http://identifiers.org/hco/12/GRCh38#123762292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124802166-C-A

123762292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5 prime UTR variant
orthologous variants: 124802166-C-T

123762306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5 prime UTR variant
orthologous variants: 124802180-G-T

123762312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5 prime UTR variant
orthologous variants: 124802186-G-A

123762327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5 prime UTR variant
orthologous variants: 124802201-G-A

123762327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5 prime UTR variant
orthologous variants: 124802201-G-T

123762373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124802264-G-A

123762373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124802264-G-T

123762381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124802272-G-A

123762381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124802272-G-T

http://identifiers.org/hco/12/GRCh38#123762395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124802286-C-A

123762395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124802286-C-G

123762395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124802286-C-T

123762397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124802288-G-A

123762397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124802288-G-T

http://identifiers.org/hco/12/GRCh38#123762444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124802335-C-A

123762444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124802335-C-T

123762483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124802374-G-A

123762483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124802374-G-T

123762498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 124802389-G-A

123762498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 124802389-G-C

123762498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 124802389-G-T

123764365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124802954-T-A

123767193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124803562-C-T

123767199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124803568-C-T

123767320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124803634-G-A

123767477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124803769-C-G

123767477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124803769-C-T

123767628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 124803911-A-T

123767718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124803990-G-A

123767751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124804013-A-G

123767755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124804017-T-C

123767756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124804018-G-A

http://identifiers.org/hco/12/GRCh38#123767760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124804021-C-A

123768032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124804205-T-C

123772849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 124807131-A-G

123772899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124807181-G-A

123772971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124807253-T-C

123772986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124807265-T-C

123772987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124807266-G-C

123773008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124807293-C-G

123773008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124807293-C-T

123774107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124808413-T-A

123774168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124808474-C-G

123774168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124808474-C-T

123774234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124808540-G-A

123774234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124808540-G-C

123774234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124808540-G-T

123774272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 124808578-T-A

123774272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 124808578-T-G

123781153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124809431-C-T

123781158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124809436-T-C

123781232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124809513-G-A

123781302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124809583-A-G

123781393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124809705-G-T

http://identifiers.org/hco/12/GRCh38#123781431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124809753-C-A

123781431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124809753-C-T

123782954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124811384-G-C

123782957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124811387-T-C

123782957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124811387-T-G

123782976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124811398-G-T

123783015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124811432-T-C

123783045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124811462-T-C

123783087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124811496-G-A

123783151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124811555-G-A

123783151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124811555-G-T

123783169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124811573-G-C

http://identifiers.org/hco/12/GRCh38#123783304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124811710-C-A

123783675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124813628-T-A

123783733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124813675-A-G

http://identifiers.org/hco/12/GRCh38#123783826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124813766-C-A

123783826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124813766-C-G

123783826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124813766-C-T

123783834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124813776-A-G

http://identifiers.org/hco/12/GRCh38#123783835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124813777-C-A

123783835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124813777-C-T

123783970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124813890-T-G

123784021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124813941-A-T

123784111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124814031-A-G

123784196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124814116-A-G

123784231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124814147-G-T

123784232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124814148-A-G

http://identifiers.org/hco/12/GRCh38#123785647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124818872-A-C

123785647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124818872-A-G

123785669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124818894-G-A

123785669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124818894-G-C

123785669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124818894-G-T

http://identifiers.org/hco/12/GRCh38#123785700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124818901-C-A

123785700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124818901-C-T

123785757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124818963-C-T

123785769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124818975-C-T

http://identifiers.org/hco/12/GRCh38#123785772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124818978-C-A

123785772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124818978-C-G

123785772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124818978-C-T

123785793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124818999-C-T

http://identifiers.org/hco/12/GRCh38#123785808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124819014-C-A

123785808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124819014-C-T

123786117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124819269-C-T

123786633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124819774-T-C

123786638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124819779-T-C

123786638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124819779-T-G

123786677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124819807-G-A

123786688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124819818-C-T

http://identifiers.org/hco/12/GRCh38#123786691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124819821-A-C

123786691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124819821-A-G

123786691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124819821-A-T

123787750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124820526-G-A

123787750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124820526-G-T

123787768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124820559-G-A

http://identifiers.org/hco/12/GRCh38#123788068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124820867-C-A

123788068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124820867-C-G

123789766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124823459-T-C

http://identifiers.org/hco/12/GRCh38#123789785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124823478-C-A

123789785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124823478-C-T

http://identifiers.org/hco/12/GRCh38#123789798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124823491-C-A

123789798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124823491-C-T

123789821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124823515-A-G

123789882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124823558-G-A

http://identifiers.org/hco/12/GRCh38#123790034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124823714-C-A

123790034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124823714-C-T

123790133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124823813-G-A

123794055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124824780-T-C

123794140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124824869-G-A

123794140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124824869-G-C

123796706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124825505-G-A

123796718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124825517-C-T

http://identifiers.org/hco/12/GRCh38#123796724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124825523-A-C

123796749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 124825548-C-T

123796751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124825550-A-G

123796775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124825574-T-C

123799204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124827783-A-G

123799204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124827783-A-T

123799239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 124827818-T-C

123799239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 124827818-T-G

123799375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124827954-C-T

http://identifiers.org/hco/12/GRCh38#123799390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124827964-C-A

123799390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124827964-C-G

123799390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124827964-C-T

123800053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124830081-G-A

123800088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124830115-A-G

123800089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124830116-G-A

123800127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124830155-T-C

123800134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124830162-T-C

123800285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124830301-G-A

123800285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124830301-G-C

123800285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124830301-G-T

123800290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124830306-C-G

123801356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124831346-G-A

http://identifiers.org/hco/12/GRCh38#123801389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124831379-A-C

123803580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124832646-T-G

123803611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124832677-G-T

123803624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124832690-G-A

123803624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124832690-G-T

http://identifiers.org/hco/12/GRCh38#123803656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124832713-C-A

123803698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124832755-T-G

123803807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124832864-A-G

123803842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124832899-G-T

123804783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124835259-T-C

http://identifiers.org/hco/12/GRCh38#123804972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124835450-C-A

123804972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124835450-C-T

http://identifiers.org/hco/12/GRCh38#123805113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124835591-A-C

123805113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124835591-A-G

123805146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124835624-G-A

123805146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124835624-G-T

123808654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124836971-C-T

123808696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124837002-T-A

123808696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124837002-T-C

http://identifiers.org/hco/12/GRCh38#123808878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124837162-C-A

123808899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, start_lost, synonymous_variant
orthologous variants: 124837183-T-C

123808899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: 124837183-T-G

123813129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124837912-A-T

123813138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124837921-T-C

123813356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124838144-C-T

123813421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124838209-T-G

123813517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124838305-A-G

http://identifiers.org/hco/12/GRCh38#123813544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124838332-A-C

123813544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124838332-A-G

123813646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124838434-C-G

123813646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124838434-C-T

123813792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124839229-T-G

123813906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124839343-C-T

http://identifiers.org/hco/12/GRCh38#123818811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124839666-C-A

123818811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124839666-C-T

123818922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124839747-T-C

123818960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124839822-C-T

123819024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124839886-T-C

123819033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124839895-T-A

123819089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124839995-T-C

123819177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124840129-A-T

123819204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124840156-T-C

123819204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124840156-T-G

123819306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124840240-T-C

123820559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124841831-A-G

123820559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124841831-A-T

123820565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124841837-G-A

123820565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124841837-G-T

http://identifiers.org/hco/12/GRCh38#123820770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124842043-C-A

123820770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124842043-C-T

123826881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124842762-C-T

123826891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124842772-A-G

123830121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124845508-T-C

123830238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124845600-T-C

123830372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124845691-G-A

http://identifiers.org/hco/12/GRCh38#123830499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124845807-C-A

123830499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124845807-C-T

123830573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124845887-G-A

123831298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124846537-G-A

http://identifiers.org/hco/12/GRCh38#123833037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124847422-A-C

123833085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124847469-T-A

123833085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124847469-T-C

http://identifiers.org/hco/12/GRCh38#123833094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124847478-C-A

123833266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124847650-A-G

123833332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124847716-A-T

123833441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124847789-G-A

123833441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124847789-G-C

123833441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124847789-G-T

123833450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124847797-T-C

123833535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124847895-G-T

123833666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124848001-A-T

123834178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124848337-G-A

123834364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124848778-T-C

123834374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124848788-G-A

123834630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124849092-T-C

http://identifiers.org/hco/12/GRCh38#123834934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124849369-A-C

123834939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124849374-G-A

123835049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124849496-G-T

123835058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124849505-A-G

123835162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124849601-C-T

123835172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124849612-T-C

123835236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124849926-T-G

123835273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124849964-T-C

http://identifiers.org/hco/12/GRCh38#123835278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124849969-C-A

123835278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124849969-C-T

123835338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124850032-G-A

123835338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124850032-G-T

123835383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124850073-A-G

http://identifiers.org/hco/12/GRCh38#123835530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124850218-C-A

123835530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: 124850218-C-G

http://identifiers.org/hco/12/GRCh38#123838380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124850363-C-A

123838380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124850363-C-G

123838380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124850363-C-T

123838433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124850413-G-A

123838444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124850425-G-A

123838629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 124850610-T-A

http://identifiers.org/hco/12/GRCh38#123838659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124850640-C-A

123838659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 124850640-C-G

http://identifiers.org/hco/12/GRCh38#123838699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124850680-C-A

123841354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124850836-T-C

123841378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124850860-G-T

123841384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124850866-C-G

123841384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124850866-C-T

http://identifiers.org/hco/12/GRCh38#123841396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124850878-A-C

123841396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124850878-A-G

123841420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 124850902-T-G

123841554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124851036-G-T

123841558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124851040-A-G

123841570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124851052-A-G

123845501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124851930-T-C

123845521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124851950-A-T

123845591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124852031-T-C

123845591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124852031-T-G

123845636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124852076-G-C

123845648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124852088-C-T

123845765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124852205-G-A

123846061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124852499-G-A

123846076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124852514-C-T

123846140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 124852578-C-G

123846140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124852578-C-T

123846190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124852605-C-T

123846209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124852624-C-T

123846814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124853006-C-G

123847076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124853249-C-T

123847123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124853313-C-T

123847454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124853770-G-A

123847454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124853770-G-T

http://identifiers.org/hco/12/GRCh38#123847827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124854109-C-A

123847827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124854109-C-G

123847827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124854109-C-T

123847863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124854139-T-G

http://identifiers.org/hco/12/GRCh38#123847872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124854148-C-A

123847872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124854148-C-T

123847897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124854172-G-T

http://identifiers.org/hco/12/GRCh38#123847934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124854196-A-C

123847934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124854196-A-G

123847976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 124854238-C-G

123848125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124854387-G-A

123848125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124854387-G-T

123848126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124854388-C-T

http://identifiers.org/hco/12/GRCh38#123848135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124854397-C-A

123848141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124854403-G-T

http://identifiers.org/hco/12/GRCh38#123848216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124854434-C-A

123848216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124854434-C-G

123848408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124854575-G-A

123848618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124854786-G-T

123848795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124854946-T-C

123848801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124854952-C-T

123848855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124855006-T-C

123850879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124856139-G-A

123851070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 124856330-G-T

123851080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124856348-G-A

123851080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124856348-G-T

123851084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 124856352-G-A

123851084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 124856352-G-C

http://identifiers.org/hco/12/GRCh38#123853092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124859216-C-A

123853092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124859216-C-T

http://identifiers.org/hco/12/GRCh38#123853095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124859219-C-A

123853123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124859261-T-C

123853131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124859269-G-T

123853143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124859278-T-C

http://identifiers.org/hco/12/GRCh38#123853195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124859321-C-A

123853195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124859321-C-T

123853322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 124859448-G-A

123853337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 124859463-C-G

123853337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 124859463-C-T

123853396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124859514-A-G

http://identifiers.org/hco/12/GRCh38#123857076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124860912-C-A

123857184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124861020-T-C

123859129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 124862191-C-T

http://identifiers.org/hco/12/GRCh38#123859186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124862248-A-C

http://identifiers.org/hco/12/GRCh38#123859194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124862256-C-A

123859194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 124862256-C-G

123859233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124862295-C-G

123859233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 124862295-C-T

http://identifiers.org/hco/12/GRCh38#123859279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124862339-C-A

123859279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124862339-C-G

123859284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124862344-G-A

123859284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124862344-G-T

123859285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124862345-T-C

123859330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124862391-G-A

123860182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124863078-T-G

123860939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124864310-T-C

123860939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124864310-T-G

123860964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124864331-C-T

123860965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124864332-A-G

123860993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 124864360-A-G

123860993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 124864360-A-T

123861196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124864565-A-G

123861196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124864565-A-T

123864558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124866778-C-G

123864607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 124866838-T-C

123864607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 124866838-T-G

123864649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 124866880-T-A

123864707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 124866938-G-C

123864749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124866980-T-A

123864753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124866984-T-A

123864859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124867078-A-G

123865014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124867346-A-G

123865068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124867419-C-T

123865821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124868596-A-G

http://identifiers.org/hco/12/GRCh38#123865822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124868597-A-C

123865822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124868597-A-G

123865822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124868597-A-T

http://identifiers.org/hco/12/GRCh38#123865887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124868656-C-A

123865887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124868656-C-G

123865887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124868656-C-T

123865931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124868696-G-A

123865931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124868696-G-T

123866150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124868910-T-C

123866928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124869446-G-C

123866928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124869446-G-T

123867354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124870775-T-C

123867365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 124870781-A-T

123867388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 124870804-T-C

123867388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 124870804-T-G

123867496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 124870906-T-A

123867505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 124870915-T-C

123867541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 124870951-T-A

123867677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124871074-G-A

123867848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124871240-G-A

http://identifiers.org/hco/12/GRCh38#123867899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124871286-C-A

123867932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 124871319-G-A

123868001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 124871388-T-C

123868102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 124871489-A-G

123868128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124871515-C-T

http://identifiers.org/hco/12/GRCh38#123868181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124871538-A-C

123868181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124871538-A-T

123868182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124871539-G-A

123868182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124871539-G-T

123868189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124871546-A-G

123868230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124871579-T-C

123868270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124871604-C-T

123868365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124871695-C-G

123868365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124871695-C-T

123869923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124872968-C-T

123869974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124873020-G-A

123869974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124873020-G-T

123869990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124873035-C-G

123870035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124873080-G-A

123870164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124873181-T-C

123870176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124873183-G-A

123870222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124873208-T-C

123870311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124873247-G-T

http://identifiers.org/hco/12/GRCh38#123870344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124873279-A-C

123870408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 124873347-G-A

123870545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124873487-G-T

123870657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124873565-C-T

123870775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124873675-C-T

123870859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124873758-G-A

123871368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124874893-T-G

123871479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 124874992-G-A

123871479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 124874992-G-T

123871617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124875130-A-G

123871637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124875150-T-A

http://identifiers.org/hco/12/GRCh38#123871723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124875231-C-A

123871810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124875313-G-A

123873626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 124876022-T-C

123873641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 124876037-C-G

123873731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124876127-G-A

123873733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124876129-G-A

123873733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124876129-G-T

123873741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124876137-G-T

123873795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124876268-A-G

123873837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124876339-A-T

http://identifiers.org/hco/12/GRCh38#123873857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124876370-C-A

123873900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124876427-C-T

123874203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124876691-T-C

123874434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124876988-T-G

123874498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124877068-C-T

123874618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124877193-T-C

123875019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124877678-G-T

123875100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124877742-A-G

123875440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 124878070-A-G

123875532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124878136-G-A

123875532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124878136-G-T

123875585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124878186-T-G

http://identifiers.org/hco/12/GRCh38#123875593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124878194-C-A

123877667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124878727-C-T

123877846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 124878887-C-T

http://identifiers.org/hco/12/GRCh38#123877905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124878946-A-C

123877905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 124878946-A-G

123877922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124878970-A-G

123878242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124879795-C-T

123878972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124880137-A-G

123878976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124880141-G-A

123879127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124880264-A-G

http://identifiers.org/hco/12/GRCh38#123879130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124880267-C-A

123879130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124880267-C-G

http://identifiers.org/hco/12/GRCh38#123879232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124880354-C-A

http://identifiers.org/hco/12/GRCh38#123879267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124880375-C-A

123879267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 124880375-C-G

123879267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 124880375-C-T

http://identifiers.org/hco/12/GRCh38#123879294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124880402-C-A

123879354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 124880462-G-C

123879354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 124880462-G-T

123879592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124880833-C-G

123879592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124880833-C-T

123879605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124880849-T-C

123879609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124880853-T-A

123879620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124880864-G-A

123879620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124880864-G-C

123879640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 124880884-C-T

123879662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 124880906-T-C

123879783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 124881027-G-A

123879798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 124881042-C-G

123880200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124881545-A-G

123880212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124881556-G-T

123880241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124881593-T-C

123880242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124881594-A-G

123880246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 124881598-A-G

http://identifiers.org/hco/12/GRCh38#123881738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124881809-C-A

123881738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 124881809-C-T

http://identifiers.org/hco/12/GRCh38#123881762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124881833-C-A

123881762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 124881833-C-T

123881765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 124881836-A-G

123881780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 124881851-T-C

123881783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 124881854-G-A

123881783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 124881854-G-C

123881783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 124881854-G-T

123881792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 124881863-T-C

123887216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124882876-A-G

123887236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124882896-C-T

123887258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124882918-T-C

123887261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124882921-C-T

123893360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 124885846-T-C

123893490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124885970-G-T

123893493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124885973-G-A

123893493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124885973-G-T

123893549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124886015-A-G

123893632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124886091-T-C

123894843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124886473-A-G

123894858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124886488-G-A

123894859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124886489-T-C

123894872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124886502-G-T

123894885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124886513-T-A

123894885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124886513-T-C

123895109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124886659-A-T

123895465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124886913-G-A

123895472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124886920-G-A

123895497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124886943-C-G

123895497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124886943-C-T

123895572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124887040-T-C

123895679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124887148-A-G

123896242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124887310-T-G

123896497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124887483-G-A

123896895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124887867-T-C

123896922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, undefined
orthologous variants: 124887894-G-A

123897255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, undefined
orthologous variants: 124888213-A-G

123897368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124888317-G-T

123897760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124888503-T-G

123897764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 124888507-C-T

123897789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124888532-G-A

123897789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124888532-G-T

123897924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124888667-C-T

http://identifiers.org/hco/12/GRCh38#123898547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124889526-A-C

123898578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124889546-G-A

123898578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124889546-G-T

123898637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124889609-T-G

http://identifiers.org/hco/12/GRCh38#123898641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124889613-C-A

http://identifiers.org/hco/12/GRCh38#123898747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124889719-C-A

123898747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124889719-C-G

123898747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124889719-C-T

http://identifiers.org/hco/12/GRCh38#123902804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124890762-C-A

123902804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124890762-C-T

123902809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124890767-T-C

123902809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124890767-T-G

123902822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124890780-T-C

123902881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124890836-G-A

123902881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124890836-G-T

123902900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124890847-T-C

123902901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124890848-G-A

123902930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124890877-A-G

http://identifiers.org/hco/12/GRCh38#123902933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124890880-C-A

123902933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 124890880-C-T

http://identifiers.org/hco/12/GRCh38#123903024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124890971-C-A

123903024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124890971-C-T

http://identifiers.org/hco/12/GRCh38#123903063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124891010-C-A

123903063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124891010-C-T

123903096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124891043-G-A

123903096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124891043-G-C

123903096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124891043-G-T

123909090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124891471-C-T

123909091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124891472-G-A

http://identifiers.org/hco/12/GRCh38#123909135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124891501-C-A

123909135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124891501-C-G

123909135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124891501-C-T

123909147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124891513-G-A

123909147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124891513-G-T

123909186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124891548-T-C

123909240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124891594-C-T

http://identifiers.org/hco/12/GRCh38#123909339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124891692-C-A

123909339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124891692-C-G

http://identifiers.org/hco/12/GRCh38#123909547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124891844-C-A

123909547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124891844-C-T

http://identifiers.org/hco/12/GRCh38#123909611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124891879-C-A

123909701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124891953-C-T

123909702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124891954-G-A

123910488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124893034-C-G

123910514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124893050-A-G

123910522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124893058-A-G

123910552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124893087-T-C

123910635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: 124893170-G-A

123910747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124893257-T-C

123913103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124894251-C-G

123913247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124894395-C-T

123913266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124894414-C-T

http://identifiers.org/hco/12/GRCh38#123913311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124894459-A-C

123914380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124894675-G-A

123914380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124894675-G-T

123914425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124894720-C-T

123914608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124894888-G-A

123914608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124894888-G-T

123914634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124894912-T-A

123914634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124894912-T-C

123914635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124894913-G-A

123914635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124894913-G-T

123914802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124895000-G-A

123914802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124895000-G-T

http://identifiers.org/hco/12/GRCh38#123914831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124895032-C-A

123914831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124895032-C-T

123914876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124895077-C-G

123914876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124895077-C-T

123914906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124895107-C-T

123915140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124895252-C-T

123915401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124895450-T-C

123915905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124895910-G-A

http://identifiers.org/hco/12/GRCh38#123916361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124896142-C-A

123916361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124896142-C-T

http://identifiers.org/hco/12/GRCh38#123916570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124896308-C-A

123916570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124896308-C-T

123916839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124896561-A-G

http://identifiers.org/hco/12/GRCh38#123916847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124896564-C-A

123916847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124896564-C-T

123917040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124896600-T-C

123917453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124896814-G-C

123917453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124896814-G-T

123917571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124896882-C-T

123917747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124897057-G-A

123917747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124897057-G-C

123917747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: synonymous variant
orthologous variants: 124897057-G-T

123917820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 124897130-A-G

123917845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124897144-A-G

123917960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124897876-G-T

http://identifiers.org/hco/12/GRCh38#123918017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124897915-C-A

123918017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124897915-C-G

123918017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124897915-C-T

123918105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron variant
orthologous variants: 124898005-A-G

123918699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124898310-G-A

123918735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124898346-T-C

123918735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124898346-T-G

123918750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124898361-A-G

123918759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 124898370-G-A

123918759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124898370-G-C

123918759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124898370-G-T

123918828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 124898439-T-G

123923465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124899663-T-C

http://identifiers.org/hco/12/GRCh38#123923475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124899674-C-A

123923484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124899678-T-C

http://identifiers.org/hco/12/GRCh38#123923650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124899813-C-A

123923650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124899813-C-T

123923737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124899890-A-G

123923751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124899904-G-T

123923758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 124899911-T-C

123923773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124899926-G-A

123923845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124899998-A-G

http://identifiers.org/hco/12/GRCh38#123923848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124900001-A-C

123923937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124900087-G-A

123923937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124900087-G-T

http://identifiers.org/hco/12/GRCh38#123924125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124900214-C-A

123924125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124900214-C-G

123924125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124900214-C-T

http://identifiers.org/hco/12/GRCh38#123924141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124900223-C-A

http://identifiers.org/hco/12/GRCh38#123924157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124900239-C-A

123924157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124900239-C-G

http://identifiers.org/hco/12/GRCh38#123924257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124900339-C-A

123924257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124900339-C-T

123924516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124900592-A-G

123924576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124900640-T-C

123924691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124901188-G-A

123924691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124901188-G-T

123925070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124901518-G-A

123925169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124901617-C-T

123926410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124903700-G-A

123926410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124903700-G-T

123926419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124903731-G-T

http://identifiers.org/hco/12/GRCh38#123926598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124903896-C-A

123926602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124903899-G-A

123926606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124903902-G-A

123927727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124904452-C-G

123927727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124904452-C-T

http://identifiers.org/hco/12/GRCh38#123928035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124904745-C-A

123928098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124904794-G-A

123928098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124904794-G-T

123928115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124904811-T-C

http://identifiers.org/hco/12/GRCh38#123928138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124904836-C-A

123928138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124904836-C-T

123928165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124904858-T-C

123928238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124904921-G-A

123928238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124904921-G-C

123928238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124904921-G-T

123928381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 124905039-G-A

123928381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 124905039-G-T

123928604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124905298-G-A

123928604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124905298-G-T

http://identifiers.org/hco/12/GRCh38#123928632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124905326-C-A

http://identifiers.org/hco/12/GRCh38#123929261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124905485-C-A

123929261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124905485-C-G

123929261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124905485-C-T

123929265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124905489-T-C

http://identifiers.org/hco/12/GRCh38#123929645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124905820-C-A

123929645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124905820-C-G

123929645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124905820-C-T

123929696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124905869-G-A

123929747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124905920-C-T

123929961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124906114-G-A

123930065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124906227-T-C

http://identifiers.org/hco/12/GRCh38#123930155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124906373-C-A

123930242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124906452-A-G

123930249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124906477-G-T

http://identifiers.org/hco/12/GRCh38#123930287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124906515-C-A

123930287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124906515-C-T

http://identifiers.org/hco/12/GRCh38#123930293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124906521-C-A

123930293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124906521-C-T

123930381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124906568-T-C

http://identifiers.org/hco/12/GRCh38#123930425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124906612-C-A

123930425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124906612-C-G

123930425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124906612-C-T

123930437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124906624-T-G

123930467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124906654-G-A

123930467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124906654-G-C

123930517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124906704-G-A

123930517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124906704-G-C

123930697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124906869-T-C

123930809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124906932-A-G

123930835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124906958-G-A

123930835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124906958-G-T

123931480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 124907230-C-T

123931586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124907333-G-A

123931603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124907359-C-T

123931724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124907479-G-C

123931729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124907484-A-G

http://identifiers.org/hco/12/GRCh38#123932201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124907925-C-A

123932201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124907925-C-T

http://identifiers.org/hco/12/GRCh38#123932287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124908005-C-A

123932635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124908335-T-A

123932695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124908389-G-A

123932760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124908451-G-T

123933213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124909426-A-G

123933213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 124909426-A-T

http://identifiers.org/hco/12/GRCh38#123933342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124909525-C-A

123933342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124909525-C-T

123933427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124909610-G-A

123933504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124909687-G-A

123933552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124909731-G-A

http://identifiers.org/hco/12/GRCh38#123933557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124909736-C-A

123933557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124909736-C-G

123933557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124909736-C-T

123933586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124909765-G-T

http://identifiers.org/hco/12/GRCh38#123933636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124909796-C-A

123933640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124909800-T-C

123933659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124909805-T-C

123934065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 124910065-G-A

123934065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 124910065-G-T

123934103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910101-G-A

123934103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910101-G-C

123934103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910101-G-T

123934366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910284-G-A

123934458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910366-T-A

123934479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910386-A-G

123934511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910391-G-A

123934511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910391-G-T

123934524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910404-A-T

123934539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910422-G-A

123934539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910422-G-C

123934539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910422-G-T

123934571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910455-G-A

123934589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910464-A-G

123934741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910609-T-C

http://identifiers.org/hco/12/GRCh38#123934802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124910662-C-A

123934865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910678-G-C

123934865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910678-G-T

123934887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910686-T-C

123934890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910689-G-T

123934975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124910770-T-C

123934999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124910794-T-C

http://identifiers.org/hco/12/GRCh38#123935220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124910936-C-A

123935220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124910936-C-G

123935261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124910975-T-G

123935291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124910999-C-T

http://identifiers.org/hco/12/GRCh38#123935311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#124911019-A-C

123935311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 124911019-A-T

123935328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 124911036-C-G

123935328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 124911036-C-T

123935403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 124911111-T-C

123935484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2941
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 124911192-T-C