90993882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3 prime UTR variant
orthologous variants: 14915614-T-A

90994489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3 prime UTR variant
orthologous variants: 14915051-T-C

http://identifiers.org/hco/8/GRCh38#90994580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14914964-C-A

90994580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3 prime UTR variant
orthologous variants: 14914964-C-T

90994590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3 prime UTR variant
orthologous variants: 14914953-A-G

90994591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3 prime UTR variant
orthologous variants: 14914952-A-G

http://identifiers.org/hco/8/GRCh38#90994757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14914791-C-A

90994757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3 prime UTR variant
orthologous variants: 14914791-C-T

90995110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3 prime UTR variant
orthologous variants: 14914418-C-T

90995408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3 prime UTR variant
orthologous variants: 14914132-A-G

http://identifiers.org/hco/8/GRCh38#90995454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14914088-C-A

90995454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3 prime UTR variant
orthologous variants: 14914088-C-T

90995590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 14913952-A-T

90995593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 14913949-A-G

90995611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 14913931-A-G

http://identifiers.org/hco/8/GRCh38#90995935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14913603-C-A

90995945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14913593-T-C

90995951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14913587-G-A

90995951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14913587-G-T

90995996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14913542-T-C

90996087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14913413-A-G

90996518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14912783-T-C

90996541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14912760-G-A

90996541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14912760-G-T

90996553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14912748-G-A

90996553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14912748-G-C

90996553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14912748-G-T

90996567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14912735-G-A

90996567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14912735-G-T

http://identifiers.org/hco/8/GRCh38#90996572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14912730-C-A

90996582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14912720-G-A

90996582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14912720-G-T

http://identifiers.org/hco/8/GRCh38#90996591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14912711-C-A

90996591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14912711-C-T

90996592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14912710-T-C

90996799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14912377-A-G

90996841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14912339-A-G

90997342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14911903-T-C

http://identifiers.org/hco/8/GRCh38#90997392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14911854-A-C

90997473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14911774-G-T

90997514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14911735-G-A

90997522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14911701-C-T

90997804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14911454-A-G

90998078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14911193-G-C

90998274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14910995-G-A

90998274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14910995-G-T

http://identifiers.org/hco/8/GRCh38#91004982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14905547-A-C

91005033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14905494-G-C

91005066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14905460-G-T

91005106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14905420-T-C

http://identifiers.org/hco/8/GRCh38#91005117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14905409-C-A

91005170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14905354-T-A

91005170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14905354-T-C

91005304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14905244-T-G

91005408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14905137-A-G

91005935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14904853-A-G

91005973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14904821-G-A

91006171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14904642-G-T

http://identifiers.org/hco/8/GRCh38#91006301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14904499-A-C

91007188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14903889-G-A

91007491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14903668-G-C

91007647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14903530-A-T

91007703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14903476-G-A

91007783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14903406-A-G

91007784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14903405-T-C

91007988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14903241-T-C

91007992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14903237-A-T

91008220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14903037-T-C

91008454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14902827-C-T

91008617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14902656-A-G

http://identifiers.org/hco/8/GRCh38#91008711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14902566-C-A

91008970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14902283-T-C

91009005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14902248-C-T

91009064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14902188-T-C

91009368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14901881-A-G

91009424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14901822-A-G

http://identifiers.org/hco/8/GRCh38#91009492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14901754-A-C

91009577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14901604-T-C

http://identifiers.org/hco/8/GRCh38#91009719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14901483-C-A

91009727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14901475-A-G

91009877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14901322-C-T

91009899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14901301-A-G

91009932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14901278-T-C

http://identifiers.org/hco/8/GRCh38#91009957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14901254-C-A

91010125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14901127-G-A

91010304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14900975-A-G

91010569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14900721-C-T

http://identifiers.org/hco/8/GRCh38#91010783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14900516-C-A

91010783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14900516-C-T

91012510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14898219-A-G

91012549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14898184-G-A

91012549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14898184-G-C

http://identifiers.org/hco/8/GRCh38#91012627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14898108-A-C

91012670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14898066-T-C

91012675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14898061-C-G

91012740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14897986-G-C

http://identifiers.org/hco/8/GRCh38#91012764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14897956-C-A

91013132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14897512-C-T

91013228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14897425-C-T

91013949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14897023-A-G

91013973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14896994-A-G

http://identifiers.org/hco/8/GRCh38#91013996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14896971-A-C

91014047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14896918-T-C

91014047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14896918-T-G

91014170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14896633-A-G

http://identifiers.org/hco/8/GRCh38#91014293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14896491-C-A

91014319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14896465-A-G

91014355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14896429-G-A

91014860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14896028-G-A

http://identifiers.org/hco/8/GRCh38#91014898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14895989-A-C

91015026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14895854-G-C

91015127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14895761-T-C

91015358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14895601-G-C

http://identifiers.org/hco/8/GRCh38#91016474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14895211-C-A

http://identifiers.org/hco/8/GRCh38#91016482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14895206-C-A

91016482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14895206-C-T

91016495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14895195-C-T

91016547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14895145-C-T

91016687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14895056-A-T

91016755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14894990-T-C

91016776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14894977-T-C

91017515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14894521-G-T

91017595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14894439-C-G

91017772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14894159-T-C

http://identifiers.org/hco/8/GRCh38#91017820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#14894112-A-C

91017974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14893967-G-A

91018056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14893883-T-C

91018310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14893698-T-C

91018310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14893698-T-G

91018382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 14893630-T-C

91018515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14893497-T-C

91018556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14893455-G-A

91018562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14893449-G-A

91018562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14893449-G-C

91018616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14893406-T-C

http://identifiers.org/hco/8/GRCh38#91018622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#14893400-A-C

http://identifiers.org/hco/8/GRCh38#91018669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14893350-C-A

91018669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14893350-C-T

91018733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14893288-T-C

http://identifiers.org/hco/8/GRCh38#91018753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14893262-C-A

91018767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14893248-T-C

91018800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14893215-G-A

91018821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14893185-G-A

91018841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14893165-T-C

91019074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14892943-G-A

91019187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14892833-T-G

91020372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14887705-T-G

91020401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14887677-G-A

91020401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14887677-G-T

91020647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14887427-T-C

http://identifiers.org/hco/8/GRCh38#91020872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14887006-C-A

http://identifiers.org/hco/8/GRCh38#91020879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14886999-A-C

91020879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14886999-A-G

91020896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14886991-T-C

91021176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14886758-T-G

91021213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14886721-C-G

http://identifiers.org/hco/8/GRCh38#91021284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14886652-A-C

91021481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14886470-T-A

91021481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14886470-T-C

http://identifiers.org/hco/8/GRCh38#91021500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14886451-A-C

91021508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14886443-A-G

91021515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14886441-T-C

91021516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14886440-T-A

91024062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14883633-A-G

http://identifiers.org/hco/8/GRCh38#91024073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14883622-A-C

91024162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14883557-T-C

http://identifiers.org/hco/8/GRCh38#91024270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14883456-C-A

91024270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14883456-C-G

91024270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14883456-C-T

91024278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14883448-T-C

91024278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14883448-T-G

91024304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14883422-A-G

91024347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 14883381-A-G

91024349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 14883379-A-G

91024350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 14883378-T-G

91025127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14882268-T-C

91025455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14881988-A-G

91025495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14881954-A-G

91025602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14881845-G-C

http://identifiers.org/hco/8/GRCh38#91025988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14881504-A-C

91026019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14881474-A-G

91026095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14881412-C-T

http://identifiers.org/hco/8/GRCh38#91026151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14881361-A-C

91026751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14880833-T-C

91026955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14880621-C-T

91026980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14880601-G-A

91026983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14880598-A-T

91026992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14880588-G-A

91026992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14880588-G-T

91027101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14880272-T-G

91027210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14880186-T-A

91027210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14880186-T-C

91027220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14880176-G-A

91027507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14879925-C-T

91027528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14879904-G-A

91027528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14879904-G-C

91029412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14876177-T-C

91029416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14876173-T-C

91031667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14875277-A-G

91031716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14875225-A-G

91031778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14875168-T-C

91033655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14874041-C-T

91033710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14873979-G-A

91033935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14873780-G-A

91033938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14873777-C-T

91034616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14872893-T-A

91034804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14872728-A-T

91034812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14872720-C-T

91036581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14870471-T-A

http://identifiers.org/hco/8/GRCh38#91036657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14870294-A-C

91037500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14869380-T-C

91038232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14867611-C-T

http://identifiers.org/hco/8/GRCh38#91038248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14867594-A-C

91038495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14866775-G-T

91038765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14866126-T-C

http://identifiers.org/hco/8/GRCh38#91038811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14866087-C-A

91038812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14866086-T-C

91038950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14865975-T-C

91039251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14865678-T-C

91039804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14865181-G-A

91039884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14865103-T-G

91039910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14865074-G-A

91039910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14865074-G-T

91040036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14864960-A-G

91040676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 14864403-G-A

91040806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 14864272-G-T

91040818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 14864260-G-A

91040818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 14864260-G-T

91040853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 14864250-T-A

91040853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 14864250-T-C

91040853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 14864250-T-G

91040857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 14864246-G-A

91040857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25452
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 14864246-G-T