31382475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148889835-C-T

31382791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148890170-A-G

31383466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148891288-T-C

31383637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148891454-A-G

31383728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148891538-A-G

31384196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148892373-T-G

31384451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148892649-T-C

31385979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148893505-T-C

http://identifiers.org/hco/12/GRCh38#31386008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148893536-C-A

31386087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148893615-C-G

31386149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148893676-C-T

http://identifiers.org/hco/12/GRCh38#31386196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148893725-C-A

31386614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148894093-T-C

31386681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148894161-G-A

31386757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148894220-T-C

31387153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148894759-G-A

31387170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148894776-G-A

31387170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148894776-G-T

31387214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148894819-G-A

31387214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148894819-G-C

31387214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148894819-G-T

31387317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148894916-G-C

31387317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3 prime UTR variant
orthologous variants: 148894916-G-T

31387809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148895409-T-C

http://identifiers.org/hco/12/GRCh38#31387812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148895412-C-A

31389246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148899678-T-A

31389246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148899678-T-C

31389246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148899678-T-G

http://identifiers.org/hco/12/GRCh38#31389283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148899715-C-A

31389283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148899715-C-T

31389395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: synonymous variant
orthologous variants: 148899826-A-G

31389526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148899957-C-T

31389895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148900422-T-C

31389950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148900471-T-C

http://identifiers.org/hco/12/GRCh38#31389969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148900490-C-A

31389977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148900498-A-G

31390023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148900541-G-T

31390204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148900712-C-T

http://identifiers.org/hco/12/GRCh38#31392176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148901327-C-A

31392176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148901327-C-G

31392191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148901342-A-G

http://identifiers.org/hco/12/GRCh38#31392417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148901573-C-A

31392509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148901911-G-A

31392510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148901912-A-G

31392592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148902076-A-G

31392629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 148902112-A-G

31392709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148902193-A-T

31392712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148902196-C-T

31393051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148902567-C-T

31393060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148902576-C-T

http://identifiers.org/hco/12/GRCh38#31393326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148902664-C-A

31393436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148902766-C-T

31398179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: synonymous variant
orthologous variants: 148906668-G-A

31398179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: missense variant
orthologous variants: 148906668-G-C

31398179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: missense variant
orthologous variants: 148906668-G-T

31398341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: synonymous variant
orthologous variants: 148906830-C-T

31398495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148907003-T-A

31398495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148907003-T-C

31398495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148907003-T-G

http://identifiers.org/hco/12/GRCh38#31399428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148907902-A-C

31399428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148907902-A-G

31399526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148908013-G-A

31399809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148908380-T-C

http://identifiers.org/hco/12/GRCh38#31399835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148908408-C-A

31399835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148908408-C-T

31400247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148908783-G-T

http://identifiers.org/hco/12/GRCh38#31400485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148909852-A-C

31401463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148910603-C-T

31401548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148910678-C-T

31402576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: synonymous variant
orthologous variants: 148911331-A-G

http://identifiers.org/hco/12/GRCh38#31402689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148911447-C-A

31407624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148914457-G-T

31409100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148915016-T-C

31409248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148915599-A-G

31409248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148915599-A-T

http://identifiers.org/hco/12/GRCh38#31409300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148915651-C-A

31409393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148915744-G-A

31409393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148915744-G-C

31409393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148915744-G-T

31413292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148918341-A-G

31413292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148918341-A-T

http://identifiers.org/hco/12/GRCh38#31413411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148918456-A-C

31413465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: synonymous variant
orthologous variants: 148918509-C-T

31415235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148920738-T-C

http://identifiers.org/hco/12/GRCh38#31415505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148920977-C-A

31424502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148928748-G-A

31424553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: missense variant
orthologous variants: 148928799-A-T

31425927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148929758-G-C

http://identifiers.org/hco/12/GRCh38#31426154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148930242-C-A

31426154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148930242-C-T

31426256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148930576-G-A

31426256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148930576-G-C

31426256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148930576-G-T

http://identifiers.org/hco/12/GRCh38#31426261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148930581-C-A

31426261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148930581-C-T

31426530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148930838-G-A

31426530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148930838-G-C

31426530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148930838-G-T

31426707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148931000-G-A

31426707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148931000-G-T

http://identifiers.org/hco/12/GRCh38#31426857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148931155-C-A

31426857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148931155-C-G

http://identifiers.org/hco/12/GRCh38#31426938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148931222-A-C

http://identifiers.org/hco/12/GRCh38#31427083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148931370-A-C

31431620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148933492-G-A

31431636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148933507-T-C

http://identifiers.org/hco/12/GRCh38#31431744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148933612-C-A

http://identifiers.org/hco/12/GRCh38#31431775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148933653-C-A

31431787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148933692-A-T

31431956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148933829-T-C

31432809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148934476-T-C

31432911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148934570-T-C

31432918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148934577-T-C

31432918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148934577-T-G

http://identifiers.org/hco/12/GRCh38#31432925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148934584-C-A

31432925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148934584-C-T

31433009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148934635-G-A

31433009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148934635-G-T

http://identifiers.org/hco/12/GRCh38#31433031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148934654-A-C

31433111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, undefined
orthologous variants: 148934720-C-T

31433188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: synonymous variant
orthologous variants: 148934797-A-G

31442570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148937748-G-A

31442570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148937748-G-T

31442789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: synonymous variant
orthologous variants: 148937898-T-C

31443343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148938272-G-A

31443747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148938495-T-C

31443750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148938498-A-G

http://identifiers.org/hco/12/GRCh38#31444034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148938707-A-C

http://identifiers.org/hco/12/GRCh38#31444116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148938786-C-A

31444159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148938828-G-T

http://identifiers.org/hco/12/GRCh38#31444980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148941191-C-A

31445052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148941260-C-T

31445375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148941488-T-C

31447526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148943002-T-A

31447526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148943002-T-C

http://identifiers.org/hco/12/GRCh38#31447887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148943356-C-A

31447887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148943356-C-T

http://identifiers.org/hco/12/GRCh38#31447987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148943454-A-C

31448070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148943542-T-C

http://identifiers.org/hco/12/GRCh38#31448093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148943565-A-C

31448126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148943577-T-A

31448577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148943734-G-A

31448771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148943838-G-A

31449118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148944080-G-A

31449179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148944166-T-A

http://identifiers.org/hco/12/GRCh38#31449231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148944217-A-C

31449328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148944319-T-C

31449333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148944324-A-T

31449599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148944593-G-C

31450849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148945084-G-A

31450849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148945084-G-C

31450967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148945196-A-G

31451219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148945417-C-T

31451570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148945669-G-A

31452018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 148946059-G-A

31452096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 148946137-T-G

31452114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, missense_variant
orthologous variants: 148946155-T-A

31454173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148950513-C-T

31457185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148953615-T-C

31457207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148953637-C-T

31458322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148954718-T-A

31459656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148955390-T-A

31459656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148955390-T-C

31459656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148955390-T-G

31459739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148955474-T-C

31460019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148956242-T-C

31460072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148956291-T-C

31460072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148956291-T-G

http://identifiers.org/hco/12/GRCh38#31460124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148956329-C-A

31460124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron variant
orthologous variants: 148956329-C-T

31460317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148956521-T-C

31460409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148956612-G-A

31460409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148956612-G-T

31460517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148956979-T-C

31460635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148957092-G-A

31460635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148957092-G-C

31461884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148957732-T-G

31464040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148960416-G-A

31464748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148961819-A-G

31474172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148966320-C-T

31474819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148967386-T-C

31474912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148967483-C-G

31475037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148967611-A-T

31478219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148968627-T-C

31478268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148968659-G-A

31478710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148968796-G-C

31478799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148968866-A-G

31478830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148968897-C-T

31479030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148969071-A-G

31479524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148969486-G-A

31479524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148969486-G-C

31479524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148969486-G-T

31479605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 148969564-G-T

31479679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 148969638-G-A

http://identifiers.org/hco/12/GRCh38#31480004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148969963-A-C

31480073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 148970032-G-A

31480250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 148970209-G-A

31480250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 148970209-G-T

31480316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148970280-T-C

31480381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148970509-A-T

31480400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148970528-T-A

31488292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148976840-T-C

31488558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148977100-G-C

http://identifiers.org/hco/12/GRCh38#31488994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148977428-C-A

31488994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148977428-C-T

31489464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148978255-G-A

http://identifiers.org/hco/12/GRCh38#31495124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148981520-C-A

31495253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148981616-T-C

31495673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148982158-G-T

http://identifiers.org/hco/12/GRCh38#31495677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148982162-C-A

31495714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148982220-T-C

31495722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148982228-G-T

http://identifiers.org/hco/12/GRCh38#31495799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148982293-A-C

31495799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148982293-A-G

31495813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148982307-G-C

31495813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148982307-G-T

http://identifiers.org/hco/12/GRCh38#31495923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148982417-C-A

31495923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 148982417-C-G

31495923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 148982417-C-T

31495947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148982445-C-G

http://identifiers.org/hco/12/GRCh38#31495959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148982469-C-A

31495959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148982469-C-T

31495994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148982568-T-A

31495994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148982568-T-C

http://identifiers.org/hco/12/GRCh38#31496038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148982655-C-A

31496038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148982655-C-T

31496136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148982846-G-A

31496291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148983042-G-A

http://identifiers.org/hco/12/GRCh38#31496916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148983680-A-C

31497544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148984649-T-C

31498106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148985012-A-G

31498544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148985399-T-C

31498936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148985609-G-A

31498942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148985615-T-C

31499215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148985919-T-C

http://identifiers.org/hco/12/GRCh38#31499486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148986256-A-C

31499486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148986256-A-G

31499741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148986497-T-A

31499741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148986497-T-C

31518514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148988121-A-G

31518518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148988126-T-C

31518518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148988126-T-G

31519448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148989151-T-C

31564271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148992564-T-C

31564325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148992618-C-T

31564326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148992619-A-G

31564352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148992644-C-T

31570533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148994287-T-C

http://identifiers.org/hco/12/GRCh38#31570585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148994321-C-A

31570785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148994865-T-A

31570785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148994865-T-C

31571507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148995569-G-A

31572298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148996448-C-T

31572348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 148996494-A-T

http://identifiers.org/hco/12/GRCh38#31573556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#148998372-C-A

31574634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 149000258-T-C

31589776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149001919-G-A

31589776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149001919-G-T

http://identifiers.org/hco/12/GRCh38#31589991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#149002112-C-A

31589991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149002112-C-T

31590115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149002257-A-G

31590174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 149002315-G-A

31590174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 149002315-G-C

31590174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 149002315-G-T

31590185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 149002318-C-G

31590185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 149002318-C-T

31590208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149002342-G-A

31590208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149002342-G-T

http://identifiers.org/hco/12/GRCh38#31590251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#149002376-C-A

31590251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149002376-C-T

http://identifiers.org/hco/12/GRCh38#31590283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#149002403-C-A

http://identifiers.org/hco/12/GRCh38#31590310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#149002430-C-A

31590310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 149002430-C-T

31590482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 149002526-G-C

http://identifiers.org/hco/12/GRCh38#31590784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#149002759-C-A

31590784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149002759-C-G

31590784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149002759-C-T

http://identifiers.org/hco/12/GRCh38#31590833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#149002808-C-A

31590833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149002808-C-T

31590875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149002849-G-A

31590875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149002849-G-T

31590908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149002933-C-T

31590950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 149002975-C-G

31591006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149003026-G-A

31591006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 149003026-G-T

http://identifiers.org/hco/12/GRCh38#31591098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#149003128-A-C

31591098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28338
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 149003128-A-G