24357254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267657-T-A

24357254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267657-T-C

24357284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267627-G-T

24357345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267592-A-G

http://identifiers.org/hco/1/GRCh38#24357361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267576-C-A

24357394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267534-G-A

24357394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267534-G-T

24357442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267494-G-A

24357442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267494-G-C

24357442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267494-G-T

http://identifiers.org/hco/1/GRCh38#24357451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267485-C-A

http://identifiers.org/hco/1/GRCh38#24357456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267480-C-A

24357456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267480-C-T

http://identifiers.org/hco/1/GRCh38#24357482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267467-C-A

24357527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267421-C-T

http://identifiers.org/hco/1/GRCh38#24357554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267394-C-A

24357554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267394-C-T

24357565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267383-T-C

http://identifiers.org/hco/1/GRCh38#24357638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267331-C-A

24357638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267331-C-T

24357685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267285-A-G

http://identifiers.org/hco/1/GRCh38#24357709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267269-C-A

24357709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267269-C-G

24357709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267269-C-T

24357713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267266-G-A

http://identifiers.org/hco/1/GRCh38#24357738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267240-C-A

24357738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267240-C-G

24357738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267240-C-T

24357936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135267092-G-T

http://identifiers.org/hco/1/GRCh38#24357985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135267053-A-C

http://identifiers.org/hco/1/GRCh38#24358169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135264251-C-A

24358215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135264202-C-T

http://identifiers.org/hco/1/GRCh38#24358406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135264061-C-A

24358406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135264061-C-T

24358507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135264003-G-T

24358638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135263873-G-T

24358670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135263837-T-G

24360772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135261204-A-T

24360789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135261187-C-G

24360812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135261164-A-G

24360813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135261163-G-T

24361117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135260860-G-T

http://identifiers.org/hco/1/GRCh38#24361125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135260852-C-A

24361125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135260852-C-G

24361125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135260852-C-T

24361149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135260835-A-T

24361167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135260821-G-A

24361167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135260821-G-C

24361167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135260821-G-T

24364912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135259701-T-C

24364983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135259630-C-T

24365246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135259341-G-C

24365644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135258845-C-T

24367482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135258744-A-T

24367499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135258727-C-G

24367859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135258556-T-C

http://identifiers.org/hco/1/GRCh38#24368156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135258325-C-A

24368891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257642-G-A

24368895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257638-G-A

24368895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257638-G-T

http://identifiers.org/hco/1/GRCh38#24368904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135257629-C-A

24368904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257629-C-T

24368968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257576-G-A

24368968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257576-G-T

24368982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257562-G-C

24369002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257487-G-A

24369002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257487-G-T

http://identifiers.org/hco/1/GRCh38#24369061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135257432-C-A

24369061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257432-C-T

24369206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257340-G-T

http://identifiers.org/hco/1/GRCh38#24369237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135257310-C-A

http://identifiers.org/hco/1/GRCh38#24369240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135257307-C-A

24369240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257307-C-T

http://identifiers.org/hco/1/GRCh38#24369298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135257249-C-A

24369298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257249-C-T

24369302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257245-G-C

http://identifiers.org/hco/1/GRCh38#24369572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135257053-C-A

24369572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135257053-C-G

http://identifiers.org/hco/1/GRCh38#24369581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135257044-C-A

24369690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135256950-T-C

24369898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135256744-A-G

24369932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135256713-C-T

http://identifiers.org/hco/1/GRCh38#24369937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135256704-C-A

24369937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135256704-C-T

http://identifiers.org/hco/1/GRCh38#24369940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135256701-C-A

24369940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135256701-C-T

24369953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135256689-T-C

24369966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135256676-G-A

24369966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135256676-G-C

24369966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135256676-G-T

24369969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135256673-C-T

24370192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135256475-T-C

24370199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135256468-C-T

24370982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135255484-T-C

24372967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135253430-G-A

24373420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135253112-G-A

24373462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135253070-A-G

http://identifiers.org/hco/1/GRCh38#24373467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135253065-A-C

24373490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135253031-G-T

24373570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252977-A-G

24373573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252969-T-C

24373581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252962-A-T

http://identifiers.org/hco/1/GRCh38#24373617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135252923-C-A

24373622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252918-T-A

24373622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252918-T-C

24373634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252906-G-A

24373634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252906-G-T

http://identifiers.org/hco/1/GRCh38#24373638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135252902-C-A

24373638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252902-C-T

24373729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135252809-C-G

24373729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135252809-C-T

24373819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252719-A-G

24373829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252709-C-T

24373935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252613-T-C

24373936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252612-G-A

24373936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252612-G-T

24373946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252602-G-A

24373946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135252602-G-T

24374987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135252074-G-A

24375024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135252033-G-A

24375141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135251925-C-T

24375480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135251535-C-T

24375481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135251534-G-A

24375744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135251284-A-G

24376517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135249837-T-C

24376574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135249781-T-C

24376661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135249730-C-T

24376736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135249661-G-A

24376818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135249601-C-T

24376884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135249541-C-T

24379640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135246764-G-C

24379640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135246764-G-T

24379641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135246763-C-T

24379701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135246703-G-A

24379831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135246574-G-C

24379858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135246550-A-G

http://identifiers.org/hco/1/GRCh38#24379878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135246530-A-C

24379878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135246530-A-G

24379969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135246237-T-A

24379969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135246237-T-C

24380010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135246196-C-T

24380607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135245509-A-T

24380647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135245492-C-G

24381298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135245090-A-T

24381427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135244991-T-C

24381428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135244990-G-A

24381428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135244990-G-T

24381584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135244855-G-A

24381706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135244738-A-G

24381831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135244622-G-A

24381836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135244617-A-G

24381903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135244523-A-T

http://identifiers.org/hco/1/GRCh38#24382051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135244297-C-A

24382254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135244088-G-A

24382309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135244043-G-A

24382549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135243818-A-G

24382575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135243783-G-A

24382728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135243661-C-T

24382736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135243653-A-T

24382737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135243652-A-G

24382749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135243640-T-C

http://identifiers.org/hco/1/GRCh38#24383492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135242666-C-A

24383705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135242478-G-A

24383780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135242403-C-T

24383799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135242385-A-G

24383804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135242380-T-C

http://identifiers.org/hco/1/GRCh38#24383918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135242278-C-A

24383918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135242278-C-G

24383946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135242250-T-C

24383996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135242200-A-G

24384129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135242072-T-C

24384147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135242054-C-T

24384278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135241907-T-C

24384347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135241862-G-T

24384388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135241821-A-G

24385129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135241157-C-T

24386395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135239511-G-C

24386497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135239427-G-A

24388535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135237750-T-C

24388729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135237587-T-G

24388848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135237463-A-G

24388904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135237397-A-G

24388911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135237390-C-T

24388983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135237326-T-C

24389041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135237278-T-C

24389094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135237224-A-G

24389127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135237191-G-A

24389129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135237189-T-A

24389287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135237065-G-A

24389982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135236338-T-C

http://identifiers.org/hco/1/GRCh38#24390014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135236306-C-A

http://identifiers.org/hco/1/GRCh38#24390039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135236280-C-A

24390039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135236280-C-G

24390046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135236273-T-C

24391446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135235446-G-A

24391446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135235446-G-T

24391586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135235340-T-C

24391586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135235340-T-G

24391616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 135235310-G-A

24391616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 135235310-G-T

24391681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 135235245-T-A

24400997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135234105-T-C

http://identifiers.org/hco/1/GRCh38#24401015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135234083-C-A

24401038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135234060-A-T

24401043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135234055-G-A

24401091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135234005-G-A

24401165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135233939-T-A

24401165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135233939-T-C

24401165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135233939-T-G

http://identifiers.org/hco/1/GRCh38#24401169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135233935-A-C

24401169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135233935-A-G

24401195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135233912-G-T

http://identifiers.org/hco/1/GRCh38#24401249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135233854-C-A

24401333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135233791-C-T

24401471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135233662-C-T

24401490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135233643-A-G

24401518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135233630-G-A

24401518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135233630-G-C

24401518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135233630-G-T

24401564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135233605-G-A

24401564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135233605-G-C

24401564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135233605-G-T

http://identifiers.org/hco/1/GRCh38#24401566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135233603-C-A

24401568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135233601-G-A

24401568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135233601-G-T

http://identifiers.org/hco/1/GRCh38#24401603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135233564-C-A

24401603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135233564-C-T

24408551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135225474-G-A

24408820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135225167-G-T

24408894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135225095-T-A

24408899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135225090-G-A

24409002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135225005-A-G

24413202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135223701-C-T

24413296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135223628-G-A

http://identifiers.org/hco/1/GRCh38#24413460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135223495-C-A

24413481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135223474-C-T

24413571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135223387-G-C

http://identifiers.org/hco/1/GRCh38#24413645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135223326-C-A

24413645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135223326-C-T

24413713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135223277-T-C

24413808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 135223187-A-G

http://identifiers.org/hco/1/GRCh38#24413827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135223168-C-A

24414470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135222812-T-C

http://identifiers.org/hco/1/GRCh38#24414526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135222759-C-A

24414850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135222747-A-G

24414869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135222728-T-C

24415105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 135222497-G-T

24415225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135222357-G-A

24415225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135222357-G-T

http://identifiers.org/hco/1/GRCh38#24415377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135222225-C-A

24415411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135222197-G-T

24415448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135222153-G-A

24415448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135222153-G-T

24415516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135222090-T-C

24415552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135222070-C-T

http://identifiers.org/hco/1/GRCh38#24415576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135222048-A-C

24415576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135222048-A-G

24415582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135222042-T-C

24415731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135221911-G-A

24415731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135221911-G-T

24416004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135221664-C-T

http://identifiers.org/hco/1/GRCh38#24416136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135221520-A-C

http://identifiers.org/hco/1/GRCh38#24416203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135221481-C-A

24416223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135221464-G-T

24416232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 135221455-G-A

24416232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 135221455-G-T

http://identifiers.org/hco/1/GRCh38#24416259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135221438-C-A

24416291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135221407-C-T

24416456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135221284-G-A

24416524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135221183-G-C

24416525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135221182-G-C

24416525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135221182-G-T

http://identifiers.org/hco/1/GRCh38#24416565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135221138-C-A

24416565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135221138-C-T

24416672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135221046-A-G

24416826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135220908-G-A

http://identifiers.org/hco/1/GRCh38#24416836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135220898-C-A

24416836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135220898-C-G

24416836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135220898-C-T

24416931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28070
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135220808-A-G