55466647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57723151-C-G

55467766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57723587-G-A

55467885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57723693-C-T

55468924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57727663-T-C

55469420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57728189-C-T

55469439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57728209-C-T

55469490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57728248-A-G

55469515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57728273-T-A

55469912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57728686-A-G

http://identifiers.org/hco/7/GRCh38#55470588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57729210-C-A

55470588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57729210-C-T

http://identifiers.org/hco/7/GRCh38#55470595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57729231-C-A

http://identifiers.org/hco/7/GRCh38#55470814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57729448-C-A

55471445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57730170-G-A

http://identifiers.org/hco/7/GRCh38#55471785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57730511-C-A

55471786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57730512-T-A

55471873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57730628-A-G

http://identifiers.org/hco/7/GRCh38#55471889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57730644-C-A

55471889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57730644-C-T

http://identifiers.org/hco/7/GRCh38#55471928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57730684-C-A

55471953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57730709-G-T

http://identifiers.org/hco/7/GRCh38#55471978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57730728-C-A

55471991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57730741-G-T

55472117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57730836-T-C

55472294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57731010-A-G

55472301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57731017-G-A

http://identifiers.org/hco/7/GRCh38#55472460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57731128-C-A

55472460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57731128-C-T

55472517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57731151-C-T

55472723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57731353-G-A

55472723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57731353-G-T

55472939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57731555-G-A

http://identifiers.org/hco/7/GRCh38#55472965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57731581-C-A

55472965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57731581-C-T

55473023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57731639-G-A

http://identifiers.org/hco/7/GRCh38#55473193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57731804-C-A

55473193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57731804-C-G

55473193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57731804-C-T

http://identifiers.org/hco/7/GRCh38#55477417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57732200-A-C

55477417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57732200-A-G

55477913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57732633-G-C

55478398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57733047-C-T

55490579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57736713-G-C

55490583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57736717-C-T

55490670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57736780-T-C

55491041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57737104-A-G

55491086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57737133-G-A

55491174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57737206-T-C

55491200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57737227-C-T

http://identifiers.org/hco/7/GRCh38#55491248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57737278-C-A

55491452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57737671-G-C

55491478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57737697-A-G

55491706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57737974-G-A

55492096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739250-G-A

55492157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739308-A-G

55492157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739308-A-T

http://identifiers.org/hco/7/GRCh38#55492190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57739338-C-A

55492210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739353-G-T

55492275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57739413-G-A

55492363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57739501-T-C

55492379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57739517-G-A

http://identifiers.org/hco/7/GRCh38#55492481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57739620-C-A

55492481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739620-C-T

55492505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739643-T-C

http://identifiers.org/hco/7/GRCh38#55492506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57739644-C-A

55492506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739644-C-G

55492506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739644-C-T

http://identifiers.org/hco/7/GRCh38#55492513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57739651-C-A

55492513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739651-C-T

http://identifiers.org/hco/7/GRCh38#55492514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57739652-C-A

55492514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739652-C-G

55492514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739652-C-T

55492554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739705-G-T

http://identifiers.org/hco/7/GRCh38#55492561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57739712-C-A

55492561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739712-C-T

http://identifiers.org/hco/7/GRCh38#55492710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57739864-A-C

55492710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739864-A-G

55492710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739864-A-T

55492734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57739884-G-A

http://identifiers.org/hco/7/GRCh38#55492852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57739977-C-A

http://identifiers.org/hco/7/GRCh38#55492911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57740035-C-A

55493266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57740295-C-G

55493327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57740339-A-G

http://identifiers.org/hco/7/GRCh38#55493341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57740354-C-A

55493341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57740354-C-T

55493389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57740380-A-G

55493470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57740465-G-A

55493591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57740584-T-G

55497045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57751236-C-T

http://identifiers.org/hco/7/GRCh38#55497054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57751245-C-A

55497065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57751260-G-A

55497133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57751348-G-T

55497147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57751383-C-T

55497604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57751687-G-C

55497604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57751687-G-T

http://identifiers.org/hco/7/GRCh38#55497609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57751692-C-A

55497609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57751692-C-G

55497639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57751722-G-A

55497639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57751722-G-C

55497639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57751722-G-T

55497647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57751730-G-A

55498087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57752007-G-A

55498249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57752171-G-A

http://identifiers.org/hco/7/GRCh38#55498358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57752249-A-C

55498368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57752259-G-A

55498427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57752323-T-C

55500037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57752549-A-G

55500037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57752549-A-T

55500284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57752728-C-G

http://identifiers.org/hco/7/GRCh38#55500688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57753117-C-A

55500768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57753161-T-C

55500768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57753161-T-G

55501201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57754182-A-G

55501247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57754238-T-A

55501329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57754330-A-G

55501351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57754410-C-T

http://identifiers.org/hco/7/GRCh38#55501355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57754414-C-A

http://identifiers.org/hco/7/GRCh38#55501368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57754427-C-A

55501368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57754427-C-T

55501417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57754882-A-G

55501608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57755064-A-G

55501657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57755112-T-C

55501931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57755335-T-A

55501967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57755367-T-C

55502045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57755452-A-T

55502101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57755508-C-G

55502262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57755696-T-C

55502614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57756053-C-G

55502759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57756173-C-T

55502790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57756204-G-A

55502869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57756279-G-A

55502945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57756349-C-T

55503195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57756576-T-C

55503214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57756595-G-A

55503517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57756888-G-A

55503638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57757185-G-A

55503967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57757489-T-C

55504993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57758704-T-C

55505389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57759065-G-A

55505460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57759148-C-T

http://identifiers.org/hco/7/GRCh38#55505708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57759311-A-C

55505708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57759311-A-G

55505819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57759416-T-C

55505889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57759489-A-G

http://identifiers.org/hco/7/GRCh38#55506075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57759655-C-A

55506322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57759887-C-T

55513389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57762813-T-C

55513389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57762813-T-G

55513448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57762865-C-T

55513763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57763115-T-C

http://identifiers.org/hco/7/GRCh38#55521242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57767134-A-C

55521242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57767134-A-G

55521254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57767144-G-A

55521254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57767144-G-T

55521275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57767168-G-T

55521425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57767414-G-C

55521474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57767460-A-T

55521499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57767485-G-A

http://identifiers.org/hco/7/GRCh38#55521516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57767502-C-A

55521516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57767502-C-T

55521520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57767506-T-A

55521520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57767506-T-C

55521520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57767506-T-G

55521549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57767536-T-C

55530203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57774492-T-C

55530209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57774498-T-C

55530209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57774498-T-G

55530667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57774968-T-C

55530740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57775039-G-T

55530742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57775041-C-T

http://identifiers.org/hco/7/GRCh38#55530766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57775066-C-A

55530766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57775066-C-T

http://identifiers.org/hco/7/GRCh38#55530773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57775073-C-A

55530773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57775073-C-T

http://identifiers.org/hco/7/GRCh38#55546761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57782280-C-A

55546891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57782396-A-G

55546954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57782462-G-A

55547053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57782536-T-A

55547053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57782536-T-C

55547108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57782590-A-G

55547167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57782663-G-A

55547217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57782716-G-A

http://identifiers.org/hco/7/GRCh38#55547412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57782896-C-A

55547671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57783561-T-C

http://identifiers.org/hco/7/GRCh38#55547704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57783595-A-C

55547711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57783602-T-C

55547760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57783651-C-T

55548730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57783825-T-C

http://identifiers.org/hco/7/GRCh38#55548979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57784081-C-A

55549026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57784128-G-A

55549152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57784259-T-C

55549228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57784289-A-T

55549245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57784307-A-G

55549278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57784340-G-A

55549630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57784429-G-A

55549693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57784491-G-A

55549693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57784491-G-C

55549980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57784728-G-T

55550014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57784760-C-T

55550210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57784956-C-T

55550218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57784964-C-T

55550219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57784965-G-A

http://identifiers.org/hco/7/GRCh38#55564777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57788909-C-A

55564777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57788909-C-G

55564781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57788913-G-C

55564875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57789030-G-A

55567218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57789610-C-G

55567599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57790073-C-T

55567708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57790170-T-G

55567754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57790232-T-C

55567920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57790370-C-T

55567923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57790373-G-C

55568006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57790458-C-T

55568635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57791064-T-C

55568768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57791164-G-A

55568768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57791164-G-C

55568768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57791164-G-T

55568943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57791291-T-C

55568943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57791291-T-G

55569206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57791573-T-C

55569288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57791649-A-G

55569296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57791656-G-A

55569317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57791666-C-G

55569402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57791768-A-G

http://identifiers.org/hco/7/GRCh38#55569492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57791855-C-A

55569492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57791855-C-T

55569751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57792088-G-A

http://identifiers.org/hco/7/GRCh38#55569992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57792321-C-A

55569992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57792321-C-T

http://identifiers.org/hco/7/GRCh38#55570043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57792371-A-C

55571335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57801226-A-G

55571478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57801377-T-A

http://identifiers.org/hco/7/GRCh38#55571615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57801520-C-A

55571615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57801520-C-T

55571620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57801525-G-A

55571620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57801525-G-C

http://identifiers.org/hco/7/GRCh38#55571660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57801555-C-A

55571671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57801566-C-G

55571671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57801566-C-T

55571675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57801569-C-G

55571830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57801665-T-C

55571952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57801693-G-A

55571952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57801693-G-T

55572204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57801870-T-C

55572204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57801870-T-G

55572375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57802007-T-C

55572643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57802231-G-A

55572643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57802231-G-T

http://identifiers.org/hco/7/GRCh38#55572692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57802249-C-A

http://identifiers.org/hco/7/GRCh38#55572723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57802280-A-C

55572760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57802313-G-A

55572760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57802313-G-T

55572779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34518
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57802320-G-A