http://identifiers.org/hco/14/GRCh38#104085760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112073311-C-A

104085760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112073311-C-T

http://identifiers.org/hco/14/GRCh38#104085795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112073350-C-A

104085795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112073350-C-T

104085815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112073370-C-T

http://identifiers.org/hco/14/GRCh38#104085881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112073442-C-A

104085881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112073442-C-T

104085892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112073453-G-A

104085892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112073453-G-T

104088133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112075260-G-A

104088252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112075373-C-T

104088579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112075648-G-A

http://identifiers.org/hco/14/GRCh38#104088591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112075660-C-A

104092391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112078355-G-A

104092578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112078554-G-A

104092583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112078559-C-T

http://identifiers.org/hco/14/GRCh38#104092599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112078586-C-A

http://identifiers.org/hco/14/GRCh38#104092664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112078657-C-A

104092669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112078662-G-A

104092669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112078662-G-T

http://identifiers.org/hco/14/GRCh38#104092679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112078672-C-A

104092679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112078672-C-T

http://identifiers.org/hco/14/GRCh38#104092703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112078696-C-A

104092703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112078696-C-T

http://identifiers.org/hco/14/GRCh38#104092766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112078759-C-A

104092766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078759-C-G

104092766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078759-C-T

104092788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078799-G-A

104092788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078799-G-T

http://identifiers.org/hco/14/GRCh38#104092805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112078818-C-A

104092809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078822-G-T

http://identifiers.org/hco/14/GRCh38#104092815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112078828-C-A

104092815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078828-C-T

104092840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078857-G-C

104092840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078857-G-T

104092849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078867-T-A

104092849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078867-T-C

104092850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078868-G-A

104092850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078868-G-T

http://identifiers.org/hco/14/GRCh38#104092856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112078874-A-C

104092903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078906-T-C

104092917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078919-A-G

104092917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078919-A-T

http://identifiers.org/hco/14/GRCh38#104092931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112078927-C-A

104092931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078927-C-T

http://identifiers.org/hco/14/GRCh38#104092983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112078986-A-C

104092983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112078986-A-G

104093133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112079116-T-C

104093133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112079116-T-G

http://identifiers.org/hco/14/GRCh38#104093162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112079144-A-C

104093162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112079144-A-G

104093162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112079144-A-T

http://identifiers.org/hco/14/GRCh38#104093164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112079146-C-A

104093164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112079146-C-G

104093164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112079146-C-T

104093192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112079187-G-A

104093192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112079187-G-T

http://identifiers.org/hco/14/GRCh38#104093198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112079193-A-C

http://identifiers.org/hco/14/GRCh38#104093269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112079239-A-C

104093269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112079239-A-G

104093269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112079239-A-T

http://identifiers.org/hco/14/GRCh38#104093276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112079246-C-A

104093276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112079246-C-T

104093290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112079259-T-C

104093290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112079259-T-G

104093407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112079348-A-G

http://identifiers.org/hco/14/GRCh38#104093408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112079349-C-A

104093415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112079356-G-A

104093415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112079356-G-T

104093499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112079423-G-A

104093500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112079424-C-T

104093688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112079573-G-A

104093688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112079573-G-C

104093688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112079573-G-T

104093949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112079679-G-C

104094820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112080348-T-G

104094928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112080429-T-G

104094929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112080430-G-A

104094929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112080430-G-C

http://identifiers.org/hco/14/GRCh38#104095442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112080691-C-A

104095442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112080691-C-G

http://identifiers.org/hco/14/GRCh38#104095492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112080756-C-A

104095492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112080756-C-T

http://identifiers.org/hco/14/GRCh38#104095514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112080792-A-C

104095514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112080792-A-G

104095623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112080906-C-T

104095676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112080947-G-C

104095676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112080947-G-T

http://identifiers.org/hco/14/GRCh38#104095758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112081013-C-A

104095758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112081013-C-G

104095758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112081013-C-T

104095861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112081148-G-A

104095861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112081148-G-T

104096047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112081335-A-G

104096137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112081402-C-T

http://identifiers.org/hco/14/GRCh38#104096139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112081404-C-A

104097172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112081695-C-T

104097405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112081895-T-C

http://identifiers.org/hco/14/GRCh38#104097407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112081897-C-A

104097407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112081897-C-T

104097426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112081911-G-A

104097426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112081911-G-T

http://identifiers.org/hco/14/GRCh38#104097468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112081922-C-A

104097468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112081922-C-T

http://identifiers.org/hco/14/GRCh38#104097520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112081967-C-A

104097520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112081967-C-T

104097565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112082012-T-C

104097653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112082102-A-G

104097661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112082110-G-A

104097661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112082110-G-T

104097675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112082122-G-C

104097679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112082126-G-A

104097679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112082126-G-T

104099956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112083636-G-A

104100016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112083693-G-T

104100722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112083888-G-A

104100722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112083888-G-C

104100996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112084111-T-A

104101291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112084376-A-G

104101665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112084728-G-A

104101891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112084919-G-A

104102462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112085434-G-A

104102600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112085539-C-G

104102989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112085866-G-A

104103145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086009-G-A

104103182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086040-C-T

104103309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086173-G-A

104103309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086173-G-C

104103415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086267-A-G

104103425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086273-G-A

104103425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086273-G-T

104103430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086275-G-T

104103503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086336-G-A

104103506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086339-G-T

http://identifiers.org/hco/14/GRCh38#104103633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112086458-C-A

104103633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112086458-C-T

104103660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112086485-G-C

104103660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112086485-G-T

104103666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112086491-T-C

104103667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112086492-G-T

http://identifiers.org/hco/14/GRCh38#104103723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112086536-C-A

104103723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086536-C-T

104103746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086567-A-G

104103758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086579-G-A

104103758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086579-G-C

104103758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086579-G-T

http://identifiers.org/hco/14/GRCh38#104103769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112086595-C-A

104103769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086595-C-T

http://identifiers.org/hco/14/GRCh38#104103770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112086596-C-A

104103770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086596-C-T

http://identifiers.org/hco/14/GRCh38#104103800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112086630-C-A

104103800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086630-C-G

104103800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086630-C-T

http://identifiers.org/hco/14/GRCh38#104103812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112086645-C-A

104103812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086645-C-T

104103848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086689-G-A

104103889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112086746-C-T

104104055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112087000-C-T

http://identifiers.org/hco/14/GRCh38#104104288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112087289-C-A

104104288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112087289-C-G

104104288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112087289-C-T

104104337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112087332-G-A

104104354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112087349-C-T

http://identifiers.org/hco/14/GRCh38#104104550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112087526-C-A

104104553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112087529-T-A

104104564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112087537-T-C

104104564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112087537-T-G

104104575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112087548-G-A

104104575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112087548-G-C

104104575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112087548-G-T

104104611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112087575-C-T

http://identifiers.org/hco/14/GRCh38#104104648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112087613-A-C

104104648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112087613-A-G

http://identifiers.org/hco/14/GRCh38#104104654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112087619-C-A

104104654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112087619-C-G

104104654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112087619-C-T

104104672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112087637-C-T

104104690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112087655-G-A

104104690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112087655-G-C

104104716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112087681-G-A

104104716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112087681-G-T

104104754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112087719-T-A

104104754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112087719-T-C

104104860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112087791-G-A

104104860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112087791-G-T

http://identifiers.org/hco/14/GRCh38#104105129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112087990-C-A

http://identifiers.org/hco/14/GRCh38#104105175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112088048-C-A

http://identifiers.org/hco/14/GRCh38#104105212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112088089-C-A

104105212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112088089-C-G

104105212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112088089-C-T

104105325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112088181-C-G

104105325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112088181-C-T

104105404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112088251-C-T

104105420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112088267-C-G

104105420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112088267-C-T

104105460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112088308-T-C

104105461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112088309-G-T

104105503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112088339-T-C

104105665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112088471-G-A

104105787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112088639-C-G

104105985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112088760-G-A

104106084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112088805-G-A

104106108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112088828-C-T

104106277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112088929-C-T

104106587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112089192-G-A

104106587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112089192-G-T

104106742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112089298-G-A

104106742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112089298-G-T

104106891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112089470-G-T

104106936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112089503-T-C

104107009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112089566-G-C

104107009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112089566-G-T

http://identifiers.org/hco/14/GRCh38#104107020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112089577-C-A

104107020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112089577-C-T

http://identifiers.org/hco/14/GRCh38#104107037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112089594-C-A

104107066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112089615-G-A

104107066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112089615-G-C

104107066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112089615-G-T

104107134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112089677-C-T

http://identifiers.org/hco/14/GRCh38#104107149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112089692-C-A

104107149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112089692-C-T

104107254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: missense variant
orthologous variants: 112089796-G-C

http://identifiers.org/hco/14/GRCh38#104107313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112089855-C-A

104107313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: synonymous variant
orthologous variants: 112089855-C-T

http://identifiers.org/hco/14/GRCh38#104107326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112089868-C-A

104107357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: 112089900-A-G

104107376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: 112089911-T-C

http://identifiers.org/hco/14/GRCh38#104108682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112090806-C-A

104108682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: 112090806-C-T

http://identifiers.org/hco/14/GRCh38#104108796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112090943-C-A

104108796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant
orthologous variants: 112090943-C-T

104108954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: 112091026-G-A

104108961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: 112091033-C-T

104109151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: 112091167-G-A

104109151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: 112091167-G-T

104109159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: 112091175-G-T

http://identifiers.org/hco/14/GRCh38#104109332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112091344-C-A

104109332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: 112091344-C-G

104109332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: 112091344-C-T

104109440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: 112091413-T-C

104109473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: 112091447-A-G

104109517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: 112091476-T-C

104110452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 112091916-T-G

104110561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 112092012-T-C

104110753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 112092139-C-T

104110880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 112092217-G-C

104110977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 112092316-G-A

104110977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 112092316-G-T

104110988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 112092324-T-A

104111258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron variant
orthologous variants: 112092498-T-C

104111532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 112092776-G-A

104111532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 112092776-G-C

104111532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 112092776-G-T

104111685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112092895-T-C

104111685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112092895-T-G

http://identifiers.org/hco/14/GRCh38#104111689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112092899-C-A

http://identifiers.org/hco/14/GRCh38#104111708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112092918-C-A

104111708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112092918-C-T

104111815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112093006-G-A

104111815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112093006-G-T

104111856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112093043-G-T

104111912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 112093088-C-T

http://identifiers.org/hco/14/GRCh38#104112019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112093188-C-A

104112019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112093188-C-T

104112026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112093195-G-A

104112026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112093195-G-C

http://identifiers.org/hco/14/GRCh38#104112124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112093296-C-A

104112156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112093323-T-C

http://identifiers.org/hco/14/GRCh38#104112366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112093457-C-A

104112366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112093457-C-T

http://identifiers.org/hco/14/GRCh38#104112481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112093566-C-A

104112481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112093566-C-T

http://identifiers.org/hco/14/GRCh38#104112541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112093610-C-A

104112572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112093638-C-T

104112623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112093829-G-T

http://identifiers.org/hco/14/GRCh38#104112647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112093935-C-A

http://identifiers.org/hco/14/GRCh38#104112724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112093998-C-A

104112764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094034-T-C

http://identifiers.org/hco/14/GRCh38#104112913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112094183-C-A

104112913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094183-C-G

104112913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094183-C-T

104112931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094196-T-A

104112931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094196-T-C

http://identifiers.org/hco/14/GRCh38#104112975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112094225-C-A

http://identifiers.org/hco/14/GRCh38#104112978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112094228-A-C

104112978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094228-A-G

104112978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094228-A-T

104113007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094242-A-G

http://identifiers.org/hco/14/GRCh38#104113011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112094246-C-A

104113011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094246-C-T

http://identifiers.org/hco/14/GRCh38#104113136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112094357-C-A

104113136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094357-C-T

104113144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094365-A-G

http://identifiers.org/hco/14/GRCh38#104113154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112094375-C-A

http://identifiers.org/hco/14/GRCh38#104113183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112094397-C-A

104113183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094397-C-G

104113183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094397-C-T

104113252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094468-C-T

http://identifiers.org/hco/14/GRCh38#104113282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112094492-A-C

104113282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094492-A-G

104113282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094492-A-T

104113286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094496-A-G

104113621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094635-G-A

104113774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094848-T-C

104113794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094868-G-A

http://identifiers.org/hco/14/GRCh38#104113796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112094870-C-A

104113796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094870-C-T

http://identifiers.org/hco/14/GRCh38#104113852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112094928-C-A

104113853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094929-A-G

104113869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094939-G-A

http://identifiers.org/hco/14/GRCh38#104113890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112094957-C-A

http://identifiers.org/hco/14/GRCh38#104113898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112094970-C-A

104113898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112094970-C-T

104113950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112095019-A-G

104114093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112095094-G-A

104114093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112095094-G-T

104114225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112095206-C-T

http://identifiers.org/hco/14/GRCh38#104114287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112095244-C-A

http://identifiers.org/hco/14/GRCh38#104114317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112095257-C-A

104114373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112095287-G-A

104114373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112095287-G-T

http://identifiers.org/hco/14/GRCh38#104114572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112095428-C-A

104114572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112095428-C-T

104114582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112095438-G-T

104114622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112095482-A-G

104114622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112095482-A-T

104115071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112095747-T-C

104115173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20123
most severe consequence: 3 prime UTR variant
orthologous variants: 112095842-C-T