http://identifiers.org/hco/11/GRCh38#74696466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99683898-A-C

74696483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 99683881-T-C

http://identifiers.org/hco/11/GRCh38#74696711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99683637-C-A

74696711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99683637-C-T

74696812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99683550-G-T

74696992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99683174-G-A

74697170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682980-C-T

http://identifiers.org/hco/11/GRCh38#74697173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99682977-C-A

74697173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99682977-C-G

74697173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99682977-C-T

74697178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99682972-G-A

74697178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99682972-G-C

74697178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99682972-G-T

http://identifiers.org/hco/11/GRCh38#74697361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99682812-C-A

74697361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682812-C-T

http://identifiers.org/hco/11/GRCh38#74697391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99682785-C-A

74697391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682785-C-G

74697391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682785-C-T

74697562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682652-G-A

74697562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682652-G-T

http://identifiers.org/hco/11/GRCh38#74697580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99682634-A-C

74697580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682634-A-G

74697580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682634-A-T

74697696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682537-A-T

http://identifiers.org/hco/11/GRCh38#74697719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99682518-A-C

74697739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682456-G-A

74697739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682456-G-T

74697778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682401-G-A

74697778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682401-G-T

74697784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682395-A-G

74697821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682289-G-T

http://identifiers.org/hco/11/GRCh38#74697827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99682283-A-C

74697827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99682283-A-G

74698271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99681752-A-T

74698396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99681648-T-C

74698431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99681619-A-G

74698446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99681604-A-T

74698505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99681579-C-T

74698515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99681569-T-C

74698516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99681568-G-A

74698516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99681568-G-T

http://identifiers.org/hco/11/GRCh38#74698544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/7/GRCm39#99681541-C-A

74698575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99681511-T-C

http://identifiers.org/hco/11/GRCh38#74698577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/7/GRCm39#99681509-C-A

74698609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99681432-G-A

74698625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99681342-G-C

74698625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99681342-G-T

74698687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99681230-A-G

74698775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99681060-A-G

74698826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99681014-G-A

74698832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99681008-A-G

74698984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680852-G-A

74698984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680852-G-T

http://identifiers.org/hco/11/GRCh38#74698990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99680848-C-A

74698990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680848-C-T

74698996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680842-A-G

74699093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680747-G-A

74699093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680747-G-T

74699108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680738-T-C

http://identifiers.org/hco/11/GRCh38#74699116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99680730-C-A

74699116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680730-C-T

74699191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680657-A-G

http://identifiers.org/hco/11/GRCh38#74699192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99680656-C-A

74699249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680604-T-C

74699296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680530-G-A

http://identifiers.org/hco/11/GRCh38#74699343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99680501-C-A

74699343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680501-C-T

74699351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680493-C-T

74699370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680473-G-A

74699370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680473-G-T

74699376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680467-A-G

74699395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680448-G-A

74699395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680448-G-T

74699413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680430-G-T

74699502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99680345-A-G

http://identifiers.org/hco/11/GRCh38#74699567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99680296-C-A

74699689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99680240-A-G

http://identifiers.org/hco/11/GRCh38#74699759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99680178-C-A

74699759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99680178-C-T

http://identifiers.org/hco/11/GRCh38#74699770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99680167-C-A

74699841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99680113-G-A

74699884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99680079-C-T

74699987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99679962-T-C

74700199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99679612-C-G

74700290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99679530-G-C

74700337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99679496-G-C

74700433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99679456-C-T

http://identifiers.org/hco/11/GRCh38#74700451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99679438-C-A

74700451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99679438-C-T

74700469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99679420-G-A

74700524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99679376-T-C

74700537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99679367-G-A

74702624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678710-C-T

74702637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99678697-C-T

74702654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678690-G-T

74702718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678628-G-A

74702743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678604-G-A

74702743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678604-G-T

74702759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678594-G-C

74702837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99678513-C-T

74703066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678282-A-T

74703073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678274-T-C

74703073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678274-T-G

74703119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678225-G-A

74703119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678225-G-T

http://identifiers.org/hco/11/GRCh38#74703157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99678199-C-A

74703157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678199-C-G

74703161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678195-T-C

74703161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678195-T-G

74703162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678194-G-C

74703162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678194-G-T

http://identifiers.org/hco/11/GRCh38#74703191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99678175-C-A

74703191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678175-C-T

http://identifiers.org/hco/11/GRCh38#74703205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99678159-C-A

74703205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99678159-C-T

74703400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99677956-T-C

http://identifiers.org/hco/11/GRCh38#74703584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99677770-C-A

74703849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99677533-C-G

74703909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99677483-C-T

74703917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99677475-T-G

74704011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99677415-C-G

74704011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99677415-C-T

74704193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99677263-C-T

74704344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99677049-G-A

74704344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99677049-G-T

74704394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99677003-A-G

74704710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99676729-G-A

74704775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99676670-G-T

74704780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99676664-G-A

74704780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99676664-G-T

74704794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99676614-G-C

74704794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99676614-G-T

74704799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99676609-A-G

74704960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99676418-A-G

74704986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99676404-G-T

74705176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99676272-A-G

74705317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99676087-G-A

74705352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99676051-G-T

74705428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99675974-C-T

74705449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99675953-G-A

74705563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99675850-G-A

74705601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99675805-C-T

74705970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99675525-A-G

74706124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99675362-G-C

74706124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99675362-G-T

74706362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99675149-G-T

74706371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99675140-G-T

http://identifiers.org/hco/11/GRCh38#74706409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99675084-C-A

74706426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99675059-G-T

74706524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99674969-G-A

74706555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99674938-A-G

74706619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99674898-T-C

74706619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99674898-T-G

74706672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99674846-A-G

74706813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99674719-G-T

http://identifiers.org/hco/11/GRCh38#74706919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99674621-A-C

74707117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99674469-G-A

74707131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99674455-T-C

74707432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99674227-A-G

74707662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99674033-G-C

74707742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99673963-C-T

74708187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99673311-G-T

74708266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99673195-G-A

74708266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99673195-G-T

http://identifiers.org/hco/11/GRCh38#74708391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99673061-C-A

74708391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99673061-C-T

http://identifiers.org/hco/11/GRCh38#74708400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99673052-C-A

74708400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99673052-C-T

74708505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99672943-G-A

74708505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99672943-G-T

74708510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99672938-G-T

74708512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99672936-G-T

74708538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99672923-A-G

74708645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99672844-G-A

http://identifiers.org/hco/11/GRCh38#74708998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99672474-C-A

74709087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99672389-A-T

74709119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99672357-C-T

74710695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99671433-G-A

http://identifiers.org/hco/11/GRCh38#74710709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99671419-C-A

74710716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99671412-T-C

74710716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99671412-T-G

74710721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99671407-T-C

74710729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99671400-G-A

74710729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99671400-G-T

74710747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99671392-T-C

74710769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99671383-C-G

74710769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99671383-C-T

http://identifiers.org/hco/11/GRCh38#74710840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99671322-A-C

74710841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99671321-G-T

74711000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 99671164-G-A

74713211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99670357-T-C

74713286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99670288-G-A

74713286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99670288-G-C

74713286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99670288-G-T

74713307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99670271-G-T

74713344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99670234-G-A

74713344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99670234-G-T

74713361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99670209-G-A

74713361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99670209-G-T

74713492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99670080-C-T

74713498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99670074-T-G

http://identifiers.org/hco/11/GRCh38#74713591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99669983-C-A

74713591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99669983-C-G

74713591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99669983-C-T

74713599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99669971-T-A

74713752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99669815-G-A

74713803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99669763-T-C

74714052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99669519-G-A

74714517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99669072-C-T

74714545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99669041-C-T

74714682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99668906-C-T

74714716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99668884-G-A

74714892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99668771-G-A

74715166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99668538-T-G

74717311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99667731-G-A

74717342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99667693-G-C

74717734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99667322-T-C

74718138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99666837-G-A

74718299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99666569-G-A

74718350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99666515-G-T

http://identifiers.org/hco/11/GRCh38#74718647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99666356-C-A

74718701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99666315-G-T

74718709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99666307-G-C

74718709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99666307-G-T

74719013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99666093-T-A

74719013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99666093-T-C

74719057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99666056-G-C

http://identifiers.org/hco/11/GRCh38#74719119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99666012-C-A

74719119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99666012-C-G

74719119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99666012-C-T

74719140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99665989-G-A

74719140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99665989-G-C

74719140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99665989-G-T

74719142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99665987-G-A

74719142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99665987-G-T

74719158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99665971-A-T

74719185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99665939-T-A

74719185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99665939-T-C

http://identifiers.org/hco/11/GRCh38#74719243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99665882-C-A

http://identifiers.org/hco/11/GRCh38#74719343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99665839-C-A

74719356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99665826-T-A

74719356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99665826-T-C

74719383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99665798-C-T

http://identifiers.org/hco/11/GRCh38#74719409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99665772-C-A

74719409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99665772-C-T

74719417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99665764-C-T

74719697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99665272-C-T

74719746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99665217-A-G

74720158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99664695-A-G

74720338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99664505-G-A

74720376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99664468-T-A

74720376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99664468-T-C

http://identifiers.org/hco/11/GRCh38#74720460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99664389-C-A

74720460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99664389-C-G

74720485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99664376-A-G

74720495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99664366-C-T

74720507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99664349-T-C

http://identifiers.org/hco/11/GRCh38#74720653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99664217-C-A

74720806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99664098-G-A

74720806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99664098-G-C

74720826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99664078-C-T

74721568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99663373-A-G

74721784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99663166-T-G

74722148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99662852-G-A

74722216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99662801-C-T

74722290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99662653-C-T

74722298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99662645-C-T

74722412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99662449-T-C

http://identifiers.org/hco/11/GRCh38#74722419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99662442-C-A

74722820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99662059-A-G

74722910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99661970-G-A

74722971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99661911-G-A

http://identifiers.org/hco/11/GRCh38#74723219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99661691-A-C

74723219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99661691-A-G

74723227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99661683-G-A

74723230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99661680-C-T

74724447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99660860-G-A

http://identifiers.org/hco/11/GRCh38#74724535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99660768-C-A

74724535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99660768-C-T

74724573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99660734-C-T

74724612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99660711-T-A

74724702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99660628-G-A

74724785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99660541-G-A

74725672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99659991-C-G

74725672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99659991-C-T

74725956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99659767-C-G

74725991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99659732-G-A

http://identifiers.org/hco/11/GRCh38#74726052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99659691-C-A

74726387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99659374-A-G

http://identifiers.org/hco/11/GRCh38#74726392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99659369-C-A

74726430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99659333-T-C

74726560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99659208-C-T

74726561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99659207-G-A

74726957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99658811-T-C

74727034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99658743-A-G

74727240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99658570-C-G

74727241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99658569-A-G

74727262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99658548-T-C

74727324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99658487-T-G

74727787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99658334-C-G

74728856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99657543-C-T

74729021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99657393-G-C

74729061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99657361-T-A

74729061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99657361-T-C

74730092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99656469-G-A

74730166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99656396-T-A

74730526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99656110-T-G

http://identifiers.org/hco/11/GRCh38#74730810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99655849-C-A

74730810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99655849-C-T

74730827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99655832-A-G

74730985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99655695-G-A

74730985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99655695-G-T

74731015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99655665-T-G

http://identifiers.org/hco/11/GRCh38#74731049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99655641-A-C

74731049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99655641-A-G

74731076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99655617-T-C

74731076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99655617-T-G

74731089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99655604-A-G

74731092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99655601-G-A

74731092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99655601-G-T

74731102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99655591-A-G

74731122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99655571-A-G

74731126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99655567-G-T

http://identifiers.org/hco/11/GRCh38#74731144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99655549-C-A

http://identifiers.org/hco/11/GRCh38#74731148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99655545-C-A

74731148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99655545-C-G

74731148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99655545-C-T

74731160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5 prime UTR variant
orthologous variants: 99655533-G-A

74731160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5 prime UTR variant
orthologous variants: 99655533-G-T

74731183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5 prime UTR variant
orthologous variants: 99655510-G-T

74731206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5 prime UTR variant
orthologous variants: 99655473-G-T

http://identifiers.org/hco/11/GRCh38#74731257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99655424-A-C

74731257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5 prime UTR variant
orthologous variants: 99655424-A-G

74731257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5 prime UTR variant
orthologous variants: 99655424-A-T

http://identifiers.org/hco/11/GRCh38#74731262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99655419-C-A

74731262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5 prime UTR variant
orthologous variants: 99655419-C-G

74731262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5 prime UTR variant
orthologous variants: 99655419-C-T

74731288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5 prime UTR variant
orthologous variants: 99655390-G-T

74731378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5 prime UTR variant
orthologous variants: 99655320-G-A

74731418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24168
most severe consequence: 5 prime UTR variant
orthologous variants: 99655292-C-T