72752324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99307326-G-A

72752331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99307333-G-C

72752331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99307333-G-T

72752397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99307393-G-A

72752416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99307412-T-C

72752555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99307535-T-C

72752555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99307535-T-G

72752556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99307536-G-C

72752626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99307604-G-C

72752626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99307604-G-T

72752641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99307619-T-C

72752725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99307713-A-G

72753379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99309727-A-G

72753379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99309727-A-T

72753386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99309734-T-A

72753416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99309766-A-G

72753421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99309771-A-G

http://identifiers.org/hco/13/GRCh38#72753509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99309850-C-A

72753509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99309850-C-T

72753536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99309861-T-C

72753568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99309887-G-A

72753568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99309887-G-T

72753695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 99310043-T-G

http://identifiers.org/hco/13/GRCh38#72753725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99310073-C-A

72753790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 99310153-T-C

http://identifiers.org/hco/13/GRCh38#72755026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99310988-C-A

http://identifiers.org/hco/13/GRCh38#72755031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99310993-C-A

72755031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99310993-C-T

http://identifiers.org/hco/13/GRCh38#72755037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99310999-C-A

72755147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 99311078-A-G

http://identifiers.org/hco/13/GRCh38#72755267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99311164-C-A

72755267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99311164-C-T

72755321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99311214-A-G

http://identifiers.org/hco/13/GRCh38#72755329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99311220-C-A

72755329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99311220-C-T

72755541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99311425-G-C

72755686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99311539-A-G

72755953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99311756-G-A

72755953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99311756-G-T

http://identifiers.org/hco/13/GRCh38#72755990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99311786-C-A

72756084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99311863-G-T

72756087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99311866-G-A

http://identifiers.org/hco/13/GRCh38#72756195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99311973-A-C

72756195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99311973-A-G

http://identifiers.org/hco/13/GRCh38#72756202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99311980-C-A

72756202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99311980-C-G

72756202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99311980-C-T

http://identifiers.org/hco/13/GRCh38#72756216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99312003-C-A

72756216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99312003-C-T

http://identifiers.org/hco/13/GRCh38#72756230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99312010-C-A

72756230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99312010-C-G

72756230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99312010-C-T

72756280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99312055-G-T

72756399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99312123-A-G

72756443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99312162-G-T

72756496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99312195-A-G

72758441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99313522-G-A

72758590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99313656-A-G

72758645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99313844-G-T

72758765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99313933-T-A

72758765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99313933-T-C

http://identifiers.org/hco/13/GRCh38#72758924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99314039-C-A

72759148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99314241-T-C

72759194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99314284-T-C

72759198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99314288-G-A

72759198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99314288-G-T

72759232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99314321-T-C

http://identifiers.org/hco/13/GRCh38#72759253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99314338-C-A

72759460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 99314512-T-C

72759485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99314537-T-G

http://identifiers.org/hco/13/GRCh38#72759490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99314542-C-A

72759490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3 prime UTR variant
orthologous variants: 99314542-C-T

72759694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 99314736-A-G

72759753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 99314788-T-C

72759792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 99314815-T-C

72759813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 99314836-C-G

http://identifiers.org/hco/13/GRCh38#72759848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99314871-A-C

72759900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99314922-G-A

72759900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99314922-G-T

http://identifiers.org/hco/13/GRCh38#72759940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99314964-A-C

http://identifiers.org/hco/13/GRCh38#72759963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99314987-C-A

72760277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99315450-T-C

http://identifiers.org/hco/13/GRCh38#72760346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99315538-A-C

http://identifiers.org/hco/13/GRCh38#72760386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99315600-C-A

http://identifiers.org/hco/13/GRCh38#72760395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99315609-C-A

http://identifiers.org/hco/13/GRCh38#72760397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99315611-A-C

72760497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99315672-T-C

72760502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99315677-A-G

72760521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 99315690-G-C

72761163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99316380-G-A

72761231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99316444-G-A

72761231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99316444-G-T

72761294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99316496-G-A

72761348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99316549-T-G

72761359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99316560-G-A

72761359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99316560-G-C

72761498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 99316699-T-C

72761498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 99316699-T-G

72762141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 99317319-T-C

72762158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99317332-A-T

72762182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99317356-A-T

72763378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99318596-T-A

72763378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99318596-T-C

72763378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99318596-T-G

72763379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99318597-G-T

http://identifiers.org/hco/13/GRCh38#72763397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99318614-A-C

72763460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 99318671-G-A

72763614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 99318825-A-T

http://identifiers.org/hco/13/GRCh38#72763631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99318843-C-A

72763631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99318843-C-T

72763699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99318898-A-G

72763699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99318898-A-T

72763763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99318960-T-C

72764598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99319412-T-C

72764695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99319488-T-C

72765909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99320029-A-T

72765923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99320043-A-G

72765938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99320058-A-G

72766004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 99320118-G-A

72766085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99320193-A-T

72766126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99320236-T-A

72766210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99320321-T-C

72766749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99320687-C-T

72768787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 99321465-T-A

72768787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 99321465-T-C

72768844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 99321522-A-G

72768853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 99321531-A-G

72768871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 99321549-T-C

72768895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 99321573-A-G

http://identifiers.org/hco/13/GRCh38#72768904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, stop_lost, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99321582-C-A

72768904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 99321582-C-T

72768926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99321604-T-C

http://identifiers.org/hco/13/GRCh38#72768936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99321615-A-C

72768936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99321615-A-G

72769227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99322162-C-T

72769286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99322204-G-C

72770103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99323001-T-C

72770872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99323281-A-G

72770997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99323403-G-A

72771075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99323477-A-G

http://identifiers.org/hco/13/GRCh38#72771140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99323542-A-C

http://identifiers.org/hco/13/GRCh38#72771222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99323619-C-A

72771222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99323619-C-T

72771228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99323625-T-C

72771691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99324013-A-T

72771926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99324955-A-G

72772038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99325066-A-G

72772058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99325082-C-G

http://identifiers.org/hco/13/GRCh38#72772093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99325099-A-C

72772093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99325099-A-G

72772852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99326357-G-T

72772947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99326461-C-G

72772947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99326461-C-T

72773849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99327277-A-G

http://identifiers.org/hco/13/GRCh38#72773851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99327287-A-C

72773892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99327348-G-C

72773927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99327384-G-A

72773927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99327384-G-C

72773927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99327384-G-T

http://identifiers.org/hco/13/GRCh38#72774077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99327532-A-C

72774085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99327540-A-G

72774092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99327548-T-C

72774152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99327608-T-C

72774179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99327635-A-G

72774189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99327644-A-G

72774605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99328069-T-C

72774667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99328120-G-A

72774829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99328263-T-C

72774887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99328340-G-A

http://identifiers.org/hco/13/GRCh38#72775174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99328732-C-A

72775265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 99328818-A-G

72775319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 99328872-A-G

72775367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 99328920-T-A

72775367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 99328920-T-C

72775367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 99328920-T-G

72775450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99328995-G-A

72775450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99328995-G-T

72775452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99328997-T-C

72775693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99329403-T-C

72775709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99329417-G-A

72775740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99329448-G-A

72775740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99329448-G-T

72775815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99329509-A-G

72775815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99329509-A-T

72775914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99332598-T-A

72775943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 99332627-G-T

72775964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 99332648-A-G

72775964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 99332648-A-T

72775979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 99332663-T-C

http://identifiers.org/hco/13/GRCh38#72776241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99332908-C-A

72776241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99332908-C-T

72776305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99332972-T-C

72776382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99333034-T-C

http://identifiers.org/hco/13/GRCh38#72776417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99333068-C-A

72776713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99333727-T-C

72776879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99333877-C-T

72777016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99334011-T-C

72777165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99334102-T-C

72777310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-A

72777310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-C

http://identifiers.org/hco/13/GRCh38#72777561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99334340-C-A

72777581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99334359-C-T

72777603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -A-G

http://identifiers.org/hco/13/GRCh38#72777604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-A

72777604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-G

72777611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -A-T

http://identifiers.org/hco/13/GRCh38#72778085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99334933-C-A

72778085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99334933-C-G

72778085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99334933-C-T

72778140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99334975-A-G

72778176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99335010-T-C

http://identifiers.org/hco/13/GRCh38#72778274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99335108-C-A

72778274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 99335108-C-T

72778458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99335291-T-A

72778458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99335291-T-C

72780503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99335818-C-G

72780528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99335843-T-G

72780628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99335931-A-G

72780681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99335978-G-C

72780854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99336127-C-G

72780854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99336127-C-T

72781023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99336300-A-G

72781029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99336306-T-C

72781032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99336309-T-C

72781056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99336337-T-C

http://identifiers.org/hco/13/GRCh38#72781178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99336445-A-C

72781178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99336445-A-G

72781189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99336459-A-G

http://identifiers.org/hco/13/GRCh38#72781421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99336695-A-C

72781423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99336697-T-A

72781423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99336697-T-G

72781451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99336742-G-A

72781451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99336742-G-C

72781451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99336742-G-T

http://identifiers.org/hco/13/GRCh38#72781469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#99336764-C-A

72781469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99336764-C-T

72781481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99336776-G-A

72781481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99336776-G-C

72781653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99336930-G-A

72781653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 99336930-G-T

http://identifiers.org/hco/13/GRCh38#72781674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99336951-C-A

72781708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99336985-G-T

72781850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 99337127-A-G

72781855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99337132-T-C

http://identifiers.org/hco/13/GRCh38#72781875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#99337139-C-A

72781875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99337139-C-T

72781885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99337149-C-G

72781885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99337149-C-T

72781897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99337161-A-G

72781926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99337179-T-G

72781999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99337245-G-A

72781999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 99337245-G-T

http://identifiers.org/hco/13/GRCh38#72782077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#99337296-C-A

72782077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20604
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99337296-C-T