http://identifiers.org/hco/3/GRCh38#154121082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62246106-C-A

154121098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62246122-G-A

154121105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62246129-A-T

http://identifiers.org/hco/3/GRCh38#154121112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62246134-C-A

154121112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62246134-C-G

154121112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62246134-C-T

154121133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62246155-T-C

154121170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62246192-G-A

154121170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62246192-G-T

http://identifiers.org/hco/3/GRCh38#154121173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62246201-C-A

154121173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62246201-C-T

154121200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62246221-T-C

http://identifiers.org/hco/3/GRCh38#154121203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62246224-C-A

154121203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62246224-C-T

http://identifiers.org/hco/3/GRCh38#154121210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62246231-A-C

154121210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62246231-A-T

154121211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62246232-C-T

154121212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62246233-G-T

http://identifiers.org/hco/3/GRCh38#154121227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62246242-C-A

154121227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62246242-C-T

154121245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62246260-T-C

154121245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62246260-T-G

154121248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62246263-G-A

154121248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62246263-G-C

154121248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62246263-G-T

154121275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62246287-T-C

154121318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62246318-G-A

154121318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62246318-G-C

154121318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62246318-G-T

154121319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62246319-A-G

154121319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62246319-A-T

http://identifiers.org/hco/3/GRCh38#154121326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62246325-C-A

154121326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62246325-C-T

154121472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 62246443-A-G

http://identifiers.org/hco/3/GRCh38#154121609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62246568-C-A

154121609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62246568-C-T

154121651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62246610-G-A

154121651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62246610-G-T

http://identifiers.org/hco/3/GRCh38#154121806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62246743-C-A

154121806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62246743-C-T

154121846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62246783-G-A

154121846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62246783-G-T

154121855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62246792-G-A

154121855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62246792-G-T

154121898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, undefined
orthologous variants: 62246835-C-T

154121969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 5 prime UTR variant
orthologous variants: 62246894-C-T

154122007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: missense variant
orthologous variants: 62246932-C-G

154122007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62246932-C-T

154122011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: missense variant
orthologous variants: 62246936-G-A

154122011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: missense variant
orthologous variants: 62246936-G-C

154122011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: missense variant
orthologous variants: 62246936-G-T

154122106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247028-G-A

154122109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247031-C-T

154122166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247088-G-A

154122166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247088-G-C

154122166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247088-G-T

154122209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: missense variant
orthologous variants: 62247131-G-T

154122213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: missense variant
orthologous variants: 62247135-G-A

154122213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: missense variant
orthologous variants: 62247135-G-T

154122347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: missense variant
orthologous variants: 62247269-G-T

154122362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: missense variant
orthologous variants: 62247284-T-C

154122400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247322-T-A

154122423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: missense variant
orthologous variants: 62247338-T-C

http://identifiers.org/hco/3/GRCh38#154122466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62247379-C-A

154122466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247379-C-G

154122466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247379-C-T

http://identifiers.org/hco/3/GRCh38#154122475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62247388-C-A

154122475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247388-C-T

http://identifiers.org/hco/3/GRCh38#154122643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62247565-C-A

154122643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247565-C-G

154122643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247565-C-T

154122679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: missense variant
orthologous variants: 62247598-G-C

154122679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: missense variant
orthologous variants: 62247598-G-T

154122832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: missense variant
orthologous variants: 62247751-C-G

154122859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247778-G-C

154122859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247778-G-T

154122979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247898-T-C

154123063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62247982-G-A

http://identifiers.org/hco/3/GRCh38#154123118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62248034-A-C

154123737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62248190-T-C

154123737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62248190-T-G

http://identifiers.org/hco/3/GRCh38#154123787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62248232-C-A

154124224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62248630-A-T

154124226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62248632-T-A

http://identifiers.org/hco/3/GRCh38#154124283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62248667-A-C

154124283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62248667-A-G

154124310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62248689-A-G

154124329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62248708-G-T

http://identifiers.org/hco/3/GRCh38#154124557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62248921-C-A

154124586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62248950-G-A

154124586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62248950-G-C

154124586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62248950-G-T

154125057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62249419-C-T

154125292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62249641-A-G

154125852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62250379-A-G

154125989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62250468-G-A

154126100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62250553-G-A

154126522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62250963-T-C

154127949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62251220-T-C

http://identifiers.org/hco/3/GRCh38#154127953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62251224-C-A

154127953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62251224-C-T

154127980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62251246-C-T

154128050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62251315-A-G

154128802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62251855-G-C

154128957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252006-C-T

154129025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252080-T-C

154129095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252148-A-G

154129175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252191-C-T

154129188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252201-G-A

154129188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252201-G-T

http://identifiers.org/hco/3/GRCh38#154129461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62252490-C-A

154129461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252490-C-G

154129461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252490-C-T

154129510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252503-A-G

154129510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252503-A-T

154129570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 62252563-G-A

154129570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 62252563-G-T

154129690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62252683-T-C

154129716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: synonymous variant
orthologous variants: 62252709-T-G

154129732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252728-C-T

154129749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252745-G-A

http://identifiers.org/hco/3/GRCh38#154129754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62252750-A-C

154129754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252750-A-G

http://identifiers.org/hco/3/GRCh38#154129771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62252767-A-C

154129771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252767-A-G

154129776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252772-A-T

154129810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252806-T-A

154129810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252806-T-C

154129836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252835-C-G

154129836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62252835-C-T

154130047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62253065-G-A

154130047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62253065-G-C

http://identifiers.org/hco/3/GRCh38#154130057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62253075-A-C

154130063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62253081-G-A

154130063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62253081-G-T

154130721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62253457-G-A

154130786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62253521-G-A

http://identifiers.org/hco/3/GRCh38#154130804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62253554-A-C

154130922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62253670-G-A

http://identifiers.org/hco/3/GRCh38#154130943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62253692-A-C

154131000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62253749-A-G

154131482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62254528-T-C

154131663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62254642-T-G

154131664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62254643-C-T

154131683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62254662-G-C

154131767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62254731-C-G

154131767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62254731-C-T

http://identifiers.org/hco/3/GRCh38#154132041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62254934-A-C

154132325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62255271-C-G

154132365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62255367-C-T

154132561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62255623-G-A

154132619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62255672-C-T

154132724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62255784-T-C

154132794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62255840-T-G

http://identifiers.org/hco/3/GRCh38#154132936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62255916-C-A

154132936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62255916-C-T

154133258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62256258-G-A

154133262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62256262-A-G

154133332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62256334-G-A

http://identifiers.org/hco/3/GRCh38#154135726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62256867-A-C

154136007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62257128-C-T

154136014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62257135-G-A

154136538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62257527-A-G

154136617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62257603-C-G

154136617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62257603-C-T

154136619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62257605-A-G

http://identifiers.org/hco/3/GRCh38#154136868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62257849-C-A

154136868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62257849-C-T

154137955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62258678-C-G

http://identifiers.org/hco/3/GRCh38#154138011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62258728-A-C

154138410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62261279-G-A

154138410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62261279-G-T

154138585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62261455-C-T

http://identifiers.org/hco/3/GRCh38#154138880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62261940-C-A

154138913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62261966-C-G

154139210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62262243-C-G

154139397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62262409-T-C

154139512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62262559-G-C

154139514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62262561-A-G

154139577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62262626-C-G

154139577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62262626-C-T

154139599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62262648-C-T

154139933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62262971-T-C

154139970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62263020-T-A

154140066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, undefined
orthologous variants: 62263088-T-C

154140540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62263537-T-C

154140641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62263613-G-A

http://identifiers.org/hco/3/GRCh38#154140678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62263644-A-C

154140678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62263644-A-G

154142190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62271266-A-G

154142215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62271291-T-C

154142426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62275149-C-G

154142447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62275170-G-A

154142485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62275208-A-G

154142585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62275308-T-C

154142585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62275308-T-G

154142837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62275567-T-C

154142966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62275692-C-G

154142990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62275720-A-G

154143198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62275906-T-C

154143437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62276383-C-G

154143777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62276930-T-C

http://identifiers.org/hco/3/GRCh38#154143785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62276938-C-A

154143852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62276979-T-A

154143852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62276979-T-G

154144424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62277823-G-T

154144585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62277970-T-A

154144585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62277970-T-C

154144629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62278015-T-G

154144772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62278140-C-T

154144779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62278147-T-G

154144797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62278165-G-T

154144826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62278194-A-G

154144942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62278338-C-T

154145114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62278487-G-T

154145407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62278746-A-G

154145477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62278824-A-G

154145480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62278827-A-G

154145535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62278881-T-C

154145535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62278881-T-G

154145965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62279257-G-A

154146017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62279309-T-C

154146059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62279352-G-A

154146121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62279413-T-C

154146134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62279427-A-G

154146144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62279436-C-G

154146144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62279436-C-T

154146205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62279497-T-C

154146223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62279515-G-T

154146256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62279630-C-T

154146314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62279788-T-G

154146329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62279803-G-A

154146741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62280164-A-G

154147053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62280438-G-A

154147128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62280515-G-C

154147444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62280748-C-G

http://identifiers.org/hco/3/GRCh38#154147484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62280789-A-C

154147484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62280789-A-G

http://identifiers.org/hco/3/GRCh38#154147493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62280798-A-C

154147758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62281569-T-C

154147858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62281653-A-G

http://identifiers.org/hco/3/GRCh38#154147998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62281764-C-A

154148130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62281880-C-T

154148183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62281932-G-T

154148549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62282296-C-T

http://identifiers.org/hco/3/GRCh38#154148751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62282495-A-C

154148881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62282629-G-A

154149016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62282756-T-C

154149558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285197-T-A

154149578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285222-T-A

154149578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285222-T-C

154149594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285237-T-C

154149595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285238-G-A

154149595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285238-G-T

http://identifiers.org/hco/3/GRCh38#154149628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62285278-A-C

154149730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285347-A-G

154149766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285380-G-A

154149867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285477-C-T

154149951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285572-T-A

154150053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285786-T-A

154150054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285787-A-G

154150060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285793-G-C

154150060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285793-G-T

154150102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285867-A-G

154150113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285878-T-C

154150117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62285882-A-T

154150303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62286064-A-T

154150394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62286144-G-A

154150580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62286428-C-T

154150638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62286483-C-T

154150828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62286691-C-G

154150938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62286782-C-T

154151499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62286970-T-A

154151620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62287119-C-G

154152220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62287780-A-G

154152629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62288162-T-A

http://identifiers.org/hco/3/GRCh38#154152777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62288257-C-A

154152777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 62288257-C-T

154152807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 62288287-T-C

http://identifiers.org/hco/3/GRCh38#154152844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62288324-A-C

http://identifiers.org/hco/3/GRCh38#154152879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62288359-C-A

154152879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 62288359-C-T

154153037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62288514-G-A

154153037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62288514-G-C

154153037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62288514-G-T

http://identifiers.org/hco/3/GRCh38#154153057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62288534-C-A

154153058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62288535-T-A

154153058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62288535-T-C

154153196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62288666-C-T

154153349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62288764-C-G

154153349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62288764-C-T

154153652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62288995-A-G

154153652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62288995-A-T

http://identifiers.org/hco/3/GRCh38#154153966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62289312-A-C

154154123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62289471-A-T

154154261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62289588-G-A

http://identifiers.org/hco/3/GRCh38#154154341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62289645-C-A

154154341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62289645-C-T

154154345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62289649-C-T

154154398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62289705-A-G

154154549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62289937-C-T

154154641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62290152-A-T

154154851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62290358-T-C

154155037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62290538-T-A

154155037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62290538-T-C

154155037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62290538-T-G

154155216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62290662-A-G

154155534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62290960-A-G

154155947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62291507-A-G

154156003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62291563-A-G

154156016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62291576-G-T

154156026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62291590-A-G

154156081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62291876-G-A

154156204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62291989-C-G

154156758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62294523-A-G

154156849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62294601-G-A

154156969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62294701-C-G

154157022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62294754-G-A

154157124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62294859-G-A

154157425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62295161-G-A

154157425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62295161-G-T

154157438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62295174-T-C

154157780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62295592-A-G

154157841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62295714-G-A

154157975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62295910-G-T

154158055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62295982-G-A

154158107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62296014-G-A

154158902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62296871-A-T

154158975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62296930-G-A

154158975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62296930-G-C

154159178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62297094-C-T

http://identifiers.org/hco/3/GRCh38#154159772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62297579-C-A

154160126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62297952-T-A

http://identifiers.org/hco/3/GRCh38#154160909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62298484-C-A

http://identifiers.org/hco/3/GRCh38#154161369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62298869-A-C

154161798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62299753-C-T

154161819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62299775-A-G

154161849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62299805-T-A

154161996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62299965-C-T

154162000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62299969-T-G

154162028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62299997-G-C

http://identifiers.org/hco/3/GRCh38#154162082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#62300047-A-C

154163455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62300600-T-G

154163543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62300711-T-A

http://identifiers.org/hco/3/GRCh38#154163743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62300956-A-C

154163743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62300956-A-T

154164492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62301708-G-A

154164685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62301898-C-G

154164757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62301959-T-C

154164953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62302308-T-C

http://identifiers.org/hco/3/GRCh38#154164992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62302343-A-C

154164992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62302343-A-G

154165021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62302372-A-G

http://identifiers.org/hco/3/GRCh38#154165213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62302520-C-A

154165266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62302565-T-C

154165269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62302568-T-A

154165269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62302568-T-C

154165278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62302577-T-G

http://identifiers.org/hco/3/GRCh38#154165580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62302835-C-A

154165580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62302835-C-G

154165615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62302870-C-G

154165634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62302889-T-C

154165807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62303059-G-A

154166323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62303427-T-C

154166474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62303553-T-G

154166557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62303617-A-G

http://identifiers.org/hco/3/GRCh38#154166852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62303909-A-C

154166925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62303968-C-G

154167024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62304042-C-T

154167048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62304062-G-A

http://identifiers.org/hco/3/GRCh38#154167115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62304255-A-C

154167226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62304440-C-G

154167226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62304440-C-T

154167366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62304582-C-T

154167580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62304762-C-G

154167614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62304805-T-G

154167747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62304933-C-T

154169483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62305741-G-A

154169588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62305855-G-A

154170048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62306449-T-G

http://identifiers.org/hco/3/GRCh38#154170075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62306476-C-A

154173087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62306891-G-A

154173095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62306899-A-G

154173110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62306914-A-G

http://identifiers.org/hco/3/GRCh38#154173192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62306974-A-C

154173192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62306974-A-G

154173992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62307717-C-G

154174384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62308126-T-A

154175055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62308916-C-T

154175117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62308975-G-T

154175187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62309035-G-A

154175218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62309067-C-T

154175290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62309132-G-A

154175300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62309154-G-A

http://identifiers.org/hco/3/GRCh38#154175304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62309158-A-C

154175583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62309497-C-T

http://identifiers.org/hco/3/GRCh38#154175686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62309636-C-A

154175803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62309805-T-A

154175933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62309927-T-C

154176148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62310113-A-G

154176243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62310163-G-T

154176272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62310182-G-T

154176573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62311151-G-T

154176582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62311160-A-G

154177099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62311718-C-G

154177182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62311797-G-A

154177355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62311977-C-T

154177455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62312081-T-C

154177803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62312400-T-C

154177904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62312497-A-G

154178344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62312619-C-T

154178385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62312662-C-T

154178634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62312886-C-T

154178643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62312898-A-G

154178787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62313044-G-A

http://identifiers.org/hco/3/GRCh38#154178806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62313061-C-A

154178882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62313135-C-T

154178965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62313217-A-G

154179111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62313339-A-G

154179175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62313410-C-T

http://identifiers.org/hco/3/GRCh38#154179243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62313468-A-C

154179292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62313518-C-T

154179331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62313561-A-G

154179618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62313799-C-T

154179786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62315156-C-T

154179972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62315329-C-T

154180048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62315383-T-C

154180077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62315415-G-A

154180098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62315436-A-G

154180374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62315629-G-C

154180582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62315858-C-T

154180904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62319646-T-G

154181284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62319987-A-G

http://identifiers.org/hco/3/GRCh38#154181959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62320674-A-C

154182155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62320783-G-A

154182163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62320791-T-C

154182339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62320968-G-A

154182463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62321087-G-A

http://identifiers.org/hco/3/GRCh38#154182514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62321133-C-A

154182514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62321133-C-T

154182627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62321234-T-A

154182646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62321250-A-G

154182649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62321253-T-A

154182797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62321433-C-G

154183129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62323687-A-G

154183193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62323752-A-G

154183236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62323807-G-C

154183565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62324170-A-G

154183683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62324286-T-C

154183887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62324488-A-G

154184306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62324605-G-T

154184386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62324686-A-G

154184509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62324809-C-G

154184760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62325000-C-G

154184927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62325131-G-T

154185011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62325204-C-T

154185410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62325363-C-T

154185511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62325468-C-T

154185988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62325951-C-T

154186096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62326045-T-C

154186840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62326386-G-T

154187582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62326839-T-C

154187582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62326839-T-G

http://identifiers.org/hco/3/GRCh38#154187597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62326872-C-A

154187597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62326872-C-T

http://identifiers.org/hco/3/GRCh38#154187598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62326873-C-A

154187598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62326873-C-T

154187652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62326939-A-G

154187652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62326939-A-T

154187748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, missense_variant
orthologous variants: 62327033-T-G

154187772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 62327057-A-G

154187772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 62327057-A-T

154187850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62327135-G-A

154187850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62327135-G-T

http://identifiers.org/hco/3/GRCh38#154187979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62327250-C-A

154187979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62327250-C-G

154187983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62327254-A-G

154187998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62327269-G-T

154188158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62327441-A-T

154188425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62327676-C-T

154188572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62327822-G-A

154188667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62327897-A-G

154188893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62328592-G-A

154188992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62328690-T-C

154189001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62328699-A-G

154189860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62329204-C-T

154190116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62329835-C-T

154190148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62329869-C-T

154190173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62329883-G-T

154190779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62330459-A-G

154190814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62330496-C-T

154190853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62330537-T-C

154191072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62330711-T-C

154191079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62330719-T-C

154191279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62330912-T-C

154191322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 62330955-A-G

http://identifiers.org/hco/3/GRCh38#154191503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62331114-A-C

154191503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62331114-A-G

154191503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62331114-A-T

154191525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62331133-A-G

http://identifiers.org/hco/3/GRCh38#154191531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62331139-C-A

154191531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62331139-C-T

154191544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62331148-G-A

154191663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62331252-A-T

http://identifiers.org/hco/3/GRCh38#154191723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62331313-A-C

154191723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62331313-A-G

http://identifiers.org/hco/3/GRCh38#154191913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62331455-A-C

154191954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62331495-C-G

154191995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62331534-A-G

154192174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62331611-G-C

154192237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62331669-T-C

154193163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62332379-G-C

154193215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62332431-G-A

154193244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62332493-G-C

154193407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62332683-T-C

154193458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62332723-T-C

154193481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62332746-A-G

154194103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62333315-C-T

http://identifiers.org/hco/3/GRCh38#154194426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62333704-A-C

154194432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62333710-A-G

154194432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62333710-A-T

154194609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62333975-A-G

154194623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62333989-T-A

154194728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62334094-G-A

154194856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62334157-A-G

154194868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62334169-T-A

154194868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62334169-T-G

154195067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62334369-T-C

154195607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62334794-G-C

154196430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62335521-C-T

154217631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62335886-C-T

154217656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62335911-A-G

154217690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62336083-C-T

http://identifiers.org/hco/3/GRCh38#154217772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62336168-C-A

154217772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62336168-C-T

http://identifiers.org/hco/3/GRCh38#154217866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62336299-C-A

154217866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 62336299-C-T

http://identifiers.org/hco/3/GRCh38#154217927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62336360-C-A

154217927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, missense_variant
orthologous variants: 62336360-C-T

154217969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62336402-A-G

154217984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62336420-G-A

154217984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62336420-G-C

154217984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62336420-G-T

154217987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62336423-C-G

http://identifiers.org/hco/3/GRCh38#154218032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62336463-C-A

154218032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62336463-C-T

154218063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62336494-G-A

154218346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62336727-A-G

http://identifiers.org/hco/3/GRCh38#154218536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62336912-A-C

154218666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62337021-G-A

154218666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62337021-G-C

154218984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62337311-G-A

154224266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62338395-T-C

http://identifiers.org/hco/3/GRCh38#154224671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62338789-A-C

154224671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62338789-A-G

154224820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62338922-T-C

154224987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62339097-A-G

http://identifiers.org/hco/3/GRCh38#154225313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62339418-A-C

154225675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62339773-A-G

154225675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62339773-A-T

154225743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62339837-A-G

154225752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron variant
orthologous variants: 62339846-A-G

154225835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62339888-T-C

154225835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62339888-T-G

154225846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62339899-C-T

154226234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62340255-C-G

154226344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62340359-A-G

154226350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62340365-G-A

154226350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62340365-G-C

154226694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62340685-C-T

154228731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62341292-T-G

154228757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62341317-G-A

154228791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62341349-A-G

http://identifiers.org/hco/3/GRCh38#154228794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62341352-C-A

154229360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62341635-T-C

154229430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62341712-G-C

154229575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62341794-A-G

154229668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62341873-G-A

154231254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62345440-C-T

154231266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62345452-C-T

154232264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62346994-G-C

154232285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62347011-T-C

154232522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62347245-G-C

154232564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62347289-T-C

154233338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62347793-A-G

154233449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62347903-T-G

154233472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62347930-C-G

154233553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62348005-G-T

154233589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62348039-G-T

154233627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62348060-G-T

154233678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62348116-A-G

154233829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62348272-G-T

154233917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62348353-A-G

154233954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62348389-G-A

154234148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62348566-C-T

154234437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62348826-A-G

154234657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62349051-C-T

154234665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62349059-C-T

154235712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62350425-A-G

154235735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62350438-T-C

154235735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62350438-T-G

154235770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62350473-A-G

154235949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62350653-T-C

154236010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62350730-T-A

154236093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62350896-T-C

154236098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62350901-T-C

154236204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62351003-T-G

http://identifiers.org/hco/3/GRCh38#154236458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62351232-C-A

154237033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62352416-G-A

154237707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62352807-A-G

154237996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62353111-G-A

154237996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62353111-G-T

154238132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62353296-C-T

154238161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62353324-C-T

154238552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62353686-G-T

154238593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62353721-A-G

154238725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62353842-T-G

154238854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62353958-C-T

154239023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62354113-A-G

154239407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62354409-C-T

154239477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62354477-T-G

154239540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62354521-C-T

154239864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62354801-C-T

http://identifiers.org/hco/3/GRCh38#154239926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62354858-C-A

http://identifiers.org/hco/3/GRCh38#154240264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62355414-C-A

154240264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62355414-C-T

http://identifiers.org/hco/3/GRCh38#154240356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62355502-C-A

154240356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62355502-C-G

154240588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62355732-A-G

154240603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62355749-T-A

http://identifiers.org/hco/3/GRCh38#154240629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62355780-C-A

154241155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62356422-T-C

154241155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62356422-T-G

154241171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62356437-G-T

154241295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62356550-G-A

154241419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62356680-T-G

154243126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62356986-C-T

154243199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62357042-C-T

154243317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62357155-T-G

154243688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62357496-G-A

154243956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62358281-G-A

154244014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62358338-G-A

154244016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62358340-A-T

154247617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62359192-G-A

154247618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62359193-C-G

154247618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62359193-C-T

154247655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62359230-G-C

154247720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62361216-T-C

154247811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62361305-A-G

154248148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62361645-C-T

154248298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62361795-G-A

154248382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62361875-C-T

154249187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62362650-G-A

154249325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62362795-C-T

154249413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62362890-A-T

154249494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62362944-C-G

154250338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62363387-T-G

154250511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62363558-T-C

154251382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62364510-G-A

154252037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62364923-A-G

154252066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62364955-T-C

154252270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62365126-G-A

154252296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62365152-G-C

154252330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62365164-G-C

154252692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62365454-A-G

154253026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62365707-G-T

154253030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62365711-G-A

154253105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62365782-C-G

154253105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62365782-C-T

154253298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 62365955-G-T

http://identifiers.org/hco/3/GRCh38#154253332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62365982-C-A

154253483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62366088-G-A

154254262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62366644-G-A

154254601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62366915-A-G

154254636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62366950-G-T

http://identifiers.org/hco/3/GRCh38#154254739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62367050-C-A

154254739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62367050-C-G

154254739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62367050-C-T

154254838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62367149-T-C

154254899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62367209-G-A

154254899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62367209-G-T

154254926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62367228-G-T

154255106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62367357-G-A

154255166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62367408-G-A

http://identifiers.org/hco/3/GRCh38#154255181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62367423-C-A

154255181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62367423-C-T

154255194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62367436-T-C

154255208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62367450-T-C

154255359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62367653-T-C

154255359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62367653-T-G

154255550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62367801-G-A

http://identifiers.org/hco/3/GRCh38#154255592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62367843-C-A

154255609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62367860-C-T

154255654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62367906-T-A

http://identifiers.org/hco/3/GRCh38#154255807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62368020-C-A

154255842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62368055-T-C

154255842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62368055-T-G

154256204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62368386-A-G

http://identifiers.org/hco/3/GRCh38#154256609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62368445-A-C

154256609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62368445-A-G

154256609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62368445-A-T

154256723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62368556-A-G

154256841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62368666-T-C

154256860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62368685-T-C

154256876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_acceptor_variant
orthologous variants: 62368700-G-A

154256969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62368791-C-G

154256969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62368791-C-T

154257021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62368828-T-C

154257083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62368883-T-C

154257100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62368900-C-T

154257137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62368931-T-A

154257137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62368931-T-C

http://identifiers.org/hco/3/GRCh38#154257182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#62368978-C-A

154257193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62368989-T-C

154257266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62369041-T-C

154257275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62369050-G-T

154257299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62369074-T-C

154257364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24490
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62369135-A-T