http://identifiers.org/hco/5/GRCh38#141653462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38105741-C-A

141653462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38105741-C-T

141653518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38105797-T-C

141653703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38105972-A-G

141653703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38105972-A-T

141653707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38105976-T-G

141653708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38105977-G-T

141653751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38106020-T-A

http://identifiers.org/hco/5/GRCh38#141653831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38106100-C-A

141653831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38106100-C-T

141653846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38106115-G-T

141653910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38106186-G-A

141653910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38106186-G-T

141653961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38106236-G-A

141653961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38106236-G-T

141653992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38106267-G-C

http://identifiers.org/hco/5/GRCh38#141654016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38106291-C-A

141654016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38106291-C-T

141654041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38106316-G-A

141654044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38106319-G-A

141654044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38106319-G-T

141654162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38106437-G-A

141654162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38106437-G-T

141654271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38106546-G-A

141654271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38106546-G-C

141654273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38106548-G-A

141654289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38106564-T-C

http://identifiers.org/hco/5/GRCh38#141654480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38106750-A-C

141654510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38106775-G-A

141654510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38106775-G-C

141654574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38106837-A-T

141654749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38107010-T-G

http://identifiers.org/hco/5/GRCh38#141655271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38107062-C-A

141655271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38107062-C-G

http://identifiers.org/hco/5/GRCh38#141655273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38107064-A-C

141655273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38107064-A-G

141655312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38107104-G-A

141655312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38107104-G-T

141655487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38107278-G-A

141655487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38107278-G-T

141655517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38107307-G-T

141655642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38107439-G-A

141655789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38107586-G-A

141655810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38107612-G-C

141655810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38107612-G-T

141655872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38107674-G-A

141655942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38107745-T-C

141656003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38108381-G-A

141656003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38108381-G-T

141656035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38108413-G-C

141656180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38108555-G-A

141656180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38108555-G-T

141656317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38108695-G-A

141656317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38108695-G-C

141656317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38108695-G-T

141656388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38108765-G-A

141656389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38108766-G-A

141656389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38108766-G-T

http://identifiers.org/hco/5/GRCh38#141656492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38108864-C-A

141656492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38108864-C-T

141656519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38108891-C-T

141656567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38108939-G-A

http://identifiers.org/hco/5/GRCh38#141656573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38108945-C-A

141656597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38108969-A-G

141656615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38108987-C-G

141656645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38109017-T-C

141656645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38109017-T-G

http://identifiers.org/hco/5/GRCh38#141656961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38109346-C-A

141657377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38110384-G-A

141657484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38110491-G-A

141657985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38111049-T-C

141658220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38111284-G-C

141658220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38111284-G-T

141658224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38111288-G-A

141658224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38111288-G-T

141658314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38111372-C-T

141658315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38111373-A-T

http://identifiers.org/hco/5/GRCh38#141658356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38111392-C-A

141658356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38111392-C-T

141658411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 38111447-C-T

141658483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 38111519-G-T

141658527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38111558-C-T

141658797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38111801-G-T

141658800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38111804-G-T

141659035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38112031-C-T

141659198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38112682-A-G

http://identifiers.org/hco/5/GRCh38#141659248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38112720-C-A

141659347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38112823-A-T

141659393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38112867-G-A

http://identifiers.org/hco/5/GRCh38#141659400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38112874-C-A

141659400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38112874-C-T

141659459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38112936-T-C

141659510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38112987-T-G

141659540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38113019-G-A

141659540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38113019-G-T

http://identifiers.org/hco/5/GRCh38#141659584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38113062-A-C

141659609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38113087-A-G

141659609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38113087-A-T

141659661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38113139-A-G

141659704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38113164-A-G

141659704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38113164-A-T

141659785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38113241-G-A

http://identifiers.org/hco/5/GRCh38#141659910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38113366-C-A

141659910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38113366-C-T

141659956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38113446-T-C

141659956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38113446-T-G

141659958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38113448-T-C

http://identifiers.org/hco/5/GRCh38#141660053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38113498-C-A

141660053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38113498-C-T

141660094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38113523-C-T

http://identifiers.org/hco/5/GRCh38#141661383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38114106-A-C

141661567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38114255-T-A

141661567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38114255-T-C

141661567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38114255-T-G

141661625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38114311-A-G

141661784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38114462-G-C

141661855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38114528-G-A

141662089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38115060-G-A

141662089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38115060-G-C

141662089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38115060-G-T

141662197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38115168-G-A

141662224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38115195-C-G

http://identifiers.org/hco/5/GRCh38#141662675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38115575-A-C

141662980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38115865-G-C

141663748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38116326-C-T

141663767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38116349-C-T

141664477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38116950-C-T

141664493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38116966-T-G

http://identifiers.org/hco/5/GRCh38#141664590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38117043-C-A

141664724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38117155-A-G

141664738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38117169-G-T

http://identifiers.org/hco/5/GRCh38#141664840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38117235-C-A

141664842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38117237-G-T

http://identifiers.org/hco/5/GRCh38#141664890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38117255-C-A

http://identifiers.org/hco/5/GRCh38#141664907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38117272-C-A

141664907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38117272-C-T

141665016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 38117381-A-T

http://identifiers.org/hco/5/GRCh38#141665036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#38117401-C-A

141665036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38117401-C-T

http://identifiers.org/hco/5/GRCh38#141665046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38117411-C-A

141665046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38117411-C-G

141665046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38117411-C-T

http://identifiers.org/hco/5/GRCh38#141665202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#38117561-C-A

141665254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38117604-G-A

141665254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38117604-G-C

http://identifiers.org/hco/5/GRCh38#141665441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#38117761-A-C

141665441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38117761-A-G

141665507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38117820-T-A

141665511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38117824-T-A

http://identifiers.org/hco/5/GRCh38#141665513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38117826-C-A

141665513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38117826-C-G

141665513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38117826-C-T

http://identifiers.org/hco/5/GRCh38#141665523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38117836-C-A

141665523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38117836-C-T

141665638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38117943-A-G

141665640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38117944-A-G

141666124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118073-T-C

141666152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118100-C-G

141666152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118100-C-T

141666165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118113-T-C

141666201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118149-A-T

141666253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118201-C-T

http://identifiers.org/hco/5/GRCh38#141666287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38118235-C-A

141666287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118235-C-G

141666287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118235-C-T

http://identifiers.org/hco/5/GRCh38#141666293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38118241-C-A

141666293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118241-C-T

141666359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118306-A-G

141666361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118309-G-A

141666361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118309-G-C

141666361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118309-G-T

141666381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118329-A-G

141666626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38118568-G-A

141666626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38118568-G-T

141666658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38118600-G-A

141666658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38118600-G-T

141666660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38118602-A-G

141666707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38118638-G-A

141666707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38118638-G-T

141666738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38118671-G-T

141666832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118759-G-A

141666832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118759-G-C

141666832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118759-G-T

http://identifiers.org/hco/5/GRCh38#141666854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38118802-C-A

141666854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118802-C-G

141666854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38118802-C-T

141668877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38119677-G-A

http://identifiers.org/hco/5/GRCh38#141668896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38119696-A-C

141668896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38119696-A-G

http://identifiers.org/hco/5/GRCh38#141669578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#38120504-C-A

141669578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38120504-C-T

http://identifiers.org/hco/5/GRCh38#141669601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#38120527-C-A

141669637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38120558-G-T

141669647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38120568-G-A

141669647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38120568-G-T

141669784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 38120683-G-A

141669840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38120739-G-A

141670050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38120941-A-T

141670087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38120972-G-A

141670135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38121019-A-G

141670138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38121022-T-C

141670145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38121029-T-C

141670271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38121144-T-C

141670395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38121259-T-G

http://identifiers.org/hco/5/GRCh38#141670397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38121261-C-A

141670397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38121261-C-T

141670553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38121409-C-T

141670687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38121551-C-T

http://identifiers.org/hco/5/GRCh38#141670766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38121630-C-A

141670766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38121630-C-T

141670768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38121632-G-A

141670768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38121632-G-T

http://identifiers.org/hco/5/GRCh38#141670854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38121690-C-A

141671122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38121958-A-G

141671122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38121958-A-T

http://identifiers.org/hco/5/GRCh38#141671177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38122022-A-C

141671214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38122059-T-C

141671214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38122059-T-G

141671245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38122089-G-A

141671251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38122095-C-G

141671251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38122095-C-T

141671338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38122185-A-T

141671528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38122373-T-G

http://identifiers.org/hco/5/GRCh38#141671744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38122590-A-C

141671817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38122659-T-C

141671997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38122841-G-A

141672019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38122842-G-A

141672232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38123059-G-A

141672232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38123059-G-C

141672309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38123136-G-A

141672341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38123166-T-C

141672491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38123503-T-C

141672518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38123531-C-T

141672602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38123615-C-T

141672663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38123676-T-G

141672664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38123677-G-A

141672715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38123729-C-G

141672819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38123833-C-T

141672852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38123866-G-A

141672852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38123866-G-T

141672943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38123952-G-C

141672957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38123968-G-C

141673180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38124186-T-A

141673180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38124186-T-C

141673184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38124190-T-A

http://identifiers.org/hco/5/GRCh38#141673343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38124319-C-A

http://identifiers.org/hco/5/GRCh38#141673359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38124343-C-A

141673359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38124343-C-G

141673391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38124371-A-G

http://identifiers.org/hco/5/GRCh38#141673397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38124377-C-A

141673397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38124377-C-G

http://identifiers.org/hco/5/GRCh38#141673777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38124761-C-A

141673777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38124761-C-T

141679152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38128803-G-A

141679333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38129004-A-T

http://identifiers.org/hco/5/GRCh38#141679424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38129103-A-C

141679493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38129183-G-A

141679493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38129183-G-T

141679508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38129201-G-A

141679693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38129412-G-A

141679693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38129412-G-T

141679745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38129466-G-A

141679878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38129579-A-T

141679964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 38129640-T-G

141679984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38129660-C-T

141680013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38129689-G-A

141680013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38129689-G-C

141680258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38129931-T-C

141680258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38129931-T-G

141680676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38130348-A-G

141680712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38130369-T-C

141680740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38130374-C-T

http://identifiers.org/hco/5/GRCh38#141680741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38130375-C-A

141680741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38130375-C-G

141680741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38130375-C-T

http://identifiers.org/hco/5/GRCh38#141680776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38130409-C-A

141680776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38130409-C-G

141680776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38130409-C-T

141680836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38130453-A-G

141680890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron variant
orthologous variants: 38130507-G-A

141680890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron variant
orthologous variants: 38130507-G-C

141680890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron variant
orthologous variants: 38130507-G-T

141680940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron variant
orthologous variants: 38130542-G-A

141680940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron variant
orthologous variants: 38130542-G-T

141680948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron variant
orthologous variants: 38130549-A-G

141680954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron variant
orthologous variants: 38130555-A-G

141680970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron variant
orthologous variants: 38130567-A-G

141680980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron variant
orthologous variants: 38130573-G-C

141681265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron variant
orthologous variants: 38130859-G-C

141681303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, undefined
orthologous variants: 38130898-C-G

141681303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron_variant, undefined
orthologous variants: 38130898-C-T

141681634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron variant
orthologous variants: 38131296-G-A

141682075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron variant
orthologous variants: 38131654-G-A

141682075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24097
most severe consequence: intron variant
orthologous variants: 38131654-G-T