34851931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113927063-C-G

34852000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113927134-T-C

34852012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113927146-T-A

34852012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113927146-T-C

34852516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113927232-T-C

http://identifiers.org/hco/15/GRCh38#34852660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113927383-C-A

34852753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113927475-A-G

34852913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113927603-G-T

http://identifiers.org/hco/15/GRCh38#34852952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113927639-A-C

34853181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113927851-T-C

34853187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113927857-G-A

34853187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113927857-G-T

34853211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113927893-C-T

34853277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113927962-T-C

34853306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113927995-G-T

34853339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113928029-G-A

34853361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113928050-C-T

34853362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113928051-A-G

34853440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113928154-T-C

34853546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113928246-A-T

http://identifiers.org/hco/15/GRCh38#34853576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#113928275-C-A

34853604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113928303-T-C

http://identifiers.org/hco/15/GRCh38#34853665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113928369-C-A

34853767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113928479-G-C

http://identifiers.org/hco/15/GRCh38#34853793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113928491-C-A

34853793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113928491-C-T

34853939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113928684-T-A

34853983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113928719-C-T

http://identifiers.org/hco/15/GRCh38#34854032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113928764-C-A

34854173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113928913-A-T

34854174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113928914-G-A

34854174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113928914-G-T

http://identifiers.org/hco/15/GRCh38#34854369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113929081-C-A

http://identifiers.org/hco/15/GRCh38#34854402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113929113-C-A

34854402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113929113-C-G

34854402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113929113-C-T

34854431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113929142-A-G

34854479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113929192-C-T

34854533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113929232-A-T

http://identifiers.org/hco/15/GRCh38#34854592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113929313-C-A

http://identifiers.org/hco/15/GRCh38#34854630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113929348-A-C

34854642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113929365-T-G

34854696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113929409-C-T

34854969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113929710-G-A

34854969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113929710-G-T

34855074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113929812-C-T

34855126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113929854-T-C

http://identifiers.org/hco/15/GRCh38#34855129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113929857-C-A

34855294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113929970-T-C

http://identifiers.org/hco/15/GRCh38#34855358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113930019-C-A

34855412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930073-G-C

34855475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930127-G-A

34855475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930127-G-C

34855475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930127-G-T

34855481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930133-A-G

34855481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930133-A-T

34855491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 113930138-T-C

34855522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930165-A-T

34855524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930167-C-T

34855675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930304-A-G

34855810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930421-A-G

34855815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930426-G-T

http://identifiers.org/hco/15/GRCh38#34855857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113930467-C-A

34856001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930566-T-A

34856001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930566-T-C

34856008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930573-G-T

34856013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930578-A-G

34856055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930598-T-C

34856078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930622-G-A

34856078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930622-G-T

34856206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113930705-T-A

34856274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113931135-T-C

34856293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113931154-T-A

34856350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113931202-G-C

34856350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3 prime UTR variant
orthologous variants: 113931202-G-T

34856392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 113931244-C-T

http://identifiers.org/hco/15/GRCh38#34856407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113931259-C-A

34856430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 113931282-G-A

34856515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 113931660-G-T

34856520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 113931665-T-G

34856521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 113931666-G-A

34856521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 113931666-G-T

34856535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 113931680-T-G

http://identifiers.org/hco/15/GRCh38#34856553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113931698-C-A

34856674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 113931804-T-C

34856706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 113931835-T-A

http://identifiers.org/hco/15/GRCh38#34856709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113931838-C-A

34856709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 113931838-C-G

34856709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 113931838-C-T

34856714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 113931846-G-A

34856714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 113931846-G-C

34856714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 113931846-G-T

34856798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113931926-G-A

34856798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113931926-G-C

34856798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113931926-G-T

http://identifiers.org/hco/15/GRCh38#34856953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113932057-A-C

34856953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113932057-A-G

34857130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113932234-G-A

34857130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113932234-G-C

34857130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113932234-G-T

34857187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113932314-A-G

34857428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113932513-T-C

34858559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113932856-A-T

34858567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113932866-G-A

34858755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113933005-G-A

34858803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113933025-T-A

34858888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113933113-A-G

34859087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113933310-T-C

34859414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113933530-T-C

34859584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113933776-T-C

34859617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113933809-T-C

34859715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113934185-A-T

34859726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113934196-G-C

34859727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113934197-G-T

34859955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113934424-G-C

34859956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113934425-G-T

http://identifiers.org/hco/15/GRCh38#34860008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113934470-C-A

34860210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113934654-A-G

34860221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113934665-T-A

34860249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113934688-G-C

34860249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113934688-G-T

34860253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113934692-A-T

34860826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113935107-T-C

34861038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113935301-A-T

34861089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113935347-A-G

34861090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113935348-T-A

34861090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113935348-T-G

http://identifiers.org/hco/15/GRCh38#34861134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113935393-A-C

http://identifiers.org/hco/15/GRCh38#34862721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113936158-C-A

34862762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113936196-T-C

34862762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113936196-T-G

http://identifiers.org/hco/15/GRCh38#34862777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113936200-A-C

http://identifiers.org/hco/15/GRCh38#34862788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113936208-C-A

http://identifiers.org/hco/15/GRCh38#34862798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113936218-C-A

34862798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113936218-C-G

34862803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113936223-A-G

34862812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113936232-T-C

http://identifiers.org/hco/15/GRCh38#34862836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113936254-C-A

34862836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113936254-C-T

34863062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113936472-A-G

34863105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113936512-T-C

34863136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113936545-T-A

34863136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113936545-T-G

34863235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113936633-T-C

http://identifiers.org/hco/15/GRCh38#34863277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113936684-C-A

34863291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113936698-A-G

34863322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113936727-G-T

34866403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113937470-T-C

34866408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113937475-A-G

34866463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113937515-A-G

34866595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113937674-G-A

34866734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113937775-G-C

34866768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113937810-T-A

34867060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113938114-G-A

34867180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113938231-A-G

34867189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113938240-T-G

34867405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113938462-A-G

34867501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113938562-T-C

34867501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113938562-T-G

34867510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113938571-T-A

34867510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113938571-T-C

34867520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113938581-G-A

34867526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 113938587-C-T

34867538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113938599-T-G

34867553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113938614-C-T

34867632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113938690-A-G

34867649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113938707-G-T

34867844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113938866-C-T

34868032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113938990-G-A

34868032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113938990-G-C

34868032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113938990-G-T

http://identifiers.org/hco/15/GRCh38#34868040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113938998-C-A

http://identifiers.org/hco/15/GRCh38#34868622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113939256-C-A

34868622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113939256-C-T

34868632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113939266-G-T

34868635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113939269-C-T

34868872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113939476-T-C

34868916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113939519-T-C

34869078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113939666-T-C

http://identifiers.org/hco/15/GRCh38#34870682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113940272-C-A

34870682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113940272-C-T

http://identifiers.org/hco/15/GRCh38#34870705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113940319-C-A

http://identifiers.org/hco/15/GRCh38#34870752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113940365-C-A

34870752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 113940365-C-G

34870752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 113940365-C-T

34870946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113940559-T-A

34870946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113940559-T-C

34870966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113940579-T-C

34870976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113940589-A-G

34870986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113940595-T-A

34870986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113940595-T-C

34871012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113940617-T-C

34871106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113940700-G-C

34871539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113940786-T-A

34871618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113940865-A-G

34871661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113940905-C-G

34871661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113940905-C-T

34871929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113941140-G-A

34871930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113941141-T-A

34871930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113941141-T-C

34871943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113941154-T-A

34871943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113941154-T-C

34872211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113941656-T-C

34872390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113941830-G-T

34872398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113941838-A-G

34872680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942096-G-A

34872777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942144-C-T

34873482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942649-C-T

34873645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942780-T-C

34873646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942781-T-C

34873665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942797-C-T

http://identifiers.org/hco/15/GRCh38#34873680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113942812-A-C

34873685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942817-G-A

34873685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942817-G-T

34873699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942831-A-G

http://identifiers.org/hco/15/GRCh38#34873704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113942836-C-A

34873704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942836-C-G

34873704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942836-C-T

34873710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942838-G-A

34873710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942838-G-T

http://identifiers.org/hco/15/GRCh38#34873783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113942917-C-A

34873811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942946-T-C

34873818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113942953-T-C

34873821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 113942956-T-A

34873821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 113942956-T-C

34873903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 113943038-C-T

http://identifiers.org/hco/15/GRCh38#34874164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113943291-C-A

34874164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943291-C-T

http://identifiers.org/hco/15/GRCh38#34874223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113943348-C-A

34874223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943348-C-T

34874224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943349-T-A

34874386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943501-T-C

34874438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943536-A-G

34874457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943549-G-A

34874486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943569-T-C

34874497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943580-A-G

34874497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943580-A-T

34874500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943583-T-A

34874582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943633-A-T

http://identifiers.org/hco/15/GRCh38#34874586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113943637-C-A

34874586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943637-C-G

34874586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943637-C-T

34874596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943647-A-G

34874596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943647-A-T

34874637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 113943674-G-C

34874817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 113943840-G-A

34874817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 113943840-G-C

34874920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113943951-T-A

34874920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113943951-T-C

34875077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944100-G-A

34875206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944189-G-C

34875220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944203-T-C

34875271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944251-A-G

34875429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944412-A-G

34875495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944477-A-G

34875509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944491-T-C

34875509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944491-T-G

34875567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944556-T-C

34875575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944564-G-A

34875576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944565-T-C

http://identifiers.org/hco/15/GRCh38#34875796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113944949-A-C

34875798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944951-T-C

34875824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944973-G-T

34875835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944984-A-T

http://identifiers.org/hco/15/GRCh38#34875837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113944986-C-A

34875837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944986-C-G

34875837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944986-C-T

34875842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944991-G-A

34875842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944991-G-T

http://identifiers.org/hco/15/GRCh38#34875848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113944997-A-C

34875848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113944997-A-G

http://identifiers.org/hco/15/GRCh38#34875878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113945018-C-A

34875878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113945018-C-T

http://identifiers.org/hco/15/GRCh38#34875882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113945022-C-A

34875882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113945022-C-T

34875924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113945050-A-G

34875931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113945057-T-C

34876024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113945148-T-C

34876030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113945154-T-C

34876035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113945158-A-G

34876047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113945170-T-G

http://identifiers.org/hco/15/GRCh38#34876055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113945178-C-A

34876055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113945178-C-G

34876572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113945540-A-G

34876586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113945554-T-G

http://identifiers.org/hco/15/GRCh38#34876647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113945611-C-A

34881198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946138-G-A

34881229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946171-G-C

34881281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946220-G-A

34881281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946220-G-C

34881419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946354-C-T

34881436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946365-C-T

34881455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946382-T-C

34881509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946434-A-G

34881726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946613-T-A

34882356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946830-G-T

34882362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946835-T-C

http://identifiers.org/hco/15/GRCh38#34882424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113946897-A-C

http://identifiers.org/hco/15/GRCh38#34882436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113946910-A-C

34882436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946910-A-G

34882437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946911-T-A

34882437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946911-T-C

34882486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946963-T-A

34882486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113946963-T-C

34882495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 113946997-T-A

34882495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 113946997-T-C

34882643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 113947145-T-C

34882643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 113947145-T-G

http://identifiers.org/hco/15/GRCh38#34882698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113947196-C-A

34882799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113947389-T-C

34883080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113947668-T-A

34883180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113947762-T-G

34883198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113947779-G-A

34883615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113948250-T-C

http://identifiers.org/hco/15/GRCh38#34883650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113948281-C-A

http://identifiers.org/hco/15/GRCh38#34883664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113948295-C-A

34883664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113948295-C-T

34883775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113948384-T-G

34883932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113948506-T-C

34884173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113948705-G-A

34884398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113949009-T-A

34884398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113949009-T-C

34884398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113949009-T-G

34884495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113949128-G-A

34884495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113949128-G-C

34885717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113949469-T-A

34886184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113949904-T-C

34886251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113949973-G-C

34886251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113949973-G-T

34886336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113950184-T-A

34886381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113950252-T-C

34886381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113950252-T-G

34886443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113950313-G-A

34886443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113950313-G-T

34886445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113950315-A-T

34886446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113950316-G-T

http://identifiers.org/hco/15/GRCh38#34886458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113950328-C-A

34886458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113950328-C-T

http://identifiers.org/hco/15/GRCh38#34886464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113950334-C-A

34886494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113950361-G-T

34886640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 113950505-A-T

http://identifiers.org/hco/15/GRCh38#34886737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113950610-A-C

http://identifiers.org/hco/15/GRCh38#34886768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113950653-A-C

34886768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113950653-A-G

34886817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113950729-C-T

34887534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951056-G-C

34889183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951138-T-C

34889233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951187-G-C

34889234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951188-C-T

34889251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951204-C-T

34889373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951316-G-A

34889400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951345-T-C

34889536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951445-T-C

34889556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951465-G-A

34889576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951485-C-T

34890039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951511-T-C

34890188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951659-C-T

34890198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951669-C-T

34890462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951969-T-C

34890463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113951970-T-A

34890602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113952104-A-G

34890633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113952135-T-C

34890648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113952150-C-T

34890767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113953284-T-C

34890768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113953285-G-C

34890939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113953450-C-G

34891089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113953627-C-G

34891089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113953627-C-T

34891933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113954349-T-C

34891935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113954351-T-C

34892308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113956205-T-C

34892365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113956262-A-G

34893638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113956347-C-G

34893638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113956347-C-T

34893641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113956350-A-G

34893784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113956492-G-A

34893834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113956530-G-A

34893834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113956530-G-C

34893906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113956589-G-A

34893906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113956589-G-T

34893912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113956595-A-G

34894043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113956659-T-C

34896997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113957538-C-T

34897010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113957552-C-T

http://identifiers.org/hco/15/GRCh38#34897109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113957651-C-A

34897109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113957651-C-T

34897302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113957806-C-T

34897609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 113958044-C-T

http://identifiers.org/hco/15/GRCh38#34897699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113958134-A-C

34897723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113958158-C-G

34897777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113958701-A-G

34897803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113958723-A-G

34897938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113958841-T-A

34900445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113960844-G-A

34900445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113960844-G-T

http://identifiers.org/hco/15/GRCh38#34900580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113960972-C-A

34900580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113960972-C-G

34900580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113960972-C-T

34900630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 113961024-G-C

34900630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 113961024-G-T

34900699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 113961093-C-G

34900699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 113961093-C-T

34900714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 113961108-T-A

34900714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 113961108-T-G

34900889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113961283-T-C

34900914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113961307-T-A

34900914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113961307-T-C

34900985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113961379-T-C

34901316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113961668-G-A

http://identifiers.org/hco/15/GRCh38#34901619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113961967-C-A

34901619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113961967-C-G

34901619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113961967-C-T

34901975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113962127-C-G

34902028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113962182-T-C

34902056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113962207-A-G

34902341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113962461-C-T

34902774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113962840-T-C

http://identifiers.org/hco/15/GRCh38#34904328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113963440-C-A

34904328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 113963440-C-T

34904414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 113963526-A-G

34904564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113963687-G-C

34904596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113963719-T-A

34904648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113963767-A-G

34905346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113964627-T-C

34906387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113965018-G-A

34906387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113965018-G-T

http://identifiers.org/hco/15/GRCh38#34906400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113965031-C-A

34906400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113965031-C-T

34906494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113965095-G-T

http://identifiers.org/hco/15/GRCh38#34907018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113965607-A-C

34907293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113965856-A-G

34909254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113966465-T-C

http://identifiers.org/hco/15/GRCh38#34909275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113966486-A-C

34909276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113966487-A-G

34909470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113966750-A-G

34909543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113966823-C-T

http://identifiers.org/hco/15/GRCh38#34909557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113966837-C-A

34909557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113966837-C-G

34909557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113966837-C-T

http://identifiers.org/hco/15/GRCh38#34909564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113966844-A-C

34909804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967039-G-A

http://identifiers.org/hco/15/GRCh38#34909858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113967101-C-A

34909899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967141-T-G

34909930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967156-G-C

34909995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967217-A-G

34910027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967244-A-T

34910067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967279-G-A

34910103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967320-A-T

34910320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 113967537-C-T

34910330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967547-G-A

34910330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967547-G-T

34911117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967665-T-C

34911156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967696-T-C

34911156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967696-T-G

http://identifiers.org/hco/15/GRCh38#34911168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113967701-C-A

34911168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967701-C-T

34911322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967857-G-A

34911416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113967939-A-G

34911525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113968021-A-T

http://identifiers.org/hco/15/GRCh38#34911695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113968186-A-C

34911697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113968187-T-C

34911771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113968224-C-T

34911791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113968244-T-A

34911820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113968279-C-G

34912233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113968847-C-G

34912233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113968847-C-T

34912245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113968859-A-G

34912260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113968871-C-T

34912290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113968895-T-A

34912310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113968915-T-C

34912319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113968924-T-C

34912418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113968986-G-T

34912661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113969204-T-A

34912686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113969216-C-T

34912944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113969458-G-T

34912964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113969471-T-C

34912964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113969471-T-G

34912994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113969500-G-A

34913042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113969545-G-A

34913237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113969731-T-A

34913243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113969736-T-C

34913410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113969867-A-G

34913970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113970455-T-C

34914008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113970492-T-C

34914074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113970542-G-C

34914086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113970554-A-T

34914100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113970569-C-T

34914315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113970752-C-T

34914413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113970848-G-A

34914617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113970994-G-A

34914651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113971013-T-C

34914790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113971128-C-G

34914790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113971128-C-T

34914827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113971165-T-C

34914845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113971184-T-C

34914873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113971212-T-G

34914904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113971239-G-T

http://identifiers.org/hco/15/GRCh38#34914975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113971288-C-A

34914975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113971288-C-G

http://identifiers.org/hco/15/GRCh38#34915142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113971454-C-A

34915142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113971454-C-T

34915175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 113971487-A-T

34916297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113972121-G-A

34916401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113972205-T-C

http://identifiers.org/hco/15/GRCh38#34918116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113973330-C-A

34918116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113973330-C-G

34918120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113973334-T-A

34918120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113973334-T-C

34918156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113973365-T-C

34918156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113973365-T-G

34918157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113973366-G-A

34918157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113973366-G-T

http://identifiers.org/hco/15/GRCh38#34918177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113973386-C-A

34918177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113973386-C-G

34918339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113973550-A-G

34918376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 113973587-T-C

34918422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113973664-T-C

34918422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113973664-T-G

34918692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113973915-T-C

34918808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113974046-T-C

34918864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113974103-C-T

http://identifiers.org/hco/15/GRCh38#34920119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113975882-A-C

34920125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113975888-T-C

34920198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113975979-A-G

34920523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113976291-A-G

http://identifiers.org/hco/15/GRCh38#34920562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113976357-C-A

34920564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113976359-G-A

http://identifiers.org/hco/15/GRCh38#34926808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113977177-C-A

34926808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113977177-C-T

34926889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113977260-A-T

http://identifiers.org/hco/15/GRCh38#34926892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113977263-C-A

http://identifiers.org/hco/15/GRCh38#34927022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113977358-C-A

34927022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113977358-C-T

34927025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113977361-G-A

34927025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113977361-G-T

34927109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113977444-G-A

34927109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113977444-G-T

34927115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113977450-A-G

34927117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 113977452-G-A

34927133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113977468-A-G

34927143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 113977478-A-G

34927166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113977490-T-C

34927474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113978701-G-A

34927492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113978719-G-C

34930212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113979368-A-T

34930213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113979369-T-C

34930230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113979383-T-C

34930253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113979415-A-G

http://identifiers.org/hco/15/GRCh38#34930407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113979569-A-C

34930413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113979575-G-C

34930413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113979575-G-T

http://identifiers.org/hco/15/GRCh38#34930469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113979638-A-C

34930585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113979756-T-A

34930629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113979797-T-A

34931233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113980142-T-G

34931236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113980145-C-T

34932111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113980635-C-T

34932167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113980696-T-A

34932167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113980696-T-C

http://identifiers.org/hco/15/GRCh38#34932179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113980708-C-A

34932189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113980718-A-T

34932212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113980741-A-G

34932295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113980859-C-T

34932348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113980910-A-G

34932423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113980985-G-A

http://identifiers.org/hco/15/GRCh38#34932471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113981032-C-A

34932471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113981032-C-T

34932492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113981052-G-T

http://identifiers.org/hco/15/GRCh38#34932563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113981096-C-A

34932656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113981201-T-C

34933001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113981402-A-G

34933167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113981562-A-G

34933192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113981586-C-T

34933243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113981614-C-T

34933399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113981728-G-C

34934502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113981940-T-A

34934502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113981940-T-C

34934512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113981951-T-G

34934513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113981952-G-A

34934513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113981952-G-T

http://identifiers.org/hco/15/GRCh38#34934641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113982070-C-A

34934641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 113982070-C-T

34934677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113982100-G-A

34934677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113982100-G-T

34934756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113982177-T-C

34934758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113982179-G-A

34934758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113982179-G-T

34934975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113982574-G-T

34935111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113982772-G-C

http://identifiers.org/hco/15/GRCh38#34935136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113982838-A-C

34935328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113983227-G-T

34935405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113983294-G-A

34935532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113983414-G-A

34938589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113985299-G-T

34938598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113985308-T-C

34938660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113985369-T-C

34938696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113985405-T-C

34938701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113985410-T-C

http://identifiers.org/hco/15/GRCh38#34938762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113985471-A-C

34938762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113985471-A-G

34938831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113985537-A-G

http://identifiers.org/hco/15/GRCh38#34938837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113985543-C-A

34938837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113985543-C-T

34938879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113985580-A-G

34938919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113985604-T-G

http://identifiers.org/hco/15/GRCh38#34938920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113985605-C-A

34940662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113986490-C-T

http://identifiers.org/hco/15/GRCh38#34940774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113986624-C-A

34940829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113986677-C-G

34940829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113986677-C-T

34940845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113986680-A-T

34940852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113986687-C-T

http://identifiers.org/hco/15/GRCh38#34940853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113986688-A-C

34941345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113987151-A-G

34941537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113987542-T-G

34941597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113987601-T-A

34941934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113987953-A-G

34941990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113988000-G-T

34942100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113988108-A-G

34942160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113988163-T-C

34942160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113988163-T-G

34943575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113988714-G-A

34943589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113988726-T-C

34943671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113988801-T-C

http://identifiers.org/hco/15/GRCh38#34944091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113989208-A-C

34944193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113989280-A-G

34944194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113989281-T-G

34944273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113989336-A-G

34944283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113989346-A-G

34944321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 113989384-T-G

34944354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113989417-A-G

34944359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 113989422-T-C

34944359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 113989422-T-G

34944386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 113989449-G-A

34944408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113989471-G-A

34944468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113989694-G-A

34944468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113989694-G-C

34944468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113989694-G-T

http://identifiers.org/hco/15/GRCh38#34944469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113989695-C-A

34944515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113989743-T-C

34944517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113989745-A-T

34944946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113990128-G-A

34945018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113990213-T-C

34945025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113990220-T-C

34945047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113990265-C-T

34945059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113990284-G-A

34945153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113990359-T-C

34945208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113990411-G-C

34945217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113990420-A-G

34945572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113991300-C-T

34945606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113991326-G-A

34945888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113991572-T-C

34945904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113991590-G-A

http://identifiers.org/hco/15/GRCh38#34948021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113991801-C-A

34948021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113991801-C-G

http://identifiers.org/hco/15/GRCh38#34948041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113991822-C-A

34948041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113991822-C-T

http://identifiers.org/hco/15/GRCh38#34948126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113991900-C-A

34948126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113991900-C-T

34948141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113991917-A-G

34948141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113991917-A-T

34948184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113991962-A-T

34948202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113991981-G-T

34948213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113991992-A-G

http://identifiers.org/hco/15/GRCh38#34948345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113992126-A-C

34948345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113992126-A-G

34948419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113992201-G-A

34949672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113992871-T-A

34952507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113996410-T-A

34952847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113996638-C-T

34952857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113996648-T-C

34952868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113996659-A-G

http://identifiers.org/hco/15/GRCh38#34952872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113996663-C-A

34952872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113996663-C-T

34952908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113996697-T-C

34952946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113996734-G-T

34952954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113996740-T-C

34952978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113996764-T-G

34952979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113996765-A-G

34952979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113996765-A-T

34953001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113996786-A-G

34953001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113996786-A-T

http://identifiers.org/hco/15/GRCh38#34953046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#113996827-A-C

34953046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113996827-A-G

34953169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113996908-A-G

34953509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113997190-T-A

34957148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113998848-G-A

34960452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114000104-C-G

http://identifiers.org/hco/15/GRCh38#34960765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114000499-C-A

34960765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114000499-C-T

http://identifiers.org/hco/15/GRCh38#34960862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114000599-A-C

http://identifiers.org/hco/15/GRCh38#34960922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114000647-C-A

http://identifiers.org/hco/15/GRCh38#34961014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114000726-A-C

34961014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114000726-A-T

34961110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114000839-T-A

34961178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114000899-G-C

34961263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114000971-C-T

34961435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114001244-C-T

http://identifiers.org/hco/15/GRCh38#34964181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114003112-C-A

34964181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114003112-C-T

http://identifiers.org/hco/15/GRCh38#34964203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114003141-C-A

34964314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114003252-G-C

34964314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114003252-G-T

34964319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114003257-T-C

34964335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114003273-T-C

34964353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114003276-G-C

34964353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114003276-G-T

http://identifiers.org/hco/15/GRCh38#34964435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114003361-A-C

34964435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114003361-A-G

34964435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114003361-A-T

34964441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114003367-G-A

34964441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114003367-G-T

http://identifiers.org/hco/15/GRCh38#34964450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#114003376-C-A

34964450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 114003376-C-T

34964520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114003449-A-G

http://identifiers.org/hco/15/GRCh38#34964521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114003450-C-A

34964521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114003450-C-G

34964521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114003450-C-T

34964536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114003457-C-G

http://identifiers.org/hco/15/GRCh38#34964544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114003465-C-A

34964580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114003485-A-G

http://identifiers.org/hco/15/GRCh38#34964601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114003507-C-A

34964601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114003507-C-T

34964634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114003540-G-C

http://identifiers.org/hco/15/GRCh38#34964757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114003655-C-A

34964782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114003689-T-C

34964816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114003717-G-A

34964816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114003717-G-C

http://identifiers.org/hco/15/GRCh38#34964841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114003742-C-A

34965058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114004181-A-T

34965059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114004182-T-C

34965067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114004190-T-C

34965071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114004194-G-C

34965122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114004240-G-A

34968591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114005008-G-A

http://identifiers.org/hco/15/GRCh38#34969471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114005510-C-A

34969471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114005510-C-T

http://identifiers.org/hco/15/GRCh38#34969476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114005515-C-A

34969477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114005516-A-G

34969533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114005567-G-T

34969596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 114005630-C-T

34969653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 114005676-C-G

http://identifiers.org/hco/15/GRCh38#34969715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#114005730-C-A

34969715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 114005730-C-G

34969715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29513
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 114005730-C-T