391721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42335971-G-T

143391831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42336081-T-C

143391883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42336127-G-A

143391883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42336127-G-T

143391959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42336201-C-T

143392212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42336378-T-C

143393100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42336926-C-T

143393194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42337006-A-G

143393564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42337370-G-T

143393603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42337412-G-A

143393628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42337438-A-T

http://identifiers.org/hco/7/GRCh38#143393679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42337487-A-C

143393690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 42337498-T-C

143393898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42337704-G-A

143393898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42337704-G-T

http://identifiers.org/hco/7/GRCh38#143394055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42337794-C-A

143394130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42337869-G-A

143394130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42337869-G-T

143394136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42337875-G-T

143394171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42337918-G-C

http://identifiers.org/hco/7/GRCh38#143394189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42337934-C-A

http://identifiers.org/hco/7/GRCh38#143395092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42338499-C-A

143395092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42338499-C-T

143395126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42338533-G-A

143395200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42338606-A-G

http://identifiers.org/hco/7/GRCh38#143395256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42338653-C-A

143395277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42338672-C-T

http://identifiers.org/hco/7/GRCh38#143395312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42338704-A-C

143395422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42338814-G-A

http://identifiers.org/hco/7/GRCh38#143395457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42338849-C-A

143395457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42338849-C-T

http://identifiers.org/hco/7/GRCh38#143395494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42338886-C-A

143395638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42338939-G-C

143395638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42338939-G-T

http://identifiers.org/hco/7/GRCh38#143395673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42338972-C-A

http://identifiers.org/hco/7/GRCh38#143395679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42338978-C-A

143395679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42338978-C-T

143395823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42339093-G-A

143396348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42339556-T-C

143396382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42339588-C-T

143396476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 42339682-G-A

143396476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 42339682-G-C

143396618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42339820-T-G

143396634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42339836-G-A

143396634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42339836-G-T

143396655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42339856-A-G

143396689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42339906-T-A

143396689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42339906-T-C

143396768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42339981-T-A

143396771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42339984-T-A

http://identifiers.org/hco/7/GRCh38#143396782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42339996-C-A

143396782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42339996-C-T

http://identifiers.org/hco/7/GRCh38#143396785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42339999-A-C

http://identifiers.org/hco/7/GRCh38#143397143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42340350-C-A

http://identifiers.org/hco/7/GRCh38#143397311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42340503-C-A

143397323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42340515-G-A

143397503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42340685-T-C

143397503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42340685-T-G

http://identifiers.org/hco/7/GRCh38#143397523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42340709-C-A

143397523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42340709-C-T

143397552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42340735-A-G

143397641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42340824-A-G

143397700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42340879-C-G

143397700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42340879-C-T

143397764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42340942-G-A

143397764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42340942-G-T

143397767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42340945-T-C

143397817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42340992-G-T

143398167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42341325-G-A

143398240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42341396-C-T

143398307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42341458-A-T

143398311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42341461-G-A

143398311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42341461-G-C

http://identifiers.org/hco/7/GRCh38#143398405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42341555-C-A

143398405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42341555-C-G

143398405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42341555-C-T

143398438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42341588-T-C

143398463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42341613-G-A

143398479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42341629-G-A

143398479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42341629-G-T

143398509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42341659-T-C

143398514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42341664-A-G

143398514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42341664-A-T

http://identifiers.org/hco/7/GRCh38#143398527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42341677-C-A

143398614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42341723-G-A

143398783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42341892-G-A

143398836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42341945-A-G

143398897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42342006-T-C

143398897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42342006-T-G

http://identifiers.org/hco/7/GRCh38#143399007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42342115-C-A

143399007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342115-C-T

143399016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342124-A-G

143399016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342124-A-T

http://identifiers.org/hco/7/GRCh38#143399038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42342140-C-A

143399043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342145-G-A

143399043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342145-G-T

143399076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342188-G-A

143399076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342188-G-T

143399172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342279-G-A

143399172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342279-G-T

143399233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342328-G-A

143399233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342328-G-T

143399480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342584-C-T

http://identifiers.org/hco/7/GRCh38#143399483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42342587-C-A

143399547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42342624-A-G

143399643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42342701-G-A

143399643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42342701-G-C

143399643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42342701-G-T

143399727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42342786-G-A

143399727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42342786-G-C

143399727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42342786-G-T

143399748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42342807-G-A

http://identifiers.org/hco/7/GRCh38#143400039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42343098-A-C

143400039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42343098-A-G

http://identifiers.org/hco/7/GRCh38#143400148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42343684-C-A

143400174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42343710-G-A

143400174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42343710-G-T

143400179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42343715-G-A

143400179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42343715-G-T

143400196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42343732-A-G

143400584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344115-A-G

143400661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344186-G-T

http://identifiers.org/hco/7/GRCh38#143400712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42344237-C-A

143400714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344240-T-C

143400714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344240-T-G

143400797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344289-T-G

143400823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344321-A-T

http://identifiers.org/hco/7/GRCh38#143400849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42344347-C-A

143400849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42344347-C-T

http://identifiers.org/hco/7/GRCh38#143400937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42344373-A-C

143400937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42344373-A-G

143400937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42344373-A-T

143401303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42344498-T-C

143401446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42344642-G-A

143401446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42344642-G-T

http://identifiers.org/hco/7/GRCh38#143401473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42344669-C-A

143401473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42344669-C-G

143401473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42344669-C-T

http://identifiers.org/hco/7/GRCh38#143401475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42344671-C-A

143401475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42344671-C-T

143401683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344845-A-T

143401696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344859-G-A

143401696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344859-G-T

143401707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344869-G-A

143401707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42344869-G-T

143402867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42345425-G-A

143402870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42345428-T-A

143402989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42345533-C-G

143403254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42345770-C-G

143403328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42345797-G-A

143403409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42345874-G-A

143403521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42345979-A-T

143403683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42346110-C-T

143403932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42346309-C-G

143403932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42346309-C-T

143404013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42346381-T-A

143404615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42347099-G-A

143404683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42347167-C-T

143404897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42347364-C-G

143404897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42347364-C-T

143405238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42347674-G-C

143405499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42347904-A-G

143405999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42348381-G-T

143406017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42348400-G-T

143406884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42348426-C-T

143407223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42348774-T-C

143407238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42348789-G-C

143407426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42348924-G-T

http://identifiers.org/hco/7/GRCh38#143407478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42348981-C-A

http://identifiers.org/hco/7/GRCh38#143407556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42349057-A-C

143407556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42349057-A-G

http://identifiers.org/hco/7/GRCh38#143407765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42349262-C-A

http://identifiers.org/hco/7/GRCh38#143407772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42349273-C-A

143407772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42349273-C-T

143407891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 42349317-G-A

143407891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 42349317-G-T

143408248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42349630-A-G

143408304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42349680-G-T

http://identifiers.org/hco/7/GRCh38#143408578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42349936-C-A

143408578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42349936-C-T

143408616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42349975-T-A

143408616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42349975-T-C

143408786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3385
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42350125-A-G